Sample records for kwh valence lithium

  1. Property:Incentive/PVResFitDolKWh | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov YouKizildere I Geothermal PwerPerkins County, Nebraska:PrecourtOid JumpEligSysSize Jump to:PVNPFitDolKWh JumpPVResFitDolKWh

  2. Property:Incentive/PVNPFitDolKWh | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov YouKizildere I Geothermal PwerPerkins County, Nebraska:PrecourtOid JumpEligSysSize Jump to:PVNPFitDolKWh Jump to:

  3. Conductive lithium storage electrode

    DOE Patents [OSTI]

    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

    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.

  4. Conductive lithium storage electrode

    DOE Patents [OSTI]

    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

    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.

  5. Hydrogen, lithium, and lithium hydride production

    DOE Patents [OSTI]

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

    2014-03-25T23:59:59.000Z

    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.

  6. High-performance batteries for electric-vehicle propulsion and stationary energy storage. Progress report, October 1978-September 1979. [40 kWh, Li-Al and Li-Si anodes

    SciTech Connect (OSTI)

    Barney, D. L.; Steunenberg, R. K.; Chilenskas, A. A.; Gay, E. C.; Battles, J. E.; Hornstra, F.; Miller, W. E.; Vissers, D. R.; Roche, M. F.; Shimotake, H.; Hudson, R.; Askew, B. A.; Sudar, S.

    1980-03-01T23:59:59.000Z

    The research, development, and management activities of the programs at Argonne National Laboratory (ANL) and at contractors' laboratories on high-temperature batteries during the period October 1978 to September 1979 are reported. These batteries are being developed for electric-vehicle propulsion and for stationary energy-storage applications. The present cells, which operate at 400 to 500/sup 0/C, are of a vertically oriented, prismatic design with one or more inner positive electrodes of FeS or FeS/sub 2/, facing negative electrodes of lithium-aluminum or lithium-silicon alloy, and molten LiCl-KC1 electrolyte. During this reporting period, cell and battery development work has continued at ANL and contractors' laboratories. A 40 kWh electric-vehicle battery (designated Mark IA) was fabricated and delivered to ANL for testing. During the initial heat-up, one of the two modules failed due to a short circuit. A failure analysis was conducted, and the Mark IA program completed. Development work on the next electric-vehicle battery (Mark II) was initiated at Eagle-Picher Industries, Inc. and Gould, Inc. Work on stationary energy-storage batteries during this period has consisted primarily of conceptual design studies. 107 figures, 67 tables.

  7. Valence Quarks Polarization from COMPASS

    E-Print Network [OSTI]

    A. Korzenev

    2007-04-26T23:59:59.000Z

    A first evaluation of the polarized valence quark distribution $\\Delta u_v(x)+\\Delta d_v(x)$ from the COMPASS experiment (CERN/SPS) is presented. The data were collected by COMPASS in the years 2002--2004 using a 160 GeV polarized muon beam scattered off a large polarized $^6$LiD target and cover the range $1< Q^2 < 100$ GeV$^2$ and $0.006valence quarks.

  8. Modeling planar 3-valence meshes

    E-Print Network [OSTI]

    Gonen, Ozgur

    2009-05-15T23:59:59.000Z

    Akleman Vinod Srinivasan Committee Members, Richard Burt Head of Department, Mark Clayton December 2007 Major Subject: Visualization Sciences iii ABSTRACT Modeling Planar 3-Valence Meshes. (December 2007) Ozgur Gonen, B.A., Istanbul Bilgi University Co... Istanbul Bilgi University in 2003. He worked as a Multimedia Developer before joining the Master of Science in Visualization Sciences program at Texas A&M University. He mostly worked with Dr. Ergun Akleman during his masters studies. He can be reached...

  9. Modeling planar 3-valence meshes

    E-Print Network [OSTI]

    Gonen, Ozgur

    2008-10-10T23:59:59.000Z

    Akleman Vinod Srinivasan Committee Members, Richard Burt Head of Department, Mark Clayton December 2007 Major Subject: Visualization Sciences iii ABSTRACT Modeling Planar 3-Valence Meshes. (December 2007) Ozgur Gonen, B.A., Istanbul Bilgi University Co... Istanbul Bilgi University in 2003. He worked as a Multimedia Developer before joining the Master of Science in Visualization Sciences program at Texas A&M University. He mostly worked with Dr. Ergun Akleman during his masters studies. He can be reached...

  10. Lithium Local Pseudopotential Using

    E-Print Network [OSTI]

    Petta, Jason

    Lithium Local Pseudopotential Using DFT Sergio Orozco Student Advisor: Chen Huang Faculty Mentor Lithium LPS Test Lithium LPS #12;Density Functional Theory (DFT) Successful quantum mechanical approach (1979) #12;Building LPS for Lithium Create a LPS using NLPS density for Lithium Test LPS by comparing

  11. Prospects for Reducing the Processing Cost of Lithium Ion Batteries

    SciTech Connect (OSTI)

    Wood III, David L [ORNL; Li, Jianlin [ORNL; Daniel, Claus [ORNL

    2014-01-01T23:59:59.000Z

    A detailed processing cost breakdown is given for lithium-ion battery (LIB) electrodes, which focuses on: 1) elimination of toxic, costly N-methylpyrrolidone (NMP) dispersion chemistry; 2) doubling the thicknesses of the anode and cathode to raise energy density; and 3) reduction of the anode electrolyte wetting and SEI-layer formation time. These processing cost reduction technologies generically adaptable to any anode or cathode cell chemistry and are being implemented at ORNL. This paper shows step by step how these cost savings can be realized in existing or new LIB manufacturing plants using a baseline case of thin (power) electrodes produced with NMP processing and a standard 10-14-day wetting and formation process. In particular, it is shown that aqueous electrode processing can cut the electrode processing cost and energy consumption by an order of magnitude. Doubling the thickness of the electrodes allows for using half of the inactive current collectors and separators, contributing even further to the processing cost savings. Finally wetting and SEI-layer formation cost savings are discussed in the context of a protocol with significantly reduced time. These three benefits collectively offer the possibility of reducing LIB pack cost from $502.8 kWh-1-usable to $370.3 kWh-1-usable, a savings of $132.5/kWh (or 26.4%).

  12. Minerals Yearbook 1989: Lithium

    SciTech Connect (OSTI)

    Ober, J.A.

    1989-01-01T23:59:59.000Z

    The United States led the world in lithium mineral and compound production and consumption. Estimated consumption increased slightly, and world production also grew. Sales increased for domestic producers, who announced price increases for the third consecutive year. Because lithium is electrochemically reactive and has other unique properties, there are many commercial lithium products. Producers sold lithium as mineral concentrate, brine, compound, or metal, depending upon the end use. Most lithium compounds were consumed in the production of ceramics, glass, and primary aluminum.

  13. 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...

  14. Molten salt lithium cells

    DOE Patents [OSTI]

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

    1980-07-18T23:59:59.000Z

    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.

  15. Molten salt lithium cells

    DOE Patents [OSTI]

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

    1982-02-09T23:59:59.000Z

    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).

  16. Molten salt lithium cells

    DOE Patents [OSTI]

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

    1983-01-01T23:59:59.000Z

    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).

  17. Block copolymer electrolytes for lithium batteries

    E-Print Network [OSTI]

    Hudson, William Rodgers

    2011-01-01T23:59:59.000Z

    facing rechargeable lithium batteries. Nature 414, 359-367 (lithium and lithium-ion batteries. Solid State Ionics 135,electrolytes for lithium-ion batteries. Advanced Materials

  18. Lithium Ion Production NDE

    E-Print Network [OSTI]

    Lithium Ion Electrode Production NDE and QC Considerations David Wood, Debasish Mohanty, Jianlin Li, and Claus Daniel 12/9/13 EERE Quality Control Workshop #12;2 Presentation name Lithium Ion Electrode to be meaningful and provide electrode and cell QC. #12;3 Presentation name New Directions in Lithium Ion Electrode

  19. Lithium ion sources

    E-Print Network [OSTI]

    Roy, Prabir K.

    2014-01-01T23:59:59.000Z

    HIFAN 1866 Lithium ion sources by Prabir K. Roy, Wayne G.No. DE-AC02-05CH11231. Lithium ion sources Prabir K. RoyUSA Abstract A 10.9 cm diameter lithium alumino-silicate ion

  20. USFOE: Extended Summary - Lithium ion batteries and their manufacturing challenges

    SciTech Connect (OSTI)

    Daniel, Claus [ORNL

    2014-01-01T23:59:59.000Z

    There is no one lithium ion battery. With the variety of materials and electrochemical couples at our disposal as shown in the previous talks, we have the opportunity to design battery cells specific for their applications. Such applications require optimization of voltage, state of charge utilization, lifetime needs, and safety considerations. Electrochemical couples allow for designing power and energy ratios and available energy for the application. Integration in a large format cell requires optimized roll to roll electrode manufacturing and active material utilization. Electrodes are coated on a current collector in a composite structure comprised of active material, binders, and conductive additives which requires careful control of colloidal chemistry, adhesion, and solidification. These added inactive materials and the cell packaging reduce energy density. Degree of porosity and compaction in the electrode can impede or enhance battery performance. Pathways are explored to bring batteries from currently commercially available 100Wh/kg and 200Wh/L at $500/kWh to 250Wh/kg and 400Wh/L at $125/kWh.

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

    E-Print Network [OSTI]

    Wilcox, James D.

    2010-01-01T23:59:59.000Z

    facing rechargeable lithium batteries. Nature, 2001. 414(of rechargeable lithium batteries, I. Lithium manganeseof rechargeable lithium batteries, II. Lithium ion

  2. Lithium purification technique

    DOE Patents [OSTI]

    Keough, R.F.; Meadows, G.E.

    1984-01-10T23:59:59.000Z

    A method for purifying liquid lithium to remove unwanted quantities of nitrogen or aluminum. The method involves precipitation of aluminum nitride by adding a reagent to the liquid lithium. The reagent will be either nitrogen or aluminum in a quantity adequate to react with the unwanted quantity of the impurity to form insoluble aluminum nitride. The aluminum nitride can be mechanically separated from the molten liquid lithium.

  3. Lithium Hexamethyldisilazide: A View of Lithium Ion Solvation

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Hexamethyldisilazide: A View of Lithium Ion Solvation through a Glass-Bottom Boat BRETT L and reactivities, we were drawn to lithium hexamethyldisilazide (LiHMDS; (Me3Si)2NLi) by its promi- nence principles of lithium ion coordination chemistry.2 Understanding how solvation influences organolithium

  4. Lithium Diisopropylamide-Mediated Ortholithiations: Lithium Chloride Catalysis

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Diisopropylamide-Mediated Ortholithiations: Lithium Chloride Catalysis Lekha Gupta, 2008 Ortholithiations of a range of arenes mediated by lithium diisopropylamide (LDA) in THF at -78 °C protocols with unpurified commercial samples of n-butyl- lithium to prepare LDA or commercially available

  5. Cathode material for lithium batteries

    DOE Patents [OSTI]

    Park, Sang-Ho; Amine, Khalil

    2013-07-23T23:59:59.000Z

    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.

  6. Side Reactions in Lithium-Ion Batteries

    E-Print Network [OSTI]

    Tang, Maureen Han-Mei

    2012-01-01T23:59:59.000Z

    experimental data from plastic lithium ion cells. Journal ofelectrolyte additive for lithium-ion batteries. Elec-A. Aging Mechanisms in Lithium-Ion Batteries. Journal of

  7. Ionic liquids for rechargeable lithium batteries

    E-Print Network [OSTI]

    Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

    2008-01-01T23:59:59.000Z

    their use in lithium-ion batteries. However, applications atresponse of lithium rechargeable batteries,” Journal of therechargeable lithium batteries (Preliminary report, Sept.

  8. Ionic liquids for rechargeable lithium batteries

    E-Print Network [OSTI]

    Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

    2008-01-01T23:59:59.000Z

    molten salts as lithium battery electrolyte,” ElectrochimicaFigure 15. Rechargeable lithium-ion battery. Figure 16 showsbattery. It is essential that an ionic liquid – lithium salt

  9. Block copolymer electrolytes for lithium batteries

    E-Print Network [OSTI]

    Hudson, William Rodgers

    2011-01-01T23:59:59.000Z

    K. M. Directions in secondary lithium battery research-and-runaway inhibitors for lithium battery electrolytes. Journalrunaway inhibitors for lithium battery electrolytes. Journal

  10. Design and Simulation of Lithium Rechargeable Batteries

    E-Print Network [OSTI]

    Doyle, C.M.

    2010-01-01T23:59:59.000Z

    of a Rechargeable Lithium Battery," J. Power Sources, 24,Wada, "Rechargeable Lithium Battery Based on Pyrolytic Car-Li-Ion Battery," Lithium Battery Symposium, Electrochemical

  11. Lithium Insertion Chemistry of Some Iron Vanadates

    E-Print Network [OSTI]

    Patoux, Sebastien; Richardson, Thomas J.

    2008-01-01T23:59:59.000Z

    in A. Nazri, G.Pistoia (Eds. ), Lithium batteries, Science &structure materials in lithium cells, for a lower limitLithium Insertion Chemistry of Some Iron Vanadates Sébastien

  12. Design and Simulation of Lithium Rechargeable Batteries

    E-Print Network [OSTI]

    Doyle, C.M.

    2010-01-01T23:59:59.000Z

    J. -P. Gabano, Ed. , Lithium Batteries, Academic Press, Newfor Rechargeable Lithium Batteries," J. Electrochem.for Rechargeable Lithium Batteries," J. Electroclzern.

  13. Lithium Insertion Chemistry of Some Iron Vanadates

    E-Print Network [OSTI]

    Patoux, Sebastien; Richardson, Thomas J.

    2008-01-01T23:59:59.000Z

    G.Pistoia (Eds. ), Lithium batteries, Science & Technology,Keywords: Lithium batteries, iron vanadates, insertionelectrode materials for lithium batteries, (mostly layered

  14. Ionic liquids for rechargeable lithium batteries

    E-Print Network [OSTI]

    Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

    2008-01-01T23:59:59.000Z

    for rechargeable lithium batteries (Preliminary report,applications using lithium batteries, we must be sure thattemperature range. For lithium batteries in hybrid vehicles,

  15. Side Reactions in Lithium-Ion Batteries

    E-Print Network [OSTI]

    Tang, Maureen Han-Mei

    2012-01-01T23:59:59.000Z

    for rechargeable lithium batteries. Advanced Materials 10,Protection of Secondary Lithium Batteries. Journal of thein Rechargeable Lithium Batteries for Overcharge Protection.

  16. Advances in lithium-ion batteries

    E-Print Network [OSTI]

    Kerr, John B.

    2003-01-01T23:59:59.000Z

    Advances in Lithium-Ion Batteries Edited by Walter A. vanpuzzling mysteries of lithium ion batteries. The book beginssuch importance to lithium ion batteries one is amazed that

  17. Block copolymer electrolytes for lithium batteries

    E-Print Network [OSTI]

    Hudson, William Rodgers

    2011-01-01T23:59:59.000Z

    polymer electrolytes for lithium batteries. Nature 394, 456-facing rechargeable lithium batteries. Nature 414, 359-367 (vanadium oxides for lithium batteries. Journal of Materials

  18. Lithium metal oxide electrodes for lithium batteries

    DOE Patents [OSTI]

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

    2008-01-01T23:59:59.000Z

    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.

  19. Block copolymer electrolytes for lithium batteries

    E-Print Network [OSTI]

    Hudson, William Rodgers

    2011-01-01T23:59:59.000Z

    D. Thin-film lithium and lithium-ion batteries. Solid StateH. Polymer electrolytes for lithium-ion batteries. AdvancedReviews, 2010). Ozawa, K. Lithium-ion rechargeable batteries

  20. Lithium metal oxide electrodes for lithium batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kang, Sun-Ho

    2010-06-08T23:59:59.000Z

    An uncycled preconditioned electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula xLi.sub.2-yH.sub.yO.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 in which 0lithium 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. The xLi.sub.2-yH.sub.y.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 material is prepared by preconditioning a precursor lithium metal oxide (i.e., xLi.sub.2M'O.sub.3.(1-x)LiMO.sub.2) with a proton-containing medium with a pH<7.0 containing an inorganic acid. Methods of preparing the electrodes are disclosed, as are electrochemical cells and batteries containing the electrodes.

  1. Electrocatalysts for Nonaqueous Lithium–Air Batteries:...

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

    Electrocatalysts for Nonaqueous Lithium–Air Batteries: Status, Challenges, and Perspective. Electrocatalysts for Nonaqueous Lithium–Air Batteries: Status, Challenges,...

  2. Stabilization of Th{sup 3+} ions into mixed-valence thorium fluoride

    SciTech Connect (OSTI)

    Dubois, Marc, E-mail: marc.dubois@univ-bpclermont.f [Clermont Universite, Universite Blaise Pascal, Laboratoire des Materiaux Inorganiques, BP 10448, F-63000 Clermont-Ferrand (France); CNRS, UMR 6002, LMI, F-63177 Aubiere (France); Dieudonne, Belto; Mesbah, Adel; Bonnet, Pierre; El-Ghozzi, Malika [Clermont Universite, Universite Blaise Pascal, Laboratoire des Materiaux Inorganiques, BP 10448, F-63000 Clermont-Ferrand (France); CNRS, UMR 6002, LMI, F-63177 Aubiere (France); Renaudin, Guillaume [Clermont Universite, ENSCCF, Laboratoire des Materiaux Inorganiques, BP 10448, F-63000 Clermont-Ferrand (France); CNRS, UMR 6002, LMI, F-63177 Aubiere (France); Avignant, Daniel [Clermont Universite, Universite Blaise Pascal, Laboratoire des Materiaux Inorganiques, BP 10448, F-63000 Clermont-Ferrand (France); CNRS, UMR 6002, LMI, F-63177 Aubiere (France)

    2011-01-15T23:59:59.000Z

    The unusual oxidation state +3 of the thorium has been stabilized into a lithium containing non-stoichiometric mixed-valence (III/IV) thorium fluorinated phase with formula Li{sub 2+x}Th{sub 12}F{sub 50} (0valence III/IV thorium fluoride. The electrochemical insertion of Li{sup +} ions into the open channels of the host matrix has been carried out at 60 {sup o}C, using an alkylcarbonate PC-LiClO{sub 4} 1 M electrolyte. The Li{sup +} and Th{sup 3+} contents, both in the starting composition and the Li{sup +} inserted ones, were investigated by high resolution solid state {sup 7}Li NMR and EPR, respectively. -- Graphical abstract: Electrochemical insertion of Li{sup +} ions into mixed-valence III/IV thorium fluoride and EPR spectra for the raw and inserted compounds. Display Omitted

  3. Valence quark distributions of the proton from maximum entropy approach

    E-Print Network [OSTI]

    Rong Wang; Xurong Chen

    2014-10-14T23:59:59.000Z

    We present an attempt of maximum entropy principle to determine valence quark distributions in the proton at very low resolution scale $Q_0^2$. The initial three valence quark distributions are obtained with limited dynamical information from quark model and QCD theory. Valence quark distributions from this method are compared to the lepton deep inelastic scattering data, and the widely used CT10 and MSTW08 data sets. The obtained valence quark distributions are consistent with experimental observations and the latest global fits of PDFs. Maximum entropy method is expected to be particularly useful in the case where relatively little information from QCD calculation is given.

  4. Valence quark distributions of the proton from maximum entropy approach

    E-Print Network [OSTI]

    Wang, Rong

    2014-01-01T23:59:59.000Z

    We present an attempt of maximum entropy principle to determine valence quark distributions in the proton at very low resolution scale $Q_0^2$. The initial three valence quark distributions are obtained with limited dynamical information from quark model and QCD theory. Valence quark distributions from this method are compared to the lepton deep inelastic scattering data, and the widely used CT10 and MSTW08 data sets. The obtained valence quark distributions are consistent with experimental observations and the latest global fits of PDFs. Maximum entropy method is expected to be particularly useful in the case where relatively little information from QCD calculation is given.

  5. Solid-state lithium battery

    DOE Patents [OSTI]

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

    2014-11-04T23:59:59.000Z

    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.

  6. Lithium battery management system

    DOE Patents [OSTI]

    Dougherty, Thomas J. (Waukesha, WI)

    2012-05-08T23:59:59.000Z

    Provided is a system for managing a lithium battery system having a plurality of cells. The battery system comprises a variable-resistance element electrically connected to a cell and located proximate a portion of the cell; and a device for determining, utilizing the variable-resistance element, whether the temperature of the cell has exceeded a predetermined threshold. A method of managing the temperature of a lithium battery system is also included.

  7. Inexpensive, Nonfluorinated Anions for Lithium Salts and Ionic...

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

    Anions for Lithium Salts and Ionic Liquids for Lithium Battery Electrolytes Inexpensive, Nonfluorinated Anions for Lithium Salts and Ionic Liquids for Lithium Battery Electrolytes...

  8. Hydrogen Outgassing from Lithium Hydride

    SciTech Connect (OSTI)

    Dinh, L N; Schildbach, M A; Smith, R A; Balazs1, B; McLean II, W

    2006-04-20T23:59:59.000Z

    Lithium hydride is a nuclear material with a great affinity for moisture. As a result of exposure to water vapor during machining, transportation, storage and assembly, a corrosion layer (oxide and/or hydroxide) always forms on the surface of lithium hydride resulting in the release of hydrogen gas. Thermodynamically, lithium hydride, lithium oxide and lithium hydroxide are all stable. However, lithium hydroxides formed near the lithium hydride substrate (interface hydroxide) and near the sample/vacuum interface (surface hydroxide) are much less thermally stable than their bulk counterpart. In a dry environment, the interface/surface hydroxides slowly degenerate over many years/decades at room temperature into lithium oxide, releasing water vapor and ultimately hydrogen gas through reaction of the water vapor with the lithium hydride substrate. This outgassing can potentially cause metal hydriding and/or compatibility issues elsewhere in the device. In this chapter, the morphology and the chemistry of the corrosion layer grown on lithium hydride (and in some cases, its isotopic cousin, lithium deuteride) as a result of exposure to moisture are investigated. The hydrogen outgassing processes associated with the formation and subsequent degeneration of this corrosion layer are described. Experimental techniques to measure the hydrogen outgassing kinetics from lithium hydride and methods employing the measured kinetics to predict hydrogen outgassing as a function of time and temperature are presented. Finally, practical procedures to mitigate the problem of hydrogen outgassing from lithium hydride are discussed.

  9. Six-Membered-Ring Malonatoborate-Based Lithium Salts as Electrolytes for Lithium Ion Batteries

    E-Print Network [OSTI]

    Yang, Li

    2014-01-01T23:59:59.000Z

    References 1. Lithium Ion Batteries: Fundamentals andProgram for Lithium Ion Batteries, U.S. Department ofas Electrolytes for Lithium Ion Batteries Li Yang a , Hanjun

  10. California Lithium Battery, Inc.

    Broader source: Energy.gov [DOE]

    California Lithium Battery (CaLBattery), based in Los Angeles, California, is developing a low-cost, advanced lithium-ion battery that employs a novel silicon graphene composite material that will substantially improve battery cycle life. When combined with other advanced battery materials, it could effectively lower battery life cycle cost by up to 70 percent. Over the next year, CALBattery will be working with Argonne National Laboratory to combine their patented silicon-graphene anode material process together with other advanced ANL cathode and electrolyte battery materials.

  11. Micro-and nanoscale domain engineering in lithium niobate and lithium tantalate

    E-Print Network [OSTI]

    Byer, Robert L.

    Micro- and nanoscale domain engineering in lithium niobate and lithium tantalate Vladimir Ya. Shur investigation of the domain evolution in lithium niobate and lithium tantalate during backswitched electric sources based on quasi-phase matching.11 Lithium niobate LiNbO3 (LN) and lithium tantalate LiTaO3 (LT

  12. Inelastic neutron scattering in valence fluctuation compounds

    SciTech Connect (OSTI)

    Jon M Lawrence

    2011-02-15T23:59:59.000Z

    The valence fluctuation compounds are rare earth intermetallics where hybridization of the nearly-localized 4f electrons with the conduction electrons leads to incorporation of the 4f's into the itinerant states. This hybridization slows down the conduction electrons and hence gives them a heavy effective mass, justifying application of the term 'heavy Fermion' (HF) to these materials. During the project period, we grew large single crystals of several such compounds and measured their properties using both standard thermodynamic probes and state-of-the-art inelastic neutron scattering. We obtained three main results. For the intermediate valence compounds CePd{sub 3} and YbAl{sub 3}, we showed that the scattering of neutrons by the fluctuations of the 4f magnetic moment does not have the momentum dependence expected for the itinerant heavy mass state; rather, the scattering is more typical of a localized spin fluctuation. We believe that incoherent scattering localizes the excitation. For the heavy Fermion compound Ce(Ni{sub 0.935}Pd{sub 0.065}){sub 2}Ge{sub 2}, which sits at a T = 0 critical point for transformation into an antiferromagnetic (AF) phase, we showed that the scattering from the AF fluctuations does not exhibit any of the divergences that are expected at a phase transition. We speculate that alloy disorder profoundly suppresses the growth of the fluctuating AF regions, leading to short range clusters rather than regions of infinite size. Finally, we explored the applicability of key concepts used to describe the behavior of rare earth heavy Fermions to uranium based HF compounds where the 5f electrons are itinerant as opposed to localized. We found that scaling laws relating the spin fluctuation energy measured in neutron scattering to the low temperature specific heat and susceptibility are valid for the uranium compounds, once corrections are made for AF fluctuations; however, the degeneracy of the high temperature moment is smaller than expected for rare-earth-like Hund's rule behavior, essentially because the orbital moment is suppressed for itinerant 5f electrons. We also found that the standard local-moment-based theory of the temperature dependence of the specific heat, susceptibility and neutron scattering fails badly for URu{sub 2}Zn{sub 20} and UCo{sub 2}Zn{sub 20}, even though the theory is phenomenally successful for the closely related rare earth compound YbFe{sub 2}Zn{sub 20}. Both these results highlight the distinction between the itineracy of the 5f's and the localization of the 4f's. It is our hope that these results are sufficiently significant as to stimulate deeper investigation of these compounds.

  13. Positron annihilation with core and valence electrons

    E-Print Network [OSTI]

    Green, D G

    2015-01-01T23:59:59.000Z

    $\\gamma$-ray spectra for positron annihilation with the core and valence electrons of the noble gas atoms Ar, Kr and Xe is calculated within the framework of diagrammatic many-body theory. The effect of positron-atom and short-range positron-electron correlations on the annihilation process is examined in detail. Short-range correlations, which are described through non-local corrections to the vertex of the annihilation amplitude, are found to significantly enhance the spectra for annihilation on the core orbitals. For Ar, Kr and Xe, the core contributions to the annihilation rate are found to be 0.55\\%, 1.5\\% and 2.2\\% respectively, their small values reflecting the difficulty for the positron to probe distances close to the nucleus. Importantly however, the core subshells have a broad momentum distribution and markedly contribute to the annihilation spectra at Doppler energy shifts $\\gtrsim3$\\,keV, and even dominate the spectra of Kr and Xe at shifts $\\gtrsim5$\\,keV. Their inclusion brings the theoretical ...

  14. Lithium disulfide battery

    DOE Patents [OSTI]

    Kaun, Thomas D. (New Lenox, IL)

    1988-01-01T23:59:59.000Z

    A negative electrode limited secondary electrochemical cell having dense FeS.sub.2 positive electrode operating exclusively on the upper plateau, a Li alloy negative electrode and a suitable lithium-containing electrolyte. The electrolyte preferably is 25 mole percent LiCl, 38 mole percent LiBr and 37 mole percent KBr. The cell may be operated isothermally.

  15. Lithium ion conducting electrolytes

    DOE Patents [OSTI]

    Angell, C. Austen (Tempe, AZ); Liu, Changle (Tempe, AZ)

    1996-01-01T23:59:59.000Z

    A liquid, predominantly lithium-conducting, ionic electrolyte having exceptionally high conductivity at temperatures of 100.degree. 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.degree. C. conductivity. Another embodiment contains up to about but not more than 10 mol percent of a molecular solvent such as acetone.

  16. Lithium ion conducting electrolytes

    DOE Patents [OSTI]

    Angell, C.A.; Liu, C.

    1996-04-09T23:59:59.000Z

    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.

  17. Advances in lithium-ion batteries

    E-Print Network [OSTI]

    Kerr, John B.

    2003-01-01T23:59:59.000Z

    Advances in Lithium-Ion Batteries Edited by Walter A. vanbook is intended for lithium-ion scientists and engineersof the state of the Lithium-ion art and in this they have

  18. Double Photoionization of excited Lithium and Beryllium

    E-Print Network [OSTI]

    Yip, Frank L.

    2010-01-01T23:59:59.000Z

    of excited Lithium and Beryllium F. L. Yip, 1 C. W. McCurdy,ion- ization of lithium and beryllium starting from aligned,DPI from aligned lithium and beryllium atoms in excited P-

  19. Side Reactions in Lithium-Ion Batteries

    E-Print Network [OSTI]

    Tang, Maureen Han-Mei

    2012-01-01T23:59:59.000Z

    simulate those in a lithium battery. Chapter 3 TransientModel for Aging of Lithium-Ion Battery Cells. Journal of TheRole in Nonaqueous Lithium-Oxygen Battery Electrochemistry.

  20. Sputter deposition of lithium silicate - lithium phosphate amorphous electrolytes

    SciTech Connect (OSTI)

    Dudney, N.J.; Bates, J.B.; Luck, C.F. (Oak Ridge National Lab., TN (USA)); Robertson, J.D. (Kentucky Univ., Lexington, KY (USA). Dept. of Chemistry)

    1991-01-01T23:59:59.000Z

    Thin films of an amorphous lithium-conducting electrolyte were deposited by rf magnetron sputtering of ceramic targets containing Li{sub 4}SiO{sub 4} and Li{sub 3}PO{sub 4}. The lithium content of the films was found to depend more strongly on the nature and composition of the targets than on many other sputtering parameters. For targets containing Li{sub 4}SiO{sub 4}, most of the lithium was found to segregate away from the sputtered area of the target. Codeposition using two sputter sources achieves a high lithium content in a controlled and reproducible film growth. 10 refs., 4 figs.

  1. Design and Simulation of Lithium Rechargeable Batteries

    E-Print Network [OSTI]

    Doyle, C.M.

    2010-01-01T23:59:59.000Z

    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

  2. Side Reactions in Lithium-Ion Batteries

    E-Print Network [OSTI]

    Tang, Maureen Han-Mei

    2012-01-01T23:59:59.000Z

    Secondary Lithium Batteries. Journal of the Electrochemicalin Rechargeable Lithium Batteries for Overcharge Protection.G. M. in Handbook of Batteries (eds Linden, D. & Reddy, T.

  3. Washington: Graphene Nanostructures for Lithium Batteries Recieves...

    Energy Savers [EERE]

    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...

  4. 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...

  5. Manganese Oxide Composite Electrodes for Lithium Batteries |...

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

    Manganese Oxide Composite Electrodes for Lithium Batteries Technology available for licensing: Improved spinel-containing "layered-layered" lithium metal oxide electrodes Materials...

  6. Lithium-based electrochromic mirrors

    E-Print Network [OSTI]

    Richardson, Thomas J.; Slack, Jonathan L.

    2003-01-01T23:59:59.000Z

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

  7. Fixed-Node Diffusion Monte Carlo of Lithium Systems

    E-Print Network [OSTI]

    Rasch, Kevin

    2015-01-01T23:59:59.000Z

    We study lithium systems over a range of number of atoms, e.g., atomic anion, dimer, metallic cluster, and body-centered cubic crystal by the diffusion Monte Carlo method. The calculations include both core and valence electrons in order to avoid any possible impact by pseudo potentials. The focus of the study is the fixed-node errors, and for that purpose we test several orbital sets in order to provide the most accurate nodal hyper surfaces. We compare our results to other high accuracy calculations wherever available and to experimental results so as to quantify the the fixed-node errors. The results for these Li systems show that fixed-node quantum Monte Carlo achieves remarkably high accuracy total energies and recovers 97-99 % of the correlation energy.

  8. Lithium Research Status and PlansLithium Research Status and Plans Charles H. Skinner, PPPL

    E-Print Network [OSTI]

    Princeton Plasma Physics Laboratory

    Lithium Research Status and PlansLithium Research Status and Plans Charles H. Skinner, PPPL Robert February 3-5, 2010 #12;NSTX PAC-27 ­ Lithium Research Status and Plans 2/15February 3-5, 2010 NSTX lithium research is an integral part of a program to develop lithium as a PFC concept for magnetic fusion NSTX w

  9. Solid lithium-ion electrolyte

    DOE Patents [OSTI]

    Zhang, Ji-Guang (Golden, CO); Benson, David K. (Golden, CO); Tracy, C. Edwin (Golden, CO)

    1998-01-01T23:59:59.000Z

    The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li.sub.2 O--CeO.sub.2 --SiO.sub.2 system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications.

  10. Solid lithium-ion electrolyte

    DOE Patents [OSTI]

    Zhang, J.G.; Benson, D.K.; Tracy, C.E.

    1998-02-10T23:59:59.000Z

    The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li{sub 2}O--CeO{sub 2}--SiO{sub 2} system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications. 12 figs.

  11. Synthesis, Characterization and Performance of Cathodes for Lithium Ion Batteries

    E-Print Network [OSTI]

    Zhu, Jianxin

    2014-01-01T23:59:59.000Z

    ion batteries In current lithium ion battery technology,ion batteries The first commercialized lithium-ion batteryfirst lithium-ion battery. Compared to the other batteries,

  12. The UC Davis Emerging Lithium Battery Test Project

    E-Print Network [OSTI]

    Burke, Andy; Miller, Marshall

    2009-01-01T23:59:59.000Z

    Characteristics of Lithium-ion Batteries of VariousMiller, M. , Emerging Lithium-ion Battery Technologies forSymposium on Large Lithium-ion Battery Technology and

  13. The UC Davis Emerging Lithium Battery Test Project

    E-Print Network [OSTI]

    Burke, Andy; Miller, Marshall

    2009-01-01T23:59:59.000Z

    The UC Davis Emerging Lithium Battery Test Project Andrewto evaluate emerging lithium battery technologies for plug-vehicles. By emerging lithium battery chemistries were meant

  14. ELLIPSOMETRY OF SURFACE LAYERS ON LEAD AND LITHIUM

    E-Print Network [OSTI]

    Peters, Richard Dudley

    2011-01-01T23:59:59.000Z

    rate. The corrosion reaction between lithium and water vaporOpen Circuit Corrosion Bo Lithium, , L A~ueous Electrolytecalculated representing corrosion of lithium in water vapor,

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

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

    Carbonate Solvents and Lithium Salts on Morphology and Coulombic Efficiency of Lithium Electrode. Effects of Carbonate Solvents and Lithium Salts on Morphology and Coulombic...

  16. ELLIPSOMETRY OF SURFACE LAYERS ON LEAD AND LITHIUM

    E-Print Network [OSTI]

    Peters, Richard Dudley

    2011-01-01T23:59:59.000Z

    Surface Layers on Lead and Lithium By Richard Dudley Peterssulfuric acid and and lithium to water, Acid concentrationsbeen observed in the reaction of lithium with water vapor. i

  17. Redox shuttle additives for overcharge protection in lithium batteries

    E-Print Network [OSTI]

    Richardson, Thomas J.; Ross Jr., P.N.

    1999-01-01T23:59:59.000Z

    Protection in Lithium Batteries”, T. J. Richardson* and P.OVERCHARGE PROTECTION IN LITHIUM BATTERIES T. J. Richardson*improve the safety of lithium batteries. ACKNOWLEDGEMENT

  18. Visualization of Charge Distribution in a Lithium Battery Electrode

    E-Print Network [OSTI]

    Liu, Jun

    2010-01-01T23:59:59.000Z

    for Rechargeable Lithium Batteries. J. Electrochem. Soc.Calculations for Lithium Batteries. J. Electrostatics 1995,Modeling of Lithium Polymer Batteries. J. Power Sources

  19. The UC Davis Emerging Lithium Battery Test Project

    E-Print Network [OSTI]

    Burke, Andy; Miller, Marshall

    2009-01-01T23:59:59.000Z

    for rechargeable lithium batteries, Journal of Powerand iron phosphate lithium batteries will be satisfactoryapplications. The cost of lithium batteries remains high ($

  20. Grafted polyelectrolyte membranes for lithium batteries and fuel cells

    E-Print Network [OSTI]

    Kerr, John B.

    2003-01-01T23:59:59.000Z

    MEMBRANES FOR LITHIUM BATTERIES AND FUEL CELLS. John Kerralso be discussed. Lithium Batteries for Transportation andpolymer membrane for lithium batteries. This paper will give

  1. Coated Silicon Nanowires as Anodes in Lithium Ion Batteries

    E-Print Network [OSTI]

    Watts, David James

    2014-01-01T23:59:59.000Z

    for rechargeable lithium batteries. J. Power Sources 139,for advanced lithium-ion batteries. J. Power Sources 174,nano-anodes for lithium rechargeable batteries. Angew. Chem.

  2. Synthesis, Characterization and Performance of Cathodes for Lithium Ion Batteries

    E-Print Network [OSTI]

    Zhu, Jianxin

    2014-01-01T23:59:59.000Z

    0 lithium batteries. J. Electrochem. Soc.for rechargeable lithium batteries. Advanced Materials 1998,for rechargeable lithium batteries. J. Electrochem. Soc.

  3. Lithium Ion Cell Development for Photovoltaic Energy Storage Applications

    SciTech Connect (OSTI)

    Susan Babinec

    2012-02-08T23:59:59.000Z

    The overall project goal is to reduce the cost of home and neighborhood photovoltaic storage systems by reducing the single largest cost component â?? the energy storage cells. Solar power is accepted as an environmentally advantaged renewable power source. Its deployment in small communities and integrated into the grid, requires a safe, reliable and low cost energy storage system. The incumbent technology of lead acid cells is large, toxic to produce and dispose of, and offer limited life even with significant maintenance. The ideal PV storage battery would have the safety and low cost of lead acid but the performance of lithium ion chemistry. Present lithium ion batteries have the desired performance but cost and safety remain the two key implementation barriers. The purpose of this project is to develop new lithium ion cells that can meet PVES cost and safety requirements using A123Systems phosphate-based cathode chemistries in commercial PHEV cell formats. The cost target is a cell design for a home or neighborhood scale at <$25/kWh. This DOE program is the continuation and expansion of an initial MPSC (Michigan Public Service Commission) program towards this goal. This program further pushes the initial limits of some aspects of the original program â?? even lower cost anode and cathode actives implemented at even higher electrode loadings, and as well explores new avenues of cost reduction via new materials â?? specifically our higher voltage cathode. The challenge in our materials development is to achieve parity in the performance metrics of cycle life and high temperature storage, and to produce quality materials at the production scale. Our new cathode material, M1X, has a higher voltage and so requires electrolyte reformulation to meet the high temperature storage requirements. The challenge of thick electrode systems is to maintain adequate adhesion and cycle life. The composite separator has been proven in systems having standard loading electrodes; the challenge with this material will be to maintain proven performance when this composite is coated onto a thicker electrode; as well the high temperature storage must meet application requirements. One continuing program challenge was the lack of specific performance variables for this PV application and so the low power requirements of PHEV/EV transportation markets were again used.

  4. Lithium niobate explosion monitor

    DOE Patents [OSTI]

    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

    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.

  5. Conflicting Roles Of Nickel In Controlling Cathode Performance In Lithium-ion Batteries

    SciTech Connect (OSTI)

    Gu, Meng; Belharouak, Ilias; Genc, Arda; Wang, Zhiguo; Wang, Dapeng; Amine, Khalil; Gao, Fei; Zhou, Guangwen; Thevuthasan, Suntharampillai; Baer, Donald R.; Zhang, Jiguang; Browning, Nigel D.; Liu, Jun; Wang, Chong M.

    2012-09-17T23:59:59.000Z

    A variety of approaches are being made to enhance the performance of lithium ion batteries. Incorporating multi-valence transition metal ions into metal oxide cathodes has been identified as an essential approach to achieve the necessary high voltage and high capacity. However, the fundamental mechanism that limits their power rate and cycling stability remains unclear. The power rate strongly depends on the lithium ion drift speed in the cathode. Crystallographically, these transition metal-based cathodes frequently have a layered structure. In the classic wisdom, it is accepted that lithium ion travels swiftly within the layers moving out/in of the cathode during the charge/discharge. Here, we report the unexpected discovery of a thermodynamically driven, yet kinetically controlled, surface modification in the widely explored lithium nickel manganese oxide cathode material, which may inhibit the battery charge/discharge rate. We found that during cathode synthesis and processing before electrochemical cycling in the cell nickel can preferentially move along the fast diffusion channels and selectively segregate at the surface facets terminated with a mix of anions and cations. This segregation essentially blocks the otherwise fast out/in pathways for lithium ions during the charge/discharge. Therefore, it appears that the transition metal dopant may help to provide high capacity and/or high voltage, but can be located in a “wrong” location that blocks or slows lithium diffusion, limiting battery performance. In this circumstance, limitations in the properties of Li-ion batteries using these cathode materials can be determined more by the materials synthesis issues than by the operation within the battery itself.

  6. Redox shuttle additives for overcharge protection in lithium batteries

    E-Print Network [OSTI]

    Richardson, Thomas J.; Ross Jr., P.N.

    1999-01-01T23:59:59.000Z

    Protection in Lithium Batteries”, T. J. Richardson* and P.PROTECTION IN LITHIUM BATTERIES T. J. Richardson* and P. N.in lithium and lithium ion batteries are now available. The

  7. Electromagnetically Restrained Lithium Blanket APEX Interim Report November, 1999

    E-Print Network [OSTI]

    California at Los Angeles, University of

    to avoid corrosion or fire. Lithium's high electrical conductivity may possibly permit efficient, compactElectromagnetically Restrained Lithium Blanket APEX Interim Report November, 1999 6-1 CHAPTER 6: ELECTROMAGNETICALLY RESTRAINED LITHIUM BLANKET Contributors Robert Woolley #12;Electromagnetically Restrained Lithium

  8. Lithium Reagents DOI: 10.1002/anie.200603038

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Reagents DOI: 10.1002/anie.200603038 Lithium Diisopropylamide: Solution Kinetics Keywords: kinetics · lithium diisopropylamide · metalation · solvent effects · synthesis design D. B: lithium diiso- propylamide (LDA). LDA has played a profound role in organic synthesis, serving as the base

  9. Lithium ion conducting ionic electrolytes

    DOE Patents [OSTI]

    Angell, C.A.; Xu, K.; Liu, C.

    1996-01-16T23:59:59.000Z

    A liquid, predominantly lithium-conducting, ionic electrolyte is described which has exceptionally high conductivity at temperatures of 100 C or lower, including room temperature. It comprises molten lithium salts or salt mixtures in which a small amount of an anionic polymer lithium salt is dissolved to stabilize the liquid against recrystallization. Further, a liquid ionic electrolyte which has been rubberized by addition of an extra proportion of anionic polymer, and which has good chemical and electrochemical stability, is described. This presents an attractive alternative to conventional salt-in-polymer electrolytes which are not cationic conductors. 4 figs.

  10. Lithium ion conducting ionic electrolytes

    DOE Patents [OSTI]

    Angell, C. Austen (Mesa, AZ); Xu, Kang (Tempe, AZ); Liu, Changle (Tulsa, OK)

    1996-01-01T23:59:59.000Z

    A liquid, predominantly lithium-conducting, ionic electrolyte is described which has exceptionally high conductivity at temperatures of 100.degree. C. or lower, including room temperature. It comprises molten lithium salts or salt mixtures in which a small amount of an anionic polymer lithium salt is dissolved to stabilize the liquid against recrystallization. Further, a liquid ionic electrolyte which has been rubberized by addition of an extra proportion of anionic polymer, and which has good chemical and electrochemical stability, is described. This presents an attractive alternative to conventional salt-in-polymer electrolytes which are not cationic conductors.

  11. Anodes for rechargeable lithium batteries

    DOE Patents [OSTI]

    Thackeray, Michael M. (Naperville, IL); Kepler, Keith D. (Mountain View, CA); Vaughey, John T. (Elmhurst, IL)

    2003-01-01T23:59:59.000Z

    A negative electrode (12) for a non-aqueous electrochemical cell (10) with an intermetallic host structure containing two or more elements selected from the metal elements and silicon, capable of accommodating lithium within its crystallographic host structure such that when the host structure is lithiated it transforms to a lithiated zinc-blende-type structure. Both active elements (alloying with lithium) and inactive elements (non-alloying with lithium) are disclosed. Electrochemical cells and batteries as well as methods of making the negative electrode are disclosed.

  12. Manufacturing of Protected Lithium Electrodes for Advanced Lithium...

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

    Steven J. Visco, CEO & CTO, PolyPlus Battery Company U.S. DOE Advanced Manufacturing Office Peer Review Meeting Washington, D.C. May 28-29, 2015 Manufacturing of Protected Lithium...

  13. Mobile linkers on DNA-coated colloids: valency without patches

    E-Print Network [OSTI]

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

    2014-08-27T23:59:59.000Z

    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.

  14. Specificity, flexibility and valence of DNA bonds guide emulsion architecture

    E-Print Network [OSTI]

    Lang Feng; Lea-Laetitia Pontani; Remi Dreyfus; Paul Chaikin; Jasna Brujic

    2013-03-25T23:59:59.000Z

    The specificity and thermal reversibility of DNA interactions have enabled the self-assembly of crystal structures, self-replicating materials and colloidal molecules. Grafting DNA onto liquid interfaces of emulsions leads to exciting new architectural possibilities due to the mobility of the DNA ligands and the patches they form between bound droplets. Here we show that the size and number of these adhesion patches (valency) can be controlled. Valence 2 leads to flexible polymers of emulsion droplets, while valence above 4 leads to rigid droplet networks. A simple thermodynamic model quantitatively describes the increase in the patch size with droplet radii, DNA concentration and the stiffness of the tether to the sticky-end. The patches are formed between droplets with complementary DNA strands or alternatively with complementary colloidal nanoparticles to mediate DNA binding between droplets. This emulsion system opens the route to directed self-assembly of more complex structures through distinct DNA bonds with varying strengths and controlled valence and flexibility.

  15. Cyanoethylated compounds as additives in lithium/lithium batteries

    DOE Patents [OSTI]

    Nagasubramanian, Ganesan (Albuquerque, NM)

    1999-01-01T23:59:59.000Z

    The power loss of lithium/lithium ion battery cells is significantly reduced, especially at low temperatures, when about 1% by weight of an additive is incorporated in the electrolyte layer of the cells. The usable additives are organic solvent soluble cyanoethylated polysaccharides and poly(vinyl alcohol). The power loss decrease results primarily from the decrease in the charge transfer resistance at the interface between the electrolyte and the cathode.

  16. Solvated electron lithium electrode for high energy density battery

    SciTech Connect (OSTI)

    Sammells, A.F.

    1987-05-26T23:59:59.000Z

    A rechargeable high energy density lithium-based cell is described comprising: a solvated electron lithium negative electrode comprising a solution of lithium dissolved in liquid ammonia; a lithium ion conducting solid electrolyte contacting the negative electrode; a liquid non-aqueous lithium ion conducting electrolyte comprising a lithium ion conducting supporting electrolyte dissolved in a non-aqueous solvent. The liquid electrolyte contacting the lithium ion conducting solid electrolyte; and a solid lithium intercalation positive electrode contacting the liquid electrolyte.

  17. Mixed valency and electronic structure in self-assembled monolayers, self-exchange, and hydrogen bonded assemblies

    E-Print Network [OSTI]

    Goeltz, John Christopher

    2011-01-01T23:59:59.000Z

    P. ”Mixed valency across hydrogen bonds” J. Am. Chem. Soc.6 Mixed valency across hydrogen bonds: a more completeMixed valency across hydrogen bonds,” by John C. Goeltz and

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

    E-Print Network [OSTI]

    Dolgopolov Stanislav Olegovich

    2014-10-21T23:59:59.000Z

    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.

  19. Rotational Mixing and Lithium Depletion

    E-Print Network [OSTI]

    Pinsonneault, M H

    2010-01-01T23:59:59.000Z

    I review basic observational features in Population I stars which strongly implicate rotation as a mixing agent; these include dispersion at fixed temperature in coeval populations and main sequence lithium depletion for a range of masses at a rate which decays with time. New developments related to the possible suppression of mixing at late ages, close binary mergers and their lithium signature, and an alternate origin for dispersion in young cool stars tied to radius anomalies observed in active young stars are discussed. I highlight uncertainties in models of Population II lithium depletion and dispersion related to the treatment of angular momentum loss. Finally, the origins of rotation are tied to conditions in the pre-main sequence, and there is thus some evidence that enviroment and planet formation could impact stellar rotational properties. This may be related to recent observational evidence for cluster to cluster variations in lithium depletion and a connection between the presence of planets and s...

  20. Development of Lithium Deposition Techniques for TFTR

    SciTech Connect (OSTI)

    Gorman, J.; Johnson, D.; Kugel, H.W.; Labik, G.; Lemunyan, G.; et al

    1997-10-01T23:59:59.000Z

    The ability to increase the quantity of lithium deposition into TFTR beyond that of the Pellet Injector while minimizing perturbations to the plasma provides interesting experimental and operational options. Two additional lithium deposition tools were developed for possible application during the 1996 Experimental Schedule: a solid lithium target probe for real-time deposition, and a lithium effusion oven for deposition between discharges. The lithium effusion oven was operated in TFTR to deposit lithium on the Inner Limiter in the absence of plasma. This resulted in the third highest power TFTR discharge.

  1. Development of lithium deposition techniques for TFTR

    SciTech Connect (OSTI)

    Kugel, H.W.; Gorman, J.; Johnson, D.; Labik, G.; Lemunyan, G.; Mansfield, D.; Timberlake, J.; Vocaturo, M.

    1997-10-01T23:59:59.000Z

    The ability to increase the quantity of lithium deposition into TFTR beyond that of the Pellet Injector while minimizing perturbations to the plasma provides interesting experimental and operational options. Two additional lithium deposition tools were developed for possible application during the 1996 Experimental Schedule: a solid lithium target probe for real-time deposition, and a lithium effusion oven for deposition between discharges. The lithium effusion oven was operated in TFTR to deposit lithium on the Inner Limiter in the absence of plasma. This resulted in the third highest power TFTR discharge.

  2. Air breathing lithium power cells

    DOE Patents [OSTI]

    Farmer, Joseph C.

    2014-07-15T23:59:59.000Z

    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.

  3. Synthesis and Electrochemical Performance of a Lithium Titanium Phosphate Anode for Aqueous Lithium-Ion Batteries

    E-Print Network [OSTI]

    Cui, Yi

    on larger scales. Im- provement of the safety of lithium-ion batteries must occur if they are to be utilized in aqueous cells. However, the choice of a suitable anode material for an aqueous lithium-ion battery is moreSynthesis and Electrochemical Performance of a Lithium Titanium Phosphate Anode for Aqueous Lithium-Ion

  4. Real-time observation of lithium fibers growth inside a nanoscale lithium-ion battery

    E-Print Network [OSTI]

    Endres. William J.

    Real-time observation of lithium fibers growth inside a nanoscale lithium-ion battery Hessam.1063/1.3643035] Lithium-ion batteries are of great interest due to their high energy density, however, various safety properties, many applications are pos- sible.10,11 One is the electrolyte of the lithium-ion batteries, where

  5. Lithium Ion Solvation: Amine and Unsaturated Hydrocarbon Solvates of Lithium Hexamethyldisilazide (LiHMDS)

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Ion Solvation: Amine and Unsaturated Hydrocarbon Solvates of Lithium Hexamethyldisilazide, and 13C NMR spectroscopic studies of 6Li-15N labeled lithium hexamethyldisilazide ([6Li,15N]- Li ligand structure and lithium amide aggregation state is a complex and sensitive function of amine alkyl

  6. SOLID STATE NMR STUDY SUPPORTING THE LITHIUM VACANCY DEFECT MODEL IN CONGRUENT LITHIUM

    E-Print Network [OSTI]

    Bluemel, Janet

    @ Pergamon SOLID STATE NMR STUDY SUPPORTING THE LITHIUM VACANCY DEFECT MODEL IN CONGRUENT LITHIUM performed on powdered and single crystal lithium niobate of defectivecongruent composition (48.4%LirO;51.6% NbrOr) using a magnetic field strength of 7.05 Tesla with the aim to distinguish between a lithium

  7. Protective lithium ion conducting ceramic coating for lithium metal anodes and associate method

    DOE Patents [OSTI]

    Bates, John B. (Oak Ridge, TN)

    1994-01-01T23:59:59.000Z

    A battery structure including a cathode, a lithium metal anode and an electrolyte disposed between the lithium anode and the cathode utilizes a thin-film layer of lithium phosphorus oxynitride overlying so as to coat the lithium anode and thereby separate the lithium anode from the electrolyte. If desired, a preliminary layer of lithium nitride may be coated upon the lithium anode before the lithium phosphorous oxynitride is, in turn, coated upon the lithium anode so that the separation of the anode and the electrolyte is further enhanced. By coating the lithium anode with this material lay-up, the life of the battery is lengthened and the performance of the battery is enhanced.

  8. Michael Thackery on Lithium-air Batteries

    ScienceCinema (OSTI)

    Michael Thackery

    2010-01-08T23:59:59.000Z

    Michael Thackery, Distinguished Fellow 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.

  9. Michael Thackery on Lithium-air Batteries

    SciTech Connect (OSTI)

    Michael Thackery

    2009-09-14T23:59:59.000Z

    Michael Thackery, Distinguished Fellow 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.

  10. Khalil Amine on Lithium-air Batteries

    SciTech Connect (OSTI)

    Khalil Amine

    2009-09-14T23:59:59.000Z

    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.

  11. Khalil Amine on Lithium-air Batteries

    ScienceCinema (OSTI)

    Khalil Amine

    2010-01-08T23:59:59.000Z

    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.

  12. Advances in lithium-ion batteries

    E-Print Network [OSTI]

    Kerr, John B.

    2003-01-01T23:59:59.000Z

    Advances in Lithium-Ion Batteries Edited by Walter A. vantolerance of these batteries this is a curious omission andmysteries of lithium ion batteries. The book begins with an

  13. Recent advances in lithium ion technology

    SciTech Connect (OSTI)

    Levy, S.C.

    1995-01-01T23:59:59.000Z

    Lithium ion technology is based on the use of lithium intercalating electrodes. Carbon is the most commonly used anode material, while the cathode materials of choice have been layered lithium metal chalcogenides (LiMX{sub 2}) and lithium spinel-type compounds. Electrolytes may be either organic liquids or polymers. Although the first practical use of graphite intercalation compounds as battery anodes was reported in 1981 for molten salt cells (1) and in 1983 for ambient temperature systems (2) it was not until Sony Energytech announced a new lithium ion rechargeable cell containing a lithium ion intercalating carbon anode in 1990, that interest peaked. The reason for this heightened interest is that these cells have the high energy density, high voltage and fight weight of metallic lithium systems plus a very long cycle life, but without the disadvantages of dendrite formation on charge and the safety considerations associated with metallic lithium.

  14. Design and Simulation of Lithium Rechargeable Batteries

    E-Print Network [OSTI]

    Doyle, C.M.

    2010-01-01T23:59:59.000Z

    Design and Simulation of Lithium Rechargeable Batteries by Christopher Marc Doyle Doctor of Philosophy in Chemical EngineeringDesign and Simulation of Lithium Rechargeable Batteries I C. Marc Doyle Department of Chemical Engineering

  15. (Lithium and lead-lithium corrosion and chemistry)

    SciTech Connect (OSTI)

    Tortorelli, P.F.

    1989-10-09T23:59:59.000Z

    Presentations on Mass Transport Processes in Li/Fe-12Cr-1MoVW Steel,'' A Lower Temperature Lithium Purification Process Incorporating Warm Trapping','' and Kinetic Analysis of Corrosion in Pb-17 at. % Li and Comparison to Pure Lithium'' were given by the traveler at the 1989 European Workshop on Lithium and Lead-Lithium Corrosion and Chemistry in Vienna, Austria. The European effort in lead-lithium appeared to be continuing unabated with a future focus on deposition and surface products reactions that can lead to corrosion control. The temperature gain realized from the use of ferritic/martensitic steels instead of austenitic steels in Pb-17 at. % Li appears to be 25--50{degrees}C. The traveler also visited the European Community's Joint Research Centre at Ispra to discuss Fe-Mn-Cr steels. He presented a seminar on Recent ORNL Results on the Development of Fe-Mn-Cr Steels,'' and toured the liquid metal laboratories. Our developmental Fe-Mn-Cr steels, which are compositionally tailored for shallow land burial, would not qualify as low activation'' materials per European standards. Because of both this and the poor sensitization resistance of these steels, our alloy development strategy for reduced activation materials should be critically reviewed.

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

    DOE Patents [OSTI]

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

    2014-05-13T23:59:59.000Z

    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.

  17. Ionic liquids for rechargeable lithium batteries

    E-Print Network [OSTI]

    Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

    2008-01-01T23:59:59.000Z

    M. Armand, “Room temperature molten salts as lithium batteryZ. Suarez, “Ionic liquid (molten salt) phase organometallic

  18. Basic features of the pion valence-quark distribution function

    E-Print Network [OSTI]

    Lei Chang; Cédric Mezrag; Hervé Moutarde; Craig D. Roberts; Jose Rodríguez-Quintero; Peter C. Tandy

    2014-06-20T23:59:59.000Z

    The impulse-approximation expression used hitherto to define the pion's valence-quark distribution function is flawed because it omits contributions from the gluons which bind quarks into the pion. A corrected leading-order expression produces the model-independent result that quarks dressed via the rainbow-ladder truncation, or any practical analogue, carry all the pion's light-front momentum at a characteristic hadronic scale. Corrections to the leading contribution may be divided into two classes, responsible for shifting dressed-quark momentum into glue and sea-quarks. Working with available empirical information, we use an algebraic model to express the principal impact of both classes of corrections. This enables a realistic comparison with experiment that allows us to highlight the basic features of the pion's measurable valence-quark distribution, $q^\\pi(x)$; namely, at a characteristic hadronic scale, $q^\\pi(x) \\sim (1-x)^2$ for $x\\gtrsim 0.85$; and the valence-quarks carry approximately two-thirds of the pion's light-front momentum.

  19. Sketching the pion's valence-quark generalised parton distribution

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Mezrag, C.; Chang, L.; Moutarde, H.; Roberts, C.D.; Rodríguez-Quintero, J.; Sabatié, F.; Schmidt, S.M.

    2015-02-01T23:59:59.000Z

    In order to learn effectively from measurements of generalised parton distributions (GPDs), it is desirable to compute them using a framework that can potentially connect empirical information with basic features of the Standard Model. We sketch an approach to such computations, based upon a rainbow-ladder (RL) truncation of QCD’s Dyson–Schwinger equations and exemplified via the pion’s valence dressed-quark GPD, Hv?(x, ?, t). Our analysis focuses primarily on ?=0, although we also capitalise on the symmetry-preserving nature of the RL truncation by connecting Hv?(x, ?=±1, t)with the pion’s valence-quark parton distribution amplitude. We explain that the impulse-approximation used hitherto to definemore »the pion’s valence dressed-quark GPD is generally invalid owing to omission of contributions from the gluons which bind dressed-quarks into the pion. A simple correction enables us to identify a practicable improvement to the approximation for Hv?(x, 0, t), expressed as the Radon transform of a single amplitude. Therewith we obtain results for Hv?(x, 0, t)and the associated impact-parameter dependent distribution, qv?(x, |#2;b?|), which provide a qualitatively sound picture of the pion’s dressed-quark structure at ahadronic scale. We evolve the distributions to a scale ?=2GeV, so as to facilitate comparisons in future with results from experiment or other nonperturbative methods.« less

  20. COSMOLOGICAL LITHIUM PROBLEM: A DIFFERENT APPROACH

    E-Print Network [OSTI]

    ?umer, Slobodan

    LITHIUM 7Li sources BBN cosmic-ray interactions (ingredients: shock waves, magnetic field, chargedCOSMOLOGICAL LITHIUM PROBLEM: A DIFFERENT APPROACH Tijana Prodanovi, University of Novi Sad Tamara Observations - boxes 4He ­ OK D ­ right on! 7Li ­ problem! Factor of 3-4 discrepancy! LITHIUM PROBLEM

  1. Solid composite electrolytes for lithium batteries

    DOE Patents [OSTI]

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

    2000-01-01T23:59:59.000Z

    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.

  2. Magnetism in Lithium–Oxygen Discharge Product

    SciTech Connect (OSTI)

    Lu, Jun; Jung, Hun-Ji; Lau, Kah Chun; Zhang, Zhengcheng; Schlueter, John A.; Du, Peng; Assary, Rajeev S.; Greeley, Jeffrey P.; Ferguson, Glen A.; Wang, Hsien-Hau; Hassoun, Jusef; Iddir, Hakim; Zhou, Jigang; Zuin, Lucia; Hu, Yongfeng; Sun, Yang-Kook; Scrosati, Bruno; Curtiss, Larry A.; Amine, Khalil

    2013-05-13T23:59:59.000Z

    Nonaqueous lithium–oxygen batteries have a much superior theoretical gravimetric energy density compared to conventional lithium-ion batteries, and thus could render long-range electric vehicles a reality. A molecular-level understanding of the reversible formation of lithium peroxide in these batteries, the properties of major/minor discharge products, and the stability of the nonaqueous electrolytes is required to achieve successful lithium–oxygen batteries. We demonstrate that the major discharge product formed in the lithium–oxygen cell, lithium peroxide, exhibits a magnetic moment. These results are based on dc-magnetization measurements and a lithium– oxygen cell containing an ether-based electrolyte. The results are unexpected because bulk lithium peroxide has a significant band gap. Density functional calculations predict that superoxide- type surface oxygen groups with unpaired electrons exist on stoichiometric lithium peroxide crystalline surfaces and on nanoparticle surfaces; these computational results are consistent with the magnetic measurement of the discharged lithium peroxide product as well as EPR measurements on commercial lithium peroxide. The presence of superoxide-type surface oxygen groups with spin can play a role in the reversible formation and decomposition of lithium peroxide as well as the reversible formation and decomposition of electrolyte molecules.

  3. Heterogeneous lithium niobate photonics on silicon substrates

    E-Print Network [OSTI]

    Fathpour, Sasan

    Heterogeneous lithium niobate photonics on silicon substrates Payam Rabiei,1,* Jichi Ma,1 Saeed-confined lithium niobate photonic devices and circuits on silicon substrates is reported based on wafer bonding high- performance lithium niobate microring optical resonators and Mach- Zehnder optical modulators

  4. Anode materials for lithium-ion batteries

    DOE Patents [OSTI]

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

    2014-12-30T23:59:59.000Z

    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.

  5. Lithium metal oxide electrodes for lithium cells and batteries

    DOE Patents [OSTI]

    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

    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

  6. The Primordial Lithium Problem

    E-Print Network [OSTI]

    Brian D. Fields

    2012-03-15T23:59:59.000Z

    Big-bang nucleosynthesis (BBN) theory, together with the precise WMAP cosmic baryon density, makes tight predictions for the abundances of the lightest elements. Deuterium and 4He measurements agree well with expectations, but 7Li observations lie a factor 3-4 below the BBN+WMAP prediction. This 4-5\\sigma\\ mismatch constitutes the cosmic "lithium problem," with disparate solutions possible. (1) Astrophysical systematics in the observations could exist but are increasingly constrained. (2) Nuclear physics experiments provide a wealth of well-measured cross-section data, but 7Be destruction could be enhanced by unknown or poorly-measured resonances, such as 7Be + 3He -> 10C^* -> p + 9B. (3) Physics beyond the Standard Model can alter the 7Li abundance, though D and 4He must remain unperturbed; we discuss such scenarios, highlighting decaying Supersymmetric particles and time-varying fundamental constants. Present and planned experiments could reveal which (if any) of these is the solution to the problem.

  7. Spatial periphery of lithium isotopes

    SciTech Connect (OSTI)

    Galanina, L. I., E-mail: galan_lidiya@mail.ru; Zelenskaja, N. S. [Moscow State University, Skobeltsyn Institute of Nuclear Physics (Russian Federation)

    2013-12-15T23:59:59.000Z

    The spatial structure of lithium isotopes is studied with the aid of the charge-exchange and (t, p) reactions on lithium nuclei. It is shown that an excited isobaric-analog state of {sup 6}Li (0{sup +}, 3.56MeV) has a halo structure formed by a proton and a neutron, that, in the {sup 9}Li nucleus, there is virtually no neutron halo, and that {sup 11}Li is a Borromean nucleus formed by a {sup 9}Li core and a two-neutron halo manifesting itself in cigar-like and dineutron configurations.

  8. Liquid Lithium Experiments in CDX-U

    SciTech Connect (OSTI)

    R. Majeski; R. Doerner; R. Kaita; G. Antar; J. Timberlake; et al

    2000-11-15T23:59:59.000Z

    The initial results of experiments involving the use of liquid lithium as a plasma facing component in the Current Drive Experiment-Upgrade (CDX-U) are reported. Studies of the interaction of a steady-state plasma with liquid lithium in the Plasma Interaction with Surface and Components Experimental Simulator (PISCES-B) are also summarized. In CDX-U a solid or liquid lithium covered rail limiter was introduced as the primary limiting surface for spherical torus discharges. Deuterium recycling was observed to be reduced, but so far not eliminated, for glow discharge-cleaned lithium surfaces. Some lithium influx was observed during tokamak operation. The PISCES-B results indicate that the rates of plasma erosion of lithium can exceed predictions by an order of magnitude at elevated temperatures. Plans to extend the CDX-U experiments to large area liquid lithium toroidal belt limiters are also described.

  9. Solid solution lithium alloy cermet anodes

    DOE Patents [OSTI]

    Richardson, Thomas J.

    2013-07-09T23:59:59.000Z

    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.

  10. LITHIUM--1997 46.1 By Joyce A. Ober

    E-Print Network [OSTI]

    LITHIUM--1997 46.1 LITHIUM By Joyce A. Ober After decades as the world's leading producer of lithium and its compounds, the United States was surpassed in 1997 when Chile became the world's largest lithium carbonate producer. Both lithium carbonate operations at the Salar de Atacama produced during

  11. Passivation of Aluminum in Lithium-ion Battery Electrolytes with LiBOB

    E-Print Network [OSTI]

    Zhang, Xueyuan; Devine, Thomas M.

    2008-01-01T23:59:59.000Z

    Passivation of Aluminum in Lithium-ion Battery Electrolytesin commercially available lithium-ion battery electrolytes,

  12. Toward a Lithium-"Air" Battery: The Effect of CO2 on the Chemistry of a Lithium-Oxygen Cell

    E-Print Network [OSTI]

    Goddard III, William A.

    Toward a Lithium-"Air" Battery: The Effect of CO2 on the Chemistry of a Lithium-Oxygen Cell Hyung as a "lithium-air battery". Most studies of lithium-air batteries have focused on demonstrating battery operations in pure oxygen conditions; such a battery should technically be described as a "lithium- dioxygen

  13. Lithium Ephedrate-Mediated Addition of a Lithium Acetylide to a Ketone: Solution Structures and Relative Reactivities of Mixed

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Ephedrate-Mediated Addition of a Lithium Acetylide to a Ketone: Solution Structures-1301 ReceiVed April 30, 1997. ReVised Manuscript ReceiVed NoVember 26, 1997 Abstract: Addition of lithiumLi and 13C NMR spectroscopies reveal lithium cyclopropylacetylide in THF to be a dimer

  14. Anode material for lithium batteries

    DOE Patents [OSTI]

    Belharouak, Ilias (Bolingbrook, IL); Amine, Khalil (Downers Grove, IL)

    2008-06-24T23:59:59.000Z

    Primary and secondary Li-ion and lithium-metal based electrochemical cell system. The suppression of gas generation is achieved through the addition of an additive or additives to the electrolyte system of respective cell, or to the cell itself whether it be a liquid, a solid- or plastized polymer electrolyte system. The gas suppression additives are primarily based on unsaturated hydrocarbons.

  15. Lithium-loaded liquid scintillators

    DOE Patents [OSTI]

    Dai, Sheng (Knoxville, TN); Kesanli, Banu (Mersin, TR); Neal, John S. (Knoxville, TN)

    2012-05-15T23:59:59.000Z

    The invention is directed to a liquid scintillating composition containing (i) one or more non-polar organic solvents; (ii) (lithium-6)-containing nanoparticles having a size of up to 10 nm and surface-capped by hydrophobic molecules; and (iii) one or more fluorophores. The invention is also directed to a liquid scintillator containing the above composition.

  16. Anode material for lithium batteries

    DOE Patents [OSTI]

    Belharouak, Ilias (Westmont, IL); Amine, Khalil (Downers Grove, IL)

    2012-01-31T23:59:59.000Z

    Primary and secondary Li-ion and lithium-metal based electrochemical cell systems. The suppression of gas generation is achieved through the addition of an additive or additives to the electrolyte system of respective cell, or to the cell itself whether it be a liquid, a solid- or plasticized polymer electrolyte system. The gas suppression additives are primarily based on unsaturated hydrocarbons.

  17. Anode material for lithium batteries

    DOE Patents [OSTI]

    Belharouak, Ilias (Bolingbrook, IL); Amine, Khalil (Oak Brook, IL)

    2011-04-05T23:59:59.000Z

    Primary and secondary Li-ion and lithium-metal based electrochemical cell systems. The suppression of gas generation is achieved through the addition of an additive or additives to the electrolyte system of respective cell, or to the cell itself whether it be a liquid, a solid- or plasticized polymer electrolyte system. The gas suppression additives are primarily based on unsaturated hydrocarbons.

  18. Lithium adsorption on armchair graphene nanoribbons Dana Krepel, Oded Hod

    E-Print Network [OSTI]

    Hod, Oded

    Lithium adsorption on armchair graphene nanoribbons Dana Krepel, Oded Hod School of Chemistry e i n f o Available online 7 December 2010 Keywords: Density functional theory Lithium Graphene Armchair graphene nanoribbon Chemical adsorption Lithium adsorption on two dimensional graphene

  19. Coated Silicon Nanowires as Anodes in Lithium Ion Batteries

    E-Print Network [OSTI]

    Watts, David James

    2014-01-01T23:59:59.000Z

    for advanced lithium-ion batteries. J. Power Sources 174,for lithium rechargeable batteries. Angew. Chem. Int. Ed.anodes for lithium-ion batteries. J. Mater. Chem. A 1,

  20. Visualization of Charge Distribution in a Lithium Battery Electrode

    E-Print Network [OSTI]

    Liu, Jun

    2010-01-01T23:59:59.000Z

    Charge Distribution in a Lithium Battery Electrode Jun Liu,Modeling of a Lithium-Polymer Battery. J. Power SourcesBehavior of a Lithium-Polymer Battery. J. Power Sources

  1. Lithium Diisopropylamide: Oligomer Structures at Low Ligand Concentrations

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Diisopropylamide: Oligomer Structures at Low Ligand Concentrations Jennifer L. Rutherford-dimensional 6Li and 15N NMR spectroscopic studies of lithium diisopropylamide (LDA) solvated ligand concentrations are discussed. Introduction Spectroscopic studies of lithium amides at low ligand

  2. Ab initio screening of lithium diffusion rates in transition metal oxide cathodes for lithium ion batteries

    E-Print Network [OSTI]

    Moore, Charles J. (Charles Jacob)

    2012-01-01T23:59:59.000Z

    A screening metric for diffusion limitations in lithium ion battery cathodes is derived using transition state theory and common materials properties. The metric relies on net activation barrier for lithium diffusion. ...

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

    SciTech Connect (OSTI)

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

    2010-01-01T23:59:59.000Z

    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.

  4. designer phase transitions in lithium-based spinels

    SciTech Connect (OSTI)

    Wouter Montfrooij

    2011-09-12T23:59:59.000Z

    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.

  5. ENDOR study of Cr3 centers substituting for lithium in lithium niobate

    E-Print Network [OSTI]

    Malovichko, Galina

    ENDOR study of Cr3¿ centers substituting for lithium in lithium niobate G. Malovichko,1, * V centers in lithium niobate crystals were investigated with the help of electron nuclear double resonance and the parameters of hyperfine and quadrupole interactions were determined. It is found that Cr3 substitutes for Li

  6. Lithium metal oxide electrodes for lithium cells and batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

    2006-11-14T23:59:59.000Z

    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 xLiMO2.(1-x)Li2M'O3 in which 0

  7. Lithium Metal Oxide Electrodes For Lithium Cells And Batteries

    DOE Patents [OSTI]

    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

    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

  8. Lithium metal oxide electrodes for lithium cells and batteries

    DOE Patents [OSTI]

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

    2008-12-23T23:59:59.000Z

    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

  9. Fact Sheet: Lithium-Ion Batteries for Stationary Energy Storage...

    Energy Savers [EERE]

    Fact Sheet: Lithium-Ion Batteries for Stationary Energy Storage (October 2012) Fact Sheet: Lithium-Ion Batteries for Stationary Energy Storage (October 2012) DOE's Energy Storage...

  10. 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...

  11. Development of Polymer Electrolytes for Advanced Lithium Batteries...

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

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

  12. Development of High Energy Lithium Batteries for Electric Vehicles...

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

    Lithium Batteries for Electric Vehicles Development of High Energy Lithium Batteries for Electric Vehicles 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program...

  13. Electrolyte additive for lithium rechargeable organic electrolyte battery

    DOE Patents [OSTI]

    Behl, Wishvender K. (Ocean, NJ); Chin, Der-Tau (Winthrop, NY)

    1989-01-01T23:59:59.000Z

    A large excess of lithium iodide in solution is used as an electrolyte adive to provide overcharge protection for a lithium rechargeable organic electrolyte battery.

  14. Electrolyte additive for lithium rechargeable organic electrolyte battery

    DOE Patents [OSTI]

    Behl, Wishvender K.; Chin, Der-Tau

    1989-02-07T23:59:59.000Z

    A large excess of lithium iodide in solution is used as an electrolyte adive to provide overcharge protection for a lithium rechargeable organic electrolyte battery.

  15. Diagnostic Studies on Lithium Battery Cells and Cell Components...

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

    Studies on Lithium Battery Cells and Cell Components Diagnostic Studies on Lithium Battery Cells and Cell Components 2012 DOE Hydrogen and Fuel Cells Program and Vehicle...

  16. Silicon sponge improves lithium-ion battery performance | EMSL

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

    sponge improves lithium-ion battery performance Silicon sponge improves lithium-ion battery performance Increasing battery's storage capacity could allow devices to run...

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

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

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

  18. Thermodynamic Investigations of Lithium- and Manganese-Rich Transition...

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

    Thermodynamic Investigations of Lithium- and Manganese-Rich Transition Metal Oxides Thermodynamic Investigations of Lithium- and Manganese-Rich Transition Metal Oxides 2013 DOE...

  19. 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...

  20. 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)...

  1. ALS Technique Gives Novel View of Lithium Battery Dendrite Growth

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

    ALS Technique Gives Novel View of Lithium Battery Dendrite Growth Print Lithium-ion batteries, popular in today's electronic devices and electric vehicles, could gain significant...

  2. 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...

  3. EV Everywhere Batteries Workshop - Next Generation Lithium Ion...

    Energy Savers [EERE]

    Next Generation Lithium Ion Batteries Breakout Session Report EV Everywhere Batteries Workshop - Next Generation Lithium Ion Batteries Breakout Session Report Breakout session...

  4. Investigations of Graphite Current Collectors and Metallic Lithium...

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

    Graphite Current Collectors and Metallic Lithium Anodes Investigations of Graphite Current Collectors and Metallic Lithium Anodes Presentation from the U.S. DOE Office of Vehicle...

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

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

    via Self-Healing Electrostatic Shield Mechanism . Dendrite-Free Lithium Deposition via Self-Healing Electrostatic Shield Mechanism . Abstract: Lithium metal batteries are called...

  6. Molecular Structure and Stability of Dissolved Lithium Polysulfide...

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

    Stability of Dissolved Lithium Polysulfide Species. Molecular Structure and Stability of Dissolved Lithium Polysulfide Species. Abstract: Ability to predict the solubility and...

  7. Designing Silicon Nanostructures for High Energy Lithium Ion...

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

    Designing Silicon Nanostructures for High Energy Lithium Ion Battery Anodes Designing Silicon Nanostructures for High Energy Lithium Ion Battery Anodes 2012 DOE Hydrogen and Fuel...

  8. 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...

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

    Energy Savers [EERE]

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

  10. EV Everywhere Batteries Workshop - Beyond Lithium Ion Breakout...

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

    Beyond Lithium Ion Breakout Session Report EV Everywhere Batteries Workshop - Beyond Lithium Ion Breakout Session Report Breakout session presentation for the EV Everywhere Grand...

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

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

    Processing Cost Barriers of High-Performance Lithium-Ion Battery Electrodes Overcoming Processing Cost Barriers of High-Performance Lithium-Ion Battery Electrodes 2012 DOE Hydrogen...

  12. Layered Electrodes for Lithium Cells and Batteries | Argonne...

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

    Layered Electrodes for Lithium Cells and Batteries Technology available for licensing: Layered lithium metal oxide compounds for ultra-high-capacity, rechargeable cathodes Lowers...

  13. Examining Hysteresis in Lithium- and Manganese-Rich Composite...

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

    Hysteresis in Lithium- and Manganese-Rich Composite Cathode Materials Examining Hysteresis in Lithium- and Manganese-Rich Composite Cathode Materials 2013 DOE Hydrogen and Fuel...

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

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

    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...

  15. 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...

  16. 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...

  17. 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...

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

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

    Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials Addressing the Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials 2012 DOE Hydrogen and...

  19. Electrode Structures and Surfaces for Lithium Batteries | Argonne...

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

    Structures and Surfaces for Lithium Batteries Technology available for licensing: Lithium-metal-oxide electrode materials with modified surfaces to protect the materials from...

  20. Optimization of mesoporous carbon structures for lithium&ndash...

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

    mesoporous carbon structures for lithium–sulfur battery applications. Optimization of mesoporous carbon structures for lithium–sulfur battery applications. Abstract:...

  1. Electrode materials and lithium battery systems

    DOE Patents [OSTI]

    Amine, Khalil (Downers Grove, IL); Belharouak, Ilias (Westmont, IL); Liu, Jun (Naperville, IL)

    2011-06-28T23:59:59.000Z

    A material comprising a lithium titanate comprising a plurality of primary particles and secondary particles, wherein the average primary particle size is about 1 nm to about 500 nm and the average secondary particle size is about 1 .mu.m to about 4 .mu.m. In some embodiments the lithium titanate is carbon-coated. Also provided are methods of preparing lithium titanates, and devices using such materials.

  2. Ternary compound electrode for lithium cells

    DOE Patents [OSTI]

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

    1980-07-30T23:59:59.000Z

    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.

  3. Ternary compound electrode for lithium cells

    DOE Patents [OSTI]

    Raistrick, Ian D. (Menlo Park, CA); Godshall, Ned A. (Stanford, CA); Huggins, Robert A. (Stanford, CA)

    1982-01-01T23:59:59.000Z

    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.degree.-500.degree. 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.

  4. Lithium Metal Anodes for Rechargeable Batteries

    SciTech Connect (OSTI)

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

    2014-02-28T23:59:59.000Z

    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.

  5. Anodes for rechargeable lithium batteries - Energy Innovation...

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

    Stories News Events Find More Like This Return to Search Anodes for rechargeable lithium batteries United States Patent Patent Number: 6,528,208 Issued: March 4, 2003...

  6. ORNL microscopy directly images problematic lithium dendrites...

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

    865.574.7308 ORNL microscopy directly images problematic lithium dendrites in batteries ORNL electron microscopy captured the first real-time nanoscale images of the nucleation and...

  7. Lithium in LMC carbon stars

    E-Print Network [OSTI]

    D. Hatzidimitriou; D. H. Morgan; R. D. Cannon; B. F. W. Croke

    2003-04-16T23:59:59.000Z

    Nineteen carbon stars that show lithium enrichment in their atmospheres have been discovered among a sample of 674 carbon stars in the Large Magellanic Cloud. Six of the Li-rich carbon stars are of J-type, i.e. with strong 13C isotopic features. No super-Li-rich carbon stars were found. The incidence of lithium enrichment among carbon stars in the LMC is much rarer than in the Galaxy, and about five times more frequent among J-type than among N-type carbon stars. The bolometric magnitudes of the Li-rich carbon stars range between -3.3 and -5.7. Existing models of Li-enrichment via the hot bottom burning process fail to account for all of the observed properties of the Li-enriched stars studied here.

  8. Spatial Distribution Of Cerium Valence In Model Planar Pd/Ce0...

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

    Distribution Of Cerium Valence In Model Planar PdCe0.7Zr0.3O2 Catalysts. Spatial Distribution Of Cerium Valence In Model Planar PdCe0.7Zr0.3O2 Catalysts. Abstract: The spatial...

  9. Emotional Valence and the Free-Energy Principle Mateus Joffily1,2

    E-Print Network [OSTI]

    Boyer, Edmond

    Emotional Valence and the Free-Energy Principle Mateus Joffily1,2 *, Giorgio Coricelli1,2,3 1 of Southern California, Los Angeles, California, United States of America Abstract The free-energy principle a definition of emotional valence in terms of the negative rate of change of free-energy over time

  10. I-Space: The Effects of Emotional Valence and Source of Music on Interpersonal Distance

    E-Print Network [OSTI]

    Sheldon, Nathan D.

    I-Space: The Effects of Emotional Valence and Source of Music on Interpersonal Distance Ana personal space, that is, the emotionally-tinged zone around the human body that people feel is ``their space''. We evaluated the effects of emotional valence (positive versus negative) and source (external

  11. A lithium oxygen secondary battery

    SciTech Connect (OSTI)

    Semkow, K.W.; Sammells, A.F.

    1987-08-01T23:59:59.000Z

    In principle the lithium-oxygen couple should provide one of the highest energy densities yet investigated for advanced battery systems. The problem to this time has been one of identifying strategies for achieving high electrochemical reversibilities at each electrode under conditions where one might anticipate to also achieve long materials lifetimes. This has been addressed in recent work by us via the application of stabilized zirconia oxygen vacancy conducting solid electrolytes, for the effective separation of respective half-cell reactions.

  12. Solid polymer electrolyte lithium batteries

    DOE Patents [OSTI]

    Alamgir, M.; Abraham, K.M.

    1993-10-12T23:59:59.000Z

    This invention pertains to Lithium batteries using Li ion (Li[sup +]) conductive solid polymer electrolytes composed of solvates of Li salts immobilized in a solid organic polymer matrix. In particular, this invention relates to Li batteries using solid polymer electrolytes derived by immobilizing solvates formed between a Li salt and an aprotic organic solvent (or mixture of such solvents) in poly(vinyl chloride). 3 figures.

  13. Solid polymer electrolyte lithium batteries

    DOE Patents [OSTI]

    Alamgir, Mohamed (Dedham, MA); Abraham, Kuzhikalail M. (Needham, MA)

    1993-01-01T23:59:59.000Z

    This invention pertains to Lithium batteries using Li ion (Li.sup.+) conductive solid polymer electrolytes composed of solvates of Li salts immobilized in a solid organic polymer matrix. In particular, this invention relates to Li batteries using solid polymer electrolytes derived by immobilizing solvates formed between a Li salt and an aprotic organic solvent (or mixture of such solvents) in poly(vinyl chloride).

  14. Electrolytes for lithium ion batteries

    DOE Patents [OSTI]

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

    2014-08-05T23:59:59.000Z

    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.

  15. max kwh | OpenEI Community

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are being directedAnnualProperty Edit withTianlinPapersWindey Wind Home Rmckeel'slinked open data Homemaps

  16. KWhOURS | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are8COaBulkTransmissionSitingProcess.pdfGetecGtelInteriasIowa: Energy ResourcesKACO Geraetetechnik GmbHKLDKSLKWhOURS

  17. OpenEI Community - max kwh

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are beingZealand Jump to: navigation, searchOfRoseConcernsCompany Oil and GasOff<div/0 en The

  18. Measurement-Based Quantum Computing with Valence-Bond-Solids

    E-Print Network [OSTI]

    Leong Chuan Kwek; Zhaohui Wei; Bei Zeng

    2011-11-22T23:59:59.000Z

    Measurement-based quantum computing (MBQC) is a model of quantum computing that proceeds by sequential measurements of individual spins in an entangled resource state. However, it remains a challenge to produce efficiently such resource states. Would it be possible to generate these states by simply cooling a quantum many-body system to its ground state? Cluster states, the canonical resource states for MBQC, do not occur naturally as unique ground states of physical systems. This inherent hurdle has led to a significant effort to identify alternative resource states that appear as ground states in spin lattices. Recently, some interesting candidates have been identified with various valence-bond-solid (VBS) states. In this review, we provide a pedagogical introduction to recent progress regarding MBQC with VBS states as possible resource states. This study has led to an interesting interdisciplinary research area at the interface of quantum information science and condensed matter physics.

  19. Measurement-Based Quantum Computing with Valence-Bond-Solids

    E-Print Network [OSTI]

    Kwek, Leong Chuan; Zeng, Bei

    2011-01-01T23:59:59.000Z

    Measurement-based quantum computing (MBQC) is a model of quantum computing that proceeds by sequential measurements of individual spins in an entangled resource state. However, it remains a challenge to produce efficiently such resource states. Would it be possible to generate these states by simply cooling a quantum many-body system to its ground state? Cluster states, the canonical resource states for MBQC, do not occur naturally as unique ground states of physical systems. This inherent hurdle has led to a significant effort to identify alternative resource states that appear as ground states in spin lattices. Recently, some interesting candidates have been identified with various valence-bond-solid (VBS) states. In this review, we provide a pedagogical introduction to recent progress regarding MBQC with VBS states as possible resource states. This study has led to an interesting interdisciplinary research area at the interface of quantum information science and condensed matter physics.

  20. Nature of the Frequency Shift of Hydrogen Valence Vibrations

    E-Print Network [OSTI]

    Zhyganiuk, I V

    2015-01-01T23:59:59.000Z

    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.

  1. XPS analysis of lithium surface and modification of surface state for uniform deposition of lithium

    SciTech Connect (OSTI)

    Kanamura, K.; Shiraishi, S.; Takehara, Z. [Kyoto Univ. (Japan)

    1995-12-31T23:59:59.000Z

    The surface modification of lithium deposited at various current densities in propylene carbonate containing 1.0 ml dm{sup {minus}3} LiClO{sub 4} was performed by addition of various amounts of HF into the electrolyte, in order to investigate the effect of the HF addition on the surface reaction of lithium. XPS and SEM analyses showed that the surface state of lithium was influenced by the concentration of HF and the electrodeposition current. These two parameters are related to the chemical reaction rate of the lithium surface with HF and the electrodeposition rate of lithium, respectively. The surface modification was highly effective in suppressing lithium dendrite formation when the chemical reaction rate with HF was greater than the electrochemical deposition rate of lithium.

  2. Nanoscale Imaging of Lithium Ion Distribution During In Situ Operation of Battery Electrode and Electrolyte

    E-Print Network [OSTI]

    Holtz, Megan E; Gunceler, Deniz; Gao, Jie; Sundararaman, Ravishankar; Schwarz, Kathleen A; Arias, Tomás A; Abruña, Héctor D; Muller, David A

    2013-01-01T23:59:59.000Z

    A major challenge in the development of new battery materials is understanding their fundamental mechanisms of operation and degradation. Their microscopically inhomogeneous nature calls for characterization tools that provide operando and localized information from individual grains and particles. Here we describe an approach that images the nanoscale distribution of ions during electrochemical charging of a battery in a transmission electron microscope liquid flow cell. We use valence energy-loss spectroscopy to track both solvated and intercalated ions, with electronic structure fingerprints of the solvated ions identified using an ab initio non-linear response theory. Equipped with the new electrochemical cell holder, nanoscale spectroscopy and theory, we have been able to determine the lithiation state of a LiFePO4 electrode and surrounding aqueous electrolyte in real time with nanoscale resolution during electrochemical charge and discharge. We follow lithium transfer between electrode and electrolyte a...

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

    SciTech Connect (OSTI)

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

    2014-05-15T23:59:59.000Z

    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.

  4. Lithium electric dipole polarizability M. Puchalski

    E-Print Network [OSTI]

    Pachucki, Krzysztof

    Lithium electric dipole polarizability M. Puchalski Faculty of Chemistry, Adam Mickiewicz, 00-681 Warsaw, Poland The electric dipole polarizability of the lithium atom in the ground state phenomena, such as van der Waals interactions in ultra-cold collisions [1­3] and Bose- Einstein condensation

  5. Jeff Chamberlain on Lithium-air batteries

    ScienceCinema (OSTI)

    Chamberlain, Jeff

    2013-04-19T23:59:59.000Z

    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

  6. Michael Thackeray on Lithium-air Batteries

    ScienceCinema (OSTI)

    Thackeray, Michael

    2013-04-19T23:59:59.000Z

    Michael Thackeray, Distinguished Fellow 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

  7. Bimetallic Cathode Materials for Lithium Based Batteries

    E-Print Network [OSTI]

    Bimetallic Cathode Materials for Lithium Based Batteries Frontiers in Materials Science Seminar / Chemistryg g g g g y University at Buffalo ­ The State University of New York (SUNY) Abstract Batteries for implantable cardiac defibrillators (ICDs) are based on the Lithium/Silver vanadium oxide (SVO, Ag2V4O11

  8. Lithium-Assisted Electrochemical Welding in Silicon Nanowire Battery Electrodes

    E-Print Network [OSTI]

    Rubloff, Gary W.

    Lithium-Assisted Electrochemical Welding in Silicon Nanowire Battery Electrodes Khim Karki, Eric-healing, interfacial lithium diffusivity, in situ TEM, lithium-ion battery Silicon is an auspicious candidate to replace today's widely utilized graphitic anodes in lithium ion batteries because its specific energy

  9. Impact of Lithium Availability on Vehicle Electrification (Presentation)

    SciTech Connect (OSTI)

    Neubauer, J.

    2011-07-01T23:59:59.000Z

    This presentation discusses the relationship between electric drive vehicles and the availability of lithium.

  10. Intense Lithium Streams in Tokamaks 1 Leonid E. Zakharov,

    E-Print Network [OSTI]

    Zakharov, Leonid E.

    Intense Lithium Streams in Tokamaks 1 Leonid E. Zakharov, Princeton University, Princeton Plasma. Temperature of the streams. 2. Lithium jets. 3. Injection into vacuum chamber. 4. Propulsion inside the vacuum chamber. 5. Stability of the lithium streams. 6. Expulsion of the lithium. 7. Summary. PRINCETON PLASMA

  11. Solvated electron lithium electrode for high energy density battery

    SciTech Connect (OSTI)

    Sammels, A.F.

    1987-08-04T23:59:59.000Z

    A solvated electron lithium negative electrode is described containing: containment means holding a solution of lithium dissolved in liquid ammonia to form a solvated electron solution, the solvated electron solution contacting a lithium intercalating membrane and providing lithium to the intercalating membrane during discharge and accepting it from the intercalating membrane during charge.

  12. Performance Characteristics of Lithium-ion Batteries of Various Chemistries for Plug-in Hybrid Vehicles

    E-Print Network [OSTI]

    Burke, Andrew; Miller, Marshall

    2009-01-01T23:59:59.000Z

    Characteristics of Lithium-ion Batteries of Variousare presented for lithium-ion cells and modules utilizingAdvisor utilizing lithium-ion batteries of the different

  13. Performance, Charging, and Second-use Considerations for Lithium Batteries for Plug-in Electric Vehicles

    E-Print Network [OSTI]

    Burke, Andrew

    2009-01-01T23:59:59.000Z

    Miller, M. , Emerging Lithium-ion Battery Technologies forCharacteristics of Lithium-ion Batteries of Variousand Simulation Results with Lithium-ion Batteries, paper

  14. Characterization of high-power lithium-ion cells-performance and diagnostic analysis

    E-Print Network [OSTI]

    2003-01-01T23:59:59.000Z

    by an arrow. Key words: Lithium ion battery, diagnostics,Development Program for Lithium-Ion Batteries: Handbook ofTechnology Development For Lithium- Ion Batteries: Gen 2

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

    E-Print Network [OSTI]

    Lin, Feng

    2014-01-01T23:59:59.000Z

    O 2 Cathode Material in Lithium Ion Batteries. Adv. Energysolvent decomposition in lithium ion batteries: first-Cathode Materials for Lithium-Ion Batteries. Adv. Funct.

  16. Characterization of an Electroactive Polymer for Overcharge Protection in Secondary Lithium Batteries

    E-Print Network [OSTI]

    Chen, Guoying; Thomas-Alyea, Karen E.; Newman, John; Richardson, Thomas J.

    2005-01-01T23:59:59.000Z

    in Secondary Lithium Batteries Guoying Chen, Karen E.protection agents in lithium batteries is relatively new,rechargeable lithium batteries with a variety of different

  17. Performance Characteristics of Lithium-ion Batteries of Various Chemistries for Plug-in Hybrid Vehicles

    E-Print Network [OSTI]

    Burke, Andrew; Miller, Marshall

    2009-01-01T23:59:59.000Z

    Whether any of the lithium battery chemistries can meetgeneral the higher cost lithium battery chemistries have thecosts for various lithium battery chemistries Electrode

  18. Synthesis and Characterization of Simultaneous Electronic and Ionic Conducting Block Copolymers for Lithium Battery Electrodes

    E-Print Network [OSTI]

    Patel, Shrayesh

    2013-01-01T23:59:59.000Z

    Copolymer: Application in Lithium Battery Electrodes. Angew.Schematic of the Proposed lithium battery electrode with aBlock Copolymers for Lithium Battery Electrodes By Shrayesh

  19. Structural Integration of Silicon Solar Cells and Lithium-ion Batteries Using Printed Electronics

    E-Print Network [OSTI]

    Kang, Jin Sung

    2012-01-01T23:59:59.000Z

    the solid state thin-film lithium battery S8-ES ( Front EdgeLithium-Ion Polymer Battery ..Mikhaylik, "Lithium-Sulfur Secondary Battery: Chemistry and

  20. MATHEMATICAL MODELING OF THE LITHIUM-ALUMINUM, IRON SULFIDE BATTERY. I. GALVONOSTATIC DISCHARGE BEHAVIOR

    E-Print Network [OSTI]

    Pollard, Richard

    2012-01-01T23:59:59.000Z

    composition profiles in lithium/sulfur battery analogues hasTHE LITHIUM-ALUMINUM, IRON SULFIDE BATTERY. I. GALVONOSTATICthe Lithium-Aluminum, Iron Sulfide Battery I. Galvanostatic

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

    E-Print Network [OSTI]

    Wilcox, James D.

    2010-01-01T23:59:59.000Z

    the lithium- transition metal electrostatic interaction. Thecation electrostatic interactions. 1 Lithium ions occupy theinteractions or by inhibiting the complete removal of lithium

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

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

    Dendrite-Free Lithium Deposition with Self-Aligned Nanorod Structure. Dendrite-Free Lithium Deposition with Self-Aligned Nanorod Structure. Abstract: Suppressing lithium (Li)...

  3. Design Principles for the Use of Electroactive Polymers for Overcharge Protection of Lithium-Ion Batteries

    E-Print Network [OSTI]

    Thomas-Alyea, Karen E.; Newman, John; Chen, Guoying; Richardson, Thomas J.

    2005-01-01T23:59:59.000Z

    Modeling of Lithium Batteries. Kluwer Academic Publishers,of interest for lithium batteries. Therefore, we can use y =and J. Newman, Advances in Lithium-Ion Batteries, ch.

  4. Studies of ionic liquids in lithium-ion battery test systems

    E-Print Network [OSTI]

    Salminen, Justin; Prausnitz, John M.; Newman, John

    2006-01-01T23:59:59.000Z

    are not useful for lithium batteries. We are therefore nowapplications using lithium batteries, we must be sure thattemperature range. For lithium batteries in hybrid vehicles,

  5. Characterization of an Electroactive Polymer for Overcharge Protection in Secondary Lithium Batteries

    E-Print Network [OSTI]

    Chen, Guoying; Thomas-Alyea, Karen E.; Newman, John; Richardson, Thomas J.

    2005-01-01T23:59:59.000Z

    Protection in Secondary Lithium Batteries Guoying Chen,protection agents in lithium batteries is relatively new,in rechargeable lithium batteries with a variety of

  6. Performance Characteristics of Lithium-ion Batteries of Various Chemistries for Plug-in Hybrid Vehicles

    E-Print Network [OSTI]

    Burke, Andrew; Miller, Marshall

    2009-01-01T23:59:59.000Z

    the manufacture of lithium batteries (References 2 and 3).Characteristics of Lithium-ion Batteries of VariousAdvisor utilizing lithium-ion batteries of the different

  7. Synthesis and Characterization of Simultaneous Electronic and Ionic Conducting Block Copolymers for Lithium Battery Electrodes

    E-Print Network [OSTI]

    Patel, Shrayesh

    2013-01-01T23:59:59.000Z

    Protection in Secondary Lithium Batteries. Electrochim. ActaFacing Rechargeable Lithium Batteries. Nature 2001, 414,for Rechargeable Lithium Batteries Using Electroactive

  8. A Failure and Structural Analysis of Block Copolymer Electrolytes for Rechargeable Lithium Metal Batteries

    E-Print Network [OSTI]

    Stone, Gregory Michael

    2012-01-01T23:59:59.000Z

    for Rechargeable Lithium Metal Batteries By Gregory Michaelfor Rechargeable Lithium Metal Batteries by Gregory Michaelin rechargeable lithium metal batteries. The block copolymer

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

    E-Print Network [OSTI]

    Lin, Feng

    2014-01-01T23:59:59.000Z

    Layered Oxides for Lithium Batteries. Nano Lett. 13, 3857–O 2 Cathode Material in Lithium Ion Batteries. Adv. Energydecomposition in lithium ion batteries: first-principles

  10. Layered manganese oxide intergrowth electrodes for rechargeable lithium batteries: Part 1-substitution with Co or Ni

    E-Print Network [OSTI]

    Dolle, Mickael; Patoux, Sebastien; Doeff, Marca M.

    2004-01-01T23:59:59.000Z

    Cathode Materials for Lithium Batteries, 2003, Massachusettsfor Rechargeable Lithium Batteries: Part 1-Substitution withelectrode materials for lithium batteries because of their

  11. Performance, Charging, and Second-use Considerations for Lithium Batteries for Plug-in Electric Vehicles

    E-Print Network [OSTI]

    Burke, Andrew

    2009-01-01T23:59:59.000Z

    Considerations for Lithium Batteries for Plug-in Electricfast charging of the lithium batteries should be possiblefast charging of the lithium batteries will be is possible

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

    E-Print Network [OSTI]

    Chen, Guoying

    2010-01-01T23:59:59.000Z

    Protection for 4 V Lithium Batteries at High Rates and LowIntroduction Rechargeable lithium batteries are known forfor rechargeable lithium batteries. When impregnated into a

  13. Cu2Sb thin film electrodes prepared by pulsed laser deposition f or lithium batteries

    E-Print Network [OSTI]

    Song, Seung-Wan; Reade, Ronald P.; Cairns, Elton J.; Vaughey, Jack T.; Thackeray, Michael M.; Striebel, Kathryn A.

    2003-01-01T23:59:59.000Z

    Laser Deposition for Lithium Batteries Seung-Wan Song, a, *in rechargeable lithium batteries. Introduction Sb-in rechargeable lithium batteries. Two advantages of

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

    E-Print Network [OSTI]

    Schmidt, Volker

    Anodes in Lithium-Ion Cells Yvonne Krämer*[a] , Claudia Birkenmaier[b] , Julian Feinauer[a,c] , Andreas lithium-ion cells is presented. Graphite anode samples were extracted from pristine and differently aged lithium-ion cells. The samples present a variety of anodes with various states of lithium plating

  15. J. Am. Chem. SOC.1991, 113,9575-9585 9575 Mixed Aggregation of Lithium Enolates and Lithium Halides

    E-Print Network [OSTI]

    Collum, David B.

    J. Am. Chem. SOC.1991, 113,9575-9585 9575 Mixed Aggregation of Lithium Enolates and Lithium Halides with Lithium 2,2,6,6-Tetramethylpiperidide(LiTMP) Patricia L. Hall, James H. Gilchrist, Aidan T. Harrison]-lithiumdi-tert-butylamide and conformationally locked [6Li]-lithium2,2,4,6,6-pentamethylpiperidide shed further light

  16. Optimization of Acetylene Black Conductive Additive and Polyvinylidene Difluoride Composition for High Power Rechargeable Lithium-Ion Cells

    E-Print Network [OSTI]

    Liu, G.; Zheng, H.; Battaglia, V.S.; Simens, A.S.; Minor, A.M.; Song, X.

    2007-01-01T23:59:59.000Z

    Lithium-Ion Battery; Electrode Design; Polymer Composite. Introduction Lithium-ion rechargeable batteries

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

    E-Print Network [OSTI]

    Wilcox, James D.

    2010-01-01T23:59:59.000Z

    Solid Solutions: Coupled Lithium-Ion and Electron Mobility.lithium batteries, II. Lithium ion rechargeable batteries.1/4)Ni(3/4)O(2) for lithium-ion batteries. Electrochimica

  18. Lithium Diisopropylamide-Mediated Ortholithiation and Anionic Fries Rearrangement of Aryl Carbamates: Role of

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Diisopropylamide-Mediated Ortholithiation and Anionic Fries Rearrangement of Aryl of the lithium diisopropylamide (LDA)-mediated anionic Fries rearrangements of aryl carbamates are described, an LDA-lithium phenolate mixed dimer, and homoaggregated lithium phenolates. The highly insoluble

  19. Lithium abundances in exoplanet-hosts stars

    E-Print Network [OSTI]

    M. Castro; S. Vauclair; O. Richard; N. C. Santos

    2008-03-20T23:59:59.000Z

    Exoplanet-host stars (EHS) are known to present surface chemical abundances different from those of stars without any detected planet (NEHS). EHS are, on the average, overmetallic compared to the Sun. The observations also show that, for cool stars, lithium is more depleted in EHS than in NEHS. The overmetallicity of EHS may be studied in the framework of two different scenarii. We have computed main sequence stellar models with various masses, metallicities and accretion rates. The results show different profiles for the lithium destruction according to the scenario. We compare these results to the spectroscopic observations of lithium.

  20. Finding Room for Improvement in Transition Metal Oxides Cathodes for Lithium-ion Batteries

    E-Print Network [OSTI]

    Kam, Kinson

    2012-01-01T23:59:59.000Z

    Metal Oxides Cathodes for Lithium-ion Batteries Kinson C.storage using rechargeable lithium-ion batteries has become

  1. Finding Room for Improvement in Transition Metal Oxides Cathodes for Lithium-ion Batteries

    E-Print Network [OSTI]

    Kam, Kinson

    2012-01-01T23:59:59.000Z

    Cathodes for Lithium-ion Batteries Kinson C. Kam and Marcarechargeable lithium-ion batteries has become an integral

  2. Passivation of Aluminum in Lithium-ion Battery Electrolytes with LiBOB

    E-Print Network [OSTI]

    Zhang, Xueyuan; Devine, Thomas M.

    2008-01-01T23:59:59.000Z

    of Aluminum in Lithium-ion Battery Electrolytes with LiBOBin commercially available lithium-ion battery electrolytes,

  3. Finding Room for Improvement in Transition Metal Oxides Cathodes for Lithium-ion Batteries

    E-Print Network [OSTI]

    Kam, Kinson

    2012-01-01T23:59:59.000Z

    Oxides Cathodes for Lithium-ion Batteries Kinson C. Kam andusing rechargeable lithium-ion batteries has become an

  4. Lithium-cation conductivity and crystal structure of lithium diphosphate

    SciTech Connect (OSTI)

    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

    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 300–1050 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) Å, b=5.2028(4) Å, c=13.3119(2) Å, ?=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.

  5. Solid State Thin Film Lithium Microbatteries

    E-Print Network [OSTI]

    Shi, Z.

    Solid state thin film lithium microbatteries fabricated by pulsed-laser deposition (PLD) are suggested. During deposition the following process parameters must be considered, which are laser energy and fluence, laser pulse ...

  6. Lithium Circuit Test Section Design and Fabrication

    SciTech Connect (OSTI)

    Godfroy, Thomas; Garber, Anne; Martin, James [NASA Marshall Space Flight Center, Nuclear Systems Engineering Analysis, Huntsville, Alabama 35812 (United States)

    2006-01-20T23:59:59.000Z

    The Early Flight Fission -- Test Facilities (EFF-TF) team has designed and built an actively pumped lithium flow circuit. Modifications were made to a circuit originally designed for NaK to enable the use of lithium that included application specific instrumentation and hardware. Component scale freeze/thaw tests were conducted to both gain experience with handling and behavior of lithium in solid and liquid form and to supply anchor data for a Generalized Fluid System Simulation Program (GFSSP) model that was modified to include the physics for freeze/thaw transitions. Void formation was investigated. The basic circuit components include: reactor segment, lithium to gas heat exchanger, electromagnetic (EM) liquid metal pump, load/drain reservoir, expansion reservoir, instrumentation, and trace heaters. This paper discusses the overall system design and build and the component testing findings.

  7. Hierarchically Structured Materials for Lithium Batteries. |...

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

    Lithium-ion battery (LIB) is one of the most promising power sources to be deployed in electric vehicles (EV), including solely battery powered vehicles, plug-in hybrid electric...

  8. NSTX Plasma Response to Lithium Coated Divertor

    SciTech Connect (OSTI)

    H.W. Kugel, M.G. Bell, J.P. Allain, R.E. Bell, S. Ding, S.P. Gerhardt, M.A. Jaworski, R. Kaita, J. Kallman, S.M. Kaye, B.P. LeBlanc, R. Maingi, R. Majeski, R. Maqueda, D.K. Mansfield, D. Mueller, R. Nygren, S.F. Paul, R. Raman, A.L. Roquemore, S.A. Sabbagh, H. Schneider, C.H. Skinner, V.A. Soukhanovskii, C.N. Taylor, J.R. Timberlak, W.R. Wampler, L.E. Zakharov, S.J. Zweben, and the NSTX Research Team

    2011-01-21T23:59:59.000Z

    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 Zeff 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.

  9. Layered electrodes for lithium cells and batteries

    DOE Patents [OSTI]

    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

    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.

  10. Lithium ion battery with improved safety

    DOE Patents [OSTI]

    Chen, Chun-hua; Hyung, Yoo Eup; Vissers, Donald R.; Amine, Khalil

    2006-04-11T23:59:59.000Z

    A lithium battery with improved safety that utilizes one or more additives in the battery electrolyte solution wherein a lithium salt is dissolved in an organic solvent, which may contain propylene, carbonate. For example, a blend of 2 wt % triphenyl phosphate (TPP), 1 wt % diphenyl monobutyl phosphate (DMP) and 2 wt % vinyl ethylene carbonate additives has been found to significantly enhance the safety and performance of Li-ion batteries using a LiPF6 salt in EC/DEC electrolyte solvent. The invention relates to both the use of individual additives and to blends of additives such as that shown in the above example at concentrations of 1 to 4-wt % in the lithium battery electrolyte. This invention relates to additives that suppress gas evolution in the cell, passivate graphite electrode and protect it from exfoliating in the presence of propylene carbonate solvents in the electrolyte, and retard flames in the lithium batteries.

  11. Side Reactions in Lithium-Ion Batteries

    E-Print Network [OSTI]

    Tang, Maureen Han-Mei

    2012-01-01T23:59:59.000Z

    Model for the Graphite Anode in Li-Ion Batteries. Journal ofgraphite Chapters 2-3 have developed a method using ferrocene to characterize the SEI in lithium- ion batteries.

  12. Lithium-Beryllium-Boron : Origin and Evolution

    E-Print Network [OSTI]

    Elisabeth Vangioni-Flam; Michel Casse; Jean Audouze

    1999-07-13T23:59:59.000Z

    The origin and evolution of Lithium-Beryllium-Boron is a crossing point between different astrophysical fields : optical and gamma spectroscopy, non thermal nucleosynthesis, Big Bang and stellar nucleosynthesis and finally galactic evolution. We describe the production and the evolution of Lithium-Beryllium-Boron from Big Bang up to now through the interaction of the Standard Galactic Cosmic Rays with the interstellar medium, supernova neutrino spallation and a low energy component related to supernova explosions in galactic superbubbles.

  13. Rechargeable lithium-ion cell

    DOE Patents [OSTI]

    Bechtold, Dieter (Bad Vilbel, DE); Bartke, Dietrich (Kelkheim, DE); Kramer, Peter (Konigstein, DE); Kretzschmar, Reiner (Kelkheim, DE); Vollbert, Jurgen (Hattersheim, DE)

    1999-01-01T23:59:59.000Z

    The invention relates to a rechargeable lithium-ion cell, a method for its manufacture, and its application. The cell is distinguished by the fact that it has a metallic housing (21) which is electrically insulated internally by two half shells (15), which cover electrode plates (8) and main output tabs (7) and are composed of a non-conductive material, where the metallic housing is electrically insulated externally by means of an insulation coating. The cell also has a bursting membrane (4) which, in its normal position, is located above the electrolyte level of the cell (1). In addition, the cell has a twisting protection (6) which extends over the entire surface of the cover (2) and provides centering and assembly functions for the electrode package, which comprises the electrode plates (8).

  14. Electrode for a lithium cell

    DOE Patents [OSTI]

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

    2008-10-14T23:59:59.000Z

    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.

  15. Predissociation dynamics of lithium iodide

    E-Print Network [OSTI]

    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

    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.

  16. Glass for sealing lithium cells

    DOE Patents [OSTI]

    Leedecke, C.J.

    1981-08-28T23:59:59.000Z

    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/.

  17. Deproto-metallation using mixed lithium-zinc and lithium-copper bases and computed CH acidity of 2-substituted quinolines

    E-Print Network [OSTI]

    Boyer, Edmond

    Deproto-metallation using mixed lithium-zinc and lithium-copper bases and computed CH acidity of 2 corresponding iodo derivatives or 2-chlorophenyl ketones using the lithium-zinc or the lithium using the lithium-zinc base. With 3-pyridyl, 2-furyl and 2-thienyl substituents, the reaction took place

  18. (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]

    , but growing through the recycling of lithium batteries. Import Sources (1994-97): Chile, 96%; and other, 4 lithium salts from battery recycling and lithium hydroxide monohydrate from former Department of Energy102 LITHIUM (Data in metric tons of contained lithium, unless otherwise noted) Domestic Production

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

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

    Initiative for Lithium-ion Battery Separator Celgard US Manufacturing Facilities Initiative for Lithium-ion Battery Separator FY 2012 Annual Progress Report for Energy Storage R&D...

  20. area liquid lithium: Topics by E-print Network

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

    liquid lithium plasma-facing surface will be used 11 Waste-Lithium-Liquid (WLL) Flow Battery for Stationary Energy Storage Applications Youngsik Kim* and Nina MahootcheianAsl...

  1. Design of novel lithium storage materials with a polyanionic framework

    E-Print Network [OSTI]

    Kim, Jae Chul, Ph. D. Massachusetts Institute of Technology

    2014-01-01T23:59:59.000Z

    Lithium ion batteries for large-scale applications demand a strict safety standard from a cathode material during operating cycles. Lithium manganese borate (LiMnBO?) that crystallizes into a hexagonal or monoclinic framework ...

  2. LITHIUM--2002 46.1 By Joyce A. Ober

    E-Print Network [OSTI]

    domestic producer of lithium carbonate from brine is Chemetall Foote's operation in Nevada. Nevada brines enriched in lithium chloride, which averaged about 300 parts per million (ppm) when Foote Mineral Co. (the

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

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

    California Geothermal Power Plant to Help Meet High Lithium Demand California Geothermal Power Plant to Help Meet High Lithium Demand September 20, 2012 - 1:15pm Addthis Ever...

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

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

    Geothermal Plant to Help Meet High Lithium Demand California: Geothermal Plant to Help Meet High Lithium Demand May 21, 2013 - 5:54pm Addthis Through funding provided by the...

  5. 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,...

  6. Novel Lithium Ion Anode Structures: Overview of New DOE BATT...

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

    Lithium Ion Anode Structures: Overview of New DOE BATT Anode Projects Novel Lithium Ion Anode Structures: Overview of New DOE BATT Anode Projects 2011 DOE Hydrogen and Fuel Cells...

  7. 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...

  8. 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...

  9. Interaction of Lithium Hydride and Ammonia Borane in THF . |...

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

    Lithium Hydride and Ammonia Borane in THF . Interaction of Lithium Hydride and Ammonia Borane in THF . Abstract: The two-step reaction between LiH and NH3BH3 in THF leads to the...

  10. Lithium-based inorganic-organic framework materials

    E-Print Network [OSTI]

    Yeung, Hamish Hei-Man

    2013-01-01T23:59:59.000Z

    This dissertation describes research into lithium-based inorganic-organic frameworks, which has led to an increased understanding of the structural diversity and properties of these materials. The crystal structures of 11 new forms of lithium...

  11. 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...

  12. aqueous lithium hydroxide: Topics by E-print Network

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

    Websites Summary: Prediction of the theoretical capacity of non-aqueous lithium-air batteries Peng Tan, Zhaohuan Wei of non-aqueous lithium-air batteries is predicted. Key...

  13. aqueous lithium bromide: Topics by E-print Network

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

    France Abstract In order to develop a LISICON separator for an aqueous lithium-air battery, a thin was coated with a lithium oxynitrured phosphorous (LiPON) thin film to...

  14. Electrochemical Isotope Effect and Lithium Isotope Separation Jay R. Black,

    E-Print Network [OSTI]

    Mcdonough, William F.

    results showing a large lithium isotope separation due to electrodeposition. The fractionation is tunable lithium were plated from solutions of 1 M LiClO4 in propylene carbonate (PC) on planar nickel electrodes

  15. Lithium-ion batteries having conformal solid electrolyte layers

    DOE Patents [OSTI]

    Kim, Gi-Heon; Jung, Yoon Seok

    2014-05-27T23:59:59.000Z

    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.

  16. Methods for making lithium vanadium oxide electrode materials

    DOE Patents [OSTI]

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

    2000-01-01T23:59:59.000Z

    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.

  17. Lithium based electrochemical cell systems having a degassing agent

    DOE Patents [OSTI]

    Hyung, Yoo-Eup (Naperville, IL); Vissers, Donald R. (Naperville, IL); Amine, Khalil (Downers Grove, IL)

    2012-05-01T23:59:59.000Z

    A lithium based electrochemical cell system includes a positive electrode; a negative electrode; an electrolyte; and a degassing agent.

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

    SciTech Connect (OSTI)

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

    2014-06-01T23:59:59.000Z

    Cerium and its technologically relevant compounds are examples of anomalous mixed valency, originating from two competing oxidation states—itinerant 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.

  19. 2008 Nature Publishing Group High-performance lithium battery

    E-Print Network [OSTI]

    Cui, Yi

    © 2008 Nature Publishing Group High-performance lithium battery anodes using silicon nanowires in lithium batteries have shown capacity fading and short battery lifetime due to pulverization and loss December 2007; doi:10.1038/nnano.2007.411 There is great interest in developing rechargeable lithium

  20. Author's personal copy Reactivity of lithium exposed graphite surface

    E-Print Network [OSTI]

    Harilal, S. S.

    on the surface [18]. Hence the effect of lithium on plasma­wall interactions is expected to dependAuthor's personal copy Reactivity of lithium exposed graphite surface S.S. Harilal a, *, J in fusion devices [1­5]. For example, wall conditioning with thin lithium layers gives rise to low hydrogen

  1. Lithium Isotope History of Cenozoic Seawater: Changes in Silicate Weathering

    E-Print Network [OSTI]

    Paytan, Adina

    Lithium Isotope History of Cenozoic Seawater: Changes in Silicate Weathering and Reverse Weathering 70 Ma · Overview of the Marine Lithium Cycle · Analytical Challenges · 68 Million Year Seawater Lithium Isotope Record (Forams) · Interpretation Standard: NIST L-SVEC Li (SRM 8545) #12;100 Ma Climate

  2. LITHIUM--2003 45.1 By Joyce A. Ober

    E-Print Network [OSTI]

    .S. operations. The single U.S. lithium carbonate producer, Chemetall Foote Corp. (a subsidiary of the German). Chemetall Foote produced lithium carbonate from brines near Silver Peak, NV. The company's other U for further processing. The only domestic producer of lithium carbonate from brine is Chemetall Foote

  3. Lithium-Mediated Benzene Adsorption on Graphene and Graphene Nanoribbons

    E-Print Network [OSTI]

    Hod, Oded

    Lithium-Mediated Benzene Adsorption on Graphene and Graphene Nanoribbons Dana Krepel and Oded Hod on lithium adsorption sites at the surface of graphene and nanoribbons thereof are investigated. The effects, bare lithium adsorption turns armchair graphene nanoribbons metallic and their zigzag counterparts half

  4. Lithium Diisopropylamide Solvated by Hexamethylphosphoramide: Substrate-Dependent

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Diisopropylamide Solvated by Hexamethylphosphoramide: Substrate-Dependent Mechanisms-1301 Received February 9, 2006; E-mail: dbc6@cornell.edu Abstract: Lithium diisopropylamide of lithium-ion solvation at a molecular level of resolution.5 Our interest in HMPA stems from studies

  5. Lithium Insertion In Silicon Nanowires: An ab Initio Study

    E-Print Network [OSTI]

    Cui, Yi

    Lithium Insertion In Silicon Nanowires: An ab Initio Study Qianfan Zhang, Wenxing Zhang, Wenhui Wan, and § School of Physics, Peking University, Beijing 100871, China ABSTRACT The ultrahigh specific lithium ion opportunities for energy storage. However, a systematic theoretical study on lithium insertion in SiNWs remains

  6. Lithium acetate transformation of yeast Maitreya Dunham August 2004

    E-Print Network [OSTI]

    Dunham, Maitreya

    Lithium acetate transformation of yeast Maitreya Dunham August 2004 Original protocol from Katja until the OD600 is around 0.7-0.8 (~7 hours). Spin down the cells. Resuspend in 5 ml lithium acetate mix. Spin. Resuspend in 0.5 ml lithium acetate mix. Transfer to an eppendorf tube. Incubate 60 minutes

  7. Lithium Diisopropylamide-Mediated Enolization: Catalysis by Hemilabile Ligands

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Diisopropylamide-Mediated Enolization: Catalysis by Hemilabile Ligands Antonio Ramirez of a lithium diisopropylamide (LDA)-mediated ester enolization. Hemilabile amino ether MeOCH2CH2NMe2, binding-based catalysis are thwarted by the occlusion of the catalyst on the lithium salt products and byproducts (eq 1

  8. 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

  9. Description: Lithium batteries are used daily in our work

    E-Print Network [OSTI]

    Description: Lithium batteries are used daily in our work activities from flashlights, cell phones containing one SureFire 3-volt non-rechargeable 123 lithium battery and one Interstate 3-volt non-rechargeable 123 lithium battery. A Garage Mechanic had the SureFire flashlight in his shirt pocket with the lens

  10. The Lithium-Ion Cell: Model, State Of Charge Estimation

    E-Print Network [OSTI]

    Schenato, Luca

    The Lithium-Ion Cell: Model, State Of Charge Estimation and Battery Management System Tutor degradation mechanisms of a Li-ion cell based on LiCoO2", Journal of Power Sources #12;Lithium ions and e and Y. Fuentes. Computer simulations of a lithium-ion polymer battery and implications for higher

  11. Liquid Lithium Wall Experiments in CDX-U R. Majeski,

    E-Print Network [OSTI]

    California at Los Angeles, University of

    Liquid Lithium Wall Experiments in CDX-U R. Kaita, a R. Majeski, a S. Luckhardt, b R. Doerner, b M ABSTRACT The concept of a flowing lithium first wall for a fusion reactor may lead to a significant advance is intensely heated and well diagnosed, and an extensive liquid lithium plasma-facing surface will be used

  12. Stabilization of tokamak plasma by lithium streams L. E. Zakharov,

    E-Print Network [OSTI]

    a stabilization mechanism independent of the plasma properties. 2. Interaction of lithium streams with externalStabilization of tokamak plasma by lithium streams L. E. Zakharov, Princeton Plasma Physics-boundary magnetohydrodynamic instabilities in tokamaks by liquid lithium streams driven by magnetic propulsion is formulated

  13. Stabilization of tokamak plasma by lithium streams L. E. Zakharov,

    E-Print Network [OSTI]

    Zakharov, Leonid E.

    a stabilization mechanism independent of the plasma properties. 2 Interaction of lithium streams with externalStabilization of tokamak plasma by lithium streams L. E. Zakharov, Princeton Plasma Physics-boundary magnetohydrodynamic instabilities in tokamaks by liquid lithium streams driven by magnetic propulsion is formulated

  14. High energy density lithium-oxygen secondary battery

    SciTech Connect (OSTI)

    Sammells, A.F.

    1989-02-07T23:59:59.000Z

    A high energy density lithium-oxygen secondary cell is described comprising a lithium-containing negative electrode; a lithium ion conducting molten salt electrolyte contacting the negative electrode; an oxygen ion conducting solid electrolyte contacting and containing the molten salt electrolyte; and an oxygen redox positive electrode contacting the oxygen ion conducting solid electrolyte.

  15. Microstructural Modeling and Design of Rechargeable Lithium-Ion Batteries

    E-Print Network [OSTI]

    García, R. Edwin

    Microstructural Modeling and Design of Rechargeable Lithium-Ion Batteries R. Edwin Garci´a,a, *,z microstructure. Experi- mental measurements are reproduced. Early models for lithium-ion batteries were developed Institute of Technology, Cambridge, Massachusetts 01239-4307, USA The properties of rechargeable lithium

  16. Mechanical Properties of Lithium-Ion Battery Separator Materials

    E-Print Network [OSTI]

    Petta, Jason

    -ion batteries like on the inside Anode Separator Cathode 500 nm 20 um20 um Anode: Graphite SeparatorMechanical Properties of Lithium-Ion Battery Separator Materials Patrick Sinko B.S. Materials and motivation ­ Why study lithium-ion batteries? ­ Lithium-ion battery fundamentals ­ Why study the mechanical

  17. Evaporated Lithium Surface Coatings in NSTX

    SciTech Connect (OSTI)

    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

    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.

  18. Cells containing solvated electron lithium negative electrodes

    SciTech Connect (OSTI)

    Uribe, F.A.; Semkow, K.W.; Sammells, A.F. (Eltron Research, Incorporated, Aurora, IL (US))

    1989-12-01T23:59:59.000Z

    Preliminary work performed on a novel solvated electron lithium negative electrode which may have application in either high energy density secondary or reserve battery systems is discussed. The lithium electrode investigated consisted of lithium initially dissolved in liquid ammonia to give a solvated electron solution. Containment of this liquid negative active material from direct contact with a liquid nonaqueous electrolyte present in the cell positive electrode compartment was addressed via the use of a lithium intercalated electronically conducting ceramic membrane of the general composition Li{sub x}WO{sub 2}(0.1{lt}x{lt} 1.0). Secondary electrochemical cells having the general configuration Li,NH{sub 3}/Li{sub x}WO{sub 2}NAE/TiS{sub 2} using nonaqueous electrolytes (NAE) based upon both propylene carbonate and 2Me-THF. Depending upon initial lithium activity in the negative electrode compartments the cell possessed an initial open-circuit potential (OCP 3.44V). Both cells, which were operated at ambient pressure (low temperature) and ambient temperature (high pressure) showed evidence for electrochemical reversibility.

  19. Optimization of Lithium Iron Phosphate Battery Charging and Performance

    E-Print Network [OSTI]

    Misic, Aleksandar

    The goal of this project is to efficiently and safely charge a 5kWh battery pack in 15 minutes. Since the project is still in progress, this report describes experiments on a 56Wh battery. Experiments were performed to ...

  20. 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)

    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

    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.

  1. A Study of the Valence Shell Photoelectron and Photoabsorption Spectra of CF?SF?

    SciTech Connect (OSTI)

    Holland, David M. P.; Shaw, David; Walker, I.C.; McEwen, I. C.; Apra, Edoardo; Guest, Martyn F.

    2005-06-28T23:59:59.000Z

    The outer valence shell photoelectron spectrum of CF?SF? has been studied experimentally and theoretically. Synchrotron radiation has been used to record angle resolved outer valence shell photoelectron spectra of CF?SF? in the photon energy range 18-60 eV. These spectra have allowed photoelectron asymmetry parameters and branching ratios to be derived. The Outer Valence Green’s Function approach has been employed to calculate the molecular orbital configuration and associated binding energies. A charge distribution analysis has also been obtained. Assignments have been proposed for the peaks observed in the photoelectron spectrum. The absolute photoabsorption cross section of CF?SF? has been measured from threshold to 40 eV, and strongly resembles that of SF6. Assignments, involving intravalence transitions, have been proposed for some of the principal features appearing in the photoabsorption spectrum of CF?SF?.

  2. Simulations of Plug-in Hybrid Vehicles Using Advanced Lithium Batteries and Ultracapacitors on Various Driving Cycles

    E-Print Network [OSTI]

    Burke, Andy; Zhao, Hengbing

    2010-01-01T23:59:59.000Z

    of ultracapacitors or even lithium-ion batteries. This isof ultracapacitors or even lithium-ion batteries. This isand Simulation Results with Lithium-ion Batteries. EET-2008

  3. The development of low cost LiFePO4-based high power lithium-ion batteries

    E-Print Network [OSTI]

    Shim, Joongpyo; Sierra, Azucena; Striebel, Kathryn A.

    2003-01-01T23:59:59.000Z

    4 , natural graphite, lithium-ion battery, diagnosticsand efficiency of pouch lithium-ion cells for constant C/24 -BASED HIGH POWER LITHIUM-ION BATTERIES Joongpyo Shim,

  4. The development of low cost LiFePO4-based high power lithium-ion batteries

    E-Print Network [OSTI]

    Shim, Joongpyo; Sierra, Azucena; Striebel, Kathryn A.

    2003-01-01T23:59:59.000Z

    HIGH POWER LITHIUM-ION BATTERIES Joongpyo Shim, Azucenaof rechargeable lithium batteries for application in hybridin consumer-size lithium batteries, such as the synthetic

  5. Simulations of Plug-in Hybrid Vehicles Using Advanced Lithium Batteries and Ultracapacitors on Various Driving Cycles

    E-Print Network [OSTI]

    Burke, Andy; Zhao, Hengbing

    2010-01-01T23:59:59.000Z

    The UC Davis Emerging Lithium Battery Test Project, Report3 for the advanced lithium battery chemistries are based onwith ultracapacitors, the LTO lithium battery should be

  6. Simulations of Plug-in Hybrid Vehicles Using Advanced Lithium Batteries and Ultracapacitors on Various Driving Cycles

    E-Print Network [OSTI]

    Burke, Andy; Zhao, Hengbing

    2010-01-01T23:59:59.000Z

    using Advanced Lithium Batteries and Ultracapacitors onusing advanced lithium batteries having energy densities ofA number of lithium batteries and ultracapacitors have been

  7. The development of low cost LiFePO4-based high power lithium-ion batteries

    E-Print Network [OSTI]

    Shim, Joongpyo; Sierra, Azucena; Striebel, Kathryn A.

    2003-01-01T23:59:59.000Z

    study of rechargeable lithium batteries for application inin consumer-size lithium batteries, such as the synthetic4 -BASED HIGH POWER LITHIUM-ION BATTERIES Joongpyo Shim,

  8. A Stable Fluorinated and Alkylated Lithium Malonatoborate Salt for Lithium Ion Battery Application

    SciTech Connect (OSTI)

    Wan, Shun [ORNL; Jiang, Xueguang [ORNL; Guo, Bingkun [ORNL; Dai, Sheng [ORNL; Sun, Xiao-Guang [ORNL

    2015-01-01T23:59:59.000Z

    A new fluorinated and alkylated lithium malonatoborate salt, lithium bis(2-methyl-2-fluoromalonato)borate (LiBMFMB), has been synthesized for lithium ion battery application. A 0.8 M LiBMFMB solution is obtained in a mixture of ethylene carbonate (EC) and ethyl methyl carbonate (EMC) (1:2 by wt.). The new LiBMFMB based electrolyte exhibits good cycling stability and rate capability in LiNi0.5Mn1.5O4 and graphite based half-cells.

  9. Deuterium Retention in NSTX with Lithium Conditioning

    SciTech Connect (OSTI)

    C.H. Skinner, J.P. Allain, W. Blanchard, H.W. Kugel, R. Maingi, L. Roquemore, V. Soukhanovskii, C.N. Taylor

    2010-06-02T23:59:59.000Z

    High (? 90%) deuterium retention was observed in NSTX gas balance measurements both withand 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 gasonly 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 showed that the binding of D atoms is fundamentally changed by lithium - in particular atoms are weakly bonded in regions near lithium atoms bound to either oxygen or the carbon matrix.

  10. Lithium metal reduction of plutonium oxide to produce plutonium metal

    DOE Patents [OSTI]

    Coops, Melvin S. (Livermore, CA)

    1992-01-01T23:59:59.000Z

    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.

  11. Lithium/water interactions: Experiments and analysis

    SciTech Connect (OSTI)

    Lomperski, S.; Corradini, M.L. (Univ. of Wisconsin, Madison, WI (United States))

    1993-08-01T23:59:59.000Z

    The interaction of molten-lithium droplets with water is studied experimentally. In one set of experiments, droplets of [approximately]10- to 15-mm diameter are injected into a vessel filled with water. The reaction is filmed, and pressure measurements are made. The initial metal and water temperatures range from 200 to 500[degrees]C and 20 to 70[degrees]C, respectively. It is found that when reactant temperatures are high, an explosive reaction often occurs. When the initial lithium temperature is >400[degrees]C and the water is >30[degrees]C, the explosive reactions become much more probable, with pressure peaks as high as 4 MPa. The reaction is modeled to explain the temperature threshold for this metal-ignition phenomena. Results with the model support the hypothesis that explosive reactions occur when the lithium droplet surface reaches its saturation temperature while the hydrogen film surrounding the drop is relatively thin. A second set of experiments measures the reaction rate of nonexplosive lithium-water reactions. The test geometry parallels that of the previous experiments, and the reactant temperature combinations are deliberately kept below the observed ignition threshold. Two separate methods are used to determine the reaction rate in each test: One uses a three-color pyrometer to measure the drop temperature as the lithium rises through the water, while the other consists of a photographic technique that measures the amount of hydrogen generated. Measured reaction rates range from [approximately]10 to 50 mol/s[center dot]m[sup 2] with good agreement between the two measurement techniques. The data do not show any significant variation in the reaction rate as a function of either the initial water or initial lithium temperature. 17 refs., 15 figs.

  12. Lithium, compression and high-pressure structure

    SciTech Connect (OSTI)

    Olinger, B.; Shaner, J.W.

    1983-03-04T23:59:59.000Z

    Lithium is found to transform from a body-centered cubic (bcc) to a face-centered cubic (fcc) structure at 6.9 gigapascals (69 kilobars) and 296 kelvin. The relative volume of the bcc structured lithium at 6.9 gigapascals is 0.718, and the fcc structure is 0.25 percent denser. The bulk modulus and its pressure derivative for the bcc structure are 11.57 gigapascals and 3.4, and for the fcc structure are 13.1 gigapascals and 2.8. Extrapolation of the bcc-fcc phase boundary and the melting curve indiactes a triple point around 15 gigapascals and 500 kelvin.

  13. Properties of lead-lithium solutions

    SciTech Connect (OSTI)

    Hoffman, N.J.; Darnell, A.; Blink, J.A.

    1980-10-01T23:59:59.000Z

    Lead-lithium solutions are of interest to liquid metal wall ICF reactor designers because Pb may be present to some extent in both heavy ion beam and laser-driven ICF targets; therefore, Pb will be present as an impurity in a flowing lithium wall. In addition, Pb-Li solutions containing approx. 80 a/o Pb are a strong candidate for a heavy ion beam driven HYLIFE converter and a viable alternative to a pure Li wall for a laser driven converter. The properties of Pb-Li solutions including the effect of hydrogen impurities are reviewed, and the reactor design implications are discussed.

  14. Corrosion Resistance of Niobium Alloys in Lithium

    SciTech Connect (OSTI)

    Ignativ, M.I.

    1986-03-01T23:59:59.000Z

    NbP1-1 niobium and NV-7, NTsU, and 5VMTs alloys, the chemical composition of which and the experimental method for were presented earlier, were investigated. The specimens were heat treated after which they were held in lithium. It was shown that in long holds of niobium alloys in lithium at temperatures below 1050/sup 0/C, the increase in their corrosion resistance is obtained not by combining the oxygen in oxides, but by the increase in the equilibrium concentration of oxygen in the investigated material by solid solution alloying of it with a metal more active toward oxygen.

  15. Electrolytic orthoborate salts for lithium batteries

    DOE Patents [OSTI]

    Angell, Charles Austen [Mesa, AZ; Xu, Wu [Tempe, AZ

    2009-05-05T23:59:59.000Z

    Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

  16. Electrolytic orthoborate salts for lithium batteries

    DOE Patents [OSTI]

    Angell, Charles Austen (Mesa, AZ); Xu, Wu (Tempe, AZ)

    2008-01-01T23:59:59.000Z

    Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

  17. Solid composite electrolytes for lithium batteries

    DOE Patents [OSTI]

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

    2001-01-01T23:59:59.000Z

    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 polymer-ceramic composite electrolyte containing poly(ethylene oxide), lithium tetrafluoroborate and titanium dioxide is provided in the form of an annealed film having a room temperature conductivity of from 10.sup.-5 S cm.sup.-1 to 10.sup.-3 S cm.sup.-1 and an activation energy of about 0.5 eV.

  18. Corrosion behaviour of materials selected for FMIT lithium system

    SciTech Connect (OSTI)

    Bazinet, G.D.; Brehm, W.F.

    1983-09-01T23:59:59.000Z

    The corrosion behavior of selected materials in a liquid lithium environment was studied in support of system and component designs for the Fusion Materials Irradiation Test (FMIT) Facility. Testing conditions ranged from about 3700 to about6500 hours of exposure to flowing lithium at temperatures from 230/sup 0/ to 270/sup 0/C and static lithium at temperatures from 200/sup 0/ to 500/sup 0/C. Principal areas of investigation included lithium corrosion/erosion effects on FMIT lithium system baseline and candidate materials. Material coupons and full-size prototypic components were evaluated to determine corrosion rates, fatigue crack growth rates, structural compatibility, and component acceptability for the lithium system. Based on the results of these studies, concerns regarding system materials and component designs were satisfactorily resolved to support a 20-year design life requirement for the FMIT lithium system.

  19. Lithium Surface Coatings for Improved Plasma Performance in NSTX

    SciTech Connect (OSTI)

    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

    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.

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

    SciTech Connect (OSTI)

    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

    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.

  1. Paper-Based Lithium-Ion Battery Nojan Aliahmad, Mangilal Agarwal, Sudhir Shrestha, and Kody Varahramyan

    E-Print Network [OSTI]

    Zhou, Yaoqi

    Paper-Based Lithium-Ion Battery Nojan Aliahmad, Mangilal Agarwal, Sudhir Shrestha, and Kody Indianapolis (IUPUI), Indianapolis, IN 46202 Lithium-ion batteries have a wide range of applications including devices. Lithium titanium oxide (Li4Ti5O12), lithium magnesium oxide (LiMn2O4) and lithium cobalt oxide

  2. Lithium Polysulfidophosphates: A Family of Lithium-Conducting Sulfur-Rich Compounds for Lithium-Sulfur Batteries

    SciTech Connect (OSTI)

    Lin, Zhan [ORNL] [ORNL; Liu, Zengcai [ORNL] [ORNL; Fu, Wujun [ORNL] [ORNL; Dudney, Nancy J [ORNL] [ORNL; Liang, Chengdu [ORNL] [ORNL

    2013-01-01T23:59:59.000Z

    Given the great potential for improving the energy density of state-of-the-art lithium-ion batteries by a factor of 5, a breakthrough in lithium-sulfur (Li-S) batteries will have a dramatic impact in a broad scope of energy related fields. Conventional Li-S batteries that use liquid electrolytes are intrinsically short-lived with low energy efficiency. The challenges stem from the poor electronic and ionic conductivities of elemental sulfur and its discharge products. We report herein lithium polysulfidophosphates (LPSP), a family of sulfur-rich compounds, as the enabler of long-lasting and energy-efficient Li-S batteries. LPSP have ionic conductivities of 3.0 10-5 S cm-1 at 25 oC, which is 8 orders of magnitude higher than that of Li2S (~10-13 S cm-1). The high Li-ion conductivity of LPSP is the salient characteristic of these compounds that impart the excellent cycling performance to Li-S batteries. In addition, the batteries are configured in an all-solid state that promises the safe cycling of high-energy batteries with metallic lithium anodes.

  3. Valence band hybridization in N-rich GaN1-xAsx alloys

    SciTech Connect (OSTI)

    Wu, J.; Walukiewicz, W.; Yu, K.M.; Denlinger, J.D.; Shan, W.; Ager III, J.W.; Kimura, A.; Tang, H.F.; Kuech, T.F.

    2004-05-04T23:59:59.000Z

    We have used photo-modulated transmission and optical absorption spectroscopies to measure the composition dependence of interband optical transitions in N-rich GaN{sub 1-x}As{sub x} alloys with x up to 0.06. The direct bandgap gradually decreases as x increases. In the dilute x limit, the observed band gap approaches 2.8 eV; this limiting value is attributed to a transition between the As localized level, which has been previously observed in As-doped GaN at 0.6 eV above the valence band maximum in As-doped GaN, and the conduction band minimum. The structure of the valence band of GaN{sub 1-x}As{sub x} is explained by the hybridization of the localized As states with the extended valence band states of GaN matrix. The hybridization is directly confirmed by soft x-ray emission experiments. To describe the electronic structure of the GaN{sub 1-x}As{sub x} alloys in the entire composition range a linear interpolation is used to combine the effects of valence band hybridization in N-rich alloys with conduction band anticrossing in As-rich alloys.

  4. Rechargeable thin-film lithium batteries

    SciTech Connect (OSTI)

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

    1993-09-01T23:59:59.000Z

    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.

  5. Lithium in LP 944-20

    E-Print Network [OSTI]

    Ya. V. Pavlenko; H. R. A. Jones; E. L. Martin; E. Guenther; M. A. Kenworthy; M. R. Zapatero Osorio

    2007-07-14T23:59:59.000Z

    We present a new estimate of the lithium abundance in the atmosphere of the brown dwarf LP 944-20. Our analysis is based on a self-consistent analysis of low, intermediate and high resolution optical and near-infrared spectra. We obtain log N(Li) = 3.25 +/-0.25 using fits of our synthetic spectra to the Li I resonance line doublet profiles observed with VLT/UVES and AAT/SPIRAL. This lithium abundance is over two orders of magnitude larger than previous estimates in the literature. In order to obtain good fits of the resonance lines of K I and Rb I and better fits to the TiO molecular absorption around the Li I resonance line, we invoke a semi-empirical model atmosphere with the dusty clouds located above the photosphere. The lithium abundance, however, is not changed by the effects of the dusty clouds. We discuss the implications of our estimate of the lithium abundance in LP 944-20 for the understanding of the properties of this benchmark brown dwarf.

  6. Electrothermal Analysis of Lithium Ion Batteries

    SciTech Connect (OSTI)

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

    2006-03-01T23:59:59.000Z

    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.

  7. Transparent lithium-ion batteries , Sangmoo Jeongb

    E-Print Network [OSTI]

    Cui, Yi

    voltage window. For example, LiCoO2 and graphite, the most common cathode and anode in Li-ion batteriesTransparent lithium-ion batteries Yuan Yanga , Sangmoo Jeongb , Liangbing Hua , Hui Wua , Seok Woo, and solar cells; however, transparent batteries, a key component in fully integrated transparent devices

  8. Implications of NSTX Lithium Results for Magnetic Fusion Research

    SciTech Connect (OSTI)

    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

    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.

  9. Lithium Depletion of Nearby Young Stellar Associations

    E-Print Network [OSTI]

    Erin Mentuch; Alexis Brandeker; Marten H. van Kerkwijk; Ray Jayawardhana; Peter H. Hauschildt

    2008-08-26T23:59:59.000Z

    We estimate cluster ages from lithium depletion in five pre-main-sequence groups found within 100 pc of the Sun: TW Hydrae Association, Eta Chamaeleontis Cluster, Beta Pictoris Moving Group, Tucanae-Horologium Association and AB Doradus Moving Group. We determine surface gravities, effective temperatures and lithium abundances for over 900 spectra through least squares fitting to model-atmosphere spectra. For each group, we compare the dependence of lithium abundance on temperature with isochrones from pre-main-sequence evolutionary tracks to obtain model dependent ages. We find that the Eta Chamaelontis Cluster and the TW Hydrae Association are the youngest, with ages of 12+/-6 Myr and 12+/-8 Myr, respectively, followed by the Beta Pictoris Moving Group at 21+/-9 Myr, the Tucanae-Horologium Association at 27+/-11 Myr, and the AB Doradus Moving Group at an age of at least 45 Myr (where we can only set a lower limit since the models -- unlike real stars -- do not show much lithium depletion beyond this age). Here, the ordering is robust, but the precise ages depend on our choice of both atmospheric and evolutionary models. As a result, while our ages are consistent with estimates based on Hertzsprung-Russell isochrone fitting and dynamical expansion, they are not yet more precise. Our observations do show that with improved models, much stronger constraints should be feasible: the intrinsic uncertainties, as measured from the scatter between measurements from different spectra of the same star, are very low: around 10 K in effective temperature, 0.05 dex in surface gravity, and 0.03 dex in lithium abundance.

  10. Diagnostic Evaluation of Detrimental Phenomena in High-Power Lithium-Ion Batteries

    E-Print Network [OSTI]

    Kostecki, Robert; Lei, Jinglei; McLarnon, Frank; Shim, Joongpyo; Striebel, Kathryn

    2005-01-01T23:59:59.000Z

    Phenomena in High-Power Lithium-Ion Batteries RobertAbstract A pouch-type lithium-ion cell, with graphite anodewith model pouch-type lithium-ion cells, with graphite

  11. Performance and degradation evaluation of five different commercial lithium-ion cells

    E-Print Network [OSTI]

    Striebel, Kathryn A.; Shim, Joongpyo

    2004-01-01T23:59:59.000Z

    Capacity Plots for 5 lithium-ion cells, normalized to aDOD cycling of five lithium-ion cells. Coulombic Ratio (Qd/Different Commercial Lithium-Ion Cells Kathryn A, Striebel

  12. Studies of ionic liquids in lithium-ion battery test systems

    E-Print Network [OSTI]

    Salminen, Justin; Prausnitz, John M.; Newman, John

    2006-01-01T23:59:59.000Z

    Studies of ionic liquids in lithium-ion battery test systemsobstacles for their use in lithium-ion batteries. However,devices. For rechargeable lithium-ion batteries, it is

  13. Failure modes in high-power lithium-ion batteries for use in hybrid electric vehicles

    E-Print Network [OSTI]

    2001-01-01T23:59:59.000Z

    for ATD 18650 GEN 1 lithium ion cells, Revision 4, DecemberFAILURE MODES IN HIGH-POWER LITHIUM-ION BATTERIES FOR USE INdevelopment of high-power lithium-ion batteries for hybrid

  14. Structural Integration of Silicon Solar Cells and Lithium-ion Batteries Using Printed Electronics

    E-Print Network [OSTI]

    Kang, Jin Sung

    2012-01-01T23:59:59.000Z

    41 Analysis on Performances of Lithium-Ion Polymerenergy for the system and lithium-ion batteries will be usedFIVE Performance of Lithium-Ion Polymer Battery Introduction

  15. Design Principles for the Use of Electroactive Polymers for Overcharge Protection of Lithium-Ion Batteries

    E-Print Network [OSTI]

    Thomas-Alyea, Karen E.; Newman, John; Chen, Guoying; Richardson, Thomas J.

    2005-01-01T23:59:59.000Z

    J. Newman, Advances in Lithium-Ion Batteries, ch. Modelingfor Overcharge Protection of Lithium-Ion Batteries Karen E.overcharge protec- tion for lithium-ion batteries. The model

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

    E-Print Network [OSTI]

    Lin, Feng

    2014-01-01T23:59:59.000Z

    Layered Oxides for Lithium Batteries. Nano Lett. 13, 3857–Material in Lithium Ion Batteries. Adv. Energy Mater. n/a–n/decomposition in lithium ion batteries: first-principles

  17. Design Principles for the Use of Electroactive Polymers for Overcharge Protection of Lithium-Ion Batteries

    E-Print Network [OSTI]

    Thomas-Alyea, Karen E.; Newman, John; Chen, Guoying; Richardson, Thomas J.

    2005-01-01T23:59:59.000Z

    and J. Newman, Advances in Lithium-Ion Batteries, ch.Modeling of Lithium Batteries. Kluwer Academic Publishers,Protection of Lithium-Ion Batteries Karen E. Thomas-Alyea,

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

    E-Print Network [OSTI]

    Chen, Guoying

    2010-01-01T23:59:59.000Z

    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

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

    E-Print Network [OSTI]

    Wilcox, James D.

    2010-01-01T23:59:59.000Z

    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

  20. Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries using Synchrotron Radiation Techniques

    E-Print Network [OSTI]

    Doeff, Marca M.

    2013-01-01T23:59:59.000Z

    Charge Distribution in a Lithium Battery Electrode. J. Phys.Aluminum is used for lithium ion battery cathodes and alland copper is used for lithium ion battery anodes. After the

  1. Characterization of nanostructured materials for lithium-ion batteries and electrochemical capacitors

    E-Print Network [OSTI]

    Augustyn, Veronica

    2013-01-01T23:59:59.000Z

    for a 2 V Rechargeable Lithium Battery. Journal of Thein a rechargeable lithium battery. Journal of Power Sourcesexception being the lithium-ion battery (Table 2.1). Table

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

    E-Print Network [OSTI]

    Wilcox, James D.

    2010-01-01T23:59:59.000Z

    of LiFePO(4) as lithium battery cathode and comparison withImproved LiFePO(4) Lithium Battery Cathode. ElectrochemicalOptimized LiFePO(4) for lithium battery cathodes. Journal of

  3. Performance, Charging, and Second-use Considerations for Lithium Batteries for Plug-in Electric Vehicles

    E-Print Network [OSTI]

    Burke, Andrew

    2009-01-01T23:59:59.000Z

    of the different lithium battery chemistries are presentedMiller, M. , Emerging Lithium-ion Battery Technologies forMid-size Full (1) Lithium-ion battery with an energy density

  4. A Failure and Structural Analysis of Block Copolymer Electrolytes for Rechargeable Lithium Metal Batteries

    E-Print Network [OSTI]

    Stone, Gregory Michael

    2012-01-01T23:59:59.000Z

    grid storage. The lithium-ion battery is the most advancedtoday [1, 2]. A lithium-ion battery is comprised of adendrite formation in lithium metal battery systems [12, 14,

  5. Lithium Diisopropylamide-Mediated Ortholithiation of 2Fluoropyridines: Rates, Mechanisms, and the Role of Autocatalysis

    E-Print Network [OSTI]

    Collum, David B.

    Lithium Diisopropylamide-Mediated Ortholithiation of 2Fluoropyridines: Rates, Mechanisms, Ithaca, New York 14853-1301, United States *S Supporting Information ABSTRACT: Lithium diisopropylamide herein mechanistic studies of the lithium diisopropylamide (LDA)-mediated ortholithiation of 2-fluoro

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

    DOE Patents [OSTI]

    Hobson, David O. (Oak Ridge, TN)

    1998-01-01T23:59:59.000Z

    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.

  7. Lithium Diffusion in Li4Ti5O12 at High Temperatures. | EMSL

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

    Lithium Diffusion in Li4Ti5O12 at High Temperatures. Lithium Diffusion in Li4Ti5O12 at High Temperatures. Abstract: Synthesis of the spinel lithium titanate Li4Ti5O12 by an...

  8. Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries using Synchrotron Radiation Techniques

    E-Print Network [OSTI]

    Doeff, Marca M.

    2013-01-01T23:59:59.000Z

    Alternatives to Current Lithium-Ion Batteries. Adv. EnergyMaterials for Lithium Ion Batteries. Materials Matters. 7 4.to the Study of Lithium Ion Batteries. J. Solid State

  9. Failure modes in high-power lithium-ion batteries for use in hybrid electric vehicles

    E-Print Network [OSTI]

    2001-01-01T23:59:59.000Z

    MODES IN HIGH-POWER LITHIUM-ION BATTERIES FOR USE IN HYBRIDof high-power lithium-ion batteries for hybrid electricthe development of lithium-ion batteries for hybrid electric

  10. 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]

    Ceder, Gerbrand

    2011-01-01T23:59:59.000Z

    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-air battery systems have the potential to provide significantly higher specific energies than current lithium

  11. (Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine in the United States was a brine

    E-Print Network [OSTI]

    94 LITHIUM (Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine in the United States was a brine operation in Nevada. The mine's production capacity was expanded in 2012, and a new lithium hydroxide plant opened in North

  12. (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]

    100 LITHIUM (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, Russia, and the United States were large producers also. Australia, Canada, and Zimbabwe were major producers of lithium

  13. (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]

    98 LITHIUM (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, Russia, and the United States were large producers also. Australia, Canada, and Zimbabwe were major producers of lithium

  14. Lithium Polymer (LiPo) Battery Usage Lithium polymer batteries are now being widely used in hobby and UAV applications. They work

    E-Print Network [OSTI]

    Langendoen, Koen

    Lithium Polymer (LiPo) Battery Usage 1 Lithium polymer batteries are now being widely used in hobby only LiPo Chargers with Error Detection - It is always recommended that you charge your lithium polymer batteries with a battery charger specifically designed for lithium polymer batteries. As an example, you

  15. Lithium 2,2,6,6-Tetramethylpiperidide and Lithium 2,2,4,6,6-Pentamethylpiperidide: Influence of TMEDA and Related

    E-Print Network [OSTI]

    Collum, David B.

    Lithium 2,2,6,6-Tetramethylpiperidide and Lithium 2,2,4,6,6-Pentamethylpiperidide: Influence,2,6,6-tetramethylpiperidide (LiTMP) and the conformationally locked (but otherwise isostructural) lithium 2 and conformational preferences of lithium 2,2,6,6-tetramethylpiperidide (LiTMP) in the solid state studied by Lappert

  16. (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]

    100 LITHIUM (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, Russia, and the United States also were major producers. Australia, Canada, and Zimbabwe were major producers of lithium

  17. (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]

    96 LITHIUM (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, Russia, and the United States were large producers also. Australia, Canada, and Zimbabwe were major producers of lithium

  18. (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]

    98 LITHIUM (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, Russia, and the United States also were major producers. Australia, Canada, and Zimbabwe were major producers of lithium

  19. (Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine operating in the United States was a

    E-Print Network [OSTI]

    94 LITHIUM (Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine operating in the United States was a brine operation in Nevada. Two companies produced a large array of downstream lithium compounds in the United States from

  20. STUDIES ON THE ROLE OF THE SUBSTRATE INTERFACE FOR GERMANIUM AND SILICON LITHIUM ION BATTERY ANODES

    E-Print Network [OSTI]

    Florida, University of

    AND SILICON LITHIUM ION BATTERY ANODES235 SEM/FIB, microstructure characterization, and local electron atom probe........................................................................................................................16 1.1 Lithium Ion Batteries

  1. Performance Characteristics of Lithium-ion Batteries of Various Chemistries for Plug-in Hybrid Vehicles

    E-Print Network [OSTI]

    Burke, Andrew; Miller, Marshall

    2009-01-01T23:59:59.000Z

    Lithium-ion battery modules for testing Table 2: BatteriesBatteries, Advanced Automotive Battery and Ultracapacitor Conference, Fourth International Symposium on Large Lithium-ion Battery

  2. Electrochemical performance of Sol-Gel synthesized LiFePO4 in lithium batteries

    E-Print Network [OSTI]

    Hu, Yaoqin; Doeff, Marca M.; Kostecki, Robert; Finones, Rita

    2003-01-01T23:59:59.000Z

    LiFePO 4 in Lithium Batteries Yaoqin Hu,* Marca M. Doeff,*material in lithium ion batteries based on environmental and

  3. Cu2Sb thin film electrodes prepared by pulsed laser deposition f or lithium batteries

    E-Print Network [OSTI]

    Song, Seung-Wan; Reade, Ronald P.; Cairns, Elton J.; Vaughey, Jack T.; Thackeray, Michael M.; Striebel, Kathryn A.

    2003-01-01T23:59:59.000Z

    The Electrochemical Society (Batteries and Energy ConversionDeposition for Lithium Batteries Seung-Wan Song, a, * Ronaldrechargeable lithium batteries. Introduction Sb-containing

  4. Performance Characteristics of Lithium-ion Batteries of Various Chemistries for Plug-in Hybrid Vehicles

    E-Print Network [OSTI]

    Burke, Andrew; Miller, Marshall

    2009-01-01T23:59:59.000Z

    on fuel cells, advanced batteries, and ultracapacitorof Lithium-ion Batteries of Various Chemistries for Plug-inAdvisor utilizing lithium-ion batteries of the different

  5. Automotive Lithium-ion Battery Supply Chain and U.S. Competitiveness...

    Office of Environmental Management (EM)

    Automotive Lithium-ion Battery Supply Chain and U.S. Competitiveness Considerations Automotive Lithium-ion Battery Supply Chain and U.S. Competitiveness Considerations This Clean...

  6. ELECTROCHEMICAL STUDIES OF THE FILM FORMATION ON LITHIUM IN PROPYLENE CARBONATE SOLUTIONS UNDER OPEN CIRCUIT CONDITIONS

    E-Print Network [OSTI]

    Geronov, Y.

    2014-01-01T23:59:59.000Z

    for film growth and lithium corrosion. The increase in LiCl0drastically decreases the lithium corrosion and reduces the

  7. Effects of Cesium Cations in Lithium Deposition via Self-Healing...

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

    Cesium Cations in Lithium Deposition via Self-Healing Electrostatic Shield Mechanism. Effects of Cesium Cations in Lithium Deposition via Self-Healing Electrostatic Shield...

  8. 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 Vehicle...

  9. au-implanted lithium niobate: Topics by E-print Network

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

    based on silicon-on-lithium-niobate photonics JEFF. By transferring large areas of thin, monocrystalline silicon to bulk lithium niobate (LiNbO3) substrates difference...

  10. Lithium: Measurement of Young's Modulus and Yield Strength

    SciTech Connect (OSTI)

    Ryan P Schultz

    2002-11-07T23:59:59.000Z

    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.

  11. Solid lithium ion conducting electrolytes and methods of preparation

    DOE Patents [OSTI]

    Narula, Chaitanya K; Daniel, Claus

    2013-05-28T23:59:59.000Z

    A composition comprised of nanoparticles of lithium ion conducting solid oxide material, wherein the solid oxide material is comprised of lithium ions, and at least one type of metal ion selected from pentavalent metal ions and trivalent lanthanide metal ions. Solution methods useful for synthesizing these solid oxide materials, as well as precursor solutions and components thereof, are also described. The solid oxide materials are incorporated as electrolytes into lithium ion batteries.

  12. Synthesis, Characterization and Performance of Cathodes for Lithium Ion Batteries

    E-Print Network [OSTI]

    Zhu, Jianxin

    2014-01-01T23:59:59.000Z

    and characterization of spinel Li 4 Ti 5 O 12 nanoparticles anode materials for lithium ion battery.Li-ion battery performance. Figure 34. Characterization of

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

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

    aqueous formulation designs by standardized dispersant selection and rheological optimization methods - Tailored Aqueous Colloids for Lithium-Ion Electrodes (TACLE) B.L....

  14. Linking Ion Solvation and Lithium Battery Electrolyte Properties...

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

    Battery Electrolyte Properties Linking Ion Solvation and Lithium Battery Electrolyte Properties 2010 DOE Vehicle Technologies and Hydrogen Programs Annual Merit Review and...

  15. Polymer Electrolytes for High Energy Density Lithium Batteries

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

    Electrolytes for High Energy Density Lithium Batteries Ashoutosh Panday Scott Mullin Nitash Balsara Proposed Battery anode (Li metal) Li Li + + e - e - Li salt in a hard solid...

  16. Synthesis, Characterization and Performance of Cathodes for Lithium Ion Batteries

    E-Print Network [OSTI]

    Zhu, Jianxin

    2014-01-01T23:59:59.000Z

    electrode in lithium-ion batteries: AFM study in an ethylenelithium-ion rechargeable batteries. Carbon 1999, 37, 165-batteries. J. Electrochem. Soc. 2001,

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

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

    Electrochemical Modeling of LMR-NMC Materials and Electrodes Addressing the Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials PHEV Battery Cost Assessment...

  18. Lithium-Ion Battery Recycling Facilities | Department of Energy

    Office of Environmental Management (EM)

    Recycling Facilities Lithium-Ion Battery Recycling Facilities 2013 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer...

  19. Development of High Energy Lithium Batteries for Electric Vehicles...

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

    Kasei * Focused on High Capacity Manganese Rich (HCMR TM ) cathodes & Silicon-Carbon composite anodes for Lithium ion batteries * Envia's high energy Li-ion battery materials...

  20. Studies on Lithium Manganese Rich MNC Composite Cathodes

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

    America Inc. 3 Presentation name Project Objectives - Relevance Undertake advanced materials research in the area of high energy (capacity) electrode materials for lithium-ion...

  1. Surface Modification Agents for Lithium-Ion Batteries | Argonne...

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

    Surface Modification Agents for Lithium-Ion Batteries Technology available for licensing: A process to modify the surface of the active material used in an electrochemical device...

  2. Lithium Ion Battery Performance of Silicon Nanowires With Carbon...

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

    Ion Battery Performance of Silicon Nanowires With Carbon Skin . Lithium Ion Battery Performance of Silicon Nanowires With Carbon Skin . Abstract: Silicon (Si) nanomaterials have...

  3. Development of Novel Electrolytes for Use in High Energy Lithium...

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

    More Documents & Publications Development of Novel Electrolytes for Use in High Energy Lithium-Ion Batteries with Wide Operating Temperature Range Development of Novel Electrolytes...

  4. Advanced Cathode Material Development for PHEV Lithium Ion Batteries...

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

    More Documents & Publications Advanced Cathode Material Development for PHEV Lithium Ion Batteries High Energy Novel Cathode Alloy Automotive Cell Develop & evaluate...

  5. Novel Redox Shuttles for Overcharge Protection of Lithium-Ion...

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

    Redox Shuttles for Overcharge Protection of Lithium-Ion Batteries Technology available for licensing: Electrolytes containing novel redox shuttles (electron transporters) for...

  6. Sandia National Laboratories: Solid-State Lithium Batteries

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

    Lithium Batteries ARPAe: Innovation Activities On November 25, 2013, in Technology Showcase Nominees Partnering with Sandia Research Facilities Current Projects Technology Showcase...

  7. 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 Our way of life is deeply intertwined with battery technologies that have enabled a mobile revolution powering cell...

  8. Intermetallic Electrodes Improve Safety and Performance in Lithium...

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

    Intermetallic Electrodes Improve Safety and Performance in Lithium-Ion Batteries Technology available for licensing: A new class of intermetallic material that can be used as a...

  9. Stabilized Lithium Metal Powder, Enabling Material and Revolutionary...

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

    Peer Evaluation es011yakovleva2011p.pdf More Documents & Publications Stabilized Lithium Metal Powder, Enabling Material and Revolutionary Technology for High Energy Li-ion...

  10. Edge Turbulence Velocity Changes with Lithium Coating on NSTX

    SciTech Connect (OSTI)

    Cao, A.; Zweben, S. J.; Stotler, D. P.; Bell, M.; Diallo, A.; Kaye, S. M.; LeBlanc, B.

    2012-08-10T23:59:59.000Z

    Lithium coating improves energy confinement and eliminates edge localized modes in NSTX, but the mechanism of this improvement is not yet well understood. We used the gas-puff-imaging (GPI) diagnostic on NSTX to measure the changes in edge turbulence which occurred during a scan with variable lithium wall coating, in order to help understand the reason for the confinement improvement with lithium. There was a small increase in the edge turbulence poloidal velocity and a decrease in the poloidal velocity fluctuation level with increased lithium. The possible effect of varying edge neutral density on turbulence damping was evaluated for these cases in NSTX. __________________________________________________

  11. Electrode Materials for Rechargeable Lithium-Ion Batteries: A...

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

    Electrode Materials for Rechargeable Lithium-Ion Batteries: A New Synthetic Approach Technology available for licensing: New high-energy cathode materials for use in rechargeable...

  12. Advanced Cathode Material Development for PHEV Lithium Ion Batteries...

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

    More Documents & Publications Advanced Cathode Material Development for PHEV Lithium Ion Batteries Vehicle Technologies Office Merit Review 2014: High Energy Novel...

  13. Redox shuttle additives for overcharge protection in lithium batteries

    E-Print Network [OSTI]

    Richardson, Thomas J.; Ross Jr., P.N.

    1999-01-01T23:59:59.000Z

    No. 5,763,119. “Redox Shuttle Additives for Overchargeprotection, electrolytes, additives, redox shuttleREDOX SHUTTLE ADDITIVES FOR OVERCHARGE PROTECTION IN LITHIUM

  14. Negative Electrodes Improve Safety in Lithium Cells and Batteries...

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

    Negative Electrodes Improve Safety in Lithium Cells and Batteries Technology available for licensing: Enhanced stability at a lower cost Lowers cost for enhanced stability...

  15. 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...

  16. Lithium In Tufas Of The Great Basin- Exploration Implications...

    Open Energy Info (EERE)

    Tufas Of The Great Basin- Exploration Implications For Geothermal Energy And Lithium Resources Jump to: navigation, search OpenEI Reference LibraryAdd to library Conference Paper:...

  17. 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...

  18. Manganese oxide composite electrodes for lithium batteries

    DOE Patents [OSTI]

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

    2009-12-22T23:59:59.000Z

    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.

  19. Manganese oxide composite electrodes for lithium batteries

    DOE Patents [OSTI]

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

    2007-12-04T23:59:59.000Z

    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.

  20. Solid polymeric electrolytes for lithium batteries

    DOE Patents [OSTI]

    Angell, Charles A.; Xu, Wu; Sun, Xiaoguang

    2006-03-14T23:59:59.000Z

    Novel conductive polyanionic polymers and methods for their preparion are provided. The polyanionic polymers comprise repeating units of weakly-coordinating anionic groups chemically linked to polymer chains. The polymer chains in turn comprise repeating spacer groups. Spacer groups can be chosen to be of length and structure to impart desired electrochemical and physical properties to the polymers. Preferred embodiments are prepared from precursor polymers comprising the Lewis acid borate tri-coordinated to a selected ligand and repeating spacer groups to form repeating polymer chain units. These precursor polymers are reacted with a chosen Lewis base to form a polyanionic polymer comprising weakly coordinating anionic groups spaced at chosen intervals along the polymer chain. The polyanionic polymers exhibit high conductivity and physical properties which make them suitable as solid polymeric electrolytes in lithium batteries, especially secondary lithium batteries.

  1. Entangled valence electron-hole dynamics revealed by stimulated attosecond x-ray Raman scattering

    SciTech Connect (OSTI)

    Healion, Daniel; Zhang, Yu; Biggs, Jason D.; Govind, Niranjan; Mukamel, Shaul

    2012-09-06T23:59:59.000Z

    We show that broadband x-ray pulses can create wavepackets of valence electrons and holes localized in the vicinity of a selected atom (nitrogen, oxygen or sulfur in cysteine) by resonant stimulated Raman scattering. The subsequent dynamics reveals highly correlated motions of entangled electrons and hole quasiparticles. This information goes beyond the time-dependent total charge density derived from x-ray diffraction.

  2. High expansion, lithium corrosion resistant sealing glasses

    DOE Patents [OSTI]

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

    1991-01-01T23:59:59.000Z

    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.

  3. Lithium-Polysulfide Flow Battery Demonstration

    SciTech Connect (OSTI)

    Zheng, Wesley

    2014-06-30T23:59:59.000Z

    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.

  4. Lithium-Polysulfide Flow Battery Demonstration

    ScienceCinema (OSTI)

    Zheng, Wesley

    2014-07-16T23:59:59.000Z

    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.

  5. Conductive polymeric compositions for lithium batteries

    DOE Patents [OSTI]

    Angell, Charles A. (Mesa, AZ); Xu, Wu (Tempe, AZ)

    2009-03-17T23:59:59.000Z

    Novel chain polymers comprising weakly basic anionic moieties chemically bound into a polyether backbone at controllable anionic separations are presented. Preferred polymers comprise orthoborate anions capped with dibasic acid residues, preferably oxalato or malonato acid residues. The conductivity of these polymers is found to be high relative to that of most conventional salt-in-polymer electrolytes. The conductivity at high temperatures and wide electrochemical window make these materials especially suitable as electrolytes for rechargeable lithium batteries.

  6. Current status of the liquid lithium target

    E-Print Network [OSTI]

    McDonald, Kirk

    in target (mm) 252 x 125Maximum beam current (mA) ~1~10~100Beam spot on the target (cm2) >2 (peak)0.52.5Beam Water direction #12;15 Be Trap Heat Exchanger Cross Section Design to remove ~12 kW Lithium tank #12;Oil cycle Flexible tubes Oil pump Heat exchanger Oil chamber Inside the lab Outside the lab #12;Elect

  7. High-discharge-rate lithium ion battery

    SciTech Connect (OSTI)

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

    2014-04-22T23:59:59.000Z

    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.

  8. High expansion, lithium corrosion resistant sealing glasses

    DOE Patents [OSTI]

    Brow, R.K.; Watkins, R.D.

    1991-06-04T23:59:59.000Z

    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.

  9. Aluminum-lithium alloys -- the next generation

    SciTech Connect (OSTI)

    Webster, D. (Advanced Material Development, Saratoga, CA (United States))

    1994-05-01T23:59:59.000Z

    The advantages of aluminum-lithium (Al-Li) alloys, such as low density and high modulus, have been well documented in the last 15 years, but their impact on the aerospace market has fallen short of initial expectations. However, vacuum refining processes have now been developed at Comalco Aluminium Ltd., Melbourne, Australia, that provide improved mechanical properties. In addition, the patented technology allows higher levels of lithium, which results in higher stiffness and lower densities. For example, alloys with 3.3% lithium and very low amounts of hydrogen and alkali metal impurities demonstrate good mechanical properties. It also exhibits good weldability, as shown in results of varestraint'' testing, which evaluates the tendency to crack during welding. The high purity of these VacLite alloys ensures that grain boundary fracture is minimized, and cleavage fracture is reduced almost to the limit of detectability. Furthermore, advanced vacuum techniques using electron beam melting at 10[sup [minus]5] torr may eventually reduce impurities to a level at which fracture occurs only in a ductile, transgranular manner.

  10. THE VALENCE OF TITANIUM IN REFRACTORY FORSTERITE. S. B. Simon1 , S. R. Sutton1,2

    E-Print Network [OSTI]

    Grossman, Lawrence

    THE VALENCE OF TITANIUM IN REFRACTORY FORSTERITE. S. B. Simon1 , S. R. Sutton1,2 and L. Grossman3 and analyzed by electron probe. Titanium K XANES spectra were collected us- ing the GSECARS X-ray microprobe

  11. Chemical overcharge protection of lithium and lithium-ion secondary batteries

    DOE Patents [OSTI]

    Abraham, Kuzhikalail M. (Needham, MA); Rohan, James F. (Cork City, IE); Foo, Conrad C. (Dedham, MA); Pasquariello, David M. (Pawtucket, RI)

    1999-01-01T23:59:59.000Z

    This invention features the use of redox reagents, dissolved in non-aqueous electrolytes, to provide overcharge protection for cells having lithium metal or lithium-ion negative electrodes (anodes). In particular, the invention features the use of a class of compounds consisting of thianthrene and its derivatives as redox shuttle reagents to provide overcharge protection. Specific examples of this invention are thianthrene and 2,7-diacetyl thianthrene. One example of a rechargeable battery in which 2,7-diacetyl thianthrene is used has carbon negative electrode (anode) and spinet LiMn.sub.2 O.sub.4 positive electrode (cathode).

  12. Chemical overcharge protection of lithium and lithium-ion secondary batteries

    DOE Patents [OSTI]

    Abraham, K.M.; Rohan, J.F.; Foo, C.C.; Pasquariello, D.M.

    1999-01-12T23:59:59.000Z

    This invention features the use of redox reagents, dissolved in non-aqueous electrolytes, to provide overcharge protection for cells having lithium metal or lithium-ion negative electrodes (anodes). In particular, the invention features the use of a class of compounds consisting of thianthrene and its derivatives as redox shuttle reagents to provide overcharge protection. Specific examples of this invention are thianthrene and 2,7-diacetyl thianthrene. One example of a rechargeable battery in which 2,7-diacetyl thianthrene is used has carbon negative electrode (anode) and spinet LiMn{sub 2}O{sub 4} positive electrode (cathode). 8 figs.

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

    SciTech Connect (OSTI)

    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

    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.

  14. The UC Davis Emerging Lithium Battery Test Project

    E-Print Network [OSTI]

    Burke, Andy; Miller, Marshall

    2009-01-01T23:59:59.000Z

    Batteries, Advanced Automotive Battery and Ultracapacitor Conference, Fourth International Symposium on Large Lithium-ion Batterybatteries with Nano-Li4Ti5O12 electrodes, Advanced Automotive Battery and Ultracapacitor Conference, Third International Symposium on Large Lithium-ion Battery

  15. Integration of Arsenic Trisulfide and Titanium Diffused Lithium Niobate Waveguides 

    E-Print Network [OSTI]

    Solmaz, Mehmet E.

    2011-08-08T23:59:59.000Z

    A chalcogenide glass (arsenic-trisulfide, As2S3) optical waveguide is vertically integrated onto titanium-diffused lithium-niobate (Ti:LiNbO3) waveguides to add optical feedback paths and to create more compact optical circuits. Lithium...

  16. LITHIUM-ION BATTERY CHARGING REPORT G. MICHAEL BARRAMEDA

    E-Print Network [OSTI]

    Ruina, Andy L.

    LITHIUM-ION BATTERY CHARGING REPORT G. MICHAEL BARRAMEDA 1. Abstract This report introduces how. Battery Pack 1 · Cycle 1 : 2334 mAh · Cycle 2: 2312 mAh #12;LITHIUM-ION BATTERY CHARGING REPORT 3 · Cycle to handle the Powerizer Li-Ion rechargeable Battery Packs. It will bring reveal battery specifications

  17. Cubic Lithium Nitride Amy Lazicki1,2

    E-Print Network [OSTI]

    Islam, M. Saif

    Cubic Lithium Nitride to 200 GPa Amy Lazicki1,2 Choong-Shik Yoo1, Warren Pickett2, Richard electrolyte material for lithium-based batteries · possible hydrogen storage material Thrust of this research ­ differences between the XRS and PDOS are indications of the presence of core-hole interactions (excitons

  18. Liquid surface skimmer apparatus for molten lithium and method

    DOE Patents [OSTI]

    Robinson, Samuel C. (Knoxville, TN); Pollard, Roy E. (Maryville, TN); Thompson, William F. (Oak Ridge, TN); Stark, Marshall W. (Gastonia, NC); Currin, Jr., Robert T. (Salisbury, NC)

    1995-01-01T23:59:59.000Z

    This invention relates to an apparatus for separating two fluids having different specific gravities. The invention also relates to a method for using the separating apparatus of the present invention. This invention particularly relates to the skimming of molten lithium metal from the surface of a fused salt electrolyte in the electrolytic production of lithium metal from a mixed fused salt.

  19. Integration of Arsenic Trisulfide and Titanium Diffused Lithium Niobate Waveguides

    E-Print Network [OSTI]

    Solmaz, Mehmet E.

    2011-08-08T23:59:59.000Z

    A chalcogenide glass (arsenic-trisulfide, As2S3) optical waveguide is vertically integrated onto titanium-diffused lithium-niobate (Ti:LiNbO3) waveguides to add optical feedback paths and to create more compact optical circuits. Lithium...

  20. Thin film method of conducting lithium-ions

    DOE Patents [OSTI]

    Zhang, Ji-Guang (Golden, CO); Benson, David K. (Golden, CO); Tracy, C. Edwin (Golden, CO)

    1998-11-10T23:59:59.000Z

    The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li.sub.2 O--CeO.sub.2 --SiO.sub.2 system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications.

  1. Thin film method of conducting lithium-ions

    DOE Patents [OSTI]

    Zhang, J.G.; Benson, D.K.; Tracy, C.E.

    1998-11-10T23:59:59.000Z

    The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li{sub 2}O-CeO{sub 2}-SiO{sub 2} system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications. 12 figs.

  2. Thin liquid lithium targets for high power density

    E-Print Network [OSTI]

    McDonald, Kirk

    High charge state High velocity flow ~60 m/s High heat capacity of Li Absorbs power depositedThin liquid lithium targets for high power density applications: heavy ion beam strippers and beta Hilton Malmö City #12;Outline Liquid Lithium Stripper idea for FRIB Brief theory of film stability

  3. Characterization of Lithium Stearate: Processing Aid for Filled Elastomers

    SciTech Connect (OSTI)

    E. Eastwood; C. Densmore

    2007-02-05T23:59:59.000Z

    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.

  4. Response of Lithium Polymer Batteries to Mechanical Loading

    E-Print Network [OSTI]

    Petta, Jason

    with graphite. · Two layers of polymer separator with electrolyte. #12;Lithium Polymer Battery Structure Cu strain of the battery. #12;Anode - Graphite Crushed Uncrushed #12;Cathode ­ LiCoO2 Crushed Uncrushed #12Response of Lithium Polymer Batteries to Mechanical Loading Karl Suabedissen1, Christina Peabody2

  5. Interconnected hollow carbon nanospheres for stable lithium metal anodes

    E-Print Network [OSTI]

    Cui, Yi

    storage, batteries with higher energy storage density than existing lithium ion batteries need metal anodes. W hen interest in secondary lithium batteries began to emerge more than four decades ago1) accommodating the large change in electrode volume during cycling (unlike graphite and silicon anodes, where

  6. Coated porous carbon cathodes for lithium ion batteries

    SciTech Connect (OSTI)

    Kercher, Andrew K [ORNL; Dudney, Nancy J [ORNL; Kiggans, Jim [ORNL; Klett, James William [ORNL

    2008-01-01T23:59:59.000Z

    Coated porous carbon cathodes for automotive lithium batteries are being developed with the goal of overcoming the problems with capacity fade and poor thermal management in conventional polymer-bonded cathodes. The active cathode material (lithium iron phosphate nanoparticles) is carbon-bonded to the porous carbon support material. Cathodes have been developed with high specific energy and power and with good cycling behavior.

  7. Lithium Lorentz Force Accelerator Thruster (LiLFA)

    E-Print Network [OSTI]

    Petta, Jason

    Argon Flow Copper Water Flow Piston/Lithium Feeding System Lithium Flow Pipes Heaters Heaters MAI Li procedure · Fire the thruster! #12;Previous Firing #12;Conclusions · Heaters and Thermocouples · Water Vacuum Pumps Thrust Stand Main Tank Water Line In Water Line Out Power Lines Computer Data Acquisition

  8. A Failure and Structural Analysis of Block Copolymer Electrolytes for Rechargeable Lithium Metal Batteries

    E-Print Network [OSTI]

    Stone, Gregory Michael

    2012-01-01T23:59:59.000Z

    lithium-ion battery is the most advanced rechargeable battery technology in use today. These batteries

  9. Optimization of lithium target for epithermal neutrons generation B. Bayanov, V. Belov, V. Kindyukb

    E-Print Network [OSTI]

    Taskaev, Sergey Yur'evich

    diffuse welding was refused, which resulted in possibility to obtain more homogeneous temperature field carrier flow and lithium layer temperature are shown. Calculation showed that the lithium target could run the temperature of lithium layer below 300 °C (Bayanov, 1998), or better below the lithium melting temperature 182

  10. Porous Doped Silicon Nanowires for Lithium Ion Battery Anode with Long Cycle Life

    E-Print Network [OSTI]

    Zhou, Chongwu

    Porous Doped Silicon Nanowires for Lithium Ion Battery Anode with Long Cycle Life Mingyuan Ge material in a lithium ion battery. Even after 250 cycles, the capacity remains stable above 2000, 1600 in energy storage has stimulated significant interest in lithium ion battery research. The lithium ion

  11. Cubic Spline Regression for the Open-Circuit Potential Curves of a Lithium-Ion Battery

    E-Print Network [OSTI]

    Cubic Spline Regression for the Open-Circuit Potential Curves of a Lithium-Ion Battery Qingzhi Guo-circuit potential OCP of an inter- calation electrode in a lithium-ion battery on the lithium concentra- tion reaction at an electrode in a lithium- ion battery depends exponentially on the difference between

  12. Kinetics of Initial Lithiation of Crystalline Silicon Electrodes of Lithium-Ion Batteries

    E-Print Network [OSTI]

    Kinetics of Initial Lithiation of Crystalline Silicon Electrodes of Lithium-Ion Batteries Matt phase. KEYWORDS: Lithium-ion batteries, silicon, kinetics, plasticity Lithium-ion batteries already at the electrolyte/lithiated silicon interface, diffusion of lithium through the lithiated phase, and the chemical

  13. Factors influencing the discharge characteristics of Na0.44MnO2-based positive electrode materials for rechargeable lithium batteries

    E-Print Network [OSTI]

    Doeff, M.M.

    2011-01-01T23:59:59.000Z

    for Rechargeable Lithium Batteries Marca M. Doeff, Kwang-For Rechargeable Lithium Batteries Marca M. Doefr*, Kwang-FOR RECHARGEABLE LITHIUM BATTERIES Marca M. Doeff * , Kwang-

  14. Analysis of the October 5, 1979 lithium spill and fire in the Lithium Processing Test Loop

    SciTech Connect (OSTI)

    Maroni, V.A.; Beatty, R.A.; Brown, H.L.; Coleman, L.F.; Foose, R.M.; McPheeters, C.C.; Slawecki, M.; Smith, D.L.; Van Deventer, E.H.; Weston, J.R.

    1981-12-01T23:59:59.000Z

    On October 5, 1979, the Lithium Processing Test Loop (LPTL) developed a lithium leak in the electromagnetic (EM) pump channel, which damaged the pump, its surrounding support structure, and the underlying floor pan. A thorough analysis of the causes and consequences of the pump failure was conducted by personnel from CEN and several other ANL divisions. Metallurgical analyses of the elliptical pump channel and adjacent piping revealed that there was a significant buildup of iron-rich crystallites and other solid material in the region of the current-carrying bus bars (region of high magnetic field), which may have resulted in a flow restriction that contributed to the deterioration of the channel walls. The location of the failure was in a region of high residual stress (due to cold work produced during channel fabrication); this failure is typical of other cold work/stress-related failures encountered in components operated in forced-circulation lithium loops. Another important result was the isolation of crystals of a compound characterized as Li/sub x/CrN/sub y/. Compounds of this type are believed to be responsible for much of the Fe, Cr, and Ni mass transfer encountered in lithium loops constructed of stainless steel. The importance of nitrogen in the mass-transfer mechanism has long been suspected, but the existence of stable ternary Li-M-N compounds (M = Fe, Cr, Ni) had not previously been verified.

  15. Lithium aluminum/iron sulfide battery having lithium aluminum and silicon as negative electrode

    DOE Patents [OSTI]

    Gilbert, Marian (Flossmoor, IL); Kaun, Thomas D. (New Lenox, IL)

    1984-01-01T23:59:59.000Z

    A method of making a negative electrode, the electrode made thereby and a secondary electrochemical cell using the electrode. Silicon powder is mixed with powdered electroactive material, such as the lithium-aluminum eutectic, to provide an improved electrode and cell.

  16. Deposition of lithium on a plasma edge probe in TFTR -- Behavior of lithium-painted walls interacting with edge plasmas

    SciTech Connect (OSTI)

    Hirooka, Y. [Univ. of California, San Diego, La Jolla, CA (United States); Ashida, K. [Toyama Univ. (Japan); Kugel, H. [Princeton Univ., NJ (United States)] [and others

    1998-05-01T23:59:59.000Z

    Recent observations have indicated that lithium pellet injection wall conditioning plays an important role in achieving the enhanced supershot regime in TFTR. However, little is understood about the behavior of lithium-coated limiter walls, interacting with edge plasmas. In the final campaign of TFTR, a cylindrical carbon fiber composite probe was inserted into the boundary plasma region and exposed to ohmically-heated deuterium discharges with lithium pellet injection. The ion-drift side probe surface exhibits a sign of codeposition of lithium, carbon, oxygen, and deuterium, whereas the electron side essentially indicates high-temperature erosion. It is found that lithium is incorporated in these codeposits in the form of oxide at the concentration of a few percent. In the electron side, lithium has been found to penetrate deeply into the probe material, presumably via rapid diffusion through interplane spaces in the graphite crystalline. Though it is not conclusive, materials mixing in the carbon and lithium system appears to be a key process in successful lithium wall conditioning.

  17. A comparative study of the corrosion resistance of an austenitic steel in lithium and the eutectic lead-lithium alloy

    SciTech Connect (OSTI)

    Gryaznov, G.M.; Evtikhin, V.A.; Kosukhin, A.Y.; Zavyal'skii, L.P.

    1986-05-01T23:59:59.000Z

    In a number of designs of thermonuclear reactors, besides liquid lithium, the use of lead-lithium alloy of the eutectic composition (Pb/sub 83/ Li/sub 17/) is envisaged for tritium breeding, heat transfer, and protecting the primary wall. The interaction of this alloy with water and air is less vigorous as compared to lithium, and the (n, 2n) type reactions involving lead atoms can ensure a tritium-breeding factor exceeding unity in the blanket at a relatively low concentration of lithium in the alloy. Tests are carried out on the 18-10 steel in convective currents of lithium and the Pb-17Li alloy in order to compare their corrosive action on the austenitic chromiumnickel steels that are promising materials for the primary wall and the blanket. Based on the obtained results, the high corrosive activity of the lead-lithium alloy as compared to pure lithium can be explained in the following way: the increased solubility of iron in lead as compared to that in lithium alone cannot ensure the observed rate of mass transfer of the steel by the lead base alloy.

  18. Electronic transport in Lithium Nickel Manganese Oxide, a high-voltage cathode material for Lithium-Ion batteries

    E-Print Network [OSTI]

    Ransil, Alan Patrick Adams

    2013-01-01T23:59:59.000Z

    Potential routes by which the energy densities of lithium-ion batteries may be improved abound. However, the introduction of Lithium Nickel Manganese Oxide (LixNi1i/2Mn3/2O4, or LNMO) as a positive electrode material appears ...

  19. The Impact Of Lithium Wall Coatings On NSTX Discharges And The Engineering Of The Lithium Tokamak eXperiment (LTX)

    SciTech Connect (OSTI)

    R. Majeski, H. Kugel and R. Kaita

    2010-03-18T23:59:59.000Z

    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 Land 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 oC 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.

  20. Lithium Abundances of the Local Thin Disk Stars

    E-Print Network [OSTI]

    David L. Lambert; Bacham E. Reddy

    2004-01-14T23:59:59.000Z

    Lithium abundances are presented for a sample of 181 nearby F and G dwarfs with accurate {\\it Hipparcos} parallaxes. The stars are on circular orbits about the Galactic centre and, hence, are identified as belonging to the thin disk. This sample is combined with two published surveys to provide a catalogue of lithium abundances, metallicities ([Fe/H]), masses, and ages for 451 F-G dwarfs, almost all belonging to the thin disk. The lithium abundances are compared and contrasted with published lithium abundances for F and G stars in local open clusters. The field stars span a larger range in [Fe/H] than the clusters for which [Fe/H] $\\simeq 0.0\\pm0.2$. The initial (i.e., interstellar) lithium abundance of the solar neighborhood, as derived from stars for which astration of lithium is believed to be unimportant, is traced from $\\log\\epsilon$(Li) = 2.2 at [Fe/H] = -1 to $\\log\\epsilon$(Li) = 3.2 at $+0.1$. This form for the evolution is dependent on the assumption that astration of lit hium is negligible for the stars defining the relation. An argument is advanced that this latter assumption may not be entirely correct, and, the evolution of lithium with [Fe/H] may be flatter than previously supposed. A sharp Hyades-like Li-dip is not seen among the field stars and appears to be replaced by a large spread among lithium abundances of stars more massive than the lower mass limit of the dip. Astration of lithium by stars of masses too low to participate in the Li-dip is discussed. These stars show little to no spread in lithium abundance at a given [Fe/H] and mass.

  1. Surface modifications for carbon lithium intercalation anodes

    DOE Patents [OSTI]

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

    2000-01-01T23:59:59.000Z

    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.

  2. Electric quadrupole transition probabilities for atomic lithium

    SciTech Connect (OSTI)

    Çelik, Gültekin, E-mail: gultekin@selcuk.edu.tr [Department of Physics, Faculty of Science, Selçuk University, Campus 42049 Konya (Turkey); Gökçe, Yasin; Y?ld?z, Murat [Department of Physics, Faculty of Science, Karamanoglu Mehmetbey University, Karaman (Turkey)

    2014-05-15T23:59:59.000Z

    Electric quadrupole transition probabilities for atomic lithium have been calculated using the weakest bound electron potential model theory (WBEPMT). We have employed numerical non-relativistic Hartree–Fock wavefunctions for expectation values of radii and the necessary energy values have been taken from the compilation at NIST. The results obtained with the present method agree very well with the Coulomb approximation results given by Caves (1975). Moreover, electric quadrupole transition probability values not existing in the literature for some highly excited levels have been obtained using the WBEPMT.

  3. Long life lithium batteries with stabilized electrodes

    DOE Patents [OSTI]

    Amine, Khalil (Downers Grove, IL); Liu, Jun (Naperville, IL); Vissers, Donald R. (Naperville, IL); Lu, Wenquan (Darien, IL)

    2009-03-24T23:59:59.000Z

    The present invention relates to non-aqueous electrolytes having electrode stabilizing additives, stabilized electrodes, and electrochemical devices containing the same. Thus the present invention provides electrolytes containing an alkali metal salt, a polar aprotic solvent, and an electrode stabilizing additive. In some embodiments the additives include a substituted or unsubstituted cyclic or spirocyclic hydrocarbon containing at least one oxygen atom and at least one alkenyl or alkynyl group. When used in electrochemical devices with, e.g., lithium manganese oxide spinel electrodes or olivine or carbon-coated olivine electrodes, the new electrolytes provide batteries with improved calendar and cycle life.

  4. Lithium Technology Corporation | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are beingZealand Jump to: navigation, searchOf KilaueaInformation Other AlternativePark, Arizona:Lithium Technology

  5. Lithium Energy Japan | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are being directedAnnual SiteofEvaluatingGroup |Jilin ZhongdiantouLichuan CityLiqcrytech LLC JumpList ofLithium Energy

  6. Determination of different valence forms of cerium in glasses using potentiometric titration

    SciTech Connect (OSTI)

    Chesnokova, S.M.; Danilova, I.Yu.; Andreev, P.A.

    1987-09-01T23:59:59.000Z

    This paper describes a potentiometric method for the quantitative determination of two cerium oxide forms--cerium dioxide and dicerium trioxide--in glasses where the oxides form a major constituent. The method uses hydroquinone as a reducing agent. Cerium valences are also determined. The sensitivity of the method is tested by analyzing known synthetic mixtures simulating the composition of the glasses. The method has been used to determine the total concentration of cerium and to monitor the redox regime in glass melting furnaces during the melting of cerium-containing glasses.

  7. Attosecond time delay in valence photoionization and photorecombination of argon: a TDLDA study

    E-Print Network [OSTI]

    Magrakvelidze, Maia; Dixit, Gopal; Ivanov, Misha; Chakraborty, Himadri S

    2015-01-01T23:59:59.000Z

    We determine and analyze the quantum phases and time delays in photoionization and photorecombination of valence 3p and 3s electrons of argon using the Kohn-Sham local density functional approach. The time-dependent local density approximation (TDLDA) is used to account for the electron correlation. Resulting attosecond Wigner-Smith time delays show excellent agreements with two recent independent experiments on argon that measured the relative 3s-3p time delay in photoionization [Physical Review Letters {\\bf 106}, 143002 (2011)] and the delay in 3p photorecombination [Physical Review Letters {\\bf 112}, 153002 (2014)

  8. Testing of Liquid Lithium Limiters in CDX-U

    SciTech Connect (OSTI)

    R. Majeski; R. Kaita; M. Boaz; P. Efthimion; T. Gray; B. Jones; D. Hoffman; H. Kugel; J. Menard; T. Munsat; A. Post-Zwicker; V. Soukhanovskii; J. Spaleta; G. Taylor; J. Timberlake; R. Woolley; L. Zakharov; M. Finkenthal; D. Stutman; G. Antar; R. Doerner; S. Luckhardt; R. Seraydarian; R. Maingi; M. Maiorano; S. Smith; D. Rodgers

    2004-07-30T23:59:59.000Z

    Part of the development of liquid metals as a first wall or divertor for reactor applications must involve the investigation of plasma-liquid metal interactions in a functioning tokamak. Most of the interest in liquid-metal walls has focused on lithium. Experiments with lithium limiters have now been conducted in the Current Drive Experiment-Upgrade (CDX-U) device at the Princeton Plasma Physics Laboratory. Initial experiments used a liquid-lithium rail limiter (L3) built by the University of California at San Diego. Spectroscopic measurements showed some reduction of impurities in CDX-U plasmas with the L3, compared to discharges with a boron carbide limiter. While no reduction in recycling was observed with the L3, which had a plasma-wet area of approximately 40 cm2, subsequent experiments with a larger area fully toroidal lithium limiter demonstrated significant reductions in both recycling and in impurity levels. Two series of experiments with the toroidal limiter have now be en performed. In each series, the area of exposed, clean lithium was increased, until in the latest experiments the liquid-lithium plasma-facing area was increased to 2000 cm2. Under these conditions, the reduction in recycling required a factor of eight increase in gas fueling in order to maintain the plasma density. The loop voltage required to sustain the plasma current was reduced from 2 V to 0.5 V. This paper summarizes the technical preparations for lithium experiments and the conditioning required to prepare the lithium surface for plasma operations. The mechanical response of the liquid metal to induced currents, especially through contact with the plasma, is discussed. The effect of the lithium-filled toroidal limiter on plasma performance is also briefly described.

  9. Hierarchically Structured Materials for Lithium Batteries

    SciTech Connect (OSTI)

    Xiao, Jie; Zheng, Jianming; Li, Xiaolin; Shao, Yuyan; Zhang, Jiguang

    2013-09-25T23:59:59.000Z

    Lithium-ion battery (LIB) is one of the most promising power sources to be deployed in electric vehicles (EV), including solely battery powered vehicles, plug-in hybrid electric vehicles, and hybrid electrical vehicles. With the increasing demand on devices of high energy densities (>500 Wh/kg) , new energy storage systems, such as lithium-oxygen (Li-O2) batteries and other emerging systems beyond the conventional LIB also attracted worldwide interest for both transportation and grid energy storage applications in recent years. It is well known that the electrochemical performances of these energy storage systems depend not only on the composition of the materials, but also on the structure of electrode materials used in the batteries. Although the desired performances characteristics of batteries often have conflict requirements on the micro/nano-structure of electrodes, hierarchically designed electrodes can be tailored to satisfy these conflict requirements. This work will review hierarchically structured materials that have been successfully used in LIB and Li-O2 batteries. Our goal is to elucidate 1) how to realize the full potential of energy materials through the manipulation of morphologies, and 2) how the hierarchical structure benefits the charge transport, promotes the interfacial properties, prolongs the electrode stability and battery lifetime.

  10. Novel carbonaceous materials for lithium secondary batteries

    SciTech Connect (OSTI)

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

    1997-07-01T23:59:59.000Z

    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.

  11. Can mirror matter solve the the cosmological lithium problem?

    SciTech Connect (OSTI)

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

    2014-05-02T23:59:59.000Z

    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.

  12. Chemical Shuttle Additives in Lithium Ion Batteries

    SciTech Connect (OSTI)

    Patterson, Mary

    2013-03-31T23:59:59.000Z

    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.

  13. Lithium As Plasma Facing Component for Magnetic Fusion Research

    SciTech Connect (OSTI)

    Masayuki Ono

    2012-09-10T23:59:59.000Z

    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.

  14. The electronic structure and optical properties of organic mixed valence anion radicals

    SciTech Connect (OSTI)

    Liberko, C.A.

    1992-01-01T23:59:59.000Z

    The electronic structure of planar and helical organic mixed valence anion radicals was studied. Cyanoimine derivatives of planar diquinones were synthesized and studied by electrochemical methods. Their anion radicals were generated electrochemically and found to be stable in air. These species had electronic absorptions in the near infrared region. The Visible and near infrared spectra as well as IR vibrational data are consistent with delocalized anion radicals. The molecular orbital energy level coefficients obtained from PPP semi-empirical molecular orbital calculations on neutral quinones, imides and cyanoimine derivatives of quinones, were used to correlate experimental data of their anion radicals. The calculation correlated the long wavelength absorptions of the anion radicals confirming that the absorptions arise from electronic transitions in delocalized species. The calculation was also valuable for assigning ESR hyperfine splittings. Including minor geometric perturbations in the calculation provides a method of predicting localization in mixed valence ion radicals. Helicene diquinones were studied by cyclic voltammetry. Their anion radicals, generated electrochemically, were studied by visible, near infrared, and ESR spectroscopies. The anion radicals were found to have electronic absorptions in the near infrared region tailing into the infrared. PPP calculations were consistent with the experimental data only if transannular interaction between the ends of the helix was included. The calculations and experimental observations are consistent with an electronic structure in which the anion radical is not only delocalized around the helix but also between the ends of the helix bonding them together in a Mobius fashion.

  15. Valence band structure of the icosahedral Ag-In-Yb quasicrystal

    SciTech Connect (OSTI)

    Sharma, H. R.; Simutis, G.; Dhanak, V. R.; Nugent, P. J.; McGrath, R. [Surface Science Research Centre and Department of Physics, University of Liverpool, Liverpool L69 3BX (United Kingdom); Cui, C. [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai 980-8577 (Japan); Shimoda, M. [National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan); Tsai, A. P. [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai 980-8577 (Japan); National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047 (Japan); Ishii, Y. [Department of Physics, Chuo University, Kasuga, Tokyo 112-8551 (Japan)

    2010-03-01T23:59:59.000Z

    The valence band structure of the icosahedral (i) Ag-In-Yb quasicrystal, which is isostructural to the binary i-Cd-Yb system, is investigated by ultraviolet photoemission spectroscopy (UPS). Experimental results are compared with electronic-structure calculations of a cubic approximant of the same phase. UPS spectra from the fivefold, threefold, and twofold i-Ag-In-Yb surfaces reveal that the valence band near to the Fermi level is dominated by Yb 4f-derived states, in agreement with calculations. The spectra also exhibit peaks which are surface core level shifted, caused by changes in the electronic structure in surface layers. Calculations yield a pseudogap in the density of states due to a hybridization of the Yb 5d band with the Ag 5p and In 5p bands. Both experimental and calculated band features are very similar to those of Cd-Yb. The modification of the band structure after surface treatment by sputtering and by oxidation is also studied. Additionally, the work function of i-Ag-In-Yb measured from the width of UPS spectrum is found to be almost unaffected by surface orientation, but increases after sputtering or oxidation.

  16. (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]

    by Joyce A. Ober, (703) 648-7717. #12;97 LITHIUM Events, Trends, and Issues: The Department of Energy (DOE produced lithium compounds for domestic consumption as well as for export to other countries. The use% of estimated domestic consumption. Other major end uses for lithium were in the manufacture of lubricants

  17. (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 Use: Chile was the largest lithium chemical producer in the world, followed by China, the United of lower production costs as compared to the costs for hard rock ores. Most of the lithium minerals mined purchased from a producer in Chile. The increased production of low-cost lithium carbonate in South America

  18. Factors influencing the discharge characteristics of Na0.44MnO2-based positive electrode materials for rechargeable lithium batteries

    E-Print Network [OSTI]

    Doeff, M.M.

    2011-01-01T23:59:59.000Z

    in rechargeable lithium battery configurations. 1,2,3 Theseprior to use in a lithium battery configuration,. Partial

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

    SciTech Connect (OSTI)

    None

    2010-08-01T23:59:59.000Z

    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. Today’s 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.

  20. Protective coating on positive lithium-metal-oxide electrodes for lithium batteries

    DOE Patents [OSTI]

    Johnson, Christopher S.; Thackeray, Michael M.; Kahaian, Arthur J.

    2006-05-23T23:59:59.000Z

    A positive electrode for a non-aqueous lithium cell comprising a LiMn2-xMxO4 spinel structure in which M is one or more metal cations with an atomic number less than 52, such that the average oxidation state of the manganese ions is equal to or greater than 3.5, and in which 0.ltoreq.x.ltoreq.0.15, having one or more lithium spine oxide LiM'2O4 or lithiated spinel oxide Li1+yM'2O4 compounds on the surface thereof in which M' are cobalt cations and in which 0.ltoreq.y.ltoreq.1.

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

    SciTech Connect (OSTI)

    R. Kaita, et. al.

    2012-07-20T23:59:59.000Z

    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.

  2. Exact valence bond entanglement entropy and probability distribution in the XXX spin chain and the Potts model

    E-Print Network [OSTI]

    Jesper Lykke Jacobsen; Hubert Saleur

    2007-11-21T23:59:59.000Z

    By relating the ground state of Temperley-Lieb hamiltonians to partition functions of 2D statistical mechanics systems on a half plane, and using a boundary Coulomb gas formalism, we obtain in closed form the valence bond entanglement entropy as well as the valence bond probability distribution in these ground states. We find in particular that for the XXX spin chain, the number N_c of valence bonds connecting a subsystem of size L to the outside goes, in the thermodynamic limit, as = (4/pi^2) ln L, disproving a recent conjecture that this should be related with the von Neumann entropy, and thus equal to 1/(3 ln 2) ln L. Our results generalize to the Q-state Potts model.

  3. Exact valence bond entanglement entropy and probability distribution in the XXX spin chain and the Potts model

    E-Print Network [OSTI]

    Jacobsen, Jesper Lykke

    2011-01-01T23:59:59.000Z

    By relating the ground state of Temperley-Lieb hamiltonians to partition functions of 2D statistical mechanics systems on a half plane, and using a boundary Coulomb gas formalism, we obtain in closed form the valence bond entanglement entropy as well as the valence bond probability distribution in these ground states. We find in particular that for the XXX spin chain, the number N_c of valence bonds connecting a subsystem of size L to the outside goes, in the thermodynamic limit, as = (4/pi^2) ln L, disproving a recent conjecture that this should be related with the von Neumann entropy, and thus equal to 1/(3 ln 2) ln L. Our results generalize to the Q-state Potts model.

  4. Optimization of Acetylene Black Conductive Additive and Polyvinylidene Difluoride Composition for High Power Rechargeable Lithium-Ion Cells

    E-Print Network [OSTI]

    Liu, G.; Zheng, H.; Battaglia, V.S.; Simens, A.S.; Minor, A.M.; Song, X.

    2007-01-01T23:59:59.000Z

    7), A365 G. M. Ehrlich, Lithium-ion Batteries, 3rd ed ed. (High Power Rechargeable Lithium-Ion Cells G. Liu a,z , H.local environment. (A) lithium-ion mass transfer in the

  5. The Effects of Various Conductive Additive and Polymeric Binder Contents on the Performance of a Lithium-ion Composite

    E-Print Network [OSTI]

    Liu, G.

    2008-01-01T23:59:59.000Z

    inactive materials weight (AB+PVDF) for lithium-ion cells.used to fabricate the lithium-ion coin cells. Figure 1. DCon the Performance of a Lithium-ion Composite Cathode G Liu

  6. An Investigation of the Effect of Graphite Degradation on the Irreversible Capacity in Lithium-ion Cells

    E-Print Network [OSTI]

    Hardwick, Laurence

    2008-01-01T23:59:59.000Z

    the Irreversible Capacity in Lithium-ion Cells Laurence J.cycling in rechargeable lithium-ion batteries. 3,4,5 This isaffect significantly lithium-ion cell long-term behaviour.

  7. New nanocrystalline manganese oxides as cathode materials for lithium batteries : electron microscopy, electrochemical and X-ray absorption studies

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    1 New nanocrystalline manganese oxides as cathode materials for lithium batteries : electron: manganese oxide, lithium batteries, nanomaterials Corresponding author: Pierre Strobel, tel. 33 476 887 940 with lithium iodide in aqueous medium at room temperature. Transmission electron microscopy (TEM) showed

  8. Lithium-Sulfur Batteries: Development of High Energy Lithium-Sulfur Cells for Electric Vehicle Applications

    SciTech Connect (OSTI)

    None

    2010-10-01T23:59:59.000Z

    BEEST Project: Sion Power is developing a lithium-sulfur (Li-S) battery, a potentially cost-effective alternative to the Li-Ion battery that could store 400% more energy per pound. All batteries have 3 key parts—a positive and negative electrode and an electrolyte—that exchange ions to store and release electricity. Using different materials for these components changes a battery’s chemistry and its ability to power a vehicle. Traditional Li-S batteries experience adverse reactions between the electrolyte and lithium-based negative electrode that ultimately limit the battery to less than 50 charge cycles. Sion Power will sandwich the lithium- and sulfur-based electrode films around a separator that protects the negative electrode and increases the number of charges the battery can complete in its lifetime. The design could eventually allow for a battery with 400% greater storage capacity per pound than Li-Ion batteries and the ability to complete more than 500 recharge cycles.

  9. Joint Center for Energy Storage Research Beyond Lithium-Ion

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

    Joint Center for Energy Storage Research Beyond Lithium-Ion 2012 2017 USE MULTIPLY-CHARGED IONS STORE ENERGY IN CHEMICAL BONDS STORE ENERGY IN LIQUIDS IN THE NEXT FIVE YEARS AT...

  10. Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications

    E-Print Network [OSTI]

    Hu, Qichao

    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 ...

  11. Arsenic Trisulfide on Lithium Niobate Devices for Infrared Integrated Optics 

    E-Print Network [OSTI]

    Xia, Xin

    2012-07-16T23:59:59.000Z

    Arsenic trisulfide (As?S?) waveguide devices on lithium niobate substrates (LiNbO?) provide a set of compact and versatile means for guiding and manipulating optical modes in infrared integrated optical circuits, including the integrated trace gas...

  12. Thermo-mechanical Behavior of Lithium-ion Battery Electrodes 

    E-Print Network [OSTI]

    An, Kai

    2013-11-25T23:59:59.000Z

    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...

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

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

    America. Lithium-ion batteries are a key component in electric vehicles and other rechargeable batteries for consumer electronics, and are used in the production of plug-in...

  14. Active primary lithium thionyl chloride battery for artillery applications

    SciTech Connect (OSTI)

    Baldwin, A.R.; Delnick, F.M. (Sandia National Labs., Albuquerque, NM (USA)); Miller, D.L. (Eagle-Picher Industries, Inc., Joplin, MO (USA))

    1990-01-01T23:59:59.000Z

    Sandia National Laboratories and Eagle Picher Industries have successfully developed an Active Lithium Thionyl Chloride (ALTC) power battery for unique artillery applications. Details of the design and the results of safety and performance will be presented. 1 ref., 5 figs.

  15. Mixed Polyanion Glasses for Lithium Ion Battery Cathodes | ornl...

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

    Mixed Polyanion Glasses for Lithium Ion Battery Cathodes May 06 2015 09:30 AM - 10:30 AM Andrew K. Kercher, Division Staff Materials Science and Technology Division Seminar...

  16. Three-Dimensional Lithium-Ion Battery Model (Presentation)

    SciTech Connect (OSTI)

    Kim, G. H.; Smith, K.

    2008-05-01T23:59:59.000Z

    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.

  17. aqueous rechargeable lithium: Topics by E-print Network

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

    batteries MIT - DSpace Summary: There has been great recent interest in lithium storage at the anode of Li-ion rechargeable battery by alloying with metals such as Al,...

  18. aqueous lithium rechargeable: Topics by E-print Network

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

    batteries MIT - DSpace Summary: There has been great recent interest in lithium storage at the anode of Li-ion rechargeable battery by alloying with metals such as Al,...

  19. Improvement in Plasma Performance with Lithium Coatings in NSTX

    SciTech Connect (OSTI)

    Kaita, R

    2009-02-17T23:59:59.000Z

    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.

  20. Improvement in Plasma Performance with Lithium Coatings in NSTX

    SciTech Connect (OSTI)

    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

    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.

  1. Lithium-ion battery modeling using non-equilibrium thermodynamics

    E-Print Network [OSTI]

    Ferguson, Todd R. (Todd Richard)

    2014-01-01T23:59:59.000Z

    The focus of this thesis work is the application of non-equilibrium thermodynamics in lithium-ion battery modeling. As the demand for higher power and longer lasting batteries increases, the search for materials suitable ...

  2. ELLIPSOMETRY OF SURFACE LAYERS ON LEAD AND LITHIUM

    E-Print Network [OSTI]

    Peters, Richard Dudley

    2011-01-01T23:59:59.000Z

    obtained from corrosion of lead in sulfuric acid. DimensionlC2.430 References L Bode, Lead teries (Wiley-Interscienceof Surface Layers on Lead and Lithium By Richard Dudley

  3. LITHIUM--1999 46.1 By Joyce A. Ober

    E-Print Network [OSTI]

    data (table 1). Chemetall Foote Corp., a subsidiary of the German company, Chemetall GmbH, produced in Kings Mountain, NC. Chemetall Foote also produced lithium carbonate at a brine deposit in Chile. FMC

  4. LITHIUM--2001 46.1 By Joyce A. Ober

    E-Print Network [OSTI]

    were withheld from publication to avoid disclosing company proprietary data (table 1). Chemetall Foote Corp. (a subsidiary of the German company Chemetall GmbH) produced lithium carbonate from brines near

  5. LITHIUM--2000 47.1 By Joyce A. Ober

    E-Print Network [OSTI]

    publication to avoid disclosing company proprietary data (table 1). Chemetall Foote Corp., a subsidiary of the German company Chemetall GmbH, produced lithium carbonate from brines near Silver Peak, NV. The company

  6. DEFECTS, PHASE TRANSFORMATIONS AND MAGNETIC PROPERTIES OF LITHIUM FERRITE

    E-Print Network [OSTI]

    Mishra, Raja Kishore

    2011-01-01T23:59:59.000Z

    International Conf. on Ferrites, Y. Hoshino, et al. , eds. ,Fine-Structure: . Lithium Ferrite (Li 20.Fe 0 )1I, Phys.Transformation in Cobalt Ferrites ll Eng. , ~'ater. Sci. H.

  7. Arsenic Trisulfide on Lithium Niobate Devices for Infrared Integrated Optics

    E-Print Network [OSTI]

    Xia, Xin

    2012-07-16T23:59:59.000Z

    Arsenic trisulfide (As?S?) waveguide devices on lithium niobate substrates (LiNbO?) provide a set of compact and versatile means for guiding and manipulating optical modes in infrared integrated optical circuits, including the integrated trace gas...

  8. Composite Electrodes for Rechargeable Lithium-Ion Batteries ...

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

    Composite Electrodes for Rechargeable Lithium-Ion Batteries Technology available for licensing: Electrodes having composite xLi2M'O3(1-x)LiMO2 structures in which an...

  9. Lithium-Titanium-Oxide Anodes Improve Battery Safety and Performance...

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

    Lithium-Titanium-Oxide Anodes Improve Battery Safety and Performance Technology available for licensing: Li4Ti5O12 spinel is a promising alternative to graphite electrodes with...

  10. Lithium sulfide compositions for battery electrolyte and battery electrode coatings

    DOE Patents [OSTI]

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

    2014-10-28T23:59:59.000Z

    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.

  11. New Opportunities for Lithium and Oxygen Spectroscopy in Working...

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

    New Opportunities for Lithium and Oxygen Spectroscopy in Working Batteries Using Inelastic X-ray Scattering T. T. Fister, P. Fenter, M. Balasubramanian, N. Karan, M. Chan, and J....

  12. Electron-nuclear entanglement in the cold lithium gas

    E-Print Network [OSTI]

    Guo-Qiang Zhu; Jun-Wen Mao; You-Quan Li

    2005-04-14T23:59:59.000Z

    We study the ground-state entanglement and thermal entanglement in the hyperfine interaction of the lithium atom. We give the relationship between the entanglement and both temperature and external magnetic fields.

  13. Autonomic Shutdown of Lithium-Ion Batteries Using Thermoresponsive...

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

    Autonomic Shutdown of Lithium-Ion Batteries Using Thermoresponsive Microcapsules M. Baginska, B.J. Blaiszik, R.J. Merriman, J.S. Moore, N. R. Sottos, and S.R. White, University of...

  14. Lithium sulfide compositions for battery electrolyte and battery electrode coatings

    SciTech Connect (OSTI)

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

    2013-12-03T23:59:59.000Z

    Methods of forming lithium-containing electrolytes are provided using wet chemical synthesis. In some examples, the lithium containing electroytes 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 or .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.

  15. Fail Safe Design for Large Capacity Lithium-ion Batteries

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

    Fail Safe Design for Large Capacity Lithium-ion Batteries NREL Commercialization & Tech Transfer Webinar March 27, 2011 Gi-Heon Kim gi-heon.kim@nrel.gov John Ireland, Kyu-Jin Lee,...

  16. New lithium cuprates for the promotion of directed organic transformations

    E-Print Network [OSTI]

    Harford, Philip James

    2014-10-07T23:59:59.000Z

    understanding. This thesis begins with a discussion of the history of DoM covering firstly monometallic lithium bases before moving to bimetallic magnesiate, zincate, aluminate, manganate bases and finally covering cuprate bases, which are the focus...

  17. Stabilized Lithium Metal Powder, Enabling Material and Revolutionary...

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

    -- Washington D.C. es011yakovleva2010o.pdf More Documents & Publications Stabilized Lithium Metal Powder, Enabling Material and Revolutionary Technology for High Energy Li-ion...

  18. Liquid Lithium Wall Experiments in CDX-U

    SciTech Connect (OSTI)

    R. Doerner; R. Kaita; R. Majeski; S. Luckhardt; et al

    1999-10-01T23:59:59.000Z

    The concept of a flowing lithium first wall for a fusion reactor may lead to a significant advance in reactor design, since it could virtually eliminate the concerns with power density and erosion, tritium retention, and cooling associated with solid walls. Sputtering and erosion tests are currently underway in the PISCES device at the University of California at San Diego (UCSD). To complement this effort, plasma interaction questions in a toroidal plasma geometry will be addressed by a proposed new groundbreaking experiment in the Current Drive eXperiment-Upgrade (CDX-U) spherical torus (ST). The CDX-U plasma is intensely heated and well diagnosed, and an extensive liquid lithium plasma-facing surface will be used for the first time with a toroidal plasma. Since CDX-U is a small ST, only approximately1 liter or less of lithium is required to produce a toroidal liquid lithium limiter target, leading to a quick and cost-effective experiment.

  19. Ab-initio study of cathode materials for lithium batteries

    E-Print Network [OSTI]

    Reed, John Stuart, 1968-

    2003-01-01T23:59:59.000Z

    Using first principles calculations the effect of electronic structure on the stability of positive electrode materials for lithium rechargeable batteries is investigated. The investigation focuses upon lithiated ?-NaFeO? ...

  20. Process for manufacturing a lithium alloy electrochemical cell

    DOE Patents [OSTI]

    Bennett, William R. (North Olmstead, OH)

    1992-10-13T23:59:59.000Z

    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.