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Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


1

max kwh | OpenEI Community  

Open Energy Info (EERE)

max kwh max kwh Home Ewilson's picture Submitted by Ewilson(53) Contributor 4 January, 2013 - 08:42 Rates with tier problems max kwh tiers I've detected that the following rates all have the improper number of "Max kWh" values (should be one less than the number of charges, since the highest tier is always "all remaining"). This is likely due to users not understanding the meaning of "Max kWh"--often I see things like: "300, 700, 1000" (derived from "first 300, next 700, greater than 1000") which should be entered as "300, 1000". This is why we need checks on input that prevent users from entering this incorrectly. Here is the list (my script only checked residential rates): Syndicate content 429 Throttled (bot load)

2

kWh | OpenEI  

Open Energy Info (EERE)

kWh kWh Dataset Summary Description This dataset contains hourly load profile data for 16 commercial building types (based off the DOE commercial reference building models) and residential buildings (based off the Building America House Simulation Protocols). This dataset also includes the Residential Energy Consumption Survey (RECS) for statistical references of building types by location. Source Commercial and Residential Reference Building Models Date Released April 18th, 2013 (9 months ago) Date Updated July 02nd, 2013 (7 months ago) Keywords building building demand building load Commercial data demand Energy Consumption energy data hourly kWh load profiles Residential Data Quality Metrics Level of Review Some Review Comment Temporal and Spatial Coverage Frequency Annually

3

Property:Incentive/PVComFitDolKWh | Open Energy Information  

Open Energy Info (EERE)

Property Property Edit with form History Facebook icon Twitter icon » Property:Incentive/PVComFitDolKWh Jump to: navigation, search Property Name Incentive/PVComFitDolKWh Property Type String Description Feed-in tariff for commercial systems. The $ amount per kWh generated such that the incentive is disbursed over time based on metered production. 100% of energy generated is exported; none is used on-site. Ex: TVA Green Power Switch $0.15/kWh; We Energies $0.225/kWh Format: $0.225 [1] References ↑ DSIRE Pages using the property "Incentive/PVComFitDolKWh" Showing 25 pages using this property. (previous 25) (next 25) A Alliant Energy (Wisconsin Power and Light) - Advanced Renewables Tariff (Wisconsin) + $0.25 + C CPS Energy - Solartricity Producer Program (Texas) + $0.27 +

4

Property:Incentive/PVResFitDolKWh | Open Energy Information  

Open Energy Info (EERE)

Property Property Edit with form History Facebook icon Twitter icon » Property:Incentive/PVResFitDolKWh Jump to: navigation, search Property Name Incentive/PVResFitDolKWh Property Type String Description Feed-in Tariff (FIT): The $ amount per kWh generated such that the incentive is disbursed over time based on metered production. 100% of energy generated is exported; none is used on-site. Ex: TVA Green Power Switch $0.15/kWh; We Energies $0.225/kWh Format: $0.225 [1] References ↑ DSIRE Pages using the property "Incentive/PVResFitDolKWh" Showing 25 pages using this property. (previous 25) (next 25) A Alliant Energy (Wisconsin Power and Light) - Advanced Renewables Tariff (Wisconsin) + $0.25 + C CPS Energy - Solartricity Producer Program (Texas) + $0.27 +

5

Property:Incentive/PVNPFitDolKWh | Open Energy Information  

Open Energy Info (EERE)

Property Property Edit with form History Facebook icon Twitter icon » Property:Incentive/PVNPFitDolKWh Jump to: navigation, search Property Name Incentive/PVNPFitDolKWh Property Type String Description Feed-in tariff for non-profit and/or government systems. The $ amount per kWh generated such that the incentive is disbursed over time based on metered production. 100% of energy generated is exported; none is used on-site. Ex: TVA Green Power Switch $0.15/kWh; We Energies $0.225/kWh Format: $0.225 [1] References ↑ DSIRE Pages using the property "Incentive/PVNPFitDolKWh" Showing 25 pages using this property. (previous 25) (next 25) A Alliant Energy (Wisconsin Power and Light) - Advanced Renewables Tariff (Wisconsin) + $0.25 + C CPS Energy - Solartricity Producer Program (Texas) + $0.27 +

6

Pairing in dense lithium  

Science Journals Connector (OSTI)

... of valence electrons. Here we report the results of first-principles calculations, indicating that lithium, the band structure of which is largely free-electron-like at ordinary densities, does ... b.c.c.) becomes unstable to a pairing of the ions. Once paired, lithium possesses an even number of electrons per primitive cell which, although not sufficient, is ...

J. B. Neaton; N. W. Ashcroft

1999-07-08T23:59:59.000Z

7

Conductive lithium storage electrode  

DOE Patents [OSTI]

A compound comprising a composition A.sub.x(M'.sub.1-aM''.sub.a).sub.y(XD.sub.4).sub.z, A.sub.x(M'.sub.1-aM''.sub.a).sub.y(DXD.sub.4).sub.z, or A.sub.x(M'.sub.1-aM''.sub.a).sub.y(X.sub.2D.sub.7).sub.z, and have values such that x, plus y(1-a) times a formal valence or valences of M', plus ya times a formal valence or valence of M'', is equal to z times a formal valence of the XD.sub.4, X.sub.2D.sub.7, or DXD.sub.4 group; or a compound comprising a composition (A.sub.1-aM''.sub.a).sub.xM'.sub.y(XD.sub.4).sub.z, (A.sub.1-aM''.sub.a).sub.xM'.sub.y(DXD.sub.4).sub.z (A.sub.1-aM''.sub.a).sub.xM'.sub.y(X.sub.2D.sub.7).sub.z and have values such that (1-a).sub.x plus the quantity ax times the formal valence or valences of M'' plus y times the formal valence or valences of M' is equal to z times the formal valence of the XD.sub.4, X.sub.2D.sub.7 or DXD.sub.4 group. In the compound, A is at least one of an alkali metal and hydrogen, M' is a first-row transition metal, X is at least one of phosphorus, sulfur, arsenic, molybdenum, and tungsten, M'' any of a Group IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB, IVB, VB, and VIB metal, D is at least one of oxygen, nitrogen, carbon, or a halogen, 0.0001lithium phosphate that can intercalate lithium or hydrogen. The compound can be used in an electrochemical device including electrodes and storage batteries and can have a gravimetric capacity of at least about 80 mAh/g while being charged/discharged at greater than about C rate of the compound.

Chiang, Yet-Ming (Framingham, MA); Chung, Sung-Yoon (Incheon, KR); Bloking, Jason T. (Mountain View, CA); Andersson, Anna M. (Vasteras, SE)

2012-04-03T23:59:59.000Z

8

Conductive lithium storage electrode  

DOE Patents [OSTI]

A compound comprising a composition A.sub.x(M'.sub.1-aM''.sub.a).sub.y(XD.sub.4).sub.z, A.sub.x(M'.sub.1-aM''.sub.a).sub.y(DXD.sub.4).sub.z, or A.sub.x(M'.sub.1-aM''.sub.a).sub.y(X.sub.2D.sub.7).sub.z, and have values such that x, plus y(1-a) times a formal valence or valences of M', plus ya times a formal valence or valence of M'', is equal to z times a formal valence of the XD.sub.4, X.sub.2D.sub.7, or DXD.sub.4 group; or a compound comprising a composition (A.sub.1-aM''.sub.a).sub.xM'.sub.y(XD.sub.4).sub.z, (A.sub.1-aM''.sub.a).sub.xM'.sub.y(DXD.sub.4).sub.z(A.sub.1-aM''.sub.a).s- ub.xM'.sub.y(X.sub.2D.sub.7).sub.z and have values such that (1-a).sub.x plus the quantity ax times the formal valence or valences of M'' plus y times the formal valence or valences of M' is equal to z times the formal valence of the XD.sub.4, X.sub.2D.sub.7 or DXD.sub.4 group. In the compound, A is at least one of an alkali metal and hydrogen, M' is a first-row transition metal, X is at least one of phosphorus, sulfur, arsenic, molybdenum, and tungsten, M'' any of a Group IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB, IVB, VB, and VIB metal, D is at least one of oxygen, nitrogen, carbon, or a halogen, 0.0001lithium phosphate that can intercalate lithium or hydrogen. The compound can be used in an electrochemical device including electrodes and storage batteries and can have a gravimetric capacity of at least about 80 mAh/g while being charged/discharged at greater than about C rate of the compound.

Chiang, Yet-Ming (Framingham, MA); Chung, Sung-Yoon (Seoul, KR); Bloking, Jason T. (Cambridge, MA); Andersson, Anna M. (Uppsala, SE)

2008-03-18T23:59:59.000Z

9

Manufacturing of Protected Lithium Electrodes for Advanced Lithium...  

Broader source: Energy.gov (indexed) [DOE]

Lithium Electrodes for Advanced Lithium-Air, Lithium-Water, and Lithium-Sulfur Batteries, April 2013 Manufacturing of Protected Lithium Electrodes for Advanced Lithium-Air,...

10

Property:Building/SPBreakdownOfElctrcityUseKwhM2Total | Open Energy  

Open Energy Info (EERE)

SPBreakdownOfElctrcityUseKwhM2Total" SPBreakdownOfElctrcityUseKwhM2Total" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 71.4577086539 + Sweden Building 05K0002 + 110.926946534 + Sweden Building 05K0003 + 72.9096074806 + Sweden Building 05K0004 + 66.0248923654 + Sweden Building 05K0005 + 54.8654809632 + Sweden Building 05K0006 + 65.291976787 + Sweden Building 05K0007 + 65.5403331042 + Sweden Building 05K0008 + 41.6418235453 + Sweden Building 05K0009 + 56.5413268466 + Sweden Building 05K0010 + 150.269021739 + Sweden Building 05K0011 + 27.5018481341 + Sweden Building 05K0012 + 37.9937990385 + Sweden Building 05K0013 + 68.8990371973 + Sweden Building 05K0014 + 166.794253904 + Sweden Building 05K0015 + 71.0813662687 + Sweden Building 05K0016 + 38.5267410327 +

11

Property:Building/SPPurchasedEngyPerAreaKwhM2Total | Open Energy  

Open Energy Info (EERE)

SPPurchasedEngyPerAreaKwhM2Total" SPPurchasedEngyPerAreaKwhM2Total" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 221.549575215 + Sweden Building 05K0002 + 213.701117318 + Sweden Building 05K0003 + 195.801526718 + Sweden Building 05K0004 + 174.148148148 + Sweden Building 05K0005 + 340.088495575 + Sweden Building 05K0006 + 211.255924171 + Sweden Building 05K0007 + 144.028151521 + Sweden Building 05K0008 + 171.282051282 + Sweden Building 05K0009 + 140.296360236 + Sweden Building 05K0010 + 300.961098398 + Sweden Building 05K0011 + 98.1045751634 + Sweden Building 05K0012 + 106.609793929 + Sweden Building 05K0013 + 175.776187637 + Sweden Building 05K0014 + 291.160427408 + Sweden Building 05K0015 + 174.193548387 + Sweden Building 05K0016 + 145.793794187 +

12

Property:Building/SPPurchasedEngyPerAreaKwhM2DstrtHeating | Open Energy  

Open Energy Info (EERE)

Property Property Edit with form History Facebook icon Twitter icon » Property:Building/SPPurchasedEngyPerAreaKwhM2DstrtHeating Jump to: navigation, search This is a property of type String. District heating Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2DstrtHeating" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 111.56331078 + Sweden Building 05K0002 + 72.7932960894 + Sweden Building 05K0003 + 111.899416255 + Sweden Building 05K0004 + 72.865497076 + Sweden Building 05K0005 + 285.840707965 + Sweden Building 05K0006 + 128.449958182 + Sweden Building 05K0007 + 63.8377147588 + Sweden Building 05K0008 + 115.128205128 + Sweden Building 05K0009 + 66.5515753129 + Sweden Building 05K0010 + 148.741418764 +

13

Property:Building/SPBreakdownOfElctrcityUseKwhM2Misc | Open Energy  

Open Energy Info (EERE)

SPBreakdownOfElctrcityUseKwhM2Misc SPBreakdownOfElctrcityUseKwhM2Misc Jump to: navigation, search This is a property of type String. Miscellaneous Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Misc" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 9.09953195331 + Sweden Building 05K0003 + 8.78442379242 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 12.9530389597 + Sweden Building 05K0008 + 6.03377747253 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 10.9950724049 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 14.2856105095 + Sweden Building 05K0014 + 27.8718727739 +

14

Property:Building/SPPurchasedEngyPerAreaKwhM2Oil-FiredBoiler | Open Energy  

Open Energy Info (EERE)

SPPurchasedEngyPerAreaKwhM2Oil-FiredBoiler SPPurchasedEngyPerAreaKwhM2Oil-FiredBoiler Jump to: navigation, search This is a property of type String. Oil-fired boiler Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2Oil-FiredBoiler" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 +

15

Property:Building/SPBreakdownOfElctrcityUseKwhM2HeatPumps | Open Energy  

Open Energy Info (EERE)

SPBreakdownOfElctrcityUseKwhM2HeatPumps SPBreakdownOfElctrcityUseKwhM2HeatPumps Jump to: navigation, search This is a property of type String. Heat pumps Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2HeatPumps" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 +

16

Property:Building/SPPurchasedEngyPerAreaKwhM2ElctrcHeating | Open Energy  

Open Energy Info (EERE)

SPPurchasedEngyPerAreaKwhM2ElctrcHeating" SPPurchasedEngyPerAreaKwhM2ElctrcHeating" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.915704329247 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.745132743363 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 25.8064516129 + Sweden Building 05K0016 + 5.89159465829 + Sweden Building 05K0017 + 0.0 + Sweden Building 05K0018 + 0.0 + Sweden Building 05K0019 + 0.0 +

17

Property:Building/SPBreakdownOfElctrcityUseKwhM2ElctrcHeating | Open Energy  

Open Energy Info (EERE)

SPBreakdownOfElctrcityUseKwhM2ElctrcHeating" SPBreakdownOfElctrcityUseKwhM2ElctrcHeating" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.915704329247 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.745132743363 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 25.8064516129 + Sweden Building 05K0016 + 5.89159465829 + Sweden Building 05K0017 + 0.0 + Sweden Building 05K0018 + 0.0 + Sweden Building 05K0019 + 0.0 +

18

Hydrogen, lithium, and lithium hydride production  

DOE Patents [OSTI]

A method of producing high purity lithium metal is provided, where gaseous-phase lithium metal is extracted from lithium hydride and condensed to form solid high purity lithium metal. The high purity lithium metal may be hydrided to provide high purity lithium hydride.

Brown, Sam W; Spencer, Larry S; Phillips, Michael R; Powell, G. Louis; Campbell, Peggy J

2014-03-25T23:59:59.000Z

19

Property:Building/SPPurchasedEngyPerAreaKwhM2OtherElctrty | Open Energy  

Open Energy Info (EERE)

OtherElctrty OtherElctrty Jump to: navigation, search This is a property of type String. Other electricity Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2OtherElctrty" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 70.305743501 + Sweden Building 05K0002 + 95.9357541899 + Sweden Building 05K0003 + 72.2496632241 + Sweden Building 05K0004 + 65.8830409357 + Sweden Building 05K0005 + 53.5026548673 + Sweden Building 05K0006 + 58.7608028994 + Sweden Building 05K0007 + 61.5607534672 + Sweden Building 05K0008 + 40.3846153846 + Sweden Building 05K0009 + 56.4810818587 + Sweden Building 05K0010 + 152.219679634 + Sweden Building 05K0011 + 25.5555555556 + Sweden Building 05K0012 + 35.8807888323 + Sweden Building 05K0013 + 61.3267863536 +

20

Property:Building/SPBreakdownOfElctrcityUseKwhM2Pumps | Open Energy  

Open Energy Info (EERE)

Pumps Pumps Jump to: navigation, search This is a property of type String. Pumps Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Pumps" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 6.37190900733 + Sweden Building 05K0002 + 6.03888185355 + Sweden Building 05K0003 + 3.38991548528 + Sweden Building 05K0004 + 4.33303636174 + Sweden Building 05K0005 + 2.75390897598 + Sweden Building 05K0006 + 7.77750996655 + Sweden Building 05K0007 + 1.66724551261 + Sweden Building 05K0008 + 3.32543498168 + Sweden Building 05K0009 + 3.08636405861 + Sweden Building 05K0010 + 14.8373684211 + Sweden Building 05K0011 + 1.47492819795 + Sweden Building 05K0012 + 3.32673206926 + Sweden Building 05K0013 + 2.63132906976 +

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Property:Building/SPBreakdownOfElctrcityUseKwhM2LargeComputersServers |  

Open Energy Info (EERE)

LargeComputersServers LargeComputersServers Jump to: navigation, search This is a property of type String. Large computers / servers Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2LargeComputersServers" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 2.88701226026 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 3.90838206628 + Sweden Building 05K0005 + 0.697674418605 + Sweden Building 05K0006 + 1.18332311465 + Sweden Building 05K0007 + 11.4098804421 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.556088941246 + Sweden Building 05K0010 + 10.0228832952 + Sweden Building 05K0011 + 0.471022727273 + Sweden Building 05K0012 + 0.774049003718 + Sweden Building 05K0013 + 0.0 +

22

Property:Building/SPBreakdownOfElctrcityUseKwhM2Elevators | Open Energy  

Open Energy Info (EERE)

Elevators Elevators Jump to: navigation, search This is a property of type String. Elevators Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Elevators" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.139664804469 + Sweden Building 05K0003 + 5.78356533453 + Sweden Building 05K0004 + 0.0116959064327 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.699648105982 + Sweden Building 05K0008 + 0.192307692308 + Sweden Building 05K0009 + 0.0661775284132 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.163674492353 + Sweden Building 05K0014 + 2.7497571546 +

23

Property:Building/SPBreakdownOfElctrcityUseKwhM2Fans | Open Energy  

Open Energy Info (EERE)

Fans Fans Jump to: navigation, search This is a property of type String. Fans Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Fans" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 5.21311928139 + Sweden Building 05K0002 + 18.5995610535 + Sweden Building 05K0003 + 20.3514016294 + Sweden Building 05K0004 + 8.08671679198 + Sweden Building 05K0005 + 16.0166245259 + Sweden Building 05K0006 + 10.358795651 + Sweden Building 05K0007 + 8.3953561818 + Sweden Building 05K0008 + 9.28527472527 + Sweden Building 05K0009 + 12.8398873749 + Sweden Building 05K0010 + 20.0966982674 + Sweden Building 05K0011 + 6.90408963585 + Sweden Building 05K0012 + 8.60719192175 + Sweden Building 05K0013 + 16.7539365907 +

24

Property:Building/SPBreakdownOfElctrcityUseKwhM2Copiers | Open Energy  

Open Energy Info (EERE)

Copiers Copiers Jump to: navigation, search This is a property of type String. Copiers Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Copiers" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.85593220339 + Sweden Building 05K0003 + 0.447247706422 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.897811865554 + Sweden Building 05K0008 + 0.9 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 7.78032036613 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 1.24104401228 + Sweden Building 05K0014 + 2.91414481058 + Sweden Building 05K0015 + 0.41935483871 +

25

Property:Building/SPPurchasedEngyPerAreaKwhM2ElctrtyTotal | Open Energy  

Open Energy Info (EERE)

ElctrtyTotal ElctrtyTotal Jump to: navigation, search This is a property of type String. Electricity, total Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2ElctrtyTotal" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 71.2214478303 + Sweden Building 05K0002 + 95.9357541899 + Sweden Building 05K0003 + 72.2496632241 + Sweden Building 05K0004 + 65.8830409357 + Sweden Building 05K0005 + 54.2477876106 + Sweden Building 05K0006 + 58.7608028994 + Sweden Building 05K0007 + 61.5607534672 + Sweden Building 05K0008 + 40.3846153846 + Sweden Building 05K0009 + 56.4810818587 + Sweden Building 05K0010 + 152.219679634 + Sweden Building 05K0011 + 25.5555555556 + Sweden Building 05K0012 + 35.8807888323 + Sweden Building 05K0013 + 61.3267863536 +

26

Property:Building/SPBreakdownOfElctrcityUseKwhM2CirculationFans | Open  

Open Energy Info (EERE)

CirculationFans CirculationFans Jump to: navigation, search This is a property of type String. Circulation fans Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2CirculationFans" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 13.3422495258 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 2.80646609789 + Sweden Building 05K0004 + 8.95823904901 + Sweden Building 05K0005 + 5.55016340076 + Sweden Building 05K0006 + 6.81308969891 + Sweden Building 05K0007 + 2.02541916787 + Sweden Building 05K0008 + 0.625641025641 + Sweden Building 05K0009 + 7.59721281624 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.757191316527 + Sweden Building 05K0012 + 6.04077487892 + Sweden Building 05K0013 + 0.767224182906 +

27

Property:Building/SPPurchasedEngyPerAreaKwhM2DstrtColg | Open Energy  

Open Energy Info (EERE)

DstrtColg DstrtColg Jump to: navigation, search This is a property of type String. District cooling Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2DstrtColg" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 38.7648166048 + Sweden Building 05K0002 + 44.9720670391 + Sweden Building 05K0003 + 11.6524472384 + Sweden Building 05K0004 + 35.3996101365 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 24.0451630889 + Sweden Building 05K0007 + 18.6296832954 + Sweden Building 05K0008 + 15.7692307692 + Sweden Building 05K0009 + 17.2637030643 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 5.09803921569 + Sweden Building 05K0012 + 15.0675825393 + Sweden Building 05K0013 + 21.4822771214 +

28

Property:Building/SPBreakdownOfElctrcityUseKwhM2AirCompressors | Open  

Open Energy Info (EERE)

AirCompressors AirCompressors Jump to: navigation, search This is a property of type String. Air compressors Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2AirCompressors" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 1.33591087145 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 1.86549707602 + Sweden Building 05K0005 + 2.04651162791 + Sweden Building 05K0006 + 1.92596566524 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.970107495214 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 1.30894886364 + Sweden Building 05K0012 + 2.01978262942 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 +

29

Property:Building/SPBreakdownOfElctrcityUseKwhM2Lighting | Open Energy  

Open Energy Info (EERE)

This is a property of type String. This is a property of type String. Lighting Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Lighting" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 13.6004313481 + Sweden Building 05K0002 + 51.2740526316 + Sweden Building 05K0003 + 25.3519773429 + Sweden Building 05K0004 + 14.5539566929 + Sweden Building 05K0005 + 17.1088606195 + Sweden Building 05K0006 + 11.7758321884 + Sweden Building 05K0007 + 16.0796522459 + Sweden Building 05K0008 + 15.7053876478 + Sweden Building 05K0009 + 19.44639866 + Sweden Building 05K0010 + 37.0625 + Sweden Building 05K0011 + 12.9336787565 + Sweden Building 05K0012 + 12.985779547 + Sweden Building 05K0013 + 21.6361810339 + Sweden Building 05K0014 + 29.853732347 +

30

Property:Building/SPBreakdownOfElctrcityUseKwhM2LargeKitchens | Open Energy  

Open Energy Info (EERE)

LargeKitchens LargeKitchens Jump to: navigation, search This is a property of type String. Large kitchens Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2LargeKitchens" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.763086941039 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.409356725146 + Sweden Building 05K0005 + 2.13953488372 + Sweden Building 05K0006 + 0.383200490497 + Sweden Building 05K0007 + 3.38701556508 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.294507436313 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.177556818182 + Sweden Building 05K0012 + 0.0953379731147 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 +

31

Property:Building/SPBreakdownOfElctrcityUseKwhM2Pcs | Open Energy  

Open Energy Info (EERE)

Pcs Pcs Jump to: navigation, search This is a property of type String. PCs Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Pcs" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 26.0998626444 + Sweden Building 05K0002 + 22.2888135593 + Sweden Building 05K0003 + 4.12075688073 + Sweden Building 05K0004 + 22.9175048733 + Sweden Building 05K0005 + 6.03962790698 + Sweden Building 05K0006 + 15.790619252 + Sweden Building 05K0007 + 5.8172794947 + Sweden Building 05K0008 + 4.66333333333 + Sweden Building 05K0009 + 8.50154616404 + Sweden Building 05K0010 + 8.05491990847 + Sweden Building 05K0011 + 2.70028409091 + Sweden Building 05K0012 + 2.19353608542 + Sweden Building 05K0013 + 8.43270214944 +

32

Property:Building/SPBreakdownOfElctrcityUseKwhM2Printers | Open Energy  

Open Energy Info (EERE)

Printers Printers Jump to: navigation, search This is a property of type String. Printers Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Printers" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.928422444931 + Sweden Building 05K0002 + 1.42372881356 + Sweden Building 05K0003 + 0.412844036697 + Sweden Building 05K0004 + 0.980506822612 + Sweden Building 05K0005 + 1.76744186047 + Sweden Building 05K0006 + 1.27988963826 + Sweden Building 05K0007 + 1.12158808933 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.765719334413 + Sweden Building 05K0010 + 1.01601830664 + Sweden Building 05K0011 + 0.774147727273 + Sweden Building 05K0012 + 1.11545428544 + Sweden Building 05K0013 + 0.549891248721 +

33

Property:Building/SPBreakdownOfElctrcityUseKwhM2SmallKitchensCoffeeRms |  

Open Energy Info (EERE)

SmallKitchensCoffeeRms SmallKitchensCoffeeRms Jump to: navigation, search This is a property of type String. Small kitchens / coffee rooms Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2SmallKitchensCoffeeRms" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 1.20677966102 + Sweden Building 05K0003 + 1.46100917431 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 2.53105456775 + Sweden Building 05K0007 + 1.08639747349 + Sweden Building 05K0008 + 0.910666666667 + Sweden Building 05K0009 + 2.06390811368 + Sweden Building 05K0010 + 3.29519450801 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 1.54234902764 +

34

Property:Building/SPBreakdownOfElctrcityUseKwhM2Refrigeration | Open Energy  

Open Energy Info (EERE)

Refrigeration Refrigeration Jump to: navigation, search This is a property of type String. Refrigeration Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Refrigeration" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 2.77390577084 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 37.1080462614 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.895094880057 + Sweden Building 05K0014 + 12.4536103016 + Sweden Building 05K0015 + 0.0 +

35

Design and testing of the HTS bearing for a 10 kWh flywheel system  

Science Journals Connector (OSTI)

Flywheels are of interest for a wide range of energy storage applications, from support of renewable resources to distributed power applications and uninterruptible power systems (UPS) (Day et al 2000 Proc. EESAT 2000 (Orlando, FL, Sept. 2000)). The use of high-temperature superconducting (HTS) bearings for such systems has significant advantages for applications requiring large amounts of energy to be stored with low parasitic losses and with minimal system maintenance. As flywheel systems increase in size, it becomes a significant challenge to provide adequate stiffness in these bearings without exceeding the strength limits of rotating magnet assemblies. The Boeing Company is designing and building a prototype flywheel of 10 kWh total stored energy and has focused much effort on the HTS bearing system. This paper will describe the general structure of the bearing and the steps taken to optimize its magnetic and structural performance and show recent test results.

A C Day; M Strasik; K E McCrary; P E Johnson; J W Gabrys; J R Schindler; R A Hawkins; D L Carlson; M D Higgins; J R Hull

2002-01-01T23:59:59.000Z

36

Property:Building/SPPurchasedEngyPerAreaKwhM2DigesterLandfillGas | Open  

Open Energy Info (EERE)

DigesterLandfillGas DigesterLandfillGas Jump to: navigation, search This is a property of type String. Digester / landfill gas Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2DigesterLandfillGas" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 +

37

Property:Building/SPBreakdownOfElctrcityUseKwhM2Laundry | Open Energy  

Open Energy Info (EERE)

Laundry Laundry Jump to: navigation, search This is a property of type String. Laundry Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2Laundry" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 + Sweden Building 05K0017 + 0.0 +

38

Property:Building/SPPurchasedEngyPerAreaKwhM2WoodChips | Open Energy  

Open Energy Info (EERE)

WoodChips WoodChips Jump to: navigation, search This is a property of type String. Wood chips Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2WoodChips" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 + Sweden Building 05K0017 + 0.0 +

39

Property:Building/SPPurchasedEngyPerAreaKwhM2Pellets | Open Energy  

Open Energy Info (EERE)

Pellets Pellets Jump to: navigation, search This is a property of type String. Pellets Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2Pellets" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 + Sweden Building 05K0017 + 0.0 +

40

Property:Building/SPPurchasedEngyPerAreaKwhM2Other | Open Energy  

Open Energy Info (EERE)

This is a property of type String. This is a property of type String. Other Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2Other" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 + Sweden Building 05K0017 + 0.0 + Sweden Building 05K0018 + 0.0 +

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Property:Building/SPPurchasedEngyPerAreaKwhM2Logs | Open Energy Information  

Open Energy Info (EERE)

Logs Logs Jump to: navigation, search This is a property of type String. Logs Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2Logs" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 + Sweden Building 05K0017 + 0.0 +

42

Property:Building/SPBreakdownOfElctrcityUseKwhM2ElctrcEngineHeaters | Open  

Open Energy Info (EERE)

ElctrcEngineHeaters ElctrcEngineHeaters Jump to: navigation, search This is a property of type String. Electric engine heaters Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2ElctrcEngineHeaters" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 2.44788473329 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.353408923575 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.835160644485 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 +

43

Property:Building/SPPurchasedEngyPerAreaKwhM2TownGas | Open Energy  

Open Energy Info (EERE)

TownGas TownGas Jump to: navigation, search This is a property of type String. Town gas Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2TownGas" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 + Sweden Building 05K0017 + 0.0 +

44

Property:Building/SPPurchasedEngyPerAreaKwhM2NaturalGas | Open Energy  

Open Energy Info (EERE)

NaturalGas NaturalGas Jump to: navigation, search This is a property of type String. Natural gas Pages using the property "Building/SPPurchasedEngyPerAreaKwhM2NaturalGas" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.0 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 + Sweden Building 05K0016 + 0.0 + Sweden Building 05K0017 + 0.0 +

45

Beyond kWh and kW demand: Understanding the new real-time electric power  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Beyond kWh and kW demand: Understanding the new real-time electric power Beyond kWh and kW demand: Understanding the new real-time electric power measurement system in LBNL Building 90 Speaker(s): Alex McEachern Date: January 14, 2010 - 12:00pm Location: 90-3122 In the Summer of 2009, LBNL researchers installed end-use sub-metering equipment and associated Energy Information System (EIS) tools to characterize energy use and comfort in Building 90. Seven of 40 key electric loads were measured using advanced meters that make sophisticated real-time measurements of dozens of power flow parameters, power disturbances, and harmonics. The talk will review some electrical engineering fundamentals, how use and interpret data measured in building 90 in real-time. The real-time data available includes power, volt-amps, VAR's, unbalance voltage and current, voltage and current distortion,

46

Lithium Iron Phosphate Composites for Lithium Batteries | Argonne...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Lithium Iron Phosphate Composites for Lithium Batteries Technology available for licensing: Inexpensive, electrochemically active phosphate compounds with high functionality for...

47

Atoms in Valence Bond. Method, implementation and application.  

E-Print Network [OSTI]

??The Atoms in Valence Bond (AiVB) approach is presented. The main goal was to develop a new and innovative approach, within the existing Valence Bond (more)

Zielinski, M.L.

2012-01-01T23:59:59.000Z

48

Lithium Insertion into Anatase Nanotubes  

Science Journals Connector (OSTI)

Lithium Insertion into Anatase Nanotubes ... Improving the Performance of Titania Nanotube Battery Materials by Surface Modification with Lithium Phosphate ...

V. Gentili; S. Brutti; L.J. Hardwick; A.R. Armstrong; S. Panero; P.G. Bruce

2012-11-01T23:59:59.000Z

49

Molten salt lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400 to 500/sup 0/C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell which may be operated at temperatures between about 100 to 170/sup 0/C. The cell is comprised of an electrolyte, which preferably includes lithium nitrate, and a lithium or lithium alloy electrode.

Raistrick, I.D.; Poris, J.; Huggins, R.A.

1980-07-18T23:59:59.000Z

50

Molten salt lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400.degree.-500.degree. C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell (10) which may be operated at temperatures between about 100.degree.-170.degree. C. Cell (10) comprises an electrolyte (16), which preferably includes lithium nitrate, and a lithium or lithium alloy electrode (12).

Raistrick, Ian D. (Menlo Park, CA); Poris, Jaime (Portola Valley, CA); Huggins, Robert A. (Stanford, CA)

1982-02-09T23:59:59.000Z

51

Lithium Supply Grows  

Science Journals Connector (OSTI)

Military-requirements are of course classified, but there is general speculation that lithium is required for the thermonuclear reactions. ...

1955-11-21T23:59:59.000Z

52

Property:Building/SPBreakdownOfElctrcityUseKwhM2HeatPumpsUsedForColg | Open  

Open Energy Info (EERE)

HeatPumpsUsedForColg HeatPumpsUsedForColg Jump to: navigation, search This is a property of type String. Heat pumps used for cooling Pages using the property "Building/SPBreakdownOfElctrcityUseKwhM2HeatPumpsUsedForColg" Showing 25 pages using this property. (previous 25) (next 25) S Sweden Building 05K0001 + 0.0 + Sweden Building 05K0002 + 0.0 + Sweden Building 05K0003 + 0.0 + Sweden Building 05K0004 + 0.0 + Sweden Building 05K0005 + 0.0 + Sweden Building 05K0006 + 0.250906049624 + Sweden Building 05K0007 + 0.0 + Sweden Building 05K0008 + 0.0 + Sweden Building 05K0009 + 0.0 + Sweden Building 05K0010 + 0.0 + Sweden Building 05K0011 + 0.0 + Sweden Building 05K0012 + 0.0 + Sweden Building 05K0013 + 0.0 + Sweden Building 05K0014 + 0.0 + Sweden Building 05K0015 + 0.0 +

53

Manufacturing of Protected Lithium Electrodes for Advanced Batteries  

Broader source: Energy.gov [DOE]

Manufacturing of Protected Lithium Electrodes for Advanced Lithium-Air, Lithium-Water, and Lithium-Sulfur Batteries

54

Chlorine hazard evaluation for the zinc-chlorine electric vehicle battery. Final technical report. [50 kWh  

SciTech Connect (OSTI)

Hazards associated with conceivable accidental chlorine releases from zinc-chlorine electric vehicle batteries are evaluated. Since commercial batteries are not yet available, this hazard assessment is based on both theoretical chlorine dispersion models and small-scale and large-scale spill tests with chlorine hydrate (which is the form of chlorine storage in the charged battery). Six spill tests involving the chlorine hydrate equivalent of a 50-kWh battery indicate that the danger zone in which chlorine vapor concentrations intermittently exceed 100 ppM extends at least 23 m directly downwind of a spill onto a warm (30 to 38/sup 0/C) road surface. Other accidental chlorine release scenarios may also cause some distress, but are not expected to produce the type of life-threatening chlorine exposures that can result from large hydrate spills. Chlorine concentration data from the hydrate spill tests compare favorably with calculations based on a quasi-steady area source dispersion model and empirical estimates of the hydrate decomposition rate. The theoretical dispersion model was combined with assumed hydrate spill probabilities and current motor vehicle accident statistics in order to project expected chlorine-induced fatality rates. These calculations indicate that expected chlorine fataility rates are several times higher in a city such as Los Angeles with a warm and calm climate than in a colder and windier city such as Boston. Calculated chlorine-induced fatality rate projections for various climates are presented as a function of hydrate spill probability in order to illustrate the degree of vehicle/battery crashworthiness required to maintain chlorine-induced fatality rates below current vehicle fatality rates due to fires and asphyxiations. 37 figures, 19 tables.

Zalosh, R. G.; Bajpai, S. N.; Short, T. P.; Tsui, R. K.

1980-04-01T23:59:59.000Z

55

Argonne, Western Lithium to develop lithium carbonate for multiple...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Laboratory as a step toward the commercialization of lithium carbonate from the Company's Kings Valley Lithium Project located in Humboldt County, Nevada, USA. Under the agreement,...

56

Photo-induced Valence Tautomerism in Co Complexes  

Science Journals Connector (OSTI)

Photo-induced Valence Tautomerism in Co Complexes ... His research interests include the development of photomagnets and phototunable photonic crystals and the design of supramolecules exhibiting photo-bistability. ... Photo-induced Valence Tautomerism in Mononuclear Compounds ...

Osamu Sato; Aili Cui; Ryotaro Matsuda; Jun Tao; Shinya Hayami

2007-04-11T23:59:59.000Z

57

Logical Effort of Higher Valency Adders David Harris  

E-Print Network [OSTI]

Logical Effort of Higher Valency Adders David Harris Harvey Mudd College 301 E. Twelfth St. Claremont, CA 91711 David_Harris@hmc.edu Abstract ­ Higher valency parallel prefix adders reduce the number

Harris, David Money

58

Precision Calculations of Atoms with Few Valence Electrons  

E-Print Network [OSTI]

Precision Calculations of Atoms with Few Valence Electrons M. G. KOZLOV Petersburg Nuclear Physics words: atoms; effective Hamiltonian; pair equations; precision calculation; valence electron for valence electrons of an atom. The low-energy part of atomic spectrum is found by solving the eigenvalue

Kozlov, Mikhail G

59

Precision Calculations of Atoms with Few Valence Electrons  

E-Print Network [OSTI]

Precision Calculations of Atoms with Few Valence Electrons M. G. KOZLOV Petersburg Nuclear Physics for valence electrons of an atom. The low-energy part of atomic spectrum is found by solving the eigenvalue­valence correlations. We tested this method on a toy model of a four-electron atom with the core 1s2 . The spectrum

Kozlov, Mikhail G

60

Cathode material for lithium batteries  

DOE Patents [OSTI]

A method of manufacture an article of a cathode (positive electrode) material for lithium batteries. The cathode material is a lithium molybdenum composite transition metal oxide material and is prepared by mixing in a solid state an intermediate molybdenum composite transition metal oxide and a lithium source. The mixture is thermally treated to obtain the lithium molybdenum composite transition metal oxide cathode material.

Park, Sang-Ho; Amine, Khalil

2013-07-23T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

American Lithium Energy Corp | Open Energy Information  

Open Energy Info (EERE)

Lithium Energy Corp Jump to: navigation, search Name: American Lithium Energy Corp Place: San Marcos, California Zip: 92069 Product: California-based developer of lithium ion...

62

Lithium metal oxide electrodes for lithium batteries  

DOE Patents [OSTI]

An uncycled electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula Li.sub.(2+2x)/(2+x)M'.sub.2x/(2+x)M.sub.(2-2x)/(2+x)O.sub.2-.delta., in which 0.ltoreq.x<1 and .delta. is less than 0.2, and in which M is a non-lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. Methods of preconditioning the electrodes are disclosed as are electrochemical cells and batteries containing the electrodes.

Thackeray, Michael M. (Naperville, IL); Kim, Jeom-Soo (Naperville, IL); Johnson, Christopher S. (Naperville, IL)

2008-01-01T23:59:59.000Z

63

Electrocatalysts for Nonaqueous LithiumAir Batteries:...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electrocatalysts for Nonaqueous LithiumAir Batteries: Status, Challenges, and Perspective. Electrocatalysts for Nonaqueous LithiumAir Batteries: Status, Challenges,...

64

Lithium Ion Accomplishments  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Lithium ion Battery Commercialization Lithium ion Battery Commercialization Johnson Controls-Saft Advanced Power Solutions, of Milwaukee, Wisconsin: Johnson Controls-Saft (JCS) will supply lithium-ion batteries to Mercedes for their S Class Hybrid to be introduced in October 2009. Technology developed with DOE support (the VL6P cell) will be used in the S Class battery. In May 2006, the Johnson Controls-Saft Joint Venture was awarded a 24 month $14.4 million contract by the DOE/USABC to develop a 40kW Li ion HEV battery system offering improved safety, low temperature performance, and cost. JCS has reported a 40% cost reduction of the 40kW system being developed in their DOE/USABC contract while maintaining performance. Lithium Ion Battery Material Commercialization Argonne National Laboratory has licensed cathode materials and associated processing

65

Solid-state lithium battery  

DOE Patents [OSTI]

The present invention is directed to a higher power, thin film lithium-ion electrolyte on a metallic substrate, enabling mass-produced solid-state lithium batteries. High-temperature thermodynamic equilibrium processing enables co-firing of oxides and base metals, providing a means to integrate the crystalline, lithium-stable, fast lithium-ion conductor lanthanum lithium tantalate (La.sub.1/3-xLi.sub.3xTaO.sub.3) directly with a thin metal foil current collector appropriate for a lithium-free solid-state battery.

Ihlefeld, Jon; Clem, Paul G; Edney, Cynthia; Ingersoll, David; Nagasubramanian, Ganesan; Fenton, Kyle Ross

2014-11-04T23:59:59.000Z

66

LITHIUM LITERATURE REVIEW: LITHIUM'S PROPERTIES AND INTERACTIONS  

Office of Scientific and Technical Information (OSTI)

HEDL-TME 78-15 HEDL-TME 78-15 uc-20 LITHIUM LITERATURE REVIEW: LITHIUM'S PROPERTIES AND INTERACTIONS Hanf ord Engineering Development Laboratory -~ - - , . .. . D.W. Jeppson J.L. Ballif W.W. Yuan B.E. Chou - - - . - . - -- r - N O T l C E n ~ h u mpon w prepared as an account of work iponrored by the United States Government. Neither the Unitcd States nor the United Stater Department of Energy. nor any of their employees, nor any of then contractor^, subcontractors. or their employees, maker any warranty, cxprcu or Implied. or anumcs any legal liability or rcrponabllity for the accuracy. cornplctcncs or uvfulnes of any information. apparatus, product or p r o a s ditclorcd. or rcpments that its u s would not infringe pnvatcly owned nghts. April 1978 HANFORD ENGINEERING DEVELOPMENT LABORATORY

67

Quantum Monte Carlo methods and lithium cluster properties  

SciTech Connect (OSTI)

Properties of small lithium clusters with sizes ranging from n = 1 to 5 atoms were investigated using quantum Monte Carlo (QMC) methods. Cluster geometries were found from complete active space self consistent field (CASSCF) calculations. A detailed development of the QMC method leading to the variational QMC (V-QMC) and diffusion QMC (D-QMC) methods is shown. The many-body aspect of electron correlation is introduced into the QMC importance sampling electron-electron correlation functions by using density dependent parameters, and are shown to increase the amount of correlation energy obtained in V-QMC calculations. A detailed analysis of D-QMC time-step bias is made and is found to be at least linear with respect to the time-step. The D-QMC calculations determined the lithium cluster ionization potentials to be 0.1982(14) [0.1981], 0.1895(9) [0.1874(4)], 0.1530(34) [0.1599(73)], 0.1664(37) [0.1724(110)], 0.1613(43) [0.1675(110)] Hartrees for lithium clusters n = 1 through 5, respectively; in good agreement with experimental results shown in the brackets. Also, the binding energies per atom was computed to be 0.0177(8) [0.0203(12)], 0.0188(10) [0.0220(21)], 0.0247(8) [0.0310(12)], 0.0253(8) [0.0351(8)] Hartrees for lithium clusters n = 2 through 5, respectively. The lithium cluster one-electron density is shown to have charge concentrations corresponding to nonnuclear attractors. The overall shape of the electronic charge density also bears a remarkable similarity with the anisotropic harmonic oscillator model shape for the given number of valence electrons.

Owen, R.K.

1990-12-01T23:59:59.000Z

68

Phenomenological theory of a single domain wall in uniaxial trigonal ferroelectrics: Lithium niobate and lithium tantalate  

E-Print Network [OSTI]

Phenomenological theory of a single domain wall in uniaxial trigonal ferroelectrics: Lithium niobate and lithium tantalate David A. Scrymgeour and Venkatraman Gopalan Department of Materials Science, lithium niobate and lithium tantalate. The contributions to the domain- wall energy from polarization

Gopalan, Venkatraman

69

Princeton Plasma Physics Lab - Lithium  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

lithium Nearly everybody knows about lithium Nearly everybody knows about lithium - a light, silvery alkali metal - used in rechargeable batteries powering everything from laptops to hybrid cars. What may not be so well known is the fact that researchers hoping to harness the energy released in fusion reactions also have used lithium to coat the walls of donut-shaped tokamak reactors. Lithium, it turns out, may help the plasmas fueling fusion reactions to retain heat for longer periods of time. This could improve the chances of producing useful energy from fusion. en COLLOQUIUM: The Lithium Tokamak eXperiment (LTX) http://www.pppl.gov/events/colloquium-lithium-tokamak-experiment-ltx

70

Lithium ion conducting electrolytes  

DOE Patents [OSTI]

A liquid, predominantly lithium-conducting, ionic electrolyte is described having exceptionally high conductivity at temperatures of 100 C or lower, including room temperature, and comprising the lithium salts selected from the group consisting of the thiocyanate, iodide, bromide, chloride, perchlorate, acetate, tetrafluoroborate, perfluoromethane sulfonate, perfluoromethane sulfonamide, tetrahaloaluminate, and heptahaloaluminate salts of lithium, with or without a magnesium-salt selected from the group consisting of the perchlorate and acetate salts of magnesium. Certain of the latter embodiments may also contain molecular additives from the group of acetonitrile (CH{sub 3}CN), succinnonitrile (CH{sub 2}CN){sub 2}, and tetraglyme (CH{sub 3}--O--CH{sub 2}--CH{sub 2}--O--){sub 2} (or like solvents) solvated to a Mg{sup +2} cation to lower the freezing point of the electrolyte below room temperature. Other particularly useful embodiments contain up to about 40, but preferably not more than about 25, mol percent of a long chain polyether polymer dissolved in the lithium salts to provide an elastic or rubbery solid electrolyte of high ambient temperature conductivity and exceptional 100 C conductivity. Another embodiment contains up to about but not more than 10 mol percent of a molecular solvent such as acetone. 2 figs.

Angell, C.A.; Liu, C.

1996-04-09T23:59:59.000Z

71

Side Reactions in Lithium-Ion Batteries  

E-Print Network [OSTI]

even with excess negative capacity, lithium can deposit ifdeposits lithium and reaches cutoff sooner. electrode excessexcess by 10%, an extension of about 0.4 mm is sufficient to prevent the onset of lithium

Tang, Maureen Han-Mei

2012-01-01T23:59:59.000Z

72

Mixed valence of iron in minerals with cation clusters  

Science Journals Connector (OSTI)

The valence and distribution of iron in vivianite, lazulite, babingtonite, rockbridgeite, acmite, aegirine-augite, hedenbergite,...2+ and Fe3+ in neighboring sites through common edges or faces is observed in all...

Georg Amthauer; George R. Rossman

1984-06-01T23:59:59.000Z

73

Polymer Electrolytes for Advanced Lithium Batteries | Department...  

Broader source: Energy.gov (indexed) [DOE]

Advanced Lithium Batteries Polymer Electrolytes for Advanced Lithium Batteries 2009 DOE Hydrogen Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation...

74

Lithium Metal Anodes for Rechargeable Batteries. | EMSL  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Metal Anodes for Rechargeable Batteries. Lithium Metal Anodes for Rechargeable Batteries. Abstract: Rechargeable lithium metal batteries have much higher energy density than those...

75

Design and Simulation of Lithium Rechargeable Batteries  

E-Print Network [OSTI]

Gabano, Ed. , Lithium Batteries, Academic Press, New York,K. V. Kordesch, "Primary Batteries 1951-1976," J. Elec- n ~.Rechargeable Lithium Batteries," J. Electrochem. Soc. , [20

Doyle, C.M.

2010-01-01T23:59:59.000Z

76

EERE Partner Testimonials - Phil Roberts, California Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Phil Roberts, California Lithium Battery (CalBattery) EERE Partner Testimonials - Phil Roberts, California Lithium Battery (CalBattery) Addthis Text Version The words "Office of...

77

Design and Simulation of Lithium Rechargeable Batteries  

E-Print Network [OSTI]

Newman, "Thermal Modeling of the LithiumIPolymer Battery I.J. Newman, "Thermal Modeling of the LithiumIPolymer Battery

Doyle, C.M.

2010-01-01T23:59:59.000Z

78

Washington: Graphene Nanostructures for Lithium Batteries Recieves...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Washington: Graphene Nanostructures for Lithium Batteries Recieves 2012 R&D 100 Award Washington: Graphene Nanostructures for Lithium Batteries Recieves 2012 R&D 100 Award February...

79

Lithium-based electrochromic mirrors  

E-Print Network [OSTI]

LITHIUM-BASED ELECTROCHROMIC MIRRORS Thomas J. Richardson*with pure antimony films. Electrochromic cycling speed andand silver. INTRODUCTION Electrochromic devices that exhibit

Richardson, Thomas J.; Slack, Jonathan L.

2003-01-01T23:59:59.000Z

80

SECONDARY BATTERIES LITHIUM RECHARGEABLE SYSTEMS LITHIUM-ION | Overview  

Science Journals Connector (OSTI)

The need to increase the specific energy and energy density of secondary batteries has become more urgent as a result of the recent rapid development of new applications, such as electric vehicles (EVs), load leveling, and various types of portable equipments, including cellular phones, personal computers, camcorders, and digital cameras. Among various types of secondary batteries, rechargeable lithium-ion batteries have been used in a wide variety of portable equipments due to their high energy density. Many researchers have contributed to develop lithium-ion batteries, and their contributions are reviewed from historical aspects onward, including the researches in primary battery with metal lithium anode, and secondary battery with metal lithium negative electrode. Researches of new materials are still very active to develop new lithium-ion batteries with higher performances. The researches of positive and negative electrode active materials and electrolytes are also reviewed historically.

J. Yamaki

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Chapter 16 - Lithium Battery Energy Storage: State of the Art Including LithiumAir and LithiumSulfur Systems  

Science Journals Connector (OSTI)

Abstract Lithium, the lightest and one of the most reactive of metals, having the greatest electrochemical potential (E0=?3.045V), provides very high energy and power densities in batteries. Rechargeable lithium-ion batteries (containing an intercalation negative electrode) have conquered the markets for portable consumer electronics and, recently, for electric vehicles. The electrolyte is usually based on a lithium salt in organic solution. Thin-film batteries use solid oxide or polymer electrolytes. As lithium metal reacts violently with water and can thus cause ignition, modern lithium-ion batteries use carbon negative electrodes and lithium metal oxide positive electrodes. Rechargeable lithium-ion batteries should not be confused with nonrechargeable lithium primary batteries (containing metallic lithium). This chapter covers all aspects of lithium battery chemistry that are pertinent to electrochemical energy storage for renewable sources and grid balancing.

Peter Kurzweil

2015-01-01T23:59:59.000Z

82

SECONDARY BATTERIES LITHIUM RECHARGEABLE SYSTEMS | Overview  

Science Journals Connector (OSTI)

Rechargeable lithium batteries have conquered the markets for portable consumer electronics and, recently, for electric vehicles. Lithium, the lightest and one of the most reactive of metals, having the greatest electrochemical potential (E=3.045V), provides very high energy and power densities in batteries. As lithium metal reacts violently with water and can ignite into flame, modern lithium-ion batteries use carbon negative electrode and lithium metal oxide positive electrode. The electrolyte is usually based on a lithium salt in organic solution. Thin-film batteries use solid oxide or polymer electrolytes. Rechargeable lithium-ion batteries (containing an intercalation negative electrode) should not be confused with nonrechargeable lithium primary batteries (containing metallic lithium). This article outlines energy storage in lithium batteries, basic cell chemistry, positive electrode materials, negative electrode materials, electrolytes, and state-of-charge (SoC) monitoring.

P. Kurzweil; K. Brandt

2009-01-01T23:59:59.000Z

83

Correlation of conductivity and angle integrated valence band photoemission  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Correlation of conductivity and angle integrated valence band photoemission Correlation of conductivity and angle integrated valence band photoemission characteristics in single crystal iron perovskites for 300 K < T < 800 K: Comparison of surface and bulk sensitive methods Title Correlation of conductivity and angle integrated valence band photoemission characteristics in single crystal iron perovskites for 300 K < T < 800 K: Comparison of surface and bulk sensitive methods Publication Type Journal Article Year of Publication 2010 Authors Braun, Artur, Bongjin S. Mun, Yun Sun, Z. Liu, Oliver Gröning, R. Mäder, Selma Erat, Xueyuan Zhang, Samuel S. Mao, Ekaterina Pomjakushina, Kazimierz Conder, and Thomas Graule Journal Journal of Electron Spectroscopy and Related Phenomena Volume 181 Issue 1 Pagination 56-62 Date Published 07/2013

84

Lithium niobate explosion monitor  

DOE Patents [OSTI]

Monitoring explosive devices is accomplished with a substantially z-cut lithium niobate crystal in abutment with the explosive device. Upon impact by a shock wave from detonation of the explosive device, the crystal emits a current pulse prior to destruction of the crystal. The current pulse is detected by a current viewing transformer and recorded as a function of time in nanoseconds. In order to self-check the crystal, the crystal has a chromium film resistor deposited thereon which may be heated by a current pulse prior to detonation. This generates a charge which is detected by a charge amplifier. 8 figs.

Bundy, C.H.; Graham, R.A.; Kuehn, S.F.; Precit, R.R.; Rogers, M.S.

1990-01-09T23:59:59.000Z

85

Lithium niobate explosion monitor  

DOE Patents [OSTI]

Monitoring explosive devices is accomplished with a substantially z-cut lithium niobate crystal in abutment with the explosive device. Upon impact by a shock wave from detonation of the explosive device, the crystal emits a current pulse prior to destruction of the crystal. The current pulse is detected by a current viewing transformer and recorded as a function of time in nanoseconds. In order to self-check the crystal, the crystal has a chromium film resistor deposited thereon which may be heated by a current pulse prior to detonation. This generates a charge which is detected by a charge amplifier.

Bundy, Charles H. (Clearwater, FL); Graham, Robert A. (Los Lunas, NM); Kuehn, Stephen F. (Albuquerque, NM); Precit, Richard R. (Albuquerque, NM); Rogers, Michael S. (Albuquerque, NM)

1990-01-01T23:59:59.000Z

86

Lattice Dynamics of Dense Lithium  

Science Journals Connector (OSTI)

We report low-frequency high-resolution Raman spectroscopy and ab-initio calculations on dense lithium from 40 to 200GPa at low temperatures. Our experimental results reveal rich first-order Raman activity in the metallic and semiconducting phases of lithium. The computed Raman frequencies are in excellent agreement with the measurements. Free energy calculations provide a quantitative description and physical explanation of the experimental phase diagram only when vibrational effect are correctly treated. The study underlines the importance of zero-point energy in determining the phase stability of compressed lithium.

F. A. Gorelli; S. F. Elatresh; C. L. Guillaume; M. Marqus; G. J. Ackland; M. Santoro; S. A. Bonev; E. Gregoryanz

2012-01-30T23:59:59.000Z

87

Lithium System Operation Dan Lev and David Stein  

E-Print Network [OSTI]

Lithium System Operation Dan Lev and David Stein March 1, 2011 (or Lithium tank for dummies) 1 #12 for Ordering . . . . . . . . . . . . . . . . . 51 9 Lithium Handling 52 9.1 Glove Box for Ordering . . . . . . . . . . . . . . . . . 57 9.2 Lithium Cleaning

88

Mobile linkers on DNA-coated colloids: valency without patches  

E-Print Network [OSTI]

Colloids coated with single-stranded DNA (ssDNA) can bind selectively to other colloids coated with complementary ssDNA. The fact that DNA-coated colloids (DNACCs) can bind to specific partners opens the prospect of making colloidal `molecules'. However, in order to design DNACC-based molecules, we must be able to control the valency of the colloids, i.e. the number of partners to which a given DNACC can bind. One obvious, but not very simple approach is to decorate the colloidal surface with patches of single-stranded DNA that selectively bind those on other colloids. Here we propose a design principle that exploits many-body effects to control the valency of otherwise isotropic colloids. Using a combination of theory and simulation, we show that we can tune the valency of colloids coated with mobile ssDNA, simply by tuning the non-specific repulsion between the particles. Our simulations show that the resulting effective interactions lead to low-valency colloids self-assembling in peculiar open structures, very different from those observed in DNACCs with immobile DNA linkers.

Stefano Angioletti-Uberti; Patrick Varilly; Bortolo M. Mognetti; Daan Frenkel

2014-08-27T23:59:59.000Z

89

Y-12 lithium-6 production  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

fusion materials on August 12, 1953. The explosion was quickly determined to be a thermonuclear-like test and was also believed to contain lithium. Y-12 chemists and engineers...

90

Pairing of valence electrons as necessary condition for energy minimization in a crystal  

E-Print Network [OSTI]

Pairing of valence electrons can lead to energy minimization of a crystal. It can be proved by use of representation of the valence electrons as plane waves in periodic potential of the crystal.

Dolgopolov Stanislav Olegovich

2014-10-21T23:59:59.000Z

91

Air breathing lithium power cells  

DOE Patents [OSTI]

A cell suitable for use in a battery according to one embodiment includes a catalytic oxygen cathode; a stabilized zirconia electrolyte for selective oxygen anion transport; a molten salt electrolyte; and a lithium-based anode. A cell suitable for use in a battery according to another embodiment includes a catalytic oxygen cathode; an electrolyte; a membrane selective to molecular oxygen; and a lithium-based anode.

Farmer, Joseph C.

2014-07-15T23:59:59.000Z

92

Lithium Technology Corporation | Open Energy Information  

Open Energy Info (EERE)

Corporation Corporation Jump to: navigation, search Name Lithium Technology Corporation Place Plymouth Meeting, Pennsylvania Zip PA 19462 Sector Vehicles Product Pennsylvania-based lithium secondary battery company manufacturing rechargeable batteries for plug-in and hybrid vehicles and for custom military and industrial applications. References Lithium Technology Corporation[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Lithium Technology Corporation is a company located in Plymouth Meeting, Pennsylvania . References ↑ "Lithium Technology Corporation" Retrieved from "http://en.openei.org/w/index.php?title=Lithium_Technology_Corporation&oldid=348412"

93

Electron delocalization in mixed-valence Keggin polyoxometalates. Ab initio calculation of the local e ective  

E-Print Network [OSTI]

Electron delocalization in mixed-valence Keggin polyoxometalates. Ab initio calculation evaluation of the in uence of the electron trans- fer on the magnetic properties of mixed-valence polyoxometalates reduced by two electrons. For that purpose, we extract from valence-spectroscopy ab initio

94

Deprotonative metallation of ferrocenes using mixed lithium-zinc and lithium-cadmium combinations  

E-Print Network [OSTI]

). It is pertinent to mention that lithium bases were previously used to deprotonate the acetal 3, albeit at lower1 Deprotonative metallation of ferrocenes using mixed lithium-zinc and lithium-cadmium combinations on the web Xth XXXXXXXXX 200X DOI: 10.1039/b000000x A mixed lithium-cadmium amide and a combination

Boyer, Edmond

95

Khalil Amine on Lithium-air Batteries  

ScienceCinema (OSTI)

Khalil Amine, materials scientist at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries.

Khalil Amine

2010-01-08T23:59:59.000Z

96

Novel Electrolytes for Lithium Ion Batteries  

SciTech Connect (OSTI)

We have been investigating three primary areas related to lithium ion battery electrolytes. First, we have been investigating the thermal stability of novel electrolytes for lithium ion batteries, in particular borate based salts. Second, we have been investigating novel additives to improve the calendar life of lithium ion batteries. Third, we have been investigating the thermal decomposition reactions of electrolytes for lithium-oxygen batteries.

Lucht, Brett L

2014-12-12T23:59:59.000Z

97

Multi-layered, chemically bonded lithium-ion and lithium/air batteries  

SciTech Connect (OSTI)

Disclosed are multilayer, porous, thin-layered lithium-ion batteries that include an inorganic separator as a thin layer that is chemically bonded to surfaces of positive and negative electrode layers. Thus, in such disclosed lithium-ion batteries, the electrodes and separator are made to form non-discrete (i.e., integral) thin layers. Also disclosed are methods of fabricating integrally connected, thin, multilayer lithium batteries including lithium-ion and lithium/air batteries.

Narula, Chaitanya Kumar; Nanda, Jagjit; Bischoff, Brian L; Bhave, Ramesh R

2014-05-13T23:59:59.000Z

98

Measurement of valence band structure in arbitrary dielectric films  

SciTech Connect (OSTI)

A new way of measuring the band structure of various dielectric materials using the secondary electron emission from Auger neutralization of ions is introduced. The first example of this measurement scheme is the magnesium oxide (MgO) films with respect to the application of the films in the display industries. The density of state in the valence bands of MgO film and MgO film with a functional layer (FL) deposited over a dielectric surface reveals that the density peak of film with a FL is considerably less than that of film, thereby indicating a better performance of MgO film with functional layer in display devices. The second example of the measurement is the boron-zinc oxide (BZO) films with respect to the application of the films to the development of solar cells. The measurement of density of state in BZO film suggests that a high concentration of boron impurity in BZO films may enhance the transition of electrons and holes through the band gap from the valence to the conduction band in zinc oxide crystals; thereby improving the conductivity of the film. Secondary electron emission by the Auger neutralization of ions is highly instrumental for the determination of the density of states in the valence band of dielectric materials.

Uhm, Han S., E-mail: hsuhm@kw.ac.kr [Department of Electrophysics, Kwangwoon University, 447-1 Wolgye-Dong, Nowon-Gu, Seoul 139-701 (Korea, Republic of); Choi, Eun H. [Department of Electrophysics, Kwangwoon University, 447-1 Wolgye-Dong, Nowon-Gu, Seoul 139-701 (Korea, Republic of)] [Department of Electrophysics, Kwangwoon University, 447-1 Wolgye-Dong, Nowon-Gu, Seoul 139-701 (Korea, Republic of)

2012-10-15T23:59:59.000Z

99

Solid composite electrolytes for lithium batteries  

DOE Patents [OSTI]

Solid composite electrolytes are provided for use in lithium batteries which exhibit moderate to high ionic conductivity at ambient temperatures and low activation energies. In one embodiment, a ceramic-ceramic composite electrolyte is provided containing lithium nitride and lithium phosphate. The ceramic-ceramic composite is also preferably annealed and exhibits an activation energy of about 0.1 eV.

Kumar, Binod (Dayton, OH); Scanlon, Jr., Lawrence G. (Fairborn, OH)

2000-01-01T23:59:59.000Z

100

Anode materials for lithium-ion batteries  

DOE Patents [OSTI]

An anode material for lithium-ion batteries is provided that comprises an elongated core structure capable of forming an alloy with lithium; and a plurality of nanostructures placed on a surface of the core structure, with each nanostructure being capable of forming an alloy with lithium and spaced at a predetermined distance from adjacent nanostructures.

Sunkara, Mahendra Kumar; Meduri, Praveen; Sumanasekera, Gamini

2014-12-30T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

Design and Simulation of Lithium Rechargeable Batteries  

E-Print Network [OSTI]

kg/m3) ! ef excess capacity of lithium foil ! rcn density ofU I read * ef ! excess capacity of lithium foil read * rcn !lx,f6.3,' ef, excess capacity of lithium foil' &/lx,f6.1,'

Doyle, C.M.

2010-01-01T23:59:59.000Z

102

Lithium metal oxide electrodes for lithium cells and batteries  

DOE Patents [OSTI]

A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Amine, Khalil (Downers Grove, IL); Kim, Jaekook (Naperville, IL)

2004-01-13T23:59:59.000Z

103

Significant influence of insufficient lithium on electrochemical performance of lithium-rich layered oxide cathodes for lithium ion batteries  

Science Journals Connector (OSTI)

Abstract With an aim to broaden the understanding of the factors that govern electrochemical performance of lithium-rich layered oxide, the influences of insufficient lithium on reversible capacity, cyclic stability and rate capability of the oxide as cathode of lithium ion battery are investigated in this study. Various concentrations of lithium precursor are introduced to synthesize a target composition Li[Li0.13Ni0.30Ni0.57]O2, and the resulting products are characterized with inductively coupled plasma spectrum, scanning electron microscope, X-ray diffraction, Raman spectroscopy, and electrochemical measurements. The results indicate that the lithium content in the resulting oxide decreases with reducing the concentration of lithium precursor from 10wt%-excess lithium to stoichiometric lithium, due to insufficient compensation for lithium volatilization during synthesis process at high temperature. However, all these oxides still exhibit typically structural and electrochemical characteristics of lithium-rich layered oxides. Interestingly, with decreasing the Li content in the oxide, its reversible capacity increases due to relatively higher content of active transition-metal ions, while the cyclic stability degrades severely because of structural instability induced by higher content of Mn3+ ions and deeper lithium extraction.

Xingde Xiang; Weishan Li

2014-01-01T23:59:59.000Z

104

Thin-film Lithium Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Thin-Film Battery with Lithium Anode Courtesy of Oak Ridge National Laboratory, Materials Science and Technology Division Thin-Film Lithium Batteries Resources with Additional Information The Department of Energy's 'Oak Ridge National Laboratory (ORNL) has developed high-performance thin-film lithium batteries for a variety of technological applications. These batteries have high energy densities, can be recharged thousands of times, and are only 10 microns thick. They can be made in essentially any size and shape. Recently, Teledyne licensed this technology from ORNL to make batteries for medical devices including electrocardiographs. In addition, new "textured" cathodes have been developed which have greatly increased the peak current capability of the batteries. This greatly expands the potential medical uses of the batteries, including transdermal applications for heart regulation.'

105

Thin-film Rechargeable Lithium Batteries  

DOE R&D Accomplishments [OSTI]

Thin film rechargeable lithium batteries using ceramic electrolyte and cathode materials have been fabricated by physical deposition techniques. The lithium phosphorous oxynitride electrolyte has exceptional electrochemical stability and a good lithium conductivity. The lithium insertion reaction of several different intercalation materials, amorphous V{sub 2}O{sub 5}, amorphous LiMn{sub 2}O{sub 4}, and crystalline LiMn{sub 2}O{sub 4} films, have been investigated using the completed cathode/electrolyte/lithium thin film battery.

Dudney, N. J.; Bates, J. B.; Lubben, D.

1995-06-00T23:59:59.000Z

106

Imaging Lithium Air Electrodes | ornl.gov  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Neutron Imaging Reveals Lithium Distribution in Lithium-Air Electrodes Neutron Imaging Reveals Lithium Distribution in Lithium-Air Electrodes Agatha Bardoel - January 01, 2013 Image produced by neutron-computed tomography. The next step in revolutionizing electric vehicle capacity Research Contacts: Hassina Bilheux, Jagjit Nanda, and S. Pannala Using neutron-computed tomography, researchers at the CG-1D neutron imaging instrument at Oak Ridge National Laboratory's High Flux Isotope Reactor (HFIR) have successfully mapped the three-dimensional spatial distribution of lithium products in electrochemically discharged lithium-air cathodes. Lithium-air chemistry promises very high-energy density that, if successful, would revolutionize the world of electric vehicles by extending their range to 500 miles or more. The high-energy density comes from

107

Solid solution lithium alloy cermet anodes  

DOE Patents [OSTI]

A metal-ceramic composite ("cermet") has been produced by a chemical reaction between a lithium compound and another metal. The cermet has advantageous physical properties, high surface area relative to lithium metal or its alloys, and is easily formed into a desired shape. An example is the formation of a lithium-magnesium nitride cermet by reaction of lithium nitride with magnesium. The reaction results in magnesium nitride grains coated with a layer of lithium. The nitride is inert when used in a battery. It supports the metal in a high surface area form, while stabilizing the electrode with respect to dendrite formation. By using an excess of magnesium metal in the reaction process, a cermet of magnesium nitride is produced, coated with a lithium-magnesium alloy of any desired composition. This alloy inhibits dendrite formation by causing lithium deposited on its surface to diffuse under a chemical potential into the bulk of the alloy.

Richardson, Thomas J.

2013-07-09T23:59:59.000Z

108

Transparent lithium-ion batteries  

Science Journals Connector (OSTI)

...computers). Typically, a battery is composed of electrode...nanotubes (5, 7), graphene (11), and organic...is not suitable for batteries, because, to our knowledge...production of 30-inch graphene films for transparent electrodes...rechargeable lithium batteries . Nature 414 : 359 367...

Yuan Yang; Sangmoo Jeong; Liangbing Hu; Hui Wu; Seok Woo Lee; Yi Cui

2011-01-01T23:59:59.000Z

109

Synthesis and structural properties of lithium titanium oxide powder  

Science Journals Connector (OSTI)

Recently, lithium titanium oxide material has gained renewed interest in electrodes for lithium ion rechargeable batteries. We investigated the influence of excess Li on the structural characteristics of lithium ...

Soo Ho Kim; Kwang Hoon Lee; Baek Seok Seong

2006-11-01T23:59:59.000Z

110

High purity lithium iron phosphate/carbon composites prepared by using secondary lithium source  

Science Journals Connector (OSTI)

Abstract Various lithium salts including lithium carbonate, lithium hydroxide, lithium acetate and lithium citrate were used as secondary lithium sources for the synthesis of lithium iron phosphate/carbon composites with cheap iron sources in the form of Fe and FePO4. Samples were characterized by X-ray diffraction, scanning electron microscopy, cyclic voltammetry and constant-current chargedischarge tests. The results showed that lithium carbonate derived product generated a high purity LiFePO4 phase with high tap densities. Furthermore, satisfactory electrochemical performance with an initial discharge capacity of 146.1mAhg?1 at 0.5C rate and good capacity retention of 95.2% after 50cycles were achieved.

Jinhan Yao; Xiaohui Wang; Pinjie Zhang; Jianbo Wang; Jian Xie; Kondo-Francois Aguey-Zinsou; Chun'An Ma; Lianbang Wang

2013-01-01T23:59:59.000Z

111

Lithium borate cluster salts as novel redox shuttles for overcharge protection of lithium-ion cells.  

SciTech Connect (OSTI)

Redox shuttle is a promising mechanism for intrinsic overcharge protection in lithium-ion cells and batteries. Two lithium borate cluster salts are reported to function as both the main salt for a nonaqueous electrolyte and the redox shuttle for overcharge protection. Lithium borate cluster salts with a tunable redox potential are promising candidates for overcharge protection for most positive electrodes in state-of-the-art lithium-ion cells.

Chen, Z.; Liu, J.; Jansen, A. N.; Casteel, B.; Amine, K.; GirishKumar, G.; Air Products and Chemicals, Inc.

2010-01-01T23:59:59.000Z

112

Lithium Metal Oxide Electrodes For Lithium Cells And Batteries  

DOE Patents [OSTI]

A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Amine, Khalil (Downers Grove, IL); Kim, Jaekook (Naperville, IL)

2004-01-20T23:59:59.000Z

113

Lithium metal oxide electrodes for lithium cells and batteries  

DOE Patents [OSTI]

A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2M'O.sub.3 in which 0

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Amine, Khalil (Oakbrook, IL)

2008-12-23T23:59:59.000Z

114

designer phase transitions in lithium-based spinels  

SciTech Connect (OSTI)

When electrons in a metal become correlated with each other, new cooperative behavior can arise. This correlation is magnified when the metal has magnetic ions embedded in it. These atomic magnets try to line up with each other, but in doing so actually create a correlation between the motions of conduction electrons. In turn, these correlated electron motions prevent the magnetic ions from aligning, even at zero Kelvin. When this competition is strongest (at the so-called quantum critical point-QCP) the response of the system can no longer be described using the text book theory for metals. In addition, a range of new phenomena has been seen to emerge in the vicinity of a QCP, such as heavy-fermion superconductivity, coexistence of magnetism and superconductivity and hyper-scaling. The main goal of our research is to try to unravel the details of the feedback mechanism between electron motion and magnetism that lies at the heart of this new physics. We have chosen lithium-based spinel structures as the most promising family of systems to achieve our goal. Known lithium-based spinels Li{sub x}M{sub 2}O{sub 4} [M=V, Ti and Mn] show a variety of ground states: heavy-fermion, superconducting, or geometrically frustrated local moment systems. Li{sub x}M{sub 2}O{sub 4} should be ideal systems for studying QCPs since their properties can easily be fine-tuned, simply by extracting some Li [which can be done without introducing disorder in the immediate surroundings of the magnetic ions]. The premise of the proposal was that since this Li-extraction can be done both in the metallic as well as in insulating compounds, that we can expand the types of quantum phase transitions that can be studied to beyond transitions in magnetic metals. The project called for developing a better understanding of quantum phase transitions by measuring all aspects of the electronic response of Li{sub x}M{sub 2}O{sub 4} by means of neutron scattering, giving microscopic information about the behavior of the individual magnetic moments and their interactions, as well as by macroscopic measurements. In addition, the aim was to synthesize new lithium-based spinel compounds by using other transition metals that exhibit both 3{sup +} and 4{sup +} valencies. Here we report on the progress we have made during the course of this grant both towards the stated goals and on new avenues that developed as a direct result of the data we collected during this grant.

Wouter Montfrooij

2011-09-12T23:59:59.000Z

115

Polymers For Advanced Lithium Batteries | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Polymers For Advanced Lithium Batteries Polymers For Advanced Lithium Batteries 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and...

116

Polymers For Advanced Lithium Batteries | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Polymers For Advanced Lithium Batteries Polymers For Advanced Lithium Batteries 2011 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and...

117

Vehicle Technologies Office Merit Review 2014: High Energy Lithium...  

Broader source: Energy.gov (indexed) [DOE]

High Energy Lithium Batteries for PHEV Applications Vehicle Technologies Office Merit Review 2014: High Energy Lithium Batteries for PHEV Applications Presentation given by...

118

Additives and Cathode Materials for High-Energy Lithium Sulfur...  

Broader source: Energy.gov (indexed) [DOE]

Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries 2013 DOE Hydrogen and Fuel Cells...

119

Development of Polymer Electrolytes for Advanced Lithium Batteries...  

Broader source: Energy.gov (indexed) [DOE]

Development of Polymer Electrolytes for Advanced Lithium Batteries Development of Polymer Electrolytes for Advanced Lithium Batteries 2013 DOE Hydrogen and Fuel Cells Program and...

120

Electrolytes - R&D for Advanced Lithium Batteries. Interfacial...  

Broader source: Energy.gov (indexed) [DOE]

R&D for Advanced Lithium Batteries. Interfacial Behavior of Electrolytes Electrolytes - R&D for Advanced Lithium Batteries. Interfacial Behavior of Electrolytes 2012 DOE Hydrogen...

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

Manipulating the Surface Reactions in Lithium Sulfur Batteries...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode Structures. Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode...

122

Interface Modifications by Anion Acceptors for High Energy Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Modifications by Anion Acceptors for High Energy Lithium Ion Batteries. Interface Modifications by Anion Acceptors for High Energy Lithium Ion Batteries. Abstract: Li-rich, Mn-rich...

123

Hierarchically Porous Graphene as a Lithium-Air Battery Electrode...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Hierarchically Porous Graphene as a Lithium-Air Battery Electrode. Hierarchically Porous Graphene as a Lithium-Air Battery Electrode. Abstract: Functionalized graphene sheets (FGS)...

124

Exploring the interaction between lithium ion and defective graphene...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Exploring the interaction between lithium ion and defective graphene surface using dispersion corrected DFT studies. Exploring the interaction between lithium ion and defective...

125

Addressing the Voltage Fade Issue with Lithium-Manganese-Rich...  

Broader source: Energy.gov (indexed) [DOE]

Addressing the Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials Addressing the Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials 2013 DOE...

126

Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

15eswise2012p.pdf More Documents & Publications Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production Expansion of Novolyte Capacity for Lithium Ion Electrolyte...

127

Celgard US Manufacturing Facilities Initiative for Lithium-ion...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Celgard US Manufacturing Facilities Initiative for Lithium-ion Battery Separator Celgard US Manufacturing Facilities Initiative for Lithium-ion...

128

Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

15eswise2011p.pdf More Documents & Publications Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production Expansion of Novolyte Capacity for Lithium Ion Electrolyte...

129

New lithium-based ionic liquid electrolytes that resist salt...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

New lithium-based ionic liquid electrolytes that resist salt concentration polarization New lithium-based ionic liquid electrolytes that resist salt concentration polarization...

130

Dendrite-Free Lithium Deposition via Self-Healing Electrostatic...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electrostatic Shield Mechanism . Abstract: Lithium metal batteries are called the holy grail of energy storage systems. However, lithium dendrite growth in these...

131

Effects of Carbonate Solvents and Lithium Salts on Morphology...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Efficiency of Lithium Electrode. Abstract: The application of lithium (Li) metal anode in rechargeable batteries is hindered by Li dendrite growth during Li deposition and...

132

High-capacity hydrogen storage in lithium and sodium amidoboranes...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

capacity hydrogen storage in lithium and sodium amidoboranes. High-capacity hydrogen storage in lithium and sodium amidoboranes. Abstract: A substantial effort worldwide has been...

133

Lithium Metal Anodes for Rechargeable Batteries  

SciTech Connect (OSTI)

Rechargeable lithium metal batteries have much higher energy density than those of lithium ion batteries using graphite anode. Unfortunately, uncontrollable dendritic lithium growth inherent in these batteries (upon repeated charge/discharge cycling) and limited Coulombic efficiency during lithium deposition/striping has prevented their practical application over the past 40 years. With the emerging of post Li-ion batteries, safe and efficient operation of lithium metal anode has become an enabling technology which may determine the fate of several promising candidates for the next generation of energy storage systems, including rechargeable Li-air battery, Li-S battery, and Li metal battery which utilize lithium intercalation compounds as cathode. In this work, various factors which affect the morphology and Coulombic efficiency of lithium anode will be analyzed. Technologies used to characterize the morphology of lithium deposition and the results obtained by modeling of lithium dendrite growth will also be reviewed. At last, recent development in this filed and urgent need in this field will also be discussed.

Xu, Wu; Wang, Jiulin; Ding, Fei; Chen, Xilin; Nasybulin, Eduard N.; Zhang, Yaohui; Zhang, Jiguang

2014-02-28T23:59:59.000Z

134

Ternary compound electrode for lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and of light weight. One type of lithium-based cell utilizes a molten salt electrolyte and normally is operated in the temperature range of about 350 to 500/sup 0/C. Such high temperature operation accelerates corrosion problems. The present invention provides an electrochemical cell in which lithium is the electroactive species. The cell has a positive electrode which includes a ternary compound generally represented as Li-M-O, wherein M is a transition metal. Corrosion of the inventive cell is considerably reduced.

Raistrick, I.D.; Godshall, N.A.; Huggins, R.A.

1980-07-30T23:59:59.000Z

135

Block copolymer electrolytes for lithium batteries  

E-Print Network [OSTI]

connecting to the solid-state lithium battery. c. An opticalbattery (discounting packaging, tabs, etc. ) demonstrate the advantage of the solid-state

Hudson, William Rodgers

2011-01-01T23:59:59.000Z

136

LITHIUM-BASED ELECTROCHROMIC MIRRORS  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

870 870 rd Presented at the 203 Meeting of the Electrochemical Society, April 28-30, 2003 in Paris, France and published in the Proceedings. Lithium-Based Electrochromic Mirrors Thomas J. Richardson and Jonathan L. Slack Lawrence Berkeley National Laboratory April 2003 This work was supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Building Technology, State and Community Programs, Office of Building Research and Standards of the U.S. Department of Energy under Contract No. DE-AC03-76SF00098. LITHIUM-BASED ELECTROCHROMIC MIRRORS Thomas J. Richardson* and Jonathan L. Slack Building Technologies Department Environmental Energy Technologies Division Lawrence Berkeley National Laboratory Berkeley, California 94720, USA

137

Electrolytes for lithium ion batteries  

SciTech Connect (OSTI)

A family of electrolytes for use in a lithium ion battery. The genus of electrolytes includes ketone-based solvents, such as, 2,4-dimethyl-3-pentanone; 3,3-dimethyl 2-butanone(pinacolone) and 2-butanone. These solvents can be used in combination with non-Lewis Acid salts, such as Li.sub.2[B.sub.12F.sub.12] and LiBOB.

Vaughey, John; Jansen, Andrew N.; Dees, Dennis W.

2014-08-05T23:59:59.000Z

138

Lithium batteries for pulse power  

SciTech Connect (OSTI)

New designs of lithium batteries having bipolar construction and thin cell components possess the very low impedance that is necessary to deliver high-intensity current pulses. The R D and understanding of the fundamental properties of these pulse batteries have reached an advanced level. Ranges of 50--300 kW/kg specific power and 80--130 Wh/kg specific energy have been demonstrated with experimental high-temperature lithium alloy/transition-metal disulfide rechargeable bipolar batteries in repeated 1- to 100-ms long pulses. Other versions are designed for repetitive power bursts that may last up to 20 or 30 s and yet may attain high specific power (1--10 kW/kg). Primary high-temperature Li-alloy/FeS{sub 2} pulse batteries (thermal batteries) are already commercially available. Other high-temperature lithium systems may use chlorine or metal-oxide positive electrodes. Also under development are low-temperature pulse batteries: a 50-kW Li/SOCl{sub 2} primary batter and an all solid-state, polymer-electrolyte secondary battery. Such pulse batteries could find use in commercial and military applications in the near future. 21 refs., 8 figs.

Redey, L.

1990-01-01T23:59:59.000Z

139

ET Parameters for Mixed-Valence Ru Complexes  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Convergence of Spectroscopic and Kinetic Electron Transfer Parameters for Convergence of Spectroscopic and Kinetic Electron Transfer Parameters for Mixed-Valence Binuclear Dipyridylamide Ruthenium Ammine Complexes Alison J. Distefano, James F. Wishart, and Stephan S. Isied Coord. Chem. Rev. 249, 507-516 (2005). [Find paper at Elsevier Science Direct] Abstract: A series of binuclear ruthenium(II,III) pentaammine complexes bridged by 4-pyridyl isonicotinamide (iso-apy) and methyl, 4-pyridyl isonicotinamide (iso-mapy), and their mononuclear congeners, were studied by spectroscopic and kinetic techniques. The amide functionality provides asymmetry between the electronic environments of the metal ions bound to the aminopyridine (apy) and pyridine carbonyl (iso) ends. The resulting difference is observed in the charge transfer spectra and the

140

Nature of the Frequency Shift of Hydrogen Valence Vibrations  

E-Print Network [OSTI]

The physical nature of a frequency shift of hydrogen valence vibrations in a water molecule due to its interaction with neighbor molecules has been studied. Electrostatic forces connected with the multipole moments of molecules are supposed to give a dominating contribution to the intermolecular interaction. The frequency shift was calculated in the case where two neighbor molecules form a dimer. The obtained result is in qualitative agreement with the frequency shifts observed for water vapor, hexagonal ice, and liquid water, as well as for aqueous solutions of alcohols. This fact testifies to the electrostatic nature of H-bonds used to describe both the specific features of the intermolecular interaction in water and the macroscopic properties of the latter.

Zhyganiuk, I V

2015-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

Configuration interaction calculation of the specific mass shift for atoms with few valence electrons.  

E-Print Network [OSTI]

) calculation. If technically Electronic address: mgk@MF1309.spb.edu possible, we allow all configurations two valence electrons. II. DETAILS OF THE CALCULATIONS In this work we calculated SMS for the low-valence correlations were included. Si II, which has a ground state configuration 3s2 3p was calculated in [1] as a one-electron

Kozlov, Mikhail G

142

A mixed-valence copper coordination polymer generated by hydrothermal metal/ligand redox reactions  

E-Print Network [OSTI]

A mixed-valence copper coordination polymer generated by hydrothermal metal/ligand redox reactions A novel coordination polymer of mixed-valence copper(I,II) with 4,4A-bipyridine and in situ oxidized and crystallographically char- acterized to be a laminated structure via weak copper(II)­ oxygen interactions. Extended

Li, Jing

143

KWhOURS | Open Energy Information  

Open Energy Info (EERE)

Zip: 1982 Sector: Services Product: Massachusetts software maker which provides mobile data collection, calculation, and report generation services that reduce cost and time...

144

Electronic states of lithium passivated germanium nanowires: An ab-initio study  

SciTech Connect (OSTI)

A study of the electronic and structural properties of germanium nanowires (GeNWs) was performed using the ab-initio Density Functional Theory within the generalized gradient approximation where electron-ion interactions are described by ultrasoft pseudopotentials. To study the effects of the lithium in the surface of the GeNWs we compare the electronic band structures of Hydrogen passivated GeNWs with those of partial and totally Li passivated GeNWs. The nanowires were constructed in the [001], [111] and [110] directions, using the supercell model to create different wire diameters. The results show that in the case of partial Li passivation there are localized orbitals near the valence band maximum, which would create a p-doped-kind of state. The total Li passivation created metallic states for all the wires.

Trejo, A.; Carvajal, E.; Vzquez-Medina, R.; Cruz-Irisson, M. [Instituto Politcnico Nacional, ESIME-Culhuacan, Av. Santa Ana 1000, 04430 D.F. (Mexico)

2014-05-15T23:59:59.000Z

145

Jeff Chamberlain on Lithium-air batteries  

ScienceCinema (OSTI)

Jeff Chamberlain, technology transfer expert at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries. More information at http://www.anl.gov/Media_Center/News/2009/batteries090915.html

Chamberlain, Jeff

2013-04-19T23:59:59.000Z

146

Jeff Chamberlain on Lithium-air batteries  

SciTech Connect (OSTI)

Jeff Chamberlain, technology transfer expert at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries. More information at http://www.anl.gov/Media_Center/News/2009/batteries090915.html

Chamberlain, Jeff

2009-01-01T23:59:59.000Z

147

Discovery of pre-galactic lithium  

Science Journals Connector (OSTI)

... so these combined in nuclear reactions to make deuterium, helium-3, helium-4 and lithium-7, production of heavier elements being aborted by the absence of stable nuclei at ... other hand, is totally destroyed in matter cycled through stars, and helium-3 and lithium-7 can be both created and destroyed, so that the net effect of stellar ...

Bernard Pagel

1982-06-10T23:59:59.000Z

148

Advanced Electrolyte Additives for PHEV/EV Lithium-ion Battery  

Broader source: Energy.gov (indexed) [DOE]

calculation method and provide insights for the next step research of advanced additives. 5 Pristine Lithium uptake Lithium removal Lithium anodes - Instantaneous...

149

Surface reconstruction and chemical evolution of stoichiometric layered cathode materials for lithium-ion batteries  

E-Print Network [OSTI]

Li-Rich Layered Oxides for Lithium Batteries. Nano Lett. 13,O 2 Cathode Material in Lithium Ion Batteries. Adv. Energysolvent decomposition in lithium ion batteries: first-

Lin, Feng

2014-01-01T23:59:59.000Z

150

Aliovalent titanium substitution in layered mixed Li Ni-Mn-Co oxides for lithium battery applications  

E-Print Network [OSTI]

indicates that some of the excess lithium is indeed presentneither the presence of excess lithium on 3b sites nor ansamples not containing excess lithium. To minimize kinetic

Kam, Kinson

2011-01-01T23:59:59.000Z

151

How should findings on antisuicidal effects of lithium be integrated into practical treatment decisions?  

Science Journals Connector (OSTI)

Beyond its prophylactic efficacy lithium has demonstrated possibly specific antisuicidal effects. Lithium significantly reduces the high excess mortality of patients with affective disorders. Appropriate lithium ...

Prof.Dr.med. B. Mller-Oerlinghausen

2003-06-01T23:59:59.000Z

152

E-Print Network 3.0 - au-implanted lithium niobate Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

lithium niobate crystals Summary: O-doped lithium niobate crystals C. L. Sonesa Optoelectronics Research Centre, University of Southampton... lithium niobate crystals induced by...

153

Doubly Excited States in Lithium  

Science Journals Connector (OSTI)

Doubly and triply excited states of lithium are considered in an effort to identify the energy levels responsible for the several narrow lines present in the optical spectrum of that element which are not classifiable in the normal singly excited spectra of that atom. Since most of these states are coupled to continuum states through the electrostatic interaction of the electrons and will thus have extremely short lifetimes, a majority of the multiply excited states can be excluded from consideration in identifying these narrow lines. The observed narrow spectral lines can be plasuibly identified on the basis of screening-theory estimates of the energies.

J. D. Garcia and J. E. Mack

1965-05-17T23:59:59.000Z

154

Ab initio valence-bond cluster model for ionic solids: Alkaline-earth oxides  

Science Journals Connector (OSTI)

A linear M-O-M (M=metal, O=oxygen) cluster embedded in a Madelung field, and also including the quantum effects of the neighboring ions, is used to represent the alkaline-earth oxides. For this model an ab initio wave function is constructed as a linear combination of Slater determinants written in an atomic orbital basis set, i.e., a valence-bond wave function. Each valence-bond determinant (or group of determinants) corresponds to a resonating valence-bond structure. We have obtained ab initio valence-bond cluster-model wave functions for the electronic ground state and the excited states involved in the optical-gap transitions. Numerical results are reasonably close to the experimental values. Moreover, the model contains the ionic model as a limiting case and can be readily extended and improved.

A. Lorda; F. Illas; J. Rubio; J. B. Torrance

1993-03-15T23:59:59.000Z

155

Frontal brain electrical activity (EEG) distinguishes valence and intensity of musical emotions  

E-Print Network [OSTI]

Frontal brain electrical activity (EEG) distinguishes valence and intensity of musical emotions (i.e., positive vs. negative) and intensity (i.e., intense vs. calm) in a group of under- graduates

Trainor, Laurel J.

156

A rapid method for the determination of lithium transference numbers  

SciTech Connect (OSTI)

Lithium ion-conducting polymer electrolytes are of increasing interest for use in lithium-polymer batteries. Lithium transference numbers, the net fraction of current carried by lithium in a cell, are key figures of merit for potential lithium battery electrolytes. The authors describe the Electrophoretic NMR (ENMR) method for the determination of lithium ion transference numbers (T{sub Li}). The work presented is a proof-of-concept of the application of the ENMR method to lithium ion transference measurements for several different lithium salts in gelled electrolytes. The NMR method allows accurate determination of T{sub Li} values, as indicated by the similarity of T{sub Li} in the gelled electrolytes to those in aqueous electrolyte solutions at low salt concentration. Based on calculated tradeoffs of various experimental parameters, they also discuss some conclusions concerning the range of applicability of the method to other electrolytes with lower lithium mobility.

Zawodzinski, T.A. Jr.; Dai, H.; Sanderson, S.; Davey, J.; Uribe, F. [Los Alamos National Lab., NM (United States). Electronics Materials and Device Research Group

1997-05-01T23:59:59.000Z

157

A Material Change: Bringing Lithium Production Back to America | Department  

Broader source: Energy.gov (indexed) [DOE]

A Material Change: Bringing Lithium Production Back to America A Material Change: Bringing Lithium Production Back to America A Material Change: Bringing Lithium Production Back to America June 29, 2012 - 5:34pm Addthis The Rockwood Lithium manufacturing facility in Kings Mountain, North Carolina. | Photo courtesy of Rockwood Lithium. The Rockwood Lithium manufacturing facility in Kings Mountain, North Carolina. | Photo courtesy of Rockwood Lithium. Niketa Kumar Niketa Kumar Public Affairs Specialist, Office of Public Affairs Between 1980 and 2009, the global demand for lithium has tripled. This metal is a key material in a number of growing industries -- including advanced vehicle batteries and consumer electronics. But more specifically, lithium-ion batteries are a vital component in electric vehicles and other rechargeable batteries for consumer electronics, and are used to produce

158

Lithium-cation conductivity and crystal structure of lithium diphosphate  

SciTech Connect (OSTI)

The electrical conductivity of lithium diphosphate Li{sub 4}P{sub 2}O{sub 7} has been measured and jump-like increasing of ionic conductivity at 913 K has been found. The crystal structure of Li{sub 4}P{sub 2}O{sub 7} has been refined using high temperature neutron diffraction at 3001050 K. At 913 K low temperature triclinic form of Li{sub 4}P{sub 2}O{sub 7} transforms into high temperature monoclinic one, space group P2{sub 1}/n, a=8.8261(4) , b=5.2028(4) , c=13.3119(2) , ?=104.372(6). The migration maps of Li{sup +} cations based on experimental data implemented into program package TOPOS have been explored. It was found that lithium cations in both low- and high temperature forms of Li{sub 4}P{sub 2}O{sub 7} migrate in three dimensions. Cross sections of the migrations channels extend as the temperature rises, but at the phase transition point have a sharp growth showing a strong crystal structure ion conductivity correlation. -- Graphical abstract: Crystal structure of Li{sub 4}P{sub 2}O{sub 7} at 950 K. Red balls represent oxygen atoms; black lines show Li{sup +} ion migration channels in the layers perpendicular to [001] direction. Highlights: Structure of Li{sub 4}P{sub 2}O{sub 7} has been refined using high temperature neutron diffraction. At 913 K triclinic form of Li{sub 4}P{sub 2}O{sub 7} transforms into high temperature monoclinic one. The migration maps of Li{sup +} implemented into program package TOPOS have been explored. Cross sections of the migrations channels at the phase transition have a sharp growth.

Voronin, V.I., E-mail: voronin@imp.uran.ru [Institute of Metal Physics Urals Branch RAS, S.Kovalevskoy Street 18, 620041 Ekaterinburg (Russian Federation); Sherstobitova, E.A. [Institute of Metal Physics Urals Branch RAS, S.Kovalevskoy Street 18, 620041 Ekaterinburg (Russian Federation); Blatov, V.A., E-mail: blatov@samsu.ru [Samara Center for Theoretical Materials Science (SCTMS), Samara State University, Ac.Pavlov Street 1, 443011 Samara (Russian Federation); Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Shekhtman, G.Sh., E-mail: shekhtman@ihte.uran.ru [Institute of High Temperature Electrochemistry Urals Branch RAS, Akademicheskaya 20, 620990 Ekaterinburg (Russian Federation)

2014-03-15T23:59:59.000Z

159

The Saft Lithium Silver Chromate Battery Performances of the LI 210 Type  

Science Journals Connector (OSTI)

After being involved in lithium power sources research since 1964, SAFT perfected in 1970 a new couple: lithium...

G. Lehmann; M. Broussely; P. Lenfant

1978-01-01T23:59:59.000Z

160

Categorical Exclusion 4497: Lithium Wet Chemistry Project  

Broader source: Energy.gov (indexed) [DOE]

8/2012 07:36 8/2012 07:36 8655749041 ENVIRONMENTAL COMPL U.S. Department of Energy Categorical Exclusion Detennination Form Proposed Action Tills: Lithium W@t Chemistry Project (4597) Program or Fi~ld Oftke: Y-12 Site Office L&cationfs) (CiWLCount:r/State): Oak Ridge, Anderson County; Tennessee Proposed Action Description: PAGE 03/04 r: :;: :: !: s .a : brnl, i ~ y. : $ ~-rtl~il : t·:~::;J The proposed action is to develop a small lithium wet chemistry operation for the following purposes: (1) to capture wet chemistry operations, (2) to provide processing path for Lithium materials such as machine dust, (3) to provide lithium based materials, and (4) to produce the littlium hydroxide needed to support production. CategQrj~l Exclusion(s) Applied

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

California Lithium Battery, Inc. | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

California California Lithium Battery, Inc. America's Next Top Energy Innovator Challenge 626 likes California Lithium Battery, Inc. Argonne National Laboratory California Lithium Battery ("CALBattery") is a start-up California company established in 2011 to develop and manufacture a breakthrough high energy density and long cycle life lithium battery for utility energy storage, transportation, and defense industries. The company is a joint venture between California-based Ionex Energy Storage Systems and CALiB Power. US production of this advanced Very Large Format (400Ah+) si-graphene LI-ion battery is scheduled to start in California in 2014. Plans are to produce the initial batteries for CALBattery JV partner Ionex Energy Storage Systems for use in 1-100MW grid scale energy storage

162

Argonne Transportation - Lithium Battery Technology Patents  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Awarded Lithium Battery Technology Patents Awarded Lithium Battery Technology Patents "Composite-structure" material is a promising battery electrode for electric vehicles Argonne National Laboratory has been granted two U.S. patents (U.S. Pat. 6,677,082 and U.S. Pat. 6,680,143) on new "composite-structure" electrode materials for rechargeable lithium-ion batteries. Electrode compositions of this type are receiving worldwide attention. Such electrodes offer superior cost and safety features over state-of-the-art LiCoO2 electrodes that power conventional lithium-ion batteries. Moreover, they demonstrate outstanding cycling stability and can be charged and discharged at high rates, making them excellent candidates to replace LiCoO2 for consumer electronic applications and hybrid electric vehicles.

163

Towards Safer Lithium-Ion Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Towards Safer Lithium-Ion Batteries Towards Safer Lithium-Ion Batteries Speaker(s): Guoying Chen Date: October 25, 2007 - 12:00pm Location: 90-3122 Seminar Host/Point of Contact: Venkat Srinivasan Safety problems associated with rechargeable lithium batteries are now well recognized. Recent spectacular fires involving cell phones, laptops, and (here at LBNL) AA cells have made the news. These events are generally caused by overcharging and subsequent development of internal shorts. Before these batteries can be used in vehicle applications, improvement in cell safety is a must. We have been active in the area of lithium battery safety for many years. For example, a versatile, inexpensive overcharge protection approach developed in our laboratory, uses an electroactive polymer to act as a reversible, self-actuating, low resistance internal

164

Rotation, inflation, and lithium in the Pleiades  

E-Print Network [OSTI]

The rapidly rotating cool dwarfs of the Pleiades are rich in lithium relative to their slowly rotating counterparts. Motivated by observations of inflated radii in young, active stars, and by calculations showing that radius inflation inhibits pre-main sequence (pre-MS) Li destruction, we test whether this pattern could arise from a connection between stellar rotation rate and radius inflation on the pre-MS. We demonstrate that pre-MS radius inflation can efficiently suppress lithium destruction by rotationally induced mixing, and that the net effect of inflation and rotational mixing is a pattern where rotation correlates with lithium abundance for $M_{*} {\\rm M}_{\\odot}$, similar to the empirical trend in the Pleiades. Next, we adopt different prescriptions for the dependence of inflation on rotation, and compare their predictions to the Pleiades lithium/rotation pattern. A connection between rotation and radius inflation naturally and generically reproduces the important qualitative features of this patte...

Somers, Garrett

2014-01-01T23:59:59.000Z

165

Layered electrodes for lithium cells and batteries  

DOE Patents [OSTI]

Lithium metal oxide compounds of nominal formula Li.sub.2MO.sub.2, in which M represents two or more positively charged metal ions, selected predominantly and preferably from the first row of transition metals are disclosed herein. The Li.sub.2MO.sub.2 compounds have a layered-type structure, which can be used as positive electrodes for lithium electrochemical cells, or as a precursor for the in-situ electrochemical fabrication of LiMO.sub.2 electrodes. The Li.sub.2MO.sub.2 compounds of the invention may have additional functions in lithium cells, for example, as end-of-discharge indicators, or as negative electrodes for lithium cells.

Johnson, Christopher S. (Naperville, IL); Thackeray, Michael M. (Naperville, IL); Vaughey, John T. (Elmhurst, IL); Kahaian, Arthur J. (Chicago, IL); Kim, Jeom-Soo (Naperville, IL)

2008-04-15T23:59:59.000Z

166

Side Reactions in Lithium-Ion Batteries  

E-Print Network [OSTI]

2.8 V vs. lithium suggests Tafel kinetics, but the bend in? a gives the slope of the Tafel region, k eff affects itsincreases, the slope of the Tafel region remains constant,

Tang, Maureen Han-Mei

2012-01-01T23:59:59.000Z

167

Design and Simulation of Lithium Rechargeable Batteries  

E-Print Network [OSTI]

A New Rechargeable Plastic Li-Ion Battery," Lithium Batteryion battery developed at Bellcore in Red Bank, NJ.1-6 The experimental prototYpe cell has the configuration: Li

Doyle, C.M.

2010-01-01T23:59:59.000Z

168

California Lithium Battery, Inc. | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

California California Lithium Battery, Inc. America's Next Top Energy Innovator Challenge 626 likes California Lithium Battery, Inc. Argonne National Laboratory California Lithium Battery ("CALBattery") is a start-up California company established in 2011 to develop and manufacture a breakthrough high energy density and long cycle life lithium battery for utility energy storage, transportation, and defense industries. The company is a joint venture between California-based Ionex Energy Storage Systems and CALiB Power. US production of this advanced Very Large Format (400Ah+) si-graphene LI-ion battery is scheduled to start in California in 2014. Plans are to produce the initial batteries for CALBattery JV partner Ionex Energy Storage Systems for use in 1-100MW grid scale energy storage

169

California Lithium Battery, Inc. | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

California California Lithium Battery, Inc. America's Next Top Energy Innovator Challenge 626 likes California Lithium Battery, Inc. Argonne National Laboratory California Lithium Battery ("CALBattery") is a start-up California company established in 2011 to develop and manufacture a breakthrough high energy density and long cycle life lithium battery for utility energy storage, transportation, and defense industries. The company is a joint venture between California-based Ionex Energy Storage Systems and CALiB Power. US production of this advanced Very Large Format (400Ah+) si-graphene LI-ion battery is scheduled to start in California in 2014. Plans are to produce the initial batteries for CALBattery JV partner Ionex Energy Storage Systems for use in 1-100MW grid scale energy storage

170

Design and simulation of lithium rechargeable batteries  

SciTech Connect (OSTI)

Lithium -based rechargeable batteries that utilize insertion electrodes are being considered for electric-vehicle applications because of their high energy density and inherent reversibility. General mathematical models are developed that apply to a wide range of lithium-based systems, including the recently commercialized lithium-ion cell. The modeling approach is macroscopic, using porous electrode theory to treat the composite insertion electrodes and concentrated solution theory to describe the transport processes in the solution phase. The insertion process itself is treated with a charge-transfer process at the surface obeying Butler-Volmer kinetics, followed by diffusion of the lithium ion into the host structure. These models are used to explore the phenomena that occur inside of lithium cells under conditions of discharge, charge, and during periods of relaxation. Also, in order to understand the phenomena that limit the high-rate discharge of these systems, we focus on the modeling of a particular system with well-characterized material properties and system parameters. The system chosen is a lithium-ion cell produced by Bellcore in Red Bank, NJ, consisting of a lithium-carbon negative electrode, a plasticized polymer electrolyte, and a lithium-manganese-oxide spinel positive electrode. This battery is being marketed for consumer electronic applications. The system is characterized experimentally in terms of its transport and thermodynamic properties, followed by detailed comparisons of simulation results with experimental discharge curves. Next, the optimization of this system for particular applications is explored based on Ragone plots of the specific energy versus average specific power provided by various designs.

Doyle, C.M.

1995-08-01T23:59:59.000Z

171

Predissociation dynamics of lithium iodide  

E-Print Network [OSTI]

The predissociation dynamics of lithium iodide (LiI) in the first excited A-state is investigated for molecules in the gas phase and embedded in helium nanodroplets, using femtosecond pump-probe photoionization spectroscopy. In the gas phase, the transient Li+ and LiI+ ion signals feature damped oscillations due to the excitation and decay of a vibrational wave packet. Based on high-level ab initio calculations of the electronic structure of LiI and simulations of the wave packet dynamics, the exponential signal decay is found to result from predissociation predominantly at the lowest avoided X-A potential curve crossing, for which we infer a coupling constant V=650(20) reciprocal cm. The lack of a pump-probe delay dependence for the case of LiI embedded in helium nanodroplets indicates fast droplet-induced relaxation of the vibrational excitation.

Schmidt, H; Stienkemeier, F; Bogomolov, A S; Baklanov, A V; Reich, D M; Skomorowski, W; Koch, C P; Mudrich, M

2015-01-01T23:59:59.000Z

172

Electrode for a lithium cell  

DOE Patents [OSTI]

This invention relates to a positive electrode for an electrochemical cell or battery, and to an electrochemical cell or battery; the invention relates more specifically to a positive electrode for a non-aqueous lithium cell or battery when the electrode is used therein. The positive electrode includes a composite metal oxide containing AgV.sub.3O.sub.8 as one component and one or more other components consisting of LiV.sub.3O.sub.8, Ag.sub.2V.sub.4O.sub.11, MnO.sub.2, CF.sub.x, AgF or Ag.sub.2O to increase the energy density of the cell, optionally in the presence of silver powder and/or silver foil to assist in current collection at the electrode and to improve the power capability of the cell or battery.

Thackeray, Michael M. (Naperville, IL); Vaughey, John T. (Elmhurst, IL); Dees, Dennis W. (Downers Grove, IL)

2008-10-14T23:59:59.000Z

173

Glass for sealing lithium cells  

DOE Patents [OSTI]

Glass compositions resistant to corrosion by lithium cell electrolyte and having an expansion coefficient of 45 to 85 x 10/sup -70/C/sup -1/ have been made with SiO/sub 2/, 25 to 55% by weight; B/sub 2/O/sub 3/, 5 to 12%; Al/sub 2/O/sub 3/, 12 to 35%; CaO, 5 to 15%; MgO, 5 to 15%; SrO, 0 to 10%; and La/sub 2/O/sub 3/, 0 to 5%. Preferred compositions within that range contain 3 to 8% SrO and 0.5 to 2.5% La/sub 2/O/sub 3/.

Leedecke, C.J.

1981-08-28T23:59:59.000Z

174

Reducing Foreign Lithium Dependence through Co-Production of Lithium from Geothermal Brine  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Foreign Lithium Dependence through Co-Production of Lithium from Foreign Lithium Dependence through Co-Production of Lithium from Geothermal Brine Kerry Klein 1 , Linda Gaines 2 1 New West Technologies LLC, Washington, DC, USA 2 Center for Transportation Research, Argonne National Laboratory, Argonne, IL, USA KEYWORDS Mineral extraction, zinc, silica, strategic metals, Imperial Valley, lithium ion batteries, electric- drive vehicles, battery recycling ABSTRACT Following a 2009 investment of $32.9 billion in renewable energy and energy efficiency research through the American Recovery and Reinvestment Act, President Obama in his January 2011 State of the Union address promised deployment of one million electric vehicles by 2015 and 80% clean energy by 2035. The United States seems poised to usher in its bright energy future,

175

Sorption of lithium from a geothermal brine by pelletized mixed aluminum-lithium hydrous oxides  

SciTech Connect (OSTI)

An inorganic ion exchanger was evaluated by the Bureau of Mines for recovering lithium from geothermal brines. The ion exchanger or sorbent was mixed hydrous oxide of aluminum and lithium that had been dried at 100 C. The dried precipitate was pelletized with a sodium silicate binder to improve flow rates in sorption tests. The sorbent was loaded to 2 mg Li/g of pellets and sorption from the solution was independent of the concentrations of Ca, Fe, Mn, and Zn. Manganese and zinc were sorbed by the pellets but did not suppress lithium sorption. Lithium was desorbed with water, but none of the washing solutions investigated removed entrained brine without stripping lithium. The complex nature of the sorption mechanisms is discussed.

Schultze, L.E.; Bauer, D.J.

1985-01-01T23:59:59.000Z

176

Molecular Structures of Polymer/Sulfur Composites for Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long Cycle Life. Molecular Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long...

177

Direct Evidence of Lithium-Induced Atomic Ordering in Amorphous...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Evidence of Lithium-Induced Atomic Ordering in Amorphous TiO2 Nanotubes . Direct Evidence of Lithium-Induced Atomic Ordering in Amorphous TiO2 Nanotubes . Abstract: In this paper,...

178

Promises and Challenges of Lithium- and Manganese-Rich Transition...  

Broader source: Energy.gov (indexed) [DOE]

Promises and Challenges of Lithium- and Manganese-Rich Transition-Metal Layered-Oxide Cathodes Promises and Challenges of Lithium- and Manganese-Rich Transition-Metal Layered-Oxide...

179

Development of Large Format Lithium Ion Cells with Higher Energy...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Large Format Lithium Ion Cells with Higher Energy Density Exceeding 500WhL Development of Large Format Lithium Ion Cells with Higher Energy Density Exceeding 500WhL 2012 DOE...

180

Mitigating Performance Degradation of High-Energy Lithium-Ion...  

Broader source: Energy.gov (indexed) [DOE]

Mitigating Performance Degradation of High-Energy Lithium-Ion Cells Mitigating Performance Degradation of High-Energy Lithium-Ion Cells 2013 DOE Hydrogen and Fuel Cells Program and...

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

Two Studies Reveal Details of Lithium-Battery Function  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Two Studies Reveal Details of Lithium-Battery Function Two Studies Reveal Details of Lithium-Battery Function Print Wednesday, 27 February 2013 00:00 Our way of life is deeply...

182

Shell Model for Atomistic Simulation of Lithium Diffusion in...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Shell Model for Atomistic Simulation of Lithium Diffusion in Mixed MnTi Oxides. Shell Model for Atomistic Simulation of Lithium Diffusion in Mixed MnTi Oxides. Abstract: Mixed...

183

Microplasticity and fatigue of some magnesium-lithium alloys  

Science Journals Connector (OSTI)

Cyclic stress-strain curves have been obtained for a series of magnesium-lithium alloys with lithium contents up to 12. 5wt%. The ... hardening exponents for stresses leading to failure in excess of 104...cycles ...

R. E. Lee; W. J. D. Jones

1974-03-01T23:59:59.000Z

184

Lithium-ion batteries having conformal solid electrolyte layers  

DOE Patents [OSTI]

Hybrid solid-liquid electrolyte lithium-ion battery devices are disclosed. Certain devices comprise anodes and cathodes conformally coated with an electron insulating and lithium ion conductive solid electrolyte layer.

Kim, Gi-Heon; Jung, Yoon Seok

2014-05-27T23:59:59.000Z

185

Nature of Bridging Bonds in Lithium and Potassium Acetate Dimers  

Science Journals Connector (OSTI)

The structures of lithium and potassium acetates were studied by the RHF/6-31G*...3COOLi)2 and (CH3COOK)2 are electrostatic in nature. The bridging lithium bond is intermediate between hydrogen and ionic, ... of ...

I. A. Panteleev; S. G. Semenov; D. N. Glebovskii

186

Loading of emulsions stacks with aqueous solutions of lithium acetate  

Science Journals Connector (OSTI)

It has been shown that thick pellicles can be loaded with lithium acetate solutions still maintaining all the desirable geometrical ... purpose of the method, that of introducing lithium atoms in the emulsion, th...

D. H. Davis; R. Levi Setti; M. Raymund; G. Tomasini

1962-11-01T23:59:59.000Z

187

Lithium carbide is prospective material for breeder of fusion reactor  

Science Journals Connector (OSTI)

It is shown that lithium carbide is a prospective material for breeder of fusion reactor. The lithium carbide equivalent dose rate reaches...?5...Sv/h) one minute after the irradiation with fusion reactor neutron...

M. V. Alenina; V. P. Kolotov; Yu. M. Platov

2014-03-01T23:59:59.000Z

188

Electrolytes - R&D for Advanced Lithium Batteries. Interfacial...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Electrolytes - R&D for Advanced Lithium Batteries. Interfacial Behavior of Electrolytes Interfacial Behavior of Electrolytes...

189

Methods for making lithium vanadium oxide electrode materials  

DOE Patents [OSTI]

A method of making vanadium oxide formulations is presented. In one method of preparing lithium vanadium oxide for use as an electrode material, the method involves: admixing a particulate form of a lithium compound and a particulate form of a vanadium compound; jet milling the particulate admixture of the lithium and vanadium compounds; and heating the jet milled particulate admixture at a temperature below the melting temperature of the admixture to form lithium vanadium oxide.

Schutts, Scott M. (Menomonie, WI); Kinney, Robert J. (Woodbury, MN)

2000-01-01T23:59:59.000Z

190

Capture of carbon dioxide over porous solid adsorbents lithium silicate, lithium aluminate and magnesium aluminate at pre-combustion temperatures  

Science Journals Connector (OSTI)

The capturing process for carbon dioxide over porous solid adsorbents such as ... resonance (NMR), and surface area. The capturing of carbon dioxide over lithium silicate, lithium aluminate, ... as exposure time,...

P. V. Korake; A. G. Gaikwad

2011-06-01T23:59:59.000Z

191

Use of Lithium Hexafluoroisopropoxide as a Mild Base for  

E-Print Network [OSTI]

Use of Lithium Hexafluoroisopropoxide as a Mild Base for Horner-Wadsworth-Emmons Olefination The weak base lithium 1,1,1,3,3,3-hexafluoroisopropoxide (LiHFI) is shown to be highly effective of base-sensitive substrates, leading to the discovery that lithium 1,1,1,3,3,3-hexafluoroisopropoxide (Li

192

RESONANT FARADAY ROTATION IN A HOT LITHIUM VAPOR  

E-Print Network [OSTI]

RESONANT FARADAY ROTATION IN A HOT LITHIUM VAPOR By SCOTT RUSSELL WAITUKAITIS A Thesis Submitted: #12;Abstract I describe a study of Faraday rotation in a hot lithium vapor. I begin by dis- cussing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 2.3 The Lithium Oven and Solenoid . . . . . . . . . . . . . . . . . 7 3 Theoretical Framework

Cronin, Alex D.

193

Proposal on Lithium Wall Experiment (LWX) on PBXM 1  

E-Print Network [OSTI]

Proposal on Lithium Wall Experiment (LWX) on PBX­M 1 Leonid E. Zakharov, Princeton University; OUTLINE 1. Mini­conference on Lithium walls and low recycling regime. 2. PBX­M Capabilities. 3. Motivation "Lithium covered walls and low recycling regimes in toka­ maks". APS meeting, October 23­27, 2000, Quebec

Zakharov, Leonid E.

194

Mechanism of Acylation of Lithium Phenylacetylide with a Weinreb Amide  

E-Print Network [OSTI]

with the excess lithium acetylide and a 1:3 (alkox- ide-rich) mixed tetramer. The stabilities of the mixedMechanism of Acylation of Lithium Phenylacetylide with a Weinreb Amide Bo Qu and David B. CollumVersity, Ithaca, New York 14853-1301 dbc6@cornell.edu ReceiVed June 14, 2006 Additions of lithium phenylacetylide

Collum, David B.

195

Lithium Ion Batteries DOI: 10.1002/anie.201103163  

E-Print Network [OSTI]

Lithium Ion Batteries DOI: 10.1002/anie.201103163 LiMn1?xFexPO4 Nanorods Grown on Graphene Sheets for Ultrahigh- Rate-Performance Lithium Ion Batteries** Hailiang Wang, Yuan Yang, Yongye Liang, Li-Feng Cui cathode materials for rechargeable lithium ion batteries (LIBs) owing to their high capacity, excellent

Cui, Yi

196

Mechanical Properties of Lithium-Ion Battery Separator Materials  

E-Print Network [OSTI]

Mechanical Properties of Lithium-Ion Battery Separator Materials Patrick Sinko B.S. Materials Science and Engineering 2013, Virginia Tech John Cannarella PhD. Candidate Mechanical and Aerospace and motivation ­ Why study lithium-ion batteries? ­ Lithium-ion battery fundamentals ­ Why study the mechanical

Petta, Jason

197

Lithium intercalated graphite : experimental Compton profile for stage one  

E-Print Network [OSTI]

L-301 Lithium intercalated graphite : experimental Compton profile for stage one G. Loupias, J différence des profils Compton est compatible avec un transfert total de l'électron de conduction du lithium électronique due à l'insertion. Abstract. 2014 Electron momentum distribution of the first stage lithium

Paris-Sud XI, Université de

198

Lithium Niobate Devices in Switching and Multiplexing [and Discussion  

Science Journals Connector (OSTI)

28 September 1989 research-article Lithium Niobate Devices in Switching and Multiplexing...Thylen Integrated-optics devices in lithium niobate have reached a significant maturity...in fibre-optic transmission systems, lithium niobate devices currently offer the only...

1989-01-01T23:59:59.000Z

199

LITHIUM--2002 46.1 By Joyce A. Ober  

E-Print Network [OSTI]

recycling operation in Trail, British Columbia, Canada. Another ToxCo subsidiary, Ozark Fluorine Specialties, the concentration of the brine increases through solar evaporation to 6,000 ppm lithium. When the lithium chloride carbonate production. Australia, Canada, and Zimbabwe were important sources of lithium concentrates

200

Evaporated Lithium Surface Coatings in NSTX  

SciTech Connect (OSTI)

Two lithium evaporators were used to evaporate more than 100 g of lithium on to the NSTX lower divertor region. Prior to each discharge, the evaporators were withdrawn behind shutters, where they also remained during the subsequent HeGDC applied for periods up to 9.5 min. After the HeGDC, the shutters were opened and the LITERs were reinserted to deposit lithium on the lower divertor target for 10 min, at rates of 10-70 mg/min, prior to the next discharge. The major improvements in plasma performance from these lithium depositions include: (1) plasma density reduction as a result of lithium deposition; (2) suppression of ELMs; (3) improvement of energy confinement in a low-triangularity shape; (4) improvement in plasma performance for standard, high-triangularity discharges: (5) reduction of the required HeGDC time between discharges; (6) increased pedestal electron and ion temperature; (7) reduced SOL plasma density; and (8) reduced edge neutral density. (C) 2009 Elsevier B.V. All rights reserved

Kugel, H. W. [Princeton Plasma Physics Laboratory (PPPL); Mansfield, D. [Princeton Plasma Physics Laboratory (PPPL); Maingi, Rajesh [ORNL; Bell, M. G. [Princeton Plasma Physics Laboratory (PPPL); Bell, R. E. [Princeton Plasma Physics Laboratory (PPPL); Allain, J. P. [Purdue University; Gates, D. [Princeton Plasma Physics Laboratory (PPPL); Gerhardt, S. P. [Princeton Plasma Physics Laboratory (PPPL); Kaita, R. [Princeton Plasma Physics Laboratory (PPPL); Kallman, J. [Princeton Plasma Physics Laboratory (PPPL); Kaye, S. [Princeton Plasma Physics Laboratory (PPPL); LeBlanc, B. P. [Princeton Plasma Physics Laboratory (PPPL); Majeski, R. [Princeton Plasma Physics Laboratory (PPPL); Menard, J. [Princeton Plasma Physics Laboratory (PPPL); Mueller, D. [Princeton Plasma Physics Laboratory (PPPL); Ono, M. [Princeton Plasma Physics Laboratory (PPPL); Paul, S. [Princeton Plasma Physics Laboratory (PPPL); Raman, R. [University of Washington, Seattle; Roquemore, A. L. [Princeton Plasma Physics Laboratory (PPPL); Ross, P. W. [Princeton Plasma Physics Laboratory (PPPL); Sabbagh, S. A. [Columbia University; Schneider, H. [Princeton Plasma Physics Laboratory (PPPL); Skinner, C. H. [Princeton Plasma Physics Laboratory (PPPL); Soukhanovskii, V. [Lawrence Livermore National Laboratory (LLNL); Stevenson, T. [Princeton Plasma Physics Laboratory (PPPL); Timberlake, J. [Princeton Plasma Physics Laboratory (PPPL); Wampler, W. R. [Sandia National Laboratories (SNL); Wilgen, John B [ORNL; Zakharov, L. E. [Princeton Plasma Physics Laboratory (PPPL)

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Evaporated Lithium Surface Coatings in NSTX  

SciTech Connect (OSTI)

Two lithium evaporators were used to evaporate more than 100 g of lithium on to the NSTX lower divertor region. Prior to each discharge, the evaporators were withdrawn behind shutters, where they also remained during the subsequent HeGDC applied for periods up to 9.5 min. After the HeGDC, the shutters were opened and the LITERs were reinserted to deposit lithium on the lower divertor target for 10 min, at rates of 10-70 mg/min, prior to the next discharge. The major improvements in plasma performance from these lithium depositions include: 1) plasma density reduction as a result of lithium deposition; 2) suppression of ELMs; 3) improvement of energy confinement in a low-triangularity shape; 4) improvement in plasma performance for standard, high-triangularity discharges; 5) reduction of the required HeGDC time between discharges; 6) increased pedestal electron and ion temperature; 7) reduced SOL plasma density; and 8) reduced edge neutral density.

Kugel, H. W.; Mansfield, D.; Maingi, R.; Bel, M. G.; Bell, R. E.; Allain, J. P.; Gates, D.; Gerhardt, S.; Kaita, R.; Kallman, J.; Kaye, S.; LeBlanc, B.; Majeski, R.; Menard, J.; Mueller, D.; Ono, M.

2009-04-09T23:59:59.000Z

202

Evaporated lithium surface coatings in NSTX.  

SciTech Connect (OSTI)

Two lithium evaporators were used to evaporate more than 100 g of lithium on to the NSTX lower divertor region. Prior to each discharge, the evaporators were withdrawn behind shutters, where they also remained during the subsequent HeGDC applied for periods up to 9.5 min. After the HeGDC, the shutters were opened and the LITERs were reinserted to deposit lithium on the lower divertor target for 10 min, at rates of 10-70 mg/min, prior to the next discharge. The major improvements in plasma performance from these lithium depositions include: (1) plasma density reduction as a result of lithium deposition; (2) suppression of ELMs; (3) improvement of energy confinement in a low-triangularity shape; (4) improvement in plasma performance for standard, high-triangularity discharges; (5) reduction of the required HeGDC time between discharges; (6) increased pedestal electron and ion temperature; (7) reduced SOL plasma density; and (8) reduced edge neutral density.

Zakharov, L. (Princeton Plasma Physics Laboratory, Princeton, NJ); Gates, D. (Princeton Plasma Physics Laboratory, Princeton, NJ); Menard, J. (Princeton Plasma Physics Laboratory, Princeton, NJ); Maingi, R. (Oak Ridge National Laboratory, Oak Ridge, TN); Schneider, H. (Princeton Plasma Physics Laboratory, Princeton, NJ); Mueller, D. (Princeton Plasma Physics Laboratory, Princeton, NJ); Wampler, William R.; Roquemore, A. L. (Princeton Plasma Physics Laboratory, Princeton, NJ); Kallman, Jeffrey K. (Princeton Plasma Physics Laboratory, Princeton, NJ); Sabbagh, S. (Columbia University, New York, NY); LeBlanc, B. (Princeton Plasma Physics Laboratory, Princeton, NJ); Raman, R. (University of Washington, Seattle, WA); Ono, M. (Princeton Plasma Physics Laboratory, Princeton, NJ); Wilgren, J. (Oak Ridge National Laboratory, Oak Ridge, TN); Allain, J.P. (Purdue University, West Lafayette, IN); Timberlake, J. (Princeton Plasma Physics Laboratory, Princeton, NJ); Stevenson, T. (Princeton Plasma Physics Laboratory, Princeton, NJ); Ross, P. W. (Princeton Plasma Physics Laboratory, Princeton, NJ); Majeski, R. (Princeton Plasma Physics Laboratory, Princeton, NJ); Kugel, Henry W. (Princeton Plasma Physics Laboratory, Princeton, NJ); Skinner, C. H. (Princeton Plasma Physics Laboratory, Princeton, NJ); Gerhardt, S. (Princeton Plasma Physics Laboratory, Princeton, NJ); Paul, S. (Princeton Plasma Physics Laboratory, Princeton, NJ); Bell, R. (Princeton Plasma Physics Laboratory, Princeton, NJ); Kaye, S. M. (Princeton Plasma Physics Laboratory, Princeton, NJ); Kaita, R. (Princeton Plasma Physics Laboratory, Princeton, NJ); Soukhanovskii, V. (Lawrence Livermore National Laboratory, Livermore, CA); Bell, Michael G. (Princeton Plasma Physics Laboratory, Princeton, NJ); Mansfield, D. (Princeton Plasma Physics Laboratory, Princeton, NJ)

2008-08-01T23:59:59.000Z

203

In Situ Ambient Pressure X-ray Photoelectron Spectroscopy Studies of Lithium-Oxygen Redox Reactions  

SciTech Connect (OSTI)

The lack of fundamental understanding of the oxygen reduction and oxygen evolution in nonaqueous electrolytes significantly hinders the development of rechargeable lithium-air batteries. Here we employ a solid-state Li4+xTi5O12/LiPON/LixV2O5 cell and examine in situ the chemistry of Li-O2 reaction products on LixV2O5 as a function of applied voltage under ultra high vacuum (UHV) and near ambient-pressure of oxygen using X-ray photoelectron spectroscopy (APXPS). Oxygen reduction and evolution reactions take place on the surface of the mixed electronic and Li+ ionic conductor, LixV2O5, which eliminate parasitic reactions between oxygen reduction/evolution reaction intermediates and aprotic electrolytes used in Li-O2 batteries reported to date. Under UHV, reversible lithium intercalation and de-intercalation from LixV2O5 was noted, where the changes in the vanadium valence state revealed from XPS in this study were comparable to that reported previously from Li/LixV2O5 thin film batteries. In presence of oxygen near ambient pressure, the LixV2O5 surface was covered gradually by the reaction product of oxygen reduction, namely lithium peroxide (Li2O2) (approximately 1-2 unit cells) upon discharge. Interestingly, the LixV2O5 surface became re-exposed upon charging, and the oxidation of Li2O2 began at much lower overpotentials (~240 mV) than the charge overpotentials of Li-O2 cells (~1000 mV) with aprotic electrolytes, which can be attributed to subnanometer-thick Li2O2 with surfaces free of contaminants such as carbonate species. Our study provides first evidence of reversible lithium peroxide formation and decomposition in situ on an oxide surface using a solid-state cell, and new insights into the reaction mechanism of Li-O2 chemistry.

Lu, Yi-chun [Massachusetts Institute of Technology (MIT); Crumlin, Ethan [Massachusetts Institute of Technology (MIT); Veith, Gabriel M [ORNL; Harding, Jonathon [Massachusetts Institute of Technology (MIT); Dudney, Nancy J [ORNL; Liu, Zhi [Lawrence Berkeley National Laboratory (LBNL); Shao-Horn, Yang [Massachusetts Institute of Technology (MIT)

2012-01-01T23:59:59.000Z

204

Mixed valency and site-preference chemistry for cerium and its compounds: A predictive density-functional theory study  

SciTech Connect (OSTI)

Cerium and its technologically relevant compounds are examples of anomalous mixed valency, originating from two competing oxidation statesitinerant Ce4+ and localized Ce3+. Under applied stress, anomalous transitions are observed but not well understood. Here we treat mixed valency as an alloy problem involving two valences with competing and numerous site-occupancy configurations. We use density-functional theory with Hubbard U (i.e., DFT+U) to evaluate the effective valence and predict properties, including controlling the valence by pseudoternary alloying. For Ce and its compounds, such as (Ce,La)2(Fe,Co)14B permanent magnets, we find a stable mixed-valent ? state near the spectroscopic value of ?s=3.53. Ce valency in compounds depends on its steric volume and local chemistry. For La doping, Ce valency shifts towards ?-like Ce3+, as expected from steric volume; for Co doping, valency depends on local Ce-site chemistry and steric volume. Our approach captures the key origins of anomalous valency and site-preference chemistry in complex compounds.

Alam, Aftab [Ames Laboratory; Johnson, Duane D. [Ames Laboratory

2014-06-01T23:59:59.000Z

205

Magnetic moment of atomic lithium  

Science Journals Connector (OSTI)

Bound-state relativistic contributions to the gJ factor of ground-state atomic lithium are calculated and compared with the experimental value gJ(Li)ge=1-(8.90.4)10-6, where ge is the free-electron g factor. This comparison is taken as the basis for judging the accuracy of several different Li wave functions taken from the literature. Most of these wave functions give agreement with the experimental value within the experimental uncertainty. A more precise experimental measurement would be desirable in order to provide a more stringent test. A wave function of the restricted Hartree-Fock type, however, leads to a value which is in disagreement with the experimental value. This is attributed to the inability of the restricted Hartree-Fock function to account for the exchange polarization of the 1s2 core electrons; the latter are found to contribute about -1.2 10-6 to gJ(Li)ge, or about 13% of the total relativistic correction. In addition to the dominant relativistic corrections of order ?2, radiative corrections (order ?3), and nuclear-mass corrections (order ?2mM) are also calculated. An isotopic shift gJ(Li6)gJ(Li7)=1+3.010-11 is predicted. The experimental measurements for Li are not yet precise enough to test these higher-order corrections.

Roger A. Hegstrom

1975-02-01T23:59:59.000Z

206

A New Method for Quantitative Marking of Deposited Lithium via Chemical Treatment on Graphite Anodes in Lithium-Ion Cells  

E-Print Network [OSTI]

A New Method for Quantitative Marking of Deposited Lithium via Chemical Treatment on Graphite Anodes in Lithium-Ion Cells Yvonne Krämer*[a] , Claudia Birkenmaier[b] , Julian Feinauer[a,c] , Andreas*[e] and Thomas Schleid[f] Abstract: A novel approach for the marking of deposited lithium on graphite anodes from

Schmidt, Volker

207

New model for the mixed-valence phenomenon in rare-earth materials  

Science Journals Connector (OSTI)

A model of a single rare-earth atom in a transition metal is derived, and terms describing screening of charge fluctuations in the resonant l=3 scattering channels by the l=2 channels are included. Using the Tomonaga approximation, in which charge fluctuations are represented by bosons, the screening channels are replaced by a boson field, and the model takes on a particularly simple form, the Anderson model of a magnetic impurity, now coupled to the boson field. The mean-field theory of this model suggests that, unlike in the original Anderson model, the impurity can be in a state of slowly fluctuating valence, which we identify with the mixed-valence phenomenon in certain rare-earth materials. These results suggest that the mixed-valence effect may be purely electronic in origin.

F. D. M. Haldane

1977-03-01T23:59:59.000Z

208

CO{sub 2} capture properties of lithium silicates with different ratios of Li{sub 2}O/SiO{sub 2}: an ab initio thermodynamic and experimental approach  

SciTech Connect (OSTI)

The lithium silicates have attracted scientific interest due to their potential use as high-temperature sorbents for CO{sub 2} capture. The electronic properties and thermodynamic stabilities of lithium silicates with different Li{sub 2}O/SiO{sub 2} ratios (Li{sub 2}O, Li{sub 8}SiO{sub 6}, Li{sub 4}SiO{sub 4}, Li{sub 6}Si{sub 2}O{sub 7}, Li{sub 2}SiO{sub 3}, Li{sub 2}Si{sub 2}O{sub 5}, Li{sub 2}Si{sub 3}O{sub 7}, and a-SiO{sub 2}) have been investigated by combining first-principles density functional theory with lattice phonon dynamics. All these lithium silicates examined are insulators with band-gaps larger than 4.5 eV. By decreasing the Li{sub 2}O/SiO{sub 2} ratio, the first valence bandwidth of the corresponding lithium silicate increases. Additionally, by decreasing the Li{sub 2}O/SiO{sub 2} ratio, the vibrational frequencies of the corresponding lithium silicates shift to higher frequencies. Based on the calculated energetic information, their CO{sub 2} absorption capabilities were extensively analyzed through thermodynamic investigations on these absorption reactions. We found that by increasing the Li{sub 2}O/SiO{sub 2} ratio when going from Li{sub 2}Si{sub 3}O{sub 7} to Li{sub 8}SiO{sub 6}, the corresponding lithium silicates have higher CO{sub 2} capture capacity, higher turnover temperatures and heats of reaction, and require higher energy inputs for regeneration. Based on our experimentally measured isotherms of the CO{sub 2} chemisorption by lithium silicates, we found that the CO{sub 2} capture reactions are two-stage processes: (1) a superficial reaction to form the external shell composed of Li{sub 2}CO{sub 3} and a metal oxide or lithium silicate secondary phase and (2) lithium diffusion from bulk to the surface with a simultaneous diffusion of CO{sub 2} into the shell to continue the CO{sub 2} chemisorption process. The second stage is the rate determining step for the capture process. By changing the mixing ratio of Li{sub 2}O and SiO{sub 2}, we can obtain different lithium silicate solids which exhibit different thermodynamic behaviors. Based on our results, three mixing scenarios are discussed to provide general guidelines for designing new CO{sub 2} sorbents to fit practical needs.

Yuhua Duan, Yuhua; Pfeiffer, Heriberto; Li, Bingyun, Romero-Ibarra, Issis C; Sorescu, Dan C; Luebke, David; Halley, J Woods

2013-06-05T23:59:59.000Z

209

Lithium metal reduction of plutonium oxide to produce plutonium metal  

DOE Patents [OSTI]

A method is described for the chemical reduction of plutonium oxides to plutonium metal by the use of pure lithium metal. Lithium metal is used to reduce plutonium oxide to alpha plutonium metal (alpha-Pu). The lithium oxide by-product is reclaimed by sublimation and converted to the chloride salt, and after electrolysis, is removed as lithium metal. Zinc may be used as a solvent metal to improve thermodynamics of the reduction reaction at lower temperatures. Lithium metal reduction enables plutonium oxide reduction without the production of huge quantities of CaO--CaCl.sub.2 residues normally produced in conventional direct oxide reduction processes.

Coops, Melvin S. (Livermore, CA)

1992-01-01T23:59:59.000Z

210

Paramagnon picture of the low-temperature susceptibility of some intermediate-valence compounds  

SciTech Connect (OSTI)

We show that the low-temperature susceptibility of Ce(In,Sn)/sub 3/ compounds has a quadratic temperature dependence with positive coefficient. We demonstrate that this behavior is well accounted for by a generalization to arbitrary band shapes of the paramagnon theory, which has been applied previously to liquid /sup 3/He. This result is relevant to the whole class of mixed-valence materials. We conclude that the previously proposed phenomenology that treats valence-fluctuation materials as heavy, nearly magnetic Fermi liquids finds further support in the present analysis.

Beal-Monod, M.T.; Lawrence, J.M.

1980-06-01T23:59:59.000Z

211

Lithium-based Technologies | Y-12 National Security Complex  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Lithium-based Technologies Lithium-based Technologies Lithium-based Technologies Y-12's 60 years of rich lithium operational history and expertise make it the clear choice for deployment of new lithium-based technologies and capabilities. There is no other U.S. site, government or commercial, that comes close to the breadth of Y-12's lithium expertise and capabilities. The Y-12 National Security Complex supplies lithium, in unclassified forms, to customers worldwide through the DOE Office of Science, Isotope Business Office. Historically, the typical order of 6Li was only gram quantities used in research and development. However, over the past three years demand has increased steadily with typical orders of around 10-20 kg each. Such increase in demand is a direct result of the use of

212

Lithium Surface Coatings for Improved Plasma Performance in NSTX  

SciTech Connect (OSTI)

NSTX high-power divertor plasma experiments have shown, for the first time, significant and frequent benefits from lithium coatings applied to plasma facing components. Lithium pellet injection on NSTX introduced lithium pellets with masses 1 to 5 mg via He discharges. Lithium coatings have also been applied with an oven that directed a collimated stream of lithium vapor toward the graphite tiles of the lower center stack and divertor. Lithium depositions from a few mg to 1 g have been applied between discharges. Benefits from the lithium coating were sometimes, but not always seen. These improvements sometimes included decreases plasma density, inductive flux consumption, and ELM frequency, and increases in electron temperature, ion temperature, energy confinement and periods of MHD quiescence. In addition, reductions in lower divertor D, C, and O luminosity were measured.

Kugel, H W; Ahn, J -W; Allain, J P; Bell, R; Boedo, J; Bush, C; Gates, D; Gray, T; Kaye, S; Kaita, R; LeBlanc, B; Maingi, R; Majeski, R; Mansfield, D; Menard, J; Mueller, D; Ono, M; Paul, S; Raman, R; Roquemore, A L; Ross, P W; Sabbagh, S; Schneider, H; Skinner, C H; Soukhanovskii, V; Stevenson, T; Timberlake, J; Wampler, W R

2008-02-19T23:59:59.000Z

213

Nanostructured lithium-aluminum alloy electrodes for lithium-ion batteries.  

SciTech Connect (OSTI)

Electrodeposited aluminum films and template-synthesized aluminum nanorods are examined as negative electrodes for lithium-ion batteries. The lithium-aluminum alloying reaction is observed electrochemically with cyclic voltammetry and galvanostatic cycling in lithium half-cells. The electrodeposition reaction is shown to have high faradaic efficiency, and electrodeposited aluminum films reach theoretical capacity for the formation of LiAl (1 Ah/g). The performance of electrodeposited aluminum films is dependent on film thickness, with thicker films exhibiting better cycling behavior. The same trend is shown for electron-beam deposited aluminum films, suggesting that aluminum film thickness is the major determinant in electrochemical performance regardless of deposition technique. Synthesis of aluminum nanorod arrays on stainless steel substrates is demonstrated using electrodeposition into anodic aluminum oxide templates followed by template dissolution. Unlike nanostructures of other lithium-alloying materials, the electrochemical performance of these aluminum nanorod arrays is worse than that of bulk aluminum.

Hudak, Nicholas S.; Huber, Dale L.

2010-12-01T23:59:59.000Z

214

Lithium pellet production (LiPP): A device for the production of small spheres of lithium  

SciTech Connect (OSTI)

With lithium as a fusion material gaining popularity, a method for producing lithium pellets relatively quickly has been developed for NSTX. The Lithium Pellet Production device is based on an injector with a sub-millimeter diameter orifice and relies on a jet of liquid lithium breaking apart into small spheres via the Plateau-Rayleigh instability. A prototype device is presented in this paper and for a pressure difference of {Delta}P= 5 Torr, spheres with diameters between 0.91 < D < 1.37 mm have been produced with an average diameter of D= 1.14 mm, which agrees with the developed theory. Successive tests performed at Princeton Plasma Physics Laboratory with Wood's metal have confirmed the dependence of sphere diameter on pressure difference as predicted.

Fiflis, P.; Andrucyzk, D.; McGuire, M.; Curreli, D.; Ruzic, D. N. [Center for Plasma Material Interactions, Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801 (United States); Roquemore, A. L. [Princeton Plasma Physics Laboratory, Princeton, New Jersey 08540 (United States)

2013-06-15T23:59:59.000Z

215

An Advanced Lithium-Ion Battery Based on a Graphene Anode and a Lithium Iron Phosphate Cathode  

Science Journals Connector (OSTI)

An Advanced Lithium-Ion Battery Based on a Graphene Anode and a Lithium Iron Phosphate Cathode ... To the best of our knowledge, complete, graphene-based, lithium ion batteries having performances comparable with those offered by the present technology are rarely reported; hence, we believe that the results disclosed in this work may open up new opportunities for exploiting graphene in the lithium-ion battery science and development. ... A full Li-ion battery (Figure 4a) is obtained by coupling the Cu-supported graphene nanoflake anode with a lithium iron phosphate, LiFePO4, that is, a cathode commonly used in commercial batteries. ...

Jusef Hassoun; Francesco Bonaccorso; Marco Agostini; Marco Angelucci; Maria Grazia Betti; Roberto Cingolani; Mauro Gemmi; Carlo Mariani; Stefania Panero; Vittorio Pellegrini; Bruno Scrosati

2014-07-15T23:59:59.000Z

216

Muon Spin Relaxation Studies of Lithium Nitridometallate Battery Materials: Muon Trapping and Lithium Ion Diffusion  

Science Journals Connector (OSTI)

Muon Spin Relaxation Studies of Lithium Nitridometallate Battery Materials: Muon Trapping and Lithium Ion Diffusion ... The muons themselves are quasi-static, most probably located in a 4h site between the [Li2N] plane and the Li(1)/Ni layer. ... The initial fall in ? results from an increase in muon hopping as the temperature is raised, while the subsequent rise originates from an increasing proportion of trapped and therefore static muons. ...

Andrew S. Powell; James S. Lord; Duncan H. Gregory; Jeremy J. Titman

2009-10-27T23:59:59.000Z

217

Novel synthesis process and structure refinements of Li4Mn5O12 for rechargeable lithium batteries  

Science Journals Connector (OSTI)

Well-crystallized Li4Mn5O12 powder with grain size of 0.10.4 ?m was prepared by heating a eutectic mixture of lithium acetate (LiOAc), and manganese nitrate (Mn(NO3)2), in an oxygen atmosphere. The structure of Li4Mn5O12 crystallites was found to be a cubic spinel using Rietveld refinement of both neutron and X-ray powder diffraction data. We confirmed that lithium ions occupy both the tetrahedral 8a sites, and part of the octahedral 16d sites, but not the 16c sites in the space group Fd3m, while all the manganese ions occupy the 16d sites. The lattice parameter was found to be sensitive to the synthesis temperature as a result of the variation in manganese valence. Samples prepared at 500 C showed better electrode performance. A rechargeable capacity of about 135 mAh/g for the cell Li/Li4Mn5O12 was obtained in the 2.53.6 V range of cell voltages.

Toshimi Takada; Hiroshi Hayakawa; Etsuo Akiba; Fujio Izumi; Bryan C. Chakoumakos

1997-01-01T23:59:59.000Z

218

Lithium: Will Short Supply Constrain Energy Technologies?  

Science Journals Connector (OSTI)

...developments have improved the storage capacity and lifetime...century. Utility electric storage-a projected 1000 units...parts per million are pumped to the surface, concentrated...area currently being pumped. Kunasz says that the...recovering lithium from seawater, although few geologists...

ALLEN L. HAMMOND

1976-03-12T23:59:59.000Z

219

Nanocarbon Networks for Advanced Rechargeable Lithium Batteries  

Science Journals Connector (OSTI)

His research focuses on energy storage and conversion with batteries, fuel cells, and solar cells. ... As an important type of secondary battery, lithium-ion batteries (LIBs) have quickly dominated the market for consumer electronics and become one of key technologies in the battery industry after their first release by Sony Company in the early 1990s. ...

Sen Xin; Yu-Guo Guo; Li-Jun Wan

2012-09-06T23:59:59.000Z

220

Rechargeable thin-film lithium batteries  

SciTech Connect (OSTI)

Rechargeable thin-film batteries consisting of lithium metal anodes, an amorphous inorganic electrolyte, and cathodes of lithium intercalation compounds have been fabricated and characterized. These include Li-TiS{sub 2}, Li-V{sub 2}O{sub 5}, and Li-Li{sub x}Mn{sub 2}O{sub 4} cells with open circuit voltages at full charge of about 2.5 V, 3.7 V, and 4.2 V, respectively. The realization of these robust cells, which can be cycled thousands of times, was possible because of the stability of the amorphous lithium electrolyte, lithium phosphorus oxynitride. This material has a typical composition of Li{sub 2.9}PO{sub 3.3}N{sub 0.46}and a conductivity at 25 C of 2 {mu}S/cm. The thin-film cells have been cycled at 100% depth of discharge using current densities of 5 to 100 {mu}A/cm{sup 2}. Over most of the charge-discharge range, the internal resistance appears to be dominated by the cathode, and the major source of the resistance is the diffusion of Li{sup +} ions from the electrolyte into the cathode. Chemical diffusion coefficients were determined from ac impedance measurements.

Bates, J.B.; Gruzalski, G.R.; Dudney, N.J.; Luck, C.F.; Yu, X.

1993-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Thin-film Rechargeable Lithium Batteries  

DOE R&D Accomplishments [OSTI]

Rechargeable thin films batteries with lithium metal anodes, an amorphous inorganic electrolyte, and cathodes of lithium intercalation compounds have been fabricated and characterized. The cathodes include TiS{sub 2}, the {omega} phase of V{sub 2}O{sub 5}, and the cubic spinel Li{sub x}Mn{sub 2}O{sub 4} with open circuit voltages at full charge of about 2.5 V, 3.7 V, and 4.2 V, respectively. The development of these robust cells, which can be cycled thousands of times, was possible because of the stability of the amorphous lithium electrolyte, lithium phosphorus oxynitride. This material has a typical composition of Li{sub 2.9}PO{sub 3.3}N{sub 0.46} and a conductivity at 25 C of 2 {mu}S/cm. Thin film cells have been cycled at 100% depth of discharge using current densities of 2 to 100 {mu}A/cm{sup 2}. The polarization resistance of the cells is due to the slow insertion rate of Li{sup +} ions into the cathode. Chemical diffusion coefficients for Li{sup +} ions in the three types of cathodes have been estimated from the analysis of ac impedance measurements.

Bates, J. B.; Gruzalski, G. R.; Dudney, N. J.; Luck, C. F.; Yu, X.

1993-11-00T23:59:59.000Z

222

NSTX plasma response to lithium coated divertor  

SciTech Connect (OSTI)

NSTX experiments have explored lithium evaporated on a graphite divertor and other plasma-facing components in both L- and H- mode confinement regimes heated by high-power neutral beams. Improvements in plasma performance have followed these lithium depositions, including a reduction and eventual elimination of the HeGDC time between discharges, reduced edge neutral density, reduced plasma density, particularly in the edge and the SOL, increased pedestal electron and ion temperature, improved energy confinement and the suppression of ELMs in the H-mode. However, with improvements in confinement and suppression of ELMs, there was a significant secular increase in the effective ion charge Z(eff) and the radiated power in H-mode plasmas as a result of increases in the carbon and medium-Z metallic impurities. Lithium itself remained at a very low level in the plasma core, < 0.1%. Initial results are reported from operation with a Liquid Lithium Divertor (LLD) recently installed. (C) 2010 Elsevier B.V. All rights reserved.

Kugel, H. W. [Princeton Plasma Physics Laboratory (PPPL); Bell, M. G. [Princeton Plasma Physics Laboratory (PPPL); Allain, J. P. [Purdue University; Bell, R. E. [Princeton Plasma Physics Laboratory (PPPL); Ding, S. [Academia Sinica, Institute of Plasma Physics, Hefei, China; Gerhardt, S. P. [Princeton Plasma Physics Laboratory (PPPL); Jaworski, M. A. [Princeton Plasma Physics Laboratory (PPPL); Kaita, R. [Princeton Plasma Physics Laboratory (PPPL); Kallman, J. [Princeton Plasma Physics Laboratory (PPPL); Kaye, S. M. [Princeton Plasma Physics Laboratory (PPPL); LeBlanc, B. P. [Princeton Plasma Physics Laboratory (PPPL); Maingi, Rajesh [ORNL; Majeski, R. [Princeton Plasma Physics Laboratory (PPPL); Maqueda, R. J. [Princeton Plasma Physics Laboratory (PPPL); Mansfield, D.K. [Princeton Plasma Physics Laboratory (PPPL); Mueller, D. [Princeton Plasma Physics Laboratory (PPPL); Nygren, R. E. [Sandia National Laboratories (SNL); Paul, S. F. [Princeton Plasma Physics Laboratory (PPPL); Raman, R [University of Washington, Seattle; Roquemore, A. L. [Princeton Plasma Physics Laboratory (PPPL); Sabbagh, S. A. [Columbia University; Schneider, H. [Princeton Plasma Physics Laboratory (PPPL); Skinner, C. H. [Princeton Plasma Physics Laboratory (PPPL); Soukhanovskii, V. A. [Lawrence Livermore National Laboratory (LLNL); Taylor, C. N. [Purdue University; Timberlake, J. [Princeton Plasma Physics Laboratory (PPPL); Wampler, W. R. [Sandia National Laboratories (SNL); Zakharov, L. E. [Princeton Plasma Physics Laboratory (PPPL); Zweben, S. J. [Princeton Plasma Physics Laboratory (PPPL)

2011-01-01T23:59:59.000Z

223

Electrothermal Analysis of Lithium Ion Batteries  

SciTech Connect (OSTI)

This report presents the electrothermal analysis and testing of lithium ion battery performance. The objectives of this report are to: (1) develop an electrothermal process/model for predicting thermal performance of real battery cells and modules; and (2) use the electrothermal model to evaluate various designs to improve battery thermal performance.

Pesaran, A.; Vlahinos, A.; Bharathan, D.; Duong, T.

2006-03-01T23:59:59.000Z

224

Mixed valence and spin fluctuations in Ce(Ni, Co)/sub 2/ and related systems  

SciTech Connect (OSTI)

The pseudobinary alloys Ce(Ni/sub x/Co/sub 1-x/)/sub 2/, (Ce/sub x/La/sub 1-x/)Ni/sub 2/ and (Ce/sub x/Y/sub 1-x/)Ni/sub 2/, where 0 < x < 1, were studied. The room-temperature lattice constant, the magnetic susceptibility in the 6 to 300 K temperature range, the low-temperature specific heat in the 0.4 to 25 K range, and the electrical resistivity in the 0.4 to 300 K range were measured. Additionally, x-ray absorption around the L/sub 3/ edge was studied using the synchroton radiation. Both thermodynamic and L/sub 3/ probes yield similar results for the changes of valence of Ce across these systems. It was established that Ce is in the saturated valence state in the Ce(Ni/sub x/Co/sub 1-x/)/sub 2/ for x < 0.25. The valence decreases with x in the 0.25 to 1 concentration range. Similarly, the valence of Ce decreases in the (Ce, Y)Ni/sub 2/ systems upon substitution of Y for Ce. The results obtained for the (Ce/sub x/La/sub 1-x/)Ni/sub 2/ system are interpreted in terms of changes of the Ce/sup 3 +/ impurity levels. Spin fluctuations due to the 3d electrons play an important role in these systems

Andraka, B.

1986-01-01T23:59:59.000Z

225

Light hadron spectroscopy using domain wall valence quarks on an asqtad sea  

E-Print Network [OSTI]

We calculate the light hadron spectrum in full QCD using two plus one flavor asqtad sea quarks and domain wall valence quarks. Meson and baryon masses are calculated on a lattice of spatial size L?2.5??fm, and a lattice ...

Walker-Loud, A.

226

Mixed-Valence Minerals of Iron and Titanium: Correlations of Structural, Mssbauer and Electronic Spectral Data  

Science Journals Connector (OSTI)

A large cariety of mixed-valence silicate and oxide minerals occur in rocks from the Earth, Moon and Meteorites, They frequently contain Fe2+ -Fe3+, Ti3+ -Ti4+ and Fe2+ -Ti4+ assemblages and often display anomalo...

Roger G. Burns; D. A. Nolet; K. M. Parkin; C. A. McCammon

1980-01-01T23:59:59.000Z

227

Composition dependent valence band order in c-oriented wurtzite AlGaN layers  

SciTech Connect (OSTI)

The valence band order of polar wurtzite aluminum gallium nitride (AlGaN) layers is analyzed for a dense series of samples, grown heteroepitaxially on sapphire substrates, covering the complete composition range. The excitonic transition energies, found by temperature dependent photoluminescence (PL) spectroscopy, were corrected to the unstrained state using input from X-ray diffraction. k?p theory yields a critical relative aluminum concentration x{sub c}=(0.090.05) for the crossing of the uppermost two valence bands for strain free material, shifting to higher values for compressively strained samples, as supported by polarization dependent PL. The analysis of the strain dependent valence band crossing reconciles the findings of other research groups, where sample strain was neglected. We found a bowing for the energy band gap to the valence band with ?{sub 9} symmetry of b{sub ?{sub 9}}=0.85eV, and propose a possible bowing for the crystal field energy of b{sub cf}=?0.12eV. A comparison of the light extraction efficiency perpendicular and parallel to the c axis of Al{sub x}Ga{sub 1-x}N/Al{sub y}Ga{sub 1-y}N quantum well structures is discussed for different compositions.

Neuschl, B., E-mail: benjamin.neuschl@uni-ulm.de; Helbing, J.; Knab, M.; Lauer, H.; Madel, M.; Thonke, K. [Institute of Quantum Matter / Semiconductor Physics Group, University of Ulm, Albert-Einstein-Allee 45, 89069 Ulm (Germany); Meisch, T.; Forghani, K.; Scholz, F. [Institute of Optoelectronics, University of Ulm, Albert-Einstein-Allee 45, 89069 Ulm (Germany); Feneberg, M. [Institut fr Experimentelle Physik, Otto-von-Guericke-Universitt Magdeburg, Universittsplatz 2, 39106 Magdeburg (Germany)

2014-09-21T23:59:59.000Z

228

Mapping the Valence States of Transition-Metal Elements Using Energy-Filtered Transmission Electron Microscopy  

E-Print Network [OSTI]

spectrum of MnO2 acquired at 200 kV using a Hitachi HF-2000 transmission electron microscope equipped lines observed in electron energy-loss spectroscopy in a transmission electron microscope (TEMMapping the Valence States of Transition-Metal Elements Using Energy-Filtered Transmission Electron

Wang, Zhong L.

229

Determination of Mn valence states in mixed-valent manganates by XANES spectroscopy  

Science Journals Connector (OSTI)

...overabsorption, many of the references were run in total electron yield mode. For others...the slope of the valence = f (energy) straight line. Therefore, the only way to improve...methylcyclopentadienyl) manganese tricarbonyl-added gasolines using XANES spectroscopy. Environmental...

Alain Manceau; Matthew A. Marcus; Sylvain Grangeon

230

Implications of NSTX Lithium Results for Magnetic Fusion Research  

SciTech Connect (OSTI)

Lithium wall coating techniques have been experimentally explored on NSTX for the last five years. The lithium experimentation on NSTX started with a few milligrams of lithium injected into the plasma as pellets and it has evolved to a lithium evaporation system which can evaporate up to ~ 100 g of lithium onto the lower divertor plates between lithium reloadings. The unique feature of the lithium research program on NSTX is that it can investigate the effects of lithium in H-mode divertor plasmas. This lithium evaporation system thus far has produced many intriguing and potentially important results; the latest of these are summarized in a companion paper by H. Kugel. In this paper, we suggest possible implications and applications of the NSTX lithium results on the magnetic fusion research which include electron and global energy confinement improvements, MHD stability enhancement at high beta, ELM control, H-mode power threshold reduction, improvements in radio frequency heating and non-inductive plasma start-up performance, innovative divertor solutions and improved operational efficiency.

M. Ono, M.G. Bell, R.E. Bell, R. Kaita, H.W. Kugel, B.P. LeBlanc, J.M. Canik, S. Diem, S.P.. Gerhardt, J. Hosea, S. Kaye, D. Mansfield, R. Maingi, J. Menard, S. F. Paul, R. Raman, S.A. Sabbagh, C.H. Skinner, V. Soukhanovskii, G. Taylor, and the NSTX Research Team

2010-01-14T23:59:59.000Z

231

Overcharge Protection for 4 V Lithium Batteries at High Rates and Low Temperature  

E-Print Network [OSTI]

Protection for 4 V Lithium Batteries at High Rates and LowRechargeable lithium batteries are known for their highBecause lithium ion batteries are especially susceptible to

Chen, Guoying

2010-01-01T23:59:59.000Z

232

STUDIES ON TWO CLASSES OF POSITIVE ELECTRODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

Linden, D. , Handbook of Batteries. 2nd ed. 1995, New York:rechargeable lithium batteries. Nature, 2001. 414(6861): p.of rechargeable lithium batteries, I. Lithium manganese

Wilcox, James D.

2010-01-01T23:59:59.000Z

233

SURFACE RECONSTRUCTION AND CHEMICAL EVOLUTION OF STOICHIOMETRIC LAYERED CATHODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

CATHODE MATERIALS FOR LITHIUM-ION BATTERIES Feng Lin, 1*As shown in Figure 2, in lithium-metal half-cells, capacitypredominantly occurs along the lithium diffusion channels,

Lin, Feng

2014-01-01T23:59:59.000Z

234

Solid state thin film battery having a high temperature lithium alloy anode  

DOE Patents [OSTI]

An improved rechargeable thin-film lithium battery involves the provision of a higher melting temperature lithium anode. Lithium is alloyed with a suitable solute element to elevate the melting point of the anode to withstand moderately elevated temperatures.

Hobson, David O. (Oak Ridge, TN)

1998-01-01T23:59:59.000Z

235

STUDIES ON TWO CLASSES OF POSITIVE ELECTRODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

around 3.5 M. A slight excess of lithium (5%) was used tothat there is a slight excess of lithium in materials withto the formation of a lithium excess surface material (Li 1+

Wilcox, James D.

2010-01-01T23:59:59.000Z

236

Flexible graphene-based lithium ion batteries with ultrafast charge and discharge rates  

Science Journals Connector (OSTI)

Flexible graphene-based lithium ion batteries with ultrafast charge and...and flexible lithium ion battery made from graphene foam, a three-dimensional...and flexible lithium ion battery made from graphene foam, a three-dimensional...

Na Li; Zongping Chen; Wencai Ren; Feng Li; Hui-Ming Cheng

2012-01-01T23:59:59.000Z

237

Stress fields in hollow coreshell spherical electrodes of lithium ion batteries  

Science Journals Connector (OSTI)

...core-shell spherical electrodes of lithium ion batteries Yingjie Liu 1 Pengyu Lv...System, Department of Mechanics and Engineering Science, College of Engineering...structure design of electrodes of lithium ion batteries. lithium ion battery...

2014-01-01T23:59:59.000Z

238

Polymers with Tailored Electronic Structure for High Capacity Lithium  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Polymers with Tailored Electronic Structure for High Capacity Lithium Polymers with Tailored Electronic Structure for High Capacity Lithium Battery Electrodes Title Polymers with Tailored Electronic Structure for High Capacity Lithium Battery Electrodes Publication Type Journal Article Year of Publication 2011 Authors Liu, Gao, Shidi Xun, Nenad Vukmirovic, Xiangyun Song, Paul Olalde-Velasco, Honghe Zheng, Vince S. Battaglia, Linwang Wang, and Wanli Yang Journal Advanced Materials Volume 23 Start Page 4679 Issue 40 Pagination 4679 - 4683 Date Published 10/2011 Keywords binders, conducting polymers, density funcational theory, lithium batteries, X-ray spectroscopy Abstract A conductive polymer is developed for solving the long-standing volume change issue in lithium battery electrodes. A combination of synthesis, spectroscopy and simulation techniques tailors the electronic structure of the polymer to enable in situ lithium doping. Composite anodes based on this polymer and commercial Si particles exhibit 2100 mAh g-1 in Si after 650 cycles without any conductive additive.

239

Lithium In Tufas Of The Great Basin- Exploration Implications For  

Open Energy Info (EERE)

In Tufas Of The Great Basin- Exploration Implications For In Tufas Of The Great Basin- Exploration Implications For Geothermal Energy And Lithium Resources Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Paper: Lithium In Tufas Of The Great Basin- Exploration Implications For Geothermal Energy And Lithium Resources Details Activities (8) Areas (4) Regions (0) Abstract: Lithium/magnesium, lithium/sodium, and to a lesser extent, potassium/magnesium ratios in calcium carbonate tufa columns provide a fingerprint for distinguishing tufa columns formed from thermal spring waters versus those formed from non-thermal spring waters. These ratios form the basis of the Mg/Li, Na/Li, and K/Mg fluid geothermometers commonly used in geothermal exploration, which are based on the fact that at elevated temperatures, due to mineral-fluid equilibria, lithium

240

Synthesis of lithium intercalation materials for rechargeable battery  

Science Journals Connector (OSTI)

Lithium-based oxides (LiMOx, where M=Ni, Co, Mn) are attractive for electrode materials, because they are capable of reversibly intercalating lithium ions for rechargeable battery without altering the main unit. We developed a novel solution-based route for the synthesis of these lithium intercalation oxides, using acetates or oxides as precursors for lithium, manganese, nickel, and cobalt, respectively with proper organic solvents. The evolution of crystal structure of these materials was analyzed by X-ray diffraction. Further analysis of LiMn2O4 samples were carried out using impedance spectroscopy and Raman spectroscopy. These studies indicate that this synthetic route, without using expensive alkoxides of solgel process, produces high-quality lithium-based oxides useful for cathode in lithium-ion rechargeable battery.

S. Nieto-Ramos; M.S. Tomar

2001-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

E-Print Network 3.0 - accumulateurs au lithium Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

au lithium Search Powered by Explorit Topic List Advanced Search Sample search results for: accumulateurs au lithium Page: << < 1 2 3 4 5 > >> 1 ACCUMULATEUR LECTRIQUE...

242

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Broader source: Energy.gov (indexed) [DOE]

CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries 2011 DOE...

243

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

& Publications Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries...

244

PolymerGraphene Nanocomposites as Ultrafast-Charge and -Discharge Cathodes for Rechargeable Lithium Batteries  

Science Journals Connector (OSTI)

PolymerGraphene Nanocomposites as Ultrafast-Charge and -Discharge Cathodes for Rechargeable Lithium Batteries ... Lithium battery; cathode; polymer; graphene; nanocomposite ...

Zhiping Song; Terrence Xu; Mikhail L. Gordin; Ying-Bing Jiang; In-Tae Bae; Qiangfeng Xiao; Hui Zhan; Jun Liu; Donghai Wang

2012-03-26T23:59:59.000Z

245

Insights into the morphological changes undergone by the anode in the lithium sulphur battery system.  

E-Print Network [OSTI]

?? In this thesis, the morphological changes of the anode surface in lithium sulphur cell, during early cycling, were simulated using symmetrical lithium electrode cells (more)

Yalamanchili, Anurag

2014-01-01T23:59:59.000Z

246

Dendrite-Free Lithium Deposition with Self-Aligned Nanorod Structure...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

with Self-Aligned Nanorod Structure. Dendrite-Free Lithium Deposition with Self-Aligned Nanorod Structure. Abstract: Suppressing lithium (Li) dendrite growth is one of the most...

247

STUDIES ON TWO CLASSES OF POSITIVE ELECTRODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

2 H 3 O 2 Li2H 2 O (lithium acetate, Sigma Aldrich), and HThe iron nitrate and lithium acetate were combined with the

Wilcox, James D.

2010-01-01T23:59:59.000Z

248

Lithium: Measurement of Young's Modulus and Yield Strength  

SciTech Connect (OSTI)

The Lithium Collection Lens is used for anti-proton collection. In analyzing the structural behavior during operation, various material properties of lithium are often needed. properties such as density, coefficient of thermal expansion, thermal conductivity, specific heat, compressability, etc.; are well known. However, to the authors knowledge there is only one published source for Young's Modulus. This paper reviews the results from the testing of Young's Modulus and the yield strength of lithium at room temperature.

Ryan P Schultz

2002-11-07T23:59:59.000Z

249

Facile synthesis of mesoporous lithium titanate spheres for high rate lithium-ion batteries  

Science Journals Connector (OSTI)

Lithium titanate is synthesized from titanium isopropoxide and lithium acetate solution under hydrothermal environment and calcinations. Introducing acidized carbon black during synthesis can produce mesoporous Li4Ti5O12. The crystalline structure and morphological observation of the as-synthesized mesoporous Li4Ti5O12 are characterized by X-ray diffraction (XRD) and scanning electron microscopy, respectively. The mesoporous structure can be directly observed through BEI images of the cross-section sample. Besides, N2 adsorption/desorption isotherm also displays a hysteresis loop, implying the beneficial evidence of mesoporous structure. The pore size distribution of mesoporous lithium titanate evaluated by BJH model is narrow, and the average size of voids is around 4nm. It is demonstrated that the electrochemical performance is significantly improved by the mesoporous structure. The mesoporous lithium titanate exhibits a stable capacity of 140mAhg?1 at 0.5C. Besides, the reversible capacity at 30C remains over half of that at 0.5C. The superior C-rate performance is associated with the mesoporous structure, facilitating lithium transportation ability during cycling.

Yu-Sheng Lin; Jenq-Gong Duh

2011-01-01T23:59:59.000Z

250

Visualization of Charge Distribution in a Lithium Battery Electrode  

E-Print Network [OSTI]

Distribution in Thin-Film Batteries. J. Electrochem. Soc.of Lithium Polymer Batteries. J. Power Sources 2002, 110,for Rechargeable Li Batteries. Chem. Mater. 2010, 15. Padhi,

Liu, Jun

2010-01-01T23:59:59.000Z

251

Sulfur@Carbon Cathodes for Lithium Sulfur Batteries > Research...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electrode Channel Flow DEMS Cell Sulfur@Carbon Cathodes for Lithium Sulfur Batteries Better Ham & Cheese: Enhanced Anodes and Cathodes for Fuel Cells Epitaxial Single...

252

Lithium/Sulfur Batteries Based on Doped Mesoporous Carbon - Energy...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Materials Advanced Materials Find More Like This Return to Search LithiumSulfur Batteries Based on Doped Mesoporous Carbon Oak Ridge National Laboratory Contact ORNL About...

253

Lithium Ion Electrode Production NDE and QC Considerations |...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

QC Considerations Lithium Ion Electrode Production NDE and QC Considerations Review of Oak Ridge process and QC activities by David Wood, Oak Ridge National Laboratory, at the...

254

Sulfur-Graphene Oxide Nanocomposite Cathodes for Lithium/Sulfur...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Advanced Materials Advanced Materials Find More Like This Return to Search Sulfur-Graphene Oxide Nanocomposite Cathodes for LithiumSulfur Cells Lawrence Berkeley National...

255

Fact #603: December 28, 2009 Where Does Lithium Come From? |...  

Broader source: Energy.gov (indexed) [DOE]

share of lithium reserves and production by country including Chile, China, Australia, Russia, Argentina, U.S. and Bolivia. For more detailed information, see the table below....

256

Physically based Impedance Modelling of Lithium-Ion Cells.  

E-Print Network [OSTI]

??In this book, a new procedure to analyze lithium-ion cells is introduced. The cells are disassembled to analyze their components in experimental cell housings. Then, (more)

Illig, Jrg

2014-01-01T23:59:59.000Z

257

Binding and Diffusion of Lithium in Graphite: Quantum Monte Carlo...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Binding and Diffusion of Lithium in Graphite: Quantum Monte Carlo Benchmarks and Validation of van der Waals Density Functional Methods P. Ganesh,* , Jeongnim Kim, Changwon...

258

JCESR: Moving Beyond Lithium-Ion | Argonne National Laboratory  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

JCESR: Moving Beyond Lithium-Ion Share Topic Energy Energy usage Energy storage Batteries Browse By - Any - Energy -Energy efficiency --Vehicles ---Alternative fuels ---Automotive...

259

Overcoming Processing Cost Barriers of High-Performance Lithium...  

Broader source: Energy.gov (indexed) [DOE]

methods - Tailored Aqueous Colloids for Lithium-Ion Electrodes (TACLE) B.L. Armstrong et al., U.S. Patent Application No. 13651,270. - Surface charge measurement,...

260

The UC Davis Emerging Lithium Battery Test Project  

E-Print Network [OSTI]

lithium titanate oxide in the negative electrode indicate cycle life in excesslithium titanate oxide in the negative electrode indicate cycle life in excess

Burke, Andy; Miller, Marshall

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

High capacity nanostructured electrode materials for lithium-ion batteries.  

E-Print Network [OSTI]

??The lithium-ion battery is currently the most widely used electrochemical storage system on the market, with applications ranging from portable electronics to electric vehicles, to (more)

Seng, Kuok H

2013-01-01T23:59:59.000Z

262

Expanded North Carolina Lithium Facility Opens, Boosting U.S...  

Broader source: Energy.gov (indexed) [DOE]

plug-in hybrids and other advanced clean energy technologies grows worldwide, rare earth elements and other critical materials, including lithium, are facing increasing global...

263

California: Geothermal Plant to Help Meet High Lithium Demand...  

Energy Savers [EERE]

technologies that extract battery materials like lithium, manganese, and zinc from geothermal brines. Simbol has the potential to power 300,000-600,000 electric vehicles per...

264

California Geothermal Power Plant to Help Meet High Lithium Demand...  

Energy Savers [EERE]

brines in California. Batteries from Brine California: Geothermal Plant to Help Meet High Lithium Demand Mineral Recovery Creates Revenue Stream for Geothermal Energy Development...

265

Overcoming Processing Cost Barriers of High-Performance Lithium...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Cost Barriers of High-Performance Lithium-Ion Battery Electrodes 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer...

266

Development of Large Format Lithium Ion Cells with Higher Energy...  

Broader source: Energy.gov (indexed) [DOE]

Overall Project Goal: To research, develop and demonstrate large format lithium ion cells with energy density > 500 WhL Barriers addressed: - Low energy density - Cost -...

267

Sandia National Laboratories: lithium-ion-based solid electrolyte...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

lithium-ion-based solid electrolyte battery Sandia Labs, Front Edge Technology, Inc., Pacific Northwest National Lab, Univ. of California-Los Angeles: Micro Power Source On March...

268

Development of Electrolytes for Lithium-ion Batteries  

Broader source: Energy.gov (indexed) [DOE]

Battaglia & J. Kerr (LBNL) * M. Payne (Novolyte) * F. Puglia & B. Ravdel (Yardney) * G. Smith & O. Borodin (U. Utah) 3 3 Develop novel electrolytes for lithium ion batteries that...

269

Fundamental Studies of Lithium-Sulfur Cell Chemistry  

Broader source: Energy.gov (indexed) [DOE]

Studies of Lithium-Sulfur Cell Chemistry PI: Nitash Balsara LBNL June 17, 2014 Project ID ESS224 This presentation does not contain any proprietary, confidential, or otherwise...

270

Electronic structure of lithium-doped anatase TiO{sub 2} prepared in ultrahigh vacuum  

SciTech Connect (OSTI)

Insertion of lithium in anatase TiO{sub 2}, giving Li{sub x}TiO{sub 2}, is performed under ultrahigh vacuum (UHV) conditions and studied using synchrotron radiation based electron spectroscopy. Core level photoemission spectra are directly compared to results obtained after electrochemical insertion, illustrating the usefulness of the UHV approach. The growth of a state of mainly Ti 3d character in the band gap is monitored and the amount of charge transferred from Li to the band gap state is quantified. The result that the Ti 3d level is occupied by 0.85{+-}0.10 electronic charge is in good agreement with theoretical predictions. Binding energy shifts of the core levels suggest that the population of the Ti 3d states does not follow a simple rigid band behavior. It is concluded that the formation of the Li-poor phase (x<2%) is associated with pinning of the Fermi level to the bottom of the conduction band. The Li-poor phase can therefore be envisaged as related to defects. Changes in the valence photoemission spectrum and O 1s x-ray absorption spectrum are interpreted in terms of a decreased O 2p-Ti 3d interaction upon Li insertion. Shifts in the sample work function are finally found to agree reasonably well with the measured cell voltage for electrochemical Li insertion into a nanoporous anatase film.

Richter, J.H.; Henningsson, A.; Karlsson, P.G.; Siegbahn, H.; Sandell, A. [Department of Physics, Uppsala University, P.O. Box 530, S-751 21 Uppsala (Sweden); Andersson, M.P.; Uvdal, P. [Chemical Physics, Department of Chemistry, Lund University, P.O. Box 124, S-221 00 Lund (Sweden)

2005-06-15T23:59:59.000Z

271

Batteries - Beyond Lithium Ion Breakout session  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

BEYOND LITHIUM ION BREAKOUT BEYOND LITHIUM ION BREAKOUT Breakout Session #1 - Discussion of Performance Targets and Barriers Comments on the Achievability of the Targets * 1 - Zn-Air possible either w/ or w/o electric-hybridization; also possible with a solid electrolyte variant * 2 - Multivalent systems (e.g Mg), potentially needing hybrid-battery * 3 - Advanced Li-ion with hybridization @ cell / molecular level for high-energy and high- power * 4 - MH-air, Li-air, Li-S, all show promise * 5 - High-energy density (e.g. Na-metal ) flow battery can meet power and energy goals * 6 - Solid-state batteries (all types) * 7 - New cathode chemistries (beyond S) to increase voltage * 8 - New high-voltage non-flammable electrolytes (both li-ion and beyond li-ion) * 9 - Power to energy ratio of >=12 needed for fast charge (10 min)  So liquid refill capable

272

Manganese oxide composite electrodes for lithium batteries  

DOE Patents [OSTI]

An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor of a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0lithium and lithia, from the precursor. A cell and battery are also disclosed incorporating the disclosed positive electrode.

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Li, Naichao (Croton on Hudson, NY)

2007-12-04T23:59:59.000Z

273

Manganese oxide composite electrodes for lithium batteries  

DOE Patents [OSTI]

An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor thereof a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0.5lithium and lithia, from the precursor. A cell and battery are also disclosed incorporating the disclosed positive electrode.

Johnson, Christopher S. (Naperville, IL); Kang, Sun-Ho (Naperville, IL); Thackeray, Michael M. (Naperville, IL)

2009-12-22T23:59:59.000Z

274

Expanding argon plasma interacting with lithium surface  

Science Journals Connector (OSTI)

Abstract In this thesis, the interaction between Ar Plasma and lithium is studied by Langmuir probe and Spectrometer. We have studied the effects of the applied discharge current, the gas flow rate, the magnetic field on emission spectrum, electron temperature and electron density. The experimental results show that spectrum intensity, electron temperature and electron density all increase with the increasing discharge current, gas flow rate or magnetic field when the other experimental conditions were fixed, and it is also found that the intensity of Li-670.78nm increases slowly at first and then increases rapidly, at last, it tends to be stable figure at the beginning of experiment. What is more, spectrum of lithium (670.78nm) is also detected at the first diagnostic window (viewing window).

X. Cao; S. Chen; W. Zhang; X. Xue; M. Lu; C. Wang; J. Wang; F. Gou; D. Yang; Ou Wei

2014-01-01T23:59:59.000Z

275

High-discharge-rate lithium ion battery  

DOE Patents [OSTI]

The present invention provides for a lithium ion battery and process for creating such, comprising higher binder to carbon conductor ratios than presently used in the industry. The battery is characterized by much lower interfacial resistances at the anode and cathode as a result of initially mixing a carbon conductor with a binder, then with the active material. Further improvements in cycleability can also be realized by first mixing the carbon conductor with the active material first and then adding the binder.

Liu, Gao; Battaglia, Vincent S; Zheng, Honghe

2014-04-22T23:59:59.000Z

276

High expansion, lithium corrosion resistant sealing glasses  

DOE Patents [OSTI]

Glass compositions containing CaO, Al.sub.2 O.sub.3, B.sub.2 O.sub.3, SrO and BaO in various combinations of mole % are provided. These compositions are capable of forming stable glass-to-metal seals with pin materials of 446 Stainless Steel and Alloy-52 rather than molybdenum, for use in harsh chemical environments, specifically in lithium batteries.

Brow, Richard K. (Albuquerque, NM); Watkins, Randall D. (Albuquerque, NM)

1991-01-01T23:59:59.000Z

277

Lithium-Polysulfide Flow Battery Demonstration  

SciTech Connect (OSTI)

In this video, Stanford graduate student Wesley Zheng demonstrates the new low-cost, long-lived flow battery he helped create. The researchers created this miniature system using simple glassware. Adding a lithium polysulfide solution to the flask immediately produces electricity that lights an LED. A utility version of the new battery would be scaled up to store many megawatt-hours of energy.

Zheng, Wesley

2014-06-30T23:59:59.000Z

278

Valence- and conduction-band structure of the sapphire (1102) surface  

Science Journals Connector (OSTI)

X-ray photoelectron (XPS) and electron-energy-loss spectroscopies have been employed to investigate the valence- and conduction-band densities of states of the sapphire (1102) surface. The photoemission spectrum of the valence-band region has been adjusted to remove cross-section effects and compared to the recent theoretical density of states calculated by Ciraci and Batra. The energy-loss data have been used to determine the bulk-plasmon energy of sapphire, 24.00.3 eV, as well as the locations of eight regions of high conduction-bandstate density within 20 eV above the conduction-band minimum. One of these regions is an empty surface state 4.0 eV below the conduction-band minimum. Several high-binding-energy satellites in the XPS core-level spectra are reported and interpreted in terms of energy losses to plasmons and interband transitions.

W. J. Gignac; R. Stanley Williams; Steven P. Kowalczyk

1985-07-15T23:59:59.000Z

279

Optical Structure near 20 meV in Valence-Fluctuation Compounds  

Science Journals Connector (OSTI)

The first measurement is reported of low-energy (20 meV) structure in the low-temperature dielectric function of two valence-fluctuation materials: CePd3 and YbCu2Si2. The structure is consistent with energy-dependent scattering of electrons off a resonant level whose width and position (relative to the Fermi level) are roughly comparable. No such structure is observed in the integral-valent materials YPd3, DyPd3, and LuCu2Si2. The valence-fluctuation compounds CeCu2Si2 and CeAl3 do not show a resonance above 4 meV.

F. E. Pinkerton; A. J. Sievers; J. W. Wilkins; M. B. Maple; B. C. Sales

1981-10-05T23:59:59.000Z

280

Interatomic decay of inner-valence ionized states in ArXe clusters: Relativistic approach  

SciTech Connect (OSTI)

In this work we investigate interatomic electronic decay processes taking place in mixed argon-xenon clusters upon the inner-valence ionization of an argon center. We demonstrate that both interatomic Coulombic decay and electron-transfer mediated decay (ETMD) are important in larger rare gas clusters as opposed to dimers. Calculated secondary electron spectra are shown to depend strongly on the spin-orbit coupling in the final states of the decay as well as the presence of polarizable environment. It follows from our calculations that ETMD is a pure interface process taking place between the argon-xenon layers. The interplay of all these effects is investigated in order to arrive at a suitable physical model for the decay of inner-valence vacancies taking place in mixed ArXe clusters.

Fasshauer, Elke; Pernpointner, Markus; Gokhberg, Kirill [Theoretische Chemie, Universitaet Heidelberg, Im Neuenheimer Feld 229, D-69120 Heidelberg (Germany)

2013-01-07T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Deuterium Retention in NSTX with Lithium Conditioning  

SciTech Connect (OSTI)

High (approximate to 90%) deuterium retention was observed in NSTX gas balance measurements both with- and without lithiumization of the carbon plasma-facing components. The gas retained in ohmic discharges was measured by comparing the vessel pressure rise after a discharge to that of a gas-only pulse with the pumping valves closed. For neutral beam heated discharges the gas input and gas pumped by the NB cryopanels were tracked. The discharges were followed by outgassing of deuterium that reduced the retention. The relationship between retention and surface chemistry was explored with a new plasma-material interface probe connected to an in vacuo surface science station that exposed four material samples to the plasma. XPS and TDS analysis demonstrated that binding of D atoms in graphite is fundamentally changed by lithium - in particular atoms are weakly bonded in regions near lithium atoms bound to either oxygen or the carbon matrix. This is in contrast to the strong ionic bonding that occurs between D and pure Li. (C) 2010 Elsevier B.V. All rights reserved.

Skinner, C. H. [Princeton Plasma Physics Laboratory (PPPL); Allain, J. P. [Purdue University; Blanchard, W. [Princeton Plasma Physics Laboratory (PPPL); Kugel, H. W. [Princeton Plasma Physics Laboratory (PPPL); Maingi, Rajesh [ORNL; Roquemore, L. [Princeton Plasma Physics Laboratory (PPPL); Soukhanovskii, V. A. [Lawrence Livermore National Laboratory (LLNL); Taylor, C. N. [Purdue University

2011-01-01T23:59:59.000Z

282

Recovery of lithium and cobalt from waste lithium ion batteries of mobile phone  

SciTech Connect (OSTI)

Graphical abstract: Recovery of valuable metals from scrap batteries of mobile phone. - Highlights: Recovery of Co and Li from spent LIBs was performed by hydrometallurgical route. Under the optimum condition, 99.1% of lithium and 70.0% of cobalt were leached. The mechanism of the dissolution of lithium and cobalt was studied. Activation energy for lithium and cobalt were found to be 32.4 kJ/mol and 59.81 kJ/mol, respectively. After metal recovery, residue was washed before disposal to the environment. - Abstract: In view of the stringent environmental regulations, availability of limited natural resources and ever increasing need of alternative energy critical elements, an environmental eco-friendly leaching process is reported for the recovery of lithium and cobalt from the cathode active materials of spent lithium-ion batteries of mobile phones. The experiments were carried out to optimize the process parameters for the recovery of lithium and cobalt by varying the concentration of leachant, pulp density, reductant volume and temperature. Leaching with 2 M sulfuric acid with the addition of 5% H{sub 2}O{sub 2} (v/v) at a pulp density of 100 g/L and 75 C resulted in the recovery of 99.1% lithium and 70.0% cobalt in 60 min. H{sub 2}O{sub 2} in sulfuric acid solution acts as an effective reducing agent, which enhance the percentage leaching of metals. Leaching kinetics of lithium in sulfuric acid fitted well to the chemical controlled reaction model i.e. 1 ? (1 ? X){sup 1/3} = k{sub c}t. Leaching kinetics of cobalt fitted well to the model ash diffusion control dense constant sizes spherical particles i.e. 1 ? 3(1 ? X){sup 2/3} + 2(1 ? X) = k{sub c}t. Metals could subsequently be separated selectively from the leach liquor by solvent extraction process to produce their salts by crystallization process from the purified solution.

Jha, Manis Kumar, E-mail: mkjha@nmlindia.org; Kumari, Anjan; Jha, Amrita Kumari; Kumar, Vinay; Hait, Jhumki; Pandey, Banshi Dhar

2013-09-15T23:59:59.000Z

283

Organic matter in the Paleogene west European rift: Bresse and Valence salt basins (France)  

SciTech Connect (OSTI)

The Bresse and Valence basins are two adjacent segments of the West European rift. They contain thick Paleogene halite sequences including intercalated and interfingering siliciclastic material and carbonate and sulfate deposits. Source rock samples in this study were mainly taken from the depocenters because of maximum sampling coverage. Organic matter (OM) is generally immature and occurs primarily within intercalated nonhalitic beds. The Bresse basin seems to contain more OM in (1) the Intermediate Salt Formation (Priabonian), composed of alternating laminated carbonate and halite beds; (2) the upper part of the Upper Salt Formation (clayey carbonate beds; Rupelian), affected by synsedimentary halite solution; and (3) the solution breccia which immediate overlies the salt sequence. In the Valence basin, the organic-rich layers are concentrated in the Subsalt Formation (carbonate beds; Priabonian), and the upper part of the Lower Salt Formation (laminates; Rupelian). In both basins, type III organic matter is associated with terrigenous facies. Type I is abundant in the Valence basin (laminites), and type II seems to be more abundant in the Bresse basin. The amount of OM varies considerably, and we suppose it is higher toward the basin margins. From studies made in evaporite basins in other region, which are also known to have significant amounts of organic matter, we find a similar range of organic composition. Such studies are of interest because of their petroleum potential and for understanding precise depositional environments and waste disposal problems (gas generation with local heat source).

Curial, A.; Dumas, D.; Moretto, R.

1988-08-01T23:59:59.000Z

284

Size-consistent wave functions for nondynamical correlation energy: The valence active space optimized orbital coupled-cluster  

E-Print Network [OSTI]

Size-consistent wave functions for nondynamical correlation energy: The valence active space 6 July 1998; accepted 15 September 1998 The nondynamical correlation energy may be defined correlation energy, as defined above, involves computational complexity that grows exponentially

Krylov, Anna I.

285

Nucleon structure from mixed action calculations using 2+1 flavors of asqtad sea and domain wall valence fermions  

E-Print Network [OSTI]

We present high statistics results for the structure of the nucleon from a mixed-action calculation using 2+1 flavors of asqtad sea and domain-wall valence fermions. We perform extrapolations of our data based on different ...

Bratt, Jonathan D.

286

Characterization of Lithium Stearate: Processing Aid for Filled Elastomers  

SciTech Connect (OSTI)

This topical report presents work completed to characterize lithium stearate so a replacement supplier could be identified. Lithium stearate from Alfa Aesar and Chemtura was obtained and characterized along with the current material from Witco. Multiple methods were used to characterize the materials including Karl Fischer, FT-IR, differential scanning calorimetry, and thermogravimetric analysis.

E. Eastwood; C. Densmore

2007-02-05T23:59:59.000Z

287

Materials Challenges and Opportunities of Lithium Ion Batteries  

Science Journals Connector (OSTI)

His research interests are in the area of materials for lithium ion batteries, fuel cells, and solar cells, including novel synthesis approaches for nanomaterials. ... Lithiumsulfur (LiS) batteries with a high theoretical energy density of ?2500 Wh kg1 are considered as one promising rechargeable battery chemistry for next-generation energy storage. ...

Arumugam Manthiram

2011-01-10T23:59:59.000Z

288

Solgel synthesis of sodium and lithium based materials  

Science Journals Connector (OSTI)

Sodium and lithium cobaltates are important materials for thermoelectric and ... the solgel synthesis of sodium- and lithium-based materials by using acetate precursors. The produced Na2/3CoO2, Li(Ni1/3Mn1/3Co1/...

Sandra Hildebrandt; Andreas Eva

2012-09-01T23:59:59.000Z

289

Lithium treatment reduces morphine self-administration in addict rats  

Science Journals Connector (OSTI)

... Lithium also has been shown to interact with morphine: it can sometimes reduce morphine-induced ... mice7'8 and potentiate morphine analgesia in rats9. We have therefore investigated the possibility that lithium may affect the amount of voluntary ingestion of morphine by addict rats.

MICHAL TOMKIEWICZ; HANNAH STEINBERG

1974-11-15T23:59:59.000Z

290

Lithium Lorentz Force Accelerator Thruster (LiLFA)  

E-Print Network [OSTI]

Lithium Lorentz Force Accelerator Thruster (LiLFA) Adam Coulon Princeton University Electric originally came from the MAI (Moscow Aviation Institute) Russia · Many Princeton graduate students have #12;LiLFA Thruster · Lithium vapor ionizes in the electric field · A current evolves in the plasma

Petta, Jason

291

Two Studies Reveal Details of Lithium-Battery Function  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Two Studies Reveal Details of Lithium-Battery Function Print Two Studies Reveal Details of Lithium-Battery Function Print Our way of life is deeply intertwined with battery technologies that have enabled a mobile revolution powering cell phones, laptops, medical devices, and cars. As conventional lithium-ion batteries approach their theoretical energy-storage limits, new technologies are emerging to address the long-term energy-storage improvements needed for mobile systems, electric vehicles in particular. Battery performance depends on the dynamics of evolving electronic and chemical states that, despite advances in material synthesis and structural probes, remain elusive and largely unexplored. At Beamlines 8.0.1 and 9.3.2, researchers studied lithium-ion and lithium-air batteries, respectively, using soft x-ray spectroscopy techniques. The detailed information they obtained about the evolution of electronic and chemical states will be indispensable for understanding and optimizing better battery materials.

292

A Better Anode Design to Improve Lithium-Ion Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

A Better Anode Design to Improve A Better Anode Design to Improve Lithium-Ion Batteries A Better Anode Design to Improve Lithium-Ion Batteries Print Friday, 23 March 2012 13:53 Lithium-ion batteries are in smart phones, laptops, most other consumer electronics, and the newest electric cars. Good as these batteries are, the need for energy storage in batteries is surpassing current technologies. In a lithium-ion battery, charge moves from the cathode to the anode, a critical component for storing energy. A team of Berkeley Lab scientists has designed a new kind of anode that absorbs eight times the lithium of current designs, and has maintained its greatly increased energy capacity after more than a year of testing and many hundreds of charge-discharge cycles. Cyclical Science Succeeds

293

China Lithium Energy Electric Vehicle Investment Group CLEEVIG | Open  

Open Energy Info (EERE)

Investment Group CLEEVIG Investment Group CLEEVIG Jump to: navigation, search Name China Lithium Energy Electric Vehicle Investment Group (CLEEVIG) Place Beijing, China Zip 100101 Product Beijing-based investment company with a focus on Electric Vehicle R&D. References China Lithium Energy Electric Vehicle Investment Group (CLEEVIG)[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. China Lithium Energy Electric Vehicle Investment Group (CLEEVIG) is a company located in Beijing, China . References ↑ "[ China Lithium Energy Electric Vehicle Investment Group (CLEEVIG)]" Retrieved from "http://en.openei.org/w/index.php?title=China_Lithium_Energy_Electric_Vehicle_Investment_Group_CLEEVIG&oldid=343507

294

Two Studies Reveal Details of Lithium-Battery Function  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Two Studies Reveal Details of Lithium-Battery Function Print Two Studies Reveal Details of Lithium-Battery Function Print Our way of life is deeply intertwined with battery technologies that have enabled a mobile revolution powering cell phones, laptops, medical devices, and cars. As conventional lithium-ion batteries approach their theoretical energy-storage limits, new technologies are emerging to address the long-term energy-storage improvements needed for mobile systems, electric vehicles in particular. Battery performance depends on the dynamics of evolving electronic and chemical states that, despite advances in material synthesis and structural probes, remain elusive and largely unexplored. At Beamlines 8.0.1 and 9.3.2, researchers studied lithium-ion and lithium-air batteries, respectively, using soft x-ray spectroscopy techniques. The detailed information they obtained about the evolution of electronic and chemical states will be indispensable for understanding and optimizing better battery materials.

295

Liquid Lithium WindowlessLiquid Lithium Windowless Targets for High Power  

E-Print Network [OSTI]

the accelerator beam line · No solid confinement structure · In vacuum ­ It's possible due to Li's low vapor/s in vacuum. #12;Why Liquid Lithium? Low Z ( = 3 )---good from nuclear considerations Large working temp compatible with accelerator vacuum (10-4 Pa or 10-6 Torr). 1000 ( ) Local peak temperature can be much

McDonald, Kirk

296

Measurement of lithium isotope ratios by quadrupole-ICP-MS: application to seawater and natural carbonates  

E-Print Network [OSTI]

Measurement of lithium isotope ratios by quadrupole-ICP-MS: application to seawater and natural method for lithium isotope ratio (7 Li/6 Li) determinations with low total lithium consumption ( lithium from all matrix elements using small volume resin (2 ml/3.4 meq AG 50W-X8) and low volume elution

Weston, Ken

297

17 Years of Lithium Brown Dwarfs 10/21/12Ringberg Brown Dwarfs 1  

E-Print Network [OSTI]

17 Years of Lithium Brown Dwarfs 10/21/12Ringberg Brown Dwarfs 1 #12;The Keck Search for Lithium 10/21/12Ringberg Brown Dwarfs 2 Lithium was not seen in objects which should have been comfortably into the brown "lithium dating". This adjustment in age meant that the inferred mass of PPl 15 rose to near the substellar

Joergens, Viki

298

Abstract--This paper describes experimental results aiming at analyzing lithium-ion batteries performances  

E-Print Network [OSTI]

years, Saft has been developing a range of lithium ion cells and batteries to cover the full spectrum. To follow such a characteristic, electrochemical impedance spectroscopy (EIS) measurements on Saft lithium or several cells. II. OVERVIEW OF EXPERIMENT A. Used lithium-ion cells The cells used are lithium-ion Saft

Boyer, Edmond

299

Lithium Ethylene Dicarbonate Identified as the Primary Product of Chemical and Electrochemical Reduction of EC in EC:EMC/1.2M LiPF6 Electrolyte  

E-Print Network [OSTI]

of synthetic lithium ethylene dicarbonate. Figure 3.structure of lithium ethylene dicarbonate (A) and dimer (B).of: a. ) synthetic lithium ethylene dicarbonate; b. ) EC

Zhuang, Guorong V.; Xu, Kang; Yang, Hui; Jow, T. Richard; Ross Jr., Philip N.

2005-01-01T23:59:59.000Z

300

Thermal Property Measurements and Enthalpy Calculation of the Lithium Bromide+Lithium Iodide+1,3-Propanediol+Water System  

Science Journals Connector (OSTI)

The lithium bromide+lithium iodide+1,3-propanediol+water [LiBr/LiI mole ratio=4 and (LiBr+LiI)/HO(CH2)3...OH mass ratio=4] solution is being considered as a potential working fluid for an absorption chiller. Heat...

J.-S. Kim; H.-S. Lee; H. Lee

2000-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

The impact of lithium wall coatings on NSTX discharges and the engineering of the Lithium Tokamak eXperiment (LTX)  

SciTech Connect (OSTI)

Recent experiments on the National Spherical Torus eXperiment (NSTX) have shown the benefits of solid lithium coatings on carbon PFC's to diverted plasma performance, in both L- and H-mode confinement regimes. Better particle control, with decreased inductive flux consumption, and increased electron temperature, ion temperature, energy confinement time, and DD neutron rate were observed. Successive increases in lithium coverage resulted in the complete suppression of ELM activity in H-mode discharges. A liquid lithium divertor (LLD), which will employ the porous molybdenum surface developed for the LTX shell, is being installed on NSTX for the 2010 run period, and will provide comparisons between liquid walls in the Lithium Tokamak eXperiment (LTX) and liquid divertor targets in NSTX. LTX, which recently began operations at the Princeton Plasma Physics Laboratory, is the world's first confinement experiment with full liquid metal plasma-facing components (PFCs). All materials and construction techniques in LTX are compatible with liquid lithium. LTX employs an inner, heated, stainless steel-faced liner or shell, which will be lithium-coated. In order to ensure that lithium adheres to the shell, it is designed to operate at up to 500-600 degrees C to promote wetting of the stainless by the lithium, providing the first hot wall in a tokamak to Operate at reactor-relevant temperatures. The engineering of LTX will be discussed. (c) 2010 Elsevier B.V. All rights reserved.

Majeski, R. [Princeton Plasma Physics Laboratory (PPPL); Kugel, H. [Princeton Plasma Physics Laboratory (PPPL); Kaita, R. [Princeton Plasma Physics Laboratory (PPPL); Avasarala, S. [Princeton Plasma Physics Laboratory (PPPL); Bell, M. G. [Princeton Plasma Physics Laboratory (PPPL); Bell, R. E. [Princeton Plasma Physics Laboratory (PPPL); Berzak, L. [Princeton Plasma Physics Laboratory (PPPL); Beiersdorfer, P. [Lawrence Livermore National Laboratory (LLNL); Gerhardt, S. P. [Princeton Plasma Physics Laboratory (PPPL); Gransted, E. [Princeton Plasma Physics Laboratory (PPPL); Gray, T. [Princeton Plasma Physics Laboratory (PPPL); Jacobson, C. [Princeton Plasma Physics Laboratory (PPPL); Kallman, J. [Princeton Plasma Physics Laboratory (PPPL); Kaye, S. [Princeton Plasma Physics Laboratory (PPPL); Kozub, T. [Princeton Plasma Physics Laboratory (PPPL); LeBlanc, B. P. [Princeton Plasma Physics Laboratory (PPPL); Lepson, J. [Lawrence Livermore National Laboratory (LLNL); Lundberg, D. P. [Princeton Plasma Physics Laboratory (PPPL); Maingi, Rajesh [ORNL; Mansfield, D. [Princeton Plasma Physics Laboratory (PPPL); Paul, S. F. [Princeton Plasma Physics Laboratory (PPPL); Pereverzev, G. V. [Max-Planck-Institut fur Plasmaphysik, EURATOM Association, Garching, Germany; Schneider, H. [Princeton Plasma Physics Laboratory (PPPL); Soukhanovskii, V. [Lawrence Livermore National Laboratory (LLNL); Strickler, T. [Princeton Plasma Physics Laboratory (PPPL); Stotler, D. [Princeton Plasma Physics Laboratory (PPPL); Timberlake, J. [Princeton Plasma Physics Laboratory (PPPL); Zakharov, L. E. [Princeton Plasma Physics Laboratory (PPPL)

2010-01-01T23:59:59.000Z

302

Surface modifications for carbon lithium intercalation anodes  

DOE Patents [OSTI]

A prefabricated carbon anode containing predetermined amounts of passivating film components is assembled into a lithium-ion rechargeable battery. The modified carbon anode enhances the reduction of the irreversible capacity loss during the first discharge of a cathode-loaded cell. The passivating film components, such as Li.sub.2 O and Li.sub.2 CO.sub.3, of a predetermined amount effective for optimal passivation of carbon, are incorporated into carbon anode materials to produce dry anodes that are essentially free of battery electrolyte prior to battery assembly.

Tran, Tri D. (Livermore, CA); Kinoshita, Kimio (Cupertino, CA)

2000-01-01T23:59:59.000Z

303

Valence-transition-induced 55 surface reconstruction of Sm(0001)  

Science Journals Connector (OSTI)

Single-crystal SM(0001) surfaces have been grown epitaxially on Mo(110). At low temperatures LEED shows a 55 surface reconstruction. This new type of valence-transition-induced reconstruction corresponds to a 25% expansion of the interatomic distances in the topmost hexagonal surface layer. At room temperature the 55 LEED pattern disappears due to a disordering of the surface. This suggests a very low melting temperature for the surface which may have implications for the understanding of the anomalous melting temperature of Sm metal.

A. Stenborg; J. N. Andersen; O. Bjrneholm; A. Nilsson; N. Mrtensson

1989-07-10T23:59:59.000Z

304

Magnetic dichroism in valence-band x-ray photoemission spectroscopy  

Science Journals Connector (OSTI)

A fully relativistic description of spin-resolved valence-band x-ray photoemission spectroscopy (VB-XPS) of magnetic solids is presented that is based on multiple scattering theory. This approach allows us to investigate possible magnetic dichroism in VB-XPS. As is demonstrated by results for CoxPt1-x, application to disordered alloys is straightforward within the framework of the coherent potential approximation alloy theory. The spin-integrated spectra for unpolarized radiation were found to be in very satisfying agreement with corresponding experimental data. For the spin-resolved spectra a pronounced magnetic circular dichroism is predicted that should be easily observed.

H. Ebert and J. Schwitalla

1997-02-01T23:59:59.000Z

305

Lithium-Ion Battery Teacher Workshop  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Lithium Ion Battery Teacher Workshop Lithium Ion Battery Teacher Workshop 2012 2 2 screw eyes 2 No. 14 rubber bands 2 alligator clips 1 plastic gear font 2 steel axles 4 nylon spacers 2 Pitsco GT-R Wheels 2 Pitsco GT-F Wheels 2 balsa wood sheets 1 No. 280 motor Also: Parts List 3 Tools Required 1. Soldering iron 2. Hobby knife or coping saw 3. Glue gun 4. Needlenose pliers 5. 2 C-clamps 6. Ruler 4 1. Using a No. 2 pencil, draw Line A down the center of a balsa sheet. Making the Chassis 5 2. Turn over the balsa sheet and draw Line B ¾ of an inch from one end of the sheet. Making the Chassis 6 3. Draw a 5/8" x ½" notch from 1" from the top of the sheet. Making the Chassis 7 4. Draw Line C 2 ½" from the other end of the same sheet of balsa. Making the Chassis 8 5. Using a sharp utility knife or a coping saw, cut

306

Novel carbonaceous materials for lithium secondary batteries  

SciTech Connect (OSTI)

Carbonaceous materials have been synthesized using pillared clays (PILCs) as templates. The PILC was loaded with organic materials such as pyrene in the liquid and vapor phase, styrene in the vapor phase, trioxane, ethylene and propylene. The samples were then pyrolyzed at 700 C in an inert atmosphere, followed by dissolution of the inorganic template by conventional demineralization methods. X-ray powder diffraction of the carbons showed broad d{sub 002} peaks in the diffraction pattern, indicative of a disordered or turbostratic system. N{sub 2} BET surface areas of the carbonaceous materials range from 10 to 100 m{sup 2}/g. There is some microporosity (r < 1 nm) in the highest surface area carbons. Most of the surface area, however, comes from a mixture of micro and mesopores with radii of 2--5 nm. Electrochemical studies were performed on these carbons. Button cells were fabricated with capacity- limiting carbon pellets electrodes as the cathode a/nd metallic lithium foil as the anode. Large reversible capacities (up to 850 mAh/g) were achieved for most of the samples. The irreversible capacity loss was less than 180 mAh/g after the first cycle, suggesting that these types of carbon materials are very stable to lithium insertion and de-insertion reactions.

Sandi, G.; Winans, R.E.; Carrado, K.A.; Johnson, C.S.

1997-07-01T23:59:59.000Z

307

(Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: Chile was the leading lithium chemical producer in the world; Argentina, China, and  

E-Print Network [OSTI]

%; primary aluminum production, 6%; continuous casting, 4%; rubber and thermoplastics, 4%; pharmaceuticals, 294 LITHIUM (Data in metric tons of lithium content unless otherwise noted) Domestic Production resources, reported production and value of production were withheld from publication to avoid disclosing

308

Chemical Shuttle Additives in Lithium Ion Batteries  

SciTech Connect (OSTI)

The goals of this program were to discover and implement a redox shuttle that is compatible with large format lithium ion cells utilizing LiNi{sub 1/3}Mn{sub 1/3}Co{sub 1/3}O{sub 2} (NMC) cathode material and to understand the mechanism of redox shuttle action. Many redox shuttles, both commercially available and experimental, were tested and much fundamental information regarding the mechanism of redox shuttle action was discovered. In particular, studies surrounding the mechanism of the reduction of the oxidized redox shuttle at the carbon anode surface were particularly revealing. The initial redox shuttle candidate, namely 2-(pentafluorophenyl)-tetrafluoro-1,3,2-benzodioxaborole (BDB) supplied by Argonne National Laboratory (ANL, Lemont, Illinois), did not effectively protect cells containing NMC cathodes from overcharge. The ANL-RS2 redox shuttle molecule, namely 1,4-bis(2-methoxyethoxy)-2,5-di-tert-butyl-benzene, which is a derivative of the commercially successful redox shuttle 2,5-di-tert-butyl-1,4-dimethoxybenzene (DDB, 3M, St. Paul, Minnesota), is an effective redox shuttle for cells employing LiFePO{sub 4} (LFP) cathode material. The main advantage of ANL-RS2 over DDB is its larger solubility in electrolyte; however, ANL-RS2 is not as stable as DDB. This shuttle also may be effectively used to rebalance cells in strings that utilize LFP cathodes. The shuttle is compatible with both LTO and graphite anode materials although the cell with graphite degrades faster than the cell with LTO, possibly because of a reaction with the SEI layer. The degradation products of redox shuttle ANL-RS2 were positively identified. Commercially available redox shuttles Li{sub 2}B{sub 12}F{sub 12} (Air Products, Allentown, Pennsylvania and Showa Denko, Japan) and DDB were evaluated and were found to be stable and effective redox shuttles at low C-rates. The Li{sub 2}B{sub 12}F{sub 12} is suitable for lithium ion cells utilizing a high voltage cathode (potential that is higher than NMC) and the DDB is useful for lithium ion cells with LFP cathodes (potential that is lower than NMC). A 4.5 V class redox shuttle provided by Argonne National Laboratory was evaluated which provides a few cycles of overcharge protection for lithium ion cells containing NMC cathodes but it is not stable enough for consideration. Thus, a redox shuttle with an appropriate redox potential and sufficient chemical and electrochemical stability for commercial use in larger format lithium ion cells with NMC cathodes was not found. Molecular imprinting of the redox shuttle molecule during solid electrolyte interphase (SEI) layer formation likely contributes to the successful reduction of oxidized redox shuttle species at carbon anodes. This helps to understand how a carbon anode covered with an SEI layer, that is supposed to be electrically insulating, can reduce the oxidized form of a redox shuttle.

Patterson, Mary

2013-03-31T23:59:59.000Z

309

Can mirror matter solve the the cosmological lithium problem?  

SciTech Connect (OSTI)

The abundance of lithium-7 confronts cosmology with a long lasting inconsistency between the predictions of standard Big Bang Nucleosynthesis with the baryonic density determined from the Cosmic Microwave Background observations on the one hand, and the spectroscopic determination of the lithium-7 abundance on the other hand. We investigated the influence of the existence of a mirror world, focusing on models in which mirror neutrons can oscillate into ordinary neutrons. Such a mechanism allows for an effective late time neutron injection, which induces an increase of the destruction of beryllium-7and thus a lower final lithium-7 abundance.

Coc, Alain [Centre de Sciences Nuclaires et de Sciences de la Matire (CSNSM), CNRS/IN2P3, Universit Paris Sud 11, UMR 8609, Btiment 104, 91405 Orsay Campus (France); Uzan, Jean-Philippe; Vangioni, Elisabeth [Institut d'Astrophysique de Paris, UMR-7095 du CNRS, Universit Pierre et Marie Curie, 98 bis bd Arago, 75014 Paris, France and Sorbonne Universits, Institut Lagrange de Paris, 98 bis bd Arago, 75014 Paris (France)

2014-05-02T23:59:59.000Z

310

PROGRESS IN DESIGNING A MUON COOLING RING WITH LITHIUM LENSES.  

SciTech Connect (OSTI)

We discuss particle tracking simulations in a storage ring with lithium lens inserts designed for the six-dimensional phase space cooling of muons by the ionization cooling. The ring design contains one or more lithium lens absorbers for transverse cooling that transmit the beam with very small beta-function values, in addition to liquid-hydrogen wedge-shaped absorbers in dispersive locations for longitudinal cooling. Such a ring could comprise the final component of a cooling system for use in a muon collider. The beam matching between dipole-quadrupole lattices and the lithium lenses is of particular interest.

FUKUI,Y.CLINE,D.B.GARREN,A.A.KIRK,H.G.

2004-03-03T23:59:59.000Z

311

Lithium As Plasma Facing Component for Magnetic Fusion Research  

SciTech Connect (OSTI)

The use of lithium in magnetic fusion confinement experiments started in the 1990's in order to improve tokamak plasma performance as a low-recycling plasma-facing component (PFC). Lithium is the lightest alkali metal and it is highly chemically reactive with relevant ion species in fusion plasmas including hydrogen, deuterium, tritium, carbon, and oxygen. Because of the reactive properties, lithium can provide strong pumping for those ions. It was indeed a spectacular success in TFTR where a very small amount (~ 0.02 gram) of lithium coating of the PFCs resulted in the fusion power output to improve by nearly a factor of two. The plasma confinement also improved by a factor of two. This success was attributed to the reduced recycling of cold gas surrounding the fusion plasma due to highly reactive lithium on the wall. The plasma confinement and performance improvements have since been confirmed in a large number of fusion devices with various magnetic configurations including CDX-U/LTX (US), CPD (Japan), HT-7 (China), EAST (China), FTU (Italy), NSTX (US), T-10, T-11M (Russia), TJ-II (Spain), and RFX (Italy). Additionally, lithium was shown to broaden the plasma pressure profile in NSTX, which is advantageous in achieving high performance H-mode operation for tokamak reactors. It is also noted that even with significant applications (up to 1,000 grams in NSTX) of lithium on PFCs, very little contamination (< 0.1%) of lithium fraction in main fusion plasma core was observed even during high confinement modes. The lithium therefore appears to be a highly desirable material to be used as a plasma PFC material from the magnetic fusion plasma performance and operational point of view. An exciting development in recent years is the growing realization of lithium as a potential solution to solve the exceptionally challenging need to handle the fusion reactor divertor heat flux, which could reach 60 MW/m2 . By placing the liquid lithium (LL) surface in the path of the main divertor heat flux (divertor strike point), the lithium is evaporated from the surface. The evaporated lithium is quickly ionized by the plasma and the ionized lithium ions can provide a strongly radiative layer of plasma ("radiative mantle"), thus could significantly reduce the heat flux to the divertor strike point surfaces, thus protecting the divertor surface. The protective effects of LL have been observed in many experiments and test stands. As a possible reactor divertor candidate, a closed LL divertor system is described. Finally, it is noted that the lithium applications as a PFC can be quite flexible and broad. The lithium application should be quite compatible with various divertor configurations, and it can be also applied to protecting the presently envisioned tungsten based solid PFC surfaces such as the ones for ITER. Lithium based PFCs therefore have the exciting prospect of providing a cost effective flexible means to improve the fusion reactor performance, while providing a practical solution to the highly challenging divertor heat handling issue confronting the steadystate magnetic fusion reactors.

Masayuki Ono

2012-09-10T23:59:59.000Z

312

Manganese valence and coordination structure in Mn,Mg-codoped {gamma}-AlON green phosphor  

SciTech Connect (OSTI)

The valence and coordination structure of manganese in a Mn,Mg-codoped {gamma}-AlON spinel-type oxynitride green phosphor were studied by synchrotron X-ray diffraction and absorption fine structure measurements. The absorption edge position of the XANES revealed the bivalency of Mn. Two cation sites are available in the spinel structure for cation doping: a tetrahedral site and an octahedral site. The pre-edge of the XANES and the distance to the nearest neighbor atoms obtained from the EXAFS measurement showed that Mn was situated at the tetrahedral site. Rietveld analysis showed that the vacancy occupied the octahedral site. The preferential occupation of the tetrahedral site by Mn and the roles of N and Mg are discussed in relation to the spinel crystal structure. - Graphical Abstract: Fourier transform of EXAFS of Mn K-edge for Mn,Mg-codoped green phosphor and Mn coordination structure. Highlights: Black-Right-Pointing-Pointer Mn, Mg-codoped {gamma}-AlON green phosphor for white LED. Black-Right-Pointing-Pointer The valence of Mn is divalent. Black-Right-Pointing-Pointer Mn occupies the tetrahedral site in the spinel structure.

Takeda, Takashi, E-mail: TAKEDA.Takashi@nims.go.jp [National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan)] [National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan); Xie, Rong-Jun; Hirosaki, Naoto [National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan)] [National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan); Matsushita, Yoshitaka [National Institute for Materials Science (NIMS), NIMS-SPring-8, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan)] [National Institute for Materials Science (NIMS), NIMS-SPring-8, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Honma, Tetuso [Japan Synchrotron Radiation Research Institute (JASRI), 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan)] [Japan Synchrotron Radiation Research Institute (JASRI), 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan)

2012-10-15T23:59:59.000Z

313

Lithium-Air Battery: High Performance Cathodes for Lithium-Air Batteries  

SciTech Connect (OSTI)

BEEST Project: Researchers at Missouri S&T are developing an affordable lithium-air (Li-Air) battery that could enable an EV to travel up to 350 miles on a single charge. Todays EVs run on Li-Ion batteries, which are expensive and suffer from low energy density compared with gasoline. This new Li-Air battery could perform as well as gasoline and store 3 times more energy than current Li-Ion batteries. A Li-Air battery uses an air cathode to breathe oxygen into the battery from the surrounding air, like a human lung. The oxygen and lithium react in the battery to produce electricity. Current Li-Air batteries are limited by the rate at which they can draw oxygen from the air. The team is designing a battery using hierarchical electrode structures to enhance air breathing and effective catalysts to accelerate electricity production.

None

2010-08-01T23:59:59.000Z

314

(Data in metric tons of contained lithium, unless otherwise noted) Domestic Production and Use: The United States was the largest producer and consumer of lithium minerals and  

E-Print Network [OSTI]

and greases and in the production of synthetic rubber. Salient Statistics--United States: 1992 1993 1994 199598 LITHIUM (Data in metric tons of contained lithium, unless otherwise noted) Domestic Production worldwide. The value of domestic lithium production was estimated to be about $115 million in 1996. Two

315

(Data in metric tons of contained lithium, unless noted) Domestic Production and Use: The United States was the largest producer and consumer of lithium minerals and  

E-Print Network [OSTI]

and greases and synthetic rubber production. Salient Statistics--United States: 1991 1992 1993 1994 1995e96 LITHIUM (Data in metric tons of contained lithium, unless noted) Domestic Production and Use. The value of domestic lithium production was estimated to be about $115 million in 1995. Two companies

316

PHYSICAL REVIEW B 84, 205446 (2011) First-principles study of the oxygen evolution reaction of lithium peroxide in the lithium-air battery  

E-Print Network [OSTI]

motivation in seeking batteries with higher specific energies and higher energy den- sities. Metal-air of lithium peroxide in the lithium-air battery Yifei Mo, Shyue Ping Ong, and Gerbrand Ceder* Department) The lithium-air chemistry is an interesting candidate for the next-generation batteries with high specific

Ceder, Gerbrand

317

Comparison of H-Mode Plasmas Diverted to Solid and Liquid Lithium Surfaces  

SciTech Connect (OSTI)

Experiments were conducted with a Liquid Lithium Divertor (LLD) in NSTX. Among the goals was to use lithium recoating to sustain deuterium (D) retention by a static liquid lithium surface, approximating the ability of flowing liquid lithium to maintain chemical reactivity. Lithium evaporators were used to deposit lithium on the LLD surface. Improvements in plasma edge conditions were similar to those with lithiated graphite plasma-facing components (PFCs), including an increase in confinement over discharges without lithiumcoated PFCs and ELM reduction during H-modes. With the outer strike point on the LLD, the D retention in the LLD was about the same as that for solid lithium coatings on graphite, or about two times that achieved without lithium PFC coatings. There were also indications of contamination of the LLD surface, possibly due erosion and redeposition of carbon from PFCs. Flowing lithium may thus be needed for chemically active PFCs during long-pulse operation.

R. Kaita, et. al.

2012-07-20T23:59:59.000Z

318

Lithium and magnetic fields in giants. HD 232862 : a magnetic and lithium-rich giant star  

E-Print Network [OSTI]

We report the detection of an unusually high lithium content in HD 232862, a field giant classified as a G8II star, and hosting a magnetic field. With the spectropolarimeters ESPaDOnS at CFHT and NARVAL at TBL, we have collected high resolution and high signal-to-noise spectra of three giants : HD 232862, KU Peg and HD 21018. From spectral synthesis we have inferred stellar parameters and measured lithium abundances that we have compared to predictions from evolutionary models. We have also analysed Stokes V signatures, looking for a magnetic field on these giants. HD 232862, presents a very high abundance of lithium (ALi = 2.45 +/- 0.25 dex), far in excess of the theoretically value expected at this spectral type and for this luminosity class (i.e, G8II). The evolutionary stage of HD 232862 has been precised, and it suggests a mass in the lower part of the [1.0 Msun ; 3.5 Msun ] mass interval, likely 1.5 to 2.0 solar mass, at the bottom of the Red Giant Branch. Besides, a time variable Stokes V signature has...

Lbre, A; Nascimento, J D do; Konstantinova-Antova, R; Kolev, D; Aurire, M; De Laverny, P; De Medeiros, J R

2009-01-01T23:59:59.000Z

319

Performance and Characterization of Lithium-Ion Type Polymer Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Performance and Characterization of Lithium-Ion Type Polymer Batteries Performance and Characterization of Lithium-Ion Type Polymer Batteries Speaker(s): Myung D. Cho Date: January 18, 2002 - 12:00pm Location: Bldg. 90 Seminar Host/Point of Contact: Frank McLarnon A new process for the preparation of lithium-polymer batteries with crosslinked gel-polymer electrolyte will be introduced. The new process employs a thermal crosslinking method rather than cell lamination, and is termed "lithium ion type polymer battery (ITPB)". This thermal crosslinking process has many advantages over the standard lamination method, such as fusing the polymer into the electrodes and better adhesion between the electrolyte and electrodes. The new method results in improved high-temperature stability and a simpler process, as well as the improved

320

Students race lithium ion battery powered cars in Pantex competition |  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

race lithium ion battery powered cars in Pantex competition | race lithium ion battery powered cars in Pantex competition | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > NNSA Blog > Students race lithium ion battery powered cars ... Students race lithium ion battery powered cars in Pantex competition Posted By Greg Cunningham, Pantex Public Affairs

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

Lithium Ion Electrode Production NDE and QC Considerations  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

3 Presentation name New Directions in Lithium Ion Electrode In-Line NDE * Low-cost IR laser thickness measurement (can be done in multiple point scans across the web or an entire...

322

Understanding Why Silicon Anodes of Lithium-Ion Batteries Are...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Understanding Why Silicon Anodes of Lithium-Ion Batteries Are Fast to Discharge but Slow to Charge December 02, 2014 Measured and calculated rate-performance of a Si thin-film (70...

323

Hierarchically Porous Graphene as a LithiumAir Battery Electrode  

Science Journals Connector (OSTI)

The lithiumair battery is one of the most promising technologies among various electrochemical energy storage systems. We demonstrate that a novel air electrode consisting of an unusual hierarchical arrangement of functionalized graphene sheets (with no ...

Jie Xiao; Donghai Mei; Xiaolin Li; Wu Xu; Deyu Wang; Gordon L. Graff; Wendy D. Bennett; Zimin Nie; Laxmikant V. Saraf; Ilhan A. Aksay; Jun Liu; Ji-Guang Zhang

2011-10-10T23:59:59.000Z

324

Lithium sulfide compositions for battery electrolyte and battery electrode coatings  

SciTech Connect (OSTI)

Method of forming lithium-containing electrolytes are provided using wet chemical synthesis. In some examples, the lithium containing electrolytes are composed of .beta.-Li.sub.3PS.sub.4 or Li.sub.4P.sub.2S.sub.7. The solid electrolyte may be a core shell material. In one embodiment, the core shell material includes a core of lithium sulfide (Li.sub.2S), a first shell of .beta.-Li.sub.3PS.sub.4 or Li.sub.4P.sub.2S.sub.7, and a second shell including one of .beta.-Li.sub.3PS.sub.4 or Li.sub.4P.sub.2S.sub.7 and carbon. The lithium containing electrolytes may be incorporated into wet cell batteries or solid state batteries.

Liang, Chengdu; Liu, Zengcai; Fu, Wujun; Lin, Zhan; Dudney, Nancy J; Howe, Jane Y; Rondinone, Adam J

2014-10-28T23:59:59.000Z

325

Thermo-mechanical Behavior of Lithium-ion Battery Electrodes  

E-Print Network [OSTI]

Developing electric vehicles is widely considered as a direct approach to resolve the energy and environmental challenges faced by the human race. As one of the most promising power solutions to electric cars, the lithium ion battery is expected...

An, Kai

2013-11-25T23:59:59.000Z

326

Generation of thermonuclear energy by fusing hydrogen and lithium atoms  

Science Journals Connector (OSTI)

A method of designing a thermonuclear reactor based on the modified Cockroft-Walton accelerator, where the lithium-proton fusion was first observed, is considered. It...15 W/cm2...to the cathode are determined. T...

V. E. Tyrsa; L. P. Burtseva

2003-07-01T23:59:59.000Z

327

Novel Electrolyte Enables Stable Graphite Anodes in Lithium Ion...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

(1) A194-A200 (2014). (1,716 KB) Technology Marketing Summary Berkeley Lab researchers led by Gao Liu have developed an improved lithium ion battery electrolyte containing a...

328

Development of Electrolytes for Lithium-ion Batteries  

Broader source: Energy.gov (indexed) [DOE]

4.75V(LNMO) 5.30V(LNMO) Similar surface species are observed on Pt to metal oxide, polyethylene carbonate and lithium fluorophosphates The metal oxide does not appear to catalyze...

329

Helium Pumping Wall for a Liquid Lithium Tokamak Richard Majeski...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Helium Pumping Wall for a Liquid Lithium Tokamak Richard Majeski This invention is designed to be a subsystem of a device, a tokamak with walls or plasma facing components of...

330

Manufacturability Study and Scale-Up for Large Format Lithium...  

Broader source: Energy.gov (indexed) [DOE]

contributions out of over 40 in FY1314 * Selected publications 1. J. Li, B.L. Armstrong, J. Kiggans, C. Daniel, and D.L. Wood, "Lithium Ion Cell Performance Enhancement...

331

Advances in 3-Volt Lithium Batteries for Electronic Applications  

Science Journals Connector (OSTI)

Significant improvements have been made in recent years in the performance, reliability and operating temperature range of 3-volt primary lithium cell systems. Because of their excellent characteristics, especially their long life, they are not only ...

R. A. Langan; V. Z. Leger; G. R. Tucholski

1985-08-01T23:59:59.000Z

332

Lithium/antiepileptic drugs/naproxen/aripiprazole/memantine interaction  

Science Journals Connector (OSTI)

A 61-year-old man developed cognition disorders during concomitant use of lithium, valproate semisodium, gabapentin, naproxen, aripiprazole and memantine [duration of treatment to reaction onset not clearly state...

2008-05-01T23:59:59.000Z

333

Three-Dimensional Lithium-Ion Battery Model (Presentation)  

SciTech Connect (OSTI)

Nonuniform battery physics can cause unexpected performance and life degradations in lithium-ion batteries; a three-dimensional cell performance model was developed by integrating an electrode-scale submodel using a multiscale modeling scheme.

Kim, G. H.; Smith, K.

2008-05-01T23:59:59.000Z

334

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications  

E-Print Network [OSTI]

Battery safety has been a very important research area over the past decade. Commercially available lithium ion batteries employ low flash point (<80 C), flammable, and volatile organic electrolytes. These organic based ...

Hu, Qichao

335

Improvement in Plasma Performance with Lithium Coatings in NSTX  

SciTech Connect (OSTI)

Lithium as a plasma-facing material has attractive features, including a reduction in the recycling of hydrogenic species and the potential for withstanding high heat and neutron fluxes in fusion reactors. Dramatic effects on plasma performance with lithium-coated plasma-facing components (PFCOs) have been demonstrated on many fusion devices, including TFTR, [1] T-11M, [2] and FT-U. [3] Using a liquid-lithium-filled tray as a limiter, the CDX-U device achieved very significant enhancement in the confinement time of ohmically heated plasmas. [4] The recent NSTX experiments reported here have demonstrated, for the first time, significant and recurring benefits of lithium PFC coatings on divertor plasma performance in both L- and H- mode regimes heated by neutral beams.

Kaita, R; Ahn, J -W; Allain, J P; Bell, M G; Bell, R; Boedo, J; Bush, C; Mansfield, D; Menard, J; Mueller, D; Ono, M; Paul, S; Raman, R; Roquemore, A L; Ross, P W; Sabbagh, S; Schneider, H; Skinner, C H; Soukhanovskii, V; Stevenson, T; Stotler, D; Timberlake, J; Wampler, W R; Wilgen, J B

2008-09-12T23:59:59.000Z

336

Improvement in Plasma Performance with Lithium Coatings in NSTX  

SciTech Connect (OSTI)

Lithium as a plasma-facing material has attractive features, including a reduction in the recycling of hydrogenic species and the potential for withstanding high heat and neutron fluxes in fusion reactors. Dramatic effects on plasma performance with lithium-coated plasma-facing components (PFC's) have been demonstrated on many fusion devices, including TFTR, T-11M, and FT-U. Using a liquid-lithium-filled tray as a limiter, the CDX-U device achieved very significant enhancement in the confinement time of ohmically heated plasmas. The recent NSTX experiments reported here have demonstrated, for the first time, significant and recurring benefits of lithium PFC coatings on divertor plasma performance in both L- and H- mode regimes heated by neutral beams.

Kaita, R

2009-02-17T23:59:59.000Z

337

Process for manufacturing a lithium alloy electrochemical cell  

DOE Patents [OSTI]

A process for manufacturing a lithium alloy, metal sulfide cell tape casts slurried alloy powders in an organic solvent containing a dissolved thermoplastic organic binder onto casting surfaces. The organic solvent is then evaporated to produce a flexible tape removable adhering to the casting surface. The tape is densified to increase its green strength and then peeled from the casting surface. The tape is laminated with a separator containing a lithium salt electrolyte and a metal sulfide electrode to form a green cell. The binder is evaporated from the green cell at a temperature lower than the melting temperature of the lithium salt electrolyte. Lithium alloy, metal sulfide and separator powders may be tape cast.

Bennett, William R. (North Olmstead, OH)

1992-10-13T23:59:59.000Z

338

Graphene-Based Composite Anodes for Lithium-Ion Batteries  

Science Journals Connector (OSTI)

Graphene has emerged as a novel, highly promising ... . As an anode material for lithium-ion batteries, it was shown that it cannot be ... cycling that leads to the failure of the batteries. To resolve this probl...

Nathalie Lavoie; Fabrice M. Courtel

2013-01-01T23:59:59.000Z

339

The application of graphene in lithium ion battery electrode materials  

Science Journals Connector (OSTI)

Graphene is composed of a single atomic layer ... concept, structure, properties, preparation methods of graphene and its application in lithium ion batteries. A continuous 3D conductive network formed by graphene

Jiping Zhu; Rui Duan; Sheng Zhang; Nan Jiang; Yangyang Zhang; Jie Zhu

2014-10-01T23:59:59.000Z

340

Hyperfine Studies of Lithium Vapor using Saturated Absorption Spectroscopy  

E-Print Network [OSTI]

the frequency of a laser with respect to an atomic spectral feature.[20] As such, saturated absorptionHyperfine Studies of Lithium Vapor using Saturated Absorption Spectroscopy? . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 3.3 Broadening Mechanisms . . . . . . . . . . . . . . . . . . . . . 15 3.4 Saturated Absorption

Cronin, Alex D.

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

Challenges and Prospects of LithiumSulfur Batteries  

Science Journals Connector (OSTI)

His research interests are in the area of materials for rechargeable batteries, fuel cells, and solar cells, including novel synthesis approaches for nanomaterials. ... Lithium-ion (Li-ion) batteries have the highest energy density among the rechargeable battery chemistries. ...

Arumugam Manthiram; Yongzhu Fu; Yu-Sheng Su

2012-10-25T23:59:59.000Z

342

Thermal Behavior and Modeling of Lithium-Ion Cuboid Battery  

Science Journals Connector (OSTI)

Thermal behaviour and model are important items should be considered when designing a battery pack cooling system. Lithium-ion battery thermal behaviour and modelling method are investigated in this paper. The te...

Hongjie Wu; Shifei Yuan

2013-01-01T23:59:59.000Z

343

Rechargeable lithium battery energy storage systems for vehicular applications.  

E-Print Network [OSTI]

??Batteries are used on-board vehicles for broadly two applications starting-lighting-ignition (SLI) and vehicle traction. This thesis examines the suitability of the rechargeable lithium battery (more)

HURIA, TARUN

2012-01-01T23:59:59.000Z

344

An improved lithium acetate method for yeast transformation  

Science Journals Connector (OSTI)

We have studied the effect on Saccharomyces cerevisiae...transformation frequency of varying several parameters of the lithium acetate-mediated transformation protocol first reported by Ito et al. (1983 a). We fo...

Stewart D. Finlayson; Christine Fleming; David R. Berry

345

Synthesis, Characterization and Performance of Cathodes for Lithium Ion Batteries  

E-Print Network [OSTI]

A new cathode material for batteries of high energy density.high-energy cathode for rechargeable lithium batteries. Advanced Materialsmaterials are promising cathodes, as they can provide high power and high energy,

Zhu, Jianxin

2014-01-01T23:59:59.000Z

346

Development of Large Format Lithium Ion Cells with Higher Energy...  

Broader source: Energy.gov (indexed) [DOE]

Hydrogen and Fuel Cells Program Review ES-127 Development of Large Format Lithium Ion Cells with Higher Energy Density Erin O'Driscoll (PI) Han Wu (Presenter) Dow Kokam May 13,...

347

Lithium Source For High Performance Li-ion Cells | Department...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Li-ion Cells Lithium Source For High Performance Li-ion Cells 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer...

348

Realization of Bose-Einstein condensation with Lithium-7 atoms  

E-Print Network [OSTI]

This thesis presents our work on developing and improving the techniques of trapping and cooling an ultra-cold cloud of Lithium-7 atoms and the realization of the Bose- Einstein condensate as a first step to study quantum ...

Yu, Yichao

2014-01-01T23:59:59.000Z

349

Lithium-rich stars in the Sloan Digital Sky Survey  

E-Print Network [OSTI]

We report the discovery of 23 lithium-rich post-main-sequence stars, identified from moderate-resolution SDSS spectroscopy and confirmed with high-resolution spectra taken at the Hobby-Eberly Telescope. These new Li-rich stars cover a broad range in mass and evolutionary phase, including bright giants and post-AGB stars. The process responsible for preserving or producing excess lithium in a small fraction of evolved stars remains unclear.

Martell, Sarah L

2012-01-01T23:59:59.000Z

350

Lithium Methyl Carbonate as a Reaction Product of Metallic Lithiumand Dimethyl Carbonate  

SciTech Connect (OSTI)

To improve the understanding of passive film formation on metallic lithium in organic electrolyte, we synthesized and characterized lithium methyl carbonate (LiOCO{sub 2}CH{sub 3}), a prototypical component of the film. The chemical structure of this compound was characterized with Nuclear Magnetic Resonance (NMR) and Fourier Transform Infrared Spectroscopy (FTIR), and its thermal stability and decomposition pathway was studied by thermo-gravimetric analysis (TGA). The FTIR spectrum of chemically synthesized compound enabled us to resolve multiple products in the passive film on lithium in dimethyl carbonate (DMC). Lithium methyl carbonate is only one of the components, the others being lithium oxalate and lithium methoxide.

Zhuang, Guorong V.; Yang, Hui; Ross Jr., Philip N.; Xu, Kang; Jow, T. Richard

2005-10-16T23:59:59.000Z

351

Recycling of Lithium-Ion Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

B. Dunn B. Dunn Center for Transportation Research Argonne National Laboratory Recycling of Lithium-Ion Batteries Plug-In 2013 San Diego, CA October 2, 2013 The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory ("Argonne"). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357. The U.S. Government retains for itself, and others acting on its behalf, a paid-up nonexclusive, irrevocable worldwide license in said article to reproduce, prepare derivative works, distribute copies to the public, and perform publicly and display publicly, by or on behalf of the Government.

352

Recent Liquid Lithium Limiter Experiments in CDX-U  

SciTech Connect (OSTI)

Recent experiments in the Current Drive eXperiment-Upgrade (CDX-U) provide a first-ever test of large area liquid lithium surfaces as a tokamak first wall, to gain engineering experience with a liquid metal first wall, and to investigate whether very low recycling plasma regimes can be accessed with lithium walls. The CDX-U is a compact (R=34 cm, a=22 cm, B{sub toroidal} = 2 kG, I{sub P} =100 kA, T{sub e}(0) {approx} 100 eV, n{sub e}(0) {approx} 5 x 10{sup 19} m{sup -3}) spherical torus at the Princeton Plasma Physics Laboratory. A toroidal liquid lithium pool limiter with an area of 2000 cm{sup 2} (half the total plasma limiting surface) has been installed in CDX-U. Tokamak discharges which used the liquid lithium pool limiter required a fourfold lower loop voltage to sustain the plasma current, and a factor of 5-8 increase in gas fueling to achieve a comparable density, indicating that recycling is strongly reduced. Modeling of the discharges demonstrated that the lithium limited discharges are consistent with Z{sub effective} < 1.2 (compared to 2.4 for the pre-lithium discharges), a broadened current channel, and a 25% increase in the core electron temperature. Spectroscopic measurements indicate that edge oxygen and carbon radiation are strongly reduced.

R. Majeski; S. Jardin; R. Kaita; T. Gray; P. Marfuta; J. Spaleta; J. Timberlake; L. Zakharov; G. Antar; R. Doerner; S. Luckhardt; R. Seraydarian; V. Soukhanovskii; R. Maingi; M. Finkenthal; D. Stutman; D. Rodgers; S. Angelini

2005-05-03T23:59:59.000Z

353

Liquid Lithium Limiter Experiments in CDX-U  

SciTech Connect (OSTI)

Recent experiments in the Current Drive Experiment-Upgrade provide a first-ever test of large area liquid lithium surfaces as a tokamak first wall, to gain engineering experience with a liquid metal first wall, and to investigate whether very low recycling plasma regimes can be accessed with lithium walls. The CDX-U is a compact (R = 34 cm, a = 22 cm, B{sub toroidal} = 2 kG, I{sub P} = 100 kA, T{sub e}(0) = 100 eV, n{sub e}(0) {approx} 5 x 10{sup 19} m{sup -3}) spherical torus at the Princeton Plasma Physics Laboratory. A toroidal liquid lithium tray limiter with an area of 2000 cm{sup 2} (half the total plasma limiting surface) has been installed in CDX-U. Tokamak discharges which used the liquid lithium limiter required a fourfold lower loop voltage to sustain the plasma current, and a factor of 5-8 increase in gas fueling to achieve a comparable density, indicating that recycling is strongly reduced. Modeling of the discharges demonstrated that the lithium-limited discharges are consistent with Z{sub effective} < 1.2 (compared to 2.4 for the pre-lithium discharges), a broadened current channel, and a 25% increase in the core electron temperature. Spectroscopic measurements indicate that edge oxygen and carbon radiation are strongly reduced.

R. Majeski; S. Jardin; R. Kaita; T. Gray; P. Marfuta; J. Spaleta; J. Timberlake; L. Zakharov; G. Antar; R. Doerner; S. Luckhardt; R. Seraydarian; V. Soukhanovskii; R. Maingi; M. Finkenthal; D. Stutman; D. Rodgers

2004-10-28T23:59:59.000Z

354

Application of lithium in molten-salt reduction processes.  

SciTech Connect (OSTI)

Metallothermic reductions have been extensively studied in the field of extractive metallurgy. At Argonne National Laboratory (ANL), we have developed a molten-salt based reduction process using lithium. This process was originally developed to reduce actinide oxides present in spent nuclear fuel. Preliminary thermodynamic considerations indicate that this process has the potential to be adapted for the extraction of other metals. The reduction is carried out at 650 C in a molten-salt (LiCl) medium. Lithium oxide (Li{sub 2}O), produced during the reduction of the actinide oxides, dissolves in the molten salt. At the end of the reduction step, the lithium is regenerated from the salt by an electrowinning process. The lithium and the salt from the electrowinning are then reused for reduction of the next batch of oxide fuel. The process cycle has been successfully demonstrated on an engineering scale in a specially designed pyroprocessing facility. This paper discusses the applicability of lithium in molten-salt reduction processes with specific reference to our process. Results are presented from our work on actinide oxides to highlight the role of lithium and its effect on process variables in these molten-salt based reduction processes.

Gourishankar, K. V.

1998-11-11T23:59:59.000Z

355

N-Doped GrapheneVO2(B) Nanosheet-Built 3D Flower Hybrid for Lithium Ion Battery  

Science Journals Connector (OSTI)

N-Doped GrapheneVO2(B) Nanosheet-Built 3D Flower Hybrid for Lithium Ion Battery ... Graphene-based electrode materials for rechargeable lithium batteries ...

C. Nethravathi; Catherine R. Rajamathi; Michael Rajamathi; Ujjal K. Gautam; Xi Wang; Dmitri Golberg; Yoshio Bando

2013-03-13T23:59:59.000Z

356

KWH_APS_DPP07_1Page.ppt  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Ion-Temperature and Rotation-Velocity Profiles from a Spatially Resolving X-Ray Crystal Spectrometer on Alcator C-Mod Ion-Temperature and Rotation-Velocity Profiles from a Spatially Resolving X-Ray Crystal Spectrometer on Alcator C-Mod K. W. Hill, 1 M. Bitter, 1 P. Beiersdorfer, 3 Ch. Broennimann, 4 E. F. Eikenberry, 4 A. Ince-Cushman, 2 Ming-Feng Gu, 3 S. G. Lee, 5 M. Reinke, 2 J. E. Rice, 2 S. D. Scott, 1 and B. Stratton 1 1 Princeton Plasma Physics Laboratory, Princeton, NJ 2 MIT Plasma Science and Fusion Center, Cambridge, MA 3 LLNL, Livermore, CA 4 DECTRIS Ltd., 5232 Villigen-PSI, Switzerland 5 NFRC, Korea Basic Science Institute, Daejeon, Korea Abstract A new x-ray crystal spectrometer capable of providing spatially (~1.5 cm) and temporally (~10 ms) resolved, high resolution spectra of He-like Ar Kα lines has been installed on Alcator C-Mod. The imaging spectrometer consists of a

357

kWh Analytics: Quality Ratings for PV  

Broader source: Energy.gov [DOE]

This presentation summarizes the information given during the SunShot Grand Challenge Summit and Technology Forum, June 13-14, 2012.

358

Comparing Mainframe and Windows Server Transactions per kWh  

E-Print Network [OSTI]

........................................................................................14 Appendix A. Platform Comparison and Conversion Factors...............................................................................................................15 Conversion Factors............................................................................................................................3 Objective: Estimate Energy Consumption for Similar Uses

Narasayya, Vivek

359

Strong Coupling between 4f Valence Instability and 3d Ferromagnetism in YbxFe4Sb12 Studied by Resonant X-Ray Emission Spectroscopy  

E-Print Network [OSTI]

electrons tends to stabilize magnetic ordered states. Permanent ferromagnets, such as Nd-Fe-B and SmStrong Coupling between 4f Valence Instability and 3d Ferromagnetism in YbxFe4Sb12 Studied valence is independent of temperature. This evidences a close interplay between the magnetic instability

Lin, Jung-Fu "Afu"

360

A linear-scaling self-consistent generalization of the multistate empirical valence bond method for multiple excess protons in aqueous  

E-Print Network [OSTI]

Grot- thuss who proposed a hydrogen­oxygen shuttling mecha- nism to explain electrolysis of water.20 multiple excess protons within the context of molecular-dynamics simulation. The computational cost molecule and forms a valence bond with that oxygen atom. Meanwhile, one of the valence-bonded hydrogen

Simons, Jack

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

Electron Energy-Loss Safe-Dose Limits for Manganese Valence Measurements in Environmentally Relevant Manganese Oxides  

E-Print Network [OSTI]

19717-1303, United States § U.S. Army Engineer Research & Development Center, 3909 Halls Ferry Road are among the strongest mineral oxidants in the environment and impose significant influence on mobility. INTRODUCTION Mn exists in the 2+, 3+, and 4+ valence states in natural environment and, most of the time, as Mn

Sparks, Donald L.

362

Valence-electron distribution in MgB2 by accurate diffraction measurements and first-principles calculations  

E-Print Network [OSTI]

-principles calculations A great challenge in the studies of condensed matter is to measure the redistribution of electrons on precision electron-diffraction measurements and DFT calculations. (h-i) DFT calculated difference chargeValence-electron distribution in MgB2 by accurate diffraction measurements and first

Homes, Christopher C.

363

Extended Near-Infrared Resonance Raman Investigations of an Organic Mixed-Valence System: Diazatetracyclodiene Radical Cation  

E-Print Network [OSTI]

Extended Near-Infrared Resonance Raman Investigations of an Organic Mixed-Valence System near-infrared region show that six modes are coupled to the intramolecular charge-transfer transition transfer (IVCT) absorption bands in the red to near- infrared region of the spectrum, which are, at least

364

Controlled Nucleation and Growth Process of Li2S2/Li2S in Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Nucleation and Growth Process of Li2S2Li2S in Lithium-Sulfur Batteries. Controlled Nucleation and Growth Process of Li2S2Li2S in Lithium-Sulfur Batteries. Abstract:...

365

Synthesis Of Nitrogen-Doped Graphene Films For Lithium Battery Application  

Science Journals Connector (OSTI)

Synthesis Of Nitrogen-Doped Graphene Films For Lithium Battery Application ... Fabrication of Nitrogen-Doped Holey Graphene Hollow Microspheres and Their Use as an Active Electrode Material for Lithium Ion Batteries ...

Arava Leela Mohana Reddy; Anchal Srivastava; Sanketh R. Gowda; Hemtej Gullapalli; Madan Dubey; Pulickel M. Ajayan

2010-10-08T23:59:59.000Z

366

Biologically enhanced cathode design for improved capacity and cycle life for lithium-oxygen batteries  

E-Print Network [OSTI]

Lithium-oxygen batteries have a great potential to enhance the gravimetric energy density of fully packaged batteries by two to three times that of lithium ion cells. Recent studies have focused on finding stable electrolytes ...

Oh, Dahyun

367

Design of Safer High-Energy Density Materials for Lithium-Ion...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Safer High-Energy Density Materials for Lithium-Ion Cells Design of Safer High-Energy Density Materials for Lithium-Ion Cells 2012 DOE Hydrogen and Fuel Cells Program and Vehicle...

368

LITHIUM ISOTOPIC COMPOSITION OF CHONDRITIC METEORITES. W. F. McDonough1 , P. B. Tomascak1  

E-Print Network [OSTI]

LITHIUM ISOTOPIC COMPOSITION OF CHONDRITIC METEORITES. W. F. McDonough1 , F- Z. Teng1 , P. B processes involving aqueous fluids, given the potential solubility of lithium [1]. In this respect, Li

Mcdonough, William F.

369

Thin film lithium-based batteries and electrochromic devices fabricated with nanocomposite electrode materials  

DOE Patents [OSTI]

Thin-film lithium-based batteries and electrochromic devices (10) are fabricated with positive electrodes (12) comprising a nanocomposite material composed of lithiated metal oxide nanoparticles (40) dispersed in a matrix composed of lithium tungsten oxide.

Gillaspie, Dane T; Lee, Se-Hee; Tracy, C. Edwin; Pitts, John Roland

2014-02-04T23:59:59.000Z

370

Post-Test Analysis of Lithium-Ion Battery Materials at Argonne...  

Broader source: Energy.gov (indexed) [DOE]

Test Analysis of Lithium-Ion Battery Materials at Argonne National Laboratory Post-Test Analysis of Lithium-Ion Battery Materials at Argonne National Laboratory 2013 DOE Hydrogen...

371

Thermal behaviors of electrolytes in lithium-ion batteries determined by differential scanning calorimeter  

Science Journals Connector (OSTI)

Lithium-ion batteries have been widely used in daily electric ... occurred from time to time. Lithium-ion batteries composed of various electrolytes (containing organic solvents ... to meet safety requirements of...

Yu-Yun Sun; Tsai-Ying Hsieh; Yih-Shing Duh

2014-06-01T23:59:59.000Z

372

E-Print Network 3.0 - aluminum-lithium alloys processed Sample...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

aluminum-lithium alloys, there is a precipitation of metastable, coherent, L1... and fracture toughness of aluminum-lithium alloys can be improved by the addition of zirconium...

373

STUDIES ON TWO CLASSES OF POSITIVE ELECTRODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

A new cathode material for batteries of high energy density.art positive electrode materials for high-energy lithium ionwhen exploring new materials for high-energy lithium ion

Wilcox, James D.

2010-01-01T23:59:59.000Z

374

E-Print Network 3.0 - all-solid-state lithium secondary Sample...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

SOC and SOH of Lithium-ion Cells A. Zenati1,* , Ph. Desprez1 , H. Razik2 and S. Rael3 1 SAFT... at analyzing lithium-ion batteries performances with aging, for different state of...

375

Advanced Electrolyte Additives for PHEV/EV Lithium-ion Battery...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Advanced Electrolyte Additives for PHEVEV Lithium-ion Battery Development of Advanced Electrolytes and Electrolyte Additives...

376

Overcharge Protection for 4 V Lithium Batteries at High Rates and Low Temperature  

E-Print Network [OSTI]

lithium batteries. Because the stoichiometric spinel LiMn204 exhibits significant capacity fading during charge/discharge cycling, excess

Chen, Guoying

2010-01-01T23:59:59.000Z

377

Adaptable SiliconCarbon Nanocables Sandwiched between Reduced Graphene Oxide Sheets as Lithium Ion Battery Anodes  

Science Journals Connector (OSTI)

Adaptable SiliconCarbon Nanocables Sandwiched between Reduced Graphene Oxide Sheets as Lithium Ion Battery Anodes ... Despite rapidly growing interest in the application of graphene in lithium ion batteries, the interaction of the graphene with lithium ions and electrolyte species during electrochemical cycling is not fully understood. ...

Bin Wang; Xianglong Li; Xianfeng Zhang; Bin Luo; Meihua Jin; Minghui Liang; Shadi A. Dayeh; S. T. Picraux; Linjie Zhi

2013-01-02T23:59:59.000Z

378

EXPERIMENTAL MEASUREMENTS OF THE INTERFACE THERMAL CONDUCTANCE OF A LITHIUM METATITANATE PEBBLE BED  

E-Print Network [OSTI]

, CA 90095 aliabousena@engineering.ucla.edu The thermal properties of the lithium ceramics pebble beds will help to create a reliable database of the thermal properties of the lithium ceramics pebble beds. I heat is transferred from the hot lithium ceramic pebble beds to the coolant. The thermal properties

Abdou, Mohamed

379

Limited lithium isotopic fractionation during progressive metamorphic dehydration in metapelites: A case study  

E-Print Network [OSTI]

Limited lithium isotopic fractionation during progressive metamorphic dehydration in metapelites-zone metamorphism far removed from the pluton to partially melted rocks adjacent to the pluton. Lithium on the aureole scale. Published by Elsevier B.V. Keywords: Lithium; Isotope fractionation; Metamorphic

Mcdonough, William F.

380

Lithium in Jack Hills zircons: Evidence for extensive weathering of Earth's earliest crust Takayuki Ushikubo a,  

E-Print Network [OSTI]

Lithium in Jack Hills zircons: Evidence for extensive weathering of Earth's earliest crust Takayuki Hills lithium weathering continental crust Hadean In situ Li analyses of 4348 to 3362 Ma detrital of REEs. The Jack Hills zircons also have fractionated lithium isotope ratios (7 Li=-19 to+13) about five

Mcdonough, William F.

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

Extreme lithium isotopic fractionation during continental weathering revealed in saprolites from South Carolina  

E-Print Network [OSTI]

Extreme lithium isotopic fractionation during continental weathering revealed in saprolites from in revised form 6 July 2004 Abstract The lithium concentration and isotopic composition of two saprolites the behavior of lithium isotopes during continental weathering. Both saprolites show a general trend

Rudnick, Roberta L.

382

Lithium in cool stellar atmospheres: Big bang nucleosynthesis and extrasolar planets  

E-Print Network [OSTI]

Lithium in cool stellar atmospheres: Big bang nucleosynthesis and extrasolar planets Matthias Steffen and Elisabetta Caffau Sternphysik In metal-poor stellar atmospheres, the Lithium line at 6707 ?-NLTE, respectively. The accurate spectroscopic determination of the Lithium abundance and in particular the 6Li/7Li

383

Lithium isotopic composition and concentration of the deep continental crust Fang-Zhen Teng a,  

E-Print Network [OSTI]

Lithium isotopic composition and concentration of the deep continental crust Fang-Zhen Teng a April 2008 Accepted 5 June 2008 Editor: B. Bourdon Keywords: Lithium Isotope fractionation Deep. Lithium concentrations of granulite xenoliths also vary widely (0.5 to 21 ppm) and are, on average, lower

Mcdonough, William F.

384

Lithium isotopic systematics of granites and pegmatites from the Black Hills, South Dakota  

E-Print Network [OSTI]

Lithium isotopic systematics of granites and pegmatites from the Black Hills, South Dakota Fang compositions may reflect Li isotopic fractionation resulting from extensive crystal-melt fractionation. Lithium fractionation in the near­surface environment of > 60 (Tomascak, 2004). Lithium isotopic fractionation has been

Rudnick, Roberta L.

385

Lithium diffusion mechanisms in layered intercalation compounds A. Van der Ven*  

E-Print Network [OSTI]

Lithium diffusion mechanisms in layered intercalation compounds A. Van der Ven* , G. Ceder; accepted 28 December 2000 Abstract We investigate the mechanisms of lithium diffusion in layered intercalation compounds from ®rst-principles. We focus on LixCoO2 and ®nd that lithium diffusion

Ceder, Gerbrand

386

Reply: Lithium and Increased Cortical Gray Matter--More Tissue or More Water?  

E-Print Network [OSTI]

Reply: Lithium and Increased Cortical Gray Matter--More Tissue or More Water? To the Editor: W e cortices, in lithium-treated patients with bipolar disorder, relative to healthy control subjects (1). Dr patients. Although lithium's effects on body water homeostasis (2) are important to consider, the absence

Thompson, Paul

387

Abstract: The deproto-metalation reactions of pyrimidine and pyrazine were regioselectively carried out using lithium  

E-Print Network [OSTI]

carried out using lithium tri(2,2,6,6-tetramethylpiperidino)cadmate in tetrahydrofuran at room temperature instead of 1/3). Key words: Metalations, Cadmium, Lithium, Heterocycles, Iodine. Procedure 1 25 mmol scale metalation of aromatic rings, and various strong bases such as alkylli- thiums and lithium dialkylamides have

Boyer, Edmond

388

Solid state thin film battery having a high temperature lithium alloy anode  

DOE Patents [OSTI]

An improved rechargeable thin-film lithium battery involves the provision of a higher melting temperature lithium anode. Lithium is alloyed with a suitable solute element to elevate the melting point of the anode to withstand moderately elevated temperatures. 2 figs.

Hobson, D.O.

1998-01-06T23:59:59.000Z

389

Local Electromechanical Response at a Single Ferroelectric Domain Wall in Lithium Niobate  

E-Print Network [OSTI]

-antisites (which are excess Nb atoms at Li locations), and lithium vacancies denoted by Li. The defect equilibriumLocal Electromechanical Response at a Single Ferroelectric Domain Wall in Lithium Niobate DAVID A electromechanical response across a single ferroelectric domain wall in congruent lithium niobate at room

Gopalan, Venkatraman

390

Fabricating Genetically Engineered High-Power Lithium-Ion Batteries Using Multiple Virus Genes  

Science Journals Connector (OSTI)

...system) and a photograph of the battery used to power a green LED...electrode in a lithium-ion battery using lithium metal foil as...nanowires as a lithium-ion battery cathode was evaluated (Fig...expected to bind favorably to the graphene surface via {pi}-stacking...

Yun Jung Lee; Hyunjung Yi; Woo-Jae Kim; Kisuk Kang; Dong Soo Yun; Michael S. Strano; Gerbrand Ceder; Angela M. Belcher

2009-05-22T23:59:59.000Z

391

Understanding structural defects in lithium-rich layered oxide cathodes Karalee A. Jarvis,a  

E-Print Network [OSTI]

the required amounts of lithium, manganese, and nickel acetates were added to this solution. The molar ratioUnderstanding structural defects in lithium-rich layered oxide cathodes Karalee A. Jarvis, Accepted 31st March 2012 DOI: 10.1039/c2jm30575e Planar defects in lithium-rich layered oxides were

Ferreira, Paulo J.

392

Abstract--This paper describes experimental results aiming at analyzing lithium-ion batteries performances  

E-Print Network [OSTI]

several years SAFT has developed a range of lithium ion cells and batteries to cover the full spectrum. To follow such a characteristic, electrochemical impedance spectroscopy (EIS) measurements on SAFT lithium-ion cells The cells used are lithium-ion SAFT power cells: VL30P which outputs a nominal capacity of 30 Ah

Paris-Sud XI, Université de

393

Molecular Structure and Stability of Dissolved Lithium Polysulfide Species  

SciTech Connect (OSTI)

Ability to predict the solubility and stability of lithium polysulfide is vital in realizing longer lasting lithium-sulfur batteries. Herein we report a combined computational and experimental spectroscopic analysis to understand the dissolution mechanism of lithium polysulfide species in an aprotic solvent medium. Multinuclear NMR and sulfur K-edge X-ray absorption (XAS) analysis reveals that the lithium exchange between polysulfide species and solvent molecule constitutes the first step in the dissolution process. Lithium exchange leads to de-lithiated polysulfide ions which subsequently forms highly reactive free radicals through disproportion reaction. The energy required for the disproportion and possible dimer formation reactions of the polysulfide species are analyzed using density functional theory (DFT) calculations. We validate our calculations with variable temperature electron spin resonance (ESR) measurements. Based on these findings, we discuss approaches to optimize the electrolyte in order to control the polysulfide solubility. The energy required for the disproportion and possible dimer formation reactions of the polysulfide species are analyzed using density functional theory (DFT) calculations. We validate our calculations with variable temperature electron spin resonance (ESR) measurements. Based on these findings, we discuss approaches to optimize the electrolyte in order to control the polysulfide solubility.

Vijayakumar, M.; Govind, Niranjan; Walter, Eric D.; Burton, Sarah D.; Shukla, Anil K.; Devaraj, Arun; Xiao, Jie; Liu, Jun; Wang, Chong M.; Karim, Ayman M.; Thevuthasan, Suntharampillai

2014-03-24T23:59:59.000Z

394

Recent advances in lithiumsulfur batteries  

Science Journals Connector (OSTI)

Abstract Lithiumsulfur (LiS) batteries have attracted much attention lately because they have very high theoretical specific energy (2500Whkg?1), five times higher than that of the commercial LiCoO2/graphite batteries. As a result, they are strong contenders for next-generation energy storage in the areas of portable electronics, electric vehicles, and storage systems for renewable energy such as wind power and solar energy. However, poor cycling life and low capacity retention are main factors limiting their commercialization. To date, a large number of electrode and electrolyte materials to address these challenges have been investigated. In this review, we present the latest fundamental studies and technological development of various nanostructured cathode materials for LiS batteries, including their preparation approaches, structure, morphology and battery performance. Furthermore, the development of other significant components of LiS batteries including anodes, electrolytes, additives, binders and separators are also highlighted. Not only does the intention of our review article comprise the summary of recent advances in LiS cells, but also we cover some of our proposals for engineering of LiS cell configurations. These systematic discussion and proposed directions can enlighten ideas and offer avenues in the rational design of durable and high performance LiS batteries in the near future.

Lin Chen; Leon L. Shaw

2014-01-01T23:59:59.000Z

395

A resolution of the cosmic Lithium problem  

E-Print Network [OSTI]

In 1982, Monique and Francois Spite discovered that the 7Li abundance in the atmosphere of old metal-poor dwarf stars in the galactic halo was independent of metallicity and temperature. Since then, 7Li abundance in the Universe has become a subject of intrigue, because there is less of it in Population II dwarf stars (by a factor of 3) than standard big bang nucleosynthesis predicts. Here we show how quark-novae (QNe) occurring in the wake of Pop. III stars, can elegantly produce an A(Li) ~ 2.2 Lithium plateau in Pop. II (low-mass) stars formed in the pristine cloud swept up by the mixed SN+QN ejecta. We also find an increase in the scatter as well as an eventual drop in A(Li) below the Spite plateau values for very low metallicity ([Fe/H] < -3) in excellent agreement with observations. We propose a solution to the discrepancy between the Big Bang Nucleosynthesis 7Li abundance and the Spite plateau and list some implications and predictions of our model.

Rachid Ouyed

2014-02-20T23:59:59.000Z

396

Lithium bromide chiller technology in gas processing  

SciTech Connect (OSTI)

Lithium Bromide (LiBr) Absorption Chillers have been in use for more than half a century, mainly in the commercial air conditioning industry. The Gas Research Institute and EnMark Natural Gas Company co-funded a field test to determine the viability of this commercial air conditioning technology in the gas industry. In 1991, a 10 MMCFC natural gas conditioning plant was constructed in Sherman, Texas. The plant was designed to use a standard, off-the-shelf chiller from Trane with a modified control scheme to maintain tight operating temperature parameters. The main objective was to obtain a 40 F dewpoint natural gas stream to meet pipeline sales specifications. Various testing performed over the past three years has proven that the chiller can be operated economically and on a continuous basis in an oilfield environment with minimal operation and maintenance costs. This paper will discuss how a LiBr absorption chiller operates, how the conditioning plant performed during testing, and what potential applications are available for LiBr chiller technology.

Huey, M.A.; Leppin, D.

1995-12-31T23:59:59.000Z

397

ABAA - 6th International Conference on Advanced Lithium Batteries for  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Greetings! Greetings! Khalil Amine Chairman Khalil Amine Dear Colleagues, Welcome to the website of the 6th International Conference on Advanced Lithium Batteries for Automotive Applications (ABAA6). As Chairman of the ABAA Conference Organizing Committee, it is my great pleasure to cordially invite you to attend ABAA6. Every year, the ABAA Conference Organizing Committee hosts distinguished speakers from all over the world in the field of lithium battery research and development with a focus on automotive applications. ABAA6's primary goal is to provide attendees from both academia and industry an opportunity to meet and exchange information on advances in lithium battery research with the aim of enabling the electrification of vehicles. This year, the conference will focus on:

398

hybrid electric vehicle and lithium polymer nev testing  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

P1.2 - Hybrid Electric Vehicle and Lithium Polymer NEV Testing P1.2 - Hybrid Electric Vehicle and Lithium Polymer NEV Testing James Edward Francfort Advanced Vehicle Testing Activity Idaho National Laboratory P.O. Box 1625, Idaho Falls, ID. 83415-3830 james.francfort@inl.gov Abstract: The U.S. Department of Energy's Advanced Vehicle Testing Activity tests hybrid electric, pure electric, and other advanced technology vehicles. As part of this testing, 28 hybrid electric vehicles (HEV) are being tested in fleet, dynamometer, and closed track environments. This paper discusses some of the HEV test results, with an emphasis on the battery performance of the HEVs. It also discusses the testing results for a small electric vehicle with a lithium polymer traction battery. Keywords: hybrid; neighborhood; electric; battery; fuel;

399

Overcharge Protection for the New Generation of Lithium Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Overcharge Protection for the New Generation of Lithium Batteries Overcharge Protection for the New Generation of Lithium Batteries Speaker(s): Thomas Richardson Date: January 18, 2001 - 12:00pm Location: Bldg 90 Seminar Host/Point of Contact: Satkartar K. Kinney Lithium batteries supplied with cellular telephones and other personal electronic devices provide unprecedented power and capacities in very small formats. They are able to deliver such high performance because they incorporate highly reactive materials in both the positive and negative electrodes, resulting in individual cell potentials of nearly 4 V. Exposure to high temperatures or abusive treatment including overcharging can cause catastrophic failure of these batteries, resulting in gas venting, fire, or even explosion. Mechanical and electronic safety devices are employed to

400

Lithium ion batteries with titania/graphene anodes  

DOE Patents [OSTI]

Lithium ion batteries having an anode comprising at least one graphene layer in electrical communication with titania to form a nanocomposite material, a cathode comprising a lithium olivine structure, and an electrolyte. The graphene layer has a carbon to oxygen ratio of between 15 to 1 and 500 to 1 and a surface area of between 400 and 2630 m.sup.2/g. The nanocomposite material has a specific capacity at least twice that of a titania material without graphene material at a charge/discharge rate greater than about 10 C. The olivine structure of the cathode of the lithium ion battery of the present invention is LiMPO.sub.4 where M is selected from the group consisting of Fe, Mn, Co, Ni and combinations thereof.

Liu, Jun; Choi, Daiwon; Yang, Zhenguo; Wang, Donghai; Graff, Gordon L; Nie, Zimin; Viswanathan, Vilayanur V; Zhang, Jason; Xu, Wu; Kim, Jin Yong

2013-05-28T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Structural analysis of lithium-excess lithium manganate cathode materials by 7Li magic-angle spinning nuclear magnetic resonance spectroscopy  

Science Journals Connector (OSTI)

The local structures of lithium-excess lithium manganese spinel oxides were studied by high-resolution solid-state 7Li magic-angle spinning (MAS) NMR spectroscopy. Two resonance lines at ?500 and ?555 ppm were observed for the spinels in 7Li MAS NMR spectra. Spinel stability tests in which spinel powder was stored in electrolyte solution were performed to analyze the changes in the lithium local structure after manganese dissolution. After the spinel stability test, the intensity of the resonance at ?500 ppm decreased, whereas new resonance line at 0 ppm was observed. The lithium content of the 0 ppm peak increases with the storage time in electrolyte. SEM and chemical analysis suggested a surface coating of non-spinel lithium compounds, the presence of defects on particles surface and fluorine incorporation into the aged spinel. In addition, about 6070% of lithium remains in the spinel framework after the storage.

Hideyuki Oka; Senshi Kasahara; Tadashi Okada; Eiichi Iwata; Masaki Okada; Takayuki Shoji; Hiroshi Ohki; Tsutomu Okuda

2001-01-01T23:59:59.000Z

402

A CarParrinello and path integral molecular dynamics study of the intramolecular lithium bond in the lithium 2-pyridyl- N -oxide acetate  

Science Journals Connector (OSTI)

Lithium bonding in lithium 2-pyridyl- N -oxide acetate has been investigated using classic CarParrinello molecular dynamics (CPMD) and the path integral approach [path integrals molecular dynamics (PIMD)]. The simulations have been performed in 300 K. Structures energies and lithium trajectories have been determined. The CPMD results show that the lithium atom is generally equidistant between heavy atoms in the ( O ? Li ? O ) bridge. Applying quantum effects through the PIMD leads to similar conclusion. The theoretical lithium 2-pyridyl- N -oxide acetate infrared spectrum has also been determined using the CPMD calculations. This shows very good agreement with available experimental results and reproduces well the broad low-frequency band observed experimentally. In order to gain deeper understanding of the nature of the lithium bonding topological analysis of the electron localization function has been applied.

Piotr Durlak; Zdzis?aw Latajka; S?awomir Berski

2009-01-01T23:59:59.000Z

403

First-principles study of graphene-lithium structures for battery applications  

Science Journals Connector (OSTI)

In order to identify the best and most promising graphene-lithium structures for battery applications we performed a systematic study of different multilayer graphene-lithium structures using first-principles density-functional theory. The most promising structure identified is a few layer compound which contains a single graphene layer and four lithium layers. In this structure lithium density is six times higher than that of intercalated graphite and high lithium density observed in recent experiments can be due to this structure. In addition we show that electron density distribution around the positive Li ions is very important to design new advanced materials for battery applications.

Alper Buldum; Gulcin Tetiker

2013-01-01T23:59:59.000Z

404

Lithium Isotope Analyses of Inorganic Constituents from the Murchison Meteorite  

Science Journals Connector (OSTI)

Aqueous processes were important modifiers of solid matter during the early stages of solar system history. Lithium isotopes are sensitive indicators of such solid-liquid interactions because 7Li passes preferentially into solution and 6Li remains behind in the solid phase. Lithium isotope ratios of inorganic phases in the Murchison meteorite reveal that the value for the whole rock is simply the average of individual components with widely different isotopic compositions. 7Li content increases from chondrules to phyllosilicate-rich matrices to carbonates, as would be expected from the relative duration each component has spent during aqueous alteration on the parent asteroid.

Mark A. Sephton; Rachael H. James; Philip A. Bland

2004-01-01T23:59:59.000Z

405

Impact of solid fuel combustion technology on valence speciation of chromium in fly ash  

Science Journals Connector (OSTI)

Abstract Fly ash (FA) generated in real furnaces was used to evaluate the impact of the kind of the solid fuel burnt and combustion technology on chromium speciation, particularly the presence of Cr(III) and Cr(VI) forms as well as readily and hardly leachable chromium(VI) species in FAs. The \\{FAs\\} originated from a pulverized coal combustion boiler (PCC boiler), a fluidized bed combustion boiler (FBC boiler), a stoker-fired boiler (SF boiler), a municipal solid waste incinerator (MSWI), a cement rotary kiln (CRK) and a modern domestic boiler (DB). The speciation analysis of chromium was carried out by means of extraction followed by catalytic cathodic stripping voltammetry with adsorption of Cr(III)-DTPA complexes (CCSV-DTPA) for determination of Cr(VI) and AAS was used for determination of Cr content. It has been revealed that the antagonistic action of alkali metal compounds and iron oxides plays a crucial role in shaping valence speciation of chromium. According to the proposed transformation path of oxidation of Cr(III) to Cr(VI), hard coal combustion in an SF boiler, an FBC boiler or a domestic boiler will generate \\{FAs\\} with a low Cr(VI) level. Replacing fuel with biomass should create favorable conditions for generating FA enriched with Cr(VI). Relatively high concentrations of Cr(VI) can also be expected in FA generated in the process of high-temperature combustion of coal in PCC boilers.

Ryszard ?wietlik; Marzena Trojanowska; Monika ?o?y?ska; Artur Molik

2014-01-01T23:59:59.000Z

406

Q-dependence of the spin fluctuations in the intermediate valence compound CePd3  

SciTech Connect (OSTI)

We report inelastic neutron scattering experiments on a single crystal of the intermediate valence compound CePd3. At 300 K the magnetic scattering is quasielastic, with half-width G = 23 meV, and is independent of momentum transfer Q. At low temperature, the Q-averaged magnetic spectrum is inelastic, exhibiting a broad peak centered near E-max = 55 meV. These results, together with the temperature dependence of the susceptibility, 4f occupation number, and specific heat, can be fit by the Kondo/Anderson impurity model. The low temperature scattering near Emax, however, shows significant variations with Q, reflecting the coherence of the 4f lattice. The intensity is maximal at (1/2, 1/2, 0), intermediate at (1/2, 0, 0) and (0, 0, 0), and weak at (1/2, 1/2, 1/2). We discuss this Q-dependence in terms of current ideas about coherence in heavy fermion systems.

Fanelli, V. R.; Lawrence, J. M.; Goremychkin, E. A.; Osborn, R.; Bauer, E. D.; McClellan, K. J.; Thompson, J. D.; Booth, C. H.; Christianson, A. D.; Riseborough, P. S.

2014-06-25T23:59:59.000Z

407

LA SPECTROSCOPIE DE PERTE D'NERGIE DES LECTRONS APPLIQUE AUX BATTERIES AU LITHIUM : EXPRIENCES ET SIMULATIONS AU SEUIL K DU LITHIUM.  

E-Print Network [OSTI]

??Ce travail combine tudes exprimentales et thoriques au seuil K du lithium dans le but de permettre une meilleure comprhension des proprits des matriaux pour (more)

Mauchamp, V.

2006-01-01T23:59:59.000Z

408

Molybdenum nitride/nitrogen-doped graphene hybrid material for lithium storage in lithium ion batteries  

Science Journals Connector (OSTI)

Abstract Molybdenum nitride and nitrogen-doped graphene nanosheets (MoN/GNS) hybrid materials are synthesized by a simple hydrothermal method combined with a heat treatment at 800C under an ammonia atmosphere. It is found by scanning and transmission electron microscopy that MoN nanoparticles ranging from 20 to 40nm in diameter are homogeneously anchored to GNS. The electrochemical performance of MoN/GNS as a possible anode material for Li-ion batteries is investigated. Galvanostatic charge/discharge experiments reveal that the hybrid materials exhibit an enhanced lithium storage capacity and excellent rate capacity as a result of its efficient electronic and ionic mixed conducting network. The electrochemical results demonstrate that the weight ratio of GNS and MoN had significant effect on the electrochemical performance.

Botao Zhang; Guanglei Cui; Kejun Zhang; Lixue Zhang; Pengxian Han; Shanmu Dong

2014-01-01T23:59:59.000Z

409

Location and valence state of strontium cations on the framework of a carbon dioxide selective porous silicoaluminophosphate  

SciTech Connect (OSTI)

A Sr{sup 2+}-SAPO-34 material that displays superior CO2 adsorption selectivity and capacity was characterized via XPS and UV-vis spectroscopy to elucidate the valence state of strontium cations and framework silicon environment. Most importantly, the location of the strontium has been estimated from a Rietveld refinement analysis of synchrotron diffraction data. The XPS analysis indicated that the apparent valence state of the strontium is less than 2, an indication of its interaction with the large anionic framework. Furthermore, UV-vis tests pointed to changes in the silicon environment, plausibly related to this valence state or framework faulting. For the refinement, the analysis found that strontium occupied two unique sites: a site Sr1 slightly displaced from six-membered rings and a site Sr2 positioned at the top or bottom of the eight-membered rings. The latter position favors the interaction of the alkaline earth metal with CO{sub 2}, probably resulting in an enhanced electric field-quadrupole moment interaction.

Zhang, Li; Rivera-Ramos, Milton E.; Hernndez-Maldonado, Arturo J. (Puerto Rico) [Puerto Rico

2014-05-28T23:59:59.000Z

410

California Geothermal Power Plant to Help Meet High Lithium Demand  

Broader source: Energy.gov [DOE]

Ever wonder how we get the materials for the advanced batteries that power our cell phones, laptops, and even some electric vehicles? The U.S. Department of Energy's Geothermal Technologies Program (GTP) is working with California's Simbol Materials to develop technologies that extract battery materials like lithium, manganese, and zinc from geothermal brines produced during the geothermal production process.

411

Non-aqueous electrolyte for lithium-ion battery  

DOE Patents [OSTI]

The present technology relates to stabilizing additives and electrolytes containing the same for use in electrochemical devices such as lithium ion batteries and capacitors. The stabilizing additives include triazinane triones and bicyclic compounds comprising succinic anhydride, such as compounds of Formulas I and II described herein.

Zhang, Lu; Zhang, Zhengcheng; Amine, Khalil

2014-04-15T23:59:59.000Z

412

Performance Projections For The Lithium Tokamak Experiment (LTX)  

SciTech Connect (OSTI)

Use of a large-area liquid lithium limiter in the CDX-U tokamak produced the largest relative increase (an enhancement factor of 5-10) in Ohmic tokamak confinement ever observed. The confinement results from CDX-U do not agree with existing scaling laws, and cannot easily be projected to the new lithium tokamak experiment (LTX). Numerical simulations of CDX-U low recycling discharges have now been performed with the ASTRA-ESC code with a special reference transport model suitable for a diffusion-based confinement regime, incorporating boundary conditions for nonrecycling walls, with fuelling via edge gas puffing. This model has been successful at reproducing the experimental values of the energy confinement (4-6 ms), loop voltage (<0.5 V), and density for a typical CDX-U lithium discharge. The same transport model has also been used to project the performance of the LTX, in Ohmic operation, or with modest neutral beam injection (NBI). NBI in LTX, with a low recycling wall of liquid lithium, is predicted to result in core electron and ion temperatures of 1-2 keV, and energy confinement times in excess of 50 ms. Finally, the unique design features of LTX are summarized.

Majeski, R.; Berzak, L.; Gray, T.; Kaita, R.; Kozub, T.; Levinton, F.; D.P. Lundberg,,; Manickam, J.; Pereverzev, G. V.; Snieckus, K.; Soukhanovskii, V.; Spaleta, J.; Stotler, D.; Strickler, T.; Timberlake, J.; Yoo, J.; Zakharov, L.

2009-06-17T23:59:59.000Z

413

Novel carbonaceous materials used as anodes in lithium ion cells  

SciTech Connect (OSTI)

The objective of this work is to synthesize disordered carbons used as anodes in lithium ion batteries, where the porosity and surface area are controlled. Both parameters are critical since the irreversible capacity obtained in the first cycle seems to be associated with the surface area (an exfoliation mechanism occurs in which the exposed surface area continues to increase).

Sandi, G.; Winans, R.E.; Carrado, K.A.

1997-09-01T23:59:59.000Z

414

Phosphorous Computer Modeling of Crystalline Electrolytes: Lithium Thiophosphates and Phosphates  

E-Print Network [OSTI]

-search algorithm · Minimum-energy migration paths were determined via the construction of a weighted graph Results: Abstract Recently, lithium thiophosphate materials suitable for usage as solid electrolytes with PAW functionals generated using atompaw, and used in pwscf and abinit) · Formation energies

Holzwarth, Natalie

415

Synthesis, Characterization and Performance of Cathodes for Lithium Ion Batteries  

E-Print Network [OSTI]

lithium ion batteries. Materials Science & Engineering R-Ion Batteries by Jianxin Zhu Doctor of Philosophy, Graduate Program in Materials Science and EngineeringIon Batteries A Dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Materials Science and Engineering

Zhu, Jianxin

2014-01-01T23:59:59.000Z

416

Synthesis and electrochemical characterisation of electrospun lithium titanate ultrafine fibres  

Science Journals Connector (OSTI)

Lithium acetate dihydrate (>99.0%, Sigma-Aldrich ... %, Sigma-Aldrich) were used for the synthesis of Li4Ti5O12. PVP (Aldrich, M w=3.6נ105) was used as the base polymer for the electrospinn...

C. P. Sandhya; Bibin John; C. Gouri

2013-09-01T23:59:59.000Z

417

Issue and challenges facing rechargeable thin film lithium batteries  

Science Journals Connector (OSTI)

New materials hold the key to fundamental advances in energy conversion and storage, both of which are vital in order to meet the challenge of global warming and the finite nature of fossil fuels. Nanomaterials in particular offer unique properties or combinations of properties as electrodes and electrolytes in a range of energy devices. Technological improvements in rechargeable solid-state batteries are being driven by an ever-increasing demand for portable electronic devices. Lithium batteries are the systems of choice, offering high energy density, flexible, lightweight design and longer lifespan than comparable battery technologies. We present a brief historical review of the development of lithium-based thin film rechargeable batteries highlight ongoing research strategies and discuss the challenges that remain regarding the discovery of nanomaterials as electrolytes and electrodes for lithium batteries also this article describes the possible evolution of lithium technology and evaluates the expected improvements, arising from new materials to cell technology. New active materials under investigation and electrode process improvements may allow an ultimate final energy density of more than 500Wh/L and 200Wh/kg, in the next 56 years, while maintaining sufficient power densities. A new rechargeable battery technology cannot be foreseen today that surpasses this. This report will provide key performance results for thin film batteries and highlight recent advances in their development.

Arun Patil; Vaishali Patil; Dong Wook Shin; Ji-Won Choi; Dong-Soo Paik; Seok-Jin Yoon

2008-01-01T23:59:59.000Z

418

High power density self-cooled lithium-vanadium blanket.  

SciTech Connect (OSTI)

A self-cooled lithium-vanadium blanket concept capable of operating with 2 MW/m{sup 2} surface heat flux and 10 MW/m{sup 2} neutron wall loading has been developed. The blanket has liquid lithium as the tritium breeder and the coolant to alleviate issues of coolant breeder compatibility and reactivity. Vanadium alloy (V-4Cr-4Ti) is used as the structural material because it can accommodate high heat loads. Also, it has good mechanical properties at high temperatures, high neutron fluence capability, low degradation under neutron irradiation, good compatibility with the blanket materials, low decay heat, low waste disposal rating, and adequate strength to accommodate the electromagnetic loads during plasma disruption events. Self-healing electrical insulator (CaO) is utilized to reduce the MHD pressure drop. A poloidal coolant flow with high velocity at the first wall is used to reduce the peak temperature of the vanadium structure and to accommodate high surface heat flux. The blanket has a simple blanket configuration and low coolant pressure to reduce the fabrication cost, to improve the blanket reliability, and to increase confidence in the blanket performance. Spectral shifter, moderator, and reflector are utilized to improve the blanket shielding capability and energy multiplication, and to reduce the radial blanket thickness. Natural lithium is used to avoid extra cost related to the lithium enrichment process.

Gohar, Y.; Majumdar, S.; Smith, D.

1999-07-01T23:59:59.000Z

419

Comparison of Cycling Performance of Lithium Ion Cell Anode Graphites  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Comparison of Cycling Performance of Lithium Ion Cell Anode Graphites Comparison of Cycling Performance of Lithium Ion Cell Anode Graphites Title Comparison of Cycling Performance of Lithium Ion Cell Anode Graphites Publication Type Journal Article Year of Publication 2012 Authors Ridgway, Paul L., Honghe Zheng, A. F. Bello, Xiangyun Song, Shidi Xun, Jin Chong, and Vincent S. Battaglia Journal Journal of The Electrochemical Society Volume 159 Issue 5 Pagination A520 Date Published 2012 ISSN 00134651 Abstract Battery grade graphite products from major suppliers to the battery industry were evaluated in 2325 coin cells with lithium counter electrodes. First and ongoing cycle efficiency, total and reversible capacity, cycle life and discharge rate performance were measured to compare these anode materials. We then ranked the graphites using a formula which incorporates these performance measures to estimate the cost of the overall system, relative to the cost of a system using MCMB. This analysis indicates that replacing MCMB with CCP-G8 (Conoco Phillips) would add little to no cost, whereas each of the other graphites would lead to a more costly system. Therefore we chose CCP-G8 as the new baseline graphite for the BATT program.

420

A Better Anode Design to Improve Lithium-Ion Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

A Better Anode Design to Improve Lithium-Ion Batteries Print A Better Anode Design to Improve Lithium-Ion Batteries Print Lithium-ion batteries are in smart phones, laptops, most other consumer electronics, and the newest electric cars. Good as these batteries are, the need for energy storage in batteries is surpassing current technologies. In a lithium-ion battery, charge moves from the cathode to the anode, a critical component for storing energy. A team of Berkeley Lab scientists has designed a new kind of anode that absorbs eight times the lithium of current designs, and has maintained its greatly increased energy capacity after more than a year of testing and many hundreds of charge-discharge cycles. Cyclical Science Succeeds The anode achievement described in this highlight provides a rare scientific showcase, combining advanced tools of synthesis, characterization, and simulation in a novel approach to materials development. Gao Liu's original research team, part of Berkeley Lab's Environmental Energy Technologies Division (EETD), got the ball rolling by designing the original series of polyfluorene-based conducting polymers. Then, Wanli Yang of the ALS suggested soft x-ray absorption spectroscopy to determine their key electronic properties. To better understand these results, and their relevance to the conductivity of the polymer, the growing team sought a theoretical explanation from Lin-Wang Wang of Berkeley Lab's Materials Sciences Division (MSD). By conducting calculations on the promising polymers at Berkeley Lab's National Energy Research Scientific Computing Center (NERSC), the team gained insight into what was really happening in the PF with the carbonyl functional group, singling it out for further development.

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

A Better Anode Design to Improve Lithium-Ion Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

A Better Anode Design to Improve Lithium-Ion Batteries Print A Better Anode Design to Improve Lithium-Ion Batteries Print Lithium-ion batteries are in smart phones, laptops, most other consumer electronics, and the newest electric cars. Good as these batteries are, the need for energy storage in batteries is surpassing current technologies. In a lithium-ion battery, charge moves from the cathode to the anode, a critical component for storing energy. A team of Berkeley Lab scientists has designed a new kind of anode that absorbs eight times the lithium of current designs, and has maintained its greatly increased energy capacity after more than a year of testing and many hundreds of charge-discharge cycles. Cyclical Science Succeeds The anode achievement described in this highlight provides a rare scientific showcase, combining advanced tools of synthesis, characterization, and simulation in a novel approach to materials development. Gao Liu's original research team, part of Berkeley Lab's Environmental Energy Technologies Division (EETD), got the ball rolling by designing the original series of polyfluorene-based conducting polymers. Then, Wanli Yang of the ALS suggested soft x-ray absorption spectroscopy to determine their key electronic properties. To better understand these results, and their relevance to the conductivity of the polymer, the growing team sought a theoretical explanation from Lin-Wang Wang of Berkeley Lab's Materials Sciences Division (MSD). By conducting calculations on the promising polymers at Berkeley Lab's National Energy Research Scientific Computing Center (NERSC), the team gained insight into what was really happening in the PF with the carbonyl functional group, singling it out for further development.

422

A Better Anode Design to Improve Lithium-Ion Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Better Anode Design to Improve Lithium-Ion Batteries Print Better Anode Design to Improve Lithium-Ion Batteries Print Lithium-ion batteries are in smart phones, laptops, most other consumer electronics, and the newest electric cars. Good as these batteries are, the need for energy storage in batteries is surpassing current technologies. In a lithium-ion battery, charge moves from the cathode to the anode, a critical component for storing energy. A team of Berkeley Lab scientists has designed a new kind of anode that absorbs eight times the lithium of current designs, and has maintained its greatly increased energy capacity after more than a year of testing and many hundreds of charge-discharge cycles. Cyclical Science Succeeds The anode achievement described in this highlight provides a rare scientific showcase, combining advanced tools of synthesis, characterization, and simulation in a novel approach to materials development. Gao Liu's original research team, part of Berkeley Lab's Environmental Energy Technologies Division (EETD), got the ball rolling by designing the original series of polyfluorene-based conducting polymers. Then, Wanli Yang of the ALS suggested soft x-ray absorption spectroscopy to determine their key electronic properties. To better understand these results, and their relevance to the conductivity of the polymer, the growing team sought a theoretical explanation from Lin-Wang Wang of Berkeley Lab's Materials Sciences Division (MSD). By conducting calculations on the promising polymers at Berkeley Lab's National Energy Research Scientific Computing Center (NERSC), the team gained insight into what was really happening in the PF with the carbonyl functional group, singling it out for further development.

423

Modeling of Spherical Torus Plasmas for Liquid Lithium Wall Experiments  

SciTech Connect (OSTI)

Liquid metal walls have the potential to solve first-wall problems for fusion reactors, such as heat load and erosion of dry walls, neutron damage and activation, and tritium inventory and breeding. In the near term, such walls can serve as the basis for schemes to stabilize magnetohydrodynamic (MHD) modes. Furthermore, the low recycling characteristics of lithium walls can be used for particle control. Liquid lithium experiments have already begun in the Current Drive eXperiment-Upgrade (CDX-U). Plasmas limited with a toroidally localized limiter have been investigated, and experiments with a fully toroidal lithium limiter are in progress. A liquid surface module (LSM) has been proposed for the National Spherical Torus Experiment (NSTX). In this larger ST, plasma currents are in excess of 1 MA and a typical discharge radius is about 68 cm. The primary motivation for the LSM is particle control, and options for mounting it on the horizontal midplane or in the divertor region are under consideration. A key consideration is the magnitude of the eddy currents at the location of a liquid lithium surface. During plasma start up and disruptions, the force due to such currents and the magnetic field can force a conducting liquid off of the surface behind it. The Tokamak Simulation Code (TSC) has been used to estimate the magnitude of this effect. This program is a two dimensional, time dependent, free boundary simulation code that solves the MHD equations for an axisymmetric toroidal plasma. From calculations that match actual ST equilibria, the eddy current densities can be determined at the locations of the liquid lithium. Initial results have shown that the effects could be significant, and ways of explicitly treating toroidally local structures are under investigation.

R. Kaita; S. Jardin; B. Jones; C. Kessel; R. Majeski; J. Spaleta; R. Woolley; L. Zakharo; B. Nelson; M. Ulrickson

2002-01-29T23:59:59.000Z

424

Accretion-induced Lithium Line Enhancements in Classical T  

Science Journals Connector (OSTI)

It is widely accepted that much of the stochastic variability of T Tauri stars is due to accretion by a circumstellar disk. The emission-line spectrum as well as the excess continuum emission are common probes of this process. In this communication, we present additional probes of the circumstellar environment in the form of resonance lines of low ionization potential elements. Using a set of 14 high-resolution echelle observations of the classical T Tauri star (CTTS) RW Aur, taken between 1986 and 1996, we carefully measure the continuum veiling at each epoch by comparing more than 500 absorption lines with those of an appropriate template. This allows us to accurately subtract out the continuum emission and to recover the underlying photospheric spectrum. In doing so, we find that selected photospheric lines are enhanced by the accretion process, namely, the resonance lines of Li I and K I. A resonance line of Ti I and a low excitation potential line of Ca I also show weak enhancements. Simple slab models and computed line bisectors lead us to propose that these line enhancements are markers of cool gas at the beginning of the accretion flow which provides an additional source of line opacity. These results suggest that published values of surface lithium abundances of classical T Tauri stars are likely to be overestimated. This would account for the various reports of surface lithium abundances in excess of meteoritic values among the extreme CTTSs. Computing LTE lithium abundances of RW Aur in a low and then high accretion state yields abundances which vary by 1 order of magnitude. The low accretion state lithium abundance is consistent with theoretical predictions for a star of this age and mass, while the high accretion state spectrum yields a supermeteoritic lithium abundance.

N. M. Stout-Batalha; C. C. Batalha; G. S. Basri

2000-01-01T23:59:59.000Z

425

Luminescence from Edge Fracture in Shocked Lithium Fluoride Crystals  

SciTech Connect (OSTI)

Light emitted from a [100] lithium fluoride crystal was characterized under shock wave compression to 28GPa followed by complete stress release at the edges. The light was examined using time-gated optical spectrometry and imaging, time-resolved optical emission measurements, and hydrodynamic modeling. The shock arrival at the circumference of the crystal was delayed relative to the center so that the two regions could be studied at different times. The majority of the light emission originated when the shock waves released at the circumference of the crystal. Unlike previously reported results for shocked lithium fluoride, we found that the light spectrum is not strictly broad band, but has spectral lines associated with atomic lithium in addition to a broad band background. Also, the emission spectrum depends strongly on the gas surrounding the sample. Based on our observations, the line emission appears to be related to fracture of the lithium fluoride crystal from the shock wave releasing at the edges. Experimenters frequently utilize lithium fluoride crystals as transparent windows for observing shock compressed samples. Because of the experimental geometries used, the shock wave in such cases often reaches the circumference of the window at nearly the same moment as when it reaches the center of the sample-window interface. Light generated at the circumference could contaminate the measurement at the interface when this light scatters into the observed region. This background light may be reduced or avoided using experimental geometries which delay the arrival of the shock wave at the edges of the crystal.

Turley, W. D. [NSTec; Stevens, G. D. [NSTec; Capelle, G. A. [NSTec; Grover, M. [NSTec; Holtkamp, D. B. [LANL; LaLone, B. M. [NSTec; Veeser, L. R. [NSTec, LANL

2013-04-01T23:59:59.000Z

426

Upward-facing Lithium Flash Evaporator for NSTX-U  

SciTech Connect (OSTI)

NSTX plasma performance has been significantly enhanced by lithium conditioning [1]. To date, the lower divertor and passive plates have been conditioned by downward facing lithium evaporators (LITER) as appropriate for lower null plasmas. The higher power operation expected from NSTX-U requires double null plasma operation in order to distribute the heat flux between the upper and lower divertors making it desirable to coat the upper divertor region with Li as well. An upward aiming LITER (U-LITER) is presently under development and will be inserted into NSTX-U using a horizontal probe drive located in a 6" upper midplane port. In the retracted position the evaporator will be loaded with up to 300 mg of Li granules utilizing one of the calibrated NSTX Li powder droppers[2]. The evaporator will then be inserted into the vessel in a location within the shadow of the RF limiters and will remain in the vessel during the discharge. About 10 seconds before a discharge, it will be rapidly heated and the lithium completely evaporated onto the upper divertor, thus avoiding the complication of a shutter that prevents evaporation during the shot when the diagnostic shutters are open. The minimal time interval between the evaporation and the start of the discharge will avoid the passivation of the lithium by residual gases and enable the study of the conditioning effects of un-passivated Li surfaces [3]. Two methods are being investigated to accomplish the rapid (few second) heating of the lithium. A resistive method relies on passing a large current through a Li filled crucible. A second method requires using a 3 kW e-beam gun to heat the Li. In this paper the evaporator systems will be described and the pros and cons of each heating method will be discussed.

Roquemore, A. L.

2013-07-09T23:59:59.000Z

427

(Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: Chile was the leading lithium chemical producer in the world; Argentina, China,  

E-Print Network [OSTI]

, vehicles with an internal combustion engine and a battery-powered electric motor. Most commercially that was prone to dangerous overheating. Interest continued in lithium batteries for hybrid electric vehicles lithium batteries were being used increasingly in portable electronic devices and electrical tools

428

(Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: Chile was the leading lithium chemical producer in the world; Argentina, China, and  

E-Print Network [OSTI]

companies were pursuing the development of lithium batteries for hybrid electric vehicles--vehicles with an internal combustion engine and a battery-powered electric motor. Most commercially available hybrid rechargeable lithium batteries were being used increasingly in portable electronic devices and electrical tools

429

(Data in metric tons of contained lithium, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world, followed by China, the  

E-Print Network [OSTI]

and greases and in the production of synthetic rubber. Salient Statistics--United States: 1995 1996 1997 1998100 LITHIUM (Data in metric tons of contained lithium, unless otherwise noted) Domestic Production States, Russia, and Argentina, in descending order of production. Australia and Canada were major

430

(Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China,  

E-Print Network [OSTI]

in the manufacture of lubricants and greases and in the production of synthetic rubber. Salient Statistics98 LITHIUM (Data in metric tons of lithium content, unless otherwise noted) Domestic Production from domestic resources, reported production and value of production data cannot be published

431

(Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China,  

E-Print Network [OSTI]

in the manufacture of lubricants and greases and in the production of synthetic rubber. Salient Statistics96 LITHIUM (Data in metric tons of lithium content, unless otherwise noted) Domestic Production from domestic resources, reported production and value of production data cannot be published

432

(Data in metric tons of contained lithium, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world, followed by China,  

E-Print Network [OSTI]

and greases and in the production of synthetic rubber. Salient Statistics--United States: 1994 1995 1996 1997102 LITHIUM (Data in metric tons of contained lithium, unless otherwise noted) Domestic Production, the United States, and Argentina, in descending order of production. Australia and Canada were major

433

(Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China,  

E-Print Network [OSTI]

in the manufacture of lubricants and greases and in the production of synthetic rubber. Salient Statistics100 LITHIUM (Data in metric tons of lithium content, unless otherwise noted) Domestic Production from domestic resources, reported production and value of production data cannot be published

434

In-situ and ex-situ observations of lithium de-intercalation from LiCoO? : atomic force microscopy and transmission electron microscopy studies  

E-Print Network [OSTI]

Lithium cobalt dioxide is the most commonly used material for positive electrodes in lithium rechargeable batteries. During lithium de-intercalation from this material, ... undergoes a number of phase transitions, which ...

Clmenon, Anne

2005-01-01T23:59:59.000Z

435

Expanded North Carolina Lithium Facility Opens, Boosting U.S. Production of  

Broader source: Energy.gov (indexed) [DOE]

Expanded North Carolina Lithium Facility Opens, Boosting U.S. Expanded North Carolina Lithium Facility Opens, Boosting U.S. Production of a Key Manufacturing Material Expanded North Carolina Lithium Facility Opens, Boosting U.S. Production of a Key Manufacturing Material June 29, 2012 - 12:28pm Addthis News Media Contact (202) 586-4940 WASHINGTON - Today, U.S. Energy Secretary Steven Chu recognized the opening of Rockwood Lithium's expanded manufacturing facility in Kings Mountain, North Carolina. Rockwood is leveraging a $28.4 million investment from the Recovery Act to expand its North Carolina lithium production facility as well as its production operations in Silver Peak, Nevada. This project will create 100 new jobs and dramatically increase the United States' capacity to produce lithium, which is a key material

436

Expanded North Carolina Lithium Facility Opens, Boosting U.S. Production of  

Broader source: Energy.gov (indexed) [DOE]

Expanded North Carolina Lithium Facility Opens, Boosting U.S. Expanded North Carolina Lithium Facility Opens, Boosting U.S. Production of a Key Manufacturing Material Expanded North Carolina Lithium Facility Opens, Boosting U.S. Production of a Key Manufacturing Material June 29, 2012 - 12:28pm Addthis News Media Contact (202) 586-4940 WASHINGTON - Today, U.S. Energy Secretary Steven Chu recognized the opening of Rockwood Lithium's expanded manufacturing facility in Kings Mountain, North Carolina. Rockwood is leveraging a $28.4 million investment from the Recovery Act to expand its North Carolina lithium production facility as well as its production operations in Silver Peak, Nevada. This project will create 100 new jobs and dramatically increase the United States' capacity to produce lithium, which is a key material

437

Exploring the interaction between lithium ion and defective graphene surface using dispersion corrected DFT studies  

SciTech Connect (OSTI)

To analyze the lithium ion interaction with realistic graphene surfaces, we carried out dispersion corrected DFT-D3 studies on graphene with common point defects and chemisorbed oxygen containing functional groups along with defect free graphene surface. Our study reveals that, the interaction between lithium ion (Li+) and graphene is mainly through the delocalized ? electron of pure graphene layer. However, the oxygen containing functional groups pose high adsorption energy for lithium ion due to the Li-O ionic bond formation. Similarly, the point defect groups interact with lithium ion through possible carbon dangling bonds and/or cation-? type interactions. Overall these defect sites render a preferential site for lithium ions compared with pure graphene layer. Based on these findings, the role of graphene surface defects in lithium battery performance were discussed.

Vijayakumar, M.; Hu, Jian Z.

2013-10-15T23:59:59.000Z

438

NANOWIRE CATHODE MATERIAL FOR LITHIUM-ION BATTERIES  

SciTech Connect (OSTI)

This project involved the synthesis of nanowire -MnO2 and characterization as cathode material for high-power lithium-ion batteries for EV and HEV applications. The nanowire synthesis involved the edge site decoration nanowire synthesis developed by Dr. Reginald Penner at UC Irvine (a key collaborator in this project). Figure 1 is an SEM image showing -MnO2 nanowires electrodeposited on highly oriented pyrolytic graphite (HOPG) electrodes. This technique is unique to other nanowire template synthesis techniques in that it produces long (>500 um) nanowires which could reduce or eliminate the need for conductive additives due to intertwining of fibers. Nanowire cathode for lithium-ion batteries with surface areas 100 times greater than conventional materials can enable higher power batteries for electric vehicles (EVs) and hybrid electric vehicles (HEVs). The synthesis of the -MnO2 nanowires was successfully achieved. However, it was not found possible to co-intercalate lithium directly in the nanowire synthesis. Based on input from proposal reviewers, the scope of the project was altered to attempt the conversion into spinel LiMn2O4 nanowire cathode material by solid state reaction of the -MnO2 nanowires with LiNO3 at elevated temperatures. Attempts to perform the conversion on the graphite template were unsuccessful due to degradation of the graphite apparently caused by oxidative attack by LiNO3. Emphasis then shifted to quantitative removal of the nanowires from the graphite, followed by the solid state reaction. Attempts to quantitatively remove the nanowires by several techniques were unsatisfactory due to co-removal of excess graphite or poor harvesting of nanowires. Intercalation of lithium into -MnO2 electrodeposited onto graphite was demonstrated, showing a partial demonstration of the -MnO2 material as a lithium-ion battery cathode material. Assuming the issues of nanowires removal can be solved, the technique does offer potential for creating high-power lithium-ion battery cathode needed for advanced EV and HEVs. Several technical advancements will still be required to meet this goal, and are likely topics for future SBIR feasibility studies.

John Olson, PhD

2004-07-21T23:59:59.000Z

439

First Principles Study of the Li[subscript 10]GeP[subscript 2]S[subscript 12] Lithium Super Ionic Conductor Material  

E-Print Network [OSTI]

The continued drive for high performance lithium batteries has imposed stricter requirements on the electrolyte materials. Solid electrolytes comprising lithium super ionic conductor materials exhibit good safety and ...

Mo, Yifei

440

B-Doped Graphene as Catalyst To Improve Charge Rate of LithiumAir Battery  

Science Journals Connector (OSTI)

B-Doped Graphene as Catalyst To Improve Charge Rate of LithiumAir Battery ... The lithiumair battery as an energy storage technology can be used in electric vehicles due to its large energy density, while its poor rate capability limits its practical usage under large current density. ... According to first-principles thermodynamics calculation, we predict B-doped graphene can be a potential catalyst to improve the charge rate of lithiumair battery. ...

Xiaodong Ren; Jinzhen Zhu; Fuming Du; Jianjun Liu; Wenqing Zhang

2014-09-10T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

Further Investigations of the Effect of Replacing Lithium by Sodium on Lithium Silicate Scintillating Glass Efficiency  

SciTech Connect (OSTI)

Ce3+ doped lithium (6Li) silicate glasses are thermal neutron detectors. Prior work showed that when sodium (Na) is substituted for Li the scintillation efficiency, under beta particle stimulation, increased and then decreased as the sodium (Na) content was increased [1]. When all the 6Li was replaced by Na no scintillation was observed. Raman spectra, acquired using a visible excitation source provided no evidence of anomalous behavior. SEM microscopy did show some phase separation, but there was no obvious correlation with the scintillation efficiency. We have reexamined these glass samples using deep UV Raman excitation which reduces fluorescence interference. The newly acquired spectra show evidence of phase separation in the glasses. Specifically we see a peak at 800 cm-1 Raman shift which can be assigned to a vitreous silica moiety that results from phase separation. There is a strong correlation between this peak's area, the scintillation efficiency, and the Na content. The observed trend suggests that phase separation enhances scintillation and addition of Na reduces the amount of phase separation. We also see evidence of at least two defect structures that can be tentatively assigned to a three-membered ring structure and an oxygen vacancy. The latter is fairly strongly correlated with enhanced scintillation efficiency.

Bliss, Mary; Aker, Pamela M.; Windisch, Charles F.

2012-02-15T23:59:59.000Z

442

In situ Raman spectroscopy of lithium electrode surface in ambient temperature lithium secondary battery. Final report  

SciTech Connect (OSTI)

Raman spectroscopy was used to characterize surface layers on lithium electrodes in different solvents such as propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), and polyethylene glycol 400 dimethyl ether (PEG400DME). Both DMC and DEC were used singly, and also mixed with either methyl acetate (MA) or methyl formate (MF). The Raman spectra showed that passive films formed on the Li surface in different solvents may have different chemical structures, which changed during the charging and discharging processes. Raman spectroscopy was also applied to characterize zinc electrode surfaces in alkaline solutions. The results suggested that ZnO and Zn(OH){sub 2} formed on the Zn electrode when a passive potential was applied. A solid film of fullerene C{sub 60}, which could be used as a cathode in Li rechargeable batteries, was examined in the PEG400DME solution by both electrochemical and Raman spectroscopy. Cyclic voltammograms (CVs) showed five redox peaks which suggested the formation of C{sub 60}{sup {minus}}, C{sub 60}{sup 2{minus}}, C{sub 60}{sup 3{minus}}, C{sub 60}{sup 4{minus}}, and C{sub 60}{sup 5{minus}}. Raman spectra obtained from a thin C{sub 60} film indicated that the thin fulleride film dissolved in the PEG400DME/LiClO{sub 4} solution at negative potentials.

Tachikawa, Hiroyasu [Jackson State Univ., MS (United States). Dept. of Chemistry

1992-09-01T23:59:59.000Z

443

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Broader source: Energy.gov (indexed) [DOE]

May 2011 CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries "This presentation does not contain any proprietary, confidential, or otherwise...

444

To bolster lithium battery life, add a little salt > EMC2 News...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

for the metal is expected to boom. Early in 2014, Tesla Motors, which makes a fully electric car, announced it would build a lithium battery "gigafactory." Concurrently, Archer...

445

Tennessee, Pennsylvania: Porous Power Technologies Improves Lithium Ion Battery, Wins R&D 100 Award  

Office of Energy Efficiency and Renewable Energy (EERE)

Porous Power Technologies, partnered with Oak Ridge National Laboratory (ORNL), developed SYMMETRIX HPX-F, a nanocomposite separator for improved lithium-ion battery technology.

446

In-situ measurement with fiber Bragg sensors in lithium batteries for safety usage  

Science Journals Connector (OSTI)

Fiber Bragg grating sensors are integrated in lithium batteries to measure temperature variations during batteries operated under normal and abnormal conditions. The thermal...

Yang, Gang; Leito, Catia; Li, Yuhong; Pinto, Joo; Jiang, Xuefan

447

E-Print Network 3.0 - advanced lithium-ion batteries Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

being undertaken at ISEM... .isem.uow.edu.au 12;Project Lithium ion batteries for Electric Vehicles (EVs) Aims To provide novel solutions... to enhance the performance ......

448

Bubbles Help Break Energy Storage Record for Lithium Air-Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Bubbles Help Break Energy Storage Record for Lithium Air-Batteries Foam-base graphene keeps oxygen flowing in batteries that holds promise for electric vehicles January...

449

Chem 115Lithium-Halogen ExchangeMyers RLi + R'X RX + R'Li  

E-Print Network [OSTI]

Chem 115Lithium-Halogen ExchangeMyers RLi + R'X RX + R'Li Lithium-halogen exchange reactions are essentially inert. 2 t-BuLi t-BuI + RLi t-BuLi isobutene + isobutane + LiI Lithium-halogen exchange reactions, and lithium iodide. H OEtBr H H OEtLi H1.1 eq n-BuLi Et2O, !80 °C Lau, K. S.; Schlosser, M. J. Org. Chem. 1978

450

ccsd00001237, Experimental Study of the BEC-BCS Crossover Region in Lithium 6  

E-Print Network [OSTI]

ccsd­00001237, version 3 ­ 2 Apr 2004 Experimental Study of the BEC-BCS Crossover Region in Lithium

451

Synthesis and Characterization of Simultaneous Electronic and Ionic Conducting Block Copolymers for Lithium Battery Electrodes  

E-Print Network [OSTI]

binder material for solid-state battery electrodes. The1.10. Proposed new solid-state lithium battery design. The

Patel, Shrayesh

2013-01-01T23:59:59.000Z

452

Post-Test Analysis of Lithium-Ion Battery Materials at Argonne...  

Broader source: Energy.gov (indexed) [DOE]

not contain any proprietary, confidential, or otherwise restricted information Post-test Analysis of Lithium-Ion Battery Materials at Argonne National Laboratory Overview...

453

Post-Test Analysis of Lithium-Ion Battery Materials at Argonne...  

Broader source: Energy.gov (indexed) [DOE]

DC This presentation contains no proprietary information. Project ID: ES166 Post-test Analysis of Lithium-Ion Battery Materials at Argonne National Laboratory Overview...

454

Graphene as a high-capacity anode material for lithium ion batteries  

Science Journals Connector (OSTI)

Graphene was produced via a soft chemistry synthetic route for lithium ion battery applications. The sample was characterized by X ... electron microscopy, respectively. The electrochemical performances of graphene

Hongdong Liu ???; Jiamu Huang ???; Xinlu Li

2013-04-01T23:59:59.000Z

455

Development of Novel Nanomaterials Based on Silicon and Graphene for Lithium Ion Battery Applications.  

E-Print Network [OSTI]

??Electrochemical energy storage is one of the important strategies to address the strong demand for clean energy. Rechargeable lithium ion batteries (LIBs) are one of (more)

Hu, Yuhai

2014-01-01T23:59:59.000Z

456

Hybrid neural net and physics based model of a lithium ion battery.  

E-Print Network [OSTI]

??Lithium ion batteries have become one of the most popular types of battery in consumer electronics as well as aerospace and automotive applications. The efficient (more)

Refai, Rehan

2011-01-01T23:59:59.000Z

457

Thermal Analysis of Lithium-Ion Battery Packs and Thermal Management Solutions.  

E-Print Network [OSTI]

??Lithium ion (Li-ion) batteries have been gaining recognition as the primary technology for energy storage in motive applications due to their improved specific energy densities, (more)

Bhatia, Padampat Chander

2013-01-01T23:59:59.000Z

458

Pressure dependence of tunneling and librational modes of coupled methyl groups in lithium acetate  

Science Journals Connector (OSTI)

The pressure dependence of the tunneling and librational modes of the coupled methyl groups in lithium acetate dihydrate was studied by inelastic neutron scattering...

A. Heidemann; J. Eckert; L. Passell

1987-01-01T23:59:59.000Z

459

Isobaric vaporliquid equilibria of binary system ethyl acetate+ethyl benzene+lithium bromide  

Science Journals Connector (OSTI)

Lithium bromide salt (99.9wt% purity) ... . The salt studied was dissolved in ethyl acetate as a solvent to the saturated level...

Zaid Ahmed Al-Anber; Munther Issa Kandah

2013-05-01T23:59:59.000Z

460

Tunneling of coupled methyl groups in lithium acetate: The isotope effect  

Science Journals Connector (OSTI)

We studied by high resolution inelastic neutron scattering the isotope effect of tunneling of coupled methyl groups in lithium acetate dihydrate (LIAC). Fully protonated, fully...

A. Heidemann; H. Friedrich; E. Gnther

1989-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

Innovative Manufacturing and Materials for Low-Cost Lithium-Ion...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Manufacturing and Materials for Low-Cost Lithium-Ion Batteries 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer...

462

Magnetic dichroism in valence-band photoemission spectroscopy of disordered bcc FexCo1-x alloys  

Science Journals Connector (OSTI)

A fully relativistic calculation of spin-resolved valence-band photoemission spectra for bcc FexCo1-x alloys is presented that is based on the Korringa-Kohn-Rostoker coherent-potential approximation method of band-structure calculation. The result for the spin-integrated spectra for unpolarized radiation was found to be in very satisfying agreement with corresponding experimental data. For the spin-resolved spectra a pronounced magnetic circular dichroism is predicted that should be observable in a corresponding experiment.

S. Ostanin and H. Ebert

1998-11-01T23:59:59.000Z

463

Valence quark and meson cloud contributions to the $?^\\ast N \\to N^\\ast(1520)$ form factors  

E-Print Network [OSTI]

The covariant spectator quark model is applied to the $\\gamma^\\ast N \\to N^\\ast(1520)$ reaction. The valence quark contributions to the electromagnetic form factors and helicity transition amplitudes are estimated from the covariant structure of the $N^\\ast(1520)$ wave function calibrated by the experimental data for large squared momentum transfer $Q^2$. The difference between the model results and the experimental data is then used to parameterize the low $Q^2$ behavior, where meson cloud effects are assumed to dominate. This parametrization can be very useful for future studies of the reaction, as well as for the extension of the transition form factors to the timelike region.

G. Ramalho; M. T. Pea

2014-05-20T23:59:59.000Z

464

Advanced Lithium Power Inc ALP | Open Energy Information  

Open Energy Info (EERE)

ALP ALP Jump to: navigation, search Name Advanced Lithium Power Inc (ALP) Place Vancouver, British Columbia, Canada Product They develop lithium ion and advanced battery control systems and their primary asset is intellectual property. Coordinates 49.26044°, -123.114034° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":49.26044,"lon":-123.114034,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

465

WATER-LITHIUM BROMIDE DOUBLE-EFFECT ABSORPTION COOLING ANALYSIS  

Office of Scientific and Technical Information (OSTI)

WATER-LITHIUM BROMIDE DOUBLE-EFFECT WATER-LITHIUM BROMIDE DOUBLE-EFFECT ABSORPTION COOLING ANALYSIS Gary C . V l i e t , Michael B . Lawson, and Rudolf0 A . Lithgow Center f o r Energy Studies The University of Texas a t Austin December 1980 Final Report f o r Contract: DE AC03-79SF10540 (Mu1 tiple-Effect Absorption Cycle Solar Cooling) with the U.S. Department of Energy DISCLAIMER This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency Thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately

466

ABAA - 6th International Conference on Advanced Lithium Batteries for  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Conference Information Conference Information About ABAA6 We cordially invite you to the 6th International Conference on Advanced Lithium Batteries for Automobile Applications (ABAA6) to be held in Chicago, Illinois, USA on September 9-11, 2013. The ABAA6 Organizing Committee is busy creating various scientific programs, as well as social activities, to advance battery knowledge with the purpose of expanding vehicle electrification. We hope you will join us at ABAA6 and have a meaningful time interacting with your fellow global experts. Previous Conferences 2008 Chicago 2009 Tokyo 2010 Seoul 2011 Beijing 2012 Istanbul Conference At-A-Glance Title 6th International Conference on Advanced Lithium Batteries for Automobile Applications (ABAA6) Theme Advanced Battery Technologies for Automotive Applications

467

Lithium bromide absorption chiller passes gas conditioning field test  

SciTech Connect (OSTI)

A lithium bromide absorption chiller has been successfully used to provide refrigeration for field conditioning of natural gas. The intent of the study was to identify a process that could provide a moderate level of refrigeration necessary to meet the quality restrictions required by natural-gas transmission companies, minimize the initial investment risk, and reduce operating expenses. The technology in the test proved comparatively less expensive to operate than a propane refrigeration plant. Volatile product prices and changes in natural-gas transmission requirements have created the need for an alternative to conventional methods of natural-gas processing. The paper describes the problems with the accumulation of condensed liquids in pipelines, gas conditioning, the lithium bromide absorption cycle, economics, performance, and operating and maintenance costs.

Lane, M.J.; Huey, M.A. [Nicol and Associates, Richardson, TX (United States)

1995-07-31T23:59:59.000Z

468

Success Stories: Solid Electrolyte Lithium Ion Batteries - Seeo, Inc.  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Solid Electrolyte May Usher in a New Generation of Solid Electrolyte May Usher in a New Generation of Rechargeable Lithium Batteries For Vehicles With sky rocketing gasoline prices and exploding laptops, there could not have been a better time for a new rechargeable battery breakthrough. Enter Lawrence Berkeley National Laboratory's (LBNL) nanostructured polymer electrolyte (NPE). NPE is a solid electrolyte designed for use in rechargeable lithium batteries. The unique material was developed by LBNL researchers Nitash Balsara, Hany Eitouni, Enrique Gomez, and Mohit Singh and licensed to startup company Seeo Inc. in 2007. With solid financial backing from Khosla Ventures, located in Menlo Park, California, and an impressive scientific team recruited from LBNL, University of California, Berkeley, and the battery industry, Seeo is now

469

Ground state hyperfine structure in muonic lithium ions  

E-Print Network [OSTI]

On the basis of perturbation theory in fine structure constant alpha and the ratio of electron to muon masses we calculate one-loop vacuum polarization, electron vertex corrections, nuclear structure and recoil corrections to hyperfine splitting of the ground state in muonic lithium ions $(\\mu\\ e\\ ^6_3Li)^+$ and $(\\mu\\ e\\ ^7_3Li)^+$. We obtain total results for the ground state small hyperfine splittings in $(\\mu\\ e\\ ^6_3Li)^+$ $\\Delta\

Martynenko, A P

2014-01-01T23:59:59.000Z

470

Integrated high quality factor lithium niobate microdisk resonators  

E-Print Network [OSTI]

Lithium Niobate (LN) is an important nonlinear optical material. Here we demonstrate LN microdisk resonators that feature optical quality factor ~ 100,000, realized using robust and scalable fabrication techniques, that operate over a wide wavelength range spanning visible and near infrared. Using our resonators, and leveraging LN's large second order optical nonlinearity, we demonstrate on-chip second harmonic generation with a conversion efficiency of 0.109 W-1.

Wang, Cheng; Lin, Zin; Atikian, Haig A; Venkataraman, Vivek; Huang, I-Chun; Stark, Peter; Lon?ar, Marko

2014-01-01T23:59:59.000Z

471

Ground state hyperfine structure in muonic lithium ions  

E-Print Network [OSTI]

On the basis of perturbation theory in fine structure constant alpha and the ratio of electron to muon masses we calculate one-loop vacuum polarization, electron vertex corrections, nuclear structure and recoil corrections to hyperfine splitting of the ground state in muonic lithium ions $(\\mu\\ e\\ ^6_3Li)^+$ and $(\\mu\\ e\\ ^7_3Li)^+$. We obtain total results for the ground state small hyperfine splittings in $(\\mu\\ e\\ ^6_3Li)^+$ $\\Delta\

A. P. Martynenko; A. A. Ulybin

2014-11-12T23:59:59.000Z

472

Novel forms of carbon as potential anodes for lithium batteries  

SciTech Connect (OSTI)

The objective of this study is to design and synthesize novel carbons as potential electrode materials for lithium rechargeable batteries. A synthetic approach which utilizes inorganic templates is described and initial characterization results are discussed. The templates also act as a catalyst enabling carbon formation at low temperatures. This synthetic approach should make it easier to control the surface and bulk characteristics of these carbons.

Winans, R.E.; Carrado, K.A.

1994-06-01T23:59:59.000Z

473

Gallium Nitride Synthesis Using Lithium Metal as a Nitrogen Fixant  

Science Journals Connector (OSTI)

This present work centers on the synthesis of white, microcrystalline gallium nitride from gallium and ammonia, using lithium to increase the solubility of nitrogen-containing species in the metal phase. ... After the acid was decanted and the product was rinsed repeatedly with water and then acetone, the resulting white powder was found to exhibit the powder X-ray diffractogram (PXRD) (Figure 2a) of crystalline gallium nitride (1). ...

Sen T. Barry; Stephen A. Ruoff; Arthur L. Ruoff

1998-08-13T23:59:59.000Z

474

Lithium Economy: Will It Get the Electric Traction?  

Science Journals Connector (OSTI)

Lithium Economy: Will It Get the Electric Traction? ... In the battle for alternative fuels for a decarbonized transportation sector, electricity has a definite edge. ... However, at the large scales of extraction required for transforming the automobile scene, the production facilities could pose severe challenges to the environment in terms of water table and fresh water supplies as well as the fallout of the extraction on the flora and fauna in the neighborhood. ...

A. K. Shukla; T. Prem Kumar

2013-02-07T23:59:59.000Z

475

Lithium silver chromate cell: a five-year story  

SciTech Connect (OSTI)

A French produced lithium silver chromate cell was first introduced in 1973 and has been used ever since as a pacemaker power source. Today, more than 370,000 cells have been produced. In five years of use, no battery-related failure has been observed in the field, giving to this system the high degree of reliability, required by this application. During this period, a study of the electrochemical aspects was maintained allowing better understanding of cell behavior. 5 refs.

Lenfant, P.; Broussely, M.; Rivault, J.P.; Grimm, M.

1980-01-01T23:59:59.000Z

476

Batteries - EnerDel Lithium-Ion Battery  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

EnerDel/Argonne Advanced High-Power Battery for Hybrid Electric Vehicles EnerDel/Argonne Advanced High-Power Battery for Hybrid Electric Vehicles EnerDel lithium-ion battery The EnerDel Lithium-Ion Battery The EnerDel/Argonne lithium-ion battery is a highly reliable and extremely safe device that is lighter in weight, more compact, more powerful and longer-lasting than the nickel-metal hydride (Ni-MH) batteries in today's hybrid electric vehicles (HEVs). The battery is expected to meet the U.S. Advanced Battery Consortium's $500 manufacturing price criterion for a 25-kilowatt battery, which is almost a sixth of the cost to make comparable Ni-MH batteries intended for use in HEVs. It is also less expensive to make than comparable Li-ion batteries. That cost reduction is expected to help make HEVs more competitive in the marketplace and enable consumers to receive an immediate payback in

477

Fabrication and Performance of a Lithium X-Ray Lens  

SciTech Connect (OSTI)

Compound refractive lenses (CRLs) are arrays of concave lenses whose simple design and ease in implementation and alignment make them an attractive optic to focus x-rays. Factors considered in designing CRLs include lens material, fabrication, and assembly. Lithium is a desirable material because it provides the largest index of refraction decrement per unit absorption length of any solid elements. Lithium is a difficult material to handle and fabricate because it is rather malleable and more importantly, it reacts with moisture, and to a lesser extent, with oxygen and nitrogen in air. It also tends to adhere to molds and dies.We report on the fabrication and performance of a parabolic lithium lens consisting of 32 lenslets. Lenslets are fabricated in a precision press using an indenter with a parabolic profile and a 100 {mu}m tip radius. The indenter is made of stainless steel and is figured using a computer numerically controlled (CNC) machine. The lens is designed to have a 1.7 m focal length at 10 keV energy. In an experiment conducted at the Advanced Photon Source (APS), a 0.5 mm x 0.5 mm monochromatic undulator beam strikes the lens. A focal length of 1.71, a focal spot size of 24 {mu}m x 34 {mu}m, and a peak intensity gain of over 18 are obtained.

Young, Kristina; Khounsary, Ali [Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439 (United States); Department of Mechanical, Materials, and Aerospace Engineering, Illinois Institute of Technology, Chicago, IL 60616 (United States); Jansen, Andrew N. [Chemical Engineering Division, Argonne National Laboratory, Argonne, IL 60439 (United States); Dufresne, Eric M. [Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439 (United States); Nash, Philip [Department of Mechanical, Materials, and Aerospace Engineering, Illinois Institute of Technology, Chicago, IL 60616 (United States)

2007-01-19T23:59:59.000Z

478

Electrical detection of liquid lithium leaks from pipe joints  

SciTech Connect (OSTI)

A test stand for flowing liquid lithium is under construction at Princeton Plasma Physics Laboratory. As liquid lithium reacts with atmospheric gases and water, an electrical interlock system for detecting leaks and safely shutting down the apparatus has been constructed. A defense in depth strategy is taken to minimize the risk and impact of potential leaks. Each demountable joint is diagnosed with a cylindrical copper shell electrically isolated from the loop. By monitoring the electrical resistance between the pipe and the copper shell, a leak of (conductive) liquid lithium can be detected. Any resistance of less than 2 k? trips a relay, shutting off power to the heaters and pump. The system has been successfully tested with liquid gallium as a surrogate liquid metal. The circuit features an extensible number of channels to allow for future expansion of the loop. To ease diagnosis of faults, the status of each channel is shown with an analog front panel LED, and monitored and logged digitally by LabVIEW.

Schwartz, J. A., E-mail: jschwart@pppl.gov; Jaworski, M. A.; Mehl, J.; Kaita, R.; Mozulay, R. [Princeton Plasma Physics Laboratory, Princeton, New Jersey 08543-0451 (United States)

2014-11-15T23:59:59.000Z

479

Hybrid of Co3Sn2@Co Nanoparticles and Nitrogen-Doped Graphene as a Lithium Ion Battery Anode  

Science Journals Connector (OSTI)

Hybrid of Co3Sn2@Co Nanoparticles and Nitrogen-Doped Graphene as a Lithium Ion Battery Anode ... VO2 Nanowires Assembled into Hollow Microspheres for High-Rate and Long-Life Lithium Batteries ...

Nasir Mahmood; Chenzhen Zhang; Fei Liu; Jinghan Zhu; Yanglong Hou

2013-10-16T23:59:59.000Z

480

Abnormal Cyclibility in Ni@Graphene CoreShell and YolkShell Nanostructures for Lithium Ion Battery Anodes  

Science Journals Connector (OSTI)

Abnormal Cyclibility in Ni@Graphene CoreShell and YolkShell Nanostructures for Lithium Ion Battery Anodes ... A new graphene-based hybrid nanostructure is designed for anode materials in lithium-ion batteries. ...

Huawei Song; Hao Cui; Chengxin Wang

2014-07-08T23:59:59.000Z

Note: This page contains sample records for the topic "kwh valence lithium" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


481

Lithium isotopes in global mid-ocean ridge basalts Paul B. Tomascak a,*, Charles H. Langmuir b  

E-Print Network [OSTI]

Lithium isotopes in global mid-ocean ridge basalts Paul B. Tomascak a,*, Charles H. Langmuir b January 2008 Abstract The lithium isotope compositions of 30 well-characterized samples of glassy lavas

Langmuir, Charles H.

482

Composition-Tailored Synthesis of Gradient Transition Metal Precursor Particles for Lithium-Ion Battery Cathode Materials  

Science Journals Connector (OSTI)

Composition-Tailored Synthesis of Gradient Transition Metal Precursor Particles for Lithium-Ion Battery Cathode Materials ... Collected particles were lithiated, and one promising material was evaluated as the active cathode component in a lithium-ion battery. ...

Gary M. Koenig, Jr.; Ilias Belharouak; Haixai Deng; Yang-Kook Sun; Khalil Amine

2011-03-09T23:59:59.000Z

483

Nano-Structured Li3V2(PO4)3 /Carbon Composite for High Rate Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Nano-Structured Li3V2(PO4)3 Carbon Composite for High Rate Lithium Ion Batteries. Nano-Structured Li3V2(PO4)3 Carbon Composite for High Rate Lithium Ion Batteries. Abstract:...

484

Effect of Lithium Enrichment on the Tritium Breeding Characteristics of Various Breeders in a Fusion Driven Hybrid Reactor  

Science Journals Connector (OSTI)

Selection of lithium containing materials is very important in the design of a deuteriumtritium (DT) fusion driven hybrid reactor in order to supply its tritium self- ... lithium-6 enrichment in the coolant of t...

Mustafa beyli

2009-09-01T23:59:59.000Z

485

Excess lithium storage and charge compensation in nanoscale Li4+xTi5O12  

Science Journals Connector (OSTI)

Lithium titanate spinel (Li4Ti5O12; LTO) is a promising candidate for anodes in lithium-ion batteries due to its excellent cyclability and safety performance, and has been known as a 'zero-strain' material that allows reversible lithium insertiondeinsertion with little change in the lattice parameters. For a better understanding of lithium reaction mechanisms in this material, it has been of great interest to identify where lithium is inserted and how it migrates during charge and discharge, which is often difficult with x-ray and electron scattering techniques due to the low scattering power of lithium. In this study, we employed atomic-resolution annular bright-field imaging to directly image the lithium on interstitial sites in nanoscale LTO, and electron energy-loss spectroscopy to measure local lithium occupancy and electronic structure at different states of charge. During lithiation, charge compensation occurs primarily at O sites, rather than at Ti sites, and no significant change was found in the projected density of states (Ti 3d) until the voltage was lowered to ~50mV or below. The Li K-edge spectra were simulated via abinitio calculations, providing a direct correlation between the near-edge fine structure and the local lithium coordination. During the initial states of discharge, lithium ions on 8a sites migrate to 16c sites (above 740mV). Further lithiation causes the partial re-occupation of 8a sites, initially in the near-surface region at ~600mV, and then in the bulk at lower voltages (~50mV). We attribute the enhanced capacity in nanostructured LTO to extra storage of lithium in the near-surface region, primarily at {111} facets.

Feng Wang; Lijun Wu; Chao Ma; Dong Su; Yimei Zhu; Jason Graetz

2013-01-01T23:59:59.000Z

486

PROPAGATION DES ONDES LASTIQUES DE SURFACE Atlas des configurations calcules pour le quartz, le tantalate de lithium,  

E-Print Network [OSTI]

, le tantalate de lithium, le niobate de lithium et le vanado-sulfure de thallium en ce qui concerne'ensemble des configurations possibles des matériaux classiques (quartz, niobate de lithium et tantalate de lithium) ainsi que d'un matériau récemment signalé le vanado-sulfure de thallium (Tl3VS4). La propagation

Paris-Sud XI, Université de

487

Prediction of Multi-Physics Behaviors of Large Lithium-Ion Batteries During Internal and External Short Circuit (Presentation)  

SciTech Connect (OSTI)

This presentation describes the multi-physics behaviors of internal and external short circuits in large lithium-ion batteries.

Kim, G. H.; Lee, K. J.; Chaney, L.; Smith, K.; Darcy, E.; Pesaran, A.; Darcy, E.

2010-11-01T23:59:59.000Z

488

Evidence for correlated pair transfer of valence nucleons in multiparticle stripping channels in the 18O+174Yb reaction  

Science Journals Connector (OSTI)

The single and multinucleon transfer cross sections in 16O, 18O+174Yb reactions were measured at Elab=83?MeV bombarding energy. The data were analyzed to obtain the variation of transfer cross sections with the number of nucleons transferred from the projectile to the target nucleus, and with respect to the ground state Q value (Qgg) of the transfer reaction. In 18O+174Yb reaction, the two-neutron stripping and the two-neutron correlated cluster transfer cross sections are strongly enhanced as compared to the 16O +174Yb reaction. The results have been discussed on the basis of the possible influence of the valence neutrons in the 18O nucleus on multiparticle transfer cross sections. The transfer probabilities of multinucleon transfers have been analyzed as a function of distance of closest approach and the results for two-neutron transfer is consistent with the supposition of correlated pair transfer of valence nucleons in the 18O+174Yb reaction.

P. K. Sahu; R. K. Choudhury; D. C. Biswas; B. K. Nayak

2001-06-14T23:59:59.000Z

489

Improved Lithium Ion Behavior Properties of TiO2@Graphitic-like Carbon Core@Shell Nanostructure  

E-Print Network [OSTI]

Improved Lithium Ion Behavior Properties of TiO2@Graphitic-like Carbon Core@Shell Nanostructure Min Intercalation Electrochemistry Capacitance Lithium Ion batteries A B S T R A C T We demonstrate TiO2@graphitic on the electrode surface and enhanced lithium ion intercalation, leading to lower charge transfer resistance

Cao, Guozhong

490

A lithium isotopic study of sub-greenschist to greenschist facies metamorphism in an accretionary prism, New Zealand  

E-Print Network [OSTI]

A lithium isotopic study of sub-greenschist to greenschist facies metamorphism in an accretionary November 2010 Editor: R.W. Carlson Keywords: lithium slab-derived fluids accretionary prism quartz veins. Introduction The fluid-mobile element lithium increasingly receives attention because of the large isotopic

Mcdonough, William F.

491

1,4-Addition of Lithium Diisopropylamide to Unsaturated Esters: Role of Rate-Limiting Deaggregation, Autocatalysis,  

E-Print Network [OSTI]

1,4-Addition of Lithium Diisopropylamide to Unsaturated Esters: Role of Rate-Limiting Deaggregation, Autocatalysis, Lithium Chloride Catalysis, and Other Mixed Aggregation Effects Yun Ma, Alexander C. Hoepker.edu Abstract: Lithium diisopropylamide (LDA) in tetrahydrofuran at -78 °C undergoes 1,4-addition

Collum, David B.

492

On the Accuracy and Simplifications of Battery Models using In Situ Measurements of Lithium Concentration in Operational Cells  

E-Print Network [OSTI]

. INTRODUCTION Accurate estimates of Lithium Ion Battery State of Charge (SOC) are critical for constraining and solid phase lithium distributions across the electrode may better utilize the battery's stored energyOn the Accuracy and Simplifications of Battery Models using In Situ Measurements of Lithium

Stefanopoulou, Anna

493

Mn3O4-Graphene Hybrid as a High-Capacity Anode Material for Lithium Ion Hailiang Wang,,  

E-Print Network [OSTI]

Mn3O4-Graphene Hybrid as a High-Capacity Anode Material for Lithium Ion Batteries Hailiang Wang hybrid materials of Mn3O4 nanoparticles on reduced graphene oxide (RGO) sheets for lithium ion battery-cost, and environ- mentally friendly anode for lithium ion batteries. Our growth-on- graphene approach should offer

Cui, Yi

494

Lithium-based surfaces controlling fusion plasma behavior at the plasma-material interface  

SciTech Connect (OSTI)

The plasma-material interface and its impact on the performance of magnetically confined thermonuclear fusion plasmas are considered to be one of the key scientific gaps in the realization of nuclear fusion power. At this interface, high particle and heat flux from the fusion plasma can limit the material's lifetime and reliability and therefore hinder operation of the fusion device. Lithium-based surfaces are now being used in major magnetic confinement fusion devices and have observed profound effects on plasma performance including enhanced confinement, suppression and control of edge localized modes (ELM), lower hydrogen recycling and impurity suppression. The critical spatial scale length of deuterium and helium particle interactions in lithium ranges between 5-100 nm depending on the incident particle energies at the edge and magnetic configuration. Lithium-based surfaces also range from liquid state to solid lithium coatings on a variety of substrates (e.g., graphite, stainless steel, refractory metal W/Mo/etc., or porous metal structures). Temperature-dependent effects from lithium-based surfaces as plasma facing components (PFC) include magnetohydrodynamic (MHD) instability issues related to liquid lithium, surface impurity, and deuterium retention issues, and anomalous physical sputtering increase at temperatures above lithium's melting point. The paper discusses the viability of lithium-based surfaces in future burning-plasma environments such as those found in ITER and DEMO-like fusion reactor devices.

Allain, Jean Paul; Taylor, Chase N. [School of Nuclear Engineering, Purdue University, 400 Central Avenue, West Lafayette, Indiana 47907 (United States)

2012-05-15T23:59:59.000Z

495

Thermal Analysis of a Lorentz Force Accelerator with an Open Lithium Heat Pipe  

E-Print Network [OSTI]

%[1]. High efficiency (above 30%) is typically reached only at high power levels (above 100 kW) (see Ref. [2 significantly raising the thrust efficiency at 1 #12;2 EMSELLEM, KODYS, CHOUEIRI: LITHIUM LFA moderately high thus causing lithium vapor to condense in the cathode. An empirically inspired solution was first

Choueiri, Edgar

496

Developments in the Understanding and Application of Lithium Isotopes in the Earth and Planetary Sciences  

Science Journals Connector (OSTI)

...Large scale enrichment of lithium for thermonuclear uses took place at the Oak Ridge National...separation with Li ionic conductors. Fusion Tech 39:654-658 Vigier N, Burton...Large scale enrichment of lithium for thermonuclear uses took place at the Oak Ridge National...

Paul B. Tomascak

497

Synthesis of na-doped lithium metatitanate and its absorption for carbon dioxide  

Science Journals Connector (OSTI)

Na-doped lithium metatitanate (Na-doped Li2TiO3) absorbent was doped with Na2CO3 and lithium metatitanate (Li2TiO3) was prepared by a solid-state reaction method from mixture of TiO2 ...

Liu Zhirong, Zhang Huan, Wang Yun, Zhan Xinxing

2014-01-01T23:59:59.000Z

498

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of LithiumSulfur Battery  

Science Journals Connector (OSTI)

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of LithiumSulfur Battery ... An amylopectin wrapped graphene oxide-sulfur composite was prepared to construct a 3-dimensionally cross-linked structure through the interaction between amylopectin and graphene oxide, for stabilizing lithium sulfur batteries. ...

Weidong Zhou; Hao Chen; Yingchao Yu; Deli Wang; Zhiming Cui; Francis J. DiSalvo; Hctor D. Abrua

2013-09-05T23:59:59.000Z

499

GrapheneNanotubeIron Hierarchical Nanostructure as Lithium Ion Battery Anode  

Science Journals Connector (OSTI)

GrapheneNanotubeIron Hierarchical Nanostructure as Lithium Ion Battery Anode ... In this study, we report a novel route via microwave irradiation to synthesize a bio-inspired hierarchical graphenenanotubeiron three-dimensional nanostructure as an anode material in lithium-ion batteries. ...

Si-Hwa Lee; Vadahanambi Sridhar; Jung-Hwan Jung; Kaliyappan Karthikeyan; Yun-Sung Lee; Rahul Mukherjee; Nikhil Koratkar; Il-Kwon Oh

2013-04-03T23:59:59.000Z

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Solution-Grown Silicon Nanowires for Lithium-Ion Battery Anodes  

E-Print Network [OSTI]

interest in using nanomaterials for advanced lithium-ion battery electrodes, par- ticularly for increasingSolution-Grown Silicon Nanowires for Lithium-Ion Battery Anodes Candace K. Chan, Reken N. Patel storage capacity (theoretical values of 4200 vs 372 mAh/g for graphite). How- ever, the insertion

Cui, Yi