National Library of Energy BETA

Sample records for li ca tion

  1. The SpallaTion

    Energy Savers [EERE]

    SpallaTion neuTron Source projecT When the Department of Energy (DOE) set out in the 1990s to develop a neutron scattering research facility that was ten times more powerful than the state of the art, the concept for the project that it chose was as ambitious as the scientific capability it sought to deliver. The Spallation Neutron Source (SNS) Project called for unprecedented collaboration among six national laboratories as well as significant research and development that would push the

  2. CUSSSFIC4TION CMUXLLq

    Office of Legacy Management (LM)

    CUSSSFIC4TION CMUXLLq RITE AUG 1 7 1962 Fcx the Atomic. Energy Commisaion~ Chief. Declaseifle@tlon Brar\qh F-mm A. B. Grsaingsr (Other ends tifmtioel) The die wae foutq3 to workvery satiafactorilywiti thlanew Qpeof incert, andncm,of tbepmvLouedsfeotaofeoo+tH&' iOitYwaslmd. D&e& ._: . . ..YG ~Kl.3. i>ro;rid3 -&I:: clcsuro on bct.k.mds of the .plece m & Die #l, is also to be tried outoo 4zgust22. Barr~l~or~~~Die~~hadalaobeenawlLfiedta' plwidesd~do~-

  3. CLASSIFICdTION CAWXL~ DAm

    Office of Legacy Management (LM)

    CLASSIFICdTION CAWXL~ DAm NAR 6 1969 For the Atomic EhergY hDh=+= ,' ROBERT L JACKSON /(\' t' for the Chief, Declassification B~Jx~

  4. Optically pumped cerium-doped LiSrAlF{sub 6} and LiCaAlF{sub 6}

    DOE Patents [OSTI]

    Marshall, C.D.; Payne, S.A.; Krupke, W.F.

    1996-05-14

    Ce{sup 3+}-doped LiSrAlF{sub 6} crystals are pumped by ultraviolet light which is polarized along the c axis of the crystals to effectively energize the laser system. In one embodiment, the polarized fourth harmonic light output from a conventional Nd:YAG laser operating at 266 nm is arranged to pump Ce:LiSrAlF{sub 6} with the pump light polarized along the c axis of the crystal. The Ce:LiSrAlF{sub 6} crystal may be placed in a laser cavity for generating tunable coherent ultraviolet radiation in the range of 280-320 nm. Additionally, Ce-doped crystals possessing the LiSrAlF{sub 6} type of chemical formula, e.g. Ce-doped LiCaAlF{sub 6} and LiSrGaF{sub 6}, can be used. Alternative pump sources include an ultraviolet-capable krypton or argon laser, or ultraviolet emitting flashlamps. The polarization of the pump light will impact operation. The laser system will operate efficiently when light in the 280-320 nm gain region is injected or recirculated in the system such that the beam is also polarized along the c axis of the crystal. The Ce:LiSrAlF{sub 6} laser system can be configured to generate ultrashort pulses, and it may be used to pump other devices, such as an optical parametric oscillator. 10 figs.

  5. Optically pumped cerium-doped LiSrAlF.sub.6 and LiCaAlF.sub.6

    DOE Patents [OSTI]

    Marshall, Christopher D. (Livermore, CA); Payne, Stephen A. (Castro Valley, CA); Krupke, William F. (Pleasanton, CA)

    1996-01-01

    Ce.sup.3+ -doped LiSrAlF.sub.6 crystals are pumped by ultraviolet light which is polarized along the c axis of the crystals to effectively energize the laser system. In one embodiment, the polarized fourth harmonic light output from a conventional Nd:YAG laser operating at 266 nm is arranged to pump Ce:LiSrAlF.sub.6 with the pump light polarized along the c axis of the crystal. The Ce:LiSrAlF.sub.6 crystal may be placed in a laser cavity for generating tunable coherent ultraviolet radiation in the range of 280-320 nm. Additionally, Ce-doped crystals possessing the LiSrAlF.sub.6 type of chemical formula, e.g. Ce-doped LiCaAlF.sub.6 and LiSrGaF.sub.6, can be used. Alternative pump sources include an ultraviolet-capable krypton or argon laser, or ultraviolet emitting flashlamps. The polarization of the pump light will impact operation. The laser system will operate efficiently when light in the 280-320 nm gain region is injected or recirculated in the system such that the beam is also polarized along the c axis of the crystal. The Ce:LiSrAlF.sub.6 laser system can be configured to generate ultrashort pulses, and it may be used to pump other devices, such as an optical parametric oscillator.

  6. Progress in the material development of LiCaAlF sub 6 :Cr sup 3+ laser crystals

    SciTech Connect (OSTI)

    Michelle D. Shinn.; Chase, L.L.; Caird, J.A.; Payne, S.A.; Atherton, L.J.; Kway, W.L.

    1990-03-01

    High Cr{sup 3+} doping levels, up to 8 mole percent, and low losses have been obtained with the tunable solid-state laser material LiCaAlF{sub 6}:Cr{sup 3+} (Cr:LiCAF). Measurements and calculations show that high pumping and extraction efficiencies are possible with the improved material. 13 refs., 4 figs., 1 tab.

  7. UTICA 4, NEW YORK COFIPOR~TION

    Office of Legacy Management (LM)

    DROf fORGE & TOOL UTICA 4, NEW YORK COFIPOR~TION PHONE 3- 2331 July 5, 1955 ?:r. E. J. Block Director of Production Division United Staton Atomic ::norgy Commission Yiashington, D. C. Dear Xr. 1310~1~: Xe had a visit last Thursday from Kr. R. C. Sale11 of the: Atomic Energy Commission who inspected our vacuum melting facilities. EIz suggested that we should get in touch with you and that you r+ht be interested in the use of our facilities for the i>roduction of uranium fuel elements. Xe

  8. Photoluminescence performance of thulium doped Li{sub 4}SrCa(SiO{sub 4}){sub 2} under irradiation of ultraviolet and vacuum ultraviolet lights

    SciTech Connect (OSTI)

    Wang, Zhaofeng; Li, Yezhou; Liu, Xiong; Wei, Xingmin; Chen, Yueling; Zhou, Fei; Wang, Yuhua

    2014-11-15

    Highlights: A novel blue-emitting phosphor Li{sub 4}SrCa(SiO{sub 4}){sub 2}:Tm{sup 3+} was reported. Li{sub 4}SrCa(SiO{sub 4}){sub 2}:Tm{sup 3+} exhibited excellent thermal and irradiation stability. Li{sub 4}SrCa(SiO{sub 4}){sub 2}:Tm{sup 3+} was found to possess high color purity. - Abstract: In this work, we synthesized Tm{sup 3+} doped Li{sub 4}SrCa(SiO{sub 4}){sub 2} phosphors and investigated their photoluminescence properties under the excitation of ultraviolet and vacuum ultraviolet lights. The crystal structure analysis and variation of cell parameters confirm that Tm{sup 3+} ions have been successfully doped in the structure of Li{sub 4}SrCa(SiO{sub 4}){sub 2} host by occupying the sites of Ca{sup 2+} with the coordination number of 6. The luminescence results suggest that Li{sub 4}SrCa(SiO{sub 4}){sub 2}:Tm{sup 3+} is a good blue-emitting phosphor when excited by ultraviolet and vacuum ultraviolet irradiations. In addition, it is observed that there is nearly no degradation for Li{sub 4}SrCa(SiO{sub 4}){sub 2}:Tm{sup 3+} after undergoing thermal and irradiation treatments. Possible mechanisms for the luminescence processes are proposed on the basis of the discussion of excitation and emission spectra. In particular, the emission color of Li{sub 4}SrCa(SiO{sub 4}){sub 2}:Tm{sup 3+} by excitation of 147 and 172 nm irradiations is very close to the standard blue color, suggesting that it could be potentially applied in plasma display panels and mercury-free fluorescence lamps.

  9. LI

    Office of Legacy Management (LM)

    \ LI g. / This document con&s of lf pages. No. 1 &of #copies, Series fl . .! ' \ ' > .b P .--r ' i ' ./' MJDIFICATION NO. k sUPPLEMENTALAMw24ENrto CONTRACT NO. A T (30-l)-1335 M O D IFICATION NO. 4 CONTRACTOR AND A D D m S : KIDIFICATION TO: -EINESTIEUTED CCSTOFWORKr TOTAT,ESTIIUTEDC~T OFWRKI INCREASEIN C O M K rSSI~ OBLlDATIONt NEMTOTALCOMMISSION OBLIOaTIONt PAYl%NTTDBEMADEBY: HORIZONS, INCORPOlZATED R-inceton, New Jersey AIBNDSCOPEOFK#tK,EXTENDTR?M AND OTflER CHANOES $&31,lbOO

  10. Viscosity and density of aqueous solutions of LiBr, LiCl, ZnBr[sub 2], CaCl[sub 2], and LiNO[sub 3]; 1: Single salt solutions

    SciTech Connect (OSTI)

    Wimby, J.M.; Berntsson, T.S. . Dept. of Heat and Power Technology)

    1994-01-01

    New experimental data for the viscosity and density of the binary systems lithium chloride + water, lithium bromide + water, calcium chloride + water, lithium nitrate + water, and zinc bromide + water are presented. Densities are presented in tabular form and as 10-parameter correlations, while kinematic and dynamic viscosities are presented in tabular form. Data are presented in the concentration range from intermediate dilution to close to room temperature crystallization concentration. The temperature ranges are 20--70 C for density and 25--90 C for viscosity. When available, literature data are compared with the new data, and some disagreement is found. New thermogravimetric curves are presented for the dehydration of CaCl[sub 2], ZnBr[sub 2], and LiBr in order to enable evaluation of drying as a composition determination technique.

  11. SANDIA COKPOK4TION SANDIA BASE, .QLDUQUERQUE. N. M.

    Office of Legacy Management (LM)

    SANDIA COKPOK4TION SANDIA BASE, .QLDUQUERQUE. N. M. To : DISTRIBUTION Re: Disposition of t h e Shoal S i t e Attached herewith i s a study which has been made s w g e s t i n g p o s s i b l e f u r t h e r uses of t h e Shoal S i t e . I - ! e have a l s o b r i e f l y described how permanent d i s p o s i t i o n might be made. The study has been made with t h e hope t h a t it w i l l evolce f u r t h e r considerc~tion of t h e s i t e and l e a d t o a plan f o r continued use and eventual

  12. Ca

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

    P O. Box 3090 Ca rlsbad, New Mexico 88221 Mr. John Kieling , Acting Bureau Chief Hazardous Waste Bureau MAY 1 6 2012 New Mexico Environment Department 2905 E. Rodeo Park Drive,...

  13. Effects of Ti-Based Additives on the Hydrogen Storage Properties of aLiBH4/CaH2Destabilized System

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

    Yang, Hongwei; Ibikunle, Adeola; Goudy, Andrew J.

    2010-01-01

    The hydrogen storage properties of a destabilizedLiBH4/CaH2system ball-milled withTiCl3,TiF3, andTiO2additives have been investigated. It is found that the system withTiCl3additive has a lower dehydrogenation temperature than the ones with other additives. Further study shows that a higher amount ofTiCl3is more effective in reducing the desorption temperature of theLiBH4/CaH2system, since it leads to a lower activation energy of dehydrogenation. The activations energies for mixtures containing 4, 10, and 25?mol% ofTiCl3are 141, 126, and 110?kJ/mol, respectively. However, the benefits of higher amounts ofTiCl3are offset by a larger reduction in hydrogen capacity of the mixtures.

  14. Ca

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

    P O. Box 3090 Ca rlsbad, New Mexico 88221 Mr. John Kieling , Acting Bureau Chief Hazardous Waste Bureau MAY 1 6 2012 New Mexico Environment Department 2905 E. Rodeo Park Drive, Bldg . 1 Santa Fe, New Mexico 87505-6303 Subject: Transmittal of the Waste Isolation Pilot Plant Revised Calendar Year 2005-2008 Culebra Potentiometric Surface Map Package Dear Mr. Kieling: On August 5 , 2011 , the New Mexico Environmental Department (NMED) approved the Groundwater Work Plan submitted as a condition to

  15. First principles DFT study of ferromagnetism in SnO{sub 2} induced by doped group 1A and 2A non-magnetic elements X (X=Li, Na, K, Be, Mg, Ca)

    SciTech Connect (OSTI)

    Chakraborty, Brahmananda Ramaniah, Lavanya M.

    2014-04-24

    Transition metal - free - ferromagnetism in diluted magnetic semiconductors (DMS) is of much current interest in the search for more efficient DMS materials for spintronic applications. Here, we report the results of our first principles density functional theory (DFT) study on impurity - induced ferromagnetism in non-magnetic SnO{sub 2} by a non-magnetic impurity. The impurities considered are sp-type of group 1A and 2A elements X (X = Li, Na, K, Be, Mg, Ca). Even a single atom of the group 1A elements makes the system magnetic, whereas for the group 2A elements Ca and Mg, a higher doping is required to induce ferromagnetism. For all the elements studied, the magnetic moment appears to increase with the doping concentration, at least at certain impurity separations, which is a positive indicator for practical applications.

  16. 07Li

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

    Li Thermal Neutron Capture Evaluated Data Measurements 1967RA24: 6Li(n, ), E thermal; measured E; deduced Q. 1968SP01: 6Li(n, ), E thermal; measured E, I; deduced Q....

  17. 08Li

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

    Thermal Neutron Capture Evaluated Data Measurements 1967RA24: 7Li(n, ), E thermal; measured E; deduced Q. 1973JUZT, 1973JUZU: 7Li(n, ), E thermal; measured (E). 7Li...

  18. 9Li

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

    deduced log ft, Gamow-Teller transition strength, level width, di-neutron, neutron halo roles. 1991LUZZ: 9Li(-); measured T12. 1992LI24: 9Li(-); measured NMR...

  19. 5Li

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

    Li Ground-State Decay Evaluated Data Measured Ground-State Γcm for 5Li Adopted value: 1.23 MeV (2002TI10) Measured Mass Excess for 5Li Adopted value: 11680 ± 50 keV (2003AU02) Measurements 1960BA45: 5Li; measured not abstracted; deduced nuclear properties. 1960BR10: 5Li; measured not abstracted; deduced nuclear properties. 1960BR19: 5Li; measured not abstracted; deduced nuclear properties. 1960HA14: 5Li; measured not abstracted; deduced nuclear properties. 1960PE14: 5Li; measured not

  20. 11Li

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

    deduced log ft, Gamow-Teller transition strength, level width, di-neutron, neutron halo roles. 1992LI24: 11Li(-); measured NMR asymmetry; deduced quadrupole moment ratio....

  1. Structure and microwave dielectric characteristics of lithium-excess Ca{sub 0.6}Nd{sub 0.8/3}TiO{sub 3}/(Li{sub 0.5}Nd{sub 0.5})TiO{sub 3} ceramics

    SciTech Connect (OSTI)

    Zhou, Changrong; Chen, Guohua; Cen, Zhenyong; Yuan, Changlai; Yang, Yun; Li, Weizhou

    2013-11-15

    Graphical abstract: - Highlights: Dense ceramics were fabricated by the conventional solid-state route. Excess-Li addition lowers sintering temperature. Excess-Li addition improves the relative density and microwave dielectric properties. - Abstract: Compositions based on (1?x)Ca{sub 0.6}Nd{sub 8/3}TiO{sub 3}?x(Li{sub 1/2}Nd{sub 1/2})TiO{sub 3} + yLi (CNLNTx + yLi, x = 0.300.60, y = 00.05), suitable for microwave applications have been developed by systematically adding excess lithium in order to tune the microwave dielectric properties and lower sintering temperature. Addition of 0.03 excess-Li simultaneously reduced the sintering temperature and improved the relative density of sintered CNLNTx ceramics. The excess Li addition can compensate the evaporation of Li during sintering process and decrease the secondary phase content. The CNLNTx (x = 0.45) ceramics with 0.03 Li excess sintered at 1190 C have single phase orthorhombic perovskite structure, together with the optimum combination of microwave dielectric properties of ?{sub r} = 129, Q f = 3600 GHz, ?{sub f} = 38 ppm/C. Obviously, excess-Li addition can efficiently decrease the sintering temperature and improve the microwave dielectric properties. The high permittivity and relatively low sintering temperatures of lithium-excess Ca{sub 0.6}Nd{sub 0.8/3}TiO{sub 3}/(Li{sub 0.5}Nd{sub 0.5})TiO{sub 3} ceramics are ideal for the development of low cost ultra-small dielectric loaded antenna.

  2. Thermal Stability of LiPF 6 Salt and Li-ion Battery Electrolytes Containing LiPF

    Office of Scientific and Technical Information (OSTI)

    Thermal Stability of LiPF 6 Salt and Li-ion Battery Electrolytes Containing LiPF 6 Hui Yang a, *, Guorong V. Zhuang b, * ,z and Philip N. Ross, Jr. b, * Environmental Energy Technologies Division a and Materials Sciences Division b Lawrence Berkeley National Laboratory University of California, Berkeley, CA 94720 Abstract The thermal stability of the neat LiPF 6 salt and of 1 molal solutions of LiPF 6 in prototypical Li-ion battery solvents was studied with thermogravimetric analysis (TGA) and

  3. 10Li

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

    measured proton spectra, (). 10Li deduced spectroscopic factors. 2007SI24: C(11Li, nx), E 264 MeVnucleon; measured neutron energies and yields, as a function of...

  4. 4Li

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

    vs relative E(3He, n), E(3He, p); deduced . 4Li deduced levels, . 1996ED02: 4He(p, nX), E 100, 200 MeV; measured inclusive (, En). 4Li deduced evidence for narrow...

  5. NMR Studies of the Vanadium Spin Dynamics and Spin Structure in LiV2O4, CaV2O4, and (LixV1-x)3BO5 (x is almost equal to 0.33, 0.40)

    SciTech Connect (OSTI)

    Xiaopeng Zong

    2007-12-01

    Strong electron correlation is believed to be an essential and unifying factor in diverse properties of condensed matter systems. Ground states that can arise due to electron correlation effects include Mott insulators, heavy fermion, ferromagnetism and antiferromagnetism, spin glasses, and high-temperature superconductivity. The electronic systems in transition metal oxide compounds are often highly correlated. In this thesis, the author presents experimental studies on three strongly correlated vanadium oxide compounds: LiV{sub 2}O{sub 4}, (Li{sub x}V{sub 1-x}){sub 3}BO{sub 5}, and CaV{sub 2}O{sub 4}, which have completely different ground states.

  6. 8Li

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

    -asymmetry, NMR; deduced polarization. 1986WA01: 8Li(-); analyzed -delayed breakup -spectra; deduced intruder states role. 8Be deduced level, , Gamow-Teller matrix...

  7. LI I

    Office of Legacy Management (LM)

    LI I (I LI 1 m r - m " P pr II II I I c - 81-r J-7 . ba OAK RCEIGE MBTSC3NAL liJM!DRAT~F-zY OPERATED OY OPERATED OY MAflTlN MAHlETTA @El&Y ?Z!SEMS, HE. MAflTlN MAHlETTA @El&Y ?Z!SEMS, HE. FOR THE UNfTEfl STATES FOR THE UNfTEfl STATES ORNL/RASA-88/59 RESULTS OF THE RADIOLOGICAL SURVEY AT DIEBOLD SAFE COMPANY, 1550 GRAND BOULEVARD, HAMILTON, OHIO (HOOol) R. D. Foley L. M. Floyd OEPARTMENT Of ENERGY This report has been reproduced directly from the best available copy. Available to DOE

  8. C: LI

    Office of Legacy Management (LM)

    C: LI c1 T - P- LI m m m c I C F II c( L e3 I 7 ,' r,L .zpl I-' . "* IL.8 -1 p @ z> Cerfification Docket for the Remedid Action Performed at the G ranite City Site in G ranite City, Illinois, June 7993 Department of Energy Former Sites Restoration Division Oak Ridge Operations O ffice September 7994 613 Printed on recycledhcydable paper. 4.1514023.6 .- CERTIFICATION DOCKET FOR THE REMEDIAL ACTION PERFORMED AT THE GRANITE CITY SITE IN GRANITE CITY, ILLINOIS, JUNE 1993 SEPTEMBER 1994

  9. F LI

    Office of Legacy Management (LM)

    >"- -- F LI c ------- RADIATION SURVEY REPORT OF THE M IDDLESEX LANDFILL SITE RADIATION SURVEY REPORT OF THE ~IDDLESEX LfiMDFI.LL S I:TE it%RCH 25 - AFRiL 4, 1374 ;)UNE 27, 1974 T.!BLE OF CONTENTS Introduction and Summary . . . . . . . . . . . . . . . 1 Conclusions. . . . . . w . . . . . . , . . . , . . . . 2 Histohcal Background0 . . . . . . . . . . . . b (I . . 2 Description of Area Surveyed . . . . . . . . I . . . * 3 Survey Findings. * *,. a . . . , . . . . . . . . . . . 4 Surface

  10. 6Li General Tables

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

    Li General Table The General Table for 6Li is subdivided into the following categories: Ground State Properties of 6Li Special States Theoretical Shell Model Cluster Models Complex...

  11. 7Li Cross Section

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

    7Li(, '): emission yield 1.0 - 3.4 1 01182012 2011YA02 7Li(, ): elastic scattering differential 1.0 - 4.5 cm 170 07192011 7Li(, p): differential...

  12. X-ray absorption studies of mixed salt polymer electrolytes: ZnBr{sub 2}/CaBr{sub 2}-PEO, ZnBr{sub 2}/LiBr-PEO, and ZnBr{sub 2}/RbBr-PEO complexes

    SciTech Connect (OSTI)

    McBreen, J.; Yang, X.Q.; Lee, H.S.; Okamoto, Y.

    1995-02-01

    Polyethylene oxide (PEO)-salt systems are an important new class of electrolytes that are being considered for many uses. X-ray absorption (XAS) studies of ZnBr{sub 2}-PEO complexes, at the Zn K edge, at temperatures between 25 and 120 C, indicate that additions of bromide salts of Li, Rb, or Ca result in the formation of ZnBr{sub 4}{sup {minus} 2} complexes with a Zn-Br bond length of 2.42 {angstrom}. XAS, at the Rb K edge, in mixed RbBr/ZnBr{sub 2}-PEO complexes with an excess of ZnBr{sub 2}, shows that the ZnBr{sub 2} causes the RbBr to dissolve in the polymer. The Rb{sup +} ions are weakly complexed with the PEO with an Rb-O bond distance of 2.93 {angstrom}.

  13. 5Li General Tables

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

    Table for 5Li is subdivided into the folowing categories: Ground State Properties Cluster Model Shell Model Special States Model Calculations Model Discussions Complex...

  14. THE HIGH TEMPERATURE CHEMICAL REACTIVITY OF LI2O

    SciTech Connect (OSTI)

    Kessinger, G.; Missimer, D.

    2009-11-13

    The ultimate purpose of this study was to investigate the use of a Li-Ca mixture for direct reduction of actinide oxides to actinide metals at temperatures below 1500 C. For such a process to be successful, the products of the reduction reaction, actinide metals, Li{sub 2}O, and CaO, must all be liquid at the reaction temperature so the resulting actinide metal can coalesce and be recovered as a monolith. Since the established melting temperature of Li{sub 2}O is in the range 1427-1700 C and the melting temperature of CaO is 2654 C, the Li{sub 2}O-CaO (lithium oxidecalcium oxide) pseudo-binary system was investigated in an attempt to identify the presence of low-melting eutectic compositions. The results of our investigation indicate that there is no evidence of ternary Li-Ca-O phases or solutions melting below 1200 C. In the 1200-1500 C range utilizing MgO crucibles, there is some evidence for the formation of a ternary phase; however, it was not possible to determine the phase composition. The results of experiments performed with ZrO{sub 2} crucibles in the same temperature range did not show the formation of the possible ternary phase seen in the earlier experiment involving MgO crucibles, so it was not possible to confirm the possibility that a ternary Li-Ca-O or Li-Mg-O phase was formed. It appears that the Li{sub 2}O-CaO materials reacted, to some extent, with all of the container materials, alumina (Al{sub 2}O{sub 3}), magnesia (MgO), zirconia (ZrO{sub 2}), and 95% Pt-5% Au; however, to clarify the situation additional experiments are required. In addition to the primary purpose of this study, the results of this investigation led to the conclusions that: (1) The melting temperature of Li{sub 2}O may be as low as 1250 C, which is considerably lower than the previously published values in the range 1427-1700 C; (2) Lithium oxide (Li{sub 2}O) vaporizes congruently; (3) Lithium carbonate and Li2O react with 95% Pt-5% Au, and also reacts with pure Pt; and (4) It is likely that some or all of the past high temperature phase behavior and vaporization experiments involving Li{sub 2}O(s) at temperatures above 1250 C have actually involved Li{sub 2}O(l). If these past measurements were actually measurements performed on Li{sub 2}O(l) instead of the solid, the thermochemical data for phases and species in the Li-O system will require reevaluation.

  15. CA.0

    Office of Legacy Management (LM)

    of_f$ergy Washington, DC 20545 *. CA.0 MAY 2 9 1987 .r ,. Hr. Carl Schafer Director of Environmental Poli,cy Office of the Deputy Assistant Secretary of Defense for Installations Pentagon . ..&&&.@.&&;-D.C. 20301 Dear Mr.~:Schafer: As you know, the Department of Ene,rgy (DOE) is implementing a program to identify sites that may be radiologically contaminated as a result of DOE predecessor operations and to correct any pioblems associated with this contamination if there is

  16. 6Li Cross Section

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

    α, X) (Current as of 02/01/2016) NSR Reaction Eα (MeV) Cross Section File X4 Dataset Date Added 1985NE05 6Li(α, γ): γ thick target yield resonance X4 02/15/2012 1966FO05 6Li(α, γ): σ 0.9 - 3.0 2 < Eγ < 4 MeV, 4 < Eγ < 7 MeV, thick target capture γ-ray yield, capture γ-ray yield of 2.43 MeV resonance 02/29/2012 1989BA24 6Li(α, γ): σ 1.085, 1.175 X4 02/15/2012 1979SP01 6Li(α, γ): thick target yield curve for 718 keV γ-rays 1140 - 1250 keV 1175 keV resonance 07/19/2011

  17. 6Li Cross Section

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

    p, X) (Current as of 12152015) NSR Reaction Ep (MeV) Cross Section File X4 Dataset Date Added 2004TU02 6Li(p, ): coincidence yields, deduced S-factors low 1, S-factors from...

  18. 7Li Cross Section

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

    p, X) (Current as of 12162015) NSR Reaction Ep (MeV) Cross Section File X4 Dataset Date Added 1997GO13 7Li(pol. p, ): total , S-factor for capture to third-excited state 0 -...

  19. 10Li General Tables

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

    Li General Table The General Table for 10Li is subdivided into the following categories: Reviews Theoretical Ground State Properties Shell Model Cluster Model Other Models Special States Astrophysical Electromagnetic Transitions Hypernuclei Photodisintegration Light-Ion and Neutron Induced Reactions These General Tables correspond to the 2003 preliminary evaluation of ``Energy Levels of Light Nuclei, A = 10''. The prepublication version of A = 10 is available on this website in PDF format: A =

  20. Jennifer Li | Photosynthetic Antenna Research Center

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

    Jennifer Li Jennifer Li Jennifer Li E-mail: jennifer.li@wustl.edu Website: Washington University Undergraduate student enrolled in the PARC/I-CARES Certificate of Accomplishment in Renewable Energy & the Environment. Undergraduate

  1. C LI CI

    Office of Legacy Management (LM)

    LI CI - - 11 C LI I I Mb II II OAK RIDGE NATIONAL LABORATORY UPERml BY M A R T IN M A R IETTA ENERGY S Y S T E M S , INC. FOR THE UNfTEG STATES OEPARTMENT OF ENERGY ORNLITM-10007 RADIOLOGICAL SURVEY OF THE PERIMETER FENCE LINE OF THE FORMER COTTER SITE, HAZELWOOD, M ISSOURI (LM002) R. F. Carrier W . D. Cottrell FILE COPY This report was prepared as an account of work sponsored by an agency of the UnitedStatesGovernment. NeithertheUnitedStatesGovernment noranyagency thereof, nor any of their

  2. Li Tec | Open Energy Information

    Open Energy Info (EERE)

    Drezden, Germany Product: Based in Kamez, near Dresden, Li-Tec produces components for lithium-ion batteries. References: Li-Tec1 This article is a stub. You can help OpenEI by...

  3. I!' L;I)

    Office of Legacy Management (LM)

    ".>;jy i.~jp.~[~~ i,Zz>-c C,+;) ir,i:%J :' 0 p 'd-i I /) f) ic.c iq -.I ,'c i - * w. 3'2 , phi ': r-t;, ; *.i .; I!' L;I) --, -II s;.,yE;J-~,~;~* I' ;, f: >,p.yg ,p ' .L (3 i!>;' !i.3 y/y!-; x>:-y rJgbf;..qp: \' :sF*:l,' 5-".13, -9 _ ..-;~c~-' ~;Li;-~~~~;, 3h' ;[;i-y ; c; ' 1' 1.b y&k' 2 1 , . ..l =i. 1; G.1 ;Tr.; .j. i-:. I qr:i.gky, M,C. Jp, 2.1 F... ii, Ross CENTRAL F ILES ~"CTIVE OF TXIP m --w- The 0' 0 jet% ive Of this trip xas to evaluate tkie !- .zalth

  4. Microsoft Word - Li_FinalReport_FASTER.doc

    Office of Scientific and Technical Information (OSTI)

    ATTN: ASR Program Managers, Drs. Dorothy Koch Climate and Environmental Sciences Division Office of Biological and Environmental Research Department of Energy 19901 Germantown Road Germantown, MD20874 Title of Research Project: Continuous Evaluation of Fast Processes in Climate Models Using ARM Measurements Investigator: Zhijin Li, Researcher Joint Institute for Regional Earth System Science and Engineering, UCLA 9258 Boelter Hall, Los Angeles, CA 90095 Phone: (310) 794-5273; Fax: (310)943-1656

  5. 7Li MRI of Li batteries reveals location of microstructural lithium...

    Office of Scientific and Technical Information (OSTI)

    SciTech Connect Search Results Journal Article: 7Li MRI of Li batteries reveals location of microstructural lithium Citation Details In-Document Search Title: 7Li MRI of Li ...

  6. DOE - Office of Legacy Management -- Berkeley CA Site - CA 03

    Office of Legacy Management (LM)

    Berkeley CA Site - CA 03 FUSRAP Considered Sites Berkeley, CA Alternate Name(s): University of California Gilman Hall, University of California CA.03-1 Location: Gilman Hall, University of California, Berkeley, California CA.03-1 Historical Operations: Performed research and development on the synthesis and production of plutonium, resulting in uranium, plutonium, cesium and americium contamination. CA.03-3 CA.03-5 Eligibility Determination: Eligible CA.03-1 CA.03-2 Radiological Survey(s):

  7. UJ LiJ

    Office of Legacy Management (LM)

    o >- tD o UJ :> LiJ o W ~ Central Nevada-23 UNITED STATES DEPARTMENT OF THE INTERIOR GEOLOGICAL SURVEY Federal Center, Denver, Colorado 80225 ANALYSIS OF HYDRAULIC TESTS IN HOT CREEK VALLEY, NEVADA June 1970 Open-file report Prepared Under Contract AT(29-2)-474 for the Nevada Operations Office U.S. Atomic Energy Commission USGS-474-82 DISCLAIMER This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor

  8. Li2ikk+

    Office of Legacy Management (LM)

    Li2ikk+ 0/-/.3~+ ' Department of Energy Washington, DC 20585 m 19 1999 Mr. William R. Augustine Deputy Chief Programs Management Division U.S. Army Corps of Engineers Depanment of the Army Washington. D.C. 203 14-1000 Dear Mr. Augustine: I am writing to you as a follow-up to discussions our staffs have had regarding two former Department of the Army facilities in the Formerly Used Defense Sites (FUDS) program where the former Atomic Energy Commission (AEC) also conducted activities. These sites

  9. A=11Li (2012KE01)

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

    E(11Li) 246 MeVA, analysis of a complete three-body kinematical measurement of 11Li breakup on a 12C target indicates the reaction mechanism is 11Li inelastic scattering to...

  10. Liang Li | Argonne National Laboratory

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

    Liang Li Postdoctoral Appointee (Supervisor, Maria Chan) Current research focuses on ab-initio theoretical studies on hybrid lithium-ion/lithium-oxygen battery materials and photocatalytic reduction of CO2. Telephone 630.252.2788 Fax 630.252.4646 E-mail liangli@anl.gov CV/Resume PDF icon Liang_Li

  11. Lithium Salts for Advanced Lithium Batteries: Li-metal, Li-O2, and Li-S

    SciTech Connect (OSTI)

    Younesi, Reza; Veith, Gabriel M; Johansson, Patrik; Edstrom, Kristina; Vegge, Tejs

    2015-01-01

    Presently lithium hexafluorophosphate (LiPF6) is the dominant Li-salt used in commercial rechargeable lithium-ion batteries (LIBs) based on a graphite anode and a 3-4 V cathode material. While LiPF6 is not the ideal Li-salt for every important electrolyte property, it has a uniquely suitable combination of properties (temperature range, passivation, conductivity, etc.) rendering it the overall best Li-salt for LIBs. However, this may not necessarily be true for other types of Li-based batteries. Indeed, next generation batteries, for example lithium-metal (Li-metal), lithium-oxygen (Li-O2), and lithium sulphur (Li-S), require a re-evaluation of Li-salts due to the different electrochemical and chemical reactions and conditions within such cells. This review explores the critical role Li-salts play in ensuring in these batteries viability.

  12. Recovery of Li from alloys of Al- Li and Li- Al using engineered scavenger compounds

    DOE Patents [OSTI]

    Riley, W. D. (Albany, OR); Jong, B. W. (Corvallis, OR); Collins, W. K. (Albany, OR); Gerdemann, S. J. (Albany, OR)

    1994-01-01

    A method of producing lithium of high purity from lithium aluminum alloys using an engineered scavenger compound, comprising: I) preparing an engineered scavenger compound by: a) mixing and heating compounds of TiO2 and Li2CO3 at a temperature sufficient to dry the compounds and convert Li.sub.2 CO.sub.3 to Li.sub.2 O; and b) mixing and heating the compounds at a temperature sufficient to produce a scavenger Li.sub.2 O.3TiO.sub.2 compound; II) loading the scavenger into one of two electrode baskets in a three electrode cell reactor and placing an Al-Li alloy in a second electrode basket of the three electrode cell reactor; III) heating the cell to a temperature sufficient to enable a mixture of KCl-LiCl contained in a crucible in the cell to reach its melting point and become a molten bath; IV) immersing the baskets in the bath until an electrical connection is made between the baskets to charge the scavenger compound with Li until there is an initial current and voltage followed by a fall off ending current and voltage; and V) making a connection between the basket electrode containing engineered scavenger compound and a steel rod electrode disposed between the basket electrodes and applying a current to cause Li to leave the scavenger compound and become electrodeposited on the steel rod electrode.

  13. A=14Li (1986AJ01)

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

    86AJ01) (Not illustrated) 14Li has not been observed. The calculated mass excess is 72.29 MeV: see (1981AJ01). 14Li is then particle unstable with respect to decay into 13Li + n and 12Li + 2n by 3.88 and 3.22 MeV, respectively

  14. A=15Li (1981AJ01)

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

    1AJ01) (Not illustrated) 15Li has not been observed: its atomic mass excess is calculated to be 81.60 MeV. It is then unstable with respect to decay into 14Li + n and 13Li + 2n by 1.24 and 3.90 MeV, respectively (1974TH01). See also 13Li

  15. A=9Li (66LA04)

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

    66LA04) (See Energy Level Diagrams for 9Li) GENERAL: See (GR64C). See also Table 9.1 Table of Energy Levels (in PDF or PS). Mass of 9Li: From the Q-value for 7Li(t, p)9Li: Q ...

  16. Women @ Energy: Yan Li | Department of Energy

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

    Yan Li Women @ Energy: Yan Li March 12, 2013 - 9:23am Addthis Yan Li is a Computational Physicist at the Computational Science Center at Brookhaven National Laboratory. Yan Li is a Computational Physicist at the Computational Science Center at Brookhaven National Laboratory. Yan Li is a Computational Physicist at the Computational Science Center at Brookhaven National Laboratory. Her work is mainly focused on developing and applying advanced computational tools to investigate material properties

  17. Women @ Energy: Yan Li | Department of Energy

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

    Yan Li Women @ Energy: Yan Li March 12, 2013 - 9:23am Addthis Yan Li is a Computational Physicist at the Computational Science Center at Brookhaven National Laboratory. Yan Li is a Computational Physicist at the Computational Science Center at Brookhaven National Laboratory. Yan Li is a Computational Physicist at the Computational Science Center at Brookhaven National Laboratory. Her work is mainly focused on developing and applying advanced computational tools to investigate material properties

  18. Anion Coordination Interactions in Solvates with the Lithium Salts LiDCTA and LiTDI

    SciTech Connect (OSTI)

    McOwen, Dennis W.; Delp, Samuel A.; Paillard, Elie; Herriot, Cristelle; Han, Sang D.; Boyle, Paul D.; Sommer, Roger D.; Henderson, Wesley A.

    2014-04-17

    Lithium 4,5-dicyano-1,2,3-triazolate (LiDCTA) and lithium 2-trifluoromethyl-4,5-dicyanoimidazole (LiTDI) are two salts proposed for lithium battery electrolyte applications, but little is known about the manner in which the DCTA- and TDI- anions coordinate Li+ cations. To explore this in-depth, crystal structures are reported here for two solvates with LiDCTA: (G2)1:LiDCTA and (G1)1:LiDCTA with diglyme and monoglyme, respectively, and seven solvates with LiTDI: (G1)2:LiTDI, (G2)2:LiTDI, (G3)1:LiTDI, (THF)1:LiTDI, (EC)1:LiTDI, (PC)1:LiTDI and (DMC)1/2:LiTDI with monoglyme, diglyme, triglyme, tetrahydrofuran, ethylene carbonate, propylene carbonate and dimethyl carbonate, respectively. These latter solvate structures are compared with the previously reported acetonitrile (AN)2:LiTDI structure. The solvates indicate that the LiTDI salt is much less associated than the LiDCTA salt and that the ions in LiTDI, when aggregated in solvates, have a very similar TDI-...Li+ cation mode of coordination through both the anion ring and cyano nitrogen atoms. Such coordination facilitates the formation of polymeric ion aggregates, instead of dimers. Insight into such ion speciation is instrumental for understanding the electrolyte properties of aprotic solvent mixtures with these salts.

  19. A=12Li (1975AJ02)

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

    75AJ02) (Not illustrated) 12Li is not observed in the 4.8 GeV proton bombardment of a uranium target: it is particle unstable (1974BO05). Its atomic mass excess is therefore > 49.0 MeV. (1974TH01) calculate the mass excess of 12Li to be 52.92 MeV. 12Li would then be unstable with respect to 11Li + n, 10Li + 2n and 9Li + 3n by 3.9, 3.68 and 3.74 MeV, respectively. See also (1972TH13, 1973BO30, 1974IR04

  20. A=12Li (1990AJ01)

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

    90AJ01) (Not illustrated) 12Li is not observed in the 4.8 GeV proton bombardment of a uranium target: it is particle unstable. The calculated value of its mass excess is 52.93 MeV [see (1980AJ01)]: 12Li would then be unstable with respect to 11Li + n ,10Li + 2n and 9Li + 3n by 4.01, 2.96 and 3.76 MeV, respectively. The ground state of 12Li is predicted to have Jπ = 2- (1988POZS, 1985PO10; theor.). See also (1980AJ01

  1. Structure of the Ca[superscript 2+]-dependent PP2A heterotrimer and

    Office of Scientific and Technical Information (OSTI)

    insights into Cdc6 dephosphorylation (Journal Article) | SciTech Connect SciTech Connect Search Results Journal Article: Structure of the Ca[superscript 2+]-dependent PP2A heterotrimer and insights into Cdc6 dephosphorylation Citation Details In-Document Search Title: Structure of the Ca[superscript 2+]-dependent PP2A heterotrimer and insights into Cdc6 dephosphorylation Authors: Wlodarchak, Nathan ; Guo, Feng ; Satyshur, Kenneth A ; Jiang, Li ; Jeffrey, Philip D ; Sun, Tingwan ; Stanevich,

  2. Ying Li | Argonne Leadership Computing Facility

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

    Ying Li Margaret Butler Postdoctoral Fellow Ying Li Argonne National Laboratory 9700 S. Cass Avenue Building 240 / Wkstn. 1D21 Argonne, IL 60439 630-252-3394 yingli

  3. A=11Li (1980AJ01)

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

    80AJ01) (See the Isobar Diagram for 11Li) 11Li has been observed in the bombardment of iridium by 24 GeV protons. Its mass excess is 40.94 ± 0.08 MeV (1975TH08). The cross section for its formation is ~ 50 μb (1976TH1A). 11Li is bound: Eb for break up into 9Li + 2n and 10Li + n are 158 ± 80 and 960 ± 250 keV, respectively [see (1979AJ01) for discussions of the masses of 9Li and 10Li]. The half-life of 11Li is 8.5 ± 0.2 msec (1974RO31): it decays to neutron unstable states of 11Be [Pn =

  4. A=18Li (1995TI07)

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

    Li (1995TI07) (Not illustrated) 18Li has not been observed. Shell model calculations described in (1988POZS) predict the ground-state magentic dipole moment and charge and matter...

  5. A=10Li (2004TI06)

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

    2004TI06) (See Energy Level Diagrams for 10Li) GENERAL: References to articles on general properties of 10Li published since the previous review (1988AJ01) are grouped into...

  6. A=5Li (2002TI10)

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

    2002TI10) (See Energy Level Diagrams for 5Li) GENERAL: References to articles on general properties of 5Li published since the previous review (1988AJ01) are grouped into...

  7. A=9Li (2004TI06)

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

    2004TI06) (See Energy Level Diagrams for 9Li) GENERAL: References to articles on general properties of 9Li published since the previous review (1988AJ01) are grouped into...

  8. A=20Li (1998TI06)

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

    Li (1998TI06) (Not observed) See (1977CE05, 1983ANZQ, 1986AN07, 1987SIZX).

  9. A=14Li (1976AJ04)

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

    76AJ04) (Not illustrated) 14Li has not been observed: it is calculated to be particle unstable with a binding energy of -2.66 MeV for decay into 13Li + n and of -3.23 MeV for decay into 12Li + 2n. The calculated mass excess is 72.29 MeV (1974TH01)

  10. A=15Li (1976AJ04)

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

    76AJ04) (Not illustrated) 15Li has not been observed: its atomic mass excess is calculated to be 81.60 MeV. It is then unstable with respect to decay into 14Li + n and 13Li + 2n by 1.24 and 3.90 MeV, respectively (1974TH01)

  11. A=15Li (1986AJ01)

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

    6AJ01) (Not illustrated) 15Li has not been observed. Its atomic mass excess is calculated to be 81.60 MeV: see (1981AJ01). It is then unstable with respect to decay into 14Li + n and 13Li + 2n by 1.24 and 3.90 MeV, repsectively

  12. A=8Li (2004TI06)

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

    p)8Li Qm 0.80079 Angular distributions have been obtained at Et 23 MeV for the proton groups to 8Li*(0, 0.98, 2.26, 6.54 0.03); cm for 8Li*(2.26, 6.54) are 35 10 and 35...

  13. A=8Li (66LA04)

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

    to the geometric value, supports the hypothesis that 7Li may be described as an ( + t) cluster (RO62C). See also (AL63N, BA63O, BR63M, VA64G). 9. 7Li(d, p)8Li Qm -0.192...

  14. A=11Li (1975AJ02)

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

    by GeV protons. Its mass excess is 40.9 0.1 MeV (1973KL1C). 11Li is bound: Eb for breakup into 9Li + 2n and 10Li + n are 0.2 and 0.3 MeV, respectively see (1974AJ01) for a...

  15. A=13Li (1976AJ04)

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

    13Li is predicted to have an atomic mass excess of 61.56 MeV: it is then unstable for breakup into 12Li + n and 11Li + 2n by 0.6 and 4.5 MeV, respectively (1974TH01). The modified...

  16. A=13Li (1981AJ01)

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

    13Li is predicted to have an atomic mass excess of 61.56 MeV: it is then unstable for breakup into 12Li + n and 11Li + 2n by 0.6 and 4.5 MeV, respectively (1974TH01). The modified...

  17. Recovery of Li from alloys of Al-Li and Li-Al using engineered scavenger compounds

    SciTech Connect (OSTI)

    Riley, W.D.; Jong, B.W.; Collins, W.K.; Gerdemann, S.J.

    1992-01-01

    The invention relates to a process for obtaining Li metal selectively recovered from Li-Al or Al-Li alloy scrap by: (1) removing Li from aluminum-lithium alloys at temperatures between about 400 C-750 C in a molten salt bath of KC1-LiCl using lithium titanate (Li2O.3TiO2) as an engineered scavenger compound (ESC); and (2) electrodepositing of Li from the loaded ESC to a stainless steel electrode. By use of the second step, the ESC is prepared for reuse. A molten salt bath is required in the invention because of the inability of molten aluminum alloys to wet the ESC.

  18. A=12Li (1985AJ01)

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

    5AJ01) (Not illustrated) 12Li is not observed in the 4.8 GeV proton bombardment of a uranium target: it is particle-unstable. The calculated value of its mass excess is 52.93 MeV [see (1980AJ01)]: 12Li would then be unstable with respect to 11Li + n, 10Li + 2n and 9Li + 3n by 3.92, 2.96 and 3.76 MeV, respectively. See also (1980AJ01) and (1982KA1D, 1983ANZQ, 1984VA06

  19. A=13Li (1986AJ01)

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

    86AJ01) (Not illustrated) 13Li has not been observed. The calculated value of its mass excess is 60.34 MeV [see (1981AJ01)]: 13Li would then be unstable with respect to 11Li + 2n by 3.26 MeV. (1980BO31) have not observed 13Li in the bombardment of 124Sn by 6.7 GeV protons but state that the statistics were poor in the region of interest and that it is not excluded that 13Li may be stable. See also (1983ANZQ

  20. A=11Li (1985AJ01)

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

    5AJ01) (See the Isobar Diagram for 11Li) GENERAL: The mass excess of 11Li is 40.94 ± 0.08 MeV (1975TH08). [(A.H. Wapstra, private communication) suggests 40.91 ± 0.11 MeV.] Using the value reported by (1975TH08) 11Li is bound with respect to 9Li + 2n by 156 ± 80 keV and with respect to 10Li + n by 966 ± 260 keV [see (1984AJ01) for the masses of 9Li and 10Li]. Systematics suggest Jπ = 1/2- for 11Lig.s.. See also (1979AZ03, 1980AZ01, 1980BO31, 1981BO1X, 1982BO1Y, 1982OG02), (1981HA2C),

  1. A=9Li (59AJ76)

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

    59AJ76) (Not illustrated) Mass of 9Li: From the threshold for 9Be(d, 2p)9Li, Ed = 19 ± 1 MeV (GA51C), the mass excess of 9Li is determined as M - A = 28.1 ± 1 MeV. 1. 9Li(β-)9Be* --> 8Be + n Qm = 12.4 9Li decays to excited states of 9Be which decay by neutron emission. The mean of the reported half-lives is 0.169 ± 0.003 sec (GA51C, HO52B). See also (SH52, FR53A, BE55D, FL56, TA58B). 2. 9Be(d, 2p)9Li Qm = -15.5 The threshold is 19 ± 1 MeV (GA51C). 3. 11B(γ, 2p)9Li Qm = -31.4 See (SH52,

  2. li(1)-98.pdf

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

    23 Radiative Forcing by Smoke Aerosols Determined from Satellite and Surface Measurements Z. Li Canada Centre for Remote Sensing Ottawa, Ontario, Canada L. Kou Intermap Technologies Ottawa, Ontario, Canada Introduction As a potential offsetting agent to the greenhouse effect, aerosols are receiving increasing attention in the atmospheric science community. Notwithstanding, our knowledge of the impact of aerosols on radiation and climate is rather poor and falls well behind that of the greenhouse

  3. li(1)-99.PDF

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

    Consistency Check of Cloud Optical Properties Derived from Satellite and Surface Observations Z. Li, A. P. Trishchenko, and F.-L. Chang Canada Center for Remote Sensing Ottawa, Canada H. W. Barker Atmospheric Environmental Service Downsview, Canada W. B. Sun Dalhousie University Halifax, Nova Scotia, Canada Introduction Much work has been done to retrieve both cloud and radiative variables using space-borne observations. Several recent studies also attempted to retrieve cloud optical depth using

  4. li(2)-98.pdf

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

    7 A Consistency Analysis of ARESE Measurements Regarding Cloud Absorption Z. Li and A. Trishchenko Canada Centre for Remote Sensing Ottawa, Ontario, Canada H. W. Barker Atmospheric Environment Service Downsview, Ontario, Canada G. L. Stephens and P. Partain Colorado State University Fort Collins, Colorado P. Minnis NASA-Langley Research Center Hampton, Virginia Introduction In an attempt to resolve the recent debate over the cloud absorption anomaly, the U.S. Department of Energy sponsored a

  5. A=12Li (1980AJ01)

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

    0AJ01) (Not illustrated) 12Li is not observed in the 4.8 GeV proton bombardment of a uranium target: it is particle unstable. Its atomic mass excess would then be > 49.0 MeV. (1974TH01) calculate the mass excess of 12Li to be 52.92 MeV, while (1975JE02) calculate 52.94 MeV. Taking the average of these two values, 12Li would then be unstable with respect to 11Li + n, 10Li + 2n and 9Li + 3n by 3.92, 2.96 and 3.76 MeV, respectively. See also (1975AJ02) and (1975BE31, 1976IR1B

  6. A=14Li (1991AJ01)

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

    91AJ01) (Not illustrated) 14Li has not been observed. The calculated mass excess is 72.29 MeV: see (1981AJ01). 14Li is then particle unstable with respect to decay into 13Li + n and 12Li + 2n by 3.9 and 3.2 MeV, respectively [see, however, 13Li]. (1985PO10) calculate [in a (0 + 1)ℏω model space] that the first four states of 14Li at 0, 0.75, 1.22 and 1.48 MeV have, respectively, Jπ = 2-, 4-, 3- and 1-. See also (1986AL09, 1989OG1B) and (1988POZS; theor.)

  7. Li-rich anti-perovskite Li3OCl films with enhanced ionic conductivity

    SciTech Connect (OSTI)

    Lu, XJ; Wu, G; Howard, JW; Chen, AP; Zhao, YS; Daemen, LL; Jia, QX

    2014-08-13

    Anti-perovskite solid electrolyte films were prepared by pulsed laser deposition, and their room-temperature ionic conductivity can be improved by more than an order of magnitude in comparison with its bulk counterpart. The cyclability of Li3OCl films in contact with lithium was evaluated using a Li/Li3OCl/Li symmetric cell, showing self-stabilization during cycling test.

  8. Microsoft PowerPoint - Electrolytic T Extraction in Molten Li-LiT_2.pptx

    Office of Environmental Management (EM)

    Electrolytic Tritium Extraction in Molten Li-LiT Luke Olson Brenda L. García-Díaz Hector Colon-Mercado Joe Teprovich Dave Babineau Savannah River National Laboratory Fall 2015 Tritium Focus Group Meeting November 3-5, 2015 SRNL-STI-2015-00605 This presentation does not contain any proprietary, confidential, or otherwise restricted information LiT Electrolysis Options LiT Electrolysis Maroni Process (Baseline Option) Improve Liquid-Liquid Extraction & Electrolysis Process Intensification

  9. A=16Li (1993TI07)

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

    Li (1993TI07) (Not illustrated) This nucleus has not been observed. Shell model studies (1988POZS) are used to predict J and the magnetic dipole moment....

  10. Nanoscale LiFePO4 and Li4Ti5O12 for High Rate Li-ion Batteries

    SciTech Connect (OSTI)

    Jaiswal, A.; Horne, C.R.; Chang, O.; Zhang, W.; Kong, W.; Wang, E.; Chern, T.; Doeff, M. M.

    2009-08-04

    The electrochemical performances of nanoscale LiFePO4 and Li4Ti5O12 materials are described in this communication. The nanomaterials were synthesized by pyrolysis of an aerosol precursor. Both compositions required moderate heat-treatment to become electrochemically active. LiFePO4 nanoparticles were coated with a uniform, 2-4 nm thick carbon-coating using an organic precursor in the heat treatment step and showed high tap density of 1.24 g/cm3, in spite of 50-100 nm particle size and 2.9 wtpercent carbon content. Li4Ti5O12 nanoparticles were between 50-200 nm in size and showed tap density of 0.8 g/cm3. The nanomaterials were tested both in half cell configurations against Li-metal and also in LiFePO4/Li4Ti5O12 full cells. Nano-LiFePO4 showed high discharge rate capability with values of 150 and 138 mAh/g at C/25 and 5C, respectively, after constant C/25 charges. Nano-Li4Ti5O12 also showed high charge capability with values of 148 and 138 mAh/g at C/25 and 5C, respectively, after constant C/25 discharges; the discharge (lithiation) capability was comparatively slower. LiFePO4/Li4Ti5O12 full cells deliver charge/discharge capacity values of 150 and 122 mAh/g at C/5 and 5C, respectively.

  11. Ca rlsbad Field Office

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

    En ergy Ca rlsbad Field Office P. O . Box 3090 Carlsbad , New Mexico 88221 AUG 2 9 2013 Mr. John E. Kieling , Chief Hazardous Waste Bureau New Mexico Environment Department 2905 Rodeo Park Drive East, Building 1 Santa Fe, New Mexico 87505-6303 Subject: Notification of Class 1 Permit Modification to the Waste Isolation Pilot Plant Hazardous Waste Facility Permit Number: NM4890139088-TSDF Dear Mr. Kieling: Enclosed is a Class 1 Permit Modification Notification for the fo ll owing items: * Revise a

  12. CA.O-O

    Office of Legacy Management (LM)

    3sR L C, C II Department of Energy -e\ ' Washington, DC 20545 CA.O-O - 0 MAY 2 9 1987 Mr. Carl Schafer Director of Environmental Policy Office of the Deputy Assistant Secretary of Defense for Installations Pentagon Washington, D.C. 20301 Dear Mr. Schafer: As you know, the Department of Energy (DOE) is implementing a program to identify sites that may be radiologically contaminated as a result of DOE predecessor operations and to correct any problems associated with this contamination if there is

  13. Microsoft Word - li_abstract

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

    3, 2011 3:45 pm Refreshment will be served at 3:30 pm A few new issues regarding the density dependence of nuclear symmetry energy Professor Bao-An Li Department of Physics and Astronomy, Texas A&M University-Commerce Abstract: The density dependence of nuclear symmetry energy is rather poorly known at both sub-saturation and supra-saturation densities. However, it is very important for understanding many interesting properties/phenomena/processes in nuclear structure, heavy-ion reactions

  14. A=11Li (68AJ02)

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

    68AJ02) (See the Isobar Diagram for 11Li) 11Li has been identified in the 5.3 GeV proton bombardment of uranium. It is particle stable (PO66H). See also (GA66C, CO67A

  15. A=8Li (1988AJ01)

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

    nuclear radius of 8Li is 2.36 0.02 fm (1985TA18) see also for derived nuclear matter, charge and neutron matter r.m.s. radii. 1. 8Li(-)8Be Qm 16.0039 The - decay is...

  16. A=9Li (1979AJ01)

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

    2.3 2.9 keV for the second T 32 state in A 9 (1975KA18). 1. 9Li(-)9Be Qm 13.607 The half-life of 9Li is 178.3 0.4 msec (1976AL02). Other recent values are 175 1...

  17. A=10Li (74AJ01)

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

    10B: see (HA68V), the mass excess of 10Li, (M - A) 33.10 0.06 MeV (AB73D). The breakup energy into 9Li + n is then -0.06 0.06 MeV. Using the calculated values suggested...

  18. Electrochemistry of LiCl-Li2O-H2O Molten Salt Systems

    SciTech Connect (OSTI)

    Natalie J. Gese; Batric Pesic

    2013-03-01

    Uranium can be recovered from uranium oxide (UO2) spent fuel through the combination of the oxide reduction and electrorefining processes. During oxide reduction, the spent fuel is introduced to molten LiCl-Li2O salt at 650 degrees C and the UO2 is reduced to uranium metal via two routes: (1) electrochemically, and (2) chemically by lithium metal (Li0) that is produced electrochemically. However, the hygroscopic nature of both LiCl and Li2O leads to the formation of LiOH, contributing hydroxyl anions (OH-), the reduction of which interferes with the Li0 generation required for the chemical reduction of UO2. In order for the oxide reduction process to be an effective method for the treatment of uranium oxide fuel, the role of moisture in the LiCl-Li2O system must be understood. The behavior of moisture in the LiCl-Li2O molten salt system was studied using cyclic voltammetry, chronopotentiometry and chronoamperometry, while reduction to hydrogen was confirmed with gas chromatography.

  19. Enabling Future Li-Ion Battery Recycling | Argonne National Laboratory

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

    Future Li-Ion Battery Recycling Title Enabling Future Li-Ion Battery Recycling Publication Type Presentation Year of Publication 2014 Authors Gaines, LL Abstract Presentation made...

  20. Atsun Solar Electric Technology Co Ang Li Tiansheng | Open Energy...

    Open Energy Info (EERE)

    Co (Ang Li Tiansheng) Place: Zaozhuang, Shandong Province, China Product: Chinese PV cell and module maker. References: Atsun Solar Electric Technology Co (Ang Li...

  1. A=8Li (59AJ76)

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

    8Li (59AJ76) (See the Energy Level Diagram for 8Li) GENERAL: See also Table 8.1 [Table of Energy Levels] (in PDF or PS). Theory: See (LA55A, KU56, FR57, KU57). 1. 8Li(β-)8Be Qm = 16.001 The weighted mean of half-lives reported in (55AJ61) is 0.848 ± 0.004 sec. A value of 0.873 ± 0.013 sec is given by (VE58A). See also (IM58). The decay is complex: see 8Be. 2. 6Li(t, p)8Li Qm = 0.803 Q0 = 0.790 ± 0.011 (AL54E). The ground state reaction has been observed by (MO52, PE52, AL54E, CU55B). (CU55B)

  2. TOUGH2/EOS7CA

    Energy Science and Technology Software Center (OSTI)

    003504MLTPL00 EOS7CA Version 1.0: TOUGH2 Module for Gas Migration in Shallow Subsurface Porous Media Systems

  3. Li2Se as a Neutron Scintillator

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

    Du, Mao-Hua; Shi, Hongliang; Singh, David J.

    2015-06-23

    We show that Li2Se:Te is a potential neutron scintillator material based on density functional calculations. Li2Se exhibits a number of properties favorable for efficient neutron detection, such as a high Li concentration for neutron absorption, a small effective atomic mass and a low density for reduced sensitivity to background gamma rays, and a small band gap for a high light yield. Our calculations show that Te doping should lead to the formation of deep acceptor complex VLi-TeSe, which can facilitate efficient light emission, similar to the emission activation in Te doped ZnSe.

  4. Antiperovskite Li 3 OCl superionic conductor films for solid-state Li-ion batteries

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

    Lü, Xujie; Howard, John W.; Chen, Aiping; Zhu, Jinlong; Li, Shuai; Wu, Gang; Dowden, Paul; Xu, Hongwu; Zhao, Yusheng; Jia, Quanxi

    2016-02-02

    We prepared antiperovskite Li3OCl superionic conductor films via pulsed laser deposition using a composite target. A significantly enhanced ionic conductivity of 2.0 × 10-4 S cm-1 at room temperature is achieved, and this value is more than two orders of magnitude higher than that of its bulk counterpart. Moreover, the applicability of Li3OCl as a solid electrolyte for Li-ion batteries is demonstrated.

  5. A=13Li (1991AJ01)

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

    91AJ01) (Not illustrated) 13Li has not been observed: see (1986AJ01). The calculated value of its mass excess is 60.34 MeV [see (1981AJ01)]: 13Li would then be unstable with respect to 11Li + 2n by 3.34 MeV. (1985PO10) calculate [in a (0 + 1)ℏω model space] that the first four states of 13Li at 0, 1.42, 2.09 and 2.77 MeV have, respectively, Jπ = 3/2-, 7/2-, 1/2-, 5/2-. See also (1987PE1C, 1989OG1B) and (1988POZS, 1988ZV1A

  6. A=15Li (1991AJ01)

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

    91AJ01) (Not illustrated) 15Li has not been observed. Its atomic mass excess is calculated to be 81.60 MeV: see (1981AJ01). It is then unstable with respect to decay into 14Li + n and 13Li + 2n by 1.2 and 5.1 MeV, respectively. (1985PO10) calculate [in a (0 + 1)ℏω model space] that the first four states of 15Li at 0, 0.73, 2.39 and 2.77 MeV have, respectively, Jπ = 3/2-, 1/2-, 7/2- and 5/2-. See also (1988POZS; theor.)

  7. A=7Li (59AJ76)

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

    59AJ76) (See the Energy Level Diagram for 7Li) GENERAL: See also Table 7.1 [Table of Energy Levels] (in PDF or PS). Theory: See (AU55, DA55, LA55A, AB56, FE56, KU56, ME56, FE57C, FR57, LE57F, MA57E, MA57J, SO57, HA58D, SK58). 1. 3H(α, γ)7Li Qm = 2.465 For Eα = 0.5 to 1.9 MeV, capture radiation is observed to 7Li(0) and 7Li*(0.48), with intensity ratio 5 : 2. The smooth rise of the cross section suggests a direct capture process. The angular distribution is not isotropic, indicating l > 0

  8. A=9Li (1984AJ01)

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

    4AJ01) (See Energy Level Diagrams for 9Li) GENERAL: See also (1979AJ01) and Table 9.1 Table of Energy Levels (in PDF or PS). Model calculations: (1979LA06). Complex reactions...

  9. A=5Li (1984AJ01)

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

    84AJ01) (See Energy Level Diagrams for 5Li) GENERAL: See also (1979AJ01) and Table 5.3 Table of Energy Levels (in PDF or PS) here. Model calculations:(1978RE1A, 1979MA1J,...

  10. A=8Li (1984AJ01)

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

    4AJ01) (See Energy Level Diagrams for 8Li) GENERAL: See also (1979AJ01) and Table 8.2 Table of Energy Levels (in PDF or PS). Special states: (1980OK01). Complex reactions...

  11. A=5Li (1974AJ01)

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

    4AJ01) (See Energy Level Diagrams for 5Li) GENERAL: See also (1966LA04) and Table 5.5 Table of Energy Levels (in PDF or PS) here. Shell model calculations: (1966FR1B, 1968GO01,...

  12. A=5Li (1979AJ01)

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

    9AJ01) (See Energy Level Diagrams for 5Li) GENERAL: See also (1974AJ01) and Table 5.3 Table of Energy Levels (in PDF or PS) here. Model calculations: (1975KR1A). Special states:...

  13. A=9Li (1988AJ01)

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

    8AJ01) (See Energy Level Diagrams for 9Li) GENERAL: See also (1984AJ01) and Table 9.1 Table of Energy Levels (in PDF or PS). Model calculations: (1983KU17, 1984CH24, 1984VA06)....

  14. A=8Li (1979AJ01)

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

    79AJ01) (See Energy Level Diagrams for 8Li) GENERAL: See also (1974AJ01) and Table 8.1 Table of Energy Levels (in PDF or PS). Nuclear models: (1975KH1A, 1977ST24). Special...

  15. A=8Li (74AJ01)

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

    cross section, comparable to the geometric value, is understood in terms of the ( + t) cluster nature of 7Li (RO62C). Cross sections for this reaction have recently been...

  16. A=4Li (1992TI02)

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

    experiments (1990BR14, 1990BR17) that detect 4Li states in the particle spectra of breakup reactions. It may even be possible that these experiments are not detecting the 2-and...

  17. A=11Li (1990AJ01)

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

    increase in matter radii with increasing A and do not support the idea of a neutron halo in 11Li (1988POZS; prelim.). See, however, (1988TA1A). Fragmentation cross sections of...

  18. Construction Consultants, L.I., Inc.

    Office of Environmental Management (EM)

    Mr. Eric Baumack Senior Project Manager Construction Consultants L.I., Inc. 36 East 2 nd Street Riverhead, New York 11901 WEL-2015-05 Dear Mr. Baumack: The Office of Enterprise Assessments' Office of Enforcement has completed an investigation into an electrical shock incident involving a worker employed by a subcontractor to Construction Consultants L.I., Inc. (CCLI) at the Brookhaven National Laboratory (BNL). CCLI is a first-tier subcontractor to Brookhaven Science Associates, LLC (BSA),

  19. Materials Data on LiCaPrTeO6 (SG:7) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  20. Materials Data on LiCaN (SG:62) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  1. Materials Data on LiCaSn (SG:156) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  2. Excitation functions of {sup 6,7}Li+{sup 7}Li reactions at low energies

    SciTech Connect (OSTI)

    Prepolec, L.; Soic, N.; Blagus, S.; Miljanic, D.; Siketic, Z.; Skukan, N.; Uroic, M.; Milin, M.

    2009-08-26

    Differential cross sections of {sup 6,7}Li+{sup 7}Li nuclear reactions have been measured at forward angles (10 deg. and 20 deg.), using particle identification detector telescopes, over the energy range 2.75-10.00 MeV. Excitation functions have been obtained for low-lying residual-nucleus states. The well pronounced peak in the excitation function of {sup 7}Li({sup 7}Li,{sup 4}He){sup 10}Be(3.37 MeV,2{sup +}) at beam energy about 8 MeV, first observed by Wyborny and Carlson in 1971 at 0 deg., has been observed at 10 deg., but is less evident at 20 deg. The cross section obtained for the {sup 7}Li({sup 7}Li,{sup 4}He){sup 10}Be(g.s,0{sup +}) reaction is about ten times smaller. The well pronounced peak in the excitation function of {sup 7}Li({sup 7}Li,{sup 4}He){sup 10}Be(3.37 MeV,2{sup +}) reaction could correspond to excited states in {sup 14}C, at excitation energies around 30 MeV.

  3. Southern CA Area | Open Energy Information

    Open Energy Info (EERE)

    CA Area Jump to: navigation, search Contents 1 Clean Energy Clusters in the Southern CA Area 1.1 Products and Services in the Southern CA Area 1.2 Research and Development...

  4. P LI I CI L I

    Office of Legacy Management (LM)

    LI I - CI L - I 111 Ir LI C C c c c Ic c L ORNL/RASA-90/8 OAK RIDGE NATIONAL LABORATORY RADIOLOGICAL SURVEY OF THE FORMER BAKER BROTHERSJNC. SITE, 2551-2555 HARLEAU PLACE, TOLEDO,OHIO (BTOOOl) MABAGEO BY MABAGEO BY MAUTIH MARIETTA ENBGY SYSTEM, INC. AWTIH MAftIETTA ENBGY SYSTEM, INC. FOR THE UNITE0 STATES FOR THE UNITE0 STATES OEPARTMENT OF EtdERGY OEPARTMENT OF EtdERGY R. D. Foley L. M. Floyd _-. This report has been reproduced directly from the best available copy. Available to DOE and DOE

  5. Batteries - Next-generation Li-ion batteries Breakout session

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

    the Other Technical Areas Being Discussed * Main point: we should consider next-gen Li-ion and beyond Li-ion together as a single portfolio of work, in which risk and...

  6. Shanghai Shen Li High Tech Co Ltd | Open Energy Information

    Open Energy Info (EERE)

    Shen Li High Tech Co Ltd Jump to: navigation, search Name: Shanghai Shen-Li High Tech Co Ltd Place: Shanghai, Shanghai Municipality, China Zip: 201400 Product: Focused on the...

  7. Hydrogen storage in LiH: A first principle study

    SciTech Connect (OSTI)

    Banger, Suman Nayak, Vikas Verma, U. P.

    2014-04-24

    First principles calculations have been performed on the Lithium hydride (LiH) using the full potential linearized augmented plane wave (FP-LAPW) method within the framework of density functional theory. We have extended our calculations for LiH+2H and LiH+6H in NaCl structure. The structural stability of three compounds have been studied. It is found that LiH with 6 added Hydrogen atoms is most stable. The obtained results for LiH are in good agreement with reported experimental data. Electronic structures of three compounds are also studied. Out of three the energy band gap in LiH is ?3.0 eV and LiH+2H and LiH+6H are metallic.

  8. Li-Ion Battery Cell Manufacturing | Department of Energy

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

    Li-Ion Battery Cell Manufacturing Li-Ion Battery Cell Manufacturing 2011 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon arravt001_es_eun_2011_p.pdf More Documents & Publications 2010 DOE, Li-Ion Battery Cell Manufacturing Construction of a Li Ion Battery (LIB) Cathode Production Plant in Elyria, Ohio Process for Low Cost Domestic Production of LIB Cathode Materials

  9. Enforcement Letter, Construction Consultants L.I., Inc. | Department of

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

    Energy Construction Consultants L.I., Inc. Enforcement Letter, Construction Consultants L.I., Inc. December 4, 2015 Worker Safety and Health Enforcement Letter issued to Construction Consultants L.I., Inc. On December 4, 2015, the U.S. Department of Energy (DOE) Office of Enterprise Assessments' Office of Enforcement issued an Enforcement Letter (WEL-2015-05) to Construction Consultants L.I., Inc., relating to an electrical shock suffered by a subcontractor while working on a meteorological

  10. Optimized Operating Range for Large-Format LiFePO4/Graphite Batteries

    SciTech Connect (OSTI)

    Jiang, Jiuchun; Shi, Wei; Zheng, Jianming; Zuo, Pengjian; Xiao, Jie; Chen, Xilin; Xu, Wu; Zhang, Jiguang

    2014-06-01

    e investigated the long-term cycling performance of large format 20Ah LiFePO4/graphite batteries when they are cycled in various state-of-charge (SOC) ranges. It is found that batteries cycled in the medium SOC range (ca. 20~80% SOC) exhibit superior cycling stability than batteries cycled at both ends (0-20% or 80-100%) of the SOC even though the capcity utilized in the medium SOC range is three times as large as those cycled at both ends of the SOC. Several non-destructive techniques, including a voltage interruption approach, model-based parameter identification, electrode impedance spectra analysis, ?Q/?V analysis, and entropy change test, were used to investigate the performance of LiFePO4/graphite batteries within different SOC ranges. The results reveal that batteries at the ends of SOC exhibit much higher polarization impedance than those at the medium SOC range. These results can be attributed to the significant structural change of cathode and anode materials as revealed by the large entropy change within these ranges. The direct correlation between the polarization impedance and the cycle life of the batteries provides an effective methodology for battery management systems to control and prolong the cycle life of LiFePO4/graphite and other batteries.

  11. Probing the failure mechanism of nanoscale LiFePO₄ for Li-ion batteries

    SciTech Connect (OSTI)

    Gu, Meng; Shi, Wei; Zheng, Jianming; Yan, Pengfei; Zhang, Ji-guang; Wang, Chongmin

    2015-05-18

    LiFePO4 is a high power rate cathode material for lithium ion battery and shows remarkable capacity retention, featuring a 91% capacity retention after 3300 cycles. In this work, we use high-resolution transmission electron microscopy (HRTEM), energy dispersive x-ray spectroscopy (EDS), and electron energy loss spectroscopy (EELS) to study the gradual capacity fading mechanism of LiFePO4 materials. We found that upon prolonged electrochemical cycling of the battery, the LiFePO4 cathode shows surface amorphization and loss of oxygen species, which directly contribute to the gradual capacity fading of the battery. The finding is of great importance for the design and improvement of new LiFePO4 cathode for high-energy and high-power rechargeable battery for electric transportation.

  12. A=07Li (66LA04)

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

    66LA04) (See Energy Level Diagrams for 7Li) GENERAL: See (HU57D, BA59K, BA59N, BR59M, FE59E, MA59E, MA59H, KU60A, PE60E, PH60A, SH60C, TA60L, BA61H, BA61N, BL61C, CL61D, KH61,...

  13. A=6Li (66LA04)

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

    66LA04) (See Energy Level Diagrams for 6Li) GENERAL: See Table 6.4 Table of Energy Levels (in PDF or PS). See also (AU55, LA55, ME56, FR57, HU57D, LE57F, PI58, BA59K, BR59M,...

  14. A=9Li (74AJ01)

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

    74AJ01) (See Energy Level Diagrams for 9Li) GENERAL: See also Table 9.1 Table of Energy Levels (in PDF or PS). Model calculations:(BA66T). Special reactions:(DO56D, GA66K, KL66C,...

  15. A=7Li (74AJ01)

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

    7Li) GENERAL: See also (66LA04) and Table 7.1 Table of Energy Levels (in PDF or PS). Shell model:(KO61L, CO65I, KU65D, VO65A, BA66T, HA66F, WI66E, BO67R, BO67V, CO67M, FA67A,...

  16. A=10Li (1988AJ01)

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

    MeV) corresponds to the ground state. 10Lig.s. would then be unbound with respect to breakup into 9Li + n by 0.80 0.25 MeV: see (1979AJ01). See also (1986GI10, 1987AB15),...

  17. A=10Li (1979AJ01)

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

    width of the ground state is 1.2 0.3 MeV. 10Lig.s. is unbound with respect to breakup into 9Li + n by 0.80 0.25 MeV (1975WI26). See also (1974BA15, 1974CE1A, 1974TH01,...

  18. A=10Li (1984AJ01)

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

    MeV) corresponds to the ground state. 10Lig.s. would the be unbound with respect to breakup into 9Li + n by 0.80 0.25 MeV (1975WI26). However (1979AB11, 1980AB16), on the...

  19. A=6Li (1984AJ01)

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

    (1978CH1D, 1978ST19, 1979CA06, 1980MA41, 1981BO1Y, 1982BA52, 1982FI13, 1982LO09). Cluster and -particle models: (1978OS07, 1978PL1A, 1978RE1A, 1978SI14, 1979BE39, 1979CA06,...

  20. Epitaxial thin film growth of LiH using a liquid-Li atomic template

    SciTech Connect (OSTI)

    Oguchi, Hiroyuki; Ikeshoji, Tamio; Orimo, Shin-ichi; Ohsawa, Takeo; Shiraki, Susumu; Hitosugi, Taro; Kuwano, Hiroki

    2014-11-24

    We report on the synthesis of lithium hydride (LiH) epitaxial thin films through the hydrogenation of a Li melt, forming abrupt LiH/MgO interface. Experimental and first-principles molecular dynamics studies reveal a comprehensive microscopic picture of the crystallization processes, which sheds light on the fundamental atomistic growth processes that have remained unknown in the vapor-liquid-solid method. We found that the periodic structure that formed, because of the liquid-Li atoms at the film/MgO-substrate interface, serves as an atomic template for the epitaxial growth of LiH crystals. In contrast, films grown on the Al{sub 2}O{sub 3} substrates indicated polycrystalline films with a LiAlO{sub 2} secondary phase. These results and the proposed growth process provide insights into the preparation of other alkaline metal hydride thin films on oxides. Further, our investigations open the way to explore fundamental physics and chemistry of metal hydrides including possible phenomena that emerge at the heterointerfaces of metal hydrides.

  1. Origin of high Li? conduction in doped Li?La?Zr?O?? garnets

    SciTech Connect (OSTI)

    Chen, Yan; Rangasamy, Ezhiylmurugan; Liang, Chengdu; An, Ke

    2015-08-06

    Substitution of a native ion in the crystals with a foreign ion that differs in valence (aliovalent doping) has been widely attempted to upgrade solid-state ionic conductors for various charge carriers including O?, H?, Li?, Na?, etc. The doping helps promote the high-conductive framework and dredge the tunnel for fast ion transport. The garnet-type Li?La?Zr?O?? (LLZO) is a fast Li? solid conductor, which received much attention as an electrolyte candidate for all-solid-state lithium ion batteries, showing great potential to offer high energy density and minimize battery safety concerns to meet extensive applications in large energy storage systems such as those for electric vehicles and aerospace. In the Li-stuffed garnet framework of LLZO, the 3D pathway formed by the incompletely occupied tetrahedral sites bridged by a single octahedron enables the superior Li? conductivity. For optimal performance, many aliovalent-doping efforts have been made throughout metal elements (Al?, Ta??) and metalloid elements (Ga?, Te??) in the periodic table with various valences to stabilize the high-conductive phase and increase the Li vacancy concentration.

  2. Making Li-air batteries rechargeable: material challenges

    SciTech Connect (OSTI)

    Shao, Yuyan; Ding, Fei; Xiao, Jie; Zhang, Jian; Xu, Wu; Park, Seh Kyu; Zhang, Jiguang; Wang, Yong; Liu, Jun

    2013-02-25

    A Li-air battery could potentially provide three to five times higher energy density/specific energy than conventional batteries, thus enable the driving range of an electric vehicle comparable to a gasoline vehicle. However, making Li-air batteries rechargeable presents significant challenges, mostly related with materials. Herein, we discuss the key factors that influence the rechargeability of Li-air batteries with a focus on nonaqueous system. The status and materials challenges for nonaqueous rechargeable Li-air batteries are reviewed. These include electrolytes, cathode (electocatalysts), lithium metal anodes, and oxygen-selective membranes (oxygen supply from air). The perspective of rechargeable Li-air batteries is provided.

  3. Ca

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

    John Kieling , Acting Bureau Chief Hazardous Waste Bureau New Mexico Environment Department 2905 Rodeo Park Drive East, Bldg. 1 Santa Fe, NM 87505-6303 FEB 2 3 2012 Subject: Transmittal of the Final Audit Report for SRS/CCP Certification Audit A-1 2-04 Dear Mr. Kieling : This letter transmits the Final Audit Report for Carlsbad Field Office Audit A-12-04 of the Savannah River Site Central Chara cterization Project (SRS/CCP) processes performed to characterize and certify waste , as required by

  4. Ca

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

    James Bearzi, Chief Hazardous Waste Bureau New Mexico Environment Department 2905 Rodeo Park Drive East, Building 1 Santa Fe, New Mexico 87505-6303 April 27, 2010 Subject: Notification of Sampling Line Loss, Waste Isolation Pilot Plant Permit Number NM4890139088-TSDF Dear Mr. Bearzi: The purpose of this letter is to transmit notification to the New Mexico Environment Department (NMED) of the loss of a hydrogen and methane monitoring sampling line and the results of the associated evaluation as

  5. Ca

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

    James Bearzi, Chief Hazardous Waste Bureau New Mexico Environment Department 2905 Rodeo Park Drive East, Building 1 Santa Fe, New Mexico 87505-6303 April 27, 2010 Subject:...

  6. Solution-processable glass LiI-Li4SnS4 superionic conductors for all-solid-state Li-ion batteries

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

    Kern Ho Park; Oh, Dae Yang; Choi, Young Eun; Nam, Young Jin; Han, Lili; Kim, Ju -Young; Xin, Huolin; Lin, Feng; Oh, Seung M.; Jung, Yoon Seok

    2015-12-22

    The new, highly conductive (4.1 × 10–4 S cm–1 at 30 °C), highly deformable, and dry-air-stable glass 0.4LiI-0.6Li4SnS4 is prepared using a homogeneous methanol solution. Furthermore, the solution process enables the wetting of any exposed surface of the active materials with highly conductive solidified electrolytes (0.4LiI-0.6Li4SnS4), resulting in considerable improvements in electrochemical performances of these electrodes over conventional mixture electrodes.

  7. FIRST_Research Perspective_Li

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

    1. Structure factor obtained from MD (a) and SAXS (b) at different temperatures: comparison of spatial heterogeneity from snapshots (c) of DILs (top) and MILs (bottom) FIRST Center Research Perspective: Nanoscale Heterogeneity and Dynamics of Room Temperature Ionic Liquids Song Li Vanderbilt University Jianchang Guo, Kee Sung Han, Jose L. Bañuelos, Edward W. Hagaman, Robert W. Shaw Oak Ridge National Laboratory Research Summary: An increase of the alkyl chain length of the cation of room

  8. Microsoft Word - li_z.doc

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

    Impact of the Vertical Variation of Cloud Droplet Size on the Estimation of Cloud Liquid Water Path and Its Potential for Rain Detection Z. Li, R. Chen, and F-L Chang Earth System Science Interdisciplinary Center, University of Maryland College Park, Maryland Introduction Liquid water path (LWP) is an important cloud microphysical property that determines the climatic effects of boundary layer clouds. Satellites provide the only means of acquiring global and long-term LWP estimates. The LWP is

  9. Insight into Sulfur Reactions in LiS Batteries

    SciTech Connect (OSTI)

    Xu, Rui; Belharouak, Ilias; Zhang, Xiaofeng; chamoun, rita; Yu, Cun; Ren, Yang; Nie, Anmin; Reza, Shahbazian-Yassar; Lu, Jun; Li, James C.M.; Amine, Khalil

    2014-12-09

    Understanding and controlling the sulfur reduction species (Li2Sx, 1 ? x ? 8) under realistic battery conditions are essential for the development of advanced practical LiS cells that can reach their full theoretical capacity. However, it has been a great challenge to probe the sulfur reduction intermediates and products because of the lack of methods. This work employed various ex situ and in situ methods to study the mechanism of the LiS redox reactions and the properties of Li2Sx and Li2S. Synchrotron high-energy X-ray diffraction analysis used to characterize dry powder deposits from lithium polysulfide solution suggests that the new crystallite phase may be lithium polysulfides. The formation of Li2S crystallites with a polyhedral structure was observed in cells with both the conventional (LiTFSI) electrolyte and polysulfide-based electrolyte. In addition, an in situ transmission electron microscopy experiment observed that the lithium diffusion to sulfur during discharge preferentially occurred at the sulfur surface and formed a solid Li2S crust. This may be the reason for the capacity fade in LiS cells (as also suggested by EIS experiment in Supporting Information). The results can be a guide for future studies and control of the sulfur species and meanwhile a baseline for approaching the theoretical capacity of the LiS battery.

  10. Floor San Francisco, CA 94104

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

    Sutter Street NEW YORK ⋅ WASHINGTON, DC ⋅ LOS ANGELES ⋅ CHICAGO ⋅ BEIJING 20 th Floor San Francisco, CA 94104 TEL 415 875-6100 FAX 415 875-6161 www.nrdc.org Testimony of Marcus Griswold, PhD, Water Resources Scientist Natural Resources Defense Council Before the Quadrennial Energy Review Task Force Public Meeting on "Water Energy Nexus" June 19, 2014 Introduction Good morning Dr. Holdren, Mr. Deputy Secretary, members of the Task Force and fellow panelists. My name is Marcus

  11. Characterization of Materials for Li-ion Batteries: Success Stories...

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

    Success Stories from the High Temperature Materials Laboratory (HTML) User Program Characterization of Materials for Li-ion Batteries: Success Stories from the High...

  12. Electrical conduction of LiF interlayers in organic diodes

    SciTech Connect (OSTI)

    Bory, Benjamin F.; Janssen, Ren A. J.; Meskers, Stefan C. J.; Gomes, Henrique L.; Leeuw, Dago M. de

    2015-04-21

    An interlayer of LiF in between a metal and an organic semiconductor is commonly used to improve the electron injection. Here, we investigate the effect of moderate bias voltages on the electrical properties of Al/LiF/poly(spirofluorene)/Ba/Al diodes by systematically varying the thickness of the LiF layer (2-50?nm). Application of forward bias V below the bandgap of LiF (V?LiF/poly(spirofluorene) hetero-junction. Electrons are trapped on the poly(spirofluorene) side of the junction, while positively charged defects accumulate in the LiF with number densities as high as 10{sup 25}/m{sup 3}. Optoelectronic measurements confirm the built-up of aggregated, ionized F centres in the LiF as the positive trapped charges. The charged defects result in efficient transport of electrons from the polymer across the LiF, with current densities that are practically independent of the thickness of the LiF layer.

  13. LiDAR (Lewicki & Oldenburg, 2005) | Open Energy Information

    Open Energy Info (EERE)

    Technique LiDAR Activity Date Usefulness useful DOE-funding Unknown References Jennifer L. Lewicki, Curtis M. Oldenburg (2005) Strategies To Detect Hidden Geothermal Systems...

  14. LiDAR (Lewicki & Oldenburg, 2004) | Open Energy Information

    Open Energy Info (EERE)

    Technique LiDAR Activity Date Usefulness useful DOE-funding Unknown References Jennifer L. Lewicki, Curtis M. Oldenburg (2004) Strategies For Detecting Hidden Geothermal Systems...

  15. Li ion Motors Corp formerly EV Innovations Inc | Open Energy...

    Open Energy Info (EERE)

    Vegas, Nevada Zip: 89110 Sector: Vehicles Product: Las Vegas - based manufacturer of lithium-powered plug-in vehicles. References: Li-ion Motors Corp (formerly EV Innovations...

  16. Predictive Models of Li-ion Battery Lifetime (Presentation) Smith...

    Office of Scientific and Technical Information (OSTI)

    Predictive Models of Li-ion Battery Lifetime (Presentation) Smith, K.; Wood, E.; Santhanagopalan, S.; Kim, G.; Shi, Y.; Pesaran, A. 25 ENERGY STORAGE; 33 ADVANCED PROPULSION...

  17. Properties of (Ga,Mn)As codoped with Li

    SciTech Connect (OSTI)

    Miyakozawa, Shohei; Chen, Lin; Matsukura, Fumihiro; Ohno, Hideo

    2014-06-02

    We grow Li codoped (Ga,Mn)As layers with nominal Mn composition up to 0.15 by molecular beam epitaxy. The layers before and after annealing are characterized by x-ray diffraction, transport, magnetization, and ferromagnetic resonance measurements. The codoping with Li reduces the lattice constant and electrical resistivity of (Ga,Mn)As after annealing. We find that (Ga,Mn)As:Li takes similar Curie temperature to that of (Ga,Mn)As, but with pronounced magnetic moments and in-plane magnetic anisotropy, indicating that the Li codoping has nontrivial effects on the magnetic properties of (Ga,Mn)As.

  18. Key Parameters Governing the Energy Density of Rechargeable Li...

    Office of Scientific and Technical Information (OSTI)

    Key Parameters Governing the Energy Density of Rechargeable LiS Batteries Citation Details In-Document Search Title: Key Parameters Governing the Energy Density of Rechargeable ...

  19. Combined Quantum Chemical/Raman Spectroscopic Analyses of Li...

    Office of Scientific and Technical Information (OSTI)

    interactions using the provided methodology, but a similar analysis of PC...Li+ ... Resource Relation: Journal Name: Journal of Power Sources, 267:821-830 Research Org: ...

  20. Primordial Li abundance and massive particles

    SciTech Connect (OSTI)

    Latin-Capital-Letter-Eth apo, H.

    2012-10-20

    The problem of the observed lithium abundance coming from the Big Bang Nucleosynthesis is as of yet unsolved. One of the proposed solutions is including relic massive particles into the Big Bang Nucleosynthesis. We investigated the effects of such particles on {sup 4}HeX{sup -}+{sup 2}H{yields}{sup 6}Li+X{sup -}, where the X{sup -} is the negatively charged massive particle. We demonstrate the dominance of long-range part of the potential on the cross-section.

  1. CI L C C I LI C

    Office of Legacy Management (LM)

    CI L C C - I LI C c C I I I I I I I L rr ORNL/RASA-94/l 0t-t. 27-6 \O [I ,-' :..L, &ml OAK RIDGE NATIONAL LABORATORY RESULTS OF THE RADIOLOGICAL SURVEY at the former HERRING-HALL-MARVIN SAFE COMPANY (3rd Floor) 1550 Grand Boulevard, Hamilton, Ohio (HOOOl) M. E. Murray C. A. Johnson MANA6ED BY MARTIN MARIETTA ENERGY SYSTEMS, INC. FOR THE UNITE0 STATES DEPARTMENT OF ENEMY This report has been reproduced directly from the best available copy. Available to DOE and DOE contractors from the Office

  2. Characterization of low-melting electrolytes for potential geothermal borehole power supplies: The LiBr-KBr-LiF eutectic

    SciTech Connect (OSTI)

    Guidotti, R.A.; Reinhardt, F.W.

    1998-05-01

    The suitability of modified thermal-battery technology for use as a potential power source for geothermal borehole applications is under investigation. As a first step, the discharge processes that take place in LiSi/LiBr-KBr-LiF/FeS{sub 2} thermal cells were studied at temperatures of 350 C and 400 C using pelletized cells with immobilized electrolyte. Incorporation of a reference electrode allowed the relative contribution of each electrode to the overall cell polarization to be determined. The results of single-cell tests are presented, along with preliminary data for cells based on a lower-melting CsBr-LiBr-KBr eutectic salt.

  3. Update on Performance Improvement of Sandia-Built Li/(CFx)n and...

    Office of Scientific and Technical Information (OSTI)

    Update on Performance Improvement of Sandia-Built Li(CFx)n and LiFePO4 Cells. Citation Details In-Document Search Title: Update on Performance Improvement of Sandia-Built Li...

  4. A=6Li (1988AJ01)

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

    1984ZW1A, 1985ER06, 1985FI1E, 1985LO1A, 1986AV08, 1986LE21, 1987KI1C, 1988WO04). Cluster and -particle models: (1981PL1A, 1982WE15, 1983CA13, 1983DZ1A, 1983FO03, 1983GA12,...

  5. Microsoft Word - Household Energy Use CA

    U.S. Energy Information Administration (EIA) Indexed Site

    0 20 40 60 80 100 US PAC CA Site Consumption million Btu $0 $500 $1,000 $1,500 $2,000 $2,500 US PAC CA Expenditures dollars ALL ENERGY average per household (excl. transportation) 0 2,000 4,000 6,000 8,000 10,000 12,000 US PAC CA Site Consumption kilowatthours $0 $250 $500 $750 $1,000 $1,250 $1,500 US PAC CA Expenditures dollars ELECTRICITY ONLY average per household  California households use 62 million Btu of energy per home, 31% less than the U.S. average. The lower than average site

  6. Microsoft Word - Household Energy Use CA

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

    0 20 40 60 80 100 US PAC CA Site Consumption million Btu $0 $500 $1,000 $1,500 $2,000 $2,500 US PAC CA Expenditures dollars ALL ENERGY average per household (excl. transportation) 0 2,000 4,000 6,000 8,000 10,000 12,000 US PAC CA Site Consumption kilowatthours $0 $250 $500 $750 $1,000 $1,250 $1,500 US PAC CA Expenditures dollars ELECTRICITY ONLY average per household  California households use 62 million Btu of energy per home, 31% less than the U.S. average. The lower than average site

  7. Enabling the Future of Li-Ion Batteries | Argonne National Laboratory

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

    Enabling the Future of Li-Ion Batteries Title Enabling the Future of Li-Ion Batteries Publication Type Presentation Year of Publication 2015 Authors Gaines, LL Abstract...

  8. Localization of vacancies and mobility of lithium ions in Li{sub 2}ZrO{sub 3} as obtained by {sup 6,7}Li NMR

    SciTech Connect (OSTI)

    Baklanova, Ya. V., E-mail: baklanovay@ihim.uran.ru [Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 91 Pervomaiskaya str., 620990 Ekaterinburg (Russian Federation); Arapova, I. Yu.; Buzlukov, A.L.; Gerashenko, A.P.; Verkhovskii, S.V.; Mikhalev, K.N. [Institute of Metal Physics, Ural Branch of the Russian Academy of Sciences, 18 Kovalevskaya str., 620990 Ekaterinburg (Russian Federation); Denisova, T.A.; Shein, I.R.; Maksimova, L.G. [Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 91 Pervomaiskaya str., 620990 Ekaterinburg (Russian Federation)

    2013-12-15

    The {sup 6,7}Li NMR spectra and the {sup 7}Li spinlattice relaxation rate were measured on polycrystalline samples of Li{sub 2}ZrO{sub 3}, synthesized at 1050 K and 1300 K. The {sup 7}Li NMR lines were attributed to corresponding structural positions of lithium Li1 and Li2 by comparing the EFG components with those obtained in the first-principles calculations of the charge density in Li{sub 2}ZrO{sub 3}. For both samples the line width of the central {sup 7}Li transition and the spinlattice relaxation time decrease abruptly at the temperature increasing above ?500 K, whereas the EFG parameters are averaged (??{sub Q}?=42 (5) kHz) owing to thermally activated diffusion of lithium ions. - Graphical abstract: Path of lithium ion hopping in lithium zirconate Li{sub 2}ZrO{sub 3}. - Highlights: Polycrystalline samples Li{sub 2}ZrO{sub 3} with monoclinic crystal structure synthesized at different temperatures were investigated by {sup 6,7}Li NMR spectroscopy. Two {sup 6,7}Li NMR lines were attributed to the specific structural positions Li1 and Li2. The distribution of vacancies was clarified for both lithium sites. The activation energy and pathways of lithium diffusion in Li{sub 2}ZrO{sub 3} were defined.

  9. Solution-processable glass LiI-Li4SnS4 superionic conductors for all-solid-state Li-ion batteries

    SciTech Connect (OSTI)

    Kern Ho Park; Oh, Dae Yang; Choi, Young Eun; Nam, Young Jin; Han, Lili; Kim, Ju -Young; Xin, Huolin; Lin, Feng; Oh, Seung M.; Jung, Yoon Seok

    2015-12-22

    The new, highly conductive (4.1 × 10–4 S cm–1 at 30 °C), highly deformable, and dry-air-stable glass 0.4LiI-0.6Li4SnS4 is prepared using a homogeneous methanol solution. Furthermore, the solution process enables the wetting of any exposed surface of the active materials with highly conductive solidified electrolytes (0.4LiI-0.6Li4SnS4), resulting in considerable improvements in electrochemical performances of these electrodes over conventional mixture electrodes.

  10. Structure of neutron-rich Isotopes {sup 8}Li and {sup 9}Li and allowance for it in elastic scattering

    SciTech Connect (OSTI)

    Ibraeva, E. T.; Zhusupov, M. A.; Imambekov, O.; Sagindykov, Sh. Sh.

    2008-07-15

    The differential cross sections for elastic proton scattering on the unstable neutron-rich nuclei {sup 8}Li and {sup 9}Li at E = 700 and 60 MeV per nucleon were considered. The {sup 8}Li nucleus was treated on the basis of the three-body {alpha}-t-n model, while the {sup 9}Li nucleus was considered within the {alpha}-t-n and {sup 7}Li-n-n models. The cross sections in question were calculated within Glauber diffraction theory. A comparison of the results with available experimental data made it possible to draw conclusions on the quality of the wave functions and potential used in the calculations.

  11. LiCl Dehumidifier LiBr absorption chiller hybrid air conditioning system with energy recovery

    DOE Patents [OSTI]

    Ko, Suk M. (Huntsville, AL)

    1980-01-01

    This invention relates to a hybrid air conditioning system that combines a solar powered LiCl dehumidifier with a LiBr absorption chiller. The desiccant dehumidifier removes the latent load by absorbing moisture from the air, and the sensible load is removed by the absorption chiller. The desiccant dehumidifier is coupled to a regenerator and the desiccant in the regenerator is heated by solar heated hot water to drive the moisture therefrom before being fed back to the dehumidifier. The heat of vaporization expended in the desiccant regenerator is recovered and used to partially preheat the driving fluid of the absorption chiller, thus substantially improving the overall COP of the hybrid system.

  12. A=6Li (59AJ76)

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

    59AJ76) (See the Energy Level Diagram for 6Li) GENERAL: See also Table 6.2 [Table of Energy Levels] (in PDF or PS). Theory: See (MO54F, AD55, AU55, BA55S, IR55, LA55, OT55, FE56, ME56, NE56D, FR57, LE57F, LY57, SO57, TA57, PI58, SK58). 1. (a) 3H(3He, d)4He Qm = 14.319 Eb = 15.790 (b) 3H(3He, p)5He Qm = 11.136 (c) 3H(3He, p)4He + n Qm = 12.093 The relative intensities (43 ± 2, 6 ± 2, 51 ± 2) of reactions (a), (b) and (c), do not vary for E(3He) = 225 to 600 keV. The deuterons are isotropic

  13. Material review of Li ion battery separators

    SciTech Connect (OSTI)

    Weber, Christoph J. Geiger, Sigrid; Falusi, Sandra; Roth, Michael

    2014-06-16

    Separators for Li Ion batteries have a strong impact on cell production, cell performance, life, as well as reliability and safety. The separator market volume is about 500 million m{sup 2} mainly based on consumer applications. It is expected to grow strongly over the next decade for mobile and stationary applications using large cells. At present, the market is essentially served by polyolefine membranes. Such membranes have some technological limitations, such as wettability, porosity, penetration resistance, shrinkage and meltdown. The development of a cell failure due to internal short circuit is potentially closely related to separator material properties. Consequently, advanced separators became an intense area of worldwide research and development activity in academia and industry. New separator technologies are being developed especially to address safety and reliability related property improvements.

  14. I I LI I L I

    Office of Legacy Management (LM)

    LI - I L I 1 II C c - ORNL/RASA-9618 OAK RlDGE NATlONAl. LA8ORATORY Results of the Independent Radiological Verification Survey at B&T Metals, 425 West Town Street, Columbus, Ohio (cooolv) M . E. Murray V. P. Patania C. A. Johnson M N M E D *wD OPEbM~ B V WUCNEEDllW?ME IWiARCH CoRpoRAng FoRTHEwITf@%tATeB ltEpAAMwTmBMeR(Ly ORNL-27 (34el ~~- L._~ This report has been reproduced directly from the best available copy. Avaiiable to DOE and DOE contractors from the Office of Scientific and

  15. Investigation of the Decomposition Mechanism of Lithium Bis(oxalate)borate (LiBOB) Salt in the Electrolyte of an Aprotic LiO2 Battery

    SciTech Connect (OSTI)

    Lau, Kah Chun; Lu, Jun; Low, John; Peng, Du; Wu, Huiming; Albishri, Hassan M.; Al-Hady, D. Abd; Curtiss, Larry A.; Amine, Khalil

    2014-04-01

    The stability of the lithium bis(oxalate) borate (LiBOB) salt against lithium peroxide (Li2O2) formation in an aprotic LiO2 (Liair) battery is investigated. From theoretical and experimental findings, we find that the chemical decomposition of LiBOB in electrolytes leads to the formation lithium oxalate during the discharge of a LiO2 cell. According to density functional theory (DFT) calculations, the formation of lithium oxalate as the reaction product is exothermic and therefore is thermodynamically feasible. This reaction seems to be independent of solvents used in the LiO2 cell, and therefore LiBOB is probably not suitable to be used as the salt in LiO2 cell electrolytes.

  16. DOE - Office of Legacy Management -- Electro Circuits Inc - CA 08

    Office of Legacy Management (LM)

    Electro Circuits Inc - CA 08 FUSRAP Considered Sites Site: Electro Circuits, Inc. (CA.08 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: None Location: 401 East Green Street , Pasadena , California CA.08-1 Evaluation Year: 1994 CA.08-2 Site Operations: Conducted ultrasonic tests on uranium ingots in the early 1950s. CA.08-3 CA.08-4 Site Disposition: Eliminated - Potential for contamination remote based on limited operations at the site CA.08-2

  17. Effects of electrolyte salts on the performance of Li-O2 batteries

    SciTech Connect (OSTI)

    Nasybulin, Eduard N.; Xu, Wu; Engelhard, Mark H.; Nie, Zimin; Burton, Sarah D.; Cosimbescu, Lelia; Gross, Mark E.; Zhang, Jiguang

    2013-02-05

    It is well known that the stability of nonaqueous electrolyte is critical for the rechargeable Li-O2 batteries. Although stability of many solvents used in the electrolytes has been investigated, considerably less attention has been paid to the stability of electrolyte salt which is the second major component. Herein, we report the systematic investigation of the stability of seven common lithium salts in tetraglyme used as electrolytes for Li-O2 batteries. The discharge products of Li-O2 reaction were analyzed by X-ray diffraction, X-ray photoelectron spectroscopy and nuclear magnetic resonance spectroscopy. The performance of Li-O2 batteries was strongly affected by the salt used in the electrolyte. Lithium tetrafluoroborate (LiBF4) and lithium bis(oxalato)borate (LiBOB) decompose and form LiF and lithium borates, respectively during the discharge of Li-O2 batteries. Several other salts, including lithium bis(trifluoromethane)sulfonamide (LiTFSI), lithium trifluoromethanesulfonate (LiTf), lithium hexafluorophosphate (LiPF6), lithium perchlorate (LiClO4) , and lithium bromide (LiBr) led to the discharge products which mainly consisted of Li2O2 and only minor signs of decomposition of LiTFSI, LiTf, LPF6 and LiClO4 were detected. LiBr showed the best stability during the discharge process. As for the cycling performance, LiTf and LiTFSI were the best among the studied salts. In addition to the instability of lithium salts, decomposition of tetraglyme solvent was a more significant factor contributing to the limited cycling stability. Thus a more stable nonaqueous electrolyte including organic solvent and lithium salt still need to be further developed to reach a fully reversible Li-O2 battery.

  18. ACS National Meeting (San Diego, CA) - JCAP

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

    ACS National Meeting (San Diego, CA) ACS National Meeting (San Diego, CA) Sun, Mar 13, 2016 7:00am 07:00 Thu, Mar 17, 2016 5:00pm 17:00 San Diego Convention Center 111 W Harbor Dr San Diego, CA 92101 Harry Atwater, "Artificial Photosynthesis: Progress, Science Prospects and Technology Outlook" Abstract: The design of highly efficient, non-biological energy conversion system that generate fuels directly from sunlight, water and carbon dioxide is both a formidable challenge and an

  19. LiDAR (Lewicki & Oldenburg) | Open Energy Information

    Open Energy Info (EERE)

    Technique LiDAR Activity Date Usefulness useful DOE-funding Unknown References Jennifer L. Lewicki, Curtis M. Oldenburg (Unknown) Near-Surface Co2 Monitoring And Analysis To...

  20. Beijing ChangLi Union Energy Company | Open Energy Information

    Open Energy Info (EERE)

    Municipality, China Product: China-based technology company that research in zinc-air batteries (fuel cells). References: Beijing ChangLi Union Energy Company1 This article is a...

  1. Qiaojia River Power Co Ltd Li County | Open Energy Information

    Open Energy Info (EERE)

    Changde City, Hainan Province, China Zip: 415500 Sector: Hydro Product: Hunan-based small hydro developer. References: Qiaojia River Power Co., Ltd, Li County1 This article is a...

  2. Transport and Failure in Li-ion Batteries | Stanford Synchrotron...

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

    in Li-ion Batteries Monday, February 13, 2012 - 1:30pm SSRL Conference Room 137-322 Stephen J. Harris, General Motors R&D While battery performance is well predicted by the...

  3. LiT Electrolysis Research at Savannah River National Laboratory (SRNL) |

    Office of Environmental Management (EM)

    Department of Energy LiT Electrolysis Research at Savannah River National Laboratory (SRNL) LiT Electrolysis Research at Savannah River National Laboratory (SRNL) Presentation from the 35th Tritium Focus Group Meeting held in Princeton, New Jersey on May 05-07, 2015. PDF icon LiT Electrolysis Research at Savannah River National Laboratory (SRNL) More Documents & Publications Electrolytic Tritium Extraction in Molten Li-LiT Composite Electrolytes to Stabilize Metallic Linium Anodes Solid

  4. Heteroclite electrochemical stability of an I based Li7P2S8I superionic conductor

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

    Rangasamy, Ezhiylmurugan; Liu, Zengcai; Gobet, Mallory; Pilar, Kartik; Sahu, Gayatri; Greenbaum, Steve; Liang, Chengdu

    2015-01-01

    Stability from Instability: A Li7P2S8I solid state Li-ion conductor derived from -Li3PS4 and LiI demonstrates exceptional electrochemical stability. The oxidation instability of I is subverted nullified via its incorporation into the coordinated structure. The inclusion of I also creates stability with metallic Li anode while simultaneously improving the interfacial kinetics. Low temperature membrane processability enables facile fabrication of dense membranes, making it suitable for industrial adoption.

  5. Investigation of critical parameters in Li-ion battery electrodes |

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

    Department of Energy critical parameters in Li-ion battery electrodes Investigation of critical parameters in Li-ion battery electrodes 2011 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon es070_cabana_2011_o.pdf More Documents & Publications Positive and Negative Electrodes: Novel and Optimized Materials Novel and Optimized Materials Phases for High Energy Density Batteries FY 2012 Annual Progress Report for Energy

  6. Predictive Models of Li-ion Battery Lifetime (Presentation) (Conference) |

    Office of Scientific and Technical Information (OSTI)

    SciTech Connect Conference: Predictive Models of Li-ion Battery Lifetime (Presentation) Citation Details In-Document Search Title: Predictive Models of Li-ion Battery Lifetime (Presentation) × You are accessing a document from the Department of Energy's (DOE) SciTech Connect. This site is a product of DOE's Office of Scientific and Technical Information (OSTI) and is provided as a public service. Visit OSTI to utilize additional information resources in energy science and technology. A

  7. Combined Quantum Chemical/Raman Spectroscopic Analyses of Li+ Cation

    Office of Scientific and Technical Information (OSTI)

    Solvation: Cyclic Carbonate Solvents - Ethylene Carbonate and Propylene Earbonate (Journal Article) | SciTech Connect Combined Quantum Chemical/Raman Spectroscopic Analyses of Li+ Cation Solvation: Cyclic Carbonate Solvents - Ethylene Carbonate and Propylene Earbonate Citation Details In-Document Search Title: Combined Quantum Chemical/Raman Spectroscopic Analyses of Li+ Cation Solvation: Cyclic Carbonate Solvents - Ethylene Carbonate and Propylene Earbonate Combined computational/Raman

  8. Automotive Li-ion Battery Cooling Requirements | Department of Energy

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

    Li-ion Battery Cooling Requirements Automotive Li-ion Battery Cooling Requirements Presents thermal management of lithium-ion battery packs for electric vehicles PDF icon cunningham.pdf More Documents & Publications Overview and Progress of the Battery Testing, Analysis, and Design Activity Vehicle Technologies Office Merit Review 2014: Overview and Progress of the Battery Testing, Design and Analysis Activity Overview of Battery R&D Activities

  9. ARM - Campaign Instrument - twin-otter-li-prof

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

    govInstrumentstwin-otter-li-prof Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Campaign Instrument : Twin Otter Lidar Profiles (TWIN-OTTER-LI-PROF) Instrument Categories Aerosols, Atmospheric Profiling, Cloud Properties Campaigns Tropical Warm Pool - International Cloud Experiment (TWP-ICE) [ Download Data ] Tropical Western Pacific, 2006.01.21 - 2006.02.13 Primary Measurements Taken The following measurements are those considered

  10. Efimov physics in {sup 6}Li atoms

    SciTech Connect (OSTI)

    Braaten, Eric; Hammer, H.-W.; Kang, Daekyoung; Platter, Lucas

    2010-01-15

    A new narrow three-atom loss resonance associated with an Efimov trimer crossing the three-atom threshold has recently been discovered in a many-body system of ultracold {sup 6}Li atoms in the three lowest hyperfine spin states at a magnetic field near 895 G. O'Hara and coworkers have used measurements of the three-body recombination rate in this region to determine the complex three-body parameter associated with Efimov physics. Using this parameter as the input, we calculate the universal predictions for the spectrum of Efimov states and for the three-body recombination rate in the universal region above 600 G where all three scattering lengths are large. We predict an atom-dimer loss resonance at 672+-2 G associated with an Efimov trimer disappearing through an atom-dimer threshold. We also predict an interference minimum in the three-body recombination rate at 759+-1 G where the three-spin mixture may be sufficiently stable to allow experimental study of the many-body system.

  11. Structural and Electrochemical Characterization of Pure LiFePO 4 and Nanocomposite C- LiFePO 4 Cathodes for Lithium Ion Rechargeable Batteries

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

    Kumar, Arun; Thomas, R.; Karan, N. K.; Saavedra-Arias, J. J.; Singh, M. K.; Majumder, S. B.; Tomar, M. S.; Katiyar, R. S.

    2009-01-01

    Pure limore » thium iron phosphate ( LiFePO 4 ) and carbon-coated LiFePO 4 (C- LiFePO 4 ) cathode materials were synthesized for Li-ion batteries. Structural and electrochemical properties of these materials were compared. X-ray diffraction revealed orthorhombic olivine structure. Micro-Raman scattering analysis indicates amorphous carbon, and TEM micrographs show carbon coating on LiFePO 4 particles. Ex situ Raman spectrum of C- LiFePO 4 at various stages of charging and discharging showed reversibility upon electrochemical cycling. The cyclic voltammograms of LiFePO 4 and C- LiFePO 4 showed only a pair of peaks corresponding to the anodic and cathodic reactions. The first discharge capacities were 63, 43, and 13 mAh/g for C/5, C/3, and C/2, respectively for LiFePO 4 where as in case of C- LiFePO 4 that were 163, 144, 118, and 70 mAh/g for C/5, C/3, C/2, and 1C, respectively. The capacity retention of pure LiFePO 4 was 69% after 25 cycles where as that of C- LiFePO 4 was around 97% after 50 cycles. These results indicate that the capacity and the rate capability improved significantly upon carbon coating.« less

  12. Structural and Electrochemical Characterization of PureLiFePO4and Nanocomposite C-LiFePO4Cathodes for Lithium Ion Rechargeable Batteries

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

    Kumar, Arun; Thomas, R.; Karan, N. K.; Saavedra-Arias, J. J.; Singh, M. K.; Majumder, S. B.; Tomar, M. S.; Katiyar, R. S.

    2009-01-01

    Pure lithium iron phosphate (LiFePO4) and carbon-coatedLiFePO4(C-LiFePO4) cathode materials were synthesized for Li-ion batteries. Structural and electrochemical properties of these materials were compared. X-ray diffraction revealed orthorhombic olivine structure. Micro-Raman scattering analysis indicates amorphous carbon, and TEM micrographs show carbon coating onLiFePO4particles. Ex situ Raman spectrum of C-LiFePO4at various stages of charging and discharging showed reversibility upon electrochemical cycling. The cyclic voltammograms ofLiFePO4and C-LiFePO4showed only a pair of peaks corresponding to the anodic and cathodic reactions. The first discharge capacities were 63, 43, and 13?mAh/g for C/5, C/3, and C/2, respectively forLiFePO4where as in case of C-LiFePO4that were 163, 144,more118, and 70?mAh/g for C/5, C/3, C/2, and 1C, respectively. The capacity retention of pureLiFePO4was 69% after 25 cycles where as that of C-LiFePO4was around 97% after 50 cycles. These results indicate that the capacity and the rate capability improved significantly upon carbon coating.less

  13. California Climate Exchange CaCX | Open Energy Information

    Open Energy Info (EERE)

    CaCX Jump to: navigation, search Name: California Climate Exchange (CaCX) Place: California Product: Aims to reducte CO2 emission in California. References: California Climate...

  14. ERSUG Meeting: January 28-29, 1997 (Berkeley, CA)

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

    ERSUG Meeting: January 28-29, 1997 (Berkeley, CA) Dates January 28-29, 1997 Location Lawerence Berkeley Nantional Laboratory Perserverence Hall 1 Cyclotron Road Berkeley, CA 94720...

  15. Influence of Li ions on the oxygen reduction reaction of platinum electrocatalyst

    SciTech Connect (OSTI)

    Liu, H; Xing, YC

    2011-06-01

    A Li-air battery can provide a much higher theoretical energy density than a Li-ion battery. The use of aqueous acidic electrolytes may prevent lithium oxide deposition from aprotic electrolytes and lithium carbonate precipitation from alkaline electrolytes. The present communication reports a study on the effect of Li ions on the oxygen reduction reaction (ORR) in sulfuric acid electrolytes. It was found that the Li ions have negligible interactions with the active surface of Pt catalysts. However, significantly lower ORR activities were found when Li ions are present in the sulfuric acid. The intrinsic kinetic activities were found to decrease with the increase of Li ion concentrations, but level off when the Li ion concentrations are larger than 1.0 M. The low activities of Pt catalysts in Li ion containing electrolytes were attributed to a constraining effect of Li ions on the diffusion of oxygen in the electrolyte solution. (C) 2011 Elsevier B.V. All rights reserved.

  16. DISCOVERY OF SUPER-Li-RICH RED GIANTS IN DWARF SPHEROIDAL GALAXIES

    SciTech Connect (OSTI)

    Kirby, Evan N.; Fu, Xiaoting; Deng, Licai; Guhathakurta, Puragra

    2012-06-10

    Stars destroy lithium (Li) in their normal evolution. The convective envelopes of evolved red giants reach temperatures of millions of kelvin, hot enough for the {sup 7}Li(p, {alpha}){sup 4}He reaction to burn Li efficiently. Only about 1% of first-ascent red giants more luminous than the luminosity function bump in the red giant branch exhibit A(Li) > 1.5. Nonetheless, Li-rich red giants do exist. We present 15 Li-rich red giants-14 of which are new discoveries-among a sample of 2054 red giants in Milky Way dwarf satellite galaxies. Our sample more than doubles the number of low-mass, metal-poor ([Fe/H] {approx}< -0.7) Li-rich red giants, and it includes the most-metal-poor Li-enhanced star known ([Fe/H] = -2.82, A(Li){sub NLTE} = 3.15). Because most of the stars have Li abundances larger than the universe's primordial value, the Li in these stars must have been created rather than saved from destruction. These Li-rich stars appear like other stars in the same galaxies in every measurable regard other than Li abundance. We consider the possibility that Li enrichment is a universal phase of evolution that affects all stars, and it seems rare only because it is brief.

  17. High performance anode for advanced Li batteries

    SciTech Connect (OSTI)

    Lake, Carla

    2015-11-02

    The overall objective of this Phase I SBIR effort was to advance the manufacturing technology for ASIs Si-CNF high-performance anode by creating a framework for large volume production and utilization of low-cost Si-coated carbon nanofibers (Si-CNF) for the battery industry. This project explores the use of nano-structured silicon which is deposited on a nano-scale carbon filament to achieve the benefits of high cycle life and high charge capacity without the consequent fading of, or failure in the capacity resulting from stress-induced fracturing of the Si particles and de-coupling from the electrode. ASIs patented coating process distinguishes itself from others, in that it is highly reproducible, readily scalable and results in a Si-CNF composite structure containing 25-30% silicon, with a compositionally graded interface at the Si-CNF interface that significantly improve cycling stability and enhances adhesion of silicon to the carbon fiber support. In Phase I, the team demonstrated the production of the Si-CNF anode material can successfully be transitioned from a static bench-scale reactor into a fluidized bed reactor. In addition, ASI made significant progress in the development of low cost, quick testing methods which can be performed on silicon coated CNFs as a means of quality control. To date, weight change, density, and cycling performance were the key metrics used to validate the high performance anode material. Under this effort, ASI made strides to establish a quality control protocol for the large volume production of Si-CNFs and has identified several key technical thrusts for future work. Using the results of this Phase I effort as a foundation, ASI has defined a path forward to commercialize and deliver high volume and low-cost production of SI-CNF material for anodes in Li-ion batteries.

  18. High Performance Cathodes for Li-Air Batteries

    SciTech Connect (OSTI)

    Xing, Yangchuan

    2013-08-22

    The overall objective of this project was to develop and fabricate a multifunctional cathode with high activities in acidic electrolytes for the oxygen reduction and evolution reactions for Li-air batteries. It should enable the development of Li-air batteries that operate on hybrid electrolytes, with acidic catholytes in particular. The use of hybrid electrolytes eliminates the problems of lithium reaction with water and of lithium oxide deposition in the cathode with sole organic electrolytes. The use of acid electrolytes can eliminate carbonate formation inside the cathode, making air breathing Li-air batteries viable. The tasks of the project were focused on developing hierarchical cathode structures and bifunctional catalysts. Development and testing of a prototype hybrid Li-air battery were also conducted. We succeeded in developing a hierarchical cathode structure and an effective bifunctional catalyst. We accomplished integrating the cathode with existing anode technologies and made a pouch prototype Li-air battery using sulfuric acid as catholyte. The battery cathodes contain a nanoscale multilayer structure made with carbon nanotubes and nanofibers. The structure was demonstrated to improve battery performance substantially. The bifunctional catalyst developed contains a conductive oxide support with ultra-low loading of platinum and iridium oxides. The work performed in this project has been documented in seven peer reviewed journal publications, five conference presentations, and filing of two U.S. patents. Technical details have been documented in the quarterly reports to DOE during the course of the project.

  19. DOE CYBER SECURITY EBK: CORE COMPETENCY TRAINING REQUIREMENTS: CA

    Broader source: Energy.gov [DOE]

    DOE CYBER SECURITY EBK: CORE COMPETENCY TRAINING REQUIREMENTS. Key Cyber Security Role: Certification Agent (CA)

  20. Development of Cell/Pack Level Models for Automotive Li-Ion Batteries...

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

    CellPack Level Models for Automotive Li-Ion Batteries with Experimental Validation Development of CellPack Level Models for Automotive Li-Ion Batteries with Experimental...

  1. Guide to Developing Air-Cooled Lithium Bromide (LiBr) Absorption...

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

    Developing Air-Cooled Lithium Bromide (LiBr) Absorption for CHP Applications, April 2005 Guide to Developing Air-Cooled Lithium Bromide (LiBr) Absorption for CHP Applications, ...

  2. Advanced Li-Ion Polymer Battery Cell Manufacturing Plant in USA...

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

    Li-Ion Polymer Battery Cell Manufacturing Plant in USA Advanced Li-Ion Polymer Battery Cell Manufacturing Plant in USA 2012 DOE Hydrogen and Fuel Cells Program and Vehicle ...

  3. Xiang Ge Li La Xian Mai Di He Hydro Power Development Co Ltd...

    Open Energy Info (EERE)

    Xiang Ge Li La Xian Mai Di He Hydro Power Development Co Ltd Jump to: navigation, search Name: Xiang Ge Li La Xian Mai Di He Hydro Power Development Co., Ltd. Place: Yunnan...

  4. LiDAR At Chocolate Mountains Area (Alm, Et Al., 2010) | Open...

    Open Energy Info (EERE)

    aerial Li-DAR survey flown over the project areas, securing over 177,000 square kilometers of <30cm accuracy digital elevation data. LiDAR data were analyzed to characterize...

  5. Significant Cost Improvement of Li-Ion Cells Through Non-NMP...

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

    of Li-Ion Cells Through Non-NMP Electrode Coating, Direct Separator Coating, and Fast Formation Technologies Significant Cost Improvement of Li-Ion Cells Through Non-NMP ...

  6. A Reactive Force Field study of Li/C Systems for Electrical Energy...

    Office of Scientific and Technical Information (OSTI)

    Reactive Force Field study of LiC Systems for Electrical Energy Storage Citation Details In-Document Search Title: A Reactive Force Field study of LiC Systems for Electrical...

  7. Electrochemical Performances of LiMnPO4 Synthesized from Non...

    Office of Scientific and Technical Information (OSTI)

    Li1.1MnPO4 exhibits the most stable cycling ability probably because of the existence of a trace amount of Li3PO4 impurity that functions as a solid-state electrolyte on...

  8. X-ray line polarization spectroscopy of Li-like satellite line...

    Office of Scientific and Technical Information (OSTI)

    Journal Article: X-ray line polarization spectroscopy of Li-like satellite line spectra Citation Details In-Document Search Title: X-ray line polarization spectroscopy of Li-like...

  9. Digital Sofcell Shanghai ShenLi Goeta solid oxide fuel cell joint...

    Open Energy Info (EERE)

    ShenLi Goeta solid oxide fuel cell joint venture Jump to: navigation, search Name: Digital Sofcell - Shanghai ShenLi - Goeta solid oxide fuel cell joint venture Place: China...

  10. The significance of Li-ion batteries in electric vehicle life...

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

    The significance of Li-ion batteries in electric vehicle life-cycle energy and emissions and recycling's role in its reduction Title The significance of Li-ion batteries in...

  11. Guide to Developing Air-Cooled Lithium Bromide (LiBr) Absorption...

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

    Guide to Developing Air-Cooled Lithium Bromide (LiBr) Absorption for CHP Applications, April 2005 Guide to Developing Air-Cooled Lithium Bromide (LiBr) Absorption for CHP...

  12. Structure and Electrochemistry of Vanadium-Modified LiFePO4 ...

    Office of Scientific and Technical Information (OSTI)

    Journal Article: Structure and Electrochemistry of Vanadium-Modified LiFePO4 Citation Details In-Document Search Title: Structure and Electrochemistry of Vanadium-Modified LiFePO4...

  13. Alternating magnetic anisotropy of Li2(Li1xTx)N(T=Mn,Fe,Co,andNi)

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

    Jesche, A.; Ke, L.; Jacobs, J. L.; Harmon, B.; Houk, R. S.; Canfield, P. C.

    2015-05-11

    Substantial amounts of the transition metals Mn, Fe, Co, and Ni can be substituted for Li in single crystalline Li2(Li1xTx)N. Isothermal and temperature-dependent magnetization measurements reveal local magnetic moments with magnitudes significantly exceeding the spin-only value. The additional contributions stem from unquenched orbital moments that lead to rare-earth-like behavior of the magnetic properties. Accordingly, extremely large magnetic anisotropies have been found. Most notably, the magnetic anisotropy alternates as easy plane?easy axis?easy plane?easy axis when progressing from T = Mn ? Fe ? Co ? Ni. This behavior can be understood based on a perturbation approach in an analytical, single-ion model.moreAs a result, the calculated magnetic anisotropies show surprisingly good agreement with the experiment and capture the basic features observed for the different transition metals.less

  14. Alternating magnetic anisotropy of Li 2 ( Li 1 - x T x ) N ( T = Mn , Fe , Co , and Ni )

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

    Jesche, A.; Ke, L.; Jacobs, J. L.; Harmon, B.; Houk, R. S.; Canfield, P. C.

    2015-05-01

    Substantial amounts of the transition metals Mn, Fe, Co, and Ni can be substituted for Li in single crystalline Li?(Li1-xTx)N. Isothermal and temperature-dependent magnetization measurements reveal local magnetic moments with magnitudes significantly exceeding the spin-only value. The additional contributions stem from unquenched orbital moments that lead to rare-earth-like behavior of the magnetic properties. Accordingly, extremely large magnetic anisotropies have been found. Most notably, the magnetic anisotropy alternates as easy plane?easy axis?easy plane?easy axis when progressing from T = Mn ? Fe ? Co ? Ni. This behavior can be understood based on a perturbation approach in an analytical, single-ion model.moreThe calculated magnetic anisotropies show surprisingly good agreement with the experiment and capture the basic features observed for the different transition metals.less

  15. Alternating magnetic anisotropy of Li2(Li1–xTx)N (T = Mn, Fe, Co, and Ni)

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

    Jesche, A.; Ke, L.; Jacobs, J. L.; Harmon, B.; Houk, R. S.; Canfield, P. C.

    2015-05-11

    Substantial amounts of the transition metals Mn, Fe, Co, and Ni can be substituted for Li in single crystalline Li2(Li1–xTx)N. Isothermal and temperature-dependent magnetization measurements reveal local magnetic moments with magnitudes significantly exceeding the spin-only value. The additional contributions stem from unquenched orbital moments that lead to rare-earth-like behavior of the magnetic properties. Accordingly, extremely large magnetic anisotropies have been found. Most notably, the magnetic anisotropy alternates as easy plane→easy axis→easy plane→easy axis when progressing from T = Mn → Fe → Co → Ni. This behavior can be understood based on a perturbation approach in an analytical, single-ion model.more » As a result, the calculated magnetic anisotropies show surprisingly good agreement with the experiment and capture the basic features observed for the different transition metals.« less

  16. Protection of Li Anodes Using Dual Phase Electrolytes | Department of

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

    Energy 1 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon es012_mikhaylik_2011_p.pdf More Documents & Publications Protection of Li Anodes Using Dual Phase Electrolytes Progress of DOE Materials, Manufacturing Process R&D, and ARRA Battery Manufacturing Grants FY 2011 Annual Prog

  17. Protection of Li Anodes Using Dual Phase Electrolytes | Department of

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

    Energy 0 DOE Vehicle Technologies and Hydrogen Programs Annual Merit Review and Peer Evaluation Meeting, June 7-11, 2010 -- Washington D.C. PDF icon es012_mikhaylik_2010_o.pdf More Documents & Publications Protection of Li Anodes Using Dual Phase Electrolytes Progress of DOE Materials, Manufacturing Process R&D, and ARRA Battery Manufacturing Grant

  18. Anode Materials for Rechargeable Li-Ion Batteries

    SciTech Connect (OSTI)

    Fultz, B.

    2001-01-12

    This research is on materials for anodes and cathodes in electrochemical cells. The work is a mix of electrochemical measurements and analysis of the materials by transmission electron microscopy and x-ray diffractometry. At present, our experimental work involves only materials for Li storage, but we have been writing papers from our previous work on hydrogen-storage materials.

  19. Li corrosion resistant glasses for headers in ambient temperature Li batteries

    DOE Patents [OSTI]

    Hellstrom, E.E.; Watkins, R.D.

    1985-10-11

    Glass compositions containing 10 to 50 mol% CaO, 10 to 50 mol% Al/sub 2/O/sub 3/, 30 to 60 mol% B/sub 2/O/sub 3/, and 0 to 30 mol% MgO are provided. These compositions are capable of forming a stable glass-to-metal seal possessing electrical insulating properties for use in a lithium battery. Also provided are lithium cells containing a stainless steel body and molybdenum center pin electrically insulated by means of a seal produced according to the invention.

  20. Performance of LiAlloy/Ag(2)CrO(4) Couples in Molten CsBr-LiBr-KBr Eutectic

    SciTech Connect (OSTI)

    GUIDOTTI,RONALD A.; REINHARDT,FREDERICK W.

    1999-10-18

    The performance of Li-alloy/CsBr-LiBr-KBr/Ag{sub 2}CrO{sub 4} systems was studied over a temperature range of 250 C to 300 C, for possible use as a power source for geothermal borehole applications. Single cells were discharged at current densities of 15.8 and 32.6 mA/cm{sup 2} using Li-Si and Li-Al anodes. When tested in 5-cell batteries, the Li-Si/CsBr-LiBr-KBr/Ag{sub 2}CrO{sub 4} system exhibited thermal runaway. Thermal analytical tests showed that the Ag{sub 2}CrO{sub 4} cathode reacted exothermically with the electrolyte on activation. Consequently, this system would not be practical for the envisioned geothermal borehole applications.

  1. Microsoft Word - Cd-CA.doc

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

    The First Cadmium Enzyme - Carbonic Anhydrase 2 from the marine diatom Thalassiosira weissflogii Todd W. Lane 1 , Mak A. Saito 2 , Graham N. George 3 , Ingrid J. Pickering 3 , Roger C. Prince 4 and François M.M. Morel 5 1 Biosystems Research Department, Sandia National Labs, Livermore, CA 2 Marine Chemistry and Geochemistry Department, Woods Hole Oceanographic Institution, Woods Hole, MA 3 Department of Geological Sciences, University of Saskatchewan, Saskatoon, Canada 4 ExxonMobil Research

  2. Pressure-induced ferroelectric to paraelectric transition in LiTaO3 and

    Office of Scientific and Technical Information (OSTI)

    (Li,Mg)TaO3 (Journal Article) | DOE PAGES Pressure-induced ferroelectric to paraelectric transition in LiTaO3 and (Li,Mg)TaO3 This content will become publicly available on February 16, 2017 Title: Pressure-induced ferroelectric to paraelectric transition in LiTaO3 and (Li,Mg)TaO3 Authors: Yamanaka, Takamitsu [1] ; Nakamoto, Yuki [2] ; Takei, Fumihiko [3] ; Ahart, Muhtar [1] ; Mao, Ho-kwang [4] ; Hemley, Russell J. [1] + Show Author Affiliations Geophysical Laboratory, Carnegie Institution

  3. Pressure-induced ferroelectric to paraelectric transition in LiTaO3 and

    Office of Scientific and Technical Information (OSTI)

    (Li,Mg)TaO3 (Journal Article) | SciTech Connect Journal Article: Pressure-induced ferroelectric to paraelectric transition in LiTaO3 and (Li,Mg)TaO3 Citation Details In-Document Search This content will become publicly available on February 16, 2017 Title: Pressure-induced ferroelectric to paraelectric transition in LiTaO3 and (Li,Mg)TaO3 Authors: Yamanaka, Takamitsu [1] ; Nakamoto, Yuki [2] ; Takei, Fumihiko [3] ; Ahart, Muhtar [1] ; Mao, Ho-kwang [4] ; Hemley, Russell J. [1] + Show Author

  4. Advanced Li-Ion Polymer Battery Cell Manufacturing Plant in USA |

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

    Department of Energy Li-Ion Polymer Battery Cell Manufacturing Plant in USA Advanced Li-Ion Polymer Battery Cell Manufacturing Plant in USA 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting PDF icon arravt001_es_koo_2012_p.pdf More Documents & Publications Advanced Li-Ion Polymer Battery Cell Manufacturing Plant in USA Li-Ion Battery Cell Manufacturing 2010 DOE, Li-Ion Battery Cell Manufacturing

  5. Electrolytes in Support of 5 V Li-ion Chemistries | Department of Energy

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

    in Support of 5 V Li-ion Chemistries Electrolytes in Support of 5 V Li-ion Chemistries 2010 DOE Vehicle Technologies and Hydrogen Programs Annual Merit Review and Peer Evaluation Meeting, June 7-11, 2010 -- Washington D.C. PDF icon es024_jow_2010_o.pdf More Documents & Publications High Voltage Electrolytes for Li-ion Batteries High Voltage Electrolytes for Li-ion Batteries Vehicle Technologies Office Merit Review 2015: Fluorinated Electrolyte for 5-V Li-Ion Chemistry

  6. Method for treating electrolyte to remove Li.sub.2 O

    DOE Patents [OSTI]

    Tomczuk, Zygmunt (Lockport, IL); Miller, William E. (Naperville, IL); Johnson, Gerald K. (Downers Grove, IL); Willit, James L. (Batavia, IL)

    1998-01-01

    A method of removing Li.sub.2 O present in an electrolyte predominantly of LiCl and KCl. The electrolyte is heated to a temperature not less than about 500.degree. C. and then Al is introduced into the electrolyte in an amount in excess of the stoichiometric amount needed to convert the Li.sub.2 O to a Li-Al alloy and lithium aluminate salt. The salt and aluminum are maintained in contact with agitation for a time sufficient to convert the Li.sub.2 O.

  7. Method for treating electrolyte to remove Li{sub 2}O

    DOE Patents [OSTI]

    Tomczuk, Z.; Miller, W.E.; Johnson, G.K.; Willit, J.L.

    1998-01-20

    A method is described for removing Li{sub 2}O present in an electrolyte predominantly of LiCl and KCl. The electrolyte is heated to a temperature not less than about 500 C and then Al is introduced into the electrolyte in an amount in excess of the stoichiometric amount needed to convert the Li{sub 2}O to a Li-Al alloy and lithium aluminate salt. The salt and aluminum are maintained in contact with agitation for a time sufficient to convert the Li{sub 2}O.

  8. First-Principles Calculations, Electrochemical and X-ray Absorption Studies of Li-Ni-PO4 Surface-Treated xLi2MnO3 (1 x)LiMO2 (M = Mn, Ni, Co) Electrodes for Li-Ion Batteries

    SciTech Connect (OSTI)

    Wolverton, Christopher; Croy, J R; Balasubramanian, M; Kang, Sun-Ho; Lopez-Rivera, C. M.; Thackeray, Michael M.

    2012-01-01

    It has been previously hypothesized that the enhanced rate capability of Li-Ni-PO{sub 4}-treated xLi{sub 2}MnO{sub 3} {center_dot} (1-x)LiMO{sub 2} positive electrodes (M = Mn, Ni, Co) in Li-ion batteries might be associated with a defect Ni-doped Li{sub 3}PO{sub 4} surface structure [i.e., Li{sub 3-2y}Ni{sub y}PO{sub 4} (0 < y < 1)], thereby promoting fast Li{sup +}-ion conduction at the xLi{sub 2}MnO{sub 3} {center_dot} (1-x)LiMO{sub 2} particle surface. In this paper, the solubility of divalent metals (Fe, Mn, Ni, Mg) in {gamma}-Li{sub 3}PO{sub 4} is predicted with the first-principles GGA+U method in an effort to understand the enhanced rate capability. The predicted solubility (x) is extremely small; this finding is consistent with experimental evidence: 1) X-ray diffraction data obtained from Li-Ni-PO{sub 4}-treated xLi{sub 2}MnO{sub 3} {center_dot} (1-x)LiMO{sub 2} electrodes that show that, after annealing at 550 C, a Li{sub 3}PO{sub 4}-like structure forms as a second phase at the electrode particle surface, and 2) X-ray absorption spectroscopy, which indicate that the nickel ions are accommodated in the transition metal layers of the Li{sub 2}MnO{sub 3} component during the annealing process. However, electrochemical studies of Li{sub 3-2y}Ni{sub y}PO{sub 4}-treated xLi{sub 2}MnO{sub 3} {center_dot} (1-x)LiMO{sub 2} electrodes indicate that their rate capability increases as a function of y over the range y = 0 (Li{sub 3}PO{sub 4}) to y = 1 (LiNiPO{sub 4}), strongly suggesting that, at some level, the nickel ions play a role in reducing electrochemical impedance and increasing electrode stability at the electrode particle surface.

  9. mRNA Transcript Abundance during Plant Growth and the Influence of Li+ Exposure

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

    Duff, M. C.; Kuhne, W. W.; Halverson, N. V.; Chang, C. -S.; Kitamura, E.; Hawthorn, L.; Martinez, N. E.; Stafford, C.; Milliken, C. E.; Caldwell, E. F.; et al

    2014-10-23

    Lithium (Li) toxicity in plants is, at a minimum, a function of Li+ concentration, exposure time, species and growth conditions. Most plant studies with Li+ focus on short-term acute exposures. This study examines short- and long-term effects of Li+ exposure in Arabidopsis with Li+ uptake studies and measured shoot mRNA transcript abundance levels in treated and control plants. Stress, pathogen-response and arabinogalactan protein genes were typically more up-regulated in older (chronic, low level) Li+-treatment plants and in the much younger plants from acute high-level exposures. The gene regulation behavior of high-level Li+ resembled prior studies due to its influence on:more »inositol synthesis, 1-aminocyclopropane-1-carboxylate synthases and membrane ion transport. In contrast, chronically-exposed plants had gene regulation responses that were indicative of pathogen, cold, and heavy-metal stress, cell wall degradation, ethylene production, signal transduction, and calcium-release modulation. Acute Li+ exposure phenocopies magnesium-deficiency symptoms and is associated with elevated expression of stress response genes that could lead to consumption of metabolic and transcriptional energy reserves and the dedication of more resources to cell development. In contrast, chronic Li+ exposure increases expression signal transduction genes. The identification of new Li+-sensitive genes and a gene-based “response plan” for acute and chronic Li+ exposure are delineated.« less

  10. mRNA Transcript Abundance during Plant Growth and the Influence of Li+ Exposure

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

    Duff, M. C.; Kuhne, W. W.; Halverson, N. V.; Chang, C. -S.; Kitamura, E.; Hawthorn, L.; Martinez, N. E.; Stafford, C.; Milliken, C. E.; Caldwell, E. F.; et al

    2014-10-23

    Lithium (Li) toxicity in plants is, at a minimum, a function of Li+ concentration, exposure time, species and growth conditions. Most plant studies with Li+ focus on short-term acute exposures. This study examines short- and long-term effects of Li+ exposure in Arabidopsis with Li+ uptake studies and measured shoot mRNA transcript abundance levels in treated and control plants. Stress, pathogen-response and arabinogalactan protein genes were typically more up-regulated in older (chronic, low level) Li+-treatment plants and in the much younger plants from acute high-level exposures. The gene regulation behavior of high-level Li+ resembled prior studies due to its influence on:more » inositol synthesis, 1-aminocyclopropane-1-carboxylate synthases and membrane ion transport. In contrast, chronically-exposed plants had gene regulation responses that were indicative of pathogen, cold, and heavy-metal stress, cell wall degradation, ethylene production, signal transduction, and calcium-release modulation. Acute Li+ exposure phenocopies magnesium-deficiency symptoms and is associated with elevated expression of stress response genes that could lead to consumption of metabolic and transcriptional energy reserves and the dedication of more resources to cell development. In contrast, chronic Li+ exposure increases expression signal transduction genes. The identification of new Li+-sensitive genes and a gene-based “response plan” for acute and chronic Li+ exposure are delineated.« less

  11. Capacity Needs Diagnostics for Renewable Energies (CaDRE) | Open...

    Open Energy Info (EERE)

    here: Handbook Toolbox Four Levels of CaDRE CaDRE is based on the idea that a governing body can successfully develop in the renewable energy sector when the following...

  12. Metropolitan Water District of S CA | Open Energy Information

    Open Energy Info (EERE)

    Metropolitan Water District of S CA Jump to: navigation, search Name: Metropolitan Water District of S CA Place: California Phone Number: (213) 217-6000 Website: www.mwdh2o.com...

  13. EIS-0439: Rice Solar Energy Project in Riverside County, CA ...

    Energy Savers [EERE]

    9: Rice Solar Energy Project in Riverside County, CA EIS-0439: Rice Solar Energy Project in Riverside County, CA March 29, 2010 EIS-0439: Notice of Intent to Prepare an ...

  14. EIS-0455: Genesis Solar Energy Project in Riverside County, CA...

    Energy Savers [EERE]

    5: Genesis Solar Energy Project in Riverside County, CA EIS-0455: Genesis Solar Energy Project in Riverside County, CA December 17, 2010 EIS-0455: Notice of Adoption of an ...

  15. ERSUG Meeting: January 8-9, 1996 (Berkeley, CA)

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

    ERSUG Meeting: January 8-9, 1996 (Berkeley, CA) Dates January 8-9, 1996 Location Lawrence Berkeley National Laboratory 1 Cyclotron Road Berkeley, CA 94720 Attendee List Minutes...

  16. File:Ca1.pdf | Open Energy Information

    Open Energy Info (EERE)

    Ca1.pdf Jump to: navigation, search File File history File usage Metadata File:Ca1.pdf Size of this preview: 463 599 pixels. Other resolution: 464 600 pixels. Go to page 1 2...

  17. Luminescent properties of Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} and its potential application in white light emitting diodes

    SciTech Connect (OSTI)

    Wang, Zhijun; Li, Panlai; Li, Ting; Zhang, Xing; Li, Qingxuan; Yang, Zhiping; Guo, Qinglin

    2013-06-01

    Graphical abstract: Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} phosphor can be effectively excited by an ultraviolet and near-ultraviolet light, and produce a bright blue emission centered at 436 nm. The CIE chromaticity coordinations (x, y) of Na{sub 2}CaSiO{sub 4}:Eu{sup 2+}(NSCE)/Li{sub 2}SrSiO{sub 4}:Eu{sup 2+}(LSSE) vary with the molar ratio of the two constituents. When NSCE/LSSE is 1:3, the CIE chromaticity coordination is (0.332, 0.346), which is close to that of the natural sunlight (0.33, 0.33). The results indicate that Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} may be a promising blue phosphor for UV chip-based multi-phosphor converted white light emitting diodes. Highlights: ? Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} shows the blue emission with a peak at 436 nm and broad excitation band in the UV/n-UV range. ? White light with CIE coordinates (0.332, 0.346) is generated by mixing the blue phosphor with the Li{sub 2}SrSiO{sub 4}:Eu{sup 2+} yellow phosphor. ? Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} would be a promising blue phosphor candidate for UV chip-based multi-phosphor converted white LEDs. - Abstract: A novel blue phosphor Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} is synthesized by a high temperature solid-state reaction, and its luminescent properties are systematically studied. Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} can be effectively excited by the 354 nm radiation, and create blue emission (436 nm). The emission intensity of Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} is influenced by the Eu{sup 2+} doping content, and the optimal doping content is 1.5%, and the concentration quenching mechanism of Eu{sup 2+} in Na{sub 2}CaSiO{sub 4} can be attributed to the multipolar interaction. The white light with CIE coordinates (0.332, 0.346) is generated by mixing the blue phosphor Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} with the yellow phosphor Li{sub 2}SrSiO{sub 4}:Eu{sup 2+}. The results indicate that Na{sub 2}CaSiO{sub 4}:Eu{sup 2+} may be a potential blue emitting phosphor for UV chip-based multi-phosphor converted white light emitting diodes.

  18. Financial Statement: IG-FS-CA-06-04

    Broader source: Energy.gov [DOE]

    Review of Actions to Correct Financial Control and Reporting Weaknesses; Audit Report No: OAS-FS/CA-06-04

  19. Effect of LiAlO{sub 2} nanoparticle filler concentration on the electrical properties of PEOLiClO{sub 4} composite

    SciTech Connect (OSTI)

    Masoud, E.M.; El-Bellihi, A.-A.; Bayoumy, W.A.; Mousa, M.A.

    2013-03-15

    Highlights: ? Structural modification of nano LiAlO{sub 2} filler increased conductivity. ? Good ionic conductivity for (LiAlO{sub 2}){sub 1.5}(PEO){sub 11}(LiClO{sub 4}) at room temperature. ? Nano LiAlO{sub 2} filler enhanced both ion migration and orientation. ? High dielectric properties for (LiAlO{sub 2}){sub 1.5}(PEO){sub 11}(LiClO{sub 4}) at room temperature. - Abstract: Nano-composite polymer electrolytes are receiving attention as potential candidates to be used as electrolyte membranes in lithium polymer batteries and other devices. In this work, polyethylene oxideLiClO{sub 4} based composite polymer electrolyte was prepared by solution casting method. The effect of LiAlO{sub 2} nanoparticle ceramic filler concentration on the structure and electrical conduction of the composite was studied. Nano-LiAlO{sub 2} was synthesized by solgel method. The samples were characterized using X-ray diffraction, Fourier Transmission-Infra Red, Differential Scanning Calorimetry, and tested by dielectric properties, Direct and Alternating current measurements as well as by impedance spectroscopy. All samples showed a behavior referring to an ionic conduction. Generally, the melting temperature of the polymer electrolyte decreased with filler concentration. Both thermal property and filler concentration influenced conductivity value. At room temperature, the highest ionic conductivity was 9.76 10{sup ?5} ohm{sup ?1} cm{sup ?1} for sample with a composition of (LiAlO{sub 2}){sub 1.5}(polyethylene oxide){sub 11}(LiClO{sub 4}). All results were correlated and discussed.

  20. CA Mr. Andrew Wallo, III, NE-23

    Office of Legacy Management (LM)

    ?9OQ, 95.5 L'E&nt Plaza, SW.. W.ashin@.m, D.C. 20024.2174, Tekphone: (202) 488AQOO 7117-03.B7.cdy.43 23 September 1987 CA Mr. Andrew Wallo, III, NE-23 Division of Facility & Site Decommissioning Projects U.S. Oepartment of Energy Germantown, Maryland 20545 Dear Mr. Wallo: ELIMINATION RECOMMENDATION -- COLLEGES AND UNIVERSITIES zh/ ! o-01 lM!tl5 ML)!o-05 PI 77!0> The attached elimination recoannendation was prepared in accordance . -1 rlL.0~ with your suggestion during our meeting on

  1. CA Mr. Wayne Klassing Klassing Hardbrake Company

    Office of Legacy Management (LM)

    s/L / ' CA _ _.- Mr. Wayne Klassing Klassing Hardbrake Company P.O. Box 860 Joliet, Illinois 60434 E- 3 --- ,"".Y.- 1 , -4 v / 1 /89 ., ._ I.. Dear Mr. Klassing: The Department of Energy (DOE) has completed its review of the preliminary radiological data from the May 1989 survey of your facility in Joliet, Illinois, which is the site of the former W. E. Pratt Manufacturing Company. We are pleased to inform you that the survey has verified that the radiological condition of your

  2. Fusion of {sup 48}Ca+{sup 48}Ca Far Below the Barrier

    SciTech Connect (OSTI)

    Scarlassara, F.; Montagnoli, G.; Mason, P.; Stefanini, A. M.; Silvestri, R.; Corradi, L.; Fioretto, E.; Guiot, B.; Courtin, S.; Haas, F.; Lebhertz, D.; Szilner, S.

    2009-08-26

    In recent years, a puzzling pattern has been observed in fusion cross sections well below the Coulomb barrier, characterized as a departure from the exponential-like behavior predicted by standard coupled-channels models, known as fusion hindrance. We report on recent fusion measurements performed at the Laboratori Nazionali di Legnaro, in particular the {sup 48}Ca+{sup 48}Ca reaction down to the level of 0.6 {mu}b. Unlike most recent results in this field, we do not observe the typical divergent behavior of the logarithmic derivative; but rather a sort of saturation, albeit at a larger value than predicted with a standard nucleus-nucleus potential.

  3. Predictive Models of Li-ion Battery Lifetime

    SciTech Connect (OSTI)

    Smith, Kandler; Wood, Eric; Santhanagopalan, Shriram; Kim, Gi-heon; Shi, Ying; Pesaran, Ahmad

    2015-06-15

    It remains an open question how best to predict real-world battery lifetime based on accelerated calendar and cycle aging data from the laboratory. Multiple degradation mechanisms due to (electro)chemical, thermal, and mechanical coupled phenomena influence Li-ion battery lifetime, each with different dependence on time, cycling and thermal environment. The standardization of life predictive models would benefit the industry by reducing test time and streamlining development of system controls.

  4. Conduction below 100 °C in nominal Li6ZnNb4O14

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

    Li, Yunchao; Paranthaman, Mariappan Parans; Gill, Lance W.; Edward W. Hagaman; Wang, Yangyang; Sokolov, Alexei P.; Dai, Sheng; Ma, Cheng; Chi, Miaofang; Veith, Gabriel M.; et al

    2015-09-15

    The increasing demand for a safe rechargeable battery with a high energy density per cell is driving a search for a novel solid electrolyte with a high Li+ or Na+ conductivity that is chemically stable in a working Li-ion or Na-ion battery. Li6ZnNb4O14 has been reported to exhibit a σ Li > 10-2 S cm-1 at 250 °C, but to disproportionate into multiple phases on cooling from 850 °C to room temperature. An investigation of the room-temperature Li-ion conductivity in a porous pellet of a multiphase product of a nominal Li6ZnNb4O14 composition is shown to have bulk σ Li 3.3more » x 10-5 S cm-1 at room temperature that increases to 1.4 x 10-4 S cm-1 by 50 °C. 7Li MAS NMR spectra were fitted to two Lorentzian lines, one of which showed a dramatic increase with increasing temperature. As a result, a test for water stability indicates that Li+ may move to the particle and grain surfaces to react with adsorbed water as occurs in the garnet Li+ conductors.« less

  5. Spectroscopy of LiΛ9 by electroproduction

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

    Urciuoli, G. M.; Cusanno, F.; Marrone, S.; Acha, A.; Ambrozewicz, P.; Aniol, K. A.; Baturin, P.; Bertin, P. Y.; Benaoum, H.; Blomqvist, K. I.; et al

    2015-03-01

    Background: In the absence of accurate data on the free two-body hyperon-nucleon interaction, the spectra of hypernuclei can provide information on the details of the effective hyperon-nucleon interaction. Purpose: To obtain a high-resolution spectrum for the 9Be(e,e'K+)9ΛLi reaction. Method: Electroproduction of the hypernucleus 9ΛLi has been studied for the first time with sub-MeV energy resolution in Hall A at Jefferson Lab on a 9Be target. In order to increase the counting rate and to provide unambiguous kaon identification, two superconducting septum magnets and a Ring Imaging CHerenkov detector (RICH) were added to the Hall A standard equipment. Results: The crossmore » section to low-lying states of 9ΛLi is concentrated within 3 MeV of the ground state and can be fitted with four peaks. The positions of the doublets agree with theory while a disagreement could exist with respect to the relative strengths of the peaks in the doublets. A Λ separation energy, BΛ, of 8.36±0.08 (stat.) ±0.08 (syst.) MeV was measured, in agreement with an earlier experiment.« less

  6. Searching for Sustainable and "Greener" Li-ion Batteries

    ScienceCinema (OSTI)

    Tarascon, Jean-Marie [University of Picardie at Aimens, France

    2010-01-08

    Lithium-ion batteries are strong candidates for powering upcoming generations of hybrid electric vehicles and plug-in hybrid electric vehicles. But improvements in safety must be achieved while keeping track of materials resources and abundances, as well as materials synthesis and recycling processes, all of which could inflict a heavy energy cost. Thus, electrode materials that have a minimum footprint in nature and are made via eco-efficient processes are sorely needed. The arrival of electrode materials based on minerals such as LiFePO4 (tryphilite) is a significant, but not sufficient, step toward the long-term demand for materials sustainability. The eco-efficient synthesis of LiFePO4 nanopowders via hydrothermal/ solvo-thermal processes using latent bases, structure directing templates, or other bio-related approaches will be presented in this talk. However, to secure sustainability and greeness, organic electrodes appear to be ideal candidates.... We took a fresh look at organic based electrodes; the results of this research into sequentially metal-organic-framework electrodes and Li-based organic electrodes (LixCyOz) will be reported and discussed.

  7. Theoretical exploration of various lithium peroxide crystal structures in a Li-air battery

    SciTech Connect (OSTI)

    Lau, Kah; Qiu, Dantong; Luo, Xiangyi; Greeley, Jeffrey; Curtiss, Larry; Lu, Jun; Amine, Khalil

    2015-01-14

    We describe a series of metastable Li?O? crystal structures involving different orientations and displacements of the O?? peroxy ions based on the known Li?O? crystal structure. Within the vicinity of the chemical potential ?G ~ 0.20 eV/Li from the thermodynamic ground state of the Li?O? crystal structure (i.e., Fppl structure), all of these newly found metastable Li?O? crystal structures are found to be insulating and high-k materials, and they have a common unique signature of an O?? O-O vibration mode (? ~ 799865 cm?), which is in the range of that commonly observed in Li-air battery experiments, regardless of the random O?? orientations and the symmetry in the crystal lattice. From XRD patterns analysis, the commercially available Li?O? powder is confirmed to be the thermodynamic ground state Fppl-like structure. However, for Li?O? compounds that are grown electrochemically under the environment of Li-O? cells, we found that the XRD patterns alone are not sufficient for structural identification of these metastable Li?O? crystalline phases due to the poor crystallinity of the sample. In addition, the commonly known Raman signal of O?? vibration mode is also found to be insufficient to validate the possible existence of these newly predicted Li?O? crystal structures, as all of them similarly share the similar O?? vibration mode. However considering that the discharge voltage in most Li-O? cells are typically several tenths of an eV below the thermodynamic equilibrium for the formation of ground state Fppl structure, the formation of these metastable Li?O? crystal structures appears to be thermodynamically feasible.

  8. Dendrite-Free Li Deposition Using Trace-Amounts of Water as an Electrolyte Additive

    SciTech Connect (OSTI)

    Qian, Jiangfeng; Xu, Wu; Bhattacharya, Priyanka; Engelhard, Mark H.; Henderson, Wesley A.; Zhang, Yaohui; Zhang, Jiguang

    2015-07-01

    Residual water presents in nonaqueous electrolytes has been widely regarded as a detrimental factor for lithium (Li) batteries. This is because water is highly reactive with the commonly used LiPF6 salt and leads to the formation of HF that corrodes battery materials. In this work, we demonstrate that a controlled trace-amount of water (25-100 ppm) can be an effective electrolyte additive for achieving dendrite-free Li metal deposition in LiPF6-based electrolytes and avoid its detrimental effect at the same time. Detailed analyses reveal that the trace amount of HF formed by the decomposition reaction of LiPF6 with water will be electrochemically reduced during initial Li deposition process to form a uniform and dense LiF-rich SEI layer on the surface of the substrate. This LiF-rich SEI layer leads to a uniform distribution of the electric field on the substrate surface and enables uniform and dendrite-free Li deposition. Meanwhile the detrimental effect of HF is diminished due to the consumption of HF in the LiF formation process. Microscopic analysis reveals that the as-deposited dendrite-free Li films exhibit a self-aligned and highly-compacted Li nanorods structure which is consistent with their charming blue color or known as structure color. These findings clearly demonstrate a novel approach to control the nucleation and grow process of Li metal films using well-controlled trace-amount of water. They also shine the light on the effect of water on other electrodeposition processes.

  9. Note: {sup 6}Li III light intensity observation for {sup 6}Li{sup 3+} ion beam operation at Hyper-Electron Cyclotron Resonance ion source

    SciTech Connect (OSTI)

    Muto, Hideshi; Ohshiro, Yukimitsu; Yamaka, Shoichi; Yamaguchi, Hidetoshi; Shimoura, Susumu; Watanabe, Shin-ichi; Oyaizu, Michihiro; Kobayashi, Kiyoshi; Kotaka, Yasuteru; Nishimura, Makoto; Kase, Masayuki; Kubono, Shigeru; Hattori, Toshiyuki

    2014-12-15

    The light intensity of {sup 6}Li III line spectrum at ? = 516.7 nm was observed during {sup 6}Li{sup 3+} beam tuning at the Hyper-Electron Cyclotron Resonance (ECR) ion source. Separation of ion species of the same charge to mass ratio with an electromagnetic mass analyzer is known to be an exceptionally complex process. However, {sup 6}Li III line intensity observation conducted in this study gives new insights into its simplification of this process. The light intensity of {sup 6}Li III line spectrum from the ECR plasma was found to have a strong correlation with the extracted {sup 6}Li{sup 3+} beam intensity from the RIKEN Azimuthal Varying Field cyclotron.

  10. Graphene Modified LiFePO4 Cathode Materials for High Power Lithium ion Batteries

    SciTech Connect (OSTI)

    Zhou, X.; Wang, F.; Zhu, Y.; Liu, Z.

    2011-01-24

    Graphene-modified LiFePO{sub 4} composite has been developed as a Li-ion battery cathode material with excellent high-rate capability and cycling stability. The composite was prepared with LiFePO{sub 4} nanoparticles and graphene oxide nanosheets by spray-drying and annealing processes. The LiFePO{sub 4} primary nanoparticles embedded in micro-sized spherical secondary particles were wrapped homogeneously and loosely with a graphene 3D network. Such a special nanostructure facilitated electron migration throughout the secondary particles, while the presence of abundant voids between the LiFePO{sub 4} nanoparticles and graphene sheets was beneficial for Li{sup +} diffusion. The composite cathode material could deliver a capacity of 70 mAh g{sup -1} at 60C discharge rate and showed a capacity decay rate of <15% when cycled under 10C charging and 20C discharging for 1000 times.

  11. Crystal structure and chemical bonding of novel Li-containing polar intermetallic compound La{sub 11}Li{sub 12}Ge{sub 16}

    SciTech Connect (OSTI)

    Jung, Yaho; Nam, Gnu; Jeon, Jieun; Kim, Youngjo; You, Tae-Soo

    2012-12-15

    A novel Li-containing polar intermetallic compound La{sub 11}Li{sub 12}Ge{sub 16} has been synthesized using the high-temperature reaction method and characterized by both powder and single-crystal X-ray diffractions. The title compound crystallized in the orthorhombic crystal system (space group Immm, Z=2, Pearson symbol oI78) with fifteen crystallographically unique atomic positions in the asymmetric unit, and the lattice parameters are refined as a=4.5244(4) A, b=6.9932(6) A, and c=53.043(5) A. The complex crystal structure of the title compound can be described as a 2:1 intergrowth of two closely related compounds: La{sub 2}Li{sub 2}Ge{sub 3} (Ce{sub 2}Li{sub 2}Ge{sub 3}-type) and La{sub 3}Li{sub 4}Ge{sub 4} (Zr{sub 3}Cu{sub 4}Si{sub 4}-type) acting like 'building-blocks' along the c-axis. Six La sites are categorized into three distinct types based on the local coordination environment showing the coordination numbers of 12-14. Three unique Li sites are placed in the centers of local tetrahedra formed by four Ge atoms which eventually construct Ge{sub 2} dimers or 1-dimensional cis-/trans-Ge chains. Theoretical investigations using the tight-binding linear muffin-tin orbital (LMTO) method provide rationales for an improved structural stability and for unique local coordination geometries established by anionic elements including [LiGe{sub 4}] tetrahedra, cis-/trans-Ge chain and Ge{sub 2} dimers. - Graphical abstract: Reported is a novel ternary Li-containing polar intermetallic compound La{sub 11}Li{sub 12}Ge{sub 16}. The complex crystal structure can be viewed as a simple combination of two closely related known compounds acting as 'building-blocks', La{sub 2}Li{sub 2}G{sub 3} and La{sub 3}Li{sub 4}Ge{sub 4}, in a 2:1 stoichiometric ratio. Highlights: Black-Right-Pointing-Pointer A novel Li-containing polar intermetallic compound La{sub 11}Li{sub 12}Ge{sub 16} was synthesized. Black-Right-Pointing-Pointer The complex crystal structure was easily explained as a combination of two known compounds. Black-Right-Pointing-Pointer Theoretical calculations indicated that the Fermi level was located near the pseudogap.

  12. Red phosphor Ca{sub 2}Ge{sub 7}O{sub 16}:Eu{sup 3+} for potential application in field emission displays and white light-emitting diodes

    SciTech Connect (OSTI)

    Wang, Ting; Xu, Xuhui; Zhou, Dacheng; Qiu, Jianbei; Yu, Xue

    2014-12-15

    Abstract: A novel red emitting phosphor of Eu{sup 3+} doped Ca{sub 2}Ge{sub 7}O{sub 16} was prepared through the solid state reaction. The luminescence properties were studied in detail by photoluminescence excitation (PLE), emission (PL) spectra and cathodoluminescence (CL). Under the excitation of ultraviolet light, Ca{sub 2}Ge{sub 7}O{sub 16}:Eu{sup 3+} phosphor shows the characteristic {sup 5}D{sub 0}-{sup 7}F{sub J}(J = 1, 2, 3, 4) transition of Eu{sup 3+} with two different emissions due to the two kinds of Eu{sup 3+} ions. The luminescent intensity could be improved by co-doping with the charge compensators R{sup +} (Li, Na, K) which partially substitute for Ca{sup 2+} crystal sites. CL spectra show that Eu{sup 3+} ions were excited by the plasma produced by the incident electrons and the CL properties of Ca{sub 2}Ge{sub 7}O{sub 16}:Eu{sup 3+}, Li{sup +} as a function of accelerating voltage and probe current were investigated. Ca{sub 2}Ge{sub 7}O{sub 16}:Eu{sup 3+} phosphor offers higher thermal stability compared with the commercial red phosphor Y{sub 2}O{sub 3}:Eu{sup 3+}. The results indicate that Ca{sub 2}Ge{sub 7}O{sub 16}:Eu{sup 3+} can be a suitable red-emitting phosphor candidate for FEDs and w-LEDs.

  13. 2010 DOE, Li-Ion Battery Cell Manufacturing | Department of Energy

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

    DOE, Li-Ion Battery Cell Manufacturing 2010 DOE, Li-Ion Battery Cell Manufacturing 2010 DOE Vehicle Technologies and Hydrogen Programs Annual Merit Review and Peer Evaluation Meeting, June 7-11, 2010 -- Washington D.C. PDF icon esarravt001_eun_2010_p.pdf More Documents & Publications USABC Program Highlights Li-Ion Battery Cell Manufacturing Process for Low Cost Domestic Production of LIB Cathode Materials

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

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

    Source For High Performance Li-ion Cells Lithium Source For High Performance Li-ion Cells 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting PDF icon es140_kepler_2012_p.pdf More Documents & Publications Lithium Source For High Performance Li-ion Cells Design and Evaluation of Novel High Capacity Cathode Materials Design and Evaluation of Novel High Capacity Cathode Materials

  15. High Voltage Electrolytes for Li-ion Batteries | Department of Energy

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

    09 DOE Hydrogen Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting, May 18-22, 2009 -- Washington D.C. PDF icon esp_20_jow.pdf More Documents & Publications Electrolytes in Support of 5 V Li-ion Chemistries Vehicle Technologies Office Merit Review 2015: Fluorinated Electrolyte for 5-V Li-Ion Chemistry Vehicle Technologies Office Merit Review 2014: Fluorinated Electrolyte for 5-V Li-Ion Chemistry

  16. Jian-Rong (Jeff) Li | Center for Gas SeparationsRelevant to Clean Energy

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

    Technologies | Blandine Jerome Jian-Rong (Jeff) Li Previous Next List Jeff Li Jian-Rong (Jeff) Li Formerly: Assistant Research Scientist, Department of Chemistry, Texas A&M University Presently: Professor, Beijing University of Technology, China PhD in Chemistry, Nankai University Postdoc in Chemistry, Miami University and Texas A&M University EFRC research: Metal-organic frameworks (MOFs) and metal-organic polyhedra (MOPs) are newly developed molecule-based materials, constructed

  17. Diagnostic Studies on Li-Battery Cells and Cell Components | Department of

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

    Energy on Li-Battery Cells and Cell Components Diagnostic Studies on Li-Battery Cells and Cell Components 2011 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon es032_abraham_2011_p.pdf More Documents & Publications Diagnostic studies on Li-battery cells and cell components Diagnostic Studies Electrochemistry Cell Model

  18. Study of novel nonflammable electrolytes in Sandia-built Li-ion cells.

    Office of Scientific and Technical Information (OSTI)

    (Conference) | SciTech Connect Study of novel nonflammable electrolytes in Sandia-built Li-ion cells. Citation Details In-Document Search Title: Study of novel nonflammable electrolytes in Sandia-built Li-ion cells. Even after decades of research, Li-ion cells still lack thermal stability. A number of approaches, including adding fire retardants or fluoro compounds to the electrolyte to mitigate fire, have been investigated. These additives improved the thermal stability of the cells (only

  19. NRELs e-Ca Test

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

    NREL's e ---Ca T est Energy Innova5on Portal Webinar Arrelaine A . Dameron March 2 7, 2 012 2 Characteriza5on o f W ater P ermea5on B arriers Barrier Ambient E nvironment Sensi*ve C omponents Vapor a dsorbs a nd dissolves i nto barrier Vapor d iffuses Vapor d esorbs/ outgasses * Barrier m anufacturers need a c haracteriza5on method t hat i s: - Reproducible - Highly s ensi*ve - Easy t o u se - Scalable 3 1 F ood P ackaging 0.1 L CDs 0.01 T FTs 10 ---3 C dTe / Thin F ilm 10 ---4 C IGS 10 ---5 10

  20. DOE - Office of Legacy Management -- Stauffer-Temescal Co - CA 12

    Office of Legacy Management (LM)

    Stauffer-Temescal Co - CA 12 FUSRAP Considered Sites Site: STAUFFER-TEMESCAL CO. (CA.12) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: Stauffer Metals Company Stauffer-Temescal Co. CA.12-1 CA.12-2 CA.12-3 Location: 1201 South 47th Street , Richmond , California CA.12-1 CA.12-4 Evaluation Year: 1990 CA.12-5 CA.12-6 Site Operations: Conducted tests to determine the capabilities of electron beam melting on the purification of uranium. CA.12-1 CA.12-3

  1. Li electrodeposition dynamics visualized in-situ via a TEM liquid...

    Office of Scientific and Technical Information (OSTI)

    Conference: Li electrodeposition dynamics visualized in-situ via a TEM liquid cell. ... Language: English Word Cloud More Like This Full Text Conferences Events Please see ...

  2. Chemical and Electrochemical Lithiation of LiVOPO4 Cathodes for Lithium-ion Batteries

    SciTech Connect (OSTI)

    Harrison, Katharine L; Bridges, Craig A; Segre, C; VernadoJr, C Daniel; Applestone, Danielle; Bielawski, Christopher W; Paranthaman, Mariappan Parans; Manthiram, Arumugam

    2014-01-01

    The theoretical capacity of LiVOPO4 could be increased from 159 to 318 mAh/g with the insertion of a second Li+ ion into the lattice to form Li2VOPO4, significantly enhancing the energy density of lithium-ion batteries. The changes accompanying the second Li+ insertion into -LiVOPO4 and -LiVOPO4 are presented here at various degrees of lithiation, employing both electrochemical and chemical lithiation. Inductively coupled plasma, X-ray absorption spectroscopy, and Fourier transform spectroscopy measurements indicate that a composition of Li2VOPO4 could be realized with an oxidation state of V3+ by the chemical lithiation process. The accompanying structural changes are evidenced by X-ray and neutron powder diffraction. Spectroscopic and diffraction data collected with the chemically lithiated samples as well as diffraction data on the electrochemically lithiated samples reveal that significant amount of lithium can be inserted into -LiVOPO4 before a more dramatic structural change occurs. In contrast, lithiation of -LiVOPO4 is more consistent with the formation of a two-phase mixture throughout most of the lithiation range. The phases observed with the ambient-temperature lithiation processes presented here are significantly different from those reported in the literature.

  3. LiDAR At Twenty-Nine Palms Area (Sabin, Et Al., 2010) | Open...

    Open Energy Info (EERE)

    Sabin, Et Al., 2010) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: LiDAR At Twenty-Nine Palms Area (Sabin, Et Al., 2010) Exploration Activity...

  4. Influence of lithium salts on the discharge chemistry of Li-air cells

    SciTech Connect (OSTI)

    Veith, Gabriel M; Nanda, Jagjit; Delmau, Laetitia Helene; Dudney, Nancy J

    2012-01-01

    In this work we show that the use of a high boiling point ether solvent (tetraglyme) promotes the formation of Li2O2 in a lithium-air cell. In addition, another major constituent in the discharge product of a Li-air cell contains halides, from the lithium salt, and the tetraglyme used as the solvent. This information is critical to the development of Li-air electrolytes which are stable and promote the formation of the desired Li2O2 products.

  5. Dendrite-Free Li Deposition Using Trace-Amounts of Water as an Electrolyte

    Office of Scientific and Technical Information (OSTI)

    Additive (Journal Article) | SciTech Connect Dendrite-Free Li Deposition Using Trace-Amounts of Water as an Electrolyte Additive Citation Details In-Document Search Title: Dendrite-Free Li Deposition Using Trace-Amounts of Water as an Electrolyte Additive Residual water presents in nonaqueous electrolytes has been widely regarded as a detrimental factor for lithium (Li) batteries. This is because water is highly reactive with the commonly used LiPF6 salt and leads to the formation of HF that

  6. Analysis of Heat Dissipation in Li-Ion Cells & Modules for Modeling of Thermal Runaway (Presentation)

    SciTech Connect (OSTI)

    Kim, G.-H.; Pesaran, A.

    2007-05-15

    The objectives of this study are: (1) To develop 3D Li-Ion battery thermal abuse ''reaction'' models for cell and module analysis; (2) To understand the mechanisms and interactions between heat transfer and chemical reactions during thermal runaway for Li-Ion cells and modules; (3) To develop a tool and methodology to support the design of abuse-tolerant Li-Ion battery systems for PHEVs/HEVs; and (4) To help battery developers accelerate delivery of abuse-tolerant Li-Ion battery systems in support of the FreedomCAR's Energy Storage Program.

  7. LiDAR At Glass Buttes Area (DOE GTP) | Open Energy Information

    Open Energy Info (EERE)

    Glass Buttes Area (DOE GTP) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: LiDAR At Glass Buttes Area (DOE GTP) Exploration Activity Details...

  8. LiDAR At Gabbs Valley Area (DOE GTP) | Open Energy Information

    Open Energy Info (EERE)

    Gabbs Valley Area (DOE GTP) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: LiDAR At Gabbs Valley Area (DOE GTP) Exploration Activity Details...

  9. Miniature all-solid-state heterostructure nanowire Li-ion batteries...

    Office of Scientific and Technical Information (OSTI)

    all-solid-state heterostructure nanowire Li-ion batteries as a tool for engineering and structural diagnostics of nanoscale electrochemical processes Citation Details In-Document...

  10. Miniature All-solid-state Heterostructure Nanowire Li-ion Batteries...

    Office of Scientific and Technical Information (OSTI)

    All-solid-state Heterostructure Nanowire Li-ion Batteries as a Toll for Engineering and Structural Diagnostics of Nanoscale Electrochemical Processes Citation Details In-Document...

  11. Platforms and Methods for In Situ Characterization of Li-ion...

    Office of Scientific and Technical Information (OSTI)

    Platforms and Methods for In Situ Characterization of Li-ion Battery Materials. Citation Details In-Document Search Title: Platforms and Methods for In Situ Characterization of...

  12. Li2S encapsulated by nitrogen-doped carbon for lithium sulfur batteries

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

    Chen, Lin; Liu, Yuzi; Ashuri, Maziar; Liu, Caihong; Shaw, Leon L.

    2014-09-26

    Using high-energy ball milling of the Li2S plus carbon black mixture followed by carbonization of pyrrole, we have established a facile approach to synthesize Li2S-plus-C composite particles of average size 400 nm, encapsulated by a nitrogen-doped carbon shell. Such an engineered core–shell structure exhibits an ultrahigh initial discharge specific capacity (1029 mAh/g), reaching 88% of the theoretical capacity (1,166 mAh/g of Li2S) and thus offering the highest utilization of Li2S in the cathode among all of the reported works for the encapsulated Li2S cathodes. This Li2S/C composite core with a nitrogen-doped carbon shell can still retain 652 mAh/g after prolongedmore » 100 cycles. These superior properties are attributed to the nitrogen-doped carbon shell that can improve the conductivity to enhance the utilization of Li2S in the cathode. As a result, fine particle sizes and the presence of carbon black within the Li2S core may also play a role in high utilization of Li2S in the cathode.« less

  13. Investigation of the Rechargeability of Li-O2 Batteries in Non-aqueous Electrolyte

    SciTech Connect (OSTI)

    Xiao, Jie; Hu, Jian Z.; Wang, Deyu; Hu, Dehong; Xu, Wu; Graff, Gordon L.; Nie, Zimin; Liu, Jun; Zhang, Jiguang

    2011-07-01

    In order to understand the nature of the limited cycle life and poor energy efficiency associated with the secondary Li-O2 batteries the discharge products of primary Li-O2 cells at different depth of discharge (DOD) are systematically analyzed in this work. It is revealed that if discharged to 2.0 V a small amount of Li2O2 coexist with Li2CO3 and RO-(C=O)-OLi) in alkyl carbonate-based electrolyte. Further discharging the air electrodes to below 2.0 V the amount of Li2CO3 and LiRCO3 increases significantly due to the severe electrolyte decomposition. There is no Li2O detected in this alkyl carbonate electrolyte regardless of DOD. It is also found that the alkyl carbonate based electrolyte begins to decompose at 4.0 V during charging under the combined influences from the high surface area carbon, the nickel metal current collector and the oxygen atmosphere. Accordingly the impedance of the Li-O2 cell continues to increase after each discharge and recharge process indicating a repeated plating of insoluble lithium salts on the carbon surface. Therefore the whole carbon electrode becomes completely insulated only after a few cycles and loses the function of providing active tri-phase regions for the Li-oxygen batteries.

  14. First-Principles Study of Novel Conversion Reactions for High-Capacity Li-Ion Battery Anodes in the Li-Mg-B-N-H System

    SciTech Connect (OSTI)

    Mason, T.H.; Graetz, J.; Liu, X.; Hong, J.; Majzoub, E.H.

    2011-07-28

    Anodes for Li-ion batteries are primarily carbon-based due to their low cost and long cycle life. However, improvements to the Li capacity of carbon anodes, LiC{sub 6} in particular, are necessary to obtain a larger energy density. State-of-the-art light-metal hydrides for hydrogen storage applications often contain Li and involve reactions requiring Li transport, and light-metal ionic hydrides are candidates for novel conversion materials. Given a set of known solid-state and gas-phase reactants, we have determined the phase diagram in the Li-Mg-B-N-H system in the grand canonical ensemble, as a function of lithium chemical potential. We present computational results for several new conversion reactions with capacities between 2400 and 4000 mAh g{sup -1} that are thermodynamically favorable and that do not involve gas evolution. We provide experimental evidence for the reaction pathway on delithiation for the compound Li{sub 4}BN{sub 3}H{sub 10}. While the predicted reactions involve multiple steps, the maximum volume increase for these materials on lithium insertion is significantly smaller than that for Si.

  15. Oestrogen directly inhibits the cardiovascular L-type Ca{sup 2+} channel Ca{sub v}1.2

    SciTech Connect (OSTI)

    Ullrich, Nina D. . E-mail: ullrich@pyl.unibe.ch; Koschak, Alexandra; MacLeod, Kenneth T.

    2007-09-21

    Oestrogen can modify the contractile function of vascular smooth muscle and cardiomyocytes. The negative inotropic actions of oestrogen on the heart and coronary vasculature appear to be mediated by L-type Ca{sup 2+} channel (Ca{sub v}1.2) inhibition, but the underlying mechanisms remain elusive. We tested the hypothesis that oestrogen directly inhibits the cardiovascular L-type Ca{sup 2+} current, I {sub CaL}. The effect of oestrogen on I {sub CaL} was measured in Ca{sub v}1.2-transfected HEK-293 cells using the whole-cell patch-clamp technique. The current revealed typical activation and inactivation profiles of nifedipine- and cadmium-sensitive I {sub CaL}. Oestrogen (50 {mu}M) rapidly reduced I {sub CaL} by 50% and shifted voltage-dependent activation and availability to more negative potentials. Furthermore, oestrogen blocked the Ca{sup 2+} channel in a rate-dependent way, exhibiting higher efficiency of block at higher stimulation frequencies. Our data suggest that oestrogen inhibits I {sub CaL} through direct interaction of the steroid with the channel protein.

  16. 11-03-2010 CA-B-10-0149

    National Nuclear Security Administration (NNSA)

    1-03-2010 CA-B-10-0149 Sandia National Laboratories/California (SNL/CA), proposes to construct and test an antineutrino detector system before eventual deployment at a Canadian commercial nuclear power facility. SNL/CA is collaborating with Lawrence Livermore National Laboratory (LLNL) on this project. ✖ Sandia Site Office Assembly and Testing of Aboveground Antineutrino Detector, Add-On Task Sandia National Laboratories - California LACY,SUSAN DOYLENE 11/03

  17. RAPID/Roadmap/1-CA-a | Open Energy Information

    Open Energy Info (EERE)

    RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower Solar Tools Contribute Contact Us Land Use Planning (1-CA-a) Land...

  18. RAPID/Roadmap/12-CA-a | Open Energy Information

    Open Energy Info (EERE)

    Bulk Transmission Geothermal Hydropower Solar Tools Contribute Contact Us California Fish and Game Process (12-CA-a) California protects certain species and habitat beyond the...

  19. RAPID/Roadmap/7-CA-f | Open Energy Information

    Open Energy Info (EERE)

    RAPIDRoadmap7-CA-f < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower...

  20. RAPID/Roadmap/18-CA-b | Open Energy Information

    Open Energy Info (EERE)

    RAPIDRoadmap18-CA-b < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal...

  1. RAPID/Roadmap/6-CA-b | Open Energy Information

    Open Energy Info (EERE)

    CA-b < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower Solar Tools...

  2. RAPID/Roadmap/13-CA-c | Open Energy Information

    Open Energy Info (EERE)

    RAPIDRoadmap13-CA-c < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal...

  3. RAPID/Roadmap/14-CA-d | Open Energy Information

    Open Energy Info (EERE)

    RAPIDRoadmap14-CA-d < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal...

  4. RAPID/Roadmap/13-CA-b | Open Energy Information

    Open Energy Info (EERE)

    Help Apps Datasets Community Login | Sign Up Search Page Edit with form History RAPIDRoadmap13-CA-b < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and...

  5. RAPID/Roadmap/3-CA-b | Open Energy Information

    Open Energy Info (EERE)

    RAPIDRoadmap3-CA-b < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower...

  6. RAPID/Roadmap/6-CA-a | Open Energy Information

    Open Energy Info (EERE)

    CA-a < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower Solar Tools...

  7. RAPID/Roadmap/8-CA-c | Open Energy Information

    Open Energy Info (EERE)

    CA-c < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower Solar Tools...

  8. RAPID/Roadmap/11-CA-a | Open Energy Information

    Open Energy Info (EERE)

    RAPIDRoadmap11-CA-a < RAPID | Roadmap Jump to: navigation, search RAPID Regulatory and Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal...

  9. File:INL-geothermal-ca.pdf | Open Energy Information

    Open Energy Info (EERE)

    ca.pdf Jump to: navigation, search File File history File usage California Geothermal Resources Size of this preview: 439 599 pixels. Other resolution: 439 600 pixels. Full...

  10. RAPID/Roadmap/19-CA-a | Open Energy Information

    Open Energy Info (EERE)

    BETA About Bulk Transmission Geothermal Hydropower Solar Tools Contribute Contact Us Water Access and Water Rights (19-CA-a) California has a hybrid water law system, containing...

  11. RAPID/Roadmap/9-CA-a | Open Energy Information

    Open Energy Info (EERE)

    Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower Solar Tools Contribute Contact Us State Environmental Review Process (9-CA-a) The...

  12. RAPID/Roadmap/14-CA-c | Open Energy Information

    Open Energy Info (EERE)

    Geothermal Hydropower Solar Tools Contribute Contact Us Underground Injection Control Permit (14-CA-c) The injection of spent (cooled) geothermal fluids and in some cases...

  13. RAPID/Roadmap/14-CA-a | Open Energy Information

    Open Energy Info (EERE)

    Contact Us Nonpoint Source Pollution (14-CA-a) The California State Water Resources Control Board (SWRCB) and the California Coastal Commission (CCC), in coordination with the...

  14. RAPID/Roadmap/4-CA-a | Open Energy Information

    Open Energy Info (EERE)

    Permitting Information Desktop Toolkit BETA About Bulk Transmission Geothermal Hydropower Solar Tools Contribute Contact Us State Exploration Process (4-CA-a) 04CAAExploration.pdf...

  15. Microsoft Word - Ca-DTPA Insert_2 Pages.doc

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

    ... Cough andor wheezing were experienced by 2 individuals receiving nebulized Ca-DTPA, one ... to aerosolized treatment (ho lung disease, cough, dyspnea, chest tightness, wheezing)? ...

  16. RAPID/Roadmap/15-CA-a | Open Energy Information

    Open Energy Info (EERE)

    BETA About Bulk Transmission Geothermal Hydropower Solar Tools Contribute Contact Us Air Quality Permit - Authority to Construct (15-CA-a) A developer seeking to construct,...

  17. RAPID/Roadmap/15-CA-b | Open Energy Information

    Open Energy Info (EERE)

    BETA About Bulk Transmission Geothermal Hydropower Solar Tools Contribute Contact Us Air Quality Permit - Operating Permit (15-CA-b) A developer operating a facility that...

  18. California Fuel Cell Partnership CaFCP | Open Energy Information

    Open Energy Info (EERE)

    fuel cell vehicles under real driving conditions and to assist in the development of a hydrogen infrastructure. References: California Fuel Cell Partnership (CaFCP)1 This...

  19. LiWall Fusion - The New Concept of Magnetic Fusion

    SciTech Connect (OSTI)

    L.E. Zakharov

    2011-01-12

    Utilization of the outstanding abilities of a liquid lithium layer in pumping hydrogen isotopes leads to a new approach to magnetic fusion, called the LiWall Fusion. It relies on innovative plasma regimes with low edge density and high temperature. The approach combines fueling the plasma by neutral injection beams with the best possible elimination of outside neutral gas sources, which cools down the plasma edge. Prevention of cooling the plasma edge suppresses the dominant, temperature gradient related turbulence in the core. Such an approach is much more suitable for controlled fusion than the present practice, relying on high heating power for compensating essentially unlimited turbulent energy losses.

  20. Fatigue crack growth behavior of Al-Li alloy 1441

    SciTech Connect (OSTI)

    Prakash, R.V.; Parida, B.K.

    1995-12-31

    Fatigue crack growth behavior of Al-Li alloy 1441 having a marginally lower lithium content, compared to 80xx and 20xx series Al-Li alloys is presented in this paper. This investigation was conducted on single edge tension--SE(T)--specimens, under constant amplitude as well as under MiniLCA flight spectrum loading with the specific objective of determining the effects of stress ratio, orientation, thickness and cladding. Three thicknesses were considered: 1.2 mm(clad and unclad), 2.0 mm(clad and unclad) and 8.0 mm unclad. Constant amplitude fatigue tests were conducted at stress ratios of {minus}0.3, 0.1 and 0.7. Testing was performed under ambient conditions and along three orientations, namely L-T, T-L and L+45 degrees. Crack growth characteristics of this alloy are compared with that of BS:L73 (2014-T4 equivalent) for assessing the possibility of replacing BS:L73. Significant effect of stress ratio on crack growth rate was observed in all thicknesses. However, in case of 1.2 and 2.0 mm thick sheets, the effect was minimal at intermediate-crack growth regime. The orientation of the specimen does not adversely affect the fatigue crack growth behavior of 8.0 mm and 2.0 mm thick specimens. However, for 1.2 mm unclad sheet crack growth resistance in L-T direction was found to be superior to that along T-L direction. In majority of test cases considered, no significant effect was observed on crack growth rate due to thickness or cladding. Crack growth characteristics of Al-Li alloy 1441 and Al-Cu alloy BS:L73 under constant amplitude as well as MiniLCA spectrum loading are similar in the low and intermediate-crack growth rate regime. Based on these observations, it is felt that this Al-Li alloy has the potential for future aerospace applications.

  1. Estimating solar access of typical residential rooftops: A case study in San Jose, CA

    SciTech Connect (OSTI)

    Levinson, Ronnen M.; Gupta, Smita; Akbari, Hashem; Pomerantz, Melvin

    2008-03-03

    Shadows cast by trees and buildings can limit the solar access of rooftop solar-energy systems, including photovoltaic panels and thermal collectors. This study characterizes rooftop shading in a residential neighborhood of San Jose, CA, one of four regions analyzed in a wider study of the solar access of California homes.High-resolution orthophotos and LiDAR (Light Detection And Ranging) measurements of surface height were used to create a digital elevation model of all trees and buildings in a 4 km2 residential neighborhood. Hourly shading of roofing planes (the flat elements of roofs) was computed geometrically from the digital elevation model. Parcel boundaries were used to determine the extent to which roofing planes were shaded by trees and buildings in neighboring parcels.In the year in which surface heights were measured (2005), shadows from all sources ("total shading") reduced the insolation received by S-, SW-, and W-facing residential roofing planes in the study area by 13 - 16percent. Shadows cast by trees and buildings in neighboring parcels reduced insolation by no more than 2percent. After 30 years of simulated maximal tree growth, annual total shading increased to 19 - 22percent, and annual extraparcel shading increased to 3 - 4percent.

  2. Lattice Mn3+ Behaviors in Li4Ti5O12/LiNi0.5Mn1.5O4 Full Cells

    SciTech Connect (OSTI)

    Zheng, Jianming; Xiao, Jie; Nie, Zimin; Zhang, Jiguang

    2013-05-28

    High voltage spinels LiNi0.5Mn1.5O4 (LNMO) with different contents of residual Mn3+ ions have been evaluated in full cells using Li4Ti5O12 (LTO) as standard anode. Greatly improved cycling stability has been observed for all spinels in LTO-limited full cell, compared with those in LNMO-limited ones, while the underlying mechanisms are quite different. It has been discovered that the participation of active Mn3+ in the extended cycling and thus its observable contribution to Li+ diffusion kinetics depend on the limiting electrode and the sufficiency of Li+ ions. Potential Mn dissolution has also been discussed to identify the key factors that need to be considered to construct full cells employing high voltage spinel as the cathode.

  3. Investigation of Mechanical Activation on Li-N-H Systems Using 6Li Magic Angle Spinning Nuclear Magnetic Resonance at Ultra-High Field

    SciTech Connect (OSTI)

    Hu, Jian Zhi; Kwak, Ja Hun; Yang, Zhenguo; Osborn, William; Markmaitree, Tippawan; Shaw, Leonard D.

    2008-07-15

    Abstract The significantly enhanced spectral resolution in the 6Li MAS NMR spectra of Li-N-H systems at ultra-high field of 21.1 tesla is exploited, for the first time, to study the detailed electronic and chemical environmental changes associated with mechanical activation of Li-N-H system using high energy balling milling. Complementary to ultra-high field studies, the hydrogen discharge dynamics are investigated using variable temperature in situ 1H MAS NMR at 7.05 tesla field. The significantly enhanced spectral resolution using ultra-high filed of 21.1 tesla was demonstrated along with several major findings related to mechanical activation, including the upfield shift of the resonances in 6Li MAS spectra induced by ball milling, more efficient mechanical activation with ball milling at liquid nitrogen temperature than with ball milling at room temperature, and greatly enhanced hydrogen discharge exhibited by the liquid nitrogen ball milled samples.

  4. Phase transitions of LiAlO{sub 2} at high pressure and high temperature

    SciTech Connect (OSTI)

    Lei Li; He Duanwei Zou Yongtao; Zhang Wei; Wang Zhao; Jiang Ming; Du Maolu

    2008-08-15

    This work presents a comprehensive study on phase transitions in LiAlO{sub 2} system at high pressures and temperatures (0.5-5.0 GPa and 300-1873 K, respectively), as well as the phase stability for polymeric phases of LiAlO{sub 2} in the studied P-T space by X-ray diffraction (XRD). Besides the previously described polymorphic hexagonal {alpha}-phase, orthorhombic {beta}-phase and tetragonal {delta}-phase, a possible new phase of LiAlO{sub 2} was observed after the tetragonal {gamma}-LiAlO{sub 2} sample was treated at 5.0 GPa and 389 K. The stable regimes of these high-pressure phases were defined through the observation of coexistence points of the polymeric phases. Our results revealed that LiAlO{sub 2} could experience structural phase transitions from {gamma}-LiAlO{sub 2} to its polymorphs at lower pressures and temperatures compared to the reported results. Hexagonal {alpha}-LiAlO{sub 2} with highly (003) preferential orientation was prepared at 5.0 GPa and 1873 K. - Graphical abstract: Constructing the pressure-temperature phase diagram for LiAlO{sub 2}.

  5. High Voltage Electrolytes for Li-ion Batteries | Department of Energy

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

    2 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting PDF icon es024_jow_2012_o.pdf More Documents & Publications High Voltage Electrolytes for Li-ion Batteries High Voltage Electrolytes for Li-ion Batteries Progress in Electrolyte Component R&D within the ABR Program, 2009 thru 2013

  6. High Voltage Electrolytes for Li-ion Batteries | Department of Energy

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

    1 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon es024_jow_2011_p.pdf More Documents & Publications High Voltage Electrolytes for Li-ion Batteries High Voltage Electrolytes for Li-ion Batteries Molecular dynamics simulation and ab intio studies of electrolytes and electrolyte/electrode interfaces

  7. 09-01-2010 CA-B-10-0134

    National Nuclear Security Administration (NNSA)

    CA-B-10-0134 SNL/CA proposes a comprehensive experimental study of the properties of nanostructured thin films and individual nanowires. ✖ Sandia Site Office Thermal Transport Properties of Nanostructured Materials for Energy Conversion Sandia National Laboratories - California LACY,SUSAN DOYLENE 09/01/2010

  8. Characterization of the LiSi/CsBr-LiBr-KBr/FeS(2) System for Potential Use as a Geothermal Borehole Power Source

    SciTech Connect (OSTI)

    GUIDOTTI, RONALD A.; REINHARDT, FREDERICK W.

    1999-10-18

    We are continuing to study the suitability of modified thermal-battery technology as a potential power source for geothermal borehole applications. Previous work focused on the LiSi/FeS{sub 2} couple over a temperature range of 350 C to 400 C with the LiBr-KBr-LiF eutectic, which melts at 324.5 C. In this work, the discharge processes that take place in LiSi/CsBr-LiBr-KBr eutectic/FeS{sub 2} thermal cells were studied at temperatures between 250 C and 400 C using pelletized cells with immobilized electrolyte. The CsBr-LiBr-KBr eutectic was selected because of its lower melting point (228.5 C). Incorporation of a quasi-reference electrode allowed the determination of the relative contribution of each electrode to the overall cell polarization. The results of single-cell tests and limited battery tests are presented, along with preliminary data for battery stacks tested in a simulated geothermal borehole environment.

  9. Scanning tunneling microscopy reveals LiMnAs is a room temperature anti-ferromagnetic semiconductor

    SciTech Connect (OSTI)

    Wijnheijmer, A. P.; Koenraad, P. M.; Marti, X.; Holy, V.; Cukr, M.; Novak, V.; Jungwirth, T.

    2012-03-12

    We performed scanning tunneling microscopy and spectroscopy on a LiMnAs(001) thin film epitaxially grown on an InAs(001) substrate by molecular beam epitaxy. While the in situ cleavage exposed only the InAs(110) non-polar planes, the cleavage continued into the LiMnAs thin layer across several facets. We combined both topography and current mappings to confirm that the facets correspond to LiMnAs. By spectroscopy we show that LiMnAs has a band gap. The band gap evidenced in this study, combined with the known Neel temperature well above room temperature, confirms that LiMnAs is a promising candidate for exploring the concepts of high temperature semiconductor spintronics based on antiferromagnets.

  10. DOE - Office of Legacy Management -- General Electric Co - San Jose - CA 13

    Office of Legacy Management (LM)

    San Jose - CA 13 FUSRAP Considered Sites Site: General Electric Co. - San Jose (CA.13 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: None Location: San Jose , California CA.13-1 Evaluation Year: 1995 CA.13-2 Site Operations: Fabricated uranium metal. CA.13-1 Site Disposition: Eliminated - No Authority - NRC licensed CA.13-2 Radioactive Materials Handled: Yes Primary Radioactive Materials Handled: Uranium CA.13-1 Radiological Survey(s): No Site

  11. DOE - Office of Legacy Management -- Santa Susana Field Laboratory - CA 09

    Office of Legacy Management (LM)

    Santa Susana Field Laboratory - CA 09 FUSRAP Considered Sites Site: SANTA SUSANA FIELD LABORATORY (CA.09 ) Eliminated from consideration under FUSRAP - Remediation and certification complete Designated Name: Not Designated Alternate Name: Rockwell International, Energy Systems Group Atomics International CA.09-1 CA.09-2 Location: Chatsworth , California CA.09-3 Evaluation Year: 1985 CA.09-3 Site Operations: Conducted sodium reactor, irradiation and fuel burn up experimentation. CA.09-3 Site

  12. ANALOG I/O MODULE TEST SYSTEM BASED ON EPICS CA PROTOCOL AND ACTIVEX CA INTERFACE

    SciTech Connect (OSTI)

    YENG,YHOFF,L.

    2003-10-13

    Analog input (ADC) and output (DAC) modules play a substantial role in device level control of accelerator and large experiment physics control system. In order to get the best performance some features of analog modules including linearity, accuracy, crosstalk, thermal drift and so on have to be evaluated during the preliminary design phase. Gain and offset error calibration and thermal drift compensation (if needed) may have to be done in the implementation phase as well. A natural technique for performing these tasks is to interface the analog VO modules and GPIB interface programmable test instruments with a computer, which can complete measurements or calibration automatically. A difficulty is that drivers of analog modules and test instruments usually work on totally different platforms (vxworks VS Windows). Developing new test routines and drivers for testing instruments under VxWorks (or any other RTOS) platform is not a good solution because such systems have relatively poor user interface and developing such software requires substantial effort. EPICS CA protocol and ActiveX CA interface provide another choice, a PC and LabVIEW based test system. Analog 110 module can be interfaced from LabVIEW test routines via ActiveX CA interface. Test instruments can be controlled via LabVIEW drivers, most of which are provided by instrument vendors or by National Instruments. Labview also provides extensive data analysis and process functions. Using these functions, users can generate powerful test routines very easily. Several applications built for Spallation Neutron Source (SNS) Beam Loss Monitor (BLM) system are described in this paper.

  13. Improved thermoelectric performance of n-type Ca and Ca-Ce filled skutterudites

    SciTech Connect (OSTI)

    Thompson, Daniel R.; Liu, Chang; Ellison, Nicole D.; Salvador, James R.; Meyer, Martin S.; Haddad, Daad B.; Wang, Hsin; Cai, W.

    2014-12-28

    Thermoelectric (TE) technology for use in automotive waste heat recovery is being advanced by General Motors with support from the US Department of Energy. Skutterudites are a very promising material for this application of TE technology due to their superior mechanical properties and good TE performance. Double-filled Yb{sub x}Ba{sub y}Co{sub 4}Sb{sub 12} with ZT values around 1.1 at 750?K are the best performing n-type skutterudites produced on a large scale using an economically viable approach of melt spinning (MS) in conjunction with spark plasma sintering (SPS). Another economical production method on the tons scale, the melt quench annealing (MQA) technique, has been recently claimed by Treibacher Industrie AG, further information is available [G. Rogl et al., Acta Mater. 76, 434448 (2014)]. A possible hurdle to commercial implementation of these materials is the use of rare earths as the fillers to reduce thermal conductivity and improve the electrical transport properties. It will be shown herein that skutterudites double-filled with Ca and Ce, both of which are lower-cost fillers, display markedly different TE properties depending on whether they are produced by MQA or MS + SPS synthesis techniques. Ca and Ce double-filled skutterudites prepared by MS + SPS have TE properties that are superior to the same compositions prepared by MQA and that are comparable to the best performing Yb and Ba filled materials. Furthermore, the results of this study suggest that the unusually poor transport properties of MQA Ca-filled skutterudites can be ascribed to deleterious secondary phases, which is contrary to reports in the literature attempting to explain these irregularities via band structure features.

  14. CA_OPPUSST - Cantera OPUS Steady State

    Energy Science and Technology Software Center (OSTI)

    2005-03-01

    The Cantera Opus Steady State (ca-opusst) applications solves steady reacting flow problems in opposed-flow geometries. It is a 1-0 application that represents axisymmetnc 3-0 physical systems that can be reduced via a similarity transformation to a 1-0 mathematical representation. The code contain solutions of the general dynamic equations for the particle distribution functions using a sectional model to describe the particle distribution function. Operators for particle nucleation, coagulation, condensation (i.e., growth/etching via reactions with themore » gas ambient), internal particle reactions. particle transport due to convection and due to molecular transport, are included in the particle general dynamics equation. Heat transport due to radiation exchange of the environment with particles in local thermal equilibrium to the surrounding gas will be included in the enthalpy conservation equation that is solved for the coupled gas! particle system in an upcoming version of the code due in June 2005. The codes use Cantera , a C++ Cal Tech code, for determination of gas phase species transport, reaction, and thermodynamics physical properties and source terms. The Codes use the Cantera Aerosol Dynamics Simulator (CADS) package, a general library for aerosol modeling, to calculate properties and source terms for the aerosol general dynamics equation, including particle formation from gas phase reactions, particle surface chemistry (growth and oxidation), bulk particle chemistry, particle transport by Brownian diffusion, thermophoresis, and diffusiophoresis, and thermal radiative transport involving particles. Also included are post-processing programs, cajost and cajrof, to extract ascii data from binary output files to produce plots.« less

  15. Comparison of LiMnPO4 made by Combustion and Hydrothermal Syntheses

    SciTech Connect (OSTI)

    Chen, Jiajun; Doeff, Marca M.; Wang, Ruigang

    2008-05-15

    Among the olivine-structured metal phosphate family, LiMnPO{sub 4} exhibits a high discharge potential (4V), which is still compatible with common electrolytes, making it interesting for use in the next generation of Li ion batteries. The extremely low electronic conductivity of this material severely limits its electrochemical performance, however. One strategy to overcome this limitation is to make LiMnPO{sub 4} nanoparticulate to decrease the diffusion distance. Another is to add a carbon or other conductive coating in intimate contact with the nanoparticles of the main phase, as is commonly done with LiFePO{sub 4}. The electrochemical performance of LiFePO{sub 4} is highly dependent on the quality of the carbon coatings on the particles [1-2], among other variables. Combustion synthesis allows the co-synthesis of nanoparticles coated with carbon in one step. Hydrothermal synthesis is used industrially to make LiFePO{sub 4} cathode materials [3] and affords a good deal of control over purity, crystallinity, and particle size. A wide range of olivine-structured materials has been successfully prepared by this technique [4], including LiMnPO{sub 4} in this study. In this paper, we report on the new synthesis of nano-LiMnPO{sub 4} by a combustion method. The purity is dependent upon the conditions used for synthesis, including the type of fuel and precursors that are chosen. The fuel to nitrate ratio influences the combustion temperature, which determines the type and amount of carbon found in the LiMnPO{sub 4} composites. This can further be modified by use of carbon structural modifiers added during a subsequent (optional) calcination step. Figure 1 shows a transmission electron microscopy (TEM) image of the spherical nano-sized LiMnPO{sub 4} particles typically formed by combustion synthesis. The average particle size is around 30 nm, in agreement with values obtained by the Rietveld refinement of XRD patterns. The small size of the particles cause the peak broadening evident in the pattern of combustion formed LiMnPO{sub 4}, shown in Figure 2. Figure 2 also shows a pattern of hydrothermally prepared LiMnPO{sub 4}, which is sub-micron in size. In this presentation, we will show how the crystallographic parameters, particle size, particle morphology, and carbon content and structure impact the electrochemical properties of the LiMnPO{sub 4}/C composites produced by these methods.

  16. Comparison of LiMnPO4 made by Combustion and Hydrothermal Syntheses

    SciTech Connect (OSTI)

    Chen, Jiajun; Doeff, Marca M.; Wang, Ruigang

    2008-10-12

    Among the olivine-structured metal phosphate family, LiMnPO{sub 4} exhibits a high discharge potential (4V), which is still compatible with common electrolytes, making it interesting for use in the next generation of Li ion batteries. The extremely low electronic conductivity of this material severely limits its electrochemical performance, however. One strategy to overcome this limitation is to make LiMnPO{sub 4} nanoparticulate to decrease the diffusion distance. Another is to add a carbon or other conductive coating in intimate contact with the nanoparticles of the main phase, as is commonly done with LiFePO{sub 4}. The electrochemical performance of LiFePO{sub 4} is highly dependent on the quality of the carbon coatings on the particles, among other variables. Combustion synthesis allows the co-synthesis of nanoparticles coated with carbon in one step. Hydrothermal synthesis is used industrially to make LiFePO{sub 4} cathode materials and affords a good deal of control over purity, crystallinity, and particle size. A wide range of olivine-structured materials has been successfully prepared by this technique, including LiMnPO{sub 4} in this study. In this paper, we report on the new synthesis of nano-LiMnPO{sub 4} by a combustion method. The purity is dependent upon the conditions used for synthesis, including the type of fuel and precursors that are chosen. The fuel to nitrate ratio influences the combustion temperature, which determines the type and amount of carbon found in the LiMnPO{sub 4} composites. This can further be modified by use of carbon structural modifiers added during a subsequent (optional) calcination step. Figure 1 shows a transmission electron microscopy (TEM) image of the spherical nano-sized LiMnPO{sub 4} particles typically formed by combustion synthesis. The average particle size is around 30 nm, in agreement with values obtained by the Rietveld refinement of XRD patterns. The small size of the particles cause the peak broadening evident in the pattern of combustion formed LiMnPO{sub 4}, shown in Figure 2. Figure 2 also shows a pattern of hydrothermally prepared LiMnPO{sub 4}, which is sub-micron in size. In this presentation, we will show how the crystallographic parameters, particle size, particle morphology, and carbon content and structure impact the electrochemical properties of the LiMnPO{sub 4}/C composites produced by these methods.

  17. Elastic Hadron Scattering on Li Isotopes at Intermediate Energies

    SciTech Connect (OSTI)

    Zhusupov, M.A.; Imambekov, O.; Ibraeva, E.T.

    2005-01-01

    The elastic scattering of hadrons (protons, charged pions, and positively charged kaons) on {sup 6,7,8}Li nuclei is analyzed on the basis of Glauber-Sitenko diffraction theory. A few nuclear-wave-function versions found within two- and three-particle potential cluster models are used in the calculations. It is shown that the application of these wave functions in diffraction theory makes it possible to describe adequately the experimental differential cross sections and analyzing powers in hadron scattering at intermediate energies. In this study, particular attention is given to a comparison of the scattering of different particles on the same target nucleus, as well as to a comparison of scattering of particles of the same sort on different target nuclei.

  18. SESAME 7363: A new Li(6)D equation of state

    SciTech Connect (OSTI)

    Sheppard, Daniel Glen; Kress, Joel David; Crockett, Scott; Collins, Lee A.; Greeff, Carl William

    2015-09-21

    A new Equation of State (EOS) for Lithium 6 Deuteride (6LiD) was created, sesame 7363. This EOS was released to the user community under “eos-developmental” as sesame 97363. The construction of this new EOS is a modification of a previously released EOS, sesame 73601. Sesame 7360 is too stiff (5-10% excess pressure) at high compressions and high temperatures (ρ = 4-110g/cm3, T = 30-10,000 eV) compared to orbital-free density-functional theory. Sesame 7363 is softer and gives a better representation of the physics over this range without compromising the agreement with the experimental and simulation data that sesame 7360 was based on.

  19. Emission Regulations Reduced Impact of Climate Change in CA

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

    Emission Regulations Reduced Impact of Climate Change in CA Emission Regulations Reduced Impact of Climate Change in CA Study shows clean diesel programs slashed black carbon, a powerful short-term contributor to global warming June 13, 2013 Jon Weiner 510-486-4014 jrweiner@lbl.gov CA-BC-graphic.jpg Sacramento - Reductions in emissions of black carbon since the late 1980s, mostly from diesel engines as a result of air quality programs, have resulted in a measurable reduction of concentrations of

  20. 229th Electrochemical Society (ECS) Meeting (San Diego, CA) - JCAP

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

    229th Electrochemical Society (ECS) Meeting (San Diego, CA) 229th Electrochemical Society (ECS) Meeting (San Diego, CA) Sun, May 29, 2016 12:00pm 12:00 Thu, Jun 2, 2016 1:00pm 13:00 San Diego, CA USA Joel A. Haber, "Development of Solar Fuels Photoanodes through Combinatorial Integration of Ni-La-Co-Ce Oxide and Ni-Fe-Co-Ce Oxide Catalysts on BiVO4" The development of an efficient photoanode remains the primary materials challenge in the establishment of a scalable technology for solar

  1. Stability of the solid electrolyte Li{sub 3}OBr to common battery solvents

    SciTech Connect (OSTI)

    Schroeder, D.J.; Hubaud, A.A.; Vaughey, J.T.

    2014-01-01

    Graphical abstract: The stability of the anti-perovskite phase Li{sub 3}OBr has been assessed in a variety of battery solvents. - Highlights: Lithium stable solid electrolyte Li{sub 3}OBr unstable to polar organic solvents. Solvation with no dissolution destroys long-range structure. Ion exchange with protons observed. - Abstract: Recently a new class of solid lithium ion conductors was reported based on the anti-perovskite structure, notably Li{sub 3}OCl and Li{sub 3}OBr. For many beyond lithium-ion battery uses, the solid electrolyte is envisioned to be in direct contact with liquid electrolytes and lithium metal. In this study we evaluated the stability of the Li{sub 3}OBr phase against common battery solvents electrolytes, including diethylcarbonate (DEC) and dimethylcarbonate (DMC), as well as a LiPF{sub 6} containing commercial electrolyte. In contact with battery-grade organic solvents, Li{sub 3}OBr was typically found to be insoluble but lost its crystallinity and reacted with available protons and in some cases with the solvent. A low temperature heat treatment was able to restore crystallinity of the samples; however evidence of proton ion exchange was conserved.

  2. Summary of mechanical properties data and correlations for Li/sub 2/O, Li/sub 4/SiO/sub 4/, LiAlO/sub 2/, and Be

    SciTech Connect (OSTI)

    Billone, M.C.; Grayhack, W.T.

    1988-04-01

    The data base for thermal expansion, elastic constants, compressive and tensile failure strengths and secondary thermal creep of leading solid-breeder (Li/sub 2/O, Li/sub 4/SiO/sub 4/, and LiAlO/sub 2/) and multiplier (Be) materials is reviewed, porosity, grain size, and stress (for thermal creep). Because the data base is rather sparse in some areas, general properties of ceramics and metals are used to help guide the formulation of the correlations. The primary purpose of the data base summary and correlation development is to pave the way for stress analysis sensitivity studies. These studies will help determine which properties are important enough to structural lifetime and deformation assessments to require more data. 18 refs., 5 figs., 20 tabs.

  3. Hao Heather Li | Center for Gas SeparationsRelevant to Clean Energy

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

    Technologies | Blandine Jerome Hao Heather Li Previous Next List Li PhD Student Department of Chemistry Texas A & M University Email: hao.li[at]chem.tamu.edu Phone: 979-587-1954 BSc in Chemistry, Wuhan University, China EFRC research: Amine modified metal-organic frameworks (MOFs) stand out as a promising porous material to capture CO2 for its strong CO2 affinity, low regeneration energy and large pore volume. We have tethered a series of alkylamines onto Cr-MIL-101-SO3H and tested their

  4. Diagnostic studies on Li-battery cells and cell components | Department of

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

    Energy studies on Li-battery cells and cell components Diagnostic studies on Li-battery cells and cell components 2009 DOE Hydrogen Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting, May 18-22, 2009 -- Washington D.C. PDF icon esp_02_abraham.pdf More Documents & Publications Vehicle Technologies Office: 2008 Energy Storage R&D Annual Progress Report Diagnostic Studies on Li-Battery Cells and Cell Components Mitigating Performance Degradation of

  5. X-ray line polarization spectroscopy of Li-like satellite line spectra

    Office of Scientific and Technical Information (OSTI)

    (Journal Article) | SciTech Connect Journal Article: X-ray line polarization spectroscopy of Li-like satellite line spectra Citation Details In-Document Search Title: X-ray line polarization spectroscopy of Li-like satellite line spectra We apply the magnetic-sublevel atomic kinetics model POLAR to the calculation of polarization properties of satellite lines in Li-like Si driven by subpicosecond-duration laser pulses. We identify spectral lines whose polarization can serve as a marker of

  6. Fusion reactions in collisions induced by Li isotopes on Sn targets

    SciTech Connect (OSTI)

    Fisichella, M.; Shotter, A. C.; Di Pietro, A.; Figuera, P.; Lattuada, M.; Marchetta, C.; Musumarra, A.; Pellegriti, M. G.; Ruiz, C.; Scuderi, V.; Strano, E.; Torresi, D.; Zadro, M.

    2012-10-20

    Fusion cross sections for the {sup 6}Li+{sup 120}Sn and {sup 7}Li+{sup 119}Sn systems have been measured. We aim to search for possible effects due to the different neutron transfer Q-values, by comparing the fusion cross sections for the two systems below the barrier. This experiment is the first step of a wider systematic aiming to study the above problems in collisions induced by stable and unstable Li isotopes on tin all forming the same compound nucleus.

  7. Guide to Developing Air-Cooled Lithium Bromide (LiBr) Absorption for CHP

    Office of Environmental Management (EM)

    Applications, April 2005 | Department of Energy Developing Air-Cooled Lithium Bromide (LiBr) Absorption for CHP Applications, April 2005 Guide to Developing Air-Cooled Lithium Bromide (LiBr) Absorption for CHP Applications, April 2005 The objective of this paper is to summarize the development status of air-cooled lithium bromide (LiBr)-water absorption chillers to guide future efforts to develop chillers for combined heat and power (CHP) applications in light-commercial buildings. The key

  8. RAPID/Roadmap/8-CA-b | Open Energy Information

    Open Energy Info (EERE)

    in a timely manner and not wait until the last day of the open window. GIDAP Best Management Practice, section 3.5. 8-CA-b.7 - Hold Scoping Meeting Within five (5) Business...

  9. RAPID/Roadmap/17-CA-a | Open Energy Information

    Open Energy Info (EERE)

    Tools Contribute Contact Us State Aesthetic Concerns (17-CA-a) Page Does Not Exist.pdf Error creating thumbnail: Page number not in range. Error creating thumbnail: Page number...

  10. Field Projects: Cañon City, Colorado

    Broader source: Energy.gov [DOE]

    In June 2000, Cotter Corporation installed a PRB at its uranium ore processing millsite in Cañon City, Colorado. The PRB contains zero-valent iron (ZVI) that treated molybdenum and uranium...

  11. RAPID/Roadmap/7-CA-e | Open Energy Information

    Open Energy Info (EERE)

    see: Green arrow.PNG 9-FD-a: BLM NEPA Process 7-CA-e.8 - Conduct Environmental, Reliability, and Mitigation Assessments At the same time that the BLM is conducting the Project...

  12. NUG Meeting June 24-25, 2004 (Berkeley, CA)

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

    NUG Meeting June 24-25, 2004 (Berkeley, CA) Dates June 24-25, 2004 Location Lawrence Berkeley National Laboratory 1 Cyclotron Road Building 54, Conference Room 130 (Perseverance...

  13. 06-14-2010 CA-B-10-0081

    National Nuclear Security Administration (NNSA)

    CA-B-10-0081 Sandia National Laboratories/California proposes to continue development and testing of a neutron scatter camera to detect special nuclear materials. ✖ ✖ Sandia Site Office Neutron Scatter Camera Measurements Sandia National Laboratories - California

  14. ERSUG Meeting: June 13 - 14, 1995 (Livermore, CA)

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

    ERSUG Meeting: June 13 - 14, 1995 (Livermore, CA) Dates ERSUG Meeting: June 13 & 14, 1995 Location Lawrence Livermore National Laboratory Livermore, CA Minutes Summary of ERSUG Meeting June 13 - 14, 1995, Livermore, California The Energy Research Supercomputer Users Group (ERSUG) June 1995 meeting was hosted by the National Energy Research Supercomputer Center (NERSC) at the Lawrence Livermore National Laboratory (LLNL). Some of the talks are summarized below. Welcome The meeting opened

  15. 05-05-2010 CA-B-10-0041

    National Nuclear Security Administration (NNSA)

    CA-B-10-0041 SNL/CA proposes to install and operate a new glove box at Building 965 to support the Gas Transfer System (GTS) program. An existing hydrogen loading station would be relocated to Building 965. Facility modifications would also be needed. ✖ Sandia Site Office Glove Box Installation and Operation in Support of Gas Transfer System Program Sandia National Laboratories - California

  16. 10-04-2010 CA-B-10-0139

    National Nuclear Security Administration (NNSA)

    0-04-2010 CA-B-10-0139 Sandia National Laboratories/California (SNL/CA) proposes to fund a Campus Executive Fellowship for a student at the University of California at Berkeley. The proposed project includes fabrication and characterization of solar water splitting metal oxide photoelectrodes to study the solar energy conversion phenomena. ✖ Sandia Site Office Nanostructured Metal Oxide Photoelectrodes for Solar Hydrogen Production Lawrence Berkeley Laboratory LACY,SUSAN DOYLENE 10/04

  17. 10-04-2010 CA-B-10-0153

    National Nuclear Security Administration (NNSA)

    3 Sandia National Laboratories/California (SNL/CA) proposes to design and make block copolymers that will self-assemble into thermodynamically favorable, ordered nano-domains suitable for chemical modification in order to control transport properties. Design, development, and fabrication of the copolymers would be conducted at existing laboratories at SNL/CA, as would initial characterization. Additional characterization would be performed at New Mexico State University, Brookhaven National

  18. 10-04-2010 CA-B-10-0154

    National Nuclear Security Administration (NNSA)

    4 Sandia National Laboratories/California (SNL/CA) will develop a novel fieldable laser-induced incandescence sensor to measure black carbon (BC) and brown carbon (BrC) organic aerosols and their optical and chemical characteristics. Fabrication and laboratory testing would be conducted at SNL/CA's Combustion Research Facility (CRF). Fabrication would consist of assembly of off-the-shelf components. Laboratory testing would involve use of a small bench top flame to generate soot and

  19. Climate Action Champions: Blue Lake Rancheria Tribe, CA | Department of

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

    Energy Blue Lake Rancheria Tribe, CA Climate Action Champions: Blue Lake Rancheria Tribe, CA The Blue Lake Rancheria, California, a federally recognized Native American tribal Government and community, is located on over 100 acres of land spanning the scenic Mad River in northwestern California. In its operational strategy, the Tribe has implemented the ‘seven generations’ philosophy, where actions taken today will have a positive impact for seven generations to come. This results

  20. Climate Action Champions: San Francisco, CA | Department of Energy

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

    San Francisco, CA Climate Action Champions: San Francisco, CA To meet the challenge of climate change, San Francisco is working with residents, businesses, community organizations, and state and federal agencies to create innovative programs and policies. To meet the challenge of climate change, San Francisco is working with residents, businesses, community organizations, and state and federal agencies to create innovative programs and policies. Climate Action Progress and Plans San Francisco

  1. EA-1638: Solyndra, Inc. Photovoltaic Manufacturing Facility in Fremont, CA

    Office of Environmental Management (EM)

    | Department of Energy 8: Solyndra, Inc. Photovoltaic Manufacturing Facility in Fremont, CA EA-1638: Solyndra, Inc. Photovoltaic Manufacturing Facility in Fremont, CA March 2, 2009 EA-1638: Final Environmental Assessment Loan Guarantee to Solyndra, Inc. for Construction of A Photovoltaic Manufacturing Facility and Leasing of an Existing Commercial Facility in Fremont, California March 31, 2009 EA-1638: Finding of No Significant Impact Loan Guarantee to Solyndra, Inc. for Construction of a

  2. EA-1798: Abengoa Solar's Mojave Solar Project near Barstow, CA |

    Office of Environmental Management (EM)

    Department of Energy 8: Abengoa Solar's Mojave Solar Project near Barstow, CA EA-1798: Abengoa Solar's Mojave Solar Project near Barstow, CA July 1, 2011 EA-1798: Final Environmental Assessment Loan Guarantee to Mojave Solar, LLC for the Abengoa Mojave Solar Project near Barstow, California July 8, 2011 EA-1798: Finding of No Significant Impact Loan Guarantee to Mojave Solar, LLC for the Abengoa Mojave Solar Project near Barstow, California March 17, 2011 Abengoa Mojave Final Biological

  3. Synthesis of nanostructured LiTi{sub 2}(PO{sub 4}){sub 3} powder by a Pechini-type polymerizable complex method

    SciTech Connect (OSTI)

    Mariappan, C.R.; Galven, C.; Crosnier-Lopez, M.-P.; Le Berre, F.; Bohnke, O. . E-mail: odile.bohnke@univ-lemans.fr

    2006-02-15

    The nanostructured NASICON-type LiTi{sub 2}(PO{sub 4}){sub 3} (LTP) material has been synthesized by Pechini-type polymerizable complex method. The use of water-soluble ammonium citratoperoxotitanate (IV) metal complex instead of alkoxides as precursor allows to prepare monophase material. Thermal analyses have been carried out on the powder precursor to check the weight loss and synthesis temperature. X-ray powder diffraction analysis (XRD) has been performed on the LTP powder obtained after heating the powder precursor over a temperature range from 550 to 1050 deg. C for 2 h. By varying the molar ratio of citric acid to metal ion (CA/Ti) and citric acid to ethylene glycol (CA/EG), the grain size of the LTP powder could be modified. The formation of small and well-crystalline grains, in the order of 50-125 nm in size, has been determined from the XRD patterns and confirmed by transmission electron microscopy.

  4. DOE - Office of Legacy Management -- Naval Ordnance Test Station - CA 06

    Office of Legacy Management (LM)

    Test Station - CA 06 FUSRAP Considered Sites Site: NAVAL ORDNANCE TEST STATION (CA.06) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: China Lake Naval Weapons Center Salt Wells Pilot Plant CA.06-1 Location: Inyokern , California CA.06-1 Evaluation Year: 1987 CA.06-1 Site Operations: Naval facility; experimental development work on shape charges and quality castings on a pilot plant scale. CA.06-1 Site Disposition: Eliminated - No indication that

  5. DOE - Office of Legacy Management -- North American Aviation Inc - CA 07

    Office of Legacy Management (LM)

    American Aviation Inc - CA 07 FUSRAP Considered Sites Site: NORTH AMERICAN AVIATION, INC. (CA.07) Eliminated from consideration under FUSRAP Designated Name: None Designated Alternate Name: None Location: Downey , California CA.07-1 Evaluation Year: 1987 CA.07-1 Site Operations: Research and development on a bench scale using a small reactor; work done during the early 1950s. CA.07-1 Site Disposition: Eliminated - Potential for contamination remote based on limited scope of operations CA.07-2

  6. Alternating magnetic anisotropy of Li2(Li1xTx)N (T = Mn, Fe, Co, and Ni)

    SciTech Connect (OSTI)

    Jesche, A.; Ke, L.; Jacobs, J. L.; Harmon, B.; Houk, R. S.; Canfield, P. C.

    2015-05-11

    Substantial amounts of the transition metals Mn, Fe, Co, and Ni can be substituted for Li in single crystalline Li2(Li1xTx)N. Isothermal and temperature-dependent magnetization measurements reveal local magnetic moments with magnitudes significantly exceeding the spin-only value. The additional contributions stem from unquenched orbital moments that lead to rare-earth-like behavior of the magnetic properties. Accordingly, extremely large magnetic anisotropies have been found. Most notably, the magnetic anisotropy alternates as easy plane?easy axis?easy plane?easy axis when progressing from T = Mn ? Fe ? Co ? Ni. This behavior can be understood based on a perturbation approach in an analytical, single-ion model. As a result, the calculated magnetic anisotropies show surprisingly good agreement with the experiment and capture the basic features observed for the different transition metals.

  7. Ultrathin Li3VO4 Nanoribbon/Graphene Sandwich-Like Nanostructures...

    Office of Scientific and Technical Information (OSTI)

    Title: Ultrathin Li3VO4 NanoribbonGraphene Sandwich-Like Nanostructures with Ultrahigh Lithium ion Storage Properties Two-dimensional (2D) "graphene-like" inorganic materials, ...

  8. Can Vanadium Be Substituted into LiFePO[subscript 4]? (Journal...

    Office of Scientific and Technical Information (OSTI)

    the solid solution LiFesub 1-3y2Vsub yPOsub 4, the a and b lattice parameters and cell volume decrease with increasing vanadium content, while the c lattice parameter...

  9. New Improved Equations For Na-K, Na-Li And Sio2 Geothermometers...

    Open Energy Info (EERE)

    Improved Equations For Na-K, Na-Li And Sio2 Geothermometers By Outlier Detection And Rejection Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal Article:...

  10. X-ray line polarization spectroscopy of Li-like satellite line...

    Office of Scientific and Technical Information (OSTI)

    properties of satellite lines in Li-like Si driven by subpicosecond-duration laser pulses. ... Resource Relation: Journal Name: Journal of Physics B Research Org: Los Alamos National ...

  11. Proceedings of the AD HOC Workshop on Ceramics for Li/FeS{sub 2} batteries

    SciTech Connect (OSTI)

    Not Available

    1993-12-31

    Representatives from industry, the U.S. Advanced Battery Consortium (USABC), DOE, national laboratories, and other govt agencies met to develop recommendations and actions for accelerating the development of ceramic components critical to the successful introduction of the Li/FeS{sub 2} bipolar battery for electric vehicles. Most of the workshop is devoted to electrode materials, bipolar designs, separators, and bipolar plates. The bulk of this document is viewographs and is divided into: ceramics, USABC overview, SAFT`s Li/FeS{sub 2} USABC program, bipolar Li/FeS{sub 2} component development, design requirements for bipolar plates, separator design requirements, compatibility of ceramic insulators with lithium, characterization of MgO for use in separators, resistivity measurements of separators, sintered AlN separators for LiMS batteries, etc.

  12. Nanocrystallization of LiCoO2 Cathodes for Thin Film Batteries Utilizing Pulse Thermal Processing

    SciTech Connect (OSTI)

    2009-04-01

    This factsheet describes a study whose focus is on the nanocrystallization of the LiCoO2 cathode thin films on polyimide substrates and evaluate the microstructural evolution and resistance as a function of PTP processing conditions.

  13. Search for Solar Axion Emission from 7Li and D(p,gamma)3He Nuclear...

    Office of Scientific and Technical Information (OSTI)

    Solar Axion Emission from 7Li and D(p,gamma)3He Nuclear Decays with the CAST gamma-ray Calorimeter Andriamonje, S.; Aune, S.; DAPNIA, Saclay; Autiero, D.; CERN Lyon, IPN; Barth,...

  14. Microsoft Word - aac2012_Li_1_WG4-SLAC-PUB-15212.doc

    Office of Scientific and Technical Information (OSTI)

    et al., "Results from Plasma Wakefield Experiments at FACET", IPAC'11, San Sebastian, Spain, 2011, SLAC-PUB-14560. 5. E. Adli et al., to be published. 6. S.Z. Li and M.J. Hogan,...

  15. Vehicle Technologies Office Merit Review 2015: A 12V Start-Stop Li Polymer Battery Pack

    Broader source: Energy.gov [DOE]

    Presentation given by LG Chem Power at 2015 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Office Annual Merit Review and Peer Evaluation Meeting about A 12V start-stop Li polymer...

  16. Second-Use Li-Ion Batteries to Aid Automotive and Utility Industries (Fact Sheet)

    SciTech Connect (OSTI)

    Not Available

    2014-01-01

    Repurposing Li-ion batteries at the end of useful life in electric drive vehicles could eliminate owners' disposal concerns and offer low-cost energy storage for certain applications.

  17. Structural Analysis of Southern Dixie Valley using LiDAR and...

    Open Energy Info (EERE)

    and characterize young faults, high resolution LiDAR and 1:12,000-scale low-sun-angle (LSA) aerial photography was acquired for the NAS Fallon study area. The LSA photos were...

  18. Calibration of LI-7500 sensor for 60m CO2/H20 flux system

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

    of LI-7500 Sensor for the CO2flx and ECOR Systems Marc L. Fischer David R. Cook Revision Date 05042007 (D. R. Cook) Introduction This...

  19. Dendrite-Free Li Deposition Using Trace-Amounts of Water as an...

    Office of Scientific and Technical Information (OSTI)

    Using Trace-Amounts of Water as an Electrolyte Additive Citation Details In-Document Search Title: Dendrite-Free Li Deposition Using Trace-Amounts of Water as an Electrolyte ...

  20. Search for Solar Axion Emission from 7Li and D(p,gamma)3He Nuclear...

    Office of Scientific and Technical Information (OSTI)

    Search for Solar Axion Emission from 7Li and D(p,gamma)3He Nuclear Decays with the CAST gamma-ray Calorimeter Citation Details In-Document Search Title: Search for Solar Axion...

  1. Insights into capacity loss mechanisms in Li-ion all-solid-state...

    Office of Scientific and Technical Information (OSTI)

    Insights into capacity loss mechanisms in Li-ion all-solid-state batteries with Al anodes Citation Details In-Document Search Title: Insights into capacity loss mechanisms in...

  2. DOE - Office of Legacy Management -- Northrup Aircraft Co Inc - CA 0-02

    Office of Legacy Management (LM)

    Northrup Aircraft Co Inc - CA 0-02 FUSRAP Considered Sites Site: NORTHRUP AIRCRAFT CO., INC (CA.0-02 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: None Location: Hawthorne , California CA.0-02-1 Evaluation Year: 1987 CA.0-02-1 CA.0-02-2 Site Operations: Participated in projects involving nuclear energy for the propulsion of aircraft. CA.0-02-1 Site Disposition: Eliminated - No Authority - NRC licensed CA.0-02-1 CA.0-02-2 Radioactive Materials

  3. Structural and Chemical Evolution of Li- and Mn-rich Layered Cathode Material

    SciTech Connect (OSTI)

    Zheng, Jianming; Xu, Pinghong; Gu, Meng; Xiao, Jie; Browning, Nigel D.; Yan, Pengfei; Wang, Chong M.; Zhang, Jiguang

    2015-02-24

    Lithium (Li)- and manganese-rich (LMR) layered-structure materials are very promising cathodes for high energy density lithium-ion batteries. However, their voltage fading mechanism and its relationships with fundamental structural changes are far from being sufficiently understood. Here we report the detailed phase transformation pathway in the LMR cathode (Li[Li0.2Ni0.2Mn0.6]O2) during cycling for the samples prepared by hydro-thermal assistant method. It is found the transformation pathway of LMR cathode is closely correlated to its initial structure and preparation conditions. The results reveal that LMR cathode prepared by HA approach experiences a phase transformation from the layered structure to a LT-LiCoO2 type defect spinel-like structure (Fd-3m space group) and then to a disordered rock-salt structure (Fm-3m space group). The voltage fade can be well correlated with the Li ion insertion into octahedral sites, rather than tetrahedral sites, in both defect spinel-like structure and disordered rock-salt structure. The reversible Li insertion/removal into/from the disordered rock-salt structure is ascribed to the Li excess environment that can satisfy the Li percolating in the disordered rock-salt structure despite the increased kinetic barrier. Meanwhile, because of the presence of a great amount of oxygen vacancies, a significant decrease of Mn valence is detected in the cycled particle, which is below that anticipated for a potentially damaging Jahn-Teller distortion (+3.5). Clarification of the phase transformation pathway, cation redistribution, oxygen vacancy and Mn valence change undoubtedly provides insights into a profound understanding on the voltage fade, and capacity degradation of LMR cathode. The results also inspire us to further enhance the reversibility of LMR cathode via improving its surface structural stability.

  4. Department of Li/sup /minus// and H/sup /minus// ion sources

    SciTech Connect (OSTI)

    Walther, S.R.

    1988-12-01

    Sources of Li/sup /minus// and H/sup /minus// ions are needed for diagnostic neutral beam and for current drive in fusion plasmas. Previous efforts to generate Li/sup /minus// beams have focused on electron capture in a gas or production on a low work function surface in a plasma. Volume production of Li/sup /minus// by dissociative attachment of optically pumped lithium molecules has also been studied. This thesis presents the first experimental results for volume production of a Li/sup /minus// ion beam from a plasma discharge. A theoretical model for volume production of Li/sup /minus// ions and separate model for Li/sub 2/ production in the lithium discharge are developed to explain the experimental results. The model is in good agreement with the experiment and shows favorable parameter scalings for further improvement of the Li/sup /minus// ion source. A /sup 6/Li/degree/ diagnostic neutral beam based on this ion source is proposed for measurement of magnetic pitch angle in the International Thermonuclear Experimental Reactor (ITER). Previous efforts in developing H/sup /minus// ion sources have concentrated on volume production in a plasma discharge. Experiments to improve the H/sup /minus// current density from a magnetically filtered multicusp ion source by seeding the discharge with cesium or barium have been conducted. A substantial (> factor of five) increase in H/sup /minus// output is achieved for both cesium and barium addition. Further experiments with barium have shown that the increase is due to H/sup /minus// production on the anode walls. The experiments with cesium are consistent with this formation mechanism. These results show that this new type of 'converterless' surface production H/sup /minus// source provides greatly improved performance when compared to a volume H/sup /minus// source. 92 refs., 47 figs.

  5. Miniature all-solid-state heterostructure nanowire Li-ion batteries as a

    Office of Scientific and Technical Information (OSTI)

    tool for engineering and structural diagnostics of nanoscale electrochemical processes. (Journal Article) | SciTech Connect Miniature all-solid-state heterostructure nanowire Li-ion batteries as a tool for engineering and structural diagnostics of nanoscale electrochemical processes. Citation Details In-Document Search Title: Miniature all-solid-state heterostructure nanowire Li-ion batteries as a tool for engineering and structural diagnostics of nanoscale electrochemical processes.

  6. Ultrathin Li3VO4 Nanoribbon/Graphene Sandwich-Like Nanostructures with

    Office of Scientific and Technical Information (OSTI)

    Ultrahigh Lithium ion Storage Properties (Journal Article) | SciTech Connect SciTech Connect Search Results Journal Article: Ultrathin Li3VO4 Nanoribbon/Graphene Sandwich-Like Nanostructures with Ultrahigh Lithium ion Storage Properties Citation Details In-Document Search Title: Ultrathin Li3VO4 Nanoribbon/Graphene Sandwich-Like Nanostructures with Ultrahigh Lithium ion Storage Properties Two-dimensional (2D) "graphene-like" inorganic materials, because of the short lithium ion

  7. New High Power Li2MTi6O14Anode Material | Department of Energy

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

    High Power Li2MTi6O14Anode Material New High Power Li2MTi6O14Anode Material 2009 DOE Hydrogen Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting, May 18-22, 2009 -- Washington D.C. PDF icon esp_21_amine.pdf More Documents & Publications Developing High Capacity, Long Life, and High Power Anodes Cathodes Engineering of high energy cathode material

  8. Significant Cost Improvement of Li-Ion Cells Through Non-NMP Electrode

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

    Coating, Direct Separator Coating, and Fast Formation Technologies | Department of Energy Significant Cost Improvement of Li-Ion Cells Through Non-NMP Electrode Coating, Direct Separator Coating, and Fast Formation Technologies Significant Cost Improvement of Li-Ion Cells Through Non-NMP Electrode Coating, Direct Separator Coating, and Fast Formation Technologies 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting PDF icon

  9. Li-Chiang Lin | Center for Gas SeparationsRelevant to Clean Energy

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

    Technologies | Blandine Jerome Li-Chiang Lin Previous Next List Li-Chiang Lin Formerly: PhD Student, Department of Chemical & Biomolecular Engineering University of California, Berkeley Presently: Postdoctoral Fellow, MIT Email: lclin [at] mit.edu BS in Chemical Engineering, National Taiwan University, Taiwan MS in Chemical Engineering, National Taiwan University, Taiwan EFRC research: Carbon capture and sequestration (CCS) is one of viable strategies for reducing the negative

  10. Changyi Li | Center for Gas SeparationsRelevant to Clean Energy

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

    Technologies | Blandine Jerome Changyi Li Previous Next List LiC PhD Student Department of Chemistry University of California Email: changyi [at] berkeley.edu Phone: 510-495-2303 BA in Chemistry, California Institute of Technology EFRC Research CO2 separation is an energy intensive process using conventional solution-phase methods. Membrane-based gas separations have the potential to be a much more efficient process. The research in our group focuses on creating hybrid

  11. Effect of an Ultrathin Coating on Stabilizing Li-ion Battery Cathodes |

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

    Stanford Synchrotron Radiation Lightsource Effect of an Ultrathin Coating on Stabilizing Li-ion Battery Cathodes Sunday, January 31, 2016 Improvements in the high-voltage cycling stability of lithium ion battery cathode materials are needed to enable the wide-spread adoption of renewable energy technologies such as electric vehicles. One cathode material which exhibits significant advantages over the commonly-used commercial material LiCoO2 in terms of higher capacity, increased thermal

  12. Characterization of Li-ion Batteries using Neutron Diffraction and Infrared

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

    Imaging Techniques | Department of Energy Li-ion Batteries using Neutron Diffraction and Infrared Imaging Techniques Characterization of Li-ion Batteries using Neutron Diffraction and Infrared Imaging Techniques 2011 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon lm044_wang_2011_p.pdf More Documents & Publications Materials Characterization Capabilities at the High Temperature Materials Laboratory and HTML User

  13. Characterization of Materials for Li-ion Batteries: Success Stories from

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

    the High Temperature Materials Laboratory (HTML) User Program | Department of Energy Materials for Li-ion Batteries: Success Stories from the High Temperature Materials Laboratory (HTML) User Program Characterization of Materials for Li-ion Batteries: Success Stories from the High Temperature Materials Laboratory (HTML) User Program 2010 DOE Vehicle Technologies and Hydrogen Programs Annual Merit Review and Peer Evaluation Meeting, June 7-11, 2010 -- Washington D.C. PDF icon

  14. Development of Cell/Pack Level Models for Automotive Li-Ion Batteries with

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

    Experimental Validation | Department of Energy Cell/Pack Level Models for Automotive Li-Ion Batteries with Experimental Validation Development of Cell/Pack Level Models for Automotive Li-Ion Batteries with Experimental Validation 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting PDF icon es120_shaffer_2012_o.pdf More Documents & Publications Vehicle Technologies Office Merit Review 2014: Development of Cell/Pack

  15. Development of High Energy Cathode for Li-ion Batteries | Department of

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

    Energy for Li-ion Batteries Development of High Energy Cathode for Li-ion Batteries 2010 DOE Vehicle Technologies and Hydrogen Programs Annual Merit Review and Peer Evaluation Meeting, June 7-11, 2010 -- Washington D.C. PDF icon es056_zhang_2010_p.pdf More Documents & Publications Phase Behavior and Solid State Chemistry in Olivines Development of High Energy Cathode Materials Interfacial Processes - Diagnostics

  16. Via E-Mail Michael Li Electricity Policy Specialist U.S. Department of Energy

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

    November 1, 2010 Via E-Mail Michael Li Electricity Policy Specialist U.S. Department of Energy Office of Electricity Delivery and Energy Reliability 1000 Independence Avenue, SW Washington, DC 20585 smartgridpolicy@hq.doe.gov Re: Smart Grid RFI: Addressing Policy And Logistical Challenges Dear Mr. Li: On behalf of the Association of Home Appliance Manufacturers (AHAM), I would like to provide our comments on the Smart Grid RFI: Addressing Policy and Logistical Challenges, 75 Fed. Reg. 57,006

  17. Thermally Stable Electrolyte For Li-ion Cells. (Conference) | SciTech

    Office of Scientific and Technical Information (OSTI)

    Connect Thermally Stable Electrolyte For Li-ion Cells. Citation Details In-Document Search Title: Thermally Stable Electrolyte For Li-ion Cells. Abstract not provided. Authors: Nagasubramanian, Ganesan ; Orendorff, Christopher J. Publication Date: 2011-09-01 OSTI Identifier: 1106400 Report Number(s): SAND2011-7083C 464734 DOE Contract Number: AC04-94AL85000 Resource Type: Conference Resource Relation: Conference: The Knowledge Foundation's 2nd Annual International Conference held November

  18. Streamlining the Optimization of Li-Ion Battery Electrodes | Department of

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

    Energy Streamlining the Optimization of Li-Ion Battery Electrodes Streamlining the Optimization of Li-Ion Battery Electrodes 2009 DOE Hydrogen Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting, May 18-22, 2009 -- Washington D.C. PDF icon esp_12_lu.pdf More Documents & Publications Screen Electrode Materials & Cell Chemistries and Streamlining Optimization of Electrode Screen Electrode Materials and Cell Chemistries FY 2011 Annual Progress Report

  19. Optimization of LiFePO4 Nanoparticle Suspensions with Polyethyleneimine for Aqueous Processing

    SciTech Connect (OSTI)

    Li, Jianlin; Armstrong, Beth L; Kiggans, Jim; Daniel, Claus; Wood III, David L

    2012-01-01

    Addition of dispersants to aqueous based lithium-ion battery electrode formulations containing LiFePO{sub 4} is critical to obtaining a stable suspension. The resulting colloidal suspensions enable dramatically improved coating deposition when processing electrodes. This research examines the colloidal chemistry modifications based on polyethyleneimine (PEI) addition and dispersion characterization required to produce high quality electrode formulations and coatings for LiFePO{sub 4} active cathode material. The isoelectric point, a key parameter in characterizing colloidal dispersion stability, of LiFePO{sub 4} and super P C45 were determined to be pH = 4.3 and 3.4, respectively. PEI, a cationic surfactant, was found to be an effective dispersant. It is demonstrated that 1.0 wt % and 0.5 wt % PEI were required to stabilize the LiFePO{sub 4} and super P C45 suspension, respectively. LiFePO{sub 4} cathode suspensions with 1.5 wt % PEI demonstrated the best dispersibility of all components, as evidenced by viscosity and agglomerate size of the suspensions and elemental distribution within dry cathodes. The addition of PEI significantly improved the LiFePO{sub 4} performance.

  20. Operando NMR and XRD study of chemically synthesized LiCx oxidation in a dry room environment

    SciTech Connect (OSTI)

    Sacci, Robert L.; Gill, Lance W.; Hagaman, Edward W.; Dudney, Nancy J.

    2015-08-01

    We test the stability of pre-lithiated graphite anodes for Li-ion batteries in a dry room battery processing room. The reaction between LiCx and laboratory air was followed using operando NMR and x-ray diffraction as these methods are sensitive to change in Li stoichiometry in graphite. There is minimal reactivity between LiC6 and N2, CO2 or O2; however, LiC6 reacts with moisture to form lithium (hydr)oxide. The reaction rate follows zero-order kinetics with respects to intercalated lithium suggesting that lithium transport through the graphite is fast. The reaction mechanism occurs by sequential formation of higher stages LiC12, then LiC18, and then LiC24 as the hydrolysis proceeds to the formation of LixOHy and graphite end products. Slowing down the formation rate of the LixOHy passivation layer stabilizes of the higher stages.

  1. Synthesis and Characterization of Lithium Bis(fluoromalonato)borate (LiBFMB) for Lithium Ion Battery Applications

    SciTech Connect (OSTI)

    Liao, Chen; Han, Kee Sung; Baggetto, Loic; Hillesheim, Daniel A; Custelcean, Radu; Lee, Dr. Eun-Sung; Guo, Bingkun; Bi, Zhonghe; Jiang, Deen; Veith, Gabriel M; Hagaman, Edward {Ed} W; Brown, Gilbert M; Bridges, Craig A; Paranthaman, Mariappan Parans; Manthiram, Arumugam; Dai, Sheng; Sun, Xiao-Guang

    2014-01-01

    A new orthochelated salt, lithium bis(monofluoromalonato)borate (LiBFMB), has been synthesized and purified for the first time for application in lithium ion batteries. The presence of fluorine in the borate anion of LiBFMB increases its oxidation potential and also facilitates ion dissociation, as reflected by the ratio of ionic conductivity measured by electrochemical impedance spectroscopy ( exp) and that by ion diffusivity coefficients obtained using pulsed field gradient nuclear magnetic resonance (PFG-NMR) technique ( NMR). Half-cell tests using 5.0 V lithium nickel manganese oxide (LiNi0.5Mn1.5O4) as a cathode and EC/DMC/DEC as a solvent reveals that the impedance of the LiBFMB cell is much larger than those of LiPF6 and LiBOB based cells, which results in lower capacity and poor cycling performance of the former. XPS spectra of the cycled cathode electrode suggest that because of the stability of the LiBFMB salt, the solid electrolyte interphase (SEI) formed on the cathode surface is significantly different from those of LiPF6 and LiBOB based electrolytes, resulting in more solvent decomposition and thicker SEI layer. Initial results also indicate that using high dielectric constant solvent PC alters the surface chemistry, reduces the interfacial impedance, and enhances the performance of LiBFMB based 5.0V cell.

  2. Cylindrical target Li-beam-driven hohlraum experiments

    SciTech Connect (OSTI)

    Derzon, M.S.; Aubert, J.; Chandler, G.A.

    1998-06-01

    The authors performed a series of experiments on the Particle Beam Fusion Accelerator II (PBFA II) in May, 1994, and obtained a brightness temperature of 61 {+-} 2 eV for an ion-beam heated hohlraum. The hohlraum was a 4-mm-diameter, right-circular cylinder with a 1.5-mm-thick gold wall, a low-density CH foam fill, and a 1.5- or 3-mm-diameter diagnostic aperture in the top. The nominal parameters of the radially-incident PBFA II Li ion beam were 9 MeV peak energy ({approximately}10 MeV at the gas cell) at the target at a peak power of 2.5 {+-} 0.3 TW/cm{sup 2} and a 15 ns pulse width. Azimuthal variations in intensity of a factor of 3, with respect to the mean, were observed. Nonuniformities in thermal x-ray emission across the area of the diagnostic hole were also observed. Time-dependent hole-closure velocities were measured: the time-averaged velocity of {approximately}2 cm/{micro}s is in good agreement with sound speed estimates. Unfolded x-ray spectra and brightness temperatures as a function of time are reported and compared to simulations. Hole closure corrections are discussed with comparisons between XRD and bolometer measurements. Temperature scaling with power on target is also presented.

  3. Lithium transition metal fluorophosphates (Li{sub 2}CoPO{sub 4}F and Li{sub 2}NiPO{sub 4}F) as cathode materials for lithium ion battery from atomistic simulation

    SciTech Connect (OSTI)

    Lee, Sanghun Park, Sung Soo

    2013-08-15

    Lithium transition metal fluorophosphates (Li{sub 2}MPO{sub 4}F, M: Co and Ni) have been investigated from atomistic simulation. In order to predict the characteristics of these materials as cathode materials for lithium ion batteries, structural property, defect chemistry, and Li{sup +} ion transportation property are characterized. The coreshell model with empirical force fields is employed to reproduce the unit-cell parameters of crystal structure, which are in good agreement with the experimental data. In addition, the formation energies of intrinsic defects (Frenkel and antisite) are determined by energetics calculation. From migration energy calculations, it is found that these flurophosphates have a 3D Li{sup +} ion diffusion network forecasting good Li{sup +} ion conducting performances. Accordingly, we expect that this study provides an atomic scale insight as cathode materials for lithium ion batteries. - Graphical abstract: Lithium transition metal fluorophosphates (Li{sub 2}CoPO{sub 4}F and Li{sub 2}NiPO{sub 4}F). Display Omitted - Highlights: Lithium transition metal fluorophosphates (Li{sub 2}MPO{sub 4}F, M: Co and Ni) are investigated from classical atomistic simulation. The unit-cell parameters from experimental studies are reproduced by the coreshell model. Li{sup +} ion conducting Li{sub 2}MPO{sub 4}F has a 3D Li{sup +} ion diffusion network. It is predicted that Li/Co or Li/Ni antisite defects are well-formed at a substantial concentration level.

  4. A novel red phosphor Ca{sub 12}Al{sub 14}O{sub 32}Cl{sub 2}:Eu{sup 3+} for near UV white light-emitting diodes

    SciTech Connect (OSTI)

    Yang, Zhigang; Zhao, Zhengyan; Shi, Yurong; Wang, Yuhua

    2013-10-15

    Graphical abstract: - Highlights: Novel red phosphor Ca{sub 12}Al{sub 14}O{sub 32}Cl{sub 2}:Eu{sup 3+} was prepared by solid-state reaction. Excitation spectra suggested an obvious absorption in near-ultraviolet region. Under 392 nm excitation, the phosphors exhibited a red emission at 614 nm. Ca{sub 12}Al{sub 14}O{sub 32}Cl{sub 2}:Eu{sup 3+} could be potentially applied in near UV white LEDs. - Abstract: A novel red phosphor Ca{sub 12}Al{sub 14}O{sub 32}Cl{sub 2}:Eu{sup 3+} was synthesized using a solid-state reaction method, and its luminescence characteristics and charge compensators effect (Li{sup +}, Na{sup +}, K{sup +}) were investigated. The excitation spectra showed a obvious absorption in near-ultraviolet region. Under 392 nm excitation, the phosphors exhibited an intense red emission at 614 nm. The Commission Internationale de lEclairage (CIE) chromaticity coordinates and quantum efficiency (QE) were (0.65, 0.35) and 62.3%, respectively. The good color saturation, high quantum efficiency and small thermal-quenching properties indicate that Ca{sub 12}Al{sub 14}O{sub 32}Cl{sub 2}:Eu{sup 3+} could be potentially applied in near UV white light-emitting diodes.

  5. Controlled Nucleation and Growth Process of Li2S2/Li2S in Lithium-Sulfur Batteries

    SciTech Connect (OSTI)

    Zheng, Jianming; Gu, Meng; Wang, Chong M.; Zuo, Pengjian; Koech, Phillip K.; Zhang, Jiguang; Liu, Jun; Xiao, Jie

    2013-09-20

    Lithium-sulfur battery is a promising next-generation energy storage system because of its potentially three to five times higher energy density than that of traditional lithium ion batteries. However, the dissolution and precipitation of soluble polysulfides during cycling initiate a series of key-chain reactions that significantly shorten battery life. Herein, we demonstrate that through a simple but effective strategy, significantly improved cycling performance is achieved for high sulfur loading electrodes through controlling the nucleation and precipitation of polysulfieds on the electrode surface. More than 400 or 760 stable cycling are successfully displayed in the cells with locked discharge capacity of 625 mAh g-1 or 500 mAh g-1, respectively. The nucleation and growth process of dissolved polysulfides has been electrochemically altered to confine the thickness of discharge products passivated on the cathode surface, increasing the utilization rate of sulfur while avoiding severe morphology changes on the electrode. More importantly, the exposure of new lithium metal surface to the S-containing electrolyte is also greatly reduced through this strategy, largely minimizing the anode corrosion caused by polysulfides. This work interlocks the electrode morphologies and its evolution with electrochemical interference to modulate cell performances by using Li-S system as a platform, providing different but critical directions for this community.

  6. Development of bulk-type all-solid-state lithium-sulfur battery using LiBH{sub 4} electrolyte

    SciTech Connect (OSTI)

    Unemoto, Atsushi, E-mail: unemoto@imr.tohoku.ac.jp; Ikeshoji, Tamio [WPI-Advanced Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Yasaku, Syun; Matsuo, Motoaki [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Nogami, Genki; Tazawa, Masaru; Taniguchi, Mitsugu [Mitsubishi Gas Chemicals Co., Ltd., 182 Tayuhama Shinwari, Kita-ku, Niigata 950-3112 (Japan); Orimo, Shin-ichi [WPI-Advanced Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan)

    2014-08-25

    Stable battery operation of a bulk-type all-solid-state lithium-sulfur battery was demonstrated by using a LiBH{sub 4} electrolyte. The electrochemical activity of insulating elemental sulfur as the positive electrode was enhanced by the mutual dispersion of elemental sulfur and carbon in the composite powders. Subsequently, a tight interface between the sulfur-carbon composite and the LiBH{sub 4} powders was manifested only by cold-pressing owing to the highly deformable nature of the LiBH{sub 4} electrolyte. The high reducing ability of LiBH{sub 4} allows using the use of a Li negative electrode that enhances the energy density. The results demonstrate the interface modification of insulating sulfur and the architecture of an all-solid-state Li-S battery configuration with high energy density.

  7. First principles treatment of structural, optical, and thermoelectric properties of Li{sub 7}MnN{sub 4} as electrode for a Li secondary battery

    SciTech Connect (OSTI)

    Khan, Wilayat; Reshak, A.H.

    2015-01-15

    The electronic structure, electronic charge density and linear optical properties of the metallic Li{sub 7}MnN{sub 4} compound, having cubic symmetry, are calculated using the full potential linearized augmented plane wave (FP-LAPW) method. The calculated band structure and density of states using the local density, generalized gradient and EngelVosko approximations, depict the metallic nature of the cubic Li{sub 7}MnN{sub 4} compound. The bands crossing the Fermi level in the calculated band structure are mainly from the Mn-d states with small support of N-p states. In addition, the Mn-d states at the Fermi level enhance the density of states, which is very useful for the electronic transport properties. The valence electronic charge density depicts strong covalent bond between Mn and two N atoms and polar covalent bond between Mn and Li atoms. The frequency dependent linear optical properties like real and imaginary part of the dielectric function, optical conductivity, reflectivity and energy loss function are calculated on the basis of the computed band structure. Both intra-band and inter-band transitions contribute to the calculated optical parameters. Using the BoltzTraP code, the thermoelectric properties like electrical and thermal conductivity, Seebeck coefficient, power coefficient and heat capacity of the Li{sub 7}MnN{sub 4} are also calculated as a function of temperature and studied.

  8. A model for HAZ hardness profiles in Al-Li-X alloys: Application to the Al-Li-Cu Alloy 2095

    SciTech Connect (OSTI)

    Rading, G.O.; Shamsuzzoha, M.; Berry, J.T.

    1998-10-01

    In a previous paper details were presented of a theoretical model describing the evolution of the hardness profiles in the heat-affected zones (HAZ) of Al-Li-X weldments. The intent of the model was to qualitatively predict the general shape of such a profile, which indicates points of double inflection. In the present paper, experimental results are presented to validate the model. Panels of Al-Li-Cu Alloy 2095 in the peak aged (T8) condition were welded by the gas tungsten arc (GTA) process using AA 2319 filler metal. Conventional transmission electron microscopy (TEM) studies were conducted on specimens taken from specific points across the HAZ to estimate the relative ratios of T{sub 1} (Al{sub 2}CuLi) and {delta}{prime} (Al{sub 3}Li) precipitates, as well as incoherent grain boundary phases. Electron probe microanalysis (EPMA) was used to determine the variation of concentrations of elements across the HAZ, while the hardness profile was determined using Vickers microhardness measurements. The hardness profile and the associated pattern of phases present agree well with the information predicted qualitatively by the previously described model.

  9. Site Environmental Report for 2014 SNL/CA

    SciTech Connect (OSTI)

    Larsen, Barbara L.

    2015-06-01

    Sandia National Laboratories, California (SNL/CA) is a government-owned/contractoroperated laboratory. Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, manages and operates the laboratory for the Department of Energy’s National Nuclear Security Administration (NNSA). The NNSA Sandia Field Office administers the contract and oversees contractor operations at the site. This Site Environmental Report for 2014 was prepared in accordance with DOE Order 231.1B, Environment, Safety and Health Reporting (DOE 2011d). The report provides a summary of environmental monitoring information and compliance activities that occurred at SNL/CA during calendar year 2014. General site and environmental program information is also included.

  10. Synthesis of spherical LiMnPO{sub 4}/C composite microparticles

    SciTech Connect (OSTI)

    Bakenov, Zhumabay; Taniguchi, Izumi

    2011-08-15

    Highlights: {yields} We could prepare LiMnPO{sub 4}/C composites by a novel preparation method. {yields} The LiMnPO{sub 4}/C composites were spherical particles with a mean diameter of 3.65 {mu}m. {yields} The LiMnPO{sub 4}/C composite cathode exhibited 112 mAh g{sup -1} at 0.05 C. {yields} It also showed a good rate capability up to 5 C at room temperature and 55 {sup o}C. -- Abstract: Spherical LiMnPO{sub 4}/C composite microparticles were prepared by a combination of spray pyrolysis and spray drying followed by heat treatment and examined as a cathode material for lithium batteries. The structure, morphology and electrochemical performance of the resulting spherical LiMnPO{sub 4}/C microparticles were characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electronic microscopy and standard electrochemical techniques. The final sample was identified as a single phase orthorhombic structure of LiMnPO{sub 4} and spherical powders with a geometric mean diameter of 3.65 {mu}m and a geometric standard deviation of 1.34. The electrochemical cells contained the spherical LiMnPO{sub 4}/C microparticles exhibited first discharge capacities of 112 and 130 mAh g{sup -1} at 0.05 C at room temperature and 55 {sup o}C, respectively. These also showed a good rate capability up to 5 C at room temperature and 55 {sup o}C.

  11. DOE - Office of Legacy Management -- Mare Island Navy Yard - CA 0-01

    Office of Legacy Management (LM)

    Mare Island Navy Yard - CA 0-01 FUSRAP Considered Sites Site: MARE ISLAND NAVY YARD (CA.0-01 ) Eliminated from consideration under FUSRAP - Referred to DoD Designated Name: Not Designated Alternate Name: None Location: Mare Island , California CA.0-01-2 Evaluation Year: 1989 CA.0-01-1 Site Operations: Naval yard and shipping station. CA.0-01-2 Site Disposition: Eliminated - Referred to DOD CA.0-01-1 CA.0-01-2 Radioactive Materials Handled: None Indicated Primary Radioactive Materials Handled:

  12. Novel Energy Sources -Material Architecture and Charge Transport in Solid State Ionic Materials for Rechargeable Li ion Batteries

    SciTech Connect (OSTI)

    Katiyar, Ram S; Gmez, M; Majumder, S B; Morell, G; Tomar, M S; Smotkin, E; Bhattacharya, P; Ishikawa, Y

    2009-01-19

    Since its introduction in the consumer market at the beginning of 1990s by Sony Corporation Li-ion rechargeable battery and LiCoO2 cathode is an inseparable couple for highly reliable practical applications. However, a separation is inevitable as Li-ion rechargeable battery industry demand more and more from this well serving cathode. Spinel-type lithium manganate (e.g., LiMn2O4), lithium-based layered oxide materials (e.g., LiNiO2) and lithium-based olivine-type compounds (e.g., LiFePO4) are nowadays being extensively studied for application as alternate cathode materials in Li-ion rechargeable batteries. Primary goal of this project was the advancement of Li-ion rechargeable battery to meet the future demands of the energy sector. Major part of the research emphasized on the investigation of electrodes and solid electrolyte materials for improving the charge transport properties in Li-ion rechargeable batteries. Theoretical computational methods were used to select electrodes and electrolyte material with enhanced structural and physical properties. The effect of nano-particles on enhancing the battery performance was also examined. Satisfactory progress has been made in the bulk form and our efforts on realizing micro-battery based on thin films is close to give dividend and work is progressing well in this direction.

  13. Li2S encapsulated by nitrogen-doped carbon for lithium sulfur batteries

    SciTech Connect (OSTI)

    Chen, Lin; Liu, Yuzi; Ashuri, Maziar; Liu, Caihong; Shaw, Leon L.

    2014-09-26

    Using high-energy ball milling of the Li2S plus carbon black mixture followed by carbonization of pyrrole, we have established a facile approach to synthesize Li2S-plus-C composite particles of average size 400 nm, encapsulated by a nitrogen-doped carbon shell. Such an engineered coreshell structure exhibits an ultrahigh initial discharge specific capacity (1029 mAh/g), reaching 88% of the theoretical capacity (1,166 mAh/g of Li2S) and thus offering the highest utilization of Li2S in the cathode among all of the reported works for the encapsulated Li2S cathodes. This Li2S/C composite core with a nitrogen-doped carbon shell can still retain 652 mAh/g after prolonged 100 cycles. These superior properties are attributed to the nitrogen-doped carbon shell that can improve the conductivity to enhance the utilization of Li2S in the cathode. As a result, fine particle sizes and the presence of carbon black within the Li2S core may also play a role in high utilization of Li2S in the cathode.

  14. DOE - Office of Legacy Management -- Arthur D Little Co - CA 01

    Office of Legacy Management (LM)

    Arthur D Little Co - CA 01 FUSRAP Considered Sites Site: Arthur D Little Co (CA.01 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: Merrill Company CA.01-1 Location: San Francisco , California CA.01-2 Evaluation Year: 1986 CA.01-1 Site Operations: Performed research and development work on the modified char process for recovery of uranium from leach acid slurries; solvent extraction from carbonate leach solutions; and air oxidation of reduced uranium

  15. DOE - Office of Legacy Management -- Dow Chemical Co - Walnut Creek - CA 02

    Office of Legacy Management (LM)

    Walnut Creek - CA 02 FUSRAP Considered Sites Site: Dow Chemical Co. - Walnut Creek (CA.02 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: None Location: 2800 Mitchell Drive , Walnut Creek , California CA.02-1 Evaluation Year: 1987 CA.02-2 CA.02-3 Site Operations: From 1947 to 1957, conducted process studies and experimental investigations on different uranium and thorium-bearing ores; pilot-scale solvent extraction of uranium from phosphoric acid;

  16. DOE - Office of Legacy Management -- Burris Park Field Station - CA 10

    Office of Legacy Management (LM)

    Burris Park Field Station - CA 10 FUSRAP Considered Sites Site: Burris Park Field Station (CA.10 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: None Location: Kingsburg , California CA.10-1 Evaluation Year: 1987 CA.10-2 Site Operations: The U.S Atomic Energy Commission contracted with the University of California to conduct experiments on decontamination of soils containing Strontium-90. CA.10-1 Site Disposition: Eliminated - Adequate remediation

  17. ALD of Al2O3 for Highly Improved Performance in Li-Ion Batteries

    SciTech Connect (OSTI)

    Dillon, A.; Jung, Y. S.; Ban, C.; Riley, L.; Cavanagh, A.; Yan, Y.; George, S.; Lee, S. H.

    2012-01-01

    Significant advances in energy density, rate capability and safety will be required for the implementation of Li-ion batteries in next generation electric vehicles. We have demonstrated atomic layer deposition (ALD) as a promising method to enable superior cycling performance for a vast variety of battery electrodes. The electrodes range from already demonstrated commercial technologies (cycled under extreme conditions) to new materials that could eventually lead to batteries with higher energy densities. For example, an Al2O3 ALD coating with a thickness of ~ 8 A was able to stabilize the cycling of unexplored MoO3 nanoparticle anodes with a high volume expansion. The ALD coating enabled stable cycling at C/2 with a capacity of ~ 900 mAh/g. Furthermore, rate capability studies showed the ALD-coated electrode maintained a capacity of 600 mAh/g at 5C. For uncoated electrodes it was only possible to observe stable cycling at C/10. Also, we recently reported that a thin ALD Al2O3 coating with a thickness of ~5 A can enable natural graphite (NG) electrodes to exhibit remarkably durable cycling at 50 degrees C. The ALD-coated NG electrodes displayed a 98% capacity retention after 200 charge-discharge cycles. In contrast, bare NG showed a rapid decay. Additionally, Al2O3 ALD films with a thickness of 2 to 4 A have been shown to allow LiCoO2 to exhibit 89% capacity retention after 120 charge-discharge cycles performed up to 4.5 V vs Li/Li+. Bare LiCoO2 rapidly deteriorated in the first few cycles. The capacity fade is likely caused by oxidative decomposition of the electrolyte at higher potentials or perhaps cobalt dissolution. Interestingly, we have recently fabricated full cells of NG and LiCoO2 where we coated both electrodes, one or the other electrode as well as neither electrode. In creating these full cells, we observed some surprising results that lead us to obtain a greater understanding of the ALD coatings. We have also recently coated a binder free LiNi0.04Mn0.04Co02O2 electrode containing 5 wt% single-walled carbon nanotubes as the conductive additive and demonstrated both high rate capability as well as the ability to cycle the cathode to 5 V vrs. Li/Li+. Finally, we coated a Celgard (TM) separator and enabled stable cycling in a high dielectric electrolyte. These results will be presented in detail.

  18. Pushing the Theoretical Limit of Li-CFx Batteries: A Tale of Bi-functional Electrolyte

    SciTech Connect (OSTI)

    Rangasamy, Ezhiylmurugan; Li, Juchuan; Sahu, Gayatri; Dudney, Nancy J; Liang, Chengdu

    2014-01-01

    In a typical battery, electrodes deliver capacities less or equal the theoretical maxima of the electrode materials.1 The inert electrolyte functions solely as the ionic conductor without contribution to the cell capacity because of its distinct mono-function in the concept of conventional batteries. Here we demonstrate that the most energy-dense Li-CFx battery2 delivers a capacity exceeding the theoretical maximum of CFx with a solid electrolyte of Li3PS4 (LPS) that has dual functions: as the inert electrolyte at the anode and the active component at the cathode. Such a bi-functional electrolyte reconciles both inert and active characteristics through a synergistic discharge mechanism of CFx and LPS. Li3PS4 is known as an inactive solid electrolyte with a broad electrochemical window over 5 V.3 The synergy at the cathode is through LiF, the discharge product of CFx, which activates the electrochemical discharge of LPS at a close electrochemical potential of CFx. Therefore, the solid-state Li-CFx batteries output 126.6% energy beyond their theoretic limits without compromising the stability of the cell voltage. The extra energy comes from the electrochemical discharge of LPS, the inert electrolyte. This bi-functional electrolyte revolutionizes the concept of conventional batteries and opens a new avenue for the design of batteries with an unprecedentedly high energy density.

  19. Synthesis of BiPbSrCaCuO superconductor

    DOE Patents [OSTI]

    Hults, William L.; Kubat-Martin, Kimberly A.; Salazar, Kenneth V.; Phillips, David S.; Peterson, Dean E.

    1994-01-01

    A process and a precursor composition for preparing a lead-doped bismuth-strontium-calcium-copper oxide superconductor of the formula Bi.sub.a Pb.sub.b Sr.sub.c Ca.sub.d Cu.sub.e O.sub.f wherein a is from about 1.7 to about 1.9, b is from about 0.3 to about 0.45, c is from about 1.6 to about 2.2, d is from about 1.6 to about 2.2, e is from about 2.97 to about 3.2 and f is 10.+-.z by reacting a mixture of Bi.sub.4 Sr.sub.3 Ca.sub.3 Cu.sub.4 O.sub.16.+-.z, an alkaline earth metal cuprate, e.g., Sr.sub.9 Ca.sub.5 Cu.sub.24 O.sub.41, and an alkaline earth metal plumbate, e.g., Ca.sub.2-x Sr.sub.x PbO.sub.4 wherein x is about 0.5, is disclosed.

  20. Synthesis of BiPbSrCaCuO superconductor

    DOE Patents [OSTI]

    Hults, W.L.; Kubat-Martin, K.A.; Salazar, K.V.; Phillips, D.S.; Peterson, D.E.

    1994-04-05

    A process and a precursor composition for preparing a lead-doped bismuth-strontium-calcium-copper oxide superconductor of the formula Bi[sub a]Pb[sub b]Sr[sub c]Ca[sub d]Cu[sub e]O[sub f] wherein a is from about 1.7 to about 1.9, b is from about 0.3 to about 0.45, c is from about 1.6 to about 2.2, d is from about 1.6 to about 2.2, e is from about 2.97 to about 3.2 and f is 10[+-]z by reacting a mixture of Bi[sub 4]Sr[sub 3]Ca[sub 3]Cu[sub 4]O[sub 16[+-]z], an alkaline earth metal cuprate, e.g., Sr[sub 9]Ca[sub 5]Cu[sub 24]O[sub 41], and an alkaline earth metal plumbate, e.g., Ca[sub 2[minus]x]Sr[sub x]PbO[sub 4] wherein x is about 0.5, is disclosed.

  1. Electrochemistry Gordon Research Seminar/Conference (Ventura, CA) - JCAP

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

    Electrochemistry Gordon Research Seminar/Conference (Ventura, CA) Sat, Jan 9, 2016 2:30pm 14:30 Fri, Jan 15, 2016 3:30pm 15:30 Sonja Francis, "Catalyst Screening for Electrochemical Carbon Dioxide Reduction" Co-authors: Daniel Torelli, Bruce Brunschwig, Nate Lewis February 28 Renewable Energy: Solar Fuels - Gordon Research Conference (Lucca, IT

  2. Thermodynamic studies of CaLaFe??O??(s)

    SciTech Connect (OSTI)

    Rakshit, S.K.; Parida, S.C.; Lilova, Kristina; Navrotsky, Alexandra

    2013-05-01

    Thermodynamic studies on CaLaFe??O??(s) were carried out using Knudsen effusion mass spectrometry and calorimetry, viz. differential scanning calorimetry and high temperature oxide melt solution calorimetry. Standard molar Gibbs free energy of formation (?{sub f}G?{sub m}), enthalpy of formation and heat capacity (C?{sub ?,m}) of the compound were calculated as a function of temperature for the first time. C?{sub ?,m}(CaLaFe??O??) was determined and used for second law analysis, from which enthalpy and entropy of formation of the compound were calculated and the respective values are: ?{sub f}H?{sub m}(298.15 K)/kJ mol?=-6057(8) and S?{sub m}(298.15 K)/J K? mol?=427(5). ?{sub f}H?{sub m}(298.15 K)/kJ mol?: -6055(6) was also calculated using oxide melt solution calorimetry, which is in close agreement with the second law value. A heat capacity anomaly was also observed at T=684 K. A table of thermodynamic data from 298.15 K to 1000 K for CaLaFe??O??(s) was also constructed to represent an optimized set of data. - graphical abstract: Variation of standard molar heat capacities of CaLaF??O??(s) and MFe??O??(s) (M=Sr, Ba and Pb) as a function of temperature. Highlights: Thermodynamic studies on CaLaFe??O??(s) were performed using KEQMS and solution calorimetry. It was synthesized using gel combustion route and characterized by XRD technique. The compound is magnetic in nature and shows a heat capacity anomaly at 684 K. Thermodynamic table was constructed from 298 K to 1000 K.

  3. mRNA Transcript Abundance during Plant Growth and the Influence of Li+ Exposure

    SciTech Connect (OSTI)

    Duff, M. C. [Savannah River National Laboratory, Aiken, SC (United States); Kuhne, W. W. [Savannah River National Laboratory, Aiken, SC (United States); Halverson, N. [Savannah River National Laboratory, Aiken, SC (United States); Chang, C. -S. [Georgia Regents University Cancer Center, Augusta, GA (United States). Integrated Genomics Core; Kitamura, E. [Georgia Regents University Cancer Center, Augusta, GA (United States). Integrated Genomics Core; Hawthorn, L. [Georgia Regents University Cancer Center, Augusta, GA (United States). Integrated Genomics Core; Milliken, C. E. [Savannah River National Laboratory, Aiken, SC (United States); Caldwell, E. F. [Savannah River National Laboratory, Aiken, SC (United States); Stieve-Caldwell, E. [Savannah River National Laboratory, Aiken, SC (United States); Martinez, N. E. [Savannah River National Laboratory, Aiken, SC (United States); Colorado State University, Ft. Collins, CO (United States). Dept. of Environmental and Radiological Health Sciences; Stafford, C. [Savannah River National Laboratory, Aiken, SC (United States); Univ. of South Carolina Medical School, Columbia, SC (United States)

    2014-12-01

    Lithium (Li) toxicity in plants is, at a minimum, a function of Li+ concentration, exposure time, species and growth conditions. Most plant studies with Li+ focus on short-term acute exposures. This study examines short- and long-term effects of Li+ exposure in Arabidopsis with Li+ uptake studies and measured shoot mRNA transcript abundance levels in treated and control plants. Stress, pathogen-response and arabinogalactan protein genes were typically more up-regulated in older (chronic, low level) Li+-treatment plants and in the much younger plants from acute high-level exposures. The gene regulation behavior of high-level Li+ resembled prior studies due to its influence on: inositol synthesis, 1-aminocyclopropane-1-carboxylate synthases and membrane ion transport. In contrast, chronically-exposed plants had gene regulation responses that were indicative of pathogen, cold, and heavy-metal stress, cell wall degradation, ethylene production, signal transduction, and calcium-release modulation. Acute Li+ exposure phenocopies magnesium-deficiency symptoms and is associated with elevated expression of stress response genes that could lead to consumption of metabolic and transcriptional energy reserves and the dedication of more resources to cell development. In contrast, chronic Li+ exposure increases expression signal transduction genes. The identification of new Li+-sensitive genes and a gene-based response plan for acute and chronic Li+ exposure are delineated.

  4. mRNA Transcript Abundance during Plant Growth and the Influence of Li+ Exposure

    SciTech Connect (OSTI)

    Duff, M. C.; Kuhne, W. W.; Halverson, N. V.; Chang, C. -S.; Kitamura, E.; Hawthorn, L.; Martinez, N. E.; Stafford, C.; Milliken, C. E.; Caldwell, E. F.; Stieve-Caldwell, E.

    2014-10-23

    Lithium (Li) toxicity in plants is, at a minimum, a function of Li+ concentration, exposure time, species and growth conditions. Most plant studies with Li+ focus on short-term acute exposures. This study examines short- and long-term effects of Li+ exposure in Arabidopsis with Li+ uptake studies and measured shoot mRNA transcript abundance levels in treated and control plants. Stress, pathogen-response and arabinogalactan protein genes were typically more up-regulated in older (chronic, low level) Li+-treatment plants and in the much younger plants from acute high-level exposures. The gene regulation behavior of high-level Li+ resembled prior studies due to its influence on: inositol synthesis, 1-aminocyclopropane-1-carboxylate synthases and membrane ion transport. In contrast, chronically-exposed plants had gene regulation responses that were indicative of pathogen, cold, and heavy-metal stress, cell wall degradation, ethylene production, signal transduction, and calcium-release modulation. Acute Li+ exposure phenocopies magnesium-deficiency symptoms and is associated with elevated expression of stress response genes that could lead to consumption of metabolic and transcriptional energy reserves and the dedication of more resources to cell development. In contrast, chronic Li+ exposure increases expression signal transduction genes. The identification of new Li+-sensitive genes and a gene-based response plan for acute and chronic Li+ exposure are delineated.

  5. The ARIES-RS power core -- Recent development in Li/V designs

    SciTech Connect (OSTI)

    Sze, D.K.; Billone, M.C.; Hua, T.Q.

    1997-04-01

    The ARIES-RS fusion power plant design study is based on reversed-shear (RS) physics with a Li/V (lithium breeder and vanadium structure) blanket. The reversed-shear discharge has been documented in many large tokamak experiments. The plasma in the RS mode has a high beta, low current, and low current drive requirements. Therefore, it is an attractive physics regime for a fusion power plant. The blanket system based on a Li/V has high temperature operating capability, good tritium breeding, excellent high heat flux removal capability, long structural life time, low activation, low after heat and good safety characteristics. For these reasons, the ARIES-RS reactor study selected Li/V as the reference blanket. The combination of attractive physics and attractive blanket engineering is expected to result in a superior power plant design. This paper summarizes the power core design of the ARIES-RS power plant study.

  6. Hartree-Fock calculation of the differential photoionization cross sections of small Li clusters

    SciTech Connect (OSTI)

    Galitskiy, S. A.; Artemyev, A. N.; Jänkälä, K.; Lagutin, B. M.; Demekhin, Ph. V.

    2015-01-21

    Cross sections and angular distribution parameters for the single-photon ionization of all electron orbitals of Li{sub 2−8} are systematically computed in a broad interval of the photoelectron kinetic energies for the energetically most stable geometry of each cluster. Calculations of the partial photoelectron continuum waves in clusters are carried out by the single center method within the Hartree-Fock approximation. We study photoionization cross sections per one electron and analyze in some details general trends in the photoionization of inner and outer shells with respect to the size and geometry of a cluster. The present differential cross sections computed for Li{sub 2} are in a good agreement with the available theoretical data, whereas those computed for Li{sub 3−8} clusters can be considered as theoretical predictions.

  7. Materials for Better Li-based Storage Systems for a "Green Energy Society"

    ScienceCinema (OSTI)

    Jean-Marie Tarascon

    2010-01-08

    Li-ion batteries are strongly considered for powering the upcoming generations of HEVs and PHEVs, but there are still the issues of safety and costs in terms of materials resources and abundances, synthesis, and recycling processes. Notions of materials having minimum footprint in nature, made via eco-efficient processes, must be integrated in our new research towards the next generation of sustainable and "greener" Li-ion batteries. In this July 13, 2009 talk sponsored by Berkeley Lab's Environental Energy Technologies Division, Jean-Marie Tarascon, a professor at the University of Picardie (Amiens), discuss Eco-efficient synthesis via hydrothermal/solvothermal processes using latent bases as well as structure directing templates or other bio-related approaches of LiFePO4 nanopowders.

  8. Detailed Hydrographic Feature Extraction from High-Resolution LiDAR Data

    SciTech Connect (OSTI)

    Danny L. Anderson

    2012-05-01

    Detailed hydrographic feature extraction from high-resolution light detection and ranging (LiDAR) data is investigated. Methods for quantitatively evaluating and comparing such extractions are presented, including the use of sinuosity and longitudinal root-mean-square-error (LRMSE). These metrics are then used to quantitatively compare stream networks in two studies. The first study examines the effect of raster cell size on watershed boundaries and stream networks delineated from LiDAR-derived digital elevation models (DEMs). The study confirmed that, with the greatly increased resolution of LiDAR data, smaller cell sizes generally yielded better stream network delineations, based on sinuosity and LRMSE. The second study demonstrates a new method of delineating a stream directly from LiDAR point clouds, without the intermediate step of deriving a DEM. Direct use of LiDAR point clouds could improve efficiency and accuracy of hydrographic feature extractions. The direct delineation method developed herein and termed mDn, is an extension of the D8 method that has been used for several decades with gridded raster data. The method divides the region around a starting point into sectors, using the LiDAR data points within each sector to determine an average slope, and selecting the sector with the greatest downward slope to determine the direction of flow. An mDn delineation was compared with a traditional grid-based delineation, using TauDEM, and other readily available, common stream data sets. Although, the TauDEM delineation yielded a sinuosity that more closely matches the reference, the mDn delineation yielded a sinuosity that was higher than either the TauDEM method or the existing published stream delineations. Furthermore, stream delineation using the mDn method yielded the smallest LRMSE.

  9. Report for in-situ 7Li NMR experiment in PNNL Phase -1

    SciTech Connect (OSTI)

    Hu, Jian Zhi

    2014-08-19

    To understand the detailed local structural evolution, an in-situ 7Li NMR study was performed. An operando identification of the lithium germanide phases under various cycling regimens permitted understanding of the kinetics of phase transition between different structural phases, including the amorphous phases, and how these correlated with capacity retention. Combining data from TEM and in-situ 7Li NMR, we discovered that the phase inter-conversion during cycling was mediated by co-existing amorphous and crystalline phases, and that the high capacity observed was correlated with an over-lithiated lithium germanide phase.

  10. Ab initio calculations of the electronic structure of silicon nanocrystals doped with shallow donors (Li, P)

    SciTech Connect (OSTI)

    Kurova, N. V. Burdov, V. A.

    2013-12-15

    The results of ab initio calculations of the electronic structure of Si nanocrystals doped with shallow donors (Li, P) are reported. It is shown that phosphorus introduces much more significant distortions into the electronic structure of the nanocrystal than lithium, which is due to the stronger central cell potential of the phosphorus ion. It is found that the Li-induced splitting of the ground state in the conduction band of the nanocrystal into the singlet, doublet, and triplet retains its inverse structure typical for bulk silicon.

  11. Rapid first-cycle lithiation strategy for enhanced performance of Li-MoS2

    Office of Scientific and Technical Information (OSTI)

    batteries as identified by in situ studies. (Journal Article) | SciTech Connect Rapid first-cycle lithiation strategy for enhanced performance of Li-MoS2 batteries as identified by in situ studies. Citation Details In-Document Search Title: Rapid first-cycle lithiation strategy for enhanced performance of Li-MoS2 batteries as identified by in situ studies. Abstract not provided. Authors: Jiayu Wan ; Wenzhong Bao ; Yang Liu ; Jiaqi Dai ; Fei Shen ; Lihui Zhou ; Xinghan Cai ; Dan Urban ;

  12. Key Parameters Governing the Energy Density of Rechargeable Li/S Batteries

    Office of Scientific and Technical Information (OSTI)

    (Journal Article) | SciTech Connect Key Parameters Governing the Energy Density of Rechargeable Li/S Batteries Citation Details In-Document Search Title: Key Parameters Governing the Energy Density of Rechargeable Li/S Batteries Authors: Gao, Jie ; Abruña, Héctor D. Publication Date: 2014-03-06 OSTI Identifier: 1161939 DOE Contract Number: SC0001086 Resource Type: Journal Article Resource Relation: Journal Name: J. Phys. Chem. Lett.; Journal Volume: 5(5); Related Information: Emc2 partners

  13. Low energy detectors: 6Li-glass scintillators (Conference) | SciTech

    Office of Scientific and Technical Information (OSTI)

    Connect Low energy detectors: 6Li-glass scintillators Citation Details In-Document Search Title: Low energy detectors: 6Li-glass scintillators Authors: Lee, Hye Young [1] ; Taddeucci, Terry N [1] + Show Author Affiliations Los Alamos National Laboratory Publication Date: 2012-03-22 OSTI Identifier: 1178711 Report Number(s): LA-UR-12-01482; LA-UR-12-1482 DOE Contract Number: AC52-06NA25396 Resource Type: Conference Resource Relation: Conference: Fission Workshop ; March 8, 2012 ; Los Alamos,

  14. A high performance hybrid battery based on aluminum anode and LiFePO4 cathode

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

    Sun, Xiao-Guang; Bi, Zhonghe; Liu, Hansan; Bridges, Craig A.; Paranthaman, Mariappan Parans; Dai, Sheng; Brown, Gilbert M.

    2015-10-07

    A unique battery hybrid utilizes an aluminum anode, a LiFePO4 cathode and an acidic ionic liquid electrolyte based on 1-ethyl-3-methylimidazolium chloride (EMImCl) and aluminum trichloride (AlCl 3) (EMImCl-AlCl 3, 1-1.1 in molar ratio) with or without LiAlCl4 is proposed. This hybrid ion battery delivers an initial high capacity of 160 mAh g-1 at a current rate of C/5. It also shows good rate capability and cycling performance.

  15. Enhancing performance of Li/(CFx)n cells at low temperatures. (Conference)

    Office of Scientific and Technical Information (OSTI)

    | SciTech Connect Enhancing performance of Li/(CFx)n cells at low temperatures. Citation Details In-Document Search Title: Enhancing performance of Li/(CFx)n cells at low temperatures. No abstract prepared. Authors: Nagasubramanian, Ganesan Publication Date: 2007-04-01 OSTI Identifier: 1028949 Report Number(s): SAND2007-2065C TRN: US201122%%624 DOE Contract Number: AC04-94AL85000 Resource Type: Conference Resource Relation: Conference: Proposed for presentation at the 25th International

  16. Fabrication and Testing Capabilities for 18650 Li/(CFx)n Cells. (Journal

    Office of Scientific and Technical Information (OSTI)

    Article) | SciTech Connect Journal Article: Fabrication and Testing Capabilities for 18650 Li/(CFx)n Cells. Citation Details In-Document Search Title: Fabrication and Testing Capabilities for 18650 Li/(CFx)n Cells. Abstract not provided. Authors: Nagasubramanian, Ganesan Publication Date: 2007-08-01 OSTI Identifier: 1147597 Report Number(s): SAND2007-5628J 521695 DOE Contract Number: DE-AC04-94AL85000 Resource Type: Journal Article Resource Relation: Journal Name: International Journal of

  17. Lithium cobalt(II) pyrophosphate, Li[subscript 1.86]CoP[subscript

    Office of Scientific and Technical Information (OSTI)

    2]O[subscript 7], from synchrotron X-ray powder data (Journal Article) | SciTech Connect SciTech Connect Search Results Journal Article: Lithium cobalt(II) pyrophosphate, Li[subscript 1.86]CoP[subscript 2]O[subscript 7], from synchrotron X-ray powder data Citation Details In-Document Search Title: Lithium cobalt(II) pyrophosphate, Li[subscript 1.86]CoP[subscript 2]O[subscript 7], from synchrotron X-ray powder data Structure refinement of high-resolution X-ray powder diffraction data of the

  18. Ab Initio Many-Body Calculations of Deuteron-4He Scattering And 6Li States

    Office of Scientific and Technical Information (OSTI)

    (Journal Article) | SciTech Connect Calculations of Deuteron-4He Scattering And 6Li States Citation Details In-Document Search Title: Ab Initio Many-Body Calculations of Deuteron-4He Scattering And 6Li States Authors: Quaglioni, S ; Navratil, P Publication Date: 2011-02-08 OSTI Identifier: 1118007 Report Number(s): LLNL-JRNL-469878 DOE Contract Number: W-7405-ENG-48 Resource Type: Journal Article Resource Relation: Journal Name: Phisical Review C, na, na, April 14, 2011, pp. 04460

  19. Chemical Bonding In Amorphous Si Coated-carbon Nanotube As Anodes For Li

    Office of Scientific and Technical Information (OSTI)

    ion Batteries: A XANES Study (Journal Article) | SciTech Connect Chemical Bonding In Amorphous Si Coated-carbon Nanotube As Anodes For Li ion Batteries: A XANES Study Citation Details In-Document Search Title: Chemical Bonding In Amorphous Si Coated-carbon Nanotube As Anodes For Li ion Batteries: A XANES Study The chemical bonding nature and its evolution upon electrochemical cycling in amorphous Si coated-carbon nanotube (Si-CNT) anode has been investigated using comprehensive X-ray

  20. Development of High Capacity Anode for Li-ion Batteries | Department of

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

    Energy High Capacity Anode for Li-ion Batteries Development of High Capacity Anode for Li-ion Batteries 2010 DOE Vehicle Technologies and Hydrogen Programs Annual Merit Review and Peer Evaluation Meeting, June 7-11, 2010 -- Washington D.C. PDF icon es065_zhang_2010_p.pdf More Documents & Publications Novel Lithium Ion Anode Structures: Overview of New DOE BATT Anode Projects Hybrid Nano Carbon Fiber/Graphene Platelet-Based High-Capacity Anodes for Lithium Ion Batteries Hybrid Nano Carbon

  1. Statistical Design of Experiment for Li-ion Cell Formation Parameters using

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

    Gen3Ž Electrode Materials: Final Summary | Department of Energy Design of Experiment for Li-ion Cell Formation Parameters using Gen3Ž Electrode Materials: Final Summary Statistical Design of Experiment for Li-ion Cell Formation Parameters using Gen3Ž Electrode Materials: Final Summary 2009 DOE Hydrogen Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting, May 18-22, 2009 -- Washington D.C. PDF icon esp_03_gering.pdf More Documents &

  2. Hard Carbon Materials for High-Capacity Li-ion Battery Anodes | Department

    Office of Environmental Management (EM)

    of Energy Hard Carbon Materials for High-Capacity Li-ion Battery Anodes Hard Carbon Materials for High-Capacity Li-ion Battery Anodes 2011 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon es104_dai_2011_o.pdf More Documents & Publications Vehicle Technologies Office Merit Review 2015: A Combined Experimental and Modeling Approach for the Design of High Coulombic Efficiency Si Electrodes In situ Characterizations of New

  3. I L S-V I I I J* I LI

    Office of Legacy Management (LM)

    L - S-V I I I J* I LI 11. LI L - OAK RlDGE NATBONAL LABORATORY <;> "J :-: ,rj _ .- ORNLnM- 12225 I: ?, .,I Radiological Survey Results at the Former Bridgeport Brass Company Facility Seymour, Connecticut R. D. Foley R. F . Carrier c MANAGED BY MARTIN MARIETTA ENERGY SYSTERlS, INC. - FOR TRE UNITED STATES DEPARTMENT OF ENERGY / l- _I. _ --..--.- This report has been reproduced directly from the best available copy. Available to DOE and DOE contractors from the Cffice of Scientific and

  4. Michael Li Electricity Policy Specialist U.S. Department of Energy

    Office of Environmental Management (EM)

    6-390 Village Blvd. Princeton, NJ 08540 609.452.8060 | www.nerc.com November 1, 2010 Michael Li Electricity Policy Specialist U.S. Department of Energy Office of Electricity Delivery and Energy Reliability 1000 Independence Avenue, SW Room 8H033 Washington, DC 20585 RE: "Smart Grid RFI: Addressing Policy and Logistical Challenges" Dear Mr. Li: I am writing in response to the Department of Energy's ("DOE") Request for Information (RFI) regarding the "Smart Grid RFI:

  5. A synthesis of LiFePO{sub 4} starting from FePO{sub 4} under reducing atmosphere

    SciTech Connect (OSTI)

    Prosini, Pier Paolo; Cento, Cinzia; Masci, Amedeo; Carewska, Maria; Gislon, Paola

    2014-06-19

    A fast and easy way to produce LiFePO{sub 4} starting from FePO{sub 4}, used as iron and phosphorus source, is proposed. 5% hydrogen is employed as a reducing agent and various compounds containing lithium as lithiation agents. The selected lithiation agents included: LiCl, CH{sub 3}COOLi, LiOH, Li{sub 2}S, LiH, and Li{sub 2}CO{sub 3}. Solid state synthesis is used for the LiFePO{sub 4} preparation and the so obtained materials are structurally characterized by XRD. The materials are used to fabricate composite electrode and their specific capacity is evaluated by low rate galvanostatic charge/discharge cycles (C/10 rate). Among the various lithium salts, the acetate give rise to the LiFePO{sub 4} with the best electrochemical performance. The morphology of this material is further investigated by SEM microscopy and the specific capacity is evaluated as a function of the discharge rate and the cycle number.

  6. Compatibility of Lithium Salts with Solvent of the Non-Aqueous Electrolyte in LiO2 Batteries

    SciTech Connect (OSTI)

    Du, Peng; Lu, Jun; Lau, Kah Chun; Luo, Xiangyi; Bareno, Javier; Zhang, Xiaoyi; Ren, Yang; Zhang, Zhengcheng; Curtiss, Larry A.; Sun, Yang-Kook; Amine, Khalil

    2013-02-20

    The stability of lithium salts, especially in the presence of reduced oxygen species, O2 and H2O (even in a small amount), plays an important role in the cyclability and capacity of LiO2 cells. This combined experimental and computational study provides evidence that the stability of the electrolyte used in LiO2 cells strongly depends on the compatibility of lithium salts with solvent. In the case of the LiPF61NM3 electrolyte, the decomposition of LiPF6 occurs in the cell as evidenced by in situ XRD, FT-IR and XPS analysis, which triggers the decomposition of 1NM3 solvent due to formation of HF from the decomposition of LiPF6. These reactions lead to degradation of the electrolyte and cause poor cyclability of the cell. The same reactions are not observed when LiTFSI and LiCF3SO3 are used as the lithium salts in 1NM3 solvent, or LiPF6 is used in TEGDME solvent.

  7. First Principles Prediction of Nitrogen-doped Carbon Nanotubes as a High-Performance Cathode for Li-S Batteries

    SciTech Connect (OSTI)

    Wang, Zhiguo; Niu, Xinyue; Xiao, Jie; Wang, Chong M.; Liu, Jun; Gao, Fei

    2013-07-16

    The insulating nature of sulfur and the solubility of the polysulfide in organic electrolyte are two main factors that limit the application of lithium sulfur (Li-S) battery systems. Enhancement of Li conductivity, identification of a strong adsorption agent of polysulfides and the improvement of the whole sulfur-based electrode are of great technological importance. The diffusion of Li atoms on the outer-wall, inner-wall and inter-wall spaces in nitrogen-doped double-walled carbon nanotubes (CNTs) and penetrations of Li and S atoms through the walls are studied using density functional theory. We find that N-doping does not alternate the diffusion behaviors of Li atoms throughout the CNTs, but the energy barrier for Li atoms to penetrate the wall is greatly decreased by N-doping (from ~9.0 eV to ~ 1.0 eV). On the other hand, the energy barrier for S atoms to penetrate the wall remains very high, which is caused by the formation of the chemical bonds between the S and nearby N atoms. The results indicate that Li atoms are able to diffuse freely, whereas S atoms can be encapsulated inside the N-doped CNTs, suggesting that the N-doped CNTs can be potentially used in high performance Li-S batteries.

  8. Operando NMR and XRD study of chemically synthesized LiCx oxidation in a dry room environment

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

    Sacci, Robert L.; Gill, Lance W.; Hagaman, Edward W.; Dudney, Nancy J.

    2015-08-01

    We test the stability of pre-lithiated graphite anodes for Li-ion batteries in a dry room battery processing room. The reaction between LiCx and laboratory air was followed using operando NMR and x-ray diffraction as these methods are sensitive to change in Li stoichiometry in graphite. There is minimal reactivity between LiC6 and N2, CO2 or O2; however, LiC6 reacts with moisture to form lithium (hydr)oxide. The reaction rate follows zero-order kinetics with respects to intercalated lithium suggesting that lithium transport through the graphite is fast. The reaction mechanism occurs by sequential formation of higher stages LiC12, then LiC18, and thenmore » LiC24 as the hydrolysis proceeds to the formation of LixOHy and graphite end products. Slowing down the formation rate of the LixOHy passivation layer stabilizes of the higher stages.« less

  9. Analytical Hartree-Fock wave functions subject to cusp and asymptotic constraints: He to Xe, Li{sup +} to Cs{sup +}, H{sup {minus}} to I{sup {minus}}

    SciTech Connect (OSTI)

    Koga, Toshikatsu; Kanayama, Katsutoshi; Watanabe, Shinya; Thakkar, A.J.

    1999-02-20

    Analytical, variational approximations to Hartree-Fock wave functions are constructed for the ground states of all the neutral atoms from He to Xe, the cations from Li{sup +} to Cs{sup +}, and the stable anions from H{sup {minus}} to I{sup {minus}}. The wave functions are constrained so that each atomic orbital agrees well with the electron-nuclear cusp condition and has good long-range behavior. Painstaking optimization of the exponents and principal quantum numbers of the Slater-type basis functions allows one to reach this goal while obtaining total energies that, at worst, are a few microHartrees above the numerical Hartree-Fock limit values. The wave functions are freely available by anonymous ftp from okapi-chem.unb,ca or upon request to the authors.

  10. DOE - Office of Legacy Management -- Shannon Luminous Metals Co - CA 0-03

    Office of Legacy Management (LM)

    Shannon Luminous Metals Co - CA 0-03 FUSRAP Considered Sites Site: SHANNON LUMINOUS METALS CO. (CA.0-03 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: Shannon Luminous Metals CA.0-03-3 Location: 7356 Santa Monica Blvd. , Hollywood , California CA.0-03-1 Evaluation Year: 1987 CA.0-03-2 Site Operations: Research and development of uranium use in luminous paint pigments in the 1950s. CA.0-03-1 Site Disposition: Eliminated - No Authority - NRC licensed

  11. Effect of fuel rate and annealing process of LiFePO{sub 4} cathode material for Li-ion batteries synthesized by flame spray pyrolysis method

    SciTech Connect (OSTI)

    Halim, Abdul; Setyawan, Heru; Machmudah, Siti; Nurtono, Tantular; Winardi, Sugeng

    2014-02-24

    In this study the effect of fuel rate and annealing on particle formation of LiFePO{sub 4} as battery cathode using flame spray pyrolysis method was investigated numerically and experimentally. Numerical study was done using ANSYS FLUENT program. In experimentally, LiFePO{sub 4} was synthesized from inorganic aqueous solution followed by annealing. LPG was used as fuel and air was used as oxidizer and carrier gas. Annealing process attempted in inert atmosphere at 700C for 240 min. Numerical result showed that the increase of fuel rate caused the increase of flame temperature. Microscopic observation using Scanning Electron Microscopy (SEM) revealed that all particles have sphere and polydisperse. Increasing fuel rate caused decreasing particle size and increasing particles crystallinity. This phenomenon attributed to the flame temperature. However, all produced particles still have more amorphous phase. Therefore, annealing needed to increase particles crystallinity. Fourier Transform Infrared (FTIR) analysis showed that all particles have PO4 function group. Increasing fuel rate led to the increase of infrared spectrum absorption corresponding to the increase of particles crystallinity. This result indicated that phosphate group vibrated easily in crystalline phase. From Electrochemical Impedance Spectroscopy (EIS) analysis, annealing can cause the increase of Li{sup +} diffusivity. The diffusivity coefficient of without and with annealing particles were 6.8439910{sup ?10} and 8.5988810{sup ?10} cm{sup 2} s{sup ?1}, respectively.

  12. Multiphoton photoluminescence contrast in switched Mg:LiNbO{sub 3} and Mg:LiTaO{sub 3} single crystals

    SciTech Connect (OSTI)

    Reichenbach, P., E-mail: philipp.reichenbach@iapp.de; Kmpfe, T.; Thiessen, A.; Haumann, A.; Eng, L. M. [Institut fr Angewandte Photophysik, Technische Universitt Dresden, George-Bhr-Str. 1, 01069 Dresden (Germany); Woike, T. [Institut fr Strukturphysik, Technische Universitt Dresden, Zellescher Weg 16, 01069 Dresden (Germany)

    2014-09-22

    We observed a multiphoton luminescence contrast between virgin and single-switched domains in Mg-doped LiNbO{sub 3} (LNO) and LiTaO{sub 3} (LTO) single crystals with different doping levels of 07?mol. % and 08?mol. %, respectively. A luminescence contrast in the range of 3% was measured between as-grown and electrically inverted domain areas in Mg:LNO samples, while the contrast reaches values of up to 30% for the Mg:LTO case. Under annealing, an exponential decay of the domain contrast was observed. The activation energy of about 1?eV being determined for the decay allowed a comparison with reported activation energies of associated defects, clearly illustrating a strong connection between thermal contrast decay and the H{sup +} and Li{sup +}-ion mobility. Finally, performing similar experiments on oxidized samples undoubtedly demonstrated that the origin of the reported luminescence contrast is strongly connected with lithium ions.

  13. Concentration of Ca in blood of amateur runners using NAA

    SciTech Connect (OSTI)

    Kovacs, L.; Zamboni, C. B.; Metairon, S.; Nunes, L. A. S.; Lourenco, T. F.; Macedo, D. V.

    2013-05-06

    In this study the Ca levels were determined in amateur runners blood at LABEX (Laboratorio de Bioquimica do Exercicio - UNICAMP, Brazil), using Neutron Activation Analyses (NAA) technique. The range established at rest (162 - 410 mgL{sup -1}) when compared with control group (51 - 439 mgL{sup -1}) suggests that there is a dependency of these limits in the function of the adopted physical training.

  14. Ca(OH).sub.2 -treated ceramic microsphere

    DOE Patents [OSTI]

    Sugama, Toshifumi (Mastic Beach, NY)

    1989-01-01

    Geothermal wells with lost circulation problems are treated with a lightweight, high temperature (i.e. 350.degree. C.) cement slurry which incorporates pressure resistant hollow microspheres into the slurry wherein the spheres have been pretreated with an alkali compound such as Ca(OH).sub.2 for up to 20 hours and at 100.degree.-300.degree. C. Preferably, the alkali solution is a saturated aqueous solution and the treatment is for 10 hours.

  15. Ca(OH).sub.2 -treated ceramic microsphere

    DOE Patents [OSTI]

    Sugama, Toshifumi (Mastic Beach, NY)

    1990-01-01

    Geothermal wells with lost circulation problems are treated with a lightweight, high temperature (i.e. 350.degree. C.) cement slurry which incorporates pressure resistant hollow microspheres into the slurry wherein the spheres have been pretreated with an alkali compound such as Ca(OH).sub.2 for up to 20 hours and at 100.degree.-300.degree. C. Preferably, the alkali solution is a saturated aqueous solution and the treatment is for 10 hours.

  16. Ca(OH)[sub 2]-treated ceramic microsphere

    DOE Patents [OSTI]

    Sugama, Toshifumi.

    1990-06-26

    Geothermal wells with lost circulation problems are treated with a lightweight, high temperature (i.e. 350 C) cement slurry which incorporates pressure resistant hollow microspheres into the slurry wherein the spheres have been pretreated with an alkali compound such as Ca(OH)[sub 2] for up to 20 hours and at 100--300 C. Preferably, the alkali solution is a saturated aqueous solution and the treatment is for 10 hours. 2 figs.

  17. Ca(OH)[sub 2]-treated ceramic microsphere

    DOE Patents [OSTI]

    Sugama, Toshifumi.

    1989-04-18

    Geothermal wells with lost circulation problems are treated with a lightweight, high temperature (i.e. 350 C) cement slurry which incorporates pressure resistant hollow microspheres into the slurry wherein the spheres have been pretreated with an alkali compound such as Ca(OH)[sub 2] for up to 20 hours and at 100--300 C. Preferably, the alkali solution is a saturated aqueous solution and the treatment is for 10 hours. 2 figs.

  18. 11-03-2010 CA-B-10-0135

    National Nuclear Security Administration (NNSA)

    1-03-2010 CA-B-10-0135 Sandia National Laboratories/California proposes to establish a university partnership LDRD to support a fellowship student whose project, titled "High-Density Nanopore Array for Selective Biomolecular Transport," develop an understanding of the nanoscale phenomena of transporting molecules with electric fields through nanopores which act like selective gates. ✖ Sandia Site Office High-Density Nanopore Array for Selective Biomolecular Transport Univ of Illinois

  19. Ca2+-Doped CeBr3 Scintillating Materials

    SciTech Connect (OSTI)

    Guss, Paul; Foster, Michael E.; Wong, Bryan M.; Doty, F. Patrick; Shah, Kanai; Squillante, Michael R.; Shirwadkar, Urmila; Hawrami, Rastgo; Tower, Josh; Yuan, Ding

    2014-01-21

    Despite the outstanding scintillation performance characteristics of cerium tribromide (CeBr3) and cerium-activated lanthanum tribromide, their commercial availability and application are limited due to the difficulties of growing large, crack-free single crystals from these fragile materials. This investigation employed aliovalent doping to increase crystal strength while maintaining the optical properties of the crystal. One divalent dopant (Ca2+) was used as a dopant to strengthen CeBr3 without negatively impacting scintillation performance. Ingots containing nominal concentrations of 1.9% of the Ca2+ dopant were grown. Preliminary scintillation measurements are presented for this aliovalently doped scintillator. Ca2+-doped CeBr3 exhibited little or no change in the peak fluorescence emission for 371 nm optical excitation for CeBr3. The structural, electronic, and optical properties of CeBr3 crystals were studied using the density functional theory within the generalized gradient approximation. The calculated lattice parameters are in good agreement with the experimental data. The energy band structures and density of states were obtained. The optical properties of CeBr3, including the dielectric function, were calculated.

  20. DOE Zero Energy Ready Home Case Study: KB Home, San Marcos, CA...

    Energy Savers [EERE]

    San Marcos, CA, Production Home DOE Zero Energy Ready Home Case Study: KB Home, San Marcos, CA, ... pump for central air in sealed attic, solar water heating and 100% LED lighting. ...

  1. File:08-CA-b - CAISO Interconnection Request Process.pdf | Open...

    Open Energy Info (EERE)

    8-CA-b - CAISO Interconnection Request Process.pdf Jump to: navigation, search File File history File usage Metadata File:08-CA-b - CAISO Interconnection Request Process.pdf Size...

  2. File:08-CA-f - Permit to Construct.pdf | Open Energy Information

    Open Energy Info (EERE)

    8-CA-f - Permit to Construct.pdf Jump to: navigation, search File File history File usage Metadata File:08-CA-f - Permit to Construct.pdf Size of this preview: 463 599 pixels....

  3. X-Ray Spectroscopy of the Mn(4) Ca Cluster in the Water-Oxidation...

    Office of Scientific and Technical Information (OSTI)

    Ca Cluster in the Water-Oxidation Complex of Photosystem II Citation Details In-Document Search Title: X-Ray Spectroscopy of the Mn(4) Ca Cluster in the Water-Oxidation Complex ...

  4. File:07-CA-e - BLM-CEC Joint Siting Process.pdf | Open Energy...

    Open Energy Info (EERE)

    07-CA-e - BLM-CEC Joint Siting Process.pdf Jump to: navigation, search File File history File usage Metadata File:07-CA-e - BLM-CEC Joint Siting Process.pdf Size of this preview:...

  5. File:08-CA-d - CPCN for Transmission Projects (2).pdf | Open...

    Open Energy Info (EERE)

    8-CA-d - CPCN for Transmission Projects (2).pdf Jump to: navigation, search File File history File usage Metadata File:08-CA-d - CPCN for Transmission Projects (2).pdf Size of this...

  6. Temperature Dependence of Aliovalent-vanadium Doping in LiFePO4 Cathodes

    SciTech Connect (OSTI)

    Harrison, Katharine L; Bridges, Craig A; Paranthaman, Mariappan Parans; Idrobo Tapia, Juan C; Manthiram, Arumugam; Goodenough, J. B.; Segre, C; Katsoudas, John; Maroni, V. A.

    2013-01-01

    Vanadium-doped olivine LiFePO4 cathode materials have been synthesized by a novel low-temperature microwave-assisted solvothermal (MW-ST) method at 300 oC. Based on chemical and powder neutron/X-ray diffraction analysis, the compositions of the synthesized materials were found to be LiFe1-3x/2Vx x/2PO4 (0 x 0.2) with the presence of a small number of lithium vacancies charge-compensated by V4+, not Fe3+, leading to an average oxidation state of ~ 3.2+ for vanadium. Heating the pristine 15 % V-doped sample in inert or reducing atmospheres led to a loss of vanadium from the olivine lattice with the concomitant formation of a Li3V2(PO4)3 impurity phase; after phase segregation, a partially V-doped olivine phase remained. For comparison, V-doped samples were also synthesized by conventional ball milling and heating, but only ~ 10 % V could be accommodated in the olivine lattice in agreement with previous studies. The higher degree of doping realized with the MW-ST samples demonstrates the temperature dependence of the aliovalent-vanadium doping in LiFePO4.

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

    SciTech Connect (OSTI)

    Kam, Kinson; Doeff, Marca M.

    2010-12-01

    Improved electrochemical characteristics are observed for Li[Ni1/3Co1/3-yMyMn1/3]O2 cathode materials when M=Ti and y<0.07, compared to the baseline material, with up to 15percent increased discharge capacity.

  8. Redox probing study of the potential dependence of charge transport through Li2O2

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

    Knudsen, Kristian B.; Luntz, Alan C.; Jensen, Søren H.; Vegge, Tejs; Hjelm, Johan

    2015-11-20

    In the field of energy storage devices the pursuit for cheap, high energy density, reliable secondary batteries is at the top of the agenda. The Li–O2 battery is one of the possible technologies that, in theory, should be able to close the gap, which exists between the present state-of-the-art Li-ion technologies and the demand placed on batteries by technologies such as electrical vehicles. Here we present a redox probing study of the charge transfer across the main deposition product lithium peroxide, Li2O2, in the Li–O2 battery using outer-sphere redox shuttles. The change in heterogeneous electron transfer exchange rate as amore » function of the potential and the Li2O2 layer thickness (~depth-of-discharge) was determined using electrochemical impedance spectroscopy. In addition, the attenuation of the electron transfer exchange rate with film thickness is dependent on the probing potential, providing evidence that hole transport is the dominant process for charge transfer through Li2O2 and showing that the origin of the sudden death observed upon discharge is due to charge transport limitations.« less

  9. Method for improving voltage regulation of batteries, particularly Li/FeS/sub 2/ thermal batteries

    DOE Patents [OSTI]

    Godshall, N.A.

    1986-06-10

    Batteries are improved, especially with respect to voltage regulation properties, by employing as anode and cathode compositions, those which fall in a thermodynamically invariant region of the metallurgical phase diagram of the combination of the constituent components. The invention is especially useful in the Li/FeS/sub 2/ system.

  10. REVERSIBLE HYDROGEN STORAGE IN A LiBH{sub 4}-C{sub 60} NANOCOMPOSITE

    SciTech Connect (OSTI)

    Teprovich, J.; Zidan, R.; Peters, B.; Wheeler, J.

    2013-08-06

    Reversible hydrogen storage in a LiBH{sub 4}:C{sub 60} nanocomposite (70:30 wt. %) synthesized by solvent-assisted mixing has been demonstrated. During the solvent-assisted mixing and nanocomposite formation, a chemical reaction occurs in which the C{sub 60} cages are significantly modified by polymerization as well as by hydrogenation (fullerane formation) in the presence of LiBH{sub 4}. We have determined that two distinct hydrogen desorption events are observed upon rehydrogenation of the material, which are attributed to the reversible formation of a fullerane (C{sub 60}H{sub x}) as well as a LiBH4 species. This system is unique in that the carbon species (C{sub 60}) actively participates in the hydrogen storage process which differs from the common practice of melt infiltration of high surface area carbon materials with LiBH{sub 4} (nanoconfinment effect). This nanocomposite demonstrated good reversible hydrogen storage properties as well as the ability to absorb hydrogen under mild conditions (pressures as low as 10 bar H{sub 2} or temperatures as low as 150?C). The nanocomposite was characterized by TGA-RGA, DSC, XRD, LDI-TOF-MS, FTIR, 1H NMR, and APPI MS.

  11. Evaluation of Li2MnSiO4 Cathode | Department of Energy

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

    11 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon es018_belharouak_2011_p.pdf More Documents & Publications Search for High Energy Density Cathode Materials Evaluation of Li2MnSiO4 Cathode Design of Safer High-Energy Density Materials for Lithium-Ion Cells

  12. Evaluation of Li2MnSiO4 Cathode | Department of Energy

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

    09 DOE Hydrogen Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting, May 18-22, 2009 -- Washington D.C. PDF icon esp_18_belharouak.pdf More Documents & Publications Search for High Energy Density Cathode Materials Evaluation of Li2MnSiO4 Cathode Vehicle Technologies Office Merit Review 2014: High-Capacity Polyanion Cathodes

  13. Electrolytes and Separators for High Voltage Li Ion Cells | Department of

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

    Energy 1 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon es100_angell_2011_o.pdf More Documents & Publications Electrolytes and Separators for High Voltage Li Ion Cells High Voltage Electrolyte for Lithium Batteries Linking Ion Solvation and Lithium Battery Electrolyte Properties

  14. Origin State>> CA CA ID ID ID IL KY MD MO NM NM NY NY OH SC

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

    MO NM NM NY NY OH SC TN TN TN, WA, CA TN TN TN TN Total Shipments by Route Lawrence Livermore National Laboratory General Atomics Batelle Energy Alliance Idaho National Laboratory Advanced Mixed Waste Treatment Project Argonne National Laboratory Paducah Gaseous Diffusion Plant Aberdeen Proving Grounds National Security Technologies Sandia National Laboratory Los Alamos National Laboratory Brookhaven National Laboratory CH2M Hill B&W West Valley, LLC Portsmouth Gaseous Diffusion Plant

  15. Origin State>> CA CA ID ID ID IL KY MD NM NM NV NY NY OH TN

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

    NM NM NV NY NY OH TN TN TN, WA, CA TN TN TN TN TX Total Shipments by Route Lawrence Livermore National Laboratory General Atomics Advanced Mixed Waste Treatment Project Batelle Energy Alliance Idaho National Laboratory Argonne National Laboratory Paducah Gaseous Diffusion Plant Aberdeen Proving Ground Los Alamos National Laboratory Sandia National Laboratory National Security Technologies Brookhaven National Laboratory West Valley Environmental Services Portsmouth Gaseous Diffusion Plant

  16. Origin State>> CA CA ID ID IL KY NJ NM NY NY NV OH OH OH SC

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

    Mix Wastew Treatment Project Argonne National Laboratory Paducah Gaseous Diffusion Plant Princeton Plasma Physics Laboratory Sandia National Laboratory Brookhaven National Laboratory West Valley Demonstration Project National Security Technologies, Inc. Mound Closure Project Portsmouth Gaseous Diffusion Plant Fernald Closure Project Savannah River Site BWXT Y-12 Plant Duratek Nuclear Fuels UT-Battelle Bechtel Jacobs Permafix M&EC EnergX (Foster Wheeler) Pantex Plant SOUTHERN I-15, CA-127,

  17. Origin State>> CA ID ID ID IL KY NV NY NY OH TN TN TN, WA, CA

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

    NV NY NY OH TN TN TN, WA, CA TN TN TN TN TX Total Shipments by Route Lawrence Livermore National Laboratory Advanced Mixed Waste Treatment Project Batelle Energy Alliance Idaho National Laboratory Argonne National Laboratory Paducah Gaseous Diffusion Plant National Security Technologies Brookhaven National Laboratory West Valley Environmental Services Portsmouth Gaseous Diffusion Plant Duratek/Energy Solutions Babcox & Wilcox Technical Services Y-12 Plant Materials & Energy Corporation

  18. Origin State>> CA ID ID ID IL MD NM NM NY OH TN TN TN, WA, CA

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

    NY OH TN TN TN, WA, CA TN TN TN TX Total Shipments by Route Lawrence Livermore National Laboratory Batelle Energy Alliance Idaho National Laboratory Advanced Mixed Waste Treatment Project Argonne National Laboratory Aberdeen Proving Ground Sandia National Laboratory Los Alamos National Laboratory Brookhaven National Laboratory Portsmouth Gaseous Diffusion Plant Duratek/Energy Solutions Babcox & Wilcox Technical Services Y-12 Plant Materials & Energy Corporation (M&EC) Perma-Fix

  19. Origin State>> CA ID ID ID IL NM NM OH TN TN TN, WA, CA TN TN

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

    NM NM OH TN TN TN, WA, CA TN TN TN TN TX Total Shipments by Route Lawrence Livermore National Laboratory Batelle Energy Alliance Idaho National Laboratory Advanced Mixed Waste Treatment Project Argonne National Laboratory Sandia National Laboratory Los Alamos National Laboratory Portsmouth Gaseous Diffusion Plant Duratek/Energy Solutions Babcox & Wilcox Technical Services Y-12 Plant Materials & Energy Corporation (M&EC) Perma-Fix Nuclear Fuels Services Wastren Advantage, Inc.

  20. Assessment of LED Technology in Ornamental Post-Top Luminaires. Sacramento, CA

    SciTech Connect (OSTI)

    Tuenge, J. R.; Bryan, M. M.; Bisbee, D. A.

    2011-12-01

    GATEWAY program report on a demonstration of LED ornamental post-top luminaires in a residential part of Sacramento, CA.

  1. EIS-0455: Genesis Solar Energy Project in Riverside County, CA | Department

    Office of Environmental Management (EM)

    of Energy 5: Genesis Solar Energy Project in Riverside County, CA EIS-0455: Genesis Solar Energy Project in Riverside County, CA December 17, 2010 EIS-0455: Notice of Adoption of an Environmental Impact Statement Genesis Solar Energy Project, Riverside County, CA August 27, 2010 EIS-0455: Final Environmental Impact Statement Genesis Solar Energy Project, Riverside County, CA September 1, 2011 EIS-0455: Record of Decision Genesis Solar Energy Project, Riverside County, California

  2. Interfacial reaction dependent performance of hollow carbon nanosphere - sulfur composite as a cathode for Li-S battery

    SciTech Connect (OSTI)

    Zheng, Jianming; Yan, Pengfei; Gu, Meng; Wagner, Michael J.; Hays, Kevin A.; Chen, Junzheng; Li, Xiaohong S.; Wang, Chong M.; Zhang, Ji -Guang; Liu, Jun; Xiao, Jie

    2015-05-26

    Lithium-sulfur (Li-S) battery is a promising energy storage system due to its high energy density, cost effectiveness and environmental friendliness of sulfur. However, there are still a number of challenges, such as low Coulombic efficiency and poor long-term cycling stability, impeding the commercialization of Li-S battery. The electrochemical performance of Li-S battery is closely related with the interfacial reactions occurring between hosting substrate and active sulfur species which are poorly conducting at fully oxidized and reduced states. Here, we correlate the relationship between the performance and interfacial reactions in the Li-S battery system, using a hollow carbon nanosphere (HCNS) with highly graphitic character as hosting substrate for sulfur. With an appropriate amount of sulfur loading, HCNS/S composite exhibits excellent electrochemical performance because of the fast interfacial reactions between HCNS and the polysulfides. However, further increase of sulfur loading leads to increased formation of highly resistive insoluble reaction products (Li2S2/Li2S) which limits the reversibility of the interfacial reactions and results in poor electrochemical performance. In conclusion, these findings demonstrate the importance of the interfacial reaction reversibility in the whole electrode system on achieving high capacity and long cycle life of sulfur cathode for Li-S batteries.

  3. Interfacial reaction dependent performance of hollow carbon nanosphere - sulfur composite as a cathode for Li-S battery

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

    Zheng, Jianming; Yan, Pengfei; Gu, Meng; Wagner, Michael J.; Hays, Kevin A.; Chen, Junzheng; Li, Xiaohong S.; Wang, Chong M.; Zhang, Ji -Guang; Liu, Jun; et al

    2015-05-26

    Lithium-sulfur (Li-S) battery is a promising energy storage system due to its high energy density, cost effectiveness and environmental friendliness of sulfur. However, there are still a number of challenges, such as low Coulombic efficiency and poor long-term cycling stability, impeding the commercialization of Li-S battery. The electrochemical performance of Li-S battery is closely related with the interfacial reactions occurring between hosting substrate and active sulfur species which are poorly conducting at fully oxidized and reduced states. Here, we correlate the relationship between the performance and interfacial reactions in the Li-S battery system, using a hollow carbon nanosphere (HCNS) withmore » highly graphitic character as hosting substrate for sulfur. With an appropriate amount of sulfur loading, HCNS/S composite exhibits excellent electrochemical performance because of the fast interfacial reactions between HCNS and the polysulfides. However, further increase of sulfur loading leads to increased formation of highly resistive insoluble reaction products (Li2S2/Li2S) which limits the reversibility of the interfacial reactions and results in poor electrochemical performance. In conclusion, these findings demonstrate the importance of the interfacial reaction reversibility in the whole electrode system on achieving high capacity and long cycle life of sulfur cathode for Li-S batteries.« less

  4. Electrolyte Solvation and Ionic Association. V. Acetonitrile-Lithium Bis(fluorosulfonyl)imide (LiFSI) Mixtures

    SciTech Connect (OSTI)

    Han, Sang D.; Borodin, Oleg; Seo, D. M.; Zhou, Zhi B.; Henderson, Wesley A.

    2014-09-30

    Electrolytes with the salt lithium bis(fluorosulfonyl)imide (LiFSI) have been evaluated relative to comparable electrolytes with other lithium salts. Acetonitrile (AN) has been used as a model electrolyte solvent. The information obtained from the thermal phase behavior, solvation/ionic association interactions, quantum chemical (QC) calculations and molecular dynamics (MD) simulations (with an APPLE&P many-body polarizable force field for the LiFSI salt) of the (AN)n-LiFSI mixtures provides detailed insight into the coordination interactions of the FSI- anions and the wide variability noted in the electrolyte transport property (i.e., viscosity and ionic conductivity).

  5. Nanoscale imaging of fundamental Li battery chemistry: solid-electrolyte interphase formation and preferential growth of lithium metal nanoclusters

    SciTech Connect (OSTI)

    Sacci, Robert L; Black, Jennifer M; Wisinger, Nina; Dudney, Nancy J.; More, Karren Leslie; Unocic, Raymond R

    2015-01-01

    The performance characteristics of Li-ion batteries are intrinsically linked to evolving nanoscale interfacial electrochemical reactions. To probe the mechanisms of solid electrolyte interphase formation and Li electrodeposition from a standard battery electrolyte, we use in situ electrochemical scanning transmission electron microscopy for controlled potential sweep-hold electrochemical measurements with simultaneous BF and ADF STEM image acquisition. Through a combined quantitative electrochemical measurement and quantitative STEM imaging approach, based upon electron scattering theory, we show that chemically sensitive ADF STEM imaging can be used to estimate the density of evolving SEI constituents and distinguish contrast mechanisms of Li-bearing components in the liquid cell.

  6. Dielectric properties of a polar ZnSnO{sub 3} with LiNbO{sub 3}-type

    Office of Scientific and Technical Information (OSTI)

    structure (Journal Article) | SciTech Connect Dielectric properties of a polar ZnSnO{sub 3} with LiNbO{sub 3}-type structure Citation Details In-Document Search Title: Dielectric properties of a polar ZnSnO{sub 3} with LiNbO{sub 3}-type structure The dielectric properties of a polar LiNbO{sub 3}-type ZnSnO{sub 3} synthesized under high-pressure have been investigated with respect to the dielectric permittivity in the relative low frequency range of 10 kHz to 1 MHz and the SHG response at an

  7. CA CAIOlf Mr. Andrew Wallo. III, NE-23

    Office of Legacy Management (LM)

    kire 7900. 955 L*E,,fa,u PLUG S. W.. Washin@ on. D.C. 20024-2174, Tekphme: (202) 488-6000 7117-03.87.cdy.43 23 September 1987 CA CAIOlf Mr. Andrew Wallo. III, NE-23 Division of Facility & Site Decommissioning Projects U.S. Department of Energy Germantown, Maryland 20545 CT.05 FL .0-o/ lti.Ob id.Or Dear Mr. Wallo: In/. O-01 flA.05 ELIMINATION RECOMMENDATION -- COLLEGES AND UNIVERSITIES Mbj.o-03 I4 v.o+ The attached elimination recommendation was prepared in accordance ML.o= with your

  8. CA M r. Andrew Wallo, III, NE-23

    Office of Legacy Management (LM)

    i900,9SS L%nfam Phm, S. W.. Washington. D.C. 20024.2174, Tlkphme: (20.7) 4S.S-M)o 7117-03.87.cdy.43 23 September 1987 CA M r. Andrew Wallo, III, NE-23 Division of Facility & Site Decommissioning Projects U.S. Department of Energy Germantown, Maryland 20545 Dear M r. Wallo: ELIMINATION RECOMMENDATION -- COLLEGES AND UNIVERSITIES I - The attached elimination recommendation was prepared in accordance M1.oS with your suggestion during our meeting on 22 September. The recommendation nO.O-02

  9. CA M r. Andrew Wallo, III. NE-23

    Office of Legacy Management (LM)

    i5W 95.5 L' E&nt plom. S. W.:. Washingr on. D.C. ZOOX2i74, Tekphm: (202) 488-6OGb 7II7-03.87.cdy.43 23 September 1987. Ii CA M r. Andrew Wallo, III. NE-23 Division of Facility & Site Decommissioning Projects U.S. Department of Energy Germantown, Maryland 20545 Dear M r. Wallo: ELIMINATION RECOMMENDATION -- COLLEGES AND UNIVERSITIES pqq.0' 05 PI ;p.03- The attached elimination recommendation was prepared in accordance ,I ML.05 with your suggestion during our meeting on 22 September. The

  10. High Rate and High Capacity Li-Ion Electrodes for Vehicular Applications

    SciTech Connect (OSTI)

    Dillon, A. C.

    2012-01-01

    Significant advances in both energy density and rate capability for Li-ion batteries are necessary for implementation in electric vehicles. We have employed two different methods to improve the rate capability of high capacity electrodes. For example, we previously demonstrated that thin film high volume expansion MoO{sub 3} nanoparticle electrodes ({approx}2 {micro}m thick) have a stable capacity of {approx}630 mAh/g, at C/2 (charge/dicharge in 2 hours). By fabricating thicker conventional electrodes, an improved reversible capacity of {approx}1000 mAh/g is achieved, but the rate capability decreases. To achieve high-rate capability, we applied a thin Al{sub 2}O{sub 3} atomic layer deposition coating to enable the high volume expansion and prevent mechanical degradation. Also, we recently reported that a thin ALD Al{sub 2}O{sub 3} coating can enable natural graphite (NG) electrodes to exhibit remarkably durable cycling at 50 C. Additionally, Al{sub 2}O{sub 3} ALD films with a thickness of 2 to 4 {angstrom} have been shown to allow LiCoO{sub 2} to exhibit 89% capacity retention after 120 charge-discharge cycles performed up to 4.5 V vs. Li/Li{sup +}. Capacity fade at this high voltage is generally caused by oxidative decomposition of the electrolyte or cobalt dissolution. We have recently fabricated full cells of NG and LiCoO{sub 2} and coated both electrodes, one or the other electrode as well as neither electrode. In creating these full cells, we observed some surprising results that lead us to obtain a greater understanding of the ALD coatings. In a different approach we have employed carbon single-wall nanotubes (SWNTs) to synthesize binder-free, high-rate capability electrodes, with 95 wt.% active materials. In one case, Fe{sub 3}O{sub 4} nanorods are employed as the active storage anode material. Recently, we have also employed this method to demonstrate improved conductivity and highly improved rate capability for a LiNi{sub 0.4}Mn{sub 0.4}Co{sub 0.2}O{sub 2} cathode material. Raman spectroscopy was employed to understand how the SWNTs function as a highly flexible conductive additive.

  11. Prediction of {sup 2}D Rydberg energy levels of {sup 6}Li and {sup 7}Li based on very accurate quantum mechanical calculations performed with explicitly correlated Gaussian functions

    SciTech Connect (OSTI)

    Bubin, Sergiy; Sharkey, Keeper L.; Adamowicz, Ludwik

    2013-04-28

    Very accurate variational nonrelativistic finite-nuclear-mass calculations employing all-electron explicitly correlated Gaussian basis functions are carried out for six Rydberg {sup 2}D states (1s{sup 2}nd, n= 6, Horizontal-Ellipsis , 11) of the {sup 7}Li and {sup 6}Li isotopes. The exponential parameters of the Gaussian functions are optimized using the variational method with the aid of the analytical energy gradient determined with respect to these parameters. The experimental results for the lower states (n= 3, Horizontal-Ellipsis , 6) and the calculated results for the higher states (n= 7, Horizontal-Ellipsis , 11) fitted with quantum-defect-like formulas are used to predict the energies of {sup 2}D 1s{sup 2}nd states for {sup 7}Li and {sup 6}Li with n up to 30.

  12. A limited role for carbonic anhydrase in C4 photosynthesis as revealed by a ca1ca2 double mutant in maize.

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

    Studer, Anthony J.; Gandin, Anthony; Kolbe, Allison R.; Wang, Lin; Cousins, Asaph B.; Brutnell, Thomas P.

    2014-04-04

    Carbonic anhydrase (CA) catalyzes the first biochemical step of the carbon concentrating mechanism of C4 plants, and in C4 monocots, it has been suggested that CA activity is near limiting for photosynthesis. Here, we test this hypothesis through the characterization of transposon induced mutant alleles of Ca1 and Ca2 in Zea mays. In addition, these two isoforms account for more than 85% of the CA transcript pool. A significant change in isotopic discrimination is observed in mutant plants, which have as little as 3% of wild-type CA activity, but surprisingly, photosynthesis is not reduced under current or elevated pCO2. However,more » growth and rates of photosynthesis under sub-ambient pCO2 are significantly impaired in the mutants. These findings suggest, that while CA is not limiting for C4 photosynthesis in Z. mays at current pCO2, it likely maintains high rates of photosynthesis when CO2 availability is reduced. Current atmospheric CO2 levels now exceed 400 ppm (~40.53 Pa) and contrast the low CO2 partial pressure (pCO2) conditions under which C4 plants expanded their range ~10 million years ago when the global atmospheric CO2 was below 300 ppm (~30.40 Pa). Thus, as CO2 levels continue to rise, selective pressures for high levels of CA may be limited to arid climates where stomatal closure reduces CO2 availability to the leaf.« less

  13. Neutron scattering study on cathode LiMn{sub 2}O{sub 4} and solid electrolyte 5(Li{sub 2}O)(P{sub 2}O{sub 5})

    SciTech Connect (OSTI)

    Kartini, E. Putra, Teguh P. Jahya, A. K. Insani, A.; Adams, S.

    2014-09-30

    Neutron scattering is very important technique in order to investigate the energy storage materials such as lithium-ion battery. The unique advantages, neutron can see the light atoms such as Hydrogen, Lithium, and Oxygen, where those elements are negligible by other corresponding X-ray method. On the other hand, the energy storage materials, such as lithium ion battery is very important for the application in the electric vehicles, electronic devices or home appliances. The battery contains electrodes (anode and cathode), and the electrolyte materials. There are many challenging to improve the existing lithium ion battery materials, in order to increase their life time, cyclic ability and also its stability. One of the most scientific challenging is to investigate the crystal structure of both electrode and electrolyte, such as cathodes LiCoO{sub 2}, LiMn{sub 2}O{sub 4} and LiFePO{sub 4}, and solid electrolyte Li{sub 3}PO{sub 4}. Since all those battery materials contain Lithium ions and Oxygen, the used of neutron scattering techniques to study their structure and related properties are very important and indispensable. This article will review some works of investigating electrodes and electrolytes, LiMn{sub 2}O{sub 4} and 5(Li{sub 2}O)(P{sub 2}O{sub 5}), by using a high resolution powder diffraction (HRPD) at the multipurpose research reactor, RSG-Sywabessy of the National Nuclear Energy Agency (BATAN), Indonesia.

  14. Vehicle Technologies Office Merit Review 2015: Real-time Metrology for Li-ion Battery R&D and Manufacturing

    Broader source: Energy.gov [DOE]

    Presentation given by Applied Spectra at 2015 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Office Annual Merit Review and Peer Evaluation Meeting about real-time metrology for Li...

  15. Effect of entropy of lithium intercalation in cathodes and anodes on Li-ion battery thermal management

    SciTech Connect (OSTI)

    Viswanathan, Vilayanur V; Choi, Daiwon; Wang, Donghai; Xu, Wu; Towne, Silas A; Williford, Ralph E; Zhang, Jiguang; Liu, Jun; Yang, Zhenguo

    2010-06-01

    The entropy changes (ΔS) in various cathode and anode materials, as well as complete Li-ion batteries, were measured using an electrochemical thermodynamic measurement system (ETMS). LiCoO2 has a much larger entropy change than electrodes based on LiNixCoyMnzO2 and LiFePO4, while lithium titanate based anode has lower entropy change compared to graphite anodes. Reversible heat generation rate was found to be a significant portion of the total heat generation rate. The appropriate combinations of cathode and anode were investigated to minimize reversible heat.

  16. Astrophysical S factor for the radiative-capture reaction p{sup 6}Li {yields} {sup 7}Be{gamma}

    SciTech Connect (OSTI)

    Dubovichenko, S. B.; Burtebaev, N. Zazulin, D. M.; Kerimkulov, Zh. K.; Amar, A. S. A.

    2011-07-15

    A new measurement of differential cross sections for elastic p{sup 6}Li scattering in the energy range 0.35-1.2 MeV was performed. A partial-wave analysis of the data obtained in this way was carried out, and potentials simulating the p{sup 6}Li interaction were constructed. Various experiments devoted to studying elastic p{sup 6}Li scattering over the broad energy range of 0.5-50 MeV were analyzed on the basis of the optical model. By using the potentials obtained from the partial-wave analysis, the possibility of describing the astrophysical S factor for radiative proton capture on {sup 6}Li at low energies was considered within the potential cluster model involving forbidden states.

  17. Vehicle Technologies Office Merit Review 2014: Advanced High Energy Li-Ion Cell for PHEV and EV Applications

    Broader source: Energy.gov [DOE]

    Presentation given by 3M at 2014 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Office Annual Merit Review and Peer Evaluation Meeting about advanced high energy Li-ion cell for PHEV...

  18. Vehicle Technologies Office Merit Review 2015: Efficient Rechargeable Li/O2 Batteries Utilizing Stable Inorganic Molten Salt Electrolytes

    Broader source: Energy.gov [DOE]

    Presentation given by Liox at 2015 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Office Annual Merit Review and Peer Evaluation Meeting about efficient rechargeable Li/O2 batteries...

  19. Thermal neutron detection using a silicon pad detector and {sup 6}LiF removable converters

    SciTech Connect (OSTI)

    Barbagallo, Massimo; Cosentino, Luigi; Marchetta, Carmelo; Pappalardo, Alfio; Scire, Carlotta; Scire, Sergio; Schillaci, Maria; Vecchio, Gianfranco; Finocchiaro, Paolo; Forcina, Vittorio; Peerani, Paolo; Vaccaro, Stefano

    2013-03-15

    A semiconductor detector coupled with a neutron converter is a good candidate for neutron detection, especially for its compactness and reliability if compared with other devices, such as {sup 3}He tubes, even though its intrinsic efficiency is rather lower. In this paper we show a neutron detector design consisting of a 3 cm Multiplication-Sign 3 cm silicon pad detector coupled with one or two external {sup 6}LiF layers, enriched in {sup 6}Li at 95%, placed in contact with the Si active surfaces. This prototype, first characterized and tested at INFN Laboratori Nazionali del Sud and then at JRC Ispra, was successfully shown to detect thermal neutrons with the expected efficiency and an outstanding gamma rejection capability.

  20. Deuteron scattering on {sup 6}Li at an energy of 25 MeV

    SciTech Connect (OSTI)

    Burtebayev, N.; Artemov, S. V.; Duisebayev, B. A.; Kerimkulov, Zh. K.; Kuranov, S. B.; Sakuta, S. B.

    2010-05-15

    At an energy of 25 MeV and in the angular range 7{sup o}-175{sup o} in the laboratory frame, angular distributions were measured for elastic deuteron scattering on {sup 6}Li nuclei and for the respective inelastic-scattering processes accompanied by the transitions to the ground state (1+) of the {sup 6}Li nucleus and to its excited state at E{sub x} = 2.186 MeV (J{sup {pi}} = 3{sup +}). The resulting data were analyzed on the basis of the optical model of the nucleus and the coupled-reaction-channel method with allowance for the mechanism of alpha-particle-cluster exchange. It is shown that only upon including, in the analysis, channel coupling and the exchange mechanism can the experimental cross sections for elastic and inelastic scattering be reproduced over the entire range of angles.

  1. The High-Resolution Lightweight Telescope for the EUV (HiLiTE)

    SciTech Connect (OSTI)

    Martinez-Galarce, D S; Boerner, P; Soufli, R; De Pontieu, B; Katz, N; Title, A; Gullikson, E M; Robinson, J C; Baker, S L

    2008-06-02

    The High-resolution Lightweight Telescope for the EUV (HiLiTE) is a Cassegrain telescope that will be made entirely of Silicon Carbide (SiC), optical substrates and metering structure alike. Using multilayer coatings, this instrument will be tuned to operate at the 465 {angstrom} Ne VII emission line, formed in solar transition region plasma at {approx}500,000 K. HiLiTE will have an aperture of 30 cm, angular resolution of {approx}0.2 arc seconds and operate at a cadence of {approx}5 seconds or less, having a mass that is about 1/4 that of one of the 20 cm aperture telescopes on the Atmospheric Imaging Assembly (AIA) instrument aboard NASA's Solar Dynamics Observatory (SDO). This new instrument technology thus serves as a path finder to a post-AIA, Explorer-class missions.

  2. NANOSTRUCTURED METAL OXIDES FOR ANODES OF LI-ION RECHARGEABLE BATTERIES

    SciTech Connect (OSTI)

    Au, M.

    2009-12-04

    The aligned nanorods of Co{sub 3}O{sub 4} and nanoporous hollow spheres (NHS) of SnO{sub 2} and Mn{sub 2}O{sub 3} were investigated as the anodes for Li-ion rechargeable batteries. The Co{sub 3}O{sub 4} nanorods demonstrated 1433 mAh/g reversible capacity. The NHS of SnO{sub 2} and Mn{sub 2}O{sub 3} delivered 400 mAh/g and 250 mAh/g capacities respectively in multiple galvonastatic discharge-charge cycles. It was found that high capacity of NHS of metal oxides is sustainable attributed to their unique structure that maintains material integrity during cycling. The nanostructured metal oxides exhibit great potential as the new anode materials for Li-ion rechargeable batteries with high energy density, low cost and inherent safety.

  3. Synthesis of rock-salt type lithium borohydride and its peculiar Li{sup +} ion conduction properties

    SciTech Connect (OSTI)

    Miyazaki, R.; Maekawa, H.; Takamura, H.

    2014-05-01

    The high energy density and excellent cycle performance of lithium ion batteries makes them superior to all other secondary batteries and explains why they are widely used in portable devices. However, because organic liquid electrolytes have a higher operating voltage than aqueous solution, they are used in lithium ion batteries. This comes with the risk of fire due to their flammability. Solid electrolytes are being investigated to find an alternative to organic liquid. However, the nature of the solid-solid point contact at the interface between the electrolyte and electrode or between the electrolyte grains is such that high power density has proven difficult to attain. We develop a new method for the fabrication of a solid electrolyte using LiBH{sub 4,} known for its super Li{sup +} ion conduction without any grain boundary contribution. The modifications to the conduction pathway achieved by stabilizing the high pressure form of this material provided a new structure with some LiBH{sub 4}, more suitable to the high rate condition. We synthesized the H.P. form of LiBH{sub 4} under ambient pressure by doping LiBH{sub 4} with the KI lattice by sintering. The formation of a KI - LiBH{sub 4} solid solution was confirmed both macroscopically and microscopically. The obtained sample was shown to be a pure Li{sup +} conductor despite its small Li{sup +} content. This conduction mechanism, where the light doping cation played a major role in ion conduction, was termed the Parasitic Conduction Mechanism. This mechanism made it possible to synthesize a new ion conductor and is expected to have enormous potential in the search for new battery materials.

  4. Preliminary Analysis on Linac Oscillation Data LI05-19 and Wake Field Energy Loss in FACET Commissioning 2012

    SciTech Connect (OSTI)

    Sun, Yipeng; /SLAC

    2012-07-23

    In this note, preliminary analysis on linac ocsillation data in FACET linac LI05-09 plus LI11-19 is presented. Several quadrupoles are identified to possibly have different strength, compared with their designed strength in the MAD optics model. The beam energy loss due to longitudinal wake fields in the S-band linac is also analytically calculated, also by LITRACK numerical simulations.

  5. Theoretical exploration of various lithium peroxide crystal structures in a Li-air battery

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

    Lau, Kah; Qiu, Dantong; Luo, Xiangyi; Greeley, Jeffrey; Curtiss, Larry; Lu, Jun; Amine, Khalil

    2015-01-14

    We describe a series of metastable Li₂O₂ crystal structures involving different orientations and displacements of the O₂²⁻ peroxy ions based on the known Li₂O₂ crystal structure. Within the vicinity of the chemical potential ΔG ~ 0.20 eV/Li from the thermodynamic ground state of the Li₂O₂ crystal structure (i.e., Föppl structure), all of these newly found metastable Li₂O₂ crystal structures are found to be insulating and high-k materials, and they have a common unique signature of an O₂²⁻ O-O vibration mode (ω ~ 799–865 cm⁻¹), which is in the range of that commonly observed in Li-air battery experiments, regardless of themore » random O₂²⁻ orientations and the symmetry in the crystal lattice. From XRD patterns analysis, the commercially available Li₂O₂ powder is confirmed to be the thermodynamic ground state Föppl-like structure. However, for Li₂O₂ compounds that are grown electrochemically under the environment of Li-O₂ cells, we found that the XRD patterns alone are not sufficient for structural identification of these metastable Li₂O₂ crystalline phases due to the poor crystallinity of the sample. In addition, the commonly known Raman signal of O₂²⁻ vibration mode is also found to be insufficient to validate the possible existence of these newly predicted Li₂O₂ crystal structures, as all of them similarly share the similar O₂²⁻ vibration mode. However considering that the discharge voltage in most Li-O₂ cells are typically several tenths of an eV below the thermodynamic equilibrium for the formation of ground state Föppl structure, the formation of these metastable Li₂O₂ crystal structures appears to be thermodynamically feasible.« less

  6. Mechanical and electrochemical response of a LiCoO2 cathode using reconstructed microstructures

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

    Mendoza, Hector; Roberts, Scott Alan; Brunini, Victor E.; Grillet, Anne M.

    2016-01-02

    As LiCoO2 cathodes are charged, delithiation of the LiCoO2 active material leads to an increase in the lattice spacing, causing swelling of the particles. When these particles are packed into a bicontinuous, percolated network, as is the case in a battery electrode, this swelling leads to the generation of significant mechanical stress. In this study we performed coupled electrochemical-mechanical simulations of the charging of a LiCoO2 cathode in order to elucidate the mechanisms of stress generation and the effect of charge rate and microstructure on these stresses. Energy dispersive spectroscopy combined with scanning electron microscopy imaging was used to createmore » 3D reconstructions of a LiCoO2 cathode, and the Conformal Decomposition Finite Element Method is used to automatically generate computational meshes on this reconstructed microstructure. Replacement of the ideal solution Fickian diffusion model, typically used in battery simulations, with a more general non-ideal solution model shows substantially smaller gradients of lithium within particles than is typically observed in the literature. Using this more general model, lithium gradients only appear at states of charge where the open-circuit voltage is relatively constant. While lithium gradients do affect the mechanical stress state in the particles, the maximum stresses are always found in the fully-charged state and are strongly affected by the local details of the microstructure and particle-to-particle contacts. These coupled electrochemical-mechanical simulations begin to yield insight into the partitioning of volume change between reducing pore space and macroscopically swelling the electrode. Lastly, preliminary studies that include the presence of the polymeric binder suggest that it can greatly impact stress generation and that it is an important area for future research.« less

  7. HASL-258 IN SITU Ge(Li) AND Nal(T1) GAMMA-RAY SPECTROMETRY

    Office of Scientific and Technical Information (OSTI)

    HASL-258 IN SITU Ge(Li) AND Nal(T1) GAMMA-RAY SPECTROMETRY September 1972 Health and Safety Laboratory (AEC) New York, New York DISCLAIMER This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency Thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus,

  8. A Safer Replacement for Highly Flammable Liquids Currently Used in Li-ion

    Office of Science (SC) Website

    Batteries | U.S. DOE Office of Science (SC) A Safer Replacement for Highly Flammable Liquids Currently Used in Li-ion Batteries Small Business Innovation Research (SBIR) and Small Business Technology Transfer (STTR) SBIR/STTR Home About Funding Opportunity Announcements (FOAs) Applicant and Awardee Resources Commercialization Assistance Other Resources Awards SBIR/STTR Highlights Reporting Fraud Contact Information Small Business Innovation Research and Small Business Technology Transfer

  9. Fail-Safe Design for Large Capacity Li-Ion Battery Systems - Energy

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

    Innovation Portal Find More Like This Return to Search Fail-Safe Design for Large Capacity Li-Ion Battery Systems National Renewable Energy Laboratory Contact NREL About This Technology Publications: PDF Document Publication Fail Safe Design for Large Capacity Lithium-ion Batteries.pdf (2,324 KB) Technology Marketing Summary Lithium-ion batteries (LIBs) are a promising candidate for energy storage of electric drive vehicles due to their high power and energy density. The total electric

  10. Tao Li | Center for Gas SeparationsRelevant to Clean Energy Technologies |

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

    Blandine Jerome Tao Li Previous Next List Postdoctoral Researcher Department of Materials Science and Engineering University of California, Berkeley Email: taoli [at] berkeley.edu Phone: 510-643-6804 PhD in Chemistry, University of Pittsburgh BS in Chemistry, Fudan University EFRC research: By embedding inorganic particles in polymer matrices, the resulting mixed matrix membranes (MMMs) can potentially combine the benefits of both materials to simultaneously achieve high selectivity, high

  11. Construction of a Li Ion Battery (LIB) Cathode Production Plant in Elyria,

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

    Ohio | Department of Energy 1 DOE Hydrogen and Fuel Cells Program, and Vehicle Technologies Program Annual Merit Review and Peer Evaluation PDF icon arravt008_es_dicarlo_2011_p.pdf More Documents & Publications Process for Low Cost Domestic Production of LIB Cathode Materials Process for Low Cost Domestic Production of LIB Cathode Materials Construction of a Li Ion Battery (LIB) Cathode Production Plant in Elyria, Ohio

  12. Microsoft PowerPoint - 17_Li_ARM07_Aerosol_Breakout.ppt [Compatibility Mode]

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

    Separating Real Aerosol Effects from p g Artifacts Using Space-borne, Air-borne and Ground Measurements and Under- and Ground Measurements and Under standing Physical Processes Using a CRM Zhanqing Li Uni ersit of Mar land University of Maryland Contributors T. Yuan, M.-J. Jeong, R. Zhang and J. Fan Objectives j * Evaluate various effects on remote sensing products from satellite and g p f m ground sensors. * Separate artifacts from the real Separate artifacts from the real effects. * Eventually

  13. Microsoft PowerPoint - Garcia-Diaz - LiT Electrolysis Projects Summary V3

    Office of Environmental Management (EM)

    * Maroni is the Baseline for LiT Electrolysis * LLNL LDRD tries to improve molten salt liquid-liquid extraction and SRNL is contributing by investigating RbCl containing salts * SRNL LDRD tries process intensification to eliminate molten salt liquid-liquid extraction using advanced solid state electrolytes 2 3 * Upper Process shows generalized process flow diagram for Maroni Process * Lower right shows the simplification in the process flow diagram through the elimination of the liquid-liquid

  14. Impedance spectroscopy study of SiO2-Li2O:Nd2O3 glasses

    SciTech Connect (OSTI)

    Pereia, R.; Gozzo, C B; Guedes, I.; Boatner, Lynn A; Terezo, A J; Costa, M M

    2014-01-01

    In the present study, neodymium-doped lithium silicate glasses have been prepared by the conventional melt-quenching technique. The dielectric properties, electric modulus and electrical conductivity of SiO2-Li2O (SiLi-0Nd) and SiO2-Li2O:Nd2O3 (SiLi-1.35Nd) have been studied from 1 Hz to 1 MHz in the 333 423 K temperature range. At a given temperature and frequency, we observe that the resistivity increases while the conductivity accordingly decreases when neodymium ions are added to the glass matrix. The activation energy of two distinct regions was evaluated from the ln( dc)=f(1/T) plot and was found to be E1(T<363K)=0.61(0.66)eV and E2(T>363K)=1.26(1.09)eV for SiLi-0Nd (SiLi-1,35Nd). The dielectric constant ( Re) decreases while the dielectric loss (tan ( )) increases under Nd2O3 doping. We also observe that for both glasses, Re and tan ( ) tend to increase with increasing temperature and decrease with increasing frequency.

  15. Effects of laser energy and wavelength on the analysis of LiFePO? using laser assisted atom probe tomography

    SciTech Connect (OSTI)

    Santhanagopalan, Dhamodaran; Khalifah, Peter; Schreiber, Daniel K.; Perea, Daniel E.; Martens, Richard L.; Janssen, Yuri; Meng, Ying Shirley

    2015-01-01

    The effects of laser wavelength (355 nm and 532 nm) and laser pulse energy on the quantitative analysis of LiFePO? by atom probe tomography are considered. A systematic investigation of ultraviolet (UV, 355 nm) and green (532 nm) laser assisted field evaporation has revealed distinctly different behaviors. With the use of a UV laser, the major issue was identified as the preferential loss of oxygen (up to 10 at%) while other elements (Li, Fe and P) were observed to be close to nominal ratios. Lowering the laser energy per pulse to 1 pJ/pulse from 50 pJ/pulse increased the observed oxygen concentration to nearer its correct stoichiometry, which was also well correlated with systematically higher concentrations of ?O?? ions. Green laser assisted field evaporation led to the selective loss of Li (33% deficiency) and a relatively minor O deficiency. The loss of Li is likely a result of selective dc evaporation of Li between or after laser pulses. Comparison of the UV and green laser data suggests that the green wavelength energy was absorbed less efficiently than the UV wavelength because of differences in absorption at 355 and 532 nm for LiFePO?. Plotting of multihit events on Saxey plots also revealed a strong neutral O? loss from molecular dissociation, but quantification of this loss was insufficient to account for the observed oxygen deficiency.

  16. Nanostructured Metal Carbides for Aprotic Li-O2 Batteries. New Insights into Interfacial Reactions and Cathode Stability

    SciTech Connect (OSTI)

    Kundu, Dipan; Black, Robert; Adams, Brian; Harrison, Katharine; Zavadil, Kevin R.; Nazar, Linda F.

    2015-05-01

    The development of nonaqueous Lioxygen batteries, which relies on the reversible reaction of Li + O2 to give lithium peroxide (Li2O2), is challenged by several factors, not the least being the high charging voltage that results when carbon is typically employed as the cathode host. We report here on the remarkably low 3.2 V potential for Li2O2 oxidation on a passivated nanostructured metallic carbide (Mo2C), carbon-free cathode host. Furthermore, online mass spectrometry coupled with X-ray photoelectron spectroscopy unequivocally demonstrates that lithium peroxide is simultaneously oxidized together with the LixMoO3-passivated conductive interface formed on the carbide, owing to their close redox potentials. We found that the process rejuvenates the surface on each cycle upon electrochemical charge by releasing LixMoO3 into the electrolyte, explaining the low charging potential.

  17. Effects of laser energy and wavelength on the analysis of LiFePO₄ using laser assisted atom probe tomography

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

    Santhanagopalan, Dhamodaran; Schreiber, Daniel K.; Perea, Daniel E.; Martens, Richard L.; Janssen, Yuri; Khalifah, Peter; Meng, Ying Shirley

    2014-09-21

    The effects of laser wavelength (355 nm and 532 nm) and laser pulse energy on the quantitative analysis of LiFePO₄ by atom probe tomography are considered. A systematic investigation of ultraviolet (UV, 355 nm) and green (532 nm) laser assisted field evaporation has revealed distinctly different behaviors. With the use of a UV laser, the major issue was identified as the preferential loss of oxygen (up to 10 at%) while other elements (Li, Fe and P) were observed to be close to nominal ratios. Lowering the laser energy per pulse to 1 pJ/pulse from 50 pJ/pulse increased the observed oxygenmore »concentration to nearer its correct stoichiometry, which was also well correlated with systematically higher concentrations of ¹⁶O₂⁺ ions. Green laser assisted field evaporation led to the selective loss of Li (33% deficiency) and a relatively minor O deficiency. The loss of Li is likely a result of selective dc evaporation of Li between or after laser pulses. Comparison of the UV and green laser data suggests that the green wavelength energy was absorbed less efficiently than the UV wavelength because of differences in absorption at 355 and 532 nm for LiFePO₄. Plotting of multihit events on Saxey plots also revealed a strong neutral O₂ loss from molecular dissociation, but quantification of this loss was insufficient to account for the observed oxygen deficiency.« less

  18. Three-dimensional graphene/LiFePO{sub 4} nanostructures as cathode materials for flexible lithium-ion batteries

    SciTech Connect (OSTI)

    Ding, Y.H., E-mail: yhding@xtu.edu.cn [College of Chemical Engineering, Xiangtan University, Hunan 411105 (China); Institute of Rheology Mechanics, Xiangtan University, Hunan 411105 (China); Ren, H.M. [Institute of Rheology Mechanics, Xiangtan University, Hunan 411105 (China); Huang, Y.Y. [BTR New Energy Materials Inc., Shenzhen 518000 (China); Chang, F.H.; Zhang, P. [Institute of Rheology Mechanics, Xiangtan University, Hunan 411105 (China)

    2013-10-15

    Graphical abstract: Graphene/LiFePO{sub 4} composites as a high-performance cathode material for flexible lithium-ion batteries have been prepared by using a co-precipitation method to synthesize graphene/LiFePO4 powders as precursors and then followed by a solvent evaporation process. - Highlights: Flexible LiFePO{sub 4}/graphene films were prepared first time by a solvent evaporation process. The flexible electrode exhibited a high discharge capacity without conductive additives. Graphene network offers the electrode adequate strength to withstand repeated flexing. - Abstract: Three-dimensional graphene/LiFePO{sub 4} nanostructures for flexible lithium-ion batteries were successfully prepared by solvent evaporation method. Structural characteristics of flexible electrodes were investigated by X-ray diffraction (XRD), atomic force microscopy (AFM) and scanning electron microscopy (SEM). Electrochemical performance of graphene/LiFePO{sub 4} was examined by a variety of electrochemical testing techniques. The graphene/LiFePO{sub 4} nanostructures showed high electrochemical properties and significant flexibility. The composites with low graphene content exhibited a high capacity of 163.7 mAh g{sup ?1} at 0.1 C and 114 mAh g{sup ?1} at 5 C without further incorporation of conductive agents.

  19. Inclusion property of Cs, Sr, and Ba impurities in LiCl crystal formed by layer-melt crystallization

    SciTech Connect (OSTI)

    Choi, Jung-Hoon; Cho, Yung-Zun; Lee, Tae-Kyo; Eun, Hee-Chul; Kim, Jun-Hong; Park, Hwan-Seo; Kim, In-Tae; Park, Geun-Il

    2013-07-01

    Pyroprocessing is one of the promising technologies enabling the recycling of spent nuclear fuels from a commercial light water reactor (LWR). In general, pyroprocessing uses dry molten salts as electrolytes. In particular, LiCl waste salt after pyroprocessing contains highly radioactive I/II group fission products mainly composed of Cs, Sr, and Ba impurities. Therefore, it is beneficial to reuse LiCl salt in the pyroprocessing as an electrolyte for economic and environmental issues. Herein, to understand the inclusion property of impurities within LiCl crystal, the physical properties such as lattice parameter change, bulk modulus, and substitution enthalpy of a LiCl crystal having 0-6 at% Cs{sup +} or Ba{sup 2+} impurities under existence of 1 at% Sr{sup 2+} impurity were calculated via the first-principles density functional theory. The substitution enthalpy of LiCl crystals having 1 at% Sr{sup 2+} showed slightly decreased value than those without Sr{sup 2+} impurity. Therefore, through the substitution enthalpy calculation, it is expected that impurities will be incorporated within LiCl crystal as co-existed form rather than as a single component form. (authors)

  20. Effects of laser energy and wavelength on the analysis of LiFePO? using laser assisted atom probe tomography

    SciTech Connect (OSTI)

    Santhanagopalan, Dhamodaran; Schreiber, Daniel K.; Perea, Daniel E.; Martens, Richard L.; Janssen, Yuri; Khalifah, Peter; Meng, Ying Shirley

    2014-09-21

    The effects of laser wavelength (355 nm and 532 nm) and laser pulse energy on the quantitative analysis of LiFePO? by atom probe tomography are considered. A systematic investigation of ultraviolet (UV, 355 nm) and green (532 nm) laser assisted field evaporation has revealed distinctly different behaviors. With the use of a UV laser, the major issue was identified as the preferential loss of oxygen (up to 10 at%) while other elements (Li, Fe and P) were observed to be close to nominal ratios. Lowering the laser energy per pulse to 1 pJ/pulse from 50 pJ/pulse increased the observed oxygen concentration to nearer its correct stoichiometry, which was also well correlated with systematically higher concentrations of ?O?? ions. Green laser assisted field evaporation led to the selective loss of Li (33% deficiency) and a relatively minor O deficiency. The loss of Li is likely a result of selective dc evaporation of Li between or after laser pulses. Comparison of the UV and green laser data suggests that the green wavelength energy was absorbed less efficiently than the UV wavelength because of differences in absorption at 355 and 532 nm for LiFePO?. Plotting of multihit events on Saxey plots also revealed a strong neutral O? loss from molecular dissociation, but quantification of this loss was insufficient to account for the observed oxygen deficiency.