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Sample records for lithium 5

  1. Lithium

    USGS Publications Warehouse

    Ober, J.A.

    2006-01-01

    In 2005, lithium consumption in the United States was at 2.5 kt of contained lithium, nearly 32% more than the estimate for 2004. World consumption was 14.1 kt of lithium contained in minerals and compounds in 2003. Exports from the US increased slightly compared with 2004. Due to strong demand for lithium compounds in 2005, both lithium carbonate plants in Chile were operating at or near capacity.

  2. Lithium

    USGS Publications Warehouse

    Jaskula, B.W.

    2010-01-01

    In 2009, lithium consumption in the United States was estimated to have been about 1.2 kt (1,300 st) of contained lithium, a 40-percent decrease from 2008. The United States was estimated to be the fourth largest consumer of lithium, and remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. Only one company, Chemetall Foote Corp. (a subsidiary of Chemetall GmbH of Germany), produced lithium compounds from domestic resources. In 2009, world lithium consumption was estimated to have been about 18.7 kt (20,600 st) of lithium contained in minerals and compounds.

  3. Lithium

    USGS Publications Warehouse

    Jaskula, B.W.

    2011-01-01

    In 2010, lithium consumption in the United States was estimated to have been about 1 kt (1,100 st) of contained lithium, a 23-percent decrease from 2009. The United States was estimated to be the fourth largest consumer of lithium. It remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. Only one company, Chemetall Foote Corp. (a subsidiary of Chemetall GmbH of Germany), produced lithium compounds from domestic resources. In 2010, world lithium consumption was estimated to have been about 21 kt (22,000 st) of lithium contained in minerals and compounds, a 12-percent increase from 2009.

  4. Lithium

    USGS Publications Warehouse

    Jaskula, B.W.

    2012-01-01

    In 2011, world lithium consumption was estimated to have been about 25 kt (25,000 st) of lithium contained in minerals and compounds, a 10-percent increase from 2010. U.S. consumption was estimated to have been about 2 kt (2,200 st) of contained lithium, a 100-percent increase from 2010. The United States was estimated to be the fourth-ranked consumer of lithium and remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. One company, Chemetall Foote Corp. (a subsidiary of Chemetall GmbH of Germany), produced lithium compounds from domestic brine resources near Silver Peak, NV.

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

    SciTech Connect

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

    1981-12-01

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

  6. Lithium

    USGS Publications Warehouse

    Ober, J.

    1998-01-01

    The lithium industry can be divided into two sectors: ore concentrate producers and chemical producers. Ore concentrate producers mine lithium minerals. They beneficiate the ores to produce material for use in ceramics and glass manufacturing.

  7. New lithium iron pyrophosphate as 3.5 V class cathode material for lithium ion battery.

    PubMed

    Nishimura, Shin-ichi; Nakamura, Megumi; Natsui, Ryuichi; Yamada, Atsuo

    2010-10-06

    A new pyrophosphate compound Li(2)FeP(2)O(7) was synthesized by a conventional solid-state reaction, and its crystal structure was determined. Its reversible electrode operation at ca. 3.5 V vs Li was identified with the capacity of a one-electron theoretical value of 110 mAh g(-1) even for ca. 1 μm particles without any special efforts such as nanosizing or carbon coating. Li(2)FeP(2)O(7) and its derivatives should provide a new platform for related lithium battery electrode research and could be potential competitors to commercial olivine LiFePO(4), which has been recognized as the most promising positive cathode for a lithium-ion battery system for large-scale applications, such as plug-in hybrid electric vehicles.

  8. Lithium

    MedlinePlus

    ... bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). Lithium ... Lithium is also sometimes used to treat depression, schizophrenia (a mental ... emotions), disorders of impulse control (inability to resist the urge ...

  9. Sol-Gel-Derived Lithium Superionic Conductor Li1.5Al0.5Ge1.5(PO4)3 Electrolyte for Solid-State Lithium-Oxygen Batteries

    DTIC Science & Technology

    2014-03-12

    AFRL-RQ-WP-TP-2015-0055 SOL-GEL-DERIVED LITHIUM SUPERIONIC CONDUCTOR LI1.5AL0.5GE1.5(PO4)3 ELECTROLYTE FOR SOLID -STATE LITHIUM -OXYGEN...2014 4. TITLE AND SUBTITLE SOL-GEL-DERIVED LITHIUM SUPERIONIC CONDUCTOR LI1.5AL0.5GE1.5(PO4)3 ELECTROLYTE FOR SOLID -STATE LITHIUM -OXYGEN BATTERIES...attracting a great deal of attention as a solid electrolyte for lithium -oxygen (Li- O2) batteries due to its high ionic conductivity. In this study, LAGP

  10. Thyroid and pituitary thyroxine-5'-deiodinase activity and thyrotrophin secretion in lithium-treated rats.

    PubMed

    Frankenfeld, T G P; Corrêa Da Costa, V M; Nascimento-Saba, C C A; Ortiga-Carvalho, T M; Santos, R M M; Lisboa, P C; Carvalho, D P; Rosenthal, D

    2002-08-01

    Some authors have reported increased serum thyrotrophin (TSH) in animals chronically treated with lithium, suggesting that lithium might decrease pituitary thyroxine (T(4))-5'-deiodinase activity. On the other hand, the effect of lithium treatment on thyroidal T(4)-5'-deiodinase activity is also unknown. The present study was undertaken to evaluate the effects of lithium treatment on pituitary and thyroid T(4)-5'-deiodinase activity. Serum and pituitary TSH levels and thyroidal and pituitary T(4)-5'-deiodinase activities were determined in 3-month-old isogenic male Dutch-Miranda rats treated with lithium for 8 weeks. Chronic lithium treatment produced a slight increase in pituitary TSH content, but no change in serum TSH, and a significant increase in the thyroidal T(4)-5'-deiodinase activity. However, the pituitary T(4)-5'-deiodinase activity was unaffected by lithium administration. As far as we know, the present data show for the first time that chronic lithium treatment can increase the thyroxine to tri-iodothyronine conversion in the murine thyroid gland, be it directly or indirectly.

  11. Dual effect of lithium on NFAT5 activity in kidney cells

    PubMed Central

    Küper, Christoph; Beck, Franz-Xaver; Neuhofer, Wolfgang

    2015-01-01

    Lithium salts are used widely for treatment of bipolar and other mental disorders. Lithium therapy is accompanied frequently by renal side effects, such as nephrogenic diabetes insipidus or chronic kidney disease (CKD), but the molecular mechanisms underlying these effects are still poorly understood. In the present study we examined the effect of lithium on the activity of the osmosensitive transcriptional activator nuclear factor of activated T cells 5 (NFAT5, also known as TonEBP), which plays a key role in renal cellular osmoprotection and urinary concentrating ability. Interestingly, we found different effects of lithium on NFAT5 activity, depending on medium osmolality and incubation time. When cells were exposed to lithium for a relative short period (24 h), NFAT5 activity was significantly increased, especially under isosmotic conditions, resulting in an enhanced expression of the NFAT5 target gene heat shock protein 70 (HSP70). Further analysis revealed that the increase of NFAT5 activity depended primarily on an enhanced activity of the c-terminal transactivation domain (TAD), while NFAT5 protein abundance was largely unaffected. Enhanced activity of the TAD is probably mediated by lithium-induced inhibitory phosphorylation of glycogen synthase kinase 3β (GSK-3β), which is in accordance with previous studies. When cells were exposed to lithium for a longer period (96 h), cellular NFAT5 activity and subsequently expression of HSP70 significantly decreased under hyperosmotic conditions, due to diminished NFAT5 protein abundance, also resulting from GSK-3β inhibition. Taken together, our results provide evidence that lithium has opposing effects on NFAT5 activity, depending on environmental osmolality and exposure duration. The potential impacts of these observations on the diverse effects of lithium on kidney function are discussed. PMID:26441681

  12. Comparative Neurocognitive Effects of 5 Psychotropic Anticonvulsants and Lithium

    PubMed Central

    Thomas Gualtieri, C.; Johnson, Lynda G.

    2006-01-01

    Context Many of the new antiepileptic drugs have psychiatric indications, and most are prescribed by psychiatrists for patients with mood disorders, even when a specific indication is absent. Epileptic drugs as a whole, even the newer ones, are known to affect cognition, sometimes in untoward ways. Research on the neurocognitive effects of antiepileptic drugs, however, has been done exclusively in normal volunteers and in patients with seizure disorders. Method A naturalistic, cross-sectional study was conducted on patients who were taking 1 of 5 different antiepileptic drugs or lithium (LIT). Cognitive status was measured by a computerized neurocognitive screening battery, CNS Vital Signs (CNSVS). Subjects One hundred fifty-nine patients with bipolar disorder, aged 18-70 years, were treated with carbamazepine (CBZ) (N = 16), lamotrigine (LMTG) (N = 38), oxcarbazepine (OCBZ) (N = 19), topiramate (TPM) (N = 19), and valproic acid (VPA) (N = 37); 30 bipolar patients were treated with LIT. Results Significant group differences were detected in tests of memory, psychomotor speed, processing speed, reaction time, cognitive flexibility, and attention. Rank-order analysis indicated superiority for LMTG (1.8) followed by OCBZ (2.1), LIT(3.3), TPM (4.3), VPA (4.5), and CBZ (5.0). Conclusion The relative neurocognitive effects of the various psychotropic antiepileptic drugs in patients with bipolar disorder were concordant with those described in the seminal literature in normal volunteers and patients with epilepsy. LMTG and OCBZ had the least neurotoxicity, and TPM, VPA, and CBZ had the most. LIT effects on neurocognition were intermediate. Choosing a mood-stabilizing drug with minimal neurocognitive effects may enhance patient compliance over the long term. PMID:17406176

  13. Lithium ion conductive Li1.5Al0.5Ge1.5(PO4)3 based inorganic-organic composite separator with enhanced thermal stability and excellent electrochemical performances in 5 V lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Shi, Junli; Xia, Yonggao; Han, Shaojie; Fang, Lifeng; Pan, Meizi; Xu, Xiaoxiong; Liu, Zhaoping

    2015-01-01

    Since 5 V lithium ion batteries have attracted more and more attentions and are deemed to be an important tendency in the future, the matched design of the separators has also become a necessary and significant work. In this work, the lithium ionic conducting glass ceramic Li1.5Al0.5Ge1.5(PO4)3-polypropylene (PP) based inorganic-organic composite separator (LAGP-PP) is prepared. Compared with the pristine PP separator, the LAGP-PP separator owns enhanced thermal stability and wettability. Meanwhile, the LAGP-PP separator shows higher ion conductivity than the traditional Al2O3 coated PP separator due to the more facile lithium ion diffusion channels in the coating layer. The superior C-rate capacity and cyclability in the LiNi0.5Mn1.5O4 based 5 V lithium ion batteries indicate that the LAGP-PP separator is a good alternative for the traditional inert inorganic ceramic coated polyolefin separators and is a kind of promising candidate separator for the high voltage lithium ion batteries.

  14. Li(V0.5Ti0.5)S2 as a 1 V lithium intercalation electrode

    NASA Astrophysics Data System (ADS)

    Clark, Steve J.; Wang, Da; Armstrong, A. Robert; Bruce, Peter G.

    2016-03-01

    Graphite, the dominant anode in rechargeable lithium batteries, operates at ~0.1 V versus Li+/Li and can result in lithium plating on the graphite surface, raising safety concerns. Titanates, for example, Li4Ti5O12, intercalate lithium at~1.6 V versus Li+/Li, avoiding problematic lithium plating at the expense of reduced cell voltage. There is interest in 1 V anodes, as this voltage is sufficiently high to avoid lithium plating while not significantly reducing cell potential. The sulfides, LiVS2 and LiTiS2, have been investigated as possible 1 V intercalation electrodes but suffer from capacity fading, large 1st cycle irreversible capacity or polarization. Here we report that the 50/50 solid solution, Li1+x(V0.5Ti0.5)S2, delivers a reversible capacity to store charge of 220 mAhg-1 (at 0.9 V), 99% of theoretical, at a rate of C/2, retaining 205 mAhg-1 at C-rate (92% of theoretical). Rate capability is excellent with 200 mAhg-1 at 3C. C-rate is discharge in 1 h. Polarization is low, 100 mV at C/2. To the best of our knowledge, the properties/performances of Li(V0.5Ti0.5)S2 exceed all previous 1 V electrodes.

  15. Space Technology-5 Lithium-Ion Battery Design, Qualification and Integration and Testing

    NASA Technical Reports Server (NTRS)

    Rao, Gopalakishna M.; Stewart, Karen; Ameen, Syed; Banfield, Peter K.

    2005-01-01

    This document is a viewgraph presentation that reviews the Lithium Ion Battery for the Space Technology-5 (ST-5) mission. Included in the document is a review of the ST-5 Mission, a review of the battery requirements, a description of the battery and the battery materials. The testing and the integration and qualification data is reviewed.

  16. LiBi3S5-A lithium bismuth sulfide with strong cation disorder

    NASA Astrophysics Data System (ADS)

    Nakhal, Suliman; Wiedemann, Dennis; Stanje, Bernhard; Dolotko, Oleksandr; Wilkening, Martin; Lerch, Martin

    2016-06-01

    Among chalcogenide semiconductors for thermoelectric applications, alkali-metal bismuth compounds occur in many complex compositions favorable for high performance. Although LiBi3S5 had been announced in 1977, the potential 1D lithium-ion conductor has hitherto eluded selective synthesis and structure determination. In this study, we present a solid-state route to phase-pure LiBi3S5 powder starting from LiBiS2 and Bi2S3. Neutron diffractograms and lithium NMR spectra reveal its crystal structure to be a cation-disordered variety of the AgBi3S5 type (synthetic pavonite; monoclinic, C2/m). Topological analyses and lithium NMR relaxometry suggest that correlated lithium-ion diffusion with activation energies up to 0.66(2) eV occurs along the channels in b direction including tetrahedral voids. Because of cation disorder, immobile bismuth(III) ions clog these pathways, making LiBi3S5 a moderate to poor ionic conductor. The synthesis route reported is nonetheless promising for new lithium bismuth sulfides with, possibly ordered, structure types of the pavonite homologous series.

  17. Power System Electronics Accommodation for a Lithium Ion Battery on the Space Technology 5 (ST5) Mission

    NASA Technical Reports Server (NTRS)

    Castell, Karen; Day, John H. (Technical Monitor)

    2001-01-01

    ST5 mission requirements include validation of Lithium-ion battery in orbit. Accommodation in the power system for Li-ion battery can be reduced with smaller amp-hour size, highly matched cells when compared to the larger amp-hour size approach. Result can be lower system mass and increased reliability.

  18. Scalable integration of Li5FeO4 towards robust, high-performance lithium-ion hybrid capacitors.

    PubMed

    Park, Min-Sik; Lim, Young-Geun; Hwang, Soo Min; Kim, Jung Ho; Kim, Jeom-Soo; Dou, Shi Xue; Cho, Jaephil; Kim, Young-Jun

    2014-11-01

    Lithium-ion hybrid capacitors have attracted great interest due to their high specific energy relative to conventional electrical double-layer capacitors. Nevertheless, the safety issue still remains a drawback for lithium-ion capacitors in practical operational environments because of the use of metallic lithium. Herein, single-phase Li5FeO4 with an antifluorite structure that acts as an alternative lithium source (instead of metallic lithium) is employed and its potential use for lithium-ion capacitors is verified. Abundant Li(+) amounts can be extracted from Li5FeO4 incorporated in the positive electrode and efficiently doped into the negative electrode during the first electrochemical charging. After the first Li(+) extraction, Li(+) does not return to the Li5FeO4 host structure and is steadily involved in the electrochemical reactions of the negative electrode during subsequent cycling. Various electrochemical and structural analyses support its superior characteristics for use as a promising lithium source. This versatile approach can yield a sufficient Li(+)-doping efficiency of >90% and improved safety as a result of the removal of metallic lithium from the cell.

  19. Nb2O5 microstructures: a high-performance anode for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Liu, Sainan; Zhou, Jiang; Cai, Zhenyang; Fang, Guozhao; Pan, Anqiang; Liang, Shuquan

    2016-11-01

    We report the synthesis of three-dimensional (3D) urchin-like Nb2O5 microstructures by a facile hydrothermal approach with subsequent annealing treatment. As anode materials for lithium-ion batteries, the 3D urchin-like Nb2O5 microstructures exhibit superior electrochemical performance with excellent rate capability as well as long-term cycling stability. The electrode delivers high capacity of 131 mA h g-1 after 1000 cycles at a high current density of 1 A g-1. The excellent electrochemical performance suggests the 3D urchin-like Nb2O5 microstructures may be a promising anode candidate for high-power lithium ion batteries.

  20. Lithium diffusion in sputter-deposited Li4Ti5O12 thin films

    NASA Astrophysics Data System (ADS)

    Wunde, F.; Berkemeier, F.; Schmitz, G.

    2012-10-01

    Li4Ti5O12 (LTO) thin films are deposited by dc-ion beam sputtering at different oxygen partial pressures and different substrate temperatures. In order to investigate, how these two parameters influence the atomic structure, the specimens are characterized by X-ray diffraction and transmission electron microscopy. Electrochemical characterization of the films is done by cyclic voltammetry and chrono-potentiometry. To determine an averaged chemical diffusion coefficient of lithium, a method is developed, evaluating c-rate tests. The results obtained by this method are compared to results obtained by the well established galvanostatic intermittent titration technique (GITT), which is used to determine a concentration dependent diffusion coefficient of lithium in LTO.

  1. All-solid-state lithium organic battery with composite polymer electrolyte and pillar[5]quinone cathode.

    PubMed

    Zhu, Zhiqiang; Hong, Meiling; Guo, Dongsheng; Shi, Jifu; Tao, Zhanliang; Chen, Jun

    2014-11-26

    The cathode capacity of common lithium ion batteries (LIBs) using inorganic electrodes and liquid electrolytes must be further improved. Alternatively, all-solid-state lithium batteries comprising the electrode of organic compounds can offer much higher capacity. Herein, we successfully fabricated an all-solid-state lithium battery based on organic pillar[5]quinone (C35H20O10) cathode and composite polymer electrolyte (CPE). The poly(methacrylate) (PMA)/poly(ethylene glycol) (PEG)-LiClO4-3 wt % SiO2 CPE has an optimum ionic conductivity of 0.26 mS cm(-1) at room temperature. Furthermore, pillar[5]quinine cathode in all-solid-state battery rendered an average operation voltage of ∼2.6 V and a high initial capacity of 418 mAh g(-1) with a stable cyclability (94.7% capacity retention after 50 cycles at 0.2C rate) through the reversible redox reactions of enolate/quinonid carbonyl groups, showing favorable prospect for the device application with high capacity.

  2. Performance tests of 4-5 year old lithium sulphur dioxide batteries

    NASA Astrophysics Data System (ADS)

    Holland, C. R.; Williams, R. L.

    1983-09-01

    Tests of a new acoustic system in the spring of 1982, using radio frequency transmission of the data, required the Naval Ocean Research and Development Activity (NORDA) to reconsider the use of lithium battery technology. A request was made to the Navy Safety Office, Naval Sea Systems Command Code 06H, for permission to utilize lithium batteries in the R&D project and for permission to use existing lithium sulphur dioxide cells, which had been purchased in previous years. The safety office tentatively approved the intended useage but subject to a performance test and evaluation of a representative sample of the existing cells. In response to the NAVSEA direction, 32 cells were randomly chosen and subjected to forming and discharge tests. The cells, as a group, performed beyond expectations and provided energy in excess of the manufacturer's original specifications for these cells. All tests were performed without safety problems or any incidents. Similar cells from the same lot were subsequently used at sea in the R&D project and performed equally as well as those tested in the laboratory. This report documents the testing procedures used to evaluate 4 to 5 year old Li/SO2 cells and the test results achieved.

  3. A super lithium-rich red-clump star in the open cluster Trumpler 5

    NASA Astrophysics Data System (ADS)

    Monaco, L.; Boffin, H. M. J.; Bonifacio, P.; Villanova, S.; Carraro, G.; Caffau, E.; Steffen, M.; Ahumada, J. A.; Beletsky, Y.; Beccari, G.

    2014-04-01

    Context. The existence of lithium-rich low-mass red giant stars still represents a challenge for stellar evolution models. Stellar clusters are privileged environments for this kind of investigation. Aims: To investigate the chemical abundance pattern of the old open cluster Trumpler 5, we observed a sample of four red-clump stars with high-resolution optical spectrographs. One of them (#3416) reveals extremely strong lithium lines in its spectrum. Methods: One-dimensional, local thermodynamic equilibrium analysis was performed on the spectra of the observed stars. A 3D-NLTE analysis was performed to derive the lithium abundance of star #3416. Results: Star #3416 is super Li-rich with A(Li) = 3.75 dex. The lack of 6Li enrichment (6Li/7Li < 2%), the low carbon isotopic ratio (12C/13C = 14 ± 3), and the lack of evidence for radial velocity variation or enhanced rotational velocity (vsini = 2.8 km s-1) all suggest that lithium production has occurred in this star through the Cameron & Fowler mechanism. Conclusions: We identified a super Li-rich core helium-burning, red-clump star in an open cluster. Internal production is the most likely cause of the observed enrichment. Given the expected short duration of a star's Li-rich phase, enrichment is likely to have occurred at the red clump or in the immediately preceding phases, namely during the He-flash at the tip of the red giant branch (RGB) or while ascending the brightest portion of the RGB. Based on observations made with ESO Telescopes at the La Silla Paranal Observatory under program ID 088.D-0045(A).Appendix A is available in electronic form at http://www.aanda.org

  4. Effects of self-assembled materials prepared from V2O5 for lithium ion electroinsertion.

    PubMed

    Galiote, Nelson A; Camargo, Maiuí N L; Iost, Rodrigo M; Crespilho, Frank; Huguenin, Fritz

    2011-10-04

    Self-assembled materials consisting of V(2)O(5), polyallylamine (PAH) and silver nanoparticles (AgNPs) were obtained by the layer-by-layer (LbL) method, aiming at their application as electrodes for lithium-ion batteries and electrochromic devices. The method employed herein allowed for linear growth of visually homogeneous films composed of V(2)O(5), V(2)O(5)/PAH, and V(2)O(5)/PAH/AgNP with 15 bilayers. According to the Fourier transform infrared spectra, interaction between the oxygen atom of the vanadyl group and the amino group should be responsible for the growth of these films. This interaction also enabled establishment of an electrostatic shield between the lithium ions and the sites with higher negative charge, thereby raising the ionic mobility and consequently increasing the energy storage capacity and reducing the response time. According to the site-saturation model and the electrochemical and spectroelectrochemical results, the presence of PAH in the self-assembled host matrix decreased the number of V(2)O(5) electroactive sites. Thus, AgNPs were stabilized in PAH and inserted into the nanoarchitecture, so as to enhance the specific capacity. This should provide new conducting pathways and connect isolated V(2)O(5) particles in the host matrix. Therefore, new nanoarchitectures for specific interactions were formed spontaneously and chosen as examples in this work, aiming to demonstrate the potentiality of the adopted self-assembled method for enhancing the charge transport rate into the host matrices. The obtained materials displayed suitable properties for use as electrodes in lithium batteries and electrochromic devices.

  5. Maintaining structural integrity of 4.5 V lithium cobalt oxide cathode with fumaronitrile as a novel electrolyte additive

    NASA Astrophysics Data System (ADS)

    Wang, Xianshu; Zheng, Xiongwen; Liao, Youhao; Huang, Qiming; Xing, Lidan; Xu, Mengqing; Li, Weishan

    2017-01-01

    The specific capacity of lithium-ion battery with lithium cobalt oxide as cathode depends on the upper limitation voltage for charge/discharge cycling, but this oxide tends to be destructed structurally when it is cycled in carbonate-based electrolyte under high voltage. We report a novel electrolyte additive, fumaronitrile (FN, CNsbnd CHdbnd CHsbnd CN), which can maintain the structural integrity of lithium cobalt oxide. Electrochemical measurements indicate that lithium cobalt oxide exhibits poor cyclic stability when it is cycled under 4.5 V (vs. Li/Li+) and the charged cathode suffers serious self-discharge in a base electrolyte, 1.0 mol L-1 LiPF6 in EC/EMC/DEC (3:5:2, by weight). These issues can be overcome effectively by adding 0.5% FN into the base electrolyte. Physical and chemical characterizations demonstrate that the poor cyclic stability and self-discharge of lithium cobalt oxide result from its structural destruction caused by HF formed from electrolyte decomposition, and FN yields a protective cathode interphase film which maintains the structural integrity of lithium cobalt oxide.

  6. Advanced Mesoporous Spinel Li4Ti5O12/rGO Composites with Increased Surface Lithium Storage Capability for High-Power Lithium-Ion Batteries.

    PubMed

    Ge, Hao; Hao, Tingting; Osgood, Hannah; Zhang, Bing; Chen, Li; Cui, Luxia; Song, Xi-Ming; Ogoke, Ogechi; Wu, Gang

    2016-04-13

    Spinel Li4Ti5O12 (LTO) and reduced graphene oxide (rGO) are attractive anode materials for lithium-ion batteries (LIBs) because of their unique electrochemical properties. Herein, we report a facile one-step hydrothermal method in preparation of a nanocomposite anode consisting of well-dispersed mesoporous LTO particles onto rGO. An important reaction step involves glucose as a novel linker agent and reducing agent during the synthesis. It was found to prevent the aggregation of LTO particles, and to yield mesoporous structures in nanocomposites. Moreover, GO is reduced to rGO by the hydroxyl groups on glucose during the hydrothermal process. When compared to previously reported LTO/graphene electrodes, the newly prepared LTO/rGO nanocomposite has mesoporous characteristics and provides additional surface lithium storage capability, superior to traditional LTO-based materials for LIBs. These unique properties lead to markedly improved electrochemical performance. In particular, the nanocomposite anode delivers an ultrahigh reversible capacity of 193 mA h g(-1) at 0.5 C and superior rate performance capable of retaining a capacity of 168 mA h g(-1) at 30 C between 1.0 and 2.5 V. Therefore, the newly prepared mesoporous LTO/rGO nanocomposite with increased surface lithium storage capability will provide a new opportunity to develop high-power anode materials for LIBs.

  7. Fabrication of Nb2O5 Nanosheets for High-rate Lithium Ion Storage Applications

    PubMed Central

    Liu, Meinan; Yan, Cheng; Zhang, Yuegang

    2015-01-01

    Nb2O5 nanosheets are successfully synthesized through a facile hydrothermal reaction and followed heating treatment in air. The structural characterization reveals that the thickness of these sheets is around 50 nm and the length of sheets is 500 ~ 800 nm. Such a unique two dimensional structure enables the nanosheet electrode with superior performance during the charge-discharge process, such as high specific capacity (~184 mAh·g−1) and rate capability. Even at a current density of 1 A·g−1, the nanosheet electrode still exhibits a specific capacity of ~90 mAh·g−1. These results suggest the Nb2O5 nanosheet is a promising candidate for high-rate lithium ion storage applications. PMID:25659574

  8. Lithium Cell Reactions.

    DTIC Science & Technology

    1985-02-01

    Page 1. INVESTIGATION OF CHEMICAL, ELECTROCHEMICAL AND PARASITIC REACTIONS IN LITHIUM - THIONYL CHLORIDE CELLS ....... ................. 1 1.1 INTRODUCTION...OF LITHIUM - THIONYL CHLORIDE CELLS. ................ 56 1.4.1 Carbon Limited Overdischarge...............56 1.4.1.1 Background... LITHIUM THIONYL - CHLORIDE CELLS. .. ............ ...... 101 1.5.1 Background. ....... ............ .... 101 1.5.2 Microphotography

  9. Structure of salts of lithium chloride and lithium hexafluorophosphate as solvates with pyridine and vinylpyridine and structural comparisons: (C5H5N)LiPF6, [p-(CH2=CH)C5H4N]LiPF6, [(C5H5N)LiCl]n, and [p-(CH2=CH)C5H4N]2Li(μ-Cl)2Li[p-(CH2=CH)C5H4N]2.

    PubMed

    Jalil, AbdelAziz; Clymer, Rebecca N; Hamilton, Clifton R; Vaddypally, Shivaiah; Gau, Michael R; Zdilla, Michael J

    2017-03-01

    Due to the flammability of liquid electrolytes used in lithium ion batteries, solid lithium ion conductors are of interest to reduce danger and increase safety. The two dominating general classes of electrolytes under exploration as alternatives are ceramic and polymer electrolytes. Our group has been exploring the preparation of molecular solvates of lithium salts as alternatives. Dissolution of LiCl or LiPF6 in pyridine (py) or vinylpyridine (VnPy) and slow vapor diffusion with diethyl ether gives solvates of the lithium salts coordinated by pyridine ligands. For LiPF6, the solvates formed in pyridine and vinylpyridine, namely tetrakis(pyridine-κN)lithium(I) hexafluorophosphate, [Li(C5H5N)4]PF6, and tetrakis(4-ethenylpyridine-κN)lithium(I) hexafluorophosphate, [Li(C7H7N)4]PF6, exhibit analogous structures involving tetracoordinated lithium ions with neighboring PF6(-) anions in the I-4 and Aea2 space groups, respectively. For LiCl solvates, two very different structures form. catena-Poly[[(pyridine-κN)lithium]-μ3-chlorido], [LiCl(C5H5N)]n, crystalizes in the P212121 space group and contains channels of edge-fused LiCl rhombs templated by rows of π-stacked pyridine ligands, while the structure of the LiCl-VnPy solvate, namely di-μ-chlorido-bis[bis(4-ethenylpyridine-κN)lithium], [Li2Cl2(C7H7N)4], is described in the P21/n space group as dinuclear (VnPy)2Li(μ-Cl)2Li(VnPy)2 units packed with neighbors via a dense array of π-π interactions.

  10. Lithium abundances in globular cluster giants: NGC 6218 (M12) and NGC 5904 (M5)

    SciTech Connect

    D'Orazi, Valentina; Angelou, George C.; Lattanzio, John C.; Gratton, Raffaele G.; Lucatello, Sara; Momany, Yazan; Bragaglia, Angela; Carretta, Eugenio

    2014-08-10

    Convergent lines of evidence suggest that globular clusters host multiple stellar populations. It appears that they experience at least two episodes of star formation whereby a fraction of first-generation stars contribute astrated ejecta to form the second generation(s). To identify the polluting progenitors, we require distinguishing chemical signatures such as that provided by lithium. Theoretical models predict that lithium can be synthesized in AGB stars, whereas no net Li production is expected from other candidates. It has been shown that in order to reproduce the abundance pattern found in M4, Li production must occur within the polluters, favoring the AGB scenario. Here, we present Li and Al abundances for a large sample of RGB stars in M12 and M5. These clusters have a very similar metallicity, while demonstrating differences in several cluster properties. Our results indicate that the first-generation and second-generation stars share the same Li content in M12; we recover an abundance pattern similar to that observed in M4. In M5, we find a higher degree of complexity, and a simple dilution model fails in reproducing the majority of the stellar population. In both clusters, we require Li production across the different stellar generations, but production seems to have occurred to different extents. We suggest that such a difference might be related to the cluster mass with the Li production being more efficient in less-massive clusters. This is the first time a statistically significant correlation between the Li spread within a GC and its luminosity has been demonstrated. Finally, although Li-producing polluters are required to account for the observed pattern, other mechanisms, such as MS depletion, might have played a role in contributing to the Li internal variation, though at a relatively low level.

  11. The lithium content and other properties of F2-G5 giants in the Hertzsprung Gap

    NASA Technical Reports Server (NTRS)

    Wallerstein, George; Bohm-Vitense, Erika; Vanture, Andrew D.; Gonzalez, Guillermo

    1994-01-01

    As stars of 2-5 solar mass evolve across the Hertzsprung Gap they should first deplete their surface lithium by convective dilution and then, when convection penetrates deeper, begin to bring CN processed material to their surfaces. To investigate this process we have observed 52 giants, 25 of which have known C/N ratios, for their Li abundances. After eliminating four stars that may actually be dwarfs and including the two components of Capella analyzed by Pilachowski and Sowell we have compared our (Li/Fe) ratios with models of Swenson. For stars showing v sin i greater than 50 km/s we find (Li/Fe) to be uneffected by mixing for B - V less than 0.7 as predicted. For stars cooler than B - V = 0.7 both v sin i and (Li/Fe) drop to smaller values. For the sharp lined stars (v sin i less than 50 km/s) we find a drop in Li between B - V = 0.45 and 0.60 which cannot be understood in terms of dilution by convection. Various possible causes of such an early depletion or dilution of surface Li are discussed including diffusion at the base of the convection zone, mass loss possibly enhanced by pulsation, and magnetic activity as in the magnetic A and B type stars. The models of Richer & Michaud (1993) with diffusion point toward a satisfactory solution. A few giants with low v sin i values stand out with much higher than expected (Li/Fe) values despite their cool effective temperatures. We do not understand why those stars have not depleted their lithium as have most giants of similar color. The correlation of (N/C) with (Li/Fe) follows expectations in so far as almost all stars with enhanced (N/C) have depleted their Li as well.

  12. Two-dimensional V2O5 sheet network as electrode for lithium-ion batteries.

    PubMed

    Xu, Yun; Dunwell, Marco; Fei, Ling; Fu, Engang; Lin, Qianglu; Patterson, Brian; Yuan, Bin; Deng, Shuguang; Andersen, Paul; Luo, Hongmei; Zou, Guifu

    2014-11-26

    Two-dimensional V2O5 and manganese-doped V2O5 sheet network were synthesized by a one-step polymer-assisted chemical solution method and characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, thermal-gravimetric analysis, and galvanostatic discharge-charge analysis. The V2O5 particles were covered with thin carbon layers, which remained after decomposition of the polymer, forming a network-like sheet structure. This V2O5 network exhibits a high capacity of about 300 and 600 mA·h/g at a current density of 100 mA/g when it was used as a cathode and anode, respectively. After doping with 5% molar ratio of manganese, the capacity of the cathode increases from 99 to 165 mA·h/g at a current density of 1 A/g (∼3 C). This unique network structure provides an interconnected transportation pathway for lithium ions. Improvement of electrochemical performance after doping manganese could be attributed to the enhancement of electronic conductivity.

  13. No association between lithium full responders and the DRD1, DRD2, DRD3, DAT1, 5-HTTLPR and HTR2A genes in a Sardinian sample.

    PubMed

    Manchia, Mirko; Congiu, Donatella; Squassina, Alessio; Lampus, Simona; Ardau, Raffaella; Chillotti, Caterina; Severino, Giovanni; Del Zompo, Maria

    2009-09-30

    Polymorphisms within the DRD1, DRD2, DRD3, DAT1, 5-HTTLPR and HTR2A genes are being studied for association with lithium prophylaxis in a sample of 155 Sardinian unrelated probands affected by bipolar disorder (BP). No significant association was shown between the polymorphisms of the genes studied and response to lithium treatment.

  14. Chemical stability of Lithium 2-trifluoromethyl-4,5-dicyanoimidazolide, an electrolyte salt for Li-ion cells

    DOE PAGES

    Shkrob, Ilya A.; Pupek, Krzysztof Z.; Gilbert, James A.; ...

    2016-12-01

    Lithium hexafluorophosphate (LiPF6) is ubiquitous in commercial lithium-ion batteries, but it is hydrolytically unstable and corrosive on electrode surfaces. Using a more stable salt would confer multiple benefits for high-voltage operation, but many such electrolyte systems facilitate anodic dissolution and pitting corrosion of aluminum current collectors that negate their advantages. Lithium 2-trifluoromethyl-4,5-dicyanoimidazolide (LiTDI) is a new salt that was designed specifically for high-voltage cells. In this study we demonstrate that in carbonate electrolytes, LiTDI prevents anodic dissolution of Al current collectors, which places it into a select group of corrosion inhibitors. However, we also demonstrate that LiTDI becomes reduced onmore » lithiated graphite, undergoing sequential defluorination and yielding a thick and resistive solid-electrolyte interphase (SEI), which increases impedance and lowers electrode capacity. The mechanistic causes for this behavior are examined using computational chemistry methods in the light of recent spectroscopic studies. Here, we demonstrate that LiTDI reduction can be prevented by certain electrolyte additives, which include fluoroethylene carbonate, vinylene carbonate and lithium bis(oxalato)borate. This beneficial action is due to preferential reduction of these additives over LiTDI at a higher potential vs. Li/Li+, so the resulting SEI can prevent the direct reduction of LiTDI at lower potentials on the graphite electrode.« less

  15. Chemical stability of Lithium 2-trifluoromethyl-4,5-dicyanoimidazolide, an electrolyte salt for Li-ion cells

    SciTech Connect

    Shkrob, Ilya A.; Pupek, Krzysztof Z.; Gilbert, James A.; Trask, Stephen E.; Abraham, Daniel P.

    2016-12-01

    Lithium hexafluorophosphate (LiPF6) is ubiquitous in commercial lithium-ion batteries, but it is hydrolytically unstable and corrosive on electrode surfaces. Using a more stable salt would confer multiple benefits for high-voltage operation, but many such electrolyte systems facilitate anodic dissolution and pitting corrosion of aluminum current collectors that negate their advantages. Lithium 2-trifluoromethyl-4,5-dicyanoimidazolide (LiTDI) is a new salt that was designed specifically for high-voltage cells. In this study we demonstrate that in carbonate electrolytes, LiTDI prevents anodic dissolution of Al current collectors, which places it into a select group of corrosion inhibitors. However, we also demonstrate that LiTDI becomes reduced on lithiated graphite, undergoing sequential defluorination and yielding a thick and resistive solid-electrolyte interphase (SEI), which increases impedance and lowers electrode capacity. The mechanistic causes for this behavior are examined using computational chemistry methods in the light of recent spectroscopic studies. Here, we demonstrate that LiTDI reduction can be prevented by certain electrolyte additives, which include fluoroethylene carbonate, vinylene carbonate and lithium bis(oxalato)borate. This beneficial action is due to preferential reduction of these additives over LiTDI at a higher potential vs. Li/Li+, so the resulting SEI can prevent the direct reduction of LiTDI at lower potentials on the graphite electrode.

  16. Li(V0.5Ti0.5)S2 as a 1 V lithium intercalation electrode

    PubMed Central

    Clark, Steve J.; Wang, Da; Armstrong, A. Robert; Bruce, Peter G.

    2016-01-01

    Graphite, the dominant anode in rechargeable lithium batteries, operates at ∼0.1 V versus Li+/Li and can result in lithium plating on the graphite surface, raising safety concerns. Titanates, for example, Li4Ti5O12, intercalate lithium at∼1.6 V versus Li+/Li, avoiding problematic lithium plating at the expense of reduced cell voltage. There is interest in 1 V anodes, as this voltage is sufficiently high to avoid lithium plating while not significantly reducing cell potential. The sulfides, LiVS2 and LiTiS2, have been investigated as possible 1 V intercalation electrodes but suffer from capacity fading, large 1st cycle irreversible capacity or polarization. Here we report that the 50/50 solid solution, Li1+x(V0.5Ti0.5)S2, delivers a reversible capacity to store charge of 220 mAhg−1 (at 0.9 V), 99% of theoretical, at a rate of C/2, retaining 205 mAhg−1 at C-rate (92% of theoretical). Rate capability is excellent with 200 mAhg−1 at 3C. C-rate is discharge in 1 h. Polarization is low, 100 mV at C/2. To the best of our knowledge, the properties/performances of Li(V0.5Ti0.5)S2 exceed all previous 1 V electrodes. PMID:26996753

  17. In situ SEM Study of Lithium Intercalation in individual V2O5 Nanowires

    DOE PAGES

    Strelcov, Evgheni; Cothren, Joshua E.; Leonard, Donovan N.; ...

    2015-01-08

    Progress in rational engineering of Li-ion batteries requires better understanding of the electrochemical processes and accompanying transformations in the electrode materials on multiple length scales. In spite of recent progress in utilizing transmission electron microscopy (TEM) to analyze these materials, in situ scanning electron microscopy (SEM) was mostly overlooked as a powerful tool that allows probing these phenomena on the nano and mesoscale. In this paper, we report on in situ SEM study of lithiation in a V2O5-based single-nanobelt battery with ionic liquid electrolyte. Coupled with cyclic voltammetry measurements, in situ SEM revealed the peculiarities of subsurface intercalation, formation ofmore » solid-electrolyte interface (SEI) and electromigration of liquid. We observed that single-crystalline vanadia nanobelts do not undergo large-scale amorphization or fracture during electrochemical cycling, but rather transform topochemically with only a slight shape distortion. Lastly, the SEI layer seems to have significant influence on the lithium ion diffusion and overall capacity of the single-nanobelt battery.« less

  18. Ultrathin Li4Ti5O12 nanosheets as anode materials for lithium and sodium storage

    SciTech Connect

    Feng, Xuyong; Zou, Hailin; Xiang, Hongfa; Guo, Xin; Zhou, Tianpei; Wu, Yucheng; Xu, Wu; Yan, Pengfei; Wang, Chong M.; Zhang, Jiguang; Yu, Yan

    2016-06-13

    Two-dimensional Li4Ti5O12 (LTO) nanosheets are prepared via a surfactant assisted hydrothermal process. Polyether (P123) was added as the surfactant to modify the surface and control the microstructure of the hydrothermal products and thus affect the electrochemical performance of the as-synthesized LTO anode material. XRD results show that the addition of P123 can restrain the growth of Li2TiO3 during the hydrothermal process, thus affecting the morphology and enhancing the rate performance of the final products. With the addition of P123, the growth of LTO can be restrained and ultrathin LTO nanosheets can be obtained after high temperature sintering, which is beneficial for the charge transfer and Li+ ion diffusion. The rate performance of these two different LTO materials is very different because of their differences in phase composition and fine morphology. The P123-assisted nanostructured LTO sample (P-LTO) shows a much higher rate capability than the LTO sample without P123, with over 130 mAh g-1 capacity retained at the charge-discharge rate of 64C when used in a lithium battery. For intercalation of larger size Na+ ions, the P-LTO still exhibit a capacity of 115 mAh g-1 at a charge (de-sodiation process) rate of 10C and maintains 96% capacity after 400 cycles

  19. Lithium use in batteries

    USGS Publications Warehouse

    Goonan, Thomas G.

    2012-01-01

    Lithium has a number of uses but one of the most valuable is as a component of high energy-density rechargeable lithium-ion batteries. Because of concerns over carbon dioxide footprint and increasing hydrocarbon fuel cost (reduced supply), lithium may become even more important in large batteries for powering all-electric and hybrid vehicles. It would take 1.4 to 3.0 kilograms of lithium equivalent (7.5 to 16.0 kilograms of lithium carbonate) to support a 40-mile trip in an electric vehicle before requiring recharge. This could create a large demand for lithium. Estimates of future lithium demand vary, based on numerous variables. Some of those variables include the potential for recycling, widespread public acceptance of electric vehicles, or the possibility of incentives for converting to lithium-ion-powered engines. Increased electric usage could cause electricity prices to increase. Because of reduced demand, hydrocarbon fuel prices would likely decrease, making hydrocarbon fuel more desirable. In 2009, 13 percent of worldwide lithium reserves, expressed in terms of contained lithium, were reported to be within hard rock mineral deposits, and 87 percent, within brine deposits. Most of the lithium recovered from brine came from Chile, with smaller amounts from China, Argentina, and the United States. Chile also has lithium mineral reserves, as does Australia. Another source of lithium is from recycled batteries. When lithium-ion batteries begin to power vehicles, it is expected that battery recycling rates will increase because vehicle battery recycling systems can be used to produce new lithium-ion batteries.

  20. An unsymmetrical lithium-ion pathway between charge and discharge processes in a two-phase stage of Li4Ti5O12.

    PubMed

    Li, De; He, Ping; Li, Huiqiao; Zhou, Haoshen

    2012-07-07

    In this work, we investigated lithium-ion diffusion in spinel Li(4)Ti(5)O(12) nano-particles with carbon coating by electrochemical impedance spectroscopy (EIS), and proposed a hybrid model of the unsymmetrical lithium-ion pathway between charge and discharge processes. In this hybrid model, the charge process still follows the core-shell model, but in the discharge process, the phase transition evolves by growth of a few nuclei on the surface. And this hybrid model is possibly attributed to the nonuniform electron conductivity inside the Li(4)Ti(5)O(12) particles. Additionally, the relaxation process and the particle morphology are also carefully discussed in the experiment to show that this hybrid model is quite practical. Thereby, this investigation presents an unsymmetrical lithium-ion pathway in Li(4)Ti(5)O(12) particles, which could be extended to other active materials in lithium ion batteries.

  1. Nb{sub 2}O{sub 5} hollow nanospheres as anode material for enhanced performance in lithium ion batteries

    SciTech Connect

    Sasidharan, Manickam; Gunawardhana, Nanda; Yoshio, Masaki; Nakashima, Kenichi

    2012-09-15

    Graphical abstract: Nb{sub 2}O{sub 5} hollow nanosphere constructed electrode delivers high capacity of 172 mAh g{sup −1} after 250 cycles and maintains structural integrity and excellent cycling stability. Highlights: ► Nb{sub 2}O{sub 5} hollow nanospheres synthesis was synthesized by soft-template. ► Nb{sub 2}O{sub 5} hollow nanospheres were investigated as anode material in Li-ion battery. ► Nanostructured electrode delivers high capacity of 172 mAh g{sup −1} after 250 cycles. ► The electrode maintains the structural integrity and excellent cycling stability. ► Nanosized shell domain facilitates fast lithium intercalation/deintercalation. -- Abstract: Nb{sub 2}O{sub 5} hollow nanospheres of average diameter ca. ∼29 nm and hollow cavity size ca. 17 nm were synthesized using polymeric micelles with core–shell–corona architecture under mild conditions. The hollow particles were thoroughly characterized by transmission electron microscope (TEM), X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermal (TG/DTA) and nitrogen adsorption analyses. Thus obtained Nb{sub 2}O{sub 5} hollow nanospheres were investigated as anode materials for lithium ion rechargeable batteries for the first time. The nanostructured electrode delivers high capacity of 172 mAh g{sup −1} after 250 cycles of charge/discharge at a rate of 0.5 C. More importantly, the hollow particles based electrodes maintains the structural integrity and excellent cycling stability even after exposing to high current density 6.25 A g{sup −1}. The enhanced electrochemical behavior is ascribed to hollow cavity coupled with nanosized Nb{sub 2}O{sub 5} shell domain that facilitates fast lithium intercalation/deintercalation kinetics.

  2. Enhanced rate performance of molybdenum-doped spinel LiNi0.5Mn1.5O4 cathode materials for lithium ion battery

    NASA Astrophysics Data System (ADS)

    Yi, Ting-Feng; Chen, Bin; Zhu, Yan-Rong; Li, Xiao-Ya; Zhu, Rong-Sun

    2014-02-01

    The Mo-doped LiNi0.5Mn1.5O4 cathodes are successfully synthesized by citric acid-assisted sol-gel method. The result demonstrates that the Mo-doped LiMn1.4Ni0.55Mo0.05O4 cathodes present the improved electrochemical performance over pristine LiNi0.5Mn1.5O4. At the 2 C rate after 80 cycles, the discharge capacities are 68.5 mAh g-1 for the pristine LiNi0.5Mn1.5O4 material (53.9% of the capacity at 0.1 C), 107.4 mAh g-1 for the LiMn1.425Ni0.5Mo0.05O4 material (82.1% at 0.1 C), and 122.7 mAh g-1 for the LiMn1.4Ni0.55Mo0.05O4 material (90.5% at 0.1 C). Mo-doping is favorable for reducing the electrode polarization, suggesting that Mo-doped LiNi0.5Mn1.5O4 electrodes have faster lithium insertion/extraction kinetics during cycling. Mo-doped LiNi0.5Mn1.5O4 electrodes show lower charge-transfer resistance and higher lithium diffusion coefficients. In addition, LiMn1.4Ni0.55Mo0.05O4 cathode exhibits the smallest particle size, the lowest charge-transfer resistance and the highest lithium diffusion coefficient among all samples, indicating that it has a high reversibility and good rate capability.

  3. High Cycle Life Cathode for High Voltage (5V) Lithium Ion Batteries

    DTIC Science & Technology

    2010-12-16

    lithium cobalt phosphate (LiCoPO4) that provides higher energy density (15% > LiFePO4 demonstrated, up to 40% greater with further R&D). •The invention...standard LiFePO4 • Higher voltage at cell level may reduce number of cells required for application • Easy and inexpensive method to prepare • Offers safety

  4. V2O5-C-SnO2 Hybrid Nanobelts as High Performance Anodes for Lithium-ion Batteries

    PubMed Central

    Zhang, Linfei; Yang, Mingyang; Zhang, Shengliang; Wu, Zefei; Amini, Abbas; Zhang, Yi; Wang, Dongyong; Bao, Shuhan; Lu, Zhouguang; Wang, Ning; Cheng, Chun

    2016-01-01

    The superior performance of metal oxide nanocomposites has introduced them as excellent candidates for emerging energy sources, and attracted significant attention in recent years. The drawback of these materials is their inherent structural pulverization which adversely impacts their performance and makes the rational design of stable nanocomposites a great challenge. In this work, functional V2O5-C-SnO2 hybrid nanobelts (VCSNs) with a stable structure are introduced where the ultradispersed SnO2 nanocrystals are tightly linked with glucose on the V2O5 surface. The nanostructured V2O5 acts as a supporting matrix as well as an active electrode component. Compared with existing carbon-V2O5 hybrid nanobelts, these hybrid nanobelts exhibit a much higher reversible capacity and architectural stability when used as anode materials for lithium-ion batteries. The superior cyclic performance of VCSNs can be attributed to the synergistic effects of SnO2 and V2O5. However, limited data are available for V2O5-based anodes in lithium-ion battery design. PMID:27677326

  5. Electrochemical performance and kinetic behavior of lithium ion in Li4Ti5O12 thin film electrodes

    NASA Astrophysics Data System (ADS)

    Deng, Jianqiu; Lu, Zhouguang; Chung, C. Y.; Han, Xiaodong; Wang, Zhongmin; Zhou, Huaiying

    2014-09-01

    Li4Ti5O12 thin film electrodes are successfully deposited on Pt/Ti/SiO2/Si substrates by pulsed laser deposition (PLD) technique. The microstructure and morphology of Li4Ti5O12 thin films are characterized by XRD and ESEM. The electrochemical properties of Li4Ti5O12 thin film electrodes are evaluated by galvanostatic cycling test. The kinetic behavior of lithium ions in Li4Ti5O12 thin film electrodes is also conducted using cyclic voltammetry (CV), galvanostatic intermittent titration technique (GITT), and electrochemical impedance spectroscopy (EIS). Li4Ti5O12 thin film electrodes show favorable specific capacities and cycle performance. The chemical diffusion coefficients are found to be in a range of 10-15 to 10-12 cm2 s-1 determined by GITT method. The kinetic parameters obtained from impedance spectra as a function of the cell voltage are investigated in details. The decrease of the charge-transfer resistance (Rct) can be explained by the two-phase transition during lithium insertion into Li4Ti5O12.

  6. V2O5-C-SnO2 Hybrid Nanobelts as High Performance Anodes for Lithium-ion Batteries

    NASA Astrophysics Data System (ADS)

    Zhang, Linfei; Yang, Mingyang; Zhang, Shengliang; Wu, Zefei; Amini, Abbas; Zhang, Yi; Wang, Dongyong; Bao, Shuhan; Lu, Zhouguang; Wang, Ning; Cheng, Chun

    2016-09-01

    The superior performance of metal oxide nanocomposites has introduced them as excellent candidates for emerging energy sources, and attracted significant attention in recent years. The drawback of these materials is their inherent structural pulverization which adversely impacts their performance and makes the rational design of stable nanocomposites a great challenge. In this work, functional V2O5-C-SnO2 hybrid nanobelts (VCSNs) with a stable structure are introduced where the ultradispersed SnO2 nanocrystals are tightly linked with glucose on the V2O5 surface. The nanostructured V2O5 acts as a supporting matrix as well as an active electrode component. Compared with existing carbon-V2O5 hybrid nanobelts, these hybrid nanobelts exhibit a much higher reversible capacity and architectural stability when used as anode materials for lithium-ion batteries. The superior cyclic performance of VCSNs can be attributed to the synergistic effects of SnO2 and V2O5. However, limited data are available for V2O5-based anodes in lithium-ion battery design.

  7. Enhanced Lithium-Ion Intercalation Properties of V[subscript 2]O[subscript 5] Xerogel Electrodes with Surface Defects

    SciTech Connect

    Liu, Dawei; Liu, Yanyi; Pan, Anquiang; Nagle, Kenneth P.; Seidler, Gerald T.; Jeong, Yoon-Ha; Cao, Guozhong

    2011-09-15

    V{sub 2}O{sub 5} xerogel films were fabricated by casting V{sub 2}O{sub 5} sols onto fluorine-doped tin oxide (FTO) glass substrates and annealing at 300 C for 3 h in different annealing atmospheres of air and nitrogen. Films prepared in different annealing conditions possess different grain sizes and crystallinity, while the vanadium ion oxidation state also varies, as identified by X-ray absorption spectroscopy. A nitrogen annealing atmosphere induces the presence of defects, such as V{sup 4+} ions, and associated oxygen vacancies. Thus, the presence of defects, whether on the film surface or in the bulk, can be controlled by using air and nitrogen annealing atmospheres in the proper order. Electrochemical impedance analyses reveal enhanced charge-transfer conductivity in films with more V{sup 4+} and oxygen vacancies on the film surface, that is, a film annealed, first, for 0.5 h in air and then for 2.5 h in nitrogen. Lithium-ion intercalation measurements show that, at a charge/discharge current density of 600 mA g{sup -1}, this film possesses a noticeably better lithium-ion storage capability than films without surface defects. This sample starts with an initial discharge capacity of 139 mA h g{sup -1}, and the capacity increases slowly to a maximum value of 156 mA h g{sup -1} in the 15th cycle, followed by a mild capacity degradation in later cycles. After 50 cycles, the discharge capacity is still as high as 136 mA h g{sup -1}. A much improved lithium-ion intercalation capacity and cyclic stability are attributed to V{sup 4+} surface defects and associated oxygen vacancies introduced by N{sub 2} annealing.

  8. Lithium Inorganic Electrolyte Battery Development.

    DTIC Science & Technology

    1971-01-01

    rjp 3.2 PRISMATIC CELLS This subsection presents the results of the investigations conducted on large prismatic lithium thionyl chloride cells, both...91 5.0 PASSIVATION 5.1 INTRODUCTION Passivation in Li/SOC12 cells consists of the surface reaction of lithium directly with thionyl chloride to...produce a film of lithium chloride (LiCI). This film prevents the complete and rapid reaction of lithium and thionyl chloride at moderate temperatures. On

  9. Lithium ionic conduction and relaxation dynamics of spark plasma sintered Li5La3Ta2O12 garnet nanoceramics.

    PubMed

    Ahmad, Mohamad M

    2015-01-01

    In the present work, nanoceramics of Li5La3Ta2O12 (LLT) lithium ion conductors with the garnet-like structure are fabricated by spark plasma sintering (SPS) technique at different temperatures of 850°C, 875°C, and 900°C (SPS-850, SPS-875, and SPS-900). The grain size of the SPS nanoceramics is in the 50 to 100 nm range, indicating minimal grain growth during the SPS experiments. The ionic conduction and relaxation properties of the current garnets are studied by impedance spectroscopy (IS) measurements. The SPS-875 garnets exhibit the highest total Li ionic conductivity of 1.25 × 10(-6) S/cm at RT, which is in the same range as the LLT garnets prepared by conventional sintering technique. The high conductivity of SPS-875 sample is due to the enhanced mobility of Li ions by one order of magnitude compared to SPS-850 and SPS-900 ceramics. The concentration of mobile Li(+) ions, n c, and their mobility are estimated from the analysis of the conductivity spectra at different temperatures. n c is found to be independent of temperature for the SPS nanoceramics, which implies that the conduction process is controlled by the Li(+) mobility. Interestingly, we found that only a small fraction of lithium ions of 3.9% out of the total lithium content are mobile and contribute to the conduction process. Moreover, the relaxation dynamics in the investigated materials have been studied through the electric modulus formalism.

  10. Cu doped V2O5 flowers as cathode material for high-performance lithium ion batteries.

    PubMed

    Yu, Hong; Rui, Xianhong; Tan, Huiteng; Chen, Jing; Huang, Xin; Xu, Chen; Liu, Weiling; Yu, Denis Y W; Hng, Huey Hoon; Hoster, Harry E; Yan, Qingyu

    2013-06-07

    Hierarchical Cu doped vanadium pentoxide (V2O5) flowers were prepared via a simple hydrothermal approach followed by an annealing process. The flower precursors are self-assembled with 1D nanobelts surrounding a central core. The morphological evolution is investigated and a plausible mechanism is proposed. As the cathode material for lithium ion batteries, the Cu doped V2O5 samples exhibit improved electrochemical performance compared to the un-doped ones. Among them Cu0.02V1.98O5 delivered higher reversible specific capacities, better cycling stabilities and excellent rate capabilities, e.g. 97 mA h g(-1) at 20.0 C.

  11. Gold coating for a high performance Li4Ti5O12 nanorod aggregates anode in lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Wang, Wei; Guo, Yuanyuan; Liu, Lixiang; Wang, Shixiong; Yang, Xiangjun; Guo, Hong

    2014-01-01

    An effective strategy by combination of alcoholysis, solid-state reaction and coating techniques is employed to prepare Au@Li4Ti5O12 nanorod aggregates as anode materials for Li-ion batteries. The lithium diffusion coefficient of resulting Au@Li4Ti5O12 is 7.32 × 10-10 cm2 s-1, and its stable reversible capacity is 169 mAh g-1 with the retention of 91.1% after 100 cycles at 5 C. Moreover, it also exhibits excellent rate-capability performance. The superior cycling performance can be attributed to the unique nanorod characteristics, structural stability, and the improved ionic and electronic conduction in the electrode due to the uniform nano coating of Au.

  12. Graphene wrapped ordered LiNi0.5Mn1.5O4 nanorods as promising cathode material for lithium-ion batteries

    PubMed Central

    Tang, Xiao; Jan, S. Savut; Qian, Yanyan; Xia, Hui; Ni, Jiangfeng; Savilov, Serguei V.; Aldoshin, Serguei M.

    2015-01-01

    LiNi0.5Mn1.5O4 nanorods wrapped with graphene nanosheets have been prepared and investigated as high energy and high power cathode material for lithium-ion batteries. The structural characterization by X-ray diffraction, Raman spectroscopy, and Fourier transform infrared spectroscopy indicates the LiNi0.5Mn1.5O4 nanorods prepared from β-MnO2 nanowires have ordered spinel structure with P4332 space group. The morphological characterization by scanning electron microscopy and transmission electron microscopy reveals that the LiNi0.5Mn1.5O4 nanorods of 100–200 nm in diameter are well dispersed and wrapped in the graphene nanosheets for the composite. Benefiting from the highly conductive matrix provided by graphene nanosheets and one-dimensional nanostructure of the ordered spinel, the composite electrode exhibits superior rate capability and cycling stability. As a result, the LiNi0.5Mn1.5O4-graphene composite electrode delivers reversible capacities of 127.6 and 80.8 mAh g−1 at 0.1 and 10 C, respectively, and shows 94% capacity retention after 200 cycles at 1 C, greatly outperforming the bare LiNi0.5Mn1.5O4 nanorod cathode. The outstanding performance of the LiNi0.5Mn1.5O4-graphene composite makes it promising as cathode material for developing high energy and high power lithium-ion batteries. PMID:26148558

  13. Depth profiling the solid electrolyte interphase on lithium titanate (Li4Ti5O12) using synchrotron-based photoelectron spectroscopy

    NASA Astrophysics Data System (ADS)

    Nordh, Tim; Younesi, Reza; Brandell, Daniel; Edström, Kristina

    2015-10-01

    The presence of a surface layer on lithium titanate (Li4Ti5O12, LTO) anodes, which has been a topic of debate in scientific literature, is here investigated with tunable high surface sensitive synchrotron-based photoelectron spectroscopy (PES) to obtain a reliable depth profile of the interphase. Li||LTO cells with electrolytes consisting of 1 M lithium hexafluorophosphate dissolved in ethylene carbonate:diethyl carbonate (LiPF6 in EC:DEC) were cycled in two different voltage windows of 1.0-2.0 V and 1.4-2.0 V. LTO electrodes were characterized after 5 and 100 cycles. Also the pristine electrode as such, and an electrode soaked in the electrolyte were analyzed by varying the photon energies enabling depth profiling of the outermost surface layer. The main components of the surface layer were found to be ethers, P-O containing compounds, and lithium fluoride.

  14. Crystallographic origin of cycle decay of the high-voltage LiNi0.5Mn1.5O4 spinel lithium-ion battery electrode.

    PubMed

    Pang, Wei Kong; Lu, Cheng-Zhang; Liu, Chia-Erh; Peterson, Vanessa K; Lin, Hsiu-Fen; Liao, Shih-Chieh; Chen, Jin-Ming

    2016-06-29

    High-voltage spinel LiNi0.5Mn1.5O4 (LNMO) is considered a potential high-power-density positive electrode for lithium-ion batteries, however, it suffers from capacity decay after extended charge-discharge cycling, severely hindering commercial application. Capacity fade is thought to occur through the significant volume change of the LNMO electrode occurring on cycling, and in this work we use operando neutron powder diffraction to compare the structural evolution of the LNMO electrode in an as-assembled 18650-type battery containing a Li4Ti5O12 negative electrode with that in an identical battery following 1000 cycles at high-current. We reveal that the capacity reduction in the battery post cycling is directly proportional to the reduction in the maximum change of the LNMO lattice parameter during its evolution. This is correlated to a corresponding reduction in the MnO6 octahedral distortion in the spinel structure in the cycled battery. Further, we find that the rate of lattice evolution, which reflects the rate of lithium insertion and removal, is ∼9 and ∼10% slower in the cycled than in the as-assembled battery during the Ni(2+)/Ni(3+) and Ni(3+)/Ni(4+) transitions, respectively.

  15. Facile synthesis of hydroxy-modified MOF-5 for improving the adsorption capacity of hydrogen by lithium doping.

    PubMed

    Kubo, Masaru; Hagi, Hayato; Shimojima, Atsushi; Okubo, Tatsuya

    2013-11-01

    A facile synthesis of partially hydroxy-modified MOF-5 and its improved H2-adsorption capacity by lithium doping are reported. The reaction of Zn(NO3)2·6H2O with a mixture of terephthalic acid (H2BDC) and 2-hydroxyterephthalic acid (H2BDC-OH) in DMF gave hydroxy-modified MOF-5 (MOF-5-OH-x), in which the molar fraction (x) of BDC-OH(2-) was up to 0.54 of the whole ligand. The MOF-5-OH-x frameworks had high BET surface areas (about 3300 m(2) g(-1)), which were comparable to that of MOF-5. We suggest that the MOF-5-OH-x frameworks are formed by the secondary growth of BDC(2-)-rich MOF-5 seed crystals, which are nucleated during the early stage of the reaction. Subsequent Li doping into MOF-5-OH-x results in increased H2 uptake at 77 K and 0.1 MPa from 1.23 to 1.39 wt.% and an increased isosteric heat of H2 adsorption from 5.1-4.2 kJ mol(-1) to 5.5-4.4 kJ mol(-1).

  16. Template-free synthesis of highly porous V2O5 cuboids with enhanced performance for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Zhang, Cheng; Fang, Guozhao; Liang, Caiwu; Zhou, Jiang; Tan, Xiaoping; Pan, Anqiang; Liang, Shuquan

    2016-07-01

    Highly porous hierarchical V2O5 cuboids have been synthesized by a template-free PVP-assisted polyxol method and the formation mechanism is studied. The cuboids are assembled from numerous mesoporous nanoplates and the preferred orientation of each single nanoplate exposes the <110> facets, facilitating lithium-ion diffusion by offering a prior channel. This material exhibits a high capacity of 143 mA h g-1, high rate capacity of 10 C and long life cycling performance up to 1000 cycles. The excellent electrochemical performance of V2O5 cuboid electrodes is due to its unique porous cuboid morphology and optimized structural stability upon cycling. This research provides an effective route to the construction of complex porous architectures assembled from nanocrystals through a surfactant-assisted synthesis method.

  17. Neuroprotective effects of chronic exposure of SH-SY5Y to low lithium concentration involve glycolysis stimulation, extracellular pyruvate accumulation and resistance to oxidative stress.

    PubMed

    Nciri, Riadh; Desmoulin, Frank; Allagui, Mohamed Saleh; Murat, Jean-Claude; Feki, Abdelfattah El; Vincent, Christian; Croute, Françoise

    2013-03-01

    Recent studies suggest that lithium protects neurons from death induced by a wide array of neurotoxic insults, stimulates neurogenesis and could be used to prevent age-related neurodegenerative diseases. In this study, SH-SY5Y human neuronal cells were cultured in the absence (Con) or in the presence (Li+) of a low lithium concentration (0.5 mm Li2CO3, i.e. 1 mm lithium ion) for 25-50 wk. In the course of treatment, growth rate of Con and Li+ cells was regularly analysed using Alamar Blue dye. Resistance to oxidative stress was investigated by evaluating: (1) the adverse effects of high concentrations of lithium (4-8 mm) or glutamate (20-90 mm) on cell growth rate; (2) the levels of lipid peroxidation (TBARS) and total glutathione; (3) the expression levels of the anti-apoptotic Bcl-2 protein. In addition, glucose metabolism was investigated by analysing selected metabolites in culture media and cell extracts by 1H-NMR spectroscopy. As compared to Con, Li+ cells multiplied faster and were more resistant to stress, as evidenced by a lower dose-dependent decrease of Alamar Blue reduction and dose-dependent increase of TBARS levels induced by toxic doses of lithium and glutamate. Total glutathione content and Bcl-2 level were increased in Li+ cells. Glucose consumption and glycolytic activity were enhanced in Li+ cells and an important release of pyruvate was observed. We conclude that chronic exposure to lithium induces adaptive changes in metabolism of SH-SY5Y cells involving a higher cell growth rate and a better resistance to oxidative stress.

  18. Ab initio study of radiation effects on the Li{sub 4}Ti{sub 5}O{sub 12} electrode used in lithium-ion batteries

    SciTech Connect

    Samin, Adib E-mail: cao.152@osu.edu; Kurth, Michael; Cao, Lei E-mail: cao.152@osu.edu

    2015-04-15

    Lithium-ion batteries are currently in wide use owing to their high energy density and enhanced capabilities. Li{sub 4}Ti{sub 5}O{sub 12} is a promising anode material for lithium-ion batteries because of its advantageous properties. Lithium-ion batteries could be exposed to radiation occurring in various conditions such as during outer space exploration and nuclear accidents. In this study, we apply density functional theory to explore the effect of radiation damage on this electrode and, ultimately, on the performance of the battery. It was found that radiation could affect the structural stability of the material. Furthermore, the electrode was shown to undergo a transition from insulator to metal, following the defects due to radiation. In addition, the effect of radiation on the intercalation potential was found to be highly dependent on the nature of the defect induced.

  19. Nano crystalline Bi2(VO5) phases in lithium bismuth borate glasses containing mixed vanadium-nickel oxides

    NASA Astrophysics Data System (ADS)

    Yadav, Arti; Khasa, S.; Dahiya, M. S.; Agarwal, A.

    2016-05-01

    Glass composition 7V2O5.23Li2O.20Bi2O3.50B2O3 and x(2NiO.V2O5).(30-x)Li2O.20Bi2O3.50B2O3, x=0, 2, 5, 7 and 10, were produced by conventional melt quenching technique. The quenched amorphous glass samples were annealed at temperatures 400°C and 500°C for 6 hours. The Bi2(VO5) crystallite were grown in all prepared glass matrix. Tn vanadium lithium bismuth borate glass (annealed), the some phrase of V2O5-crystal were observed along with the nano crystalline Bi2(VO5) phase. The sharp peaks in FTTR spectra of all annealed compositions were also compatible with the XRD diffraction peaks of the system under investigation. Average crystalline size (D) of the Bi2(VO5) nano-crystallite was ~30nm for samples annealed at 400°C and ~42nm for samples annealed at 500°C. Lattice parameter and the lattice strain for all the samples was also calculated corresponding to the (113) plane of Bi2(VO5) crystallite.

  20. Heterogeneous TiO2/V2O5/Carbon Nanotube Electrodes for Lithium-Ion Batteries.

    PubMed

    Kurttepeli, Mert; Deng, Shaoren; Mattelaer, Felix; Cott, Daire J; Vereecken, Philippe; Dendooven, Jolien; Detavernier, Christophe; Bals, Sara

    2017-03-08

    Vanadium pentoxide (V2O5) is proposed and investigated as a cathode material for lithium-ion (Li-ion) batteries. However, the dissolution of V2O5 during the charge/discharge remains as an issue at the V2O5-electrolyte interface. In this work, we present a heterogeneous nanostructure with carbon nanotubes supported V2O5/titanium dioxide (TiO2) multilayers as electrodes for thin-film Li-ion batteries. Atomic layer deposition of V2O5 on carbon nanotubes provides enhanced Li storage capacity and high rate performance. An additional TiO2 layer leads to increased morphological stability and in return higher electrochemical cycling performance of V2O5/carbon nanotubes. The physical and chemical properties of TiO2/V2O5/carbon nanotubes are characterized by cyclic voltammetry and charge/discharge measurements as well as electron microscopy. The detailed mechanism of the protective TiO2 layer to improve the electrochemical cycling stability of the V2O5 is unveiled.

  1. Investigating the all-solid-state batteries based on lithium garnets and a high potential cathode - LiMn1.5Ni0.5O4.

    PubMed

    Hänsel, Christian; Afyon, Semih; Rupp, Jennifer L M

    2016-11-03

    All-solid-state Li-ion batteries based on lithium garnets give new prospects for safer battery operations avoiding liquids, and could enable the integration of high energy density electrode materials. Herein, we critically investigate the structural and chemical stability of the high voltage cathode material, LiMn1.5Ni0.5O4, based on the solid lithium garnet electrolyte LLZO (c-Li6.4Ga0.2La3Zr2O12) for all-solid Li-ion batteries. We manufacture battery cells based on nano-grained synthesized LLZO and composite cathodes (LiMn1.5Ni0.5O4/LLZO/C) fabricated via direct slurry casting of the cathode material and additives on sintered LLZO pellets against metallic Li anodes. The galvanostatic tests of such all-solid-state batteries up to 4.9 V at 95 °C reveal the incompatibility of the solid electrolyte and the cathode material under given conditions. Post-mortem analyses of the all-solid-state batteries demonstrate the formation of new inactive phases at the LLZO/LiMn1.5Ni0.5O4 interfacial region through an irreversible reaction starting at ∼3.8 V during charging. The discovered limited chemical stability under the investigated conditions raises the question if LLZO could be a promising solid-electrolyte for future all-solid-state Li-ion batteries especially at higher operation potentials and demanding operation conditions.

  2. Oxygen-participated electrochemistry of new lithium-rich layered oxides Li3MRuO5 (M = Mn, Fe).

    PubMed

    Laha, S; Natarajan, S; Gopalakrishnan, J; Morán, E; Sáez-Puche, R; Alario-Franco, M Á; Dos Santos-Garcia, A J; Pérez-Flores, J C; Kuhn, A; García-Alvarado, F

    2015-02-07

    We describe the synthesis, crystal structure and lithium deinsertion-insertion electrochemistry of two new lithium-rich layered oxides, Li3MRuO5 (M = Mn, Fe), related to rock salt based Li2MnO3 and LiCoO2. The Li3MnRuO5 oxide adopts a structure related to Li2MnO3 (C2/m) where Li and (Li0.2Mn0.4Ru0.4) layers alternate along the c-axis, while the Li3FeRuO5 oxide adopts a near-perfect LiCoO2 (R3[combining macron]m) structure where Li and (Li0.2Fe0.4Ru0.4) layers are stacked alternately. Magnetic measurements indicate for Li3MnRuO5 the presence of Mn(3+) and low spin configuration for Ru(4+) where the itinerant electrons occupy a π*-band. The onset of a net maximum in the χ vs. T plot at 9.5 K and the negative value of the Weiss constant (θ) of -31.4 K indicate the presence of antiferromagnetic superexchange interactions according to different pathways. Lithium electrochemistry shows a similar behaviour for both oxides and related to the typical behaviour of Li-rich layered oxides where participation of oxide ions in the electrochemical processes is usually found. A long first charge process with capacities of 240 mA h g(-1) (2.3 Li per f.u.) and 144 mA h g(-1) (1.38 Li per f.u.) is observed for Li3MnRuO5 and Li3FeRuO5, respectively. An initial sloping region (OCV to ca. 4.1 V) is followed by a long plateau (ca. 4.3 V). Further discharge-charge cycling points to partial reversibility (ca. 160 mA h g(-1) and 45 mA h g(-1) for Mn and Fe, respectively). Nevertheless, just after a few cycles, cell failure is observed. X-ray photoelectron spectroscopy (XPS) characterisation of both pristine and electrochemically oxidized Li3MRuO5 reveals that in the Li3MnRuO5 oxide, Mn(3+) and Ru(4+) are partially oxidized to Mn(4+) and Ru(5+) in the sloping region at low voltage, while in the long plateau, O(2-) is also oxidized. Oxygen release likely occurs which may be the cause for failure of cells upon cycling. Interestingly, some other Li-rich layered oxides have been reported to

  3. Aqueous chemistry of lithium hydroxide and boric acid and corrosion of Zircaloy-4 and Zr-2.5Nb alloys

    SciTech Connect

    Ramasubramanian, N.; Balakrishnan, P.V.

    1994-12-31

    The chemistry of the aqueous solution, surface chemistry of zirconium oxide (ZrO{sub 2}), and the physical structure of the corrosion film have to be considered for an understanding of the mechanism of corrosion of zirconium alloys in aqueous solutions. Based on information available in all these areas, the authors are proposing a model for oxide growth on Zircaloy-4 fuel cladding and Zr-2.5Nb pressure tube material, in lithium hydroxide (LiOH) solutions with and without added boric acid (H{sub 3}BO{sub 3}). Corrosion exposures were at 360 C and were short term of four-day duration. Concentration of lithium covered the range 0.7 to 3,500 ppm and boron was added at 300, 600 and 1,200 ppm. Weight gain, Fourier Transform InfraRed (FTIR) spectroscopy, and Secondary ion Mass Spectrometry (SIMS) were used to characterize the oxide films. Potentiodynamic polarization measurements were made in separate tests at 315 C. The chemistry of LiOH-H{sub 3}BO{sub 3} system at 300 to 360 C was evaluated from the ionization constants of water, LiOH, and H{sub 3}BO{sub 3}. There is no simple relationship between pH and corrosion. In the absence of boron acceleration in corrosion, in these short-term tests, is observed at concentrations >350 ppm Li for Zircaloy-4 and at >60 ppm Li for Zr-2.5Nb. According to the model proposed for oxide growth, the corrosion behavior can be classified into two categories: (1) growth of post-transition type films under acceleration conditions where solution had access into the oxide and (2) growth of pre-transition films under non-acceleration conditions where the solution had not gained access into the oxide.

  4. Research Progress in Improving the Cycling Stability of High-Voltage LiNi0.5Mn1.5O4 Cathode in Lithium-Ion Battery

    NASA Astrophysics Data System (ADS)

    Xu, XiaoLong; Deng, SiXu; Wang, Hao; Liu, JingBing; Yan, Hui

    2017-04-01

    High-voltage lithium-ion batteries (HVLIBs) are considered as promising devices of energy storage for electric vehicle, hybrid electric vehicle, and other high-power equipment. HVLIBs require their own platform voltages to be higher than 4.5 V on charge. Lithium nickel manganese spinel LiNi0.5Mn1.5O4 (LNMO) cathode is the most promising candidate among the 5 V cathode materials for HVLIBs due to its flat plateau at 4.7 V. However, the degradation of cyclic performance is very serious when LNMO cathode operates over 4.2 V. In this review, we summarize some methods for enhancing the cycling stability of LNMO cathodes in lithium-ion batteries, including doping, cathode surface coating, electrolyte modifying, and other methods. We also discuss the advantages and disadvantages of different methods.

  5. Role of V2O5 coating on LiNiO2-based materials for lithium ion battery

    NASA Astrophysics Data System (ADS)

    Xiong, Xunhui; Wang, Zhixing; Yan, Guochun; Guo, Huajun; Li, Xinhai

    2014-01-01

    X-ray diffraction (XRD), transmission electron microscope (TEM), energy dispersive spectrometer (EDX) and X-ray photoelectron spectroscopy (XPS) are used to demonstrate that V2O5 is successfully coated on LiNiO2-based materials. The V2O5 layer will react with Li impurities on surface, which will reduce the pH value and rapid moisture uptake ability of LiNiO2-based materials. Cells tests indicate that V2O5-coating layer works as HF inhibitor and/or HF scavenger, which contributes a significant improvement in cycling performance and storage characteristics in electrolyte. In the mean time, V2O5 acts as isolating layer when cathode material contacts with electrolyte especially cycling at high voltage. Structural analysis shows that V2O5-coating layer has more advantage over other oxide coating in delaying Ni3+/Ni2+ transformation and lithium extraction from bulk surface, which benefits from the properties of V2O5 reacting with LiOH/Li2CO3 impurities on surface.

  6. Investigation of Lithium Ion Storage

    NASA Technical Reports Server (NTRS)

    Lee, Leonine; Rao, Gopalkrishna M.

    1999-01-01

    NASA/GSFC is interested in flying lithium ion cells for geosynchronous earth orbit (GEO) satellites. To determine the preferred solstice storage conditions for the lithium ion chemistry, we have been studying either a constant current storage with a maximum voltage clamp or storage with only a voltage clamp. The cells used for this study are two 4Ah SAFT cylindrical lithium ion cells, two 1.5Ah Wilson Great Batch lithium ion cells, and one 8Ah Lithium Technology lithium polymer cell. In each pair, one cell is clamped at 4V, and the other is trickle charged at C/500 with a 4.lV clamp. The Lithium Technology cell is only undergoing voltage clamped storage testing. After each storage period the cells are subjected to a capacity test (C/2 discharge, C/10 charge) and a charge retention test at room temperature. Results after 4 weeks and 8 weeks of storage testing will be presented here.

  7. Temperature-dependent oxygen behavior of LixNi0.5Mn1.5O4 cathode material for lithium battery

    NASA Astrophysics Data System (ADS)

    Choi, Hyun Woo; Kim, Su Jae; Jeong, Myung Yung; Lee, Seongsu; Rim, Young Hoon; Yang, Yong Suk

    2016-11-01

    We have investigated the temperature-dependent oxygen behavior in the lithium battery cathode LixNi0.5Mn1.5O4 (LNMO) materials in the temperature range 30-1000 °C. As the temperature increases, oxygen release occurs and the change of crystal structures from the face centered cubic spinel at 30 °C to other phases follows. The amount of released oxygen and the changed crystalline phases are dependent on Li content and temperature. These phenomena are reversible against temperature in air, but not in vacuum and argon gas environments. This study illustrates the important role of temperature and atmospheric environments in synthesizing the LNMO battery materials.

  8. Controllable Preparation of V2O5/Graphene Nanocomposites as Cathode Materials for Lithium-Ion Batteries

    NASA Astrophysics Data System (ADS)

    Liu, Yanglin; Wang, Yaping; Zhang, Yifang; Liang, Shuquan; Pan, Anqiang

    2016-12-01

    Transition metal oxides and graphene composites have been widely reported in energy storage and conversion systems. However, the controllable synthesis of graphene-based nanocomposites with tunable morphologies is far less reported. In this work, we report the fabrication of V2O5 and reduced graphene oxide composites with nanosheet or nanoparticle-assembled subunits by adjusting the solvothermal solution. As cathode materials for lithium-ion batteries, the nanosheet-assembled V2O5/graphene composite exhibits better rate capability and long-term cycling stability. The V2O5/graphene composites can deliver discharge capacities of 133, 131, and 122 mAh g-1 at 16 C, 32 C, and 64 C, respectively, in the voltage range of 2.5-4.0 V vs. Li/Li+. Moreover, the electrodes can retain 85% of their original capacity at 1C rate after 500 cycles. The superior electrochemical performances are attributed to the porous structures created by the connected V2O5 nanosheets and the electron conductivity improvement by graphene.

  9. Computational study of structural, elastic and electronic properties of lithium disilicate (Li(2)Si(2)O(5)) glass-ceramic.

    PubMed

    Biskri, Zine Elabidine; Rached, Habib; Bouchear, Merzoug; Rached, Djamel

    2014-04-01

    The objective of this study is to investigate theoretically the structural, elastic and electronic properties of Lithium Disilicate (LD) crystal (Li2Si2O5), using the pseudo potential method based on Density Functional Theory (DFT) with the Local Density Approximation (LDA) and the Generalized Gradient Approximation (GGA). The calculated structural properties namely the equilibrium lattice parameters and cell volume are in good agreement with the available experimental results. However, for the LD crystal elastic moduli: Shear modulus G, Young's modulus E and Poisson's ratio ν we have found a discrepancy between our theoretical values and experimental ones reported in polycrystalline sample containing LD crystals. The calculated elastic properties show that LD is more rigid compared with other components. We also investigated the mechanical stability of Li2Si2O5 compound and we have noticed that this compound is stable against elastic deformations. On the basis of shear to bulk modulus ratio analysis, we inferred that Li2Si2O5 compound is brittle in nature. In order to complete the fundamental characteristics of this compound we have measured the elastic anisotropy. Our results for the energy band structure and Density of States (DOS) show that Li2Si2O5 compound has an insulator characteristic.

  10. Lithium Combustion: A Review

    DTIC Science & Technology

    1990-12-01

    lithium vapors generated with air formed an intense white flame that produced branched- chain condensation aerosol particles, of concentrations 򓆄 mg/im3...generated chain -aggregate lithium combustion aerosols in dry, COg-free air prior to reaction with 0, 0.10, 0.50, 1.0, 1.75, or 5.0% CO in air at a...In order to burn in gaseous chlorine or in bromine or iodine vapor, lithium needs to be heated. With iodine vapor, the reaction is accompanied by

  11. Lithium cell test results

    NASA Technical Reports Server (NTRS)

    Bragg, B. J.

    1977-01-01

    Three lithium SO2 cells, two lithium CF cells, and a vinyl chloride cell, all with crimped seals, and all strictly experimental, were independently discharged on resistors. Three temperatures were used and several different storage temperatures. Discharge rate generally on the nominal discharges were 0.1 amp, 0.5 amp, and 1 amp. Tests results show that the crimp seals are inadequate, especially for the SO2 cells. Normal discharges present no hazards. All cells discharge to zero. The problem of lithium cell explosions, such as occurred during off-limits testing, is discussed.

  12. Investigation on preparation and performance of spinel LiNi0.5Mn1.5O4 with different microstructures for lithium-ion batteries.

    PubMed

    Xue, Yuan; Wang, Zhenbo; Zheng, Lili; Yu, Fuda; Liu, Baosheng; Zhang, Yin; Ke, Ke

    2015-08-24

    The high voltage spinel LiNi0.5Mn1.5O4 is a promising cathode material in next generation of lithium ion batteries. In this study, LiNi0.5Mn1.5O4 with various particle microstructures are prepared by controlling the microstructures of precursors. LiNi0.5Mn1.5O4 spinel samples with solid, hollow and hierarchical microstructures are prepared with solid MnCO3, hollow MnO2 and hierarchical Mn2O3 as precursor, respectively. The homemade spinel materials are investigated and the results show that the content of Mn(3+) and impurity phase differ much in these three spinel samples obtained under the same calcining and annealing conditions. It is revealed for the first time that an inhomogeneous migration of atoms may introduce Mn(3+) and impurity phase in the spinel. The hierarchical microstructure with the primary particles interconnected is optimal for electrode materials because this microstructure has a higher conductivity between the interconnected primary particles and appropriate specific surface area. LiNi0.5Mn1.5O4 in this microstructure has the best rate capability and also the best long-term cycling stability.

  13. Na0.282V2O5: A high-performance cathode material for rechargeable lithium batteries and sodium batteries

    NASA Astrophysics Data System (ADS)

    Cai, Yangsheng; Zhou, Jiang; Fang, Guozhao; Cai, Gemei; Pan, Anqiang; Liang, Shuquan

    2016-10-01

    Na0.282V2O5 nanorods have been successfully prepared using a facile hydrothermal reaction followed by a calcination treatment, which is then used as a cathode for lithium batteries and sodium batteries for the first time. The crystal structure is refined to be a monoclinic lattice, which contains 3D tunnels along the b-axis. The Na ions are located inside the tunnels and form "pillar effect" to prevent the collapse of the crystal structure. As cathode material for lithium batteries, the Na0.282V2O5 nanorods deliver a high discharge specific capacity of 264, 186, 191 and 149 mA h g-1 at the current density of 50, 500, 1000 and 1500 mA g-1, respectively. The Na0.282V2O5 nanorods demonstrate the excellent cycling performance up to 400 cycles at 1 and 1.5 A g-1. Importantly, as cathode material for sodium batteries, Na0.282V2O5 exhibits superior long-term cyclic stability up to 1000 cycles at 0.3 A g-1. The results of ex-situ XRD, EIS and first-principle calculation indicate that the Na0.282V2O5 possesses good electrical conductivity and structural stability. Our work demonstrates that the Na0.282V2O5 material could be considered as a potential cathode for lithium-ion batteries, and even sodium ion batteries.

  14. Khalil Amine on Lithium-air Batteries

    SciTech Connect

    Khalil Amine

    2009-09-14

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

  15. Michael Thackeray on Lithium-air Batteries

    ScienceCinema

    Thackeray, Michael

    2016-07-12

    Michael Thackeray, Distinguished Fellow at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries.

  16. Khalil Amine on Lithium-air Batteries

    ScienceCinema

    Khalil Amine

    2016-07-12

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

  17. Hydrogen, lithium, and lithium hydride production

    DOEpatents

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

    2014-03-25

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

  18. Carbon coating of Li4Ti5O12 using amphiphilic carbonaceous material for improvement of lithium-ion battery performance

    NASA Astrophysics Data System (ADS)

    Guo, Xuefei; Wang, Chengyang; Chen, Mingming; Wang, Jiuzhou; Zheng, Jiaming

    2012-09-01

    Carbon coating of fine particles of Li4Ti5O12 synthesized under hydrothermal condition is carried out by amphiphilic carbonaceous material (ACM) in aqueous solution, followed by carbonization at 800 °C for 2 h. The particles prepared are comprised of highly-crystalline spinel-type Li4Ti5O12 with the size in the range of 100-400 nm without any agglomeration, of which surface is uniformly covered by a thin carbon layer. Their electrochemical performance as an anode in lithium-ion batteries is evaluated. The initial discharge capacity of carbon-coated Li4Ti5O12 at 20 C rate is 137 mA h g-1 and remains as high as 125 mA h g-1 after 100 cycles (91% retention), exhibiting good rate and cyclic performance. Carbon coating by using ACM as carbon precursor gives the Li4Ti5O12 particles an enhanced performance as an anode in lithium-ion batteries, owing to the improvement in electrical conductivity, polarization and ability of dispersion. This non-organic coating process may present a new economic, facile, and green pathway for the preparation of carbon-coated Li4Ti5O12 as a high power anode material in lithium-ion batteries.

  19. Lithium and Autophagy

    PubMed Central

    2014-01-01

    Lithium, a drug used to treat bipolar disorders, has a variety of neuroprotective mechanisms, including autophagy regulation, in various neuropsychiatric conditions. In neurodegenerative diseases, lithium enhances degradation of aggregate-prone proteins, including mutated huntingtin, phosphorylated tau, and α-synuclein, and causes damaged mitochondria to degrade, while in a mouse model of cerebral ischemia and Alzheimer’s disease autophagy downregulation by lithium is observed. The signaling pathway of lithium as an autophagy enhancer might be associated with the mammalian target of rapamycin (mTOR)-independent pathway, which is involved in myo-inositol-1,4,5-trisphosphate (IP3) in Huntington’s disease and Parkinson’s disease. However, the mTOR-dependent pathway might be involved in inhibiting glycogen synthase kinase-3β (GSK3β) in other diseases. Lithium’s autophagy-enhancing property may contribute to the therapeutic benefit of patients with neuropsychiatric disorders. PMID:24738557

  20. Observation of lithium pick-up ions in the 5- to 20-keV energy range following the AMPTE solar wind releases

    SciTech Connect

    Moebius, E.; Hovestadt, D.; Klecker, B.; Scholer, M.; Gloeckler, G.; Ipavich, F.M.; Luehr, H.

    1986-02-01

    Newly created 5- to 20-keV lithium ions were observed for limited time periods following the first Active Magnetospheric Particle Tracer Explorers (AMPTE) lithium release in the solar wind on September 11, 1984. The detection of these so-called ''pick-up'' ions by the time-of-flight spectrometer SULEICA (suprathermal energy ionic charge analyzer) on the AMPTE/IRM satellite depends critically on the orientation of the interplanetary magnetic field with respect to the directions of the solar wind and the spin axis of the IRM spacecraft, which was favorable only during the short time when these ions were seen. Our observations are compatible with a shell-like expansion of the Li cloud with velocities of about 2.5 km/s. The signatures by which the artificial pick-up ions are identified can also be used to detect and investigate natural pick-up ions.

  1. A 3.5 V lithium-iodine hybrid redox battery with vertically aligned carbon nanotube current collector.

    PubMed

    Zhao, Yu; Hong, Misun; Bonnet Mercier, Nadège; Yu, Guihua; Choi, Hee Cheul; Byon, Hye Ryung

    2014-02-12

    A lithium-iodine (Li-I2) cell using the triiodide/iodide (I3(-)/I(-)) redox couple in an aqueous cathode has superior gravimetric and volumetric energy densities (∼ 330 W h kg(-1) and ∼ 650 W h L(-1), respectively, from saturated I2 in an aqueous cathode) to the reported aqueous Li-ion batteries and aqueous cathode-type batteries, which provides an opportunity to construct cost-effective and high-performance energy storage. To apply this I3(-)/I(-) aqueous cathode for a portable and compact 3.5 V battery, unlike for grid-scale storage as general target of redox flow batteries, we use a three-dimensional and millimeter thick carbon nanotube current collector for the I3(-)/I(-) redox reaction, which can shorten the diffusion length of the redox couple and provide rapid electron transport. These endeavors allow the Li-I2 battery to enlarge its specific capacity, cycling retention, and maintain a stable potential, thereby demonstrating a promising candidate for an environmentally benign and reusable portable battery.

  2. Monodispersed Li4Ti5O12 with Controlled Morphology as High Power Lithium Ion Battery Anodes

    DOE PAGES

    Li, Yunchao; Fu, Guoyi; Watson, Mark; ...

    2016-05-31

    Monodispersed Li4Ti5O12 (LTO) nanoparticles with controlled microstructure were successfully synthesized by a combination of hydrolysis and hydrothermal method followed by a post-annealing process. The scanning electron microscopy images showed that particles with a size of 30-40 nm were precisely controlled throughout the synthesis process. The electrochemical tests of the as-prepared LTO electrodes in a half-cell proved its high rate performance and outstanding cyclability which benefits from the preserved well-controlled nanoparticle size and morphology. LTO electrodes were also tested in a full cell configuration in pairing with LiFePO4 cathodes, which demonstrated a capacity of 147.3 mAh g-1. In addition, we havemore » also demonstrated that LTO materials prepared using lithium salts separated from geothermal brine solutions had good cyclability. These demonstrations provide a promising way for making low-cost, large-scale LTO electrode materials for energy storage applications.« less

  3. Photorefractive effect in iron-doped lithium niobate crystals induced by femtosecond pulses of 1.5 {mu}m wavelength

    SciTech Connect

    Beyer, O.; Breunig, I.; Kalkum, F.; Buse, K.

    2006-01-30

    Illumination of iron-doped lithium crystals (LiNbO{sub 3}:Fe) with femtosecond pulses of 1.5 {mu}m wavelength results in large refractive index changes {delta}n in the order of 10{sup -3}. The sign of the refractive index changes depends on the polarization of the recording light. The results can be very useful for fabrication of tailored holographic components for telecommunication.

  4. Cr0.5Nb24.5O62 Nanowires with High Electronic Conductivity for High-Rate and Long-Life Lithium-Ion Storage.

    PubMed

    Yang, Chao; Yu, Shu; Lin, Chunfu; Lv, Fan; Wu, Shunqing; Yang, Yong; Wang, Wei; Zhu, Zi-Zhong; Li, Jianbao; Wang, Ning; Guo, Shaojun

    2017-04-03

    Intercalation-type TiNbxO2+2.5x (x = 2, 5, and 24) anode materials have recently become more interesting for lithium-ion batteries (LIBs) due to their large theoretical capacities of 388-402 mAh g(-1). However, the Ti(4+)/Nb(5+) ions in TiNbxO2+2.5x with empty 3d/4d orbitals usually lead to extremely low electronic conductivity of <10(-9) S cm(-1), greatly restricting their practical capacity and rate capability. Herein, we report a class of highly conductive Cr0.5Nb24.5O62 nanowires as an intercalation-type anode material for high-performance LIBs. The as-made Cr0.5Nb24.5O62 nanowires show an open shear ReO3 crystal structure (C2 space group) with 4% tetrahedra and a conducting characteristic with ultrahigh electronic conductivity of 3.6 × 10(-2) S cm(-1) and a large Li(+)-ion diffusion coefficient of 2.19 × 10(-13) cm(2) s(-1). These important characteristics make them deliver outstanding electrochemical properties in term of the largest reversible capacity (344 mAh g(-1) at 0.1 C) in all the known niobium- and titanium-based anode materials, safe working potential (∼1.65 V vs Li/Li(+)), high first-cycle Coulombic efficiency (90.8%), superior rate capability (209 mAh g(-1) at 30 C), and excellent cycling stability, making them among the best for LIBs in niobium- and titanium-based anode materials.

  5. A Safe High-Performance All-Solid-State Lithium-Vanadium Battery with a Freestanding V2O5 Nanowire Composite Paper Cathode.

    PubMed

    Zhang, Yue; Lai, Jingyuan; Gong, Yudong; Hu, Yongming; Liu, Jin; Sun, Chunwen; Wang, Zhong Lin

    2016-12-21

    The electronic conductivity and structural stability are still challenges for vanadium pentoxide (V2O5) as cathode materials in batteries. Here, we report a V2O5 nanowire-reduced graphene oxide (rGO) composite paper for direct use as a cathode without any additives for high-temperature and high-safety solid polymer electrolyte [PEO-MIL-53(Al)-LiTFSI] lithium-vanadium batteries. The batteries can show a fast and stable lithium-ion-storage performance in a wide voltage window of 1.0-4.0 V versus Li(+)/Li at 80 °C, in which with an average capacity of 329.2 mAh g(-1) at 17 mA g(-1) and a stable cycling performance over 40 cycles are achieved. The excellent electrochemical performance is mainly ascribed to integration of the electronic conductivity of rGO and interconnected networks of the V2O5 nanowires and solid electrolyte. This is a promising lithium battery for flexible and highly safe energy-storage devices.

  6. A Comparative Study of Structural Stability and Mechanical and Optical Properties of Fluorapatite (Ca5(PO4)3F) and Lithium Disilicate (Li2Si2O5) Components Forming Dental Glass-Ceramics: First Principles Study

    NASA Astrophysics Data System (ADS)

    Biskri, Z. E.; Rached, H.; Bouchear, M.; Rached, D.; Aida, M. S.

    2016-10-01

    The aim of this paper is a comparative study of structural stability and mechanical and optical properties of fluorapatite (FA) (Ca5(PO4)3F) and lithium disilicate (LD) (Li2Si2O5), using the first principles pseudopotential method based on density functional theory (DFT) within the generalized gradient approximation (GGA). The stability of fluorapatite and lithium disilicate compounds has been evaluated on the basis of their formation enthalpies. The results show that fluorapatite is more energetically stable than lithium disilicate. The independent elastic constants and related mechanical properties, including bulk modulus ( B), shear modulus ( G), Young's modulus ( E) and Poisson's ratio ( ν) as well as the Vickers hardness ( H v), have been calculated for fluorapatite compound and compared with other theoretical and experimental results. The obtained values of the shear modulus, Young's modulus and Vickers hardness are smaller in comparison with those of lithium disilicate compound, implying that lithium disilicate is more rigid than fluorapatite. The brittle and ductile properties were also discussed using B/ G ratio and Poisson's ratio. Optical properties such as refractive index n( ω), extinction coefficient k( ω), absorption coefficient α( ω) and optical reflectivity R( ω) have been determined from the calculations of the complex dielectric function ɛ( ω), and interpreted on the basis of the electronic structures of both compounds. The calculated values of static dielectric constant ɛ 1(0) and static refractive index n(0) show that the Li2Si2O5 compound has larger values compared to those of the Ca5(PO4)3F compound. The results of the extinction coefficient show that Li2Si2O5 compound exhibits a much stronger ultraviolet absorption. According to the absorption and reflectivity spectra, we inferred that both compounds are theoretically the best visible and infrared transparent materials.

  7. MAS-NMR investigations of the crystallization behaviour of lithium aluminum silicate (LAS) glasses containing P 2O 5 and TiO 2 nucleants

    NASA Astrophysics Data System (ADS)

    Ananthanarayanan, A.; Kothiyal, G. P.; Montagne, L.; Revel, B.

    2010-06-01

    Lithium aluminum silicate (LAS) glass of composition (mol%) 20.4Li 2O-4.0Al 2O 3-68.6SiO 2-3.0K 2O-2.6B 2O 3-0.5P 2O 5-0.9TiO 2 was prepared by melt quenching. The glass was then nucleated and crystallized based on differential thermal analysis (DTA) data and was characterized by 29Si, 31P, 11B and 27Al MAS-NMR. XRD and 29Si NMR showed that lithium metasilicate (Li 2SiO 3) is the first phase to c form followed by cristobalite (SiO 2) and lithium disilicate (Li 2Si 2O 5). 29Si MAS-NMR revealed a change in the network structure already for the glasses nucleated at 550 °C. Since crystalline Li 3PO 4, as observed by 31P MAS-NMR, forms concurrently with the silicate phases, we conclude that crystalline Li 3PO 4 does not act as a nucleating agent for lithium silicate phases. Moreover, 31P NMR indicates the formation of M-PO 4 ( M=B, Al or Ti) complexes. The presence of BO 3 and BO 4 structural units in all the glass/glass-ceramic samples is revealed through 11B MAS-NMR. B remains in the residual glass and the crystallization of silicate phases causes a reduction in the number of alkali ions available for charge compensation. As a result, the number of trigonally coordinated B (BO 3) increases at the expense of tetrahedrally coordinated B (BO 4). The 27Al MAS-NMR spectra indicate the presence of tetrahedrally coordinated Al species, which are only slightly perturbed by the crystallization.

  8. Fabrication and performance testing of CaO insulator coatings on V-5%Cr-5%Ti in liquid lithium

    SciTech Connect

    Park, J.H.; Dragel, G.

    1995-04-01

    Corrosion resistance of structural materials, and the magnetohydrodynamic (MHD) force and its influence on thermal hydraulics and corrosion, are major concerns in the design of liquid-metal blankets for magnetic fusion reactors (MFRs). The objective of this study is to develop in-situ stable coatings at the liquid-metal/structural-material interface, with emphasis on coatings that can be converted to an electrically insulating film to prevent adverse currents that are generated by the MHD force from passing through the structural walls. The electrical resistance of CaO coatings produced on V-5Cr-5Ti by exposure of the alloy to liquid Li that contained 0.5 - 8.5 wt.% dissolved Ca was measured as a function of time at temperatures between 250 and 600{degree}C. The solute element, Ca in liquid Li, reacted with the alloy substrate at 400-420{degree}C to produce a CaO coating.

  9. Effect of carbon segregation on performance of inhomogeneous SiCyO6/5 as anode materials for lithium-ion battery: A first-principles study

    NASA Astrophysics Data System (ADS)

    Liao, Ningbo; Zheng, Beirong; Zhou, Hongming; Xue, Wei

    2016-12-01

    Amorphous Silicon oxycarbide (SiCO) shows excellent electrochemical and cycling performance upon lithium intercalation, and is a promising anode material for future lithium-ion batteries. Carbon segregation is a unique molecular structure of SiCO and may plays a key role in its properties, a deep understanding of structure-performance relationship is crutial for reational design of SiCO anode. In this work, first principle calculations were used to investigate the effect of carbon segregation on performance of SiCyO6/5 as anode materials. Based on the calculations results, carbon segregation made small contribution on lithium capacity, while it stablized the whole system by forming three dimensional network, resulting in small volume expansion and stable mechanical properties. The theoretical capacities of SiCO with free carbon were obtained based on the most stable compositions of the lithiated structures, the predicted reversible capacities are comparable to the experimental data. The structure with higher carbon content presents larger Young's modulus during the whole lithiation process, and the saturation points of SiCyO6/5 can also be inferred from the Li content -Young's modulus curves.

  10. Lithium nephrotoxicity.

    PubMed

    Oliveira, Jobson Lopes de; Silva Júnior, Geraldo Bezerra da; Abreu, Krasnalhia Lívia Soares de; Rocha, Natália de Albuquerque; Franco, Luiz Fernando Leonavicius G; Araújo, Sônia Maria Holanda Almeida; Daher, Elizabeth de Francesco

    2010-01-01

    Lithium has been widely used in the treatment of bipolar disorder. Its renal toxicity includes impaired urinary concentrating ability and natriuresis, renal tubular acidosis, tubulointerstitial nephritis progressing to chronic kidney disease and hypercalcemia. The most common adverse effect is nephrogenic diabetes insipidus, which affects 20-40% of patients within weeks of lithium initiation. Chronic nephropathy correlates with duration of lithium therapy. Early detection of renal dysfunction should be achieved by rigorous monitoring of patients and close collaboration between psychiatrists and nephrologists. Recent experimental and clinical studies begin to clarify the mechanisms by which lithium induces changes in renal function. The aim of this study was to review the pathogenesis, clinical presentation, histopathological aspects and treatment of lithium-induced nephrotoxicity.

  11. Evaluation of Saft Ultra High Power Lithium Ion Cells (VL5U)

    DTIC Science & Technology

    2009-02-01

    Engineering Center Approved for public release; distribution unlimited. ii REPORT DOCUMENTATION PAGE Form...evaluated Saft Ultra High Power ( UHP ) cells (Saft designation VL5U) to determine their rate capability, low temperature performance, storage, and cycle...Figures Figure 1. Configuration of Saft UHP cell during discharge. The cell was discharged inside an environmental chamber and the exterior temperature

  12. Capacity fade in thin-film lithium-V{sub 2}O{sub 5} cells

    SciTech Connect

    Kwak, B.S.; Bates, J.B.; Hart, F.X.

    1996-01-01

    Capacity fade with cycling of thin-film rechargeable Li/Lipon/V{sub 2}O{sub 5} cells, formed as electrochromic mirrors with ITO current collectors, has been studied by optical and impedance spectroscopy and extended cycling experiments. An irreversible decrease in the reflectivity observed in cells cycled between 3.6 to 1.5 V was attributed to a roughening of the Li surface at the Li-Lipon interface. Although the consequent loss of contact area might be the source of increasing cell resistance responsible for the capacity fade, this possibility was ruled out because of the large variability observed in the cycling performance of cells with different cathodes and the constancy of the reflectivity when the cutoff voltage was increased to 2.5 V. It was concluded from the analysis of impedance data that a decrease in Li{sup +} ion diffusivity in the cathode and the cathode-electrolyte interface with cycling is the major cause of capacity fade.

  13. Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells

    SciTech Connect

    Lee, Eungje; Blauwkamp, Joel; Castro, Fernando C.; Wu, Jinsong; Dravid, Vinayak P.; Yan, Pengfei; Wang, Chongmin; Kim, Soo; Wolverton, Christopher; Benedek, Roy; Dogan, Fulya; Park, Joong Sun; Croy, Jason R.; Thackeray, Michael M.

    2016-10-19

    Recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi2MnO3(1-x)LiMO2 (M=Ni, Mn, Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. These findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to manganese and nickel ions in close-packed oxides and (2) their higher potential (~3.6 V vs. Li0) relative to manganese oxide spinels (~2.9 V vs. Li0) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we have revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO2 (0x0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. The results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNixO2 structures, when prepared in air between 400 and 800 C, and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentration, offer the possibility of improving the cycling stability, energy, and power of high energy (≥3.5 V) lithium-ion cells.

  14. Exploring Lithium-Cobalt-Nickel-Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells.

    PubMed

    Lee, Eungje; Blauwkamp, Joel; Castro, Fernando C; Wu, Jinsong; Dravid, Vinayak P; Yan, Pengfei; Wang, Chongmin; Kim, Soo; Wolverton, Christopher; Benedek, Roy; Dogan, Fulya; Park, Joong Sun; Croy, Jason R; Thackeray, Michael Makepeace

    2016-10-04

    Recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi2MnO3●(1-x)LiMO2 (M=Ni, Mn, Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. These findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to manganese and nickel ions in close-packed oxides and (2) their higher potential (~3.6 V vs. Li(0)) relative to manganese oxide spinels (~2.9 V vs. Li(0)) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we have revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO2 (0≤x≤0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. The results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNixO2 structures, when prepared in air between 400 and 800 °C, and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentration, offer the possibility of improving the cycling stability, energy, and power of high energy (≥3.5 V) lithium-ion cells.

  15. Mesoporous Li4Ti5O12 nanoclusters anchored on super-aligned carbon nanotubes as high performance electrodes for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Sun, Li; Kong, Weibang; Wu, Hengcai; Wu, Yang; Wang, Datao; Zhao, Fei; Jiang, Kaili; Li, Qunqing; Wang, Jiaping; Fan, Shoushan

    2015-12-01

    Mesoporous lithium titanate (LTO) nanoclusters are in situ synthesized in a network of super aligned carbon nanotubes (SACNTs) via a solution-based method followed by heat treatment in air. In the LTO-CNT composite, SACNTs not only serve as the skeleton to support a binder-free electrode, but also render the composite with high conductivity, flexibility, and mechanical strength. The homogeneously dispersed LTO nanoclusters among the SACNTs allow each LTO grain to effectively access the electrolyte and the conductive network, benefiting both ion and electron transport. By the incorporation of LTO into the CNT network, mechanical reinforcement is also achieved. When serving as a negative electrode for lithium ion batteries, such a robust composite-network architecture provides the electrodes with effective charge transport and structural integrity, leading to high-performance flexible electrodes with high capacity, high rate capability, and excellent cycling stability.Mesoporous lithium titanate (LTO) nanoclusters are in situ synthesized in a network of super aligned carbon nanotubes (SACNTs) via a solution-based method followed by heat treatment in air. In the LTO-CNT composite, SACNTs not only serve as the skeleton to support a binder-free electrode, but also render the composite with high conductivity, flexibility, and mechanical strength. The homogeneously dispersed LTO nanoclusters among the SACNTs allow each LTO grain to effectively access the electrolyte and the conductive network, benefiting both ion and electron transport. By the incorporation of LTO into the CNT network, mechanical reinforcement is also achieved. When serving as a negative electrode for lithium ion batteries, such a robust composite-network architecture provides the electrodes with effective charge transport and structural integrity, leading to high-performance flexible electrodes with high capacity, high rate capability, and excellent cycling stability. Electronic supplementary information

  16. Lithium stimulates glutamate "release" and inositol 1,4,5-trisphosphate accumulation via activation of the N-methyl-D-aspartate receptor in monkey and mouse cerebral cortex slices.

    PubMed Central

    Dixon, J F; Los, G V; Hokin, L E

    1994-01-01

    Beginning at therapeutic concentrations (1-1.5 mM), the anti-manic-depressive drug lithium stimulated the release of glutamate, a major excitatory neurotransmitter in the brain, in monkey cerebral cortex slices in a time- and concentration-dependent manner, and this was associated with increased inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] accumulation. (+/-)-3-(2-Carboxypiperazin-4-yl)propyl-1-phosphoric acid (CPP), dizocilpine (MK-801), ketamine, and Mg(2+)-antagonists to the N-methyl-D-aspartate (NMDA) receptor/channel complex selectively inhibited lithium-stimulated Ins(1,4,5)P3 accumulation. Antagonists to cholinergic-muscarinic, alpha 1-adrenergic, 5-hydroxytryptamine2 (serotoninergic), and H1 histaminergic receptors had no effect. Antagonists to non-NMDA glutamate receptors had no effect on lithium-stimulated Ins(1,4,5)P3 accumulation. Possible reasons for this are discussed. Similar results were obtained in mouse cerebral cortex slices. Carbetapentane, which inhibits glutamate release, inhibited lithium-induced Ins(1,4,5)P3 accumulation in this model. It is concluded that the primary effect of lithium in the cerebral cortex slice model is stimulation of glutamate release, which, presumably via activation of the NMDA receptor, leads to Ca2+ entry. Ins(1,4,5)P3 accumulation increases due to the presumed increased influx of intracellular Ca2+, which activates phospholipase C. These effects may have relevance to the therapeutic action of lithium in the treatment of manic depression as well as its toxic effects, especially at lithium blood levels above 1.5 mM. Images PMID:8078888

  17. Low-cost synthesis of hierarchical V2O5 microspheres as high-performance cathode for lithium-ion batteries.

    PubMed

    Shao, Jie; Li, Xinyong; Wan, Zhongming; Zhang, Longfei; Ding, Yuanlei; Zhang, Li; Qu, Qunting; Zheng, Honghe

    2013-08-28

    Hierarchical V2O5 microspheres composed of stacked platelets are fabricated through a facile, low-cost, and energy-saving approach. The preparation procedure involves a room-temperature precipitation of precursor microspheres in aqueous solution and subsequent calcination. Because of this unique structure, V2O5 microspheres manifest a high capacity (266 mA h g(-1)), excellent rate capability (223 mA h g(-1) at a current density 2400 mA g(-1)), and good cycling stability (200 mA h g(-1) after 100 cycles) as cathode materials for lithium-ion batteries.

  18. New MOF based on lithium tetrahydrofuran-2,3,4,5-tetracarboxylate: Its structure and conductivity behavior

    SciTech Connect

    Zima, Vitezslav; Patil, Deepak S.; Raja, Duraisamy Senthil; Chang, Ting-Guang; Lin, Chia-Her; Shimakawa, Koichi; Wagner, Tomas

    2014-09-15

    A novel metal–organic framework, [Li{sub 6}(HTFTA){sub 2}(H{sub 2}O){sub 3}]·3H{sub 2}O (LiTFTA, H{sub 4}TFTA is tetrahydrofuran-2,3,4,5-tetracarboxylic acid), has been synthesized under solvothermal conditions and its structure was determined by single-crystal X-ray diffraction studies. It has six different LiO{sub 4} tetrahedra which forms two kinds of tetranuclear clusters that are coordinated to the ligands and form an overall three-dimensional structure with channels running along the crystallographic a axis. Some of the carboxylate groups of the ligand moiety jut out into the channels and the channels are occupied by water molecules. The proton conductivity behavior of LiTFTA with respect to temperature and relative humidity was analyzed by our newly developed impedance data analysis method called a random-walk approach. The results were compared with the data obtained by an analysis using an equivalent electric circuit model. Based on the physical parameters obtained by the random-walk method and the known structure we suggested the mechanism of the proton conductivity in this material. The proton conduction proceeds most probably by a vehicle conduction mechanism which employs mainly water molecules of crystallization present in the channels of LiTFTA. The value of the diffusion coefficient increases with temperature whereas the number of charge carriers remains constant. On the other hand, both the number of charge carriers and diffusion coefficient increase with increasing relative humidity. - Graphical abstract: Structure of a new metal organic framework was determined and its ionic conductivity was evaluated using a random-walk approach. - Highlights: • Lithium tetrahydrofuran-2,3,4,5-tetracarboxylate is a MOF with water-filled pores. • The impedance spectra indicate that this material is ion conductive. • Conductivity was evaluated using a random walk approach. • The number of charge carriers and diffusion coefficient was determined.

  19. [Lithium nephropathy].

    PubMed

    Kaczmarczyk, Ireneusz; Sułowicz, Władysław

    2013-01-01

    Lithium salts are the first-line drug therapy in the treatment of uni- and bipolar disorder since the sixties of the twentieth century. In the mid-70s, the first information about their nephrotoxicity appeared. Lithium salts have a narrow therapeutic index. Side effects during treatment are polyuria, polydipsia and nephrogenic diabetes insipidus. Accidental intoxication can cause acute renal failure requiring renal replacement therapy while receiving long-term lithium salt can lead to the development of chronic kidney disease. The renal biopsy changes revealed a type of chronic tubulointerstitial nephropathy. The imaging studies revealed the presence of numerous symmetric microcysts. Care of the patient receiving lithium should include regular determination of serum creatinine, creatinine clearance and monitoring of urine volume. In case of deterioration of renal function reducing the dose should be considered.

  20. Lithium toxicity

    MedlinePlus

    ... Lithonate Note: Lithium is also commonly found in batteries, lubricants, high performance metal alloys, and soldering supplies. ... Kidney failure Memory problems Movement disorders Problems ... your body Psychosis (disturbed thought processes, unpredictable ...

  1. Thin-film rechargeable lithium batteries

    SciTech Connect

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

    1995-06-01

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

  2. Thin-film Rechargeable Lithium Batteries

    DOE R&D Accomplishments Database

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

    1995-06-01

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

  3. Development of lithium powder based anode with conductive carbon materials for lithium batteries

    NASA Astrophysics Data System (ADS)

    Park, Man Su

    electrode design, electrically isolated super-p carbon agglomerates in the electrode were effectively reduced by adding conductive fillers such as graphite and further improvement in cycling performance and safety was also verified. The lithium powder based anode with conductive carbon materials is very useful concept as an alternative anode design instead of pure lithium metal anode for high energy density lithium batteries such as lithium-sulfur and lithium-air. As shown in Chapter 5, this electrode concept can be further developed and optimized through the application of new carbon materials and structure.

  4. Scalable synthesis of hierarchical hollow Li4Ti5O12 microspheres assembled by zigzag-like nanosheets for high rate lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Zhu, Kunxu; Gao, Hanyang; Hu, Guoxin; Liu, Mengjing; Wang, Haochen

    2017-02-01

    Electrochemical performance, abundance and cost are three crucial criteria to comprehensively evaluate the feasibility of Li4Ti5O12 as an electrode material for lithium-ion batteries (LIBs). Herein, hierarchical hollow Li4Ti5O12 microspheres (HLTOMs) assembled by zigzag-like nanosheets are synthesized by hydrothermal treatment of scalable lithium peroxotitanate complex solution using low-cost commercial H2TiO3 particles as titanium sources, followed by a calcination treatment. Precursor solution concentration, Li/Ti ratio, hydrothermal temperature and duration are found correlative and should be optimized to obtain pure Li4Ti5O12 products. A high yield of HLTOMs up to 120 g L-1 was achieved. Due to the unique morphology, the HLTOMs deliver an outstanding rate capability of 139, 125 and 108 mA h g-1 at 10, 20 and 30 C, respectively, and exhibit 94% capacity retention after 1000 cycles at 30C indicating excellent stability. These values are much superior to those of commercial Li4Ti5O12 particles (CLTOPs), showing HLTOMs are promising anode materials for LIBs.

  5. Ambient Temperature Rechargeable Lithium Battery.

    DTIC Science & Technology

    1982-08-01

    AD-AI O297 EIC LA BS INC NEWTON MA F/6 10/3 AMB IENT TEMPERATURE RECHARGEABLE LITHIUM BATTERAU AG(MARHMU)L TI ARI AK IC07 UNCLASSIFIED C-655DEE TB6...036FL -T Research and Development Technical Report -N DELET-TR-81-0378-F AMBIENT TEMPERATURE RECHARGEABLE LITHIUM BATTERY K. M. Abraham D. L. Natwig...WORDS (Cenimne an revee filf Of ~"#amp Pu l41"lfr bg’ 61WA amober) Rechargeable lithium battery, CrO.5VO.5S2 positive electrode, 2Me-THF/LiAsF6, cell

  6. Electronic and Electrochemical Properties of Li 1–x Mn 1.5 Ni 0.5 O 4 Spinel Cathodes As a Function of Lithium Content and Cation Ordering

    DOE PAGES

    Moorhead-Rosenberg, Zach; Huq, Ashfia; Goodenough, John B.; ...

    2015-10-05

    The electronic and electrochemical properties of the high-voltage spinel LiMn1.5Ni0.5O4 as a function of cation ordering and lithium content have been investigated. Conductivity and activation energy measurements confirm that charge transfer occurs by small polaron hopping and the charge carrier conduction is easier in the Ni:3d band than in the in Mn:3d band. Seebeck coefficient data reveal that the Ni2+/3+. and Ni3+/4+ redox couples are combined in a single,3d band, and that maximum charge carrier concentration occurs where the average Ni oxidation state is close to 3+, corresponding to x = 0.5 in Li Li1-xMn1.5Ni0.5O4. Furthermore, maximum electronic conductivity ismore » found at x = 0.5, regardless of cation ordering. The thermodynamically stable phases formed during cycling were investigated by recording the X-ray diffraction (XRD) of chemically delithiated powders. The more ordered spinels maintained two separate two-phase regions upon lithium extraction, while the more disordered samples exhibited a solid-solubility region from LiMn1.5Ni0.5O4 to Li0.5Mn1.5Ni0.5O4. The conductivity and phase-transformation data of four samples with varying degrees of cation ordering were compared to the electrochemical data collected with lithium cells. Only the most ordered spinel showed inferior rate performance, while the sample annealed for a shorter time performed comparable to the unannealed or disordered samples. Our results challenge the most common beliefs about high-voltage spinel: (i) low Mn3+ content is responsible for poor rate performance and (ii) thermodynamically stable solid-solubility is critical for fast kinetics.« less

  7. Li2ZrO3-coated Li4Ti5O12 with nanoscale interface for high performance lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Zhang, Han; Liu, Yang; Wang, Ting; Yang, Yang; Shi, Shaojun; Yang, Gang

    2016-04-01

    Zr doped sample of Li4Ti4.99Zr0.01O12 (LZTO) and Li2ZrO3 (LZO) coated Li4Ti5O12 (LTO) are prepared by a solid-state method. The lattice structure of LTO is remained after doping element of Zr and coating layer of LZO. The crystal structure and electrochemical performance of the material are investigated by X-ray diffractometry (XRD), high-resolution transmission electron microscopy (HRTEM), cyclic voltammetry (CV), galvanostatic intermittent titration technique (GITT) and charge-discharge tests, respectively. Zr-doping and LZO coating play the positive role in improving the diffusion ability of lithium cations. LZTO and LZO-LTO show much improved specific capacity and rate capability compared with pristine sample of LTO. LZO-LTO has the smallest voltage differential (ΔV) of the redox peaks because the coating of Li2ZrO3 is helpful for the diffusion ability of lithium ions during charge/discharge processes. LZTO and LZO-LTO as electrode deliver the initial capacities of 164.8, 168.1 mAh g-1, respectively, which are much higher than 150.2 mAh g-1 of intrinsic sample of LTO. Even at the current density of 2 A g-1, LTZO and LZO-LTO offer capacity of 96 and 106 mAh g-1, which are much higher than 33 mAh g-1 of LTO. The improved electrochemical performance is attributed to the improved diffusion ability of lithium. During the whole discharge process, the lowest value of LTO is 5.97 × 10-17 cm2 s-1 that is much lower than 7.80 × 10-16 cm2 s-1 in LZTO and 1.85 × 10-15 cm2 s-1 in LZO-LTO, respectively.

  8. Effect of Graphene Modified Cu Current Collector on the Performance of Li4Ti5O12 Anode for Lithium-Ion Batteries.

    PubMed

    Jiang, Jiangmin; Nie, Ping; Ding, Bing; Wu, Wenxin; Chang, Zhi; Wu, Yuting; Dou, Hui; Zhang, Xiaogang

    2016-11-16

    Interface design between current collector and electroactive materials plays a key role in the electrochemical process for lithium-ion batteries. Here, a thin graphene film has been successfully synthesized on the surface of Cu current collector by a large-scale low-pressure chemical vapor deposition (LPCVD) process. The modified Cu foil was used as a current collector to support spinel Li4Ti5O12 anode directly. Electrochemical test results demonstrated that graphene coating Cu foil could effectively improve overall Li storage performance of Li4Ti5O12 anode. Especially under high current rate (e.g., 10 C), the Li4Ti5O12 electrode using modified current collector maintained a favorable capacity, which is 32% higher than that electrode using bare current collector. In addition, cycling performance has been improved using the new type current collector. The enhanced performance can be attributed to the reduced internal resistance and improved charge transfer kinetics of graphene film by increasing electron collection and decreasing lithium ion interfacial diffusion. Furthermore, the graphene film adhered on the Cu foil surface could act as an effective protective film to avoid oxidization, which can effectively improve chemical stability of Cu current collector.

  9. Navy Lithium Battery Safety

    DTIC Science & Technology

    2010-07-14

    lithium -sulfur dioxide (Li-SO2), lithium - thionyl chloride (Li- SOCL2), and lithium -sulfuryl chloride (Li-S02CL2...and 1980’s with active primary cells: Lithium -sulfur dioxide (Li-SO2) Lithium - thionyl chloride (Li-SOCL2) Lithium -sulfuryl chloride (Li-S0 CL ) 2 2...DISTRIBUTION A. Approved for public release; distribution unlimited. NAVY LITHIUM BATTERY SAFETY John Dow1 and Chris Batchelor2 Naval

  10. Dual phase Li4Ti5O12-TiO2 hierarchical hollow microspheres as anode materials for high rate lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Zhu, Kunxu; Hu, Guoxin

    2017-01-01

    Dual phase Li4Ti5O12-TiO2 hierarchical hollow microspheres composed of nanosheets are successfully fabricated by the calcination of hydrothermal product obtained from lithium peroxotitanate complex solution. Low-cost industrial H2TiO3 particles are chosen as titanium sources, which is significant for the inexpensive and large-scale production of Li4Ti5O12-TiO2 composite material. The Li4Ti5O12-TiO2 electrode yields excellent rate capability (151, 139 and 134 mA h g-1 at 10, 20 and 25 C, respectively) and good cycling stability (96% capacity retention after 500 cycles at 10 C). The mesoporous hierarchical morphology and high grain boundary density are likely the contributing factors to the excellent electrochemical performance of Li4Ti5O12-TiO2 composite.

  11. Study of structural and ferromagnetic resonance properties of spinel lithium ferrite (LiFe{sub 5}O{sub 8}) single crystals

    SciTech Connect

    Pachauri, Neha; Khodadadi, Behrouz; Mewes, Tim; Althammer, Matthias; Singh, Amit V.; Gupta, Arunava; Loukya, B.; Datta, Ranjan; Iliev, Milko; Bezmaternykh, Leonard; Gudim, Irina

    2015-06-21

    The effect of B-site cation ordering on the room temperature structural and ferromagnetic resonance (FMR) properties of single crystal spinel lithium ferrite (LiFe{sub 5}O{sub 8}, LFO) have been investigated. A detailed microstructural analysis is done through X-ray diffraction, polarized Raman spectroscopy, and transmission electron microscopy (TEM) to examine the effect of post-annealing on the B-site cation ordering. The X-ray diffraction pattern of the as-grown crystal indicates a disordered state of the crystal. However, the annealed sample shows additional superlattice reflections corresponding to the ordered phase. This ordering is further confirmed by Raman spectra and TEM images, which reveal ordering of Li and Fe ions at the octahedral sites contrasting with the relatively high degree of octahedral site disorder in the as-grown crystal. To study the effect of B-site ordering on the magnetic properties and FMR linewidth, vibrating sample magnetometry and broadband FMR measurements have been performed for both the ordered and disordered phases of lithium ferrite. The value of saturation magnetization for both phases is ∼290 emu/cm{sup 3}. A single mode FMR profile is observed for both phases with little distortion. The linewidth characteristics of the ordered and disordered phases of lithium ferrite phases are compared, and it is observed that the linewidth is independent of the cation ordering. Both the phases exhibit a low linewidth (∼26 Oe at 30 GHz) and the effective damping parameter for the as-grown and annealed samples is determined to be 0.0021 ± 0.0001.

  12. Facile synthesis of hierarchical micro/nanostructured MnO material and its excellent lithium storage property and high performance as anode in a MnO/LiNi0.5Mn1.5O(4-δ) lithium ion battery.

    PubMed

    Xu, Gui-Liang; Xu, Yue-Feng; Fang, Jun-Chuan; Fu, Fang; Sun, Hui; Huang, Ling; Yang, Shihe; Sun, Shi-Gang

    2013-07-10

    Hierarchical micro/nanostructured MnO material is synthesized from a precursor of MnCO3 with olive shape that is obtained through a facile one-pot hydrothermal procedure. The hierarchical micro/nanostructured MnO is served as anode of lithium ion battery together with a cathode of spinel LiNi0.5Mn1.5O(4-δ) material, which is synthesized also from the precursor of MnCO3 with olive shape through a different calcination process. The structures and compositions of the as-prepared materials are characterized by TGA, XRD, BET, SEM, and TEM. Electrochemical tests of the MnO materials demonstrate that it exhibit excellent lithium storage property. The MnO material in a MnO/Li half cell can deliver a reversible capacity of 782.8 mAh g(-1) after 200 cycles at a rate of 0.13 C, and a stable discharge capacity of 350 mAh g(-1) at a high rate of 2.08 C. Based on the outstanding electrochemical property of the MnO material and the LiNi0.5Mn1.5O(4-δ) as well, the MnO/LiNi0.5Mn1.5O(4-δ) full cell has demonstrated a high discharge specific energy ca. 350 Wh kg(-1) after 30 cycles at 0.1 C with an average high working voltage at 3.5 V and a long cycle stability. It can release a discharge specific energy of 227 Wh kg(-1) after 300 cycles at a higher rate of 0.5 C. Even at a much higher rate of 20 C, the MnO/LiNi0.5Mn1.5O(4-δ) full cell can still deliver a discharge specific energy of 145.5 Wh kg(-1). The excellent lithium storage property of the MnO material and its high performance as anode in the MnO/LiNi0.5Mn1.5O(4-δ) lithium ion battery is mainly attributed to its hierarchical micro/nanostructure, which could buffer the volume change and shorten the diffusion length of Li(+) during the charge/discharge processes.

  13. Topotactic insertion of lithium in the layered structure Li{sub 4}VO(PO{sub 4}){sub 2}: The tunnel structure Li{sub 5}VO(PO{sub 4}){sub 2}

    SciTech Connect

    Satya Kishore, M.; Pralong, V. Caignaert, V.; Malo, S.; Hebert, S.; Varadaraju, U.V.; Raveau, B.

    2008-04-15

    A new V(III) lithium phosphate Li{sub 5}VO(PO{sub 4}){sub 2} has been synthesized by electrochemical insertion of lithium into Li{sub 4}VO(PO{sub 4}){sub 2}. This phase, which crystallizes in the space group I4/mcm, exhibits a tunnel structure closely related to the layered structure of Li{sub 4}VO(PO{sub 4}){sub 2} and to the tunnel structure of VO(H{sub 2}PO{sub 4}){sub 2}. The topotactic reactions that take place during lithium exchange and intercalation, starting from VO(H{sub 2}PO{sub 4}){sub 2} and going to the final phase Li{sub 5}VO(PO{sub 4}){sub 2} are explained on the basis of the flexible coordinations of V{sup 4+} and V{sup 3+} species. The electrochemical and magnetic properties of this new phase are also presented and explained on the basis of the structure dimensionality. - Graphical abstract: Electrochemical synthesis of a new 3D V(III) lithium phosphate, Li{sub 5}VO(PO{sub 4}){sub 2}. Starting from the 2D Li{sub 4}VO(PO{sub 4}){sub 2}, the topotactic reaction that take place during lithium intercalation is explained on the basis of the flexible coordinations of V{sup 4+} and V{sup 3+} species.

  14. High-pressure synthesis and crystal structure of the lithium borate HP-LiB{sub 3}O{sub 5}

    SciTech Connect

    Neumair, Stephanie C.; Vanicek, Stefan; Kaindl, Reinhard; Toebbens, Daniel M.; Wurst, Klaus; Huppertz, Hubert

    2011-09-15

    The new lithium borate HP-LiB{sub 3}O{sub 5} was synthesized under high-pressure/high-temperature conditions of 6 GPa and 1050 deg. C in a multianvil press with a Walker-type module. The compound crystallizes in the space group Pnma (no. 62) with the lattice parameters a=829.7(2), b=759.6(2), and c=1726.8(4) pm (Z=16). The high-pressure compound HP-LiB{sub 3}O{sub 5} is built up from a three-dimensional network of BO{sub 4} tetrahedra and BO{sub 3} groups, which incorporates Li{sup +} ions in channels along the b-axis. Band assignments of measured IR- and Raman spectra were done via quantum-mechanical calculations. Additionally, the thermal behavior of HP-LiB{sub 3}O{sub 5} was investigated. - Graphical abstract: The new high-pressure compound HP-LiB{sub 3}O{sub 5} is built up from a three-dimensional network of BO4 tetrahedra and BO{sub 3} groups, which incorporates Li{sup +} ions in channels along the b-axis. In this paper, the synthesis, the crystal structure, and the properties of HP-LiB{sub 3}O{sub 5} are described. Highlights: > Synthesis of a new lithium borate with the composition HP-LiB{sub 3}O{sub 5} at high pressure. > In contrast to the non-centrosymmetric phase LiB{sub 3}O{sub 5}, this high-pressure phase is centrosymmetric. > First example of ternary alkali borates exhibiting threefold bridging oxygen atoms.

  15. Study of lithium absorption by users of spas treated with lithium ion.

    PubMed

    McCarty, J D; Carter, S P; Fletcher, M J; Reape, M J

    1994-05-01

    This study examines the possible dermal absorption of lithium ion into the blood serum of spa/hot tub bathers. Fifty-three participants (28 males and 25 females) spent 20 minutes per day, 4 days per week for 2 consecutive weeks in one of two assigned spas. The participants were randomly assigned to one of the two spas after matching based on sex, age, and use of oral contraceptives. The test spa contained 40 +/- 5 ppm lithium ion, while the control spa contained no additional lithium ion above the background levels of approximately 0.02 ppm. The exposure in the spa treated with lithium ion (from lithium chloride) simulated the maximum exposure that would be expected in a spa sanitized with lithium hypochlorite. The two spas were maintained at 101 +/- 2 degrees F. Serum lithium ion levels before and after spa use were determined using graphite-furnace atomic absorption spectroscopy with a minimum detectable level of lithium ion in serum of 2 micrograms l-1 (ppb). There was no statistically significant difference in serum lithium levels between the control and treatment group at any stage. We conclude that dermal exposure to lithium ion (as would be present after treatment of a spa with lithium hypochlorite) did not result in a detectable increase in the serum lithium ion level.

  16. Preparation of Li2S-P2S5 solid electrolyte from N-methylformamide solution and application for all-solid-state lithium battery

    NASA Astrophysics Data System (ADS)

    Teragawa, Shingo; Aso, Keigo; Tadanaga, Kiyoharu; Hayashi, Akitoshi; Tatsumisago, Masahiro

    2014-02-01

    Electrode-solid electrolyte composite materials for all-solid-state lithium batteries were prepared by coating of the Li2S-P2S5 solid electrolyte onto LiCoO2 particles using a N-methylformamide (NMF) solution of 80Li2S·20P2S5 (mol%) solid electrolyte. SEM and EDX analysis showed that the Li2S-P2S5 solid electrolyte was uniformly coated on LiCoO2 particles. The all-solid-state cell using the LiCoO2 particles coated with the solid electrolyte showed higher charge-discharge capacity than the cells using uncoated LiCoO2 particles.

  17. Poly(methyl methacrylate-acrylonitrile-ethyl acrylate) terpolymer based gel electrolyte for LiNi0.5Mn1.5O4 cathode of high voltage lithium ion battery

    NASA Astrophysics Data System (ADS)

    Sun, Ping; Liao, Youhao; Xie, Huili; Chen, Tingting; Rao, Mumin; Li, Weishan

    2014-12-01

    A novel gel polymer electrolyte (GPE), based on poly(methyl methacrylate-acrylonitrile-ethyl acrylate) (P(MMA-AN-EA)) terpolymer, is designed to match LiNi0.5Mn1.5O4 cathode of 5 V lithium ion battery. The performances of the synthesized P(MMA-AN-EA) terpolymer and the corresponding membrane and GPE are investigated by scanning electron microscope, energy dispersive spectroscopy, nuclear magnetic resonance spectra, Fourier transform infrared spectra, thermogravimetric analyzer, electrochemical impedance spectroscopy, linear sweep voltammetry, and charge/discharge test. It is found that the pore structure of P(MMA-AN-EA) membrane is affected by the dose of pore forming agent, polyethylene glycol (PEG400). The membrane with 3 wt% PEG400 presents the best pore structure, in which pores are dispersed uniformly and interconnected, and exhibits the largest electrolyte uptake, resulting in the highest ionic conductivity of 3.82 × 10-3 S cm-1 for the corresponding GPE at room temperature. The GPE has improved compatibility with lithium anode and is electrochemically stable up to 5.2 V (vs. Li/Li+). The high voltage LiNi0.5Mn1.5O4 cathode using the resulting GPE exhibits excellent cyclic stability, maintaining 97.9% of its initial discharge capacity after 100 cycles compared to that of 79.7% for the liquid electrolyte at 0.5 C.

  18. Fabrication of core-shell α-Fe(2)O(3)@ Li(4)Ti(5)O(12) composite and its application in the lithium ion batteries.

    PubMed

    Chen, Ming; Li, Wei; Shen, Xiao; Diao, Guowang

    2014-03-26

    In this work, a novel carbon-free core-shell α-iron oxide (α-Fe2O3)@ spinel lithium titanate (Li4Ti5O12, LTO) composite has been synthesized via a facile hydrothermal process. Element mapping confirmed the core-shell structure of α-Fe2O3@LTO. The effects of various experimental parameters, including thickness of TiO2 coating, reaction temperature, and time on the morphologies of the resulted products, were systematically investigated. The electrochemical measurements demonstrate that uniform α-Fe2O3 ellipsoids are coated with LTO to avoid forming a solid electrolyte interface (SEI) layer, to reduce initial capacity loss, and to improve the reversibility of α-Fe2O3 for Li ion storage. Compared with naked α-Fe2O3 ellipsoids, the α-Fe2O3@LTO composites exhibit lower initial capacity loss, higher reversible capacity, and better cycling performance for lithium storage. The electrochemical performance of α-Fe2O3@LTO composite heavily depends on the thickness and density of LTO coating shells. The carbon-free coating of LTO is highly effective in improving the electrochemical performance of α-Fe2O3, promising advanced batteries with high surface stability and excellent security.

  19. Synthesis of graphitized carbon, nanodiamond and graphene supported Li4Ti5O12 and comparison of their electrochemical performance as anodes for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Yang, Shuai; Miao, Juan; Wang, Qiufen; Lu, Mengwei; Sun, Jiufang; Wen, Tao

    2016-12-01

    Graphitized carbon (GC), nanodiamond (ND) and graphene (GE) supported Li4Ti5O12 (LTO) composites have been synthesized via a solid-state reaction, respectively. The particle sizes of LTO/GC, LTO/ND and LTO/GE are smaller than pure LTO. When tested as the anode for lithium ion batteries, the discharge capacities of LTO, LTO/GC, LTO/ND and LTO/GE composites are 100.1 mAh g-1, 150.4 mAh g-1, 90.4 mAh g-1 and 218.3 mAh g-1 at the current density of 175 mA g-1 after 500 cycles. Their rate capacities retain 59.8%, 80.0%, 81.0% and 85.7% at the current density of 175 mA g-1, 438 mA g-1, 875 mA g-1 and 175 mA g-1, respectively. Moreover, the recovery rates of their rate capacities are 78.6%, 83.4%, 88.9% and 90.1% when returned to the current density of 175 mA g-1, respectively. The reasons can be attributed to the synergistic effect between GC (ND and GE) and LTO as well as the features of the different carbon supports. This strategy, with the carbon constituting a good supporting structure, is an effective way to improve the cycling performance of anode materials for lithium ion batteries.

  20. Compatibility of poly(bisAEA4)-LiTFSI-MPPipTFSI ionic liquid gel polymer electrolyte with Li4Ti5O12 lithium ion battery anode

    NASA Astrophysics Data System (ADS)

    Stepniak, Izabela

    2014-02-01

    This paper presents the use of Li4Ti5O12 (LTO) as anode with ionic liquid gel polymer electrolyte (IL-GPE) for application in lithium ion batteries. IL-GPE was obtained by in situ photopolymerization method of a mixture of ethoxylated bisphenol A diacrylate (bis(AEA4) and 0.4 M solution of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) in N-methyl-N-propylpiperidinium bis(trifluoromethanesulfonyl)imide (MPPipTFSI). The surface morphology of the IL-GPE was studied using scanning electron microscopy (SEM). Stable, porous and flexible gel polymer electrolyte characterized high ionic conductivity (0.64 mS cm-1 at 25 °C) and a wide electrochemical stability window (ESW) (4.8 V). The performances of LTO/IL-GPE/Li cell were tested by using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge/discharge. Good charge/discharge capacities and low capacity loss at medium C rates preliminary cycling was obtained.

  1. catena-Poly[[(3,5-dicarb­oxy­pyrazine-2,6-dicarboxyl­ato-κ3 O 2,N 1,O 6)lithium(I)]-μ-aqua-[triaqua­lithium(I)]-μ-aqua

    PubMed Central

    Starosta, Wojciech; Leciejewicz, Janusz

    2010-01-01

    The title coordination polymer, [Li2(C8H2N2O8)(H2O)5]n contains two symmetry-independent Li+ ions; one is coordin­ated by five water O atoms, the other by an O,N,O′-tridentate doubly deprotonated pyrazine-2,3,5,6-tetra­carboxyl­ate ligand and two water O atoms. Water mol­ecules bridge adjacent Li+ ions into ribbons propagating in [100]; an alternative analysis of the structure considers it to contain alternating [Li(C8H2N2O8)(H2O)2]− anions and [Li(H2O)3]+ cations. In the polymeric model, both lithium ions show distorted trigonal–bipyramidal coordination geometries. Within the ligand, the carboxyl H atoms participate in short, almost symmetric O⋯H⋯O hydrogen bonds in which the non-coordinated carboxyl­ate O atoms are donors and acceptors. In the crystal, the ribbons inter­act via a network of O—H⋯O hydrogen bonds in which the coordinated water mol­ecules act as donors and ligand carboxyl­ate O atoms as acceptors. PMID:21589251

  2. High-temperature X-ray analysis of phase evolution in lithium ion conductor Li{sub 1.5}Al{sub 0.5}Ge{sub 1.5}(PO{sub 4}){sub 3}

    SciTech Connect

    He, Kun Wang, Yanhang; Zu, Chengkui Liu, Yonghua; Zhao, Huifeng; Chen, Jiang; Han, Bin; Ma, Juanrong

    2013-06-15

    Series of Li{sub 1.5}Al{sub 0.5}Ge{sub 1.5}(PO{sub 4}){sub 3} glass ceramic samples were prepared in this work through the change of heat treatment temperature from 650 to 1050 °C. The structures of glass ceramic samples were characterized by means of high temperature X-ray diffraction and Field Emission Scanning Electron Microscope. And the lithium ionic conductivity was analyzed through AC impedance spectroscopy. Through heat treatment at 850 °C for 4 h for the base glass sample, we obtained a maximum conductivity of 5.8 × 10{sup −4} S/cm at room temperature. - Graphical Abstract: High temperature X-ray diffraction (HT-XRD) and Rietveld refinement of Li{sub 1.5}Al{sub 0.5}Ge{sub 1.5}(PO{sub 4}){sub 3} (LAGP) glass-ceramics were recorded to investigate the phase transformation, cell parameters and the mass fraction of each crystal phase, which occur in the glass to glass-ceramics process during different crystallization temperatures. The relationship between the average grain size and conductivity that originate from and relate to the crystallization temperature was analyzed by SEM micrograph and AC impedance spectroscopy. - Highlights: • Li{sub 1.5}Al{sub 0.5}Ge{sub 1.5}(PO{sub 4}){sub 3} glass-ceramics were prepared from as-prepared glass. • The phases decomposition and mass fraction of each phase were analyzed by HT-XRD. • Conductivity is relate to grain size that influenced by crystallization temperature.

  3. Rapid charge-discharge property of Li4Ti5O12-TiO2 nanosheet and nanotube composites as anode material for power lithium-ion batteries.

    PubMed

    Yi, Ting-Feng; Fang, Zi-Kui; Xie, Ying; Zhu, Yan-Rong; Yang, Shuang-Yuan

    2014-11-26

    Well-defined Li4Ti5O12-TiO2 nanosheet and nanotube composites have been synthesized by a solvothermal process. The combination of in situ generated rutile-TiO2 in Li4Ti5O12 nanosheets or nanotubes is favorable for reducing the electrode polarization, and Li4Ti5O12-TiO2 nanocomposites show faster lithium insertion/extraction kinetics than that of pristine Li4Ti5O12 during cycling. Li4Ti5O12-TiO2 electrodes also display lower charge-transfer resistance and higher lithium diffusion coefficients than pristine Li4Ti5O12. Therefore, Li4Ti5O12-TiO2 electrodes display lower charge-transfer resistance and higher lithium diffusion coefficients. This reveals that the in situ TiO2 modification improves the electronic conductivity and electrochemical activity of the electrode in the local environment, resulting in its relatively higher capacity at high charge-discharge rate. Li4Ti5O12-TiO2 nanocomposite with a Li/Ti ratio of 3.8:5 exhibits the lowest charge-transfer resistance and the highest lithium diffusion coefficient among all samples, and it shows a much improved rate capability and specific capacity in comparison with pristine Li4Ti5O12 when charging and discharging at a 10 C rate. The improved high-rate capability, cycling stability, and fast charge-discharge performance of Li4Ti5O12-TiO2 nanocomposites can be ascribed to the improvement of electrochemical reversibility, lithium ion diffusion, and conductivity by in situ TiO2 modification.

  4. Low temperature biosynthesis of Li2O-MgO-P2O5-TiO2 nanocrystalline glass with mesoporous structure exhibiting fast lithium ion conduction.

    PubMed

    Du, Xiaoyong; He, Wen; Zhang, Xudong; Ma, Jinyun; Wang, Chonghai; Li, Chuanshan; Yue, Yuanzheng

    2013-04-01

    We demonstrate a biomimetic synthesis methodology that allows us to create Li2O-MgO-P2O5-TiO2 nanocrystalline glass with mesoporous structure at lower temperature. We design a 'nanocrystal-glass' configuration to build a nanoarchitecture by means of yeast cell templates self-assembly followed by the controlled in-situ biomineralization of materials on the cell wall. Electrochemically active nanocrystals are used as the lamellar building blocks of mesopores, and the semiconductive glass phase can act both as the 'glue' between nanocrystals and functionalized component. The Li2O-MgO-P2O5-TiO2 nanocrystalline glass exhibits outstanding thermal stability, high conductivity and wide potential window. This approach could be applied to many other multicomponent glass-ceramics to fabricate mesoporous conducting materials for solid-state lithium batteries.

  5. Enhanced Performance of "Flower-like" Li4Ti5O12 Motifs as Anode Materials for High-Rate Lithium-Ion Batteries.

    PubMed

    Wang, Lei; Zhang, Yiman; Scofield, Megan E; Yue, Shiyu; McBean, Coray; Marschilok, Amy C; Takeuchi, Kenneth J; Takeuchi, Esther S; Wong, Stanislaus S

    2015-10-12

    "Flower-like" motifs of Li4Ti5O12 were synthesized by using a facile and large-scale hydrothermal process involving unique Ti foil precursors followed by a short, relatively low-temperature calcination in air. Moreover, a detailed time-dependent growth mechanism and a reasonable reaction scheme were proposed to clearly illustrate and highlight the structural evolution and subsequent formation of this material. Specifically, the resulting "flower-like" Li4Ti5O12 microspheres consisting of thin nanosheets provide for an enhanced surface area and a reduced lithium-ion diffusion distance. The high surface areas of the exposed roughened, thin petal-like component nanosheets are beneficial for the interaction of the electrolyte with Li4Ti5O12 , which thereby ultimately provides for improved high-rate performance and favorable charge/discharge dynamics. Electrochemical studies of the as-prepared nanostructured Li4Ti5O12 clearly revealed their promising potential as an enhanced anode material for lithium-ion batteries, as they present both excellent rate capabilities (delivering 148, 141, 137, 123, and 60 mAh g(-1) under discharge rates of 0.2, 10, 20, 50, and 100 C, at cycles of 50, 55, 60, 65, and 70, respectively) and stable cycling performance (exhibiting a capacity retention of ≈97 % from cycles 10-100, under a discharge rate of 0.2 C, and an impressive capacity retention of ≈87 % by using a more rigorous discharge rate of 20 C from cycles 101-300).

  6. Electrochemical Performance of LiNi0.5Mn1.5O4 by Sol-gel Self-combustion Reaction Method in Different Kinds of Electrolyte for High-voltage Rechargeable Lithium Cells

    NASA Astrophysics Data System (ADS)

    Liang, Xinghua; Shi, Lin; Liu, Yusi; Zeng, Shuaibo; Ye, Chaochao

    2015-07-01

    LiNi0.5Mn1.5O4 cathode material was synthesized through sol-gel self-combustion reaction method. LiNi0.5Mn1.5O4 powders were subsequently characterized as cathode materials in a Li-ion coin cell comprising a Li anode with electrolyte A or electrolyte B. 1.0 mol/L Lithium Hexafluorophosphate (LiPF6) dissolved in volume ration of ethylene carbonate (EC) to ethyl methyl carbonate (EMC) to diethyl carbonate (DEC) corresponded to 4:3:3as electrolyte A, 1.0 mol/L LiPF6 dissolved in volume ration of EC to EMC to DEC corresponded to 4:2:4 as electrolyte B. Electrochemical performance of lithium cells was evaluated. These tests showed that no matter the cells with electrolyte A or electrolyte B has good discharge platform in 4.7V range (3.5V-4.75V) at the rate of 0.1C, the initial discharge capacity of cell with electrolyte B was higher than that with electrolyte A.

  7. Lithium in 2012

    USGS Publications Warehouse

    Jaskula, B.W.

    2013-01-01

    In 2012, estimated world lithium consumption was about 28 kt (31,000 st) of lithium contained in minerals and compounds, an 8 percent increase from that of 2011. Estimated U.S. consumption was about 2 kt (2,200 st) of contained lithium, the same as that of 2011. The United States was thought to rank fourth in consumption of lithium and remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. One company, Rockwood Lithium Inc., produced lithium compounds from domestic brine resources near Silver Peak, NV.

  8. The effect of 0.025 Al-doped in Li4Ti5O12 material on the performance of half cell lithium ion battery

    NASA Astrophysics Data System (ADS)

    Priyono, Slamet; Triwibowo, Joko; Prihandoko, Bambang

    2016-02-01

    The effect of 0.025 Al-doped Li4Ti5O12 as anode material for Lithium Ion battery had been studied. The pure and 0.025 Al-doped Li4Ti5O12 were synthesized through solid state process in air atmosphere. Physical characteristics of all samples were observed by XRD, FTIR, and PSA. The XRD analysis revealed that the obtained particle was highly crystalline and had a face-centered cubic spinel structure. The XRD pattern also showed that the 0.025 Al-doped on the Li4Ti5O12 did not change crystal structure of Li4Ti5O12. FTIR analysis confirmed that the spinel structure in fingerprint region was unchanged when the structure was doped by 0.025 Al. However the doping of 0.025 Al increased particle size significantly. The electrochemical performance was studied by using cyclic voltammetry (CV) and charge-discharge (CD) curves. Electrochemical analysis showed that pure Li4Ti5O12 has higher capacity than 0.025 Al-doped Li4Ti5O12 had. But 0.025 Al-doped Li4Ti5O12 possesses a better cycling stability than pure Li4Ti5O12.

  9. Lithium-aluminum-iron electrode composition

    DOEpatents

    Kaun, Thomas D.

    1979-01-01

    A negative electrode composition is presented for use in a secondary electrochemical cell. The cell also includes an electrolyte with lithium ions such as a molten salt of alkali metal halides or alkaline earth metal halides that can be used in high-temperature cells. The cell's positive electrode contains a a chalcogen or a metal chalcogenide as the active electrode material. The negative electrode composition includes up to 50 atom percent lithium as the active electrode constituent in an alloy of aluminum-iron. Various binary and ternary intermetallic phases of lithium, aluminum and iron are formed. The lithium within the intermetallic phase of Al.sub.5 Fe.sub.2 exhibits increased activity over that of lithium within a lithium-aluminum alloy to provide an increased cell potential of up to about 0.25 volt.

  10. Preparation and electrochemical performance of La3+ and F- co-doped Li4Ti5O12 anode material for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Ji, Mandi; Xu, Yunlong; Zhao, Zhen; Zhang, Huang; Liu, Dong; Zhao, Chongjun; Qian, Xiuzhen; Zhao, Chunhua

    2014-10-01

    La3+ and F- co-doped Li4Ti5O12 (LTO) anode materials are synthesized successfully via a solid state reaction. The structure and morphology are characterized by XRD, SEM and EDS. The results indicate that La3+ and F- ions were uniformly dispersed in Li4Ti5O12 lattice without changing the structure and morphology of Li4Ti5O12. Li3.95La0.05Ti5O11.7F0.3 (La005-F03) exhibits an outstanding electrochemical performance among all the samples in a potential range from 0.5 to 2.5 V, and delivers a discharge capacity of 103 mAh g-1 at 10C rate, whereas the LTO only gives 62.5 mAh g-1. The sample La005-F03 retains a discharge capacity of 170.1 mAh g-1 after 100 cycles at 1C rate. The improved electrochemical performance could be attributed to the appropriate co-doping with La3+ and F-, which can increase the amount of Ti3+/Ti4+ mixing as charge compensation, leading to the decrease of the charge transfer resistance and improvement of the electronic conductivity and lithium ion diffusion coefficient.

  11. Free-standing LiNi0.5Mn1.5O4/carbon nanofiber network film as lightweight and high-power cathode for lithium ion batteries.

    PubMed

    Fang, Xin; Ge, Mingyuan; Rong, Jiepeng; Zhou, Chongwu

    2014-05-27

    Lightweight and high-power LiNi0.5Mn1.5O4/carbon nanofiber (CNF) network electrodes are developed as a high-voltage cathode for lithium ion batteries. The LiNi0.5Mn1.5O4/CNF network electrodes are free-standing and can be used as a cathode without using any binder, carbon black, or metal current collector, and hence the total weight of the electrode is highly reduced while keeping the same areal loading of active materials. Compared with conventional electrodes, the LiNi0.5Mn1.5O4/CNF network electrodes can yield up to 55% reduction in total weight and 2.2 times enhancement in the weight percentage of active material in the whole electrode. Moreover, the LiNi0.5Mn1.5O4/carbon nanofiber (CNF) network electrodes showed excellent current rate capability in the large-current test up to 20C (1C = 140 mAh/g), when the conventional electrodes showed almost no capacity at the same condition. Further analysis of polarization resistance confirmed the favorable conductivity from the CNF network compared with the conventional electrode structure. By reducing the weight, increasing the working voltage, and improving the large-current rate capability simultaneously, the LiNi0.5Mn1.5O4/CNF electrode structure can highly enhance the energy/power density of lithium ion batteries and thus holds great potential to be used with ultrathin, ultralight electronic devices as well as electric vehicles and hybrid electric vehicles.

  12. Chemical and morphological characteristics of lithium electrode surfaces

    NASA Technical Reports Server (NTRS)

    Yen, S. P. S.; Shen, D.; Vasquez, R. P.; Grunthaner, F. J.; Somoano, R. B.

    1981-01-01

    Lithium electrode surfaces were analyzed for chemical and morphological characteristics, using electron spectroscopy chemical analysis (ESCA) and scanning electron microscopy (SEM). Samples included lithium metal and lithium electrodes which were cycled in a 1.5 M lithium arsenic hexafluoride/two-methyl tetrahydrofuran electrolyte. Results show that the surface of the as-received lithium metal was already covered by a film composed of LiO2 and an Li2O/CO2 adduct with a thickness of approximately 100-200 A. No evidence of Ni3 was found. Upon exposure of the lithium electrode to a 1.5 M LiAsF6/2-Me-THF electrochemical environment, a second film was observed to form on the surface, consisting primarily of As, Si, and F, possibly in the form of lithium arsenic oxyfluorides or lithium fluorosilicates. It is suggested that the film formation may be attributed to salt degradation.

  13. Er3+-doped strontium lithium bismuth borate glasses for broadband 1.5 μm emission - optical properties

    NASA Astrophysics Data System (ADS)

    Rajesh, D.; Balakrishna, A.; Ratnakaram, Y. C.

    2013-02-01

    Strontium lithium bismuth borate glasses (SLBiB) doped with various concentrations of Er3+ were prepared using conventional melt quench technique and investigated their optical properties. The amorphous nature of the prepared glass samples was confirmed by X-ray diffraction and SEM analysis. Optical properties were studied by measuring the optical absorption and near infrared luminescence spectra at room temperature. Judd-Ofelt (J-O) theory has been applied for the f.f transitions of Er3+ ions to evaluate J-O intensity parameters, Ωλ (λ = 2, 4 and 6). Using the J-O intensity parameters, radiative properties such as transition probabilities (AR), branching ratios (β) and radiative lifetimes (τ) are estimated for certain transitions. From the emission spectra, peak emission-cross sections (σp) and products of stimulated emission cross-section and full width at half maximum (σp×FWHM) were calculated for the observed emission transition, 4I13/2→4I15/2.

  14. A novel porous coral-like Zn0.5Ni0.5Co2O4 as an anode material for lithium ion batteries with excellent rate performance

    NASA Astrophysics Data System (ADS)

    Song, Xiong; Ru, Qiang; Mo, Yudi; Guo, Lingyun; Hu, Shejun; An, Bonan

    2014-12-01

    A novel porous coral-like Zn0.5Ni0.5Co2O4 (ZNCO) is prepared by a facile co-precipitation method using oxalic acid as complex agent, and the ZnCo2O4 (ZCO) nanospheres and NiCo2O4 (NCO) nanoflakes are also prepared for comparison. The obtained products are systematically characterized by powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The results demonstrate that the controlled metallic elements doping has significant effects on the nanostructure and electrochemical performance of the samples. Compared with the ZCO nanospheres and NCO nanoflakes, the coral-like ZNCO materials with enough free space as anodes in lithium ion batteries (LIBs) exhibit a high initial coulombic efficiency of 84%, a high specific capacity of ∼1445 mAh g-1 at a current rate of 100 mA g-1 after 50 cycles, and ∼730 mAh g-1 at a current rate of 1500 mA g-1 after 200 cycles, as well as an excellent rate capability at elevated current rates, such as, ∼1080 and ∼425 mAh g-1 at current rates of 500 and 6000 mA g-1, respectively. This work presents a meaningful way for the preparation of mixed metal oxides with porous nanostructure as superior anodes for lithium ion batteries.

  15. Enhanced performance of spherical natural graphite coated by Li4Ti5O12 as anode for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Lu, Mi; Tian, Yanyan; Zheng, Xiaodong; Gao, Jun; Huang, Bing

    2012-12-01

    The natural graphite (NG) is coated with Li4Ti5O12 (LTO) and the composite shows a markedly enhanced rate performance due to the decrease of charge transfer resistance after LTO coating. The specific capacity of the NG charge-discharged at 2 C is increased by 60.3% (128.7 vs. 80.3 mAh g-1) by coating it with 1 wt.% of Li4Ti5O12 (LTO). The comparison of the NG and that coated with 1 wt.% LTO at 0.1 C shows that the initial reversible capacity is increased from 318.1 mAh g-1 to 357.5 mAh g-1 after coating, while the total irreversible capacity loss after 50 cycles is decreased from 122.8 mAh g-1 to 103.9 mAh g-1. The composite improves the energy and power densities, safety, cycle life and lowers the price of the lithium-ion battery while avoiding the gas-swelling of full battery caused by Ti4+ because the final coating material is the lithiated LTO (Li7Ti5O12 or Li9Ti5O12).

  16. Microwave-Assisted Solvothermal Synthesis of VO2 Hollow Spheres and Their Conversion into V2O5 Hollow Spheres with Improved Lithium Storage Capability.

    PubMed

    Pan, Jing; Zhong, Li; Li, Ming; Luo, Yuanyuan; Li, Guanghai

    2016-01-22

    Monodispersed hierarchically structured V2O5 hollow spheres were successfully obtained from orthorhombic VO2 hollow spheres, which are in turn synthesized by a simple template-free microwave-assisted solvothermal method. The structural evolution of VO2 hollow spheres has been studied and explained by a chemically induced self-transformation process. The reaction time and water content in the reaction solution have a great influence on the morphology and phase structure of the resulting products in the solvothermal reaction. The diameter of the VO2 hollow spheres can be regulated simply by changing vanadium ion content in the reaction solution. The VO2 hollow spheres can be transformed into V2O5 hollow spheres with nearly no morphological change by annealing in air. The nanorods composed of V2O5 hollow spheres have an average length of about 70 nm and width of about 19 nm. When used as a cathode material for lithium-ion batteries, the V2O5 hollow spheres display a diameter-dependent electrochemical performance, and the 440 nm hollow spheres show the highest specific discharge capacity of 377.5 mAhg(-1) at a current density of 50 mAg(-1) , and are better than the corresponding solid spheres and nanorod assemblies.

  17. Lithium-associated hyperthyroidism.

    PubMed

    Siyam, Fadi F; Deshmukh, Sanaa; Garcia-Touza, Mariana

    2013-08-01

    Goiters and hypothyroidism are well-known patient complications of the use of lithium for treatment of bipolar disease. However, the occurrence of lithium-induced hyperthyroidism is a more rare event. Many times, the condition can be confused with a flare of mania. Monitoring through serial biochemical measurement of thyroid function is critical in patients taking lithium. Hyperthyroidism induced by lithium is a condition that generally can be controlled medically without the patient having to discontinue lithium therapy, although in some circumstances, discontinuation of lithium therapy may be indicated. We report on a patient case of lithium-associated hyperthyroidism that resolved after discontinuation of the medication.

  18. Jeff Chamberlain on Lithium-air batteries

    ScienceCinema

    Chamberlain, Jeff

    2016-07-12

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

  19. Lithium plating in lithium-ion batteries investigated by voltage relaxation and in situ neutron diffraction

    NASA Astrophysics Data System (ADS)

    von Lüders, Christian; Zinth, Veronika; Erhard, Simon V.; Osswald, Patrick J.; Hofmann, Michael; Gilles, Ralph; Jossen, Andreas

    2017-02-01

    In this work, lithium plating is investigated by means of voltage relaxation and in situ neutron diffraction in commercial lithium-ion batteries. We can directly correlate the voltage curve after the lithium plating with the ongoing phase transformation from LiC12 to LiC6 according to the neutron diffraction data during the relaxation. Above a threshold current of C/2 at a temperature of -2 °C, lithium plating increases dramatically. The results indicate that the intercalation rate of deposited lithium seems to be constant, independent of the deposited amount. It can be observed that the amount of plating correlates with the charging rate, whereas a charging current of C/2 leads to a deposited amount of lithium of 5.5% of the charge capacity and a current of 1C to 9.0%.

  20. Li4Ti5O12-TiO2 nanowire arrays constructed with stacked nanocrystals for high-rate lithium and sodium ion batteries

    NASA Astrophysics Data System (ADS)

    Gao, Lin; Wang, Lichuan; Dai, Sirui; Cao, Minglei; Zhong, Zhicheng; Shen, Yan; Wang, Mingkui

    2017-03-01

    This work reports on nanoparticle-stacked Li4Ti5O12-TiO2 nanowire arrays (SLTO) as anode for lithium and sodium ion battery (NIB). Our finding shows that the pseudocapacitive effect partly contributes to the performance for the NIBs based on the SLTO electrode due to a large size volume of Na+ ions. More importantly, the SLTO nanowires constituting of the nanoparticles efficiently shorten ion diffusion length, thereafter accelerate ion insertion/extraction reaction and improve the rate capability. For the SLTO electrode, a specific capacity of 199.7 mAh g-1 can be achieved in the LIBs at a current rate of 0.75 C (voltage range of 1.0-3.0 V) and a specific capacity of 94.2 mAh g-1 is obtained in the NIBs at a high current rate of 15 C (voltage range of 0.5-2.5 V). Most importantly, the sodium ion full battery based on SLTO as anode and Na3V2(PO4)3 as cathode materials shows stable cycling performance with tiny capacity degradation (90.1 mAh g-1) after 200 cycles at a current rate of 4 C (voltage range of 1.0-4.0 V), simultaneously possessing a high energy density of 136.5 Wh kg-1 at the power density of 312 W kg-1.

  1. Morphological Evolution of High-Voltage Spinel LiNi(0.5)Mn(1.5)O4 Cathode Materials for Lithium-Ion Batteries: The Critical Effects of Surface Orientations and Particle Size.

    PubMed

    Liu, Haidong; Wang, Jun; Zhang, Xiaofei; Zhou, Dong; Qi, Xin; Qiu, Bao; Fang, Jianhui; Kloepsch, Richard; Schumacher, Gerhard; Liu, Zhaoping; Li, Jie

    2016-02-01

    An evolution panorama of morphology and surface orientation of high-voltage spinel LiNi(0.5)Mn(1.5)O4 cathode materials synthesized by the combination of the microwave-assisted hydrothermal technique and a postcalcination process is presented. Nanoparticles, octahedral and truncated octahedral particles with different preferential growth of surface orientations are obtained. The structures of different materials are studied by X-ray diffraction (XRD), Raman spectroscopy, X-ray absorption near edge spectroscopy (XANES), and transmission electron microscopy (TEM). The influence of various morphologies (including surface orientations and particle size) on kinetic parameters, such as electronic conductivity and Li(+) diffusion coefficients, are investigated as well. Moreover, electrochemical measurements indicate that the morphological differences result in divergent rate capabilities and cycling performances. They reveal that appropriate surface-tailoring can satisfy simultaneously the compatibility of power capability and long cycle life. The morphology design for optimizing Li(+) transport and interfacial stability is very important for high-voltage spinel material. Overall, the crystal chemistry, kinetics and electrochemical performance of the present study on various morphologies of LiNi(0.5)Mn(1.5)O4 spinel materials have implications for understanding the complex impacts of electrode interface and electrolyte and rational design of rechargeable electrode materials for lithium-ion batteries. The outstanding performance of our truncated octahedral LiNi(0.5)Mn(1.5)O4 materials makes them promising as cathode materials to develop long-life, high energy and high power lithium-ion batteries.

  2. Density Optimization of Lithium Lanthanum Titanate Ceramics for Lightweight Lithium-Air Batteries

    DTIC Science & Technology

    2014-11-01

    Thangadurai V, Weppner W. Lithium lanthanum titanates: a review. Chemistry of Materials. 2003;15:3974–3990. 4. Knauth P. Inorganic solid Li ion conductors...an overview. Solid State Ionics. 2009;180:911–916. 5. Ban CW, Choi GM. The effect of sintering on the grain boundary conductivity of lithium ...lanthanum titanates. Solid State Ionics. 2001;140:285–292. 6. Inada R, Kimura K, Kusakabe K, Tojo T, Sakurai Y. Synthesis and lithium -ion conductivity

  3. Hierarchical carbon-coated acanthosphere-like Li4Ti5O12 microspheres for high-power lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Sha, Yujing; Xu, Xiaomin; Li, Li; Cai, Rui; Shao, Zongping

    2016-05-01

    In this work, carbon-coated hierarchical acanthosphere-like Li4Ti5O12 microspheres (denoted as AM-LTO) were prepared via a two-step hydrothermal process with low-cost glucose as the organic carbon source. The hierarchical porous microspheres had open structures with diameters of 4-6 μm, which consisted of a bunch of willow leaf-like nanosheets. Each nanosheet was comprised of Li4Ti5O12 nanoparticles that are 20 nm in size and coated by a thin carbon layer. When applied as the anode material for lithium-ion batteries (LIBs), the AM-LTO presented outstanding rate and cycling performance due to its unique morphologies. A high capacity of 145.6 mAh g-1 was achieved for AM-LTO at a rate of 40C (1C = 175 mAh g-1). In contrast, the sample synthesized without glucose as carbon source (denoted as S-LTO) experienced an obvious structural collapse during the hydrothermal reaction and presented a specific capacity of only 67 mAh g-1 at 1C, which further decreased to 14 mAh g-1 at 40C. Further morphological growth of the acanthosphere-like Li4Ti5O12 microspheres and their excellent performance as an anode in LIBs were also discussed in this work.

  4. Polysulfide Anchoring Mechanism Revealed by Atomic Layer Deposition of V2O5 and Sulfur-Filled Carbon Nanotubes for Lithium-Sulfur Batteries.

    PubMed

    Carter, Rachel; Oakes, Landon; Muralidharan, Nitin; Cohn, Adam P; Douglas, Anna; Pint, Cary L

    2017-03-01

    Despite the promise of surface engineering to address the challenge of polysulfide shuttling in sulfur-carbon composite cathodes, melt infiltration techniques limit mechanistic studies correlating engineered surfaces and polysulfide anchoring. Here, we present a controlled experimental demonstration of polysulfide anchoring using vapor phase isothermal processing to fill the interior of carbon nanotubes (CNTs) after assembly into binder-free electrodes and atomic layer deposition (ALD) coating of polar V2O5 anchoring layers on the CNT surfaces. The ultrathin submonolayer V2O5 coating on the CNT exterior surface balances the adverse effect of polysulfide shuttling with the necessity for high sulfur utilization due to binding sites near the conductive CNT surface. The sulfur loaded into the CNT interior provides a spatially separated control volume enabling high sulfur loading with direct sulfur-CNT electrical contact for efficient sulfur conversion. By controlling ALD coating thickness, high initial discharge capacity of 1209 mAh/gS at 0.1 C and exceptional cycling at 0.2 C with 87% capacity retention after 100 cycles and 73% at 450 cycles is achieved and correlated to an optimal V2O5 anchoring layer thickness. This provides experimental evidence that surface engineering approaches can be effective to overcome polysulfide shuttling by controlled design of molecular-scale building blocks for efficient binder free lithium sulfur battery cathodes.

  5. The excitation energies and term energies of the excited states 1s2ns (n=3,4,5) and 1s2nf (n=4,5) of lithium-like systems of Z=11-20

    NASA Astrophysics Data System (ADS)

    Ge, Zi-Ming; Wang, Zhi-Wen; Zhou, Ya-Jun; He, Li-Ming; Liu, Guo-Guang

    2003-05-01

    In this paper, the full-core plus correlation (FCPC) and the Ritz method is extended to calculate the non-relativistic energies of 1s2ns (n=3,4,5) and 1s2nf (n=4,5) states and the wavefunctions of the lithium-like systems from Z=11-20. The mass-polarization and the relativistic correction including the kinetic-energy correction, the Darwin term, the electron-electron contact term and the orbit-orbit interaction are evaluated perturbatively as the first-order correction. The contribution from quantum electrodynamic is also included by using the effective nuclear charge formula. The excited energies, the term-energy and fine structure, are given and compared with the other theoretical calculation and experimental results. It is shown that the correlative wave in the FCPC method embodies well the strong correlation between the 1s2 core and the valence electron.

  6. Investigation of carbon-coated lithiated Li{sub 4+x}Ti{sub 5}O{sub 12}/C for lithium-ion batteries

    SciTech Connect

    Pan, Mengjie; Zhang, Lin; Gong, Lijun; Liu, Hongbo; Chen, Yuxi

    2015-11-15

    Highlights: • Lithiated Li{sub 4+x}Ti{sub 5}O{sub 12}/C with pre-stored active Li ions has been synthesized. • The first-cycle coulombic efficiency of Li{sub 4+x}Ti{sub 5}O{sub 12}/C is over 100%. • Li{sub 4+x}Ti{sub 5}O{sub 12}/C displays excellent cyclic stability and capacity retention. • TiO{sub 2} nanoparticles and carbon coating are necessary for formation of Li{sub 4+x}Ti{sub 5}O{sub 12}/C. - Abstract: Carbon-coated Li{sub 4}Ti{sub 5}O{sub 12} and lithiated Li{sub 4+x}Ti{sub 5}O{sub 12} anode materials have been synthesized using nanosized anatase TiO{sub 2} and commercial TiO{sub 2} with mixed structure as Ti sources, respectively. Microstructural investigation indicates that Li{sub 4}Ti{sub 5}O{sub 12} and Li{sub 4+x}Ti{sub 5}O{sub 12} are covered by amorphous carbon layers with thickness of 2–3 nm. Their electrochemical performance has been evaluated, which indicates that an amount of active Li ions have been pre-stored in the Li{sub 4+x}Ti{sub 5}O{sub 12} lattice during solid-state synthesis, resulting in its first-cycle coulombic efficiency over 100%. Further, Li{sub 4+x}Ti{sub 5}O{sub 12}/C exhibits higher cyclic capacities than Li{sub 4}Ti{sub 5}O{sub 12}/C at different current density. The reversible charge capacity retention of Li{sub 4+x}Ti{sub 5}O{sub 12}/C reaches 98.5% after 100 cycles, which indicates that Li{sub 4+x}Ti{sub 5}O{sub 12}/C is promising candidate anode material for long lifetime lithium-ion batteries. The formation mechanism of Li{sub 4+x}Ti{sub 5}O{sub 12}/C has been discussed, in which the nanosized anatase TiO{sub 2} with high chemical activity and the carbon coating play key roles for the formation of Li{sub 4+x}Ti{sub 5}O{sub 12}/C.

  7. Monodispersed mesoporous Li4Ti5O12 submicrospheres as anode materials for lithium-ion batteries: morphology and electrochemical performances

    NASA Astrophysics Data System (ADS)

    Lin, Chunfu; Fan, Xiaoyong; Xin, Yuelong; Cheng, Fuquan; Lai, Man On; Zhou, Henghui; Lu, Li

    2014-05-01

    Although nanosizing Li4Ti5O12 (LTO) materials is an effective way to improve their rate performances, their low tap density and first cycle coulombic efficiency limit their practical applications. To tackle these problems while preserving the advanced rate performances, monodispersed mesoporous LTO submicrospheres are developed here. These submicrospheres are synthesized via a solvothermal method using TiO2 submicrospheres and LiOH as precursors followed by a mild calcinations. The roles of the solvent used in the solvothermal process and calcination temperature are systematically investigated and optimized. The LTO submicrospheres fabricated by the solvothermal process using a water-ethanol (60 vol%) solvent followed by a calcination process at 600 °C reveal a large sphere size of 660 +/- 30 nm with a small primary particle size of 20-100 nm, a large specific surface area of 15.5 m2 g-1, an appropriate pore size of 4.5 nm and an ultra-high tap density of 1.62 g cm-3. Furthermore, they show high crystallinity and no blockage of Li+ ion transportation pathways. Due to the novel morphology and ideal crystal structure, these submicrospheres exhibit outstanding electrochemical performances. They display a high first cycle coulombic efficiency of 93.5% and a high charge capacity of 179 mA h g-1 at 0.5 C between 1.0 and 2.5 V (vs. Li/Li+), surpassing the theoretical capacity of LTO. Their charge capacity at 10 C is as high as 109 mA h g-1 with a capacity retention of 97.8% over 100 cycles. Therefore, this LTO material can be a superior and practical candidate for the anodes of high-power lithium-ion batteries.Although nanosizing Li4Ti5O12 (LTO) materials is an effective way to improve their rate performances, their low tap density and first cycle coulombic efficiency limit their practical applications. To tackle these problems while preserving the advanced rate performances, monodispersed mesoporous LTO submicrospheres are developed here. These submicrospheres are

  8. End-stage renal disease associated with prophylactic lithium treatment.

    PubMed

    Aiff, Harald; Attman, Per-Ola; Aurell, Mattias; Bendz, Hans; Schön, Staffan; Svedlund, Jan

    2014-04-01

    The primary aim of this study was to estimate the prevalence of lithium associated end-stage renal disease (ESRD) and to compare the relative risk of ESRD in lithium users versus non-lithium users. Second, the role of lithium in the pathogenesis of ESRD was evaluated. We used the Swedish Renal Registry to search for lithium-treated patients with ESRD among 2644 patients with chronic renal replacement therapy (RRT)-either dialysis or transplantation, within two defined geographical areas in Sweden with 2.8 million inhabitants. The prevalence date was December 31, 2010. We found 30 ESRD patients with a history of lithium treatment. ESRD with RRT was significantly more prevalent among lithium users than among non-lithium users (p<0.001). The prevalence of ESRD with RRT in the lithium user population was 15.0‰ (95% CI 9.7-20.3), and close to two percent of the RRT population were lithium users. The relative risk of ESRD with RRT in the lithium user population compared with the general population was 7.8 (95% CI 5.4-11.1). Out of those 30 patients, lithium use was classified, based on chart reviews, as being the sole (n=14) or main (n=10) cause of ESRD in 24 cases. Their mean age at the start of RRT was 66 years (46-82), their mean time on lithium 27 years (12-39), and 22 of them had been on lithium for 15 years or more. We conclude that lithium-associated ESRD is an uncommon but not rare complication of lithium treatment.

  9. Highly-crystalline ultrathin gadolinium doped and carbon-coated Li4Ti5O12 nanosheets for enhanced lithium storage

    NASA Astrophysics Data System (ADS)

    Xu, G. B.; Yang, L. W.; Wei, X. L.; Ding, J. W.; Zhong, J. X.; Chu, P. K.

    2015-11-01

    Highly-crystalline gadolinium doped and carbon-coated ultrathin Li4Ti5O12 (LTO) nanosheets (denoted as LTO-Gd-C) as an anode material for Li-ion batteries (LIBs) are synthesized on large scale by controlling the amount of carbon precursor in the topotactic transformation of layered ultrathin Li1.81H0.19Ti2O5·xH2O (H-LTO) nanosheets at 700 °C. The characterizations of structure and morphology reveal that the gadolinium doped and carbon-coated ultrathin LTO nanosheets have high crystallinity with a thickness of about 10 nm. Gadolinium doping allows the spinel LTO products to be stabilized, thereby preserving the precursor's sheet morphology and single crystal structure. Carbon encapsulation serves dual functions by restraining crystal growth of the LTO primary nanoparticles in the LTO-Gd-C nanosheets and decreasing the external electron transport resistance. Owing to the synergistic effects rendered by ultrathin nanosheets with high crystallinity, gadolinium doping and carbon coating, the developed ultrathin LTO nanosheets possess excellent specific capacity, cycling performance, and rate capability compared with reference materials, when evaluated as an anode material for lithium ion batteries (LIBs). The simple and effective strategy encompassing nanoscale morphological engineering, surface modification, and doping improves the performance of LTO-based anode materials for high energy density and high power LIBs applied in large scale energy storage.

  10. Advanced electrochemical performance of Li4Ti5O12-based materials for lithium-ion battery: Synergistic effect of doping and compositing

    NASA Astrophysics Data System (ADS)

    Lin, Chunfu; Ding, Bo; Xin, Yuelong; Cheng, Fuquan; Lai, Man On; Lu, Li; Zhou, Henghui

    2014-02-01

    To improve the rate performance of Li4Ti5O12 (LTO), we employ a doping-compositing synergistic strategy that utilizes Cu2+ to alter intrinsic property and carbon nanotubes (CNTs) to engineer extrinsic conductivity. To realize cost-effective fabrication, solid state processing is adopted in the fabrication of the composite. X-ray diffraction measurement combined with Rietveld refinement shows that all doped samples have a spinel structure with Fd 3 bar m space group without any impurities, and that both lattice parameter and occupancy of non-Li+ ions in 8a sites increase with the amount of Cu2+ dopant. Through the Cu2+ doping, the electronic conductivity and Li+ diffusion coefficient of the particles are improved by at least two orders of magnitude and four times, respectively. Through further CNTs compositing, the electrical conduction between the particles is enhanced. Between 1.0 and 2.5 V vs. Li/Li+, the specific capacity of Li3.8Cu0.3Ti4.9O12/CNTs composite at 10 C is as high as 114 mAh g-1 with little loss after 100 cycles, whereas that of pristine one is only 11 mAh g-1. The excellent electrochemical performance can be ascribed to its higher electronic conductivity and enhanced lithium ion conductivity in the particles, as well as its improved electrical conduction between the particles.

  11. Fabrication of nanoscale patterns in lithium fluoride crystal using a 13.5 nm Schwarzschild objective and a laser produced plasma source.

    PubMed

    Wang, Xin; Mu, Baozhong; Jiang, Li; Zhu, Jingtao; Yi, Shengzhen; Wang, Zhanshan; He, Pengfei

    2011-12-01

    Lithium fluoride (LiF) crystal is a radiation sensitive material widely used as EUV and soft x-ray detector. The LiF-based detector has high resolution, in principle limited by the point defect size, large field of view, and wide dynamic range. Using LiF crystal as an imaging detector, a resolution of 900 nm was achieved by a projection imaging of test meshes with a Schwarzschild objective operating at 13.5 nm. In addition, by imaging of a pinhole illuminated by the plasma, an EUV spot of 1.5 μm diameter in the image plane of the objective was generated, which accomplished direct writing of color centers with resolution of 800 nm. In order to avoid sample damage and contamination due to the influence of huge debris flux produced by the plasma source, a spherical normal-incidence condenser was used to collect EUV radiation. Together with a description of experimental results, the development of the Schwarzschild objective, the influence of condenser on energy density and the alignment of the imaging system are also reported.

  12. Molten salt lithium cells

    DOEpatents

    Raistrick, Ian D.; Poris, Jaime; Huggins, Robert A.

    1983-01-01

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

  13. Molten salt lithium cells

    DOEpatents

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

    1980-07-18

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

  14. Molten salt lithium cells

    DOEpatents

    Raistrick, Ian D.; Poris, Jaime; Huggins, Robert A.

    1982-02-09

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

  15. Lithium Ion Testing at NSWC Crane in Support of NASA Goddard Space Flight Center

    NASA Technical Reports Server (NTRS)

    Brown, Harry; Jung, David; Lee, Leonine

    2010-01-01

    This viewgraph presentation reviews Lithium Ion Cell testing at the Naval Surface Warfare Center in Crane, India. The contents include: 1) Quallion 15 Ahr Lithium-Ion Cells, LEO Life Cycle Test; 2) Lithion 50 Ahr Lithium-Ion Cells, LEO Life Cycle Test; 3) ABSL 5 Ahr Lithium-Ion Battery, LRO-LLO Life Cycle Test, SDO-GEO Life Cycle Test; and 4) A123 40 Ahr Lithium-Ion Battery, GPM Life Cycle Test, MMS Life Cycle Test.

  16. Novel peapoded Li4Ti5O12 nanoparticles for high-rate and ultralong-life rechargeable lithium ion batteries at room and lower temperatures

    NASA Astrophysics Data System (ADS)

    Peng, Liang; Zhang, Huijuan; Fang, Ling; Zhang, Yan; Wang, Yu

    2016-01-01

    In this paper, a novel peapod-like Li4Ti5O12-C composite architecture with high conductivity is firstly designed and synthesized to be used as anode materials for lithium-ion batteries. In the synthesis, Na2Ti3O7 nanotubes act as precursors and sacrificial templates, and glucose molecules serve as the green carbon source, thus the peapod-like Li4Ti5O12-C composite can be fabricated by a facile hydrothermal reaction and the subsequent solid-state process. Compared to the previous reports, the as-prepared samples obtained by our new strategy exhibit excellent electrochemical performances, such as outstanding rate capability (an extremely reversible capability of 148 mA h g-1, 125 mA h g-1 at 30 C and 90 C, respectively) as well as excellent cycling performance (about 5% capacity loss after 5000 cycles at 10 C with 152 mA h g-1 capacity retained). The low-temperature measurements also demonstrate that the electrochemical performances of the peapod-like Li4Ti5O12-C composite are remarkably improved at various rate currents (at the low-temperature of -25 °C, a high Coulombic efficiency of about 99% can be achieved after 500 cycles at 10 C).In this paper, a novel peapod-like Li4Ti5O12-C composite architecture with high conductivity is firstly designed and synthesized to be used as anode materials for lithium-ion batteries. In the synthesis, Na2Ti3O7 nanotubes act as precursors and sacrificial templates, and glucose molecules serve as the green carbon source, thus the peapod-like Li4Ti5O12-C composite can be fabricated by a facile hydrothermal reaction and the subsequent solid-state process. Compared to the previous reports, the as-prepared samples obtained by our new strategy exhibit excellent electrochemical performances, such as outstanding rate capability (an extremely reversible capability of 148 mA h g-1, 125 mA h g-1 at 30 C and 90 C, respectively) as well as excellent cycling performance (about 5% capacity loss after 5000 cycles at 10 C with 152 mA h g-1 capacity

  17. Lithium-associated kidney microcysts.

    PubMed

    Tuazon, Jennifer; Casalino, David; Syed, Ehteshamuddin; Batlle, Daniel

    2008-08-31

    Long-term lithium therapy is associated with impairment in concentrating ability and, occasionally, progression to advanced chronic kidney disease from tubulointerstitial nephropathy. Biopsy findings in patients with lithium-induced chronic tubulointerstitial nephropathy include tubular atrophy and interstitial fibrosis interspersed with tubular cysts and dilatations. Recent studies have shown that cysts are seen in 33-62.5% of the patients undergoing lithium therapy. MR imaging is highly capable of defining renal morphological features and has been demonstrated to be superior to US and CT scan for the visualization of small renal cysts. The microcysts are found in both cortex and medulla, particularly in the regions with extensive atrophy and fibrosis, and can be multiple and bilateral. They tend to be sparse and do not normally exceed 1-2 mm in diameter. The renal microcysts in the image here reported are subtle, but consistent with lithium-induced chronic nephropathy. An MRI of the kidneys provides noninvasive evidence that strengthens the diagnosis of lithium-induced nephropathy.

  18. Lithium intercalation mechanism into FeF3·0.5H2O as a highly stable composite cathode material

    PubMed Central

    Ali, Ghulam; Lee, Ji–Hoon; Chang, Wonyoung; Cho, Byung-Won; Jung, Hun-Gi; Nam, Kyung-Wan; Chung, Kyung Yoon

    2017-01-01

    The growing demand for lithium-ion batteries (LIBs) requires investigation of high-performance electrode materials with the advantages of being environmentally friendly and cost-effective. In this study, a nanocomposite of open-pyrochlore-structured FeF3·0.5H2O and reduced graphene oxide (RGO) is synthesized for use as a high-performance cathode in LIBs, where RGO provides high electrical conductivity to the composite material. The morphology of the composite shows that FeF3·0.5H2O spheres are embedded into RGO layers and high-resolution TEM image shows that those spheres are composed of primary nanoparticles with a size of ~5 nm. The cycling performance indicates that the composite electrode delivers an initial high discharge capacity of 223 mAh g−1 at 0.05 C, a rate capability up to a high C-rate of 10 C (47 mAh g−1) and stable cycle performance at 0.05 C (145 mAh g−1 after 100 cycles) and 0.2 C (93 mAh g−1 after 100 cycles) while maintaining high electrochemical reversibility. Furthermore, the responsible electrochemical reaction is investigated using in-situ XRD and synchrotron-based X-ray absorption spectroscopy (XAS), and the XRD results show that FeF3·0.5H2O transitions to an amorphous-like phase through a lithiation process. However, a reversible oxidation change of Fe3+ ↔ Fe2+ is identified by the XAS results. PMID:28169373

  19. Lithium intercalation mechanism into FeF3·0.5H2O as a highly stable composite cathode material

    NASA Astrophysics Data System (ADS)

    Ali, Ghulam; Lee, Ji–Hoon; Chang, Wonyoung; Cho, Byung-Won; Jung, Hun-Gi; Nam, Kyung-Wan; Chung, Kyung Yoon

    2017-02-01

    The growing demand for lithium-ion batteries (LIBs) requires investigation of high-performance electrode materials with the advantages of being environmentally friendly and cost-effective. In this study, a nanocomposite of open-pyrochlore-structured FeF3·0.5H2O and reduced graphene oxide (RGO) is synthesized for use as a high-performance cathode in LIBs, where RGO provides high electrical conductivity to the composite material. The morphology of the composite shows that FeF3·0.5H2O spheres are embedded into RGO layers and high-resolution TEM image shows that those spheres are composed of primary nanoparticles with a size of ~5 nm. The cycling performance indicates that the composite electrode delivers an initial high discharge capacity of 223 mAh g‑1 at 0.05 C, a rate capability up to a high C-rate of 10 C (47 mAh g‑1) and stable cycle performance at 0.05 C (145 mAh g‑1 after 100 cycles) and 0.2 C (93 mAh g‑1 after 100 cycles) while maintaining high electrochemical reversibility. Furthermore, the responsible electrochemical reaction is investigated using in-situ XRD and synchrotron-based X-ray absorption spectroscopy (XAS), and the XRD results show that FeF3·0.5H2O transitions to an amorphous-like phase through a lithiation process. However, a reversible oxidation change of Fe3+ ↔ Fe2+ is identified by the XAS results.

  20. High-performance lithium-ion batteries with 1.5 μm thin copper nanowire foil as a current collector

    NASA Astrophysics Data System (ADS)

    Chu, Hsun-Chen; Tuan, Hsing-Yu

    2017-04-01

    Cu Foil, a thin sheet of Cu, is the common anode current collector in commercial lithium ion batteries (LIBs) which accounts for ∼ 10 wt% of the total cell weight. However, thickness reduction of LIB-based Cu foils below 6 μm has been limited by the incapability of conventional rolling annealing or electrodeposition process. We here report a new type of Cu foil, so called Cu nanowire foil (CuNW foil), for use as an LIB anode current collector. We fabricate Cu NW foils by rolling press Cu nanowire fabric to reduce the thickness down to ∼1.5 μm with an areal weight down to ∼1.2 mg cm-2 and a density approximately 96% to that of bulk Cu. The rough surface and porous structure of CuNW foil enable better wetting and adhering properties of graphite slurry on foil. In full cell examination, a cell of a areal capacity of 3 mAh cm-2 exhibits 83.6% capacity retention for 600 cycles at 0.6 C that meets the standard specification of most commercial LIBs. As a proof-of-concept of demonstration, we fabricate a 700 mA pouch-type battery implemented with graphite-Cu NWs foil anodes to serve as energy supply to operate electronic devices.

  1. Zr4+ doping in Li4Ti5O12 anode for lithium-ion batteries: open Li+ diffusion paths through structural imperfection.

    PubMed

    Kim, Jae-Geun; Park, Min-Sik; Hwang, Soo Min; Heo, Yoon-Uk; Liao, Ting; Sun, Ziqi; Park, Jong Hwan; Kim, Ki Jae; Jeong, Goojin; Kim, Young-Jun; Kim, Jung Ho; Dou, Shi Xue

    2014-05-01

    One-dimensional nanomaterials have short Li(+) diffusion paths and promising structural stability, which results in a long cycle life during Li(+) insertion and extraction processes in lithium rechargeable batteries. In this study, we fabricated one-dimensional spinel Li4Ti5O12 (LTO) nanofibers using an electrospinning technique and studied the Zr(4+) doping effect on the lattice, electronic structure, and resultant electrochemical properties of Li-ion batteries (LIBs). Accommodating a small fraction of Zr(4+) ions in the Ti(4+) sites of the LTO structure gave rise to enhanced LIB performance, which was due to structural distortion through an increase in the average lattice constant and thereby enlarged Li(+) diffusion paths rather than changes to the electronic structure. Insulating ZrO2 nanoparticles present between the LTO grains due to the low Zr(4+) solubility had a negative effect on the Li(+) extraction capacity, however. These results could provide key design elements for LTO anodes based on atomic level insights that can pave the way to an optimal protocol to achieve particular functionalities.

  2. Influence of Sc3+ doping in B-site on electrochemical performance of Li4Ti5O12 anode materials for lithium-ion battery

    NASA Astrophysics Data System (ADS)

    Zhang, Yaoyao; Zhang, Chunming; Lin, Ye; Xiong, Ding-Bang; Wang, Dan; Wu, Xiaoyan; He, Dannong

    2014-03-01

    Anode materials Li4Ti5O12 (LTO) and Sc-doped Li4Ti4.95Sc0.05O12-δ (LTSO) for lithium-ion batteries are both successfully synthesized by the modified sol-gel method with ethylene diamine tetraacetic acid (EDTA) and citric acid (CA) as a bi-components chelating agent. The samples are characterized by XRD, BET, XPS, EDX and SEM. The dopant Sc totally enters into the 16d sites of the spinel structure of LTO, and then further affects its morphology and property. The LTSO powder exhibits a 3D network morphology and its grain size is about 200 nm. The LTSO electrode material exhibits an excellent initial discharge capacities of 174 and 94 mAh g-1 at 1 C and 40 C, respectively. The reversible capacities of LTSO at different current rates remain nearly 100% after 50 cycles, which are compared with the capacities of the second cycles. Sc3+ doping can greatly improve the electronic conductivity of LTO which is demonstrated by electrochemical impedance spectroscopy. Cyclic voltammetry measurements also reveal that LTSO has small polarization resistance due to the high electrical conductivity and Li-ion apparent diffusion rate.

  3. Charge-discharge characteristics of all-solid-state thin-filmed lithium-ion batteries using amorphous Nb 2O 5 negative electrodes

    NASA Astrophysics Data System (ADS)

    Nakazawa, Hiromi; Sano, Kimihiro; Abe, Takashi; Baba, Mamoru; Kumagai, Naoaki

    All-solid-state thin-filmed lithium-ion rechargeable batteries composed of amorphous Nb 2O 5 negative electrode with the thickness of 50-300 nm and amorphous Li 2Mn 2O 4 positive electrode with a constant thickness of 200 nm, and amorphous Li 3PO 4- xN x electrolyte (100 nm thickness), have been fabricated on glass substrates with a 50 mm × 50 mm size by a sputtering method, and their electrochemical characteristics were investigated. The charge-discharge capacity based on the volume of positive electrode increased with increasing thickness of negative electrode, reaching about 600 mAh cm -3 for the battery with the negative electrode thickness of 200 nm. But the capacity based on the volume of both the positive and negative electrodes was the maximum value of about 310 mAh cm -3 for the battery with the negative electrode thickness of 100 nm. The shape of charge-discharge curve consisted of a two-step for the batteries with the negative electrode thickness more than 200 nm, but that with the thickness of 100 nm was a smooth S-shape curve during 500 cycles.

  4. Poly(2,5-dimercapto-1,3,4-thiadiazole) as a cathode for rechargeable lithium batteries with dramatically improved performance.

    PubMed

    Gao, Jie; Lowe, Michael A; Conte, Sean; Burkhardt, Stephen E; Abruña, Héctor D

    2012-07-02

    Organosulfur compounds with multiple thiol groups are promising for high gravimetric energy density electrochemical energy storage. We have synthesized a poly(2,5-dimercapto-1,3,4-thiadiazole) (PDMcT)/poly(3,4-ethylenedioxythiophene) (PEDOT) composite cathode for lithium-ion batteries with a new method and investigated its electrochemical behavior by charge/discharge cycles and cyclic voltammetry (CV) in an ether-based electrolyte. Based on a comparison of the electrochemical performance with a carbonate-based electrolyte, we found a much higher discharge capacity, but also a very attractive cycling performance of PDMcT by using a tetra(ethylene glycol) dimethyl ether (TEGDME)-based electrolyte. The first discharge capacity of the as-synthesized PDMcT/PEDOT composite approached 210 mAh g(-1) in the TEGDME-based electrolyte. CV results clearly show that the redox reactions of PDMcT are highly reversible in this TEGDME-based electrolyte. The reversible capacity remained around 120 mAh g(-1) after 20 charge/discharge cycles. With improved cycling performance and very low cost, PDMcT could become a very promising cathode material when combined with a TEGDME-based electrolyte. The poor capacity in the carbonate-based electrolyte is a consequence of the irreversible reaction of the DMcT monomer and dimer with the solvent, emphasizing the importance of electrolyte chemistry when studying molecular-based battery materials.

  5. Monodispersed Li4Ti5O12 with Controlled Morphology as High Power Lithium Ion Battery Anodes

    SciTech Connect

    Li, Yunchao; Fu, Guoyi; Watson, Mark; Harrison, Stephen; Paranthaman, M. Parans

    2016-05-31

    Monodispersed Li4Ti5O12 (LTO) nanoparticles with controlled microstructure were successfully synthesized by a combination of hydrolysis and hydrothermal method followed by a post-annealing process. The scanning electron microscopy images showed that particles with a size of 30-40 nm were precisely controlled throughout the synthesis process. The electrochemical tests of the as-prepared LTO electrodes in a half-cell proved its high rate performance and outstanding cyclability which benefits from the preserved well-controlled nanoparticle size and morphology. LTO electrodes were also tested in a full cell configuration in pairing with LiFePO4 cathodes, which demonstrated a capacity of 147.3 mAh g-1. In addition, we have also demonstrated that LTO materials prepared using lithium salts separated from geothermal brine solutions had good cyclability. These demonstrations provide a promising way for making low-cost, large-scale LTO electrode materials for energy storage applications.

  6. In situ SEM Study of Lithium Intercalation in individual V2O5 Nanowires

    SciTech Connect

    Strelcov, Evgheni; Cothren, Joshua E.; Leonard, Donovan N.; Borisevich, Albina Y.; Kolmakov, Andrei

    2015-01-08

    Progress in rational engineering of Li-ion batteries requires better understanding of the electrochemical processes and accompanying transformations in the electrode materials on multiple length scales. In spite of recent progress in utilizing transmission electron microscopy (TEM) to analyze these materials, in situ scanning electron microscopy (SEM) was mostly overlooked as a powerful tool that allows probing these phenomena on the nano and mesoscale. In this paper, we report on in situ SEM study of lithiation in a V2O5-based single-nanobelt battery with ionic liquid electrolyte. Coupled with cyclic voltammetry measurements, in situ SEM revealed the peculiarities of subsurface intercalation, formation of solid-electrolyte interface (SEI) and electromigration of liquid. We observed that single-crystalline vanadia nanobelts do not undergo large-scale amorphization or fracture during electrochemical cycling, but rather transform topochemically with only a slight shape distortion. Lastly, the SEI layer seems to have significant influence on the lithium ion diffusion and overall capacity of the single-nanobelt battery.

  7. Lithium nephropathy: unique sonographic findings.

    PubMed

    Di Salvo, Donald N; Park, Joseph; Laing, Faye C

    2012-04-01

    This case series describes a unique sonographic appearance consisting of numerous microcysts and punctate echogenic foci seen on renal sonograms of 10 adult patients receiving chronic lithium therapy. Clinically, chronic renal insufficiency was present in 6 and nephrogenic diabetes insipidus in 2. Sonography showed numerous microcysts and punctate echogenic foci. Computed tomography in 5 patients confirmed microcysts and microcalcifications, which were fewer in number than on sonography. Magnetic resonance imaging in 2 patients confirmed microcysts in each case. Renal biopsy in 1 patient showed chronic interstitial nephritis, microcysts, and tubular dilatation. The diagnosis of lithium nephropathy should be considered when sonography shows these findings.

  8. Lithium Battery Diaper Ulceration.

    PubMed

    Maridet, Claire; Taïeb, Alain

    2016-01-01

    We report a case of lithium battery diaper ulceration in a 16-month-old girl. Gastrointestinal and ear, nose, and throat lesions after lithium battery ingestion have been reported, but skin involvement has not been reported to our knowledge.

  9. Lithium electric dipole polarizability

    SciTech Connect

    Puchalski, M.; KePdziera, D.; Pachucki, K.

    2011-11-15

    The electric dipole polarizability of the lithium atom in the ground state is calculated including relativistic and quantum electrodynamics corrections. The obtained result {alpha}{sub E}=164.0740(5) a.u. is in good agreement with the less accurate experimental value of 164.19(1.08) a.u. The small uncertainty of about 3 parts per 10{sup 6} comes from the approximate treatment of quantum electrodynamics corrections. Our theoretical result can be considered as a benchmark for more general atomic structure methods and may serve as a reference value for the relative measurement of polarizabilities of the other alkali-metal atoms.

  10. Lithium Cell Reactions.

    DTIC Science & Technology

    1983-12-01

    SUPPLEMENTARY NOTES It. KEY WORDS (Continue on reverse .,ide if necessary and Identify by block number) Batteries Thionyl Chloride Batteries Lithium ...Batteries Lithium Cells Primary Batteries Thionyl Chloride Cells Non Rechargeable Batteries Electrochemical Reactions 20. ABSTRACT (Continue on reverse...INVESTIGATION OF CHEMICAL, ELECTROCHEMICAL AND PARASITIC REACTIONS IN LITHIUM - THIONYL CHLORIDE CELLS .......................................... 1 1.0 IN TRO D UC

  11. Comparison of LiVPO4F to Li4Ti5O12 as anode materials for lithium-ion batteries.

    PubMed

    Ma, Rui; Shao, Lianyi; Wu, Kaiqiang; Shui, Miao; Wang, Dongjie; Pan, Jianguo; Long, Nengbing; Ren, Yuanlong; Shu, Jie

    2013-09-11

    In this paper, we reported on a comparison of LiVPO4F to Li4Ti5O12 as anode materials for lithium-ion batteries. Combined with powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, galvanostatic discharge/charge tests and in situ X-ray diffraction technologies, we explore and compare the insertion/extraction mechanisms of LiVPO4F based on the V3+/V2+/V+ redox couples and Li4Ti5O12 based on the Ti4+/Ti3+ redox couple cycled in 1.0-3.0 V and 0.0-3.0 V. The electrochemical results indicate that both LiVPO4F and Li4Ti5O12 are solid electrolyte interphase free materials in 1.0-3.0 V. The insertion/extraction mechanisms of LiVPO4F and Li4Ti5O12 are similar with each other in 1.0-3.0 V as proved by in situ X-ray diffraction. It also demonstrates that both samples possess stable structure in 0.0-3.0 V. Additionally, the electrochemical performance tests of LiVPO4F and Li4Ti5O12 indicate that both samples cycled in 0.0-3.0 V exhibit much higher capacities than those cycled in 1.0-3.0 V but display worse cycle performance. The rate performance of Li4Ti5O12 far exceeds that of LiVPO4F in the same electrochemical potential window. In particular, the capacity retention of Li4Ti5O12 cycled in 1.0-3.0 V is as high as 98.2% after 20 cycles. By contrast, Li4Ti5O12 is expected to be a candidate anode material considering its high working potential, structural zero-strain property, and excellent cycle stability and rate performance.

  12. A new iron V[sub 2]O[sub 5] bronze as electrode material for rechargeable lithium batteries

    SciTech Connect

    Maingot, S.; Baffier, N. . Lab. de Chimie Appliquee de l'Etat Solide); Baddour, R.; Pereira-Ramos, J.P. . Lab. d'Electrochimie); Willmann, P. )

    1993-11-01

    A new iron V[sub 2]O[sub 5] bronze, Fe[sub 0.12]V[sub 2]O[sub 5], has been prepared via a sol-gel process. This compound exhibits an orthorhombic structure which closely resembles that of the parent oxide V[sub 2]O[sub 5]. A preliminary investigation of its electrochemical properties as rechargeable cathodic material for Li batteries is performed. The results are discussed in relation with the electrochemical behavior known for V[sub 2]O[sub 5]. Three reversible insertion steps appear in the potential range 3.8 to 2 V vs Li/Li[sup +]. They correspond to a high faradaic yield of 2.5 F. per mole of bronze mainly due to the unusually wide Li concentration range involved in the third process located near 2.3 V ([Delta]X = 1.5). The presence of ferric ions in the orthorhombic host lattice is seen to induce interesting features especially in terms of cycle life (potential range: 3.8 to 2 V; C/4 discharge-charge rate) with a specific capacity of about 200 Ah/kg after 40 cycles.

  13. Vitis labrusca extract effects on cellular dynamics and redox modulations in a SH-SY5Y neuronal cell model: a similar role to lithium.

    PubMed

    Scola, Gustavo; Laliberte, Victoria Louise Marina; Kim, Helena Kyunghee; Pinguelo, Arsene; Salvador, Mirian; Young, L Trevor; Andreazza, Ana Cristina

    2014-12-01

    Oxidative stress and calcium imbalance are consistently reported in bipolar disorder (BD). Polymorphism of voltage-dependent calcium channel, L type, alpha 1C subunit (CACNA1c), which is responsible for the regulation of calcium influx, was also shown to have a strong association with BD. These alterations can lead to a number of different consequences in the cell including production of reactive species causing oxidative damage to proteins, lipids and DNA. Lithium is the most frequent medication used for the treatment of BD. Despite lithium's effects, long-term use can result in many negative side effects. Therefore, there is an urgent need for the development of drugs that may have similar biological effects as lithium without the negative consequences. Moreover, polyphenols are secondary metabolites of plants that present multi-faceted molecular abilities, such as regulation of cellular responses. Vitis labrusca extract (VLE), a complex mixture of polyphenols obtained from seeds of winery wastes of V. labrusca, was previously characterized by our group. This extract presented powerful antioxidant and neuroprotective properties. Therefore, the ability of VLE to ameliorate the consequences of hydrogen peroxide (H2O2)-induced redox alterations to cell viability, intracellular calcium levels and the relative levels of the calcium channel CACNA1c in comparison to lithium's effects were evaluated using a neuroblastoma cell model. H2O2 treatment increased cell mortality through apoptotic and necrotic pathways leading to an increase in intracellular calcium levels and alterations to relative CACNA1c levels. VLE and lithium were found to similarly ameliorate cell mortality through regulation of the apoptotic/necrotic pathways, decreasing intracellular calcium levels and preventing alterations to the relative levels of CACNA1c. The findings of this study suggest that VLE exhibits protective properties against oxidative stress-induced alterations similar to that of lithium

  14. Intermetallic insertion anodes for lithium batteries.

    SciTech Connect

    Thackeray, M. M.; Vaughey, J.; Johnson, C. S.; Kepler, K. D.

    1999-11-12

    Binary intermetallic compounds containing lithium, or lithium alloys, such as Li{sub x}Al, Li{sub x}Si and Li{sub x}Sn have been investigated in detail in the past as negative electrode materials for rechargeable lithium batteries. It is generally acknowledged that the major limitation of these systems is the large volumetric expansion that occurs when lithium reacts with the host metal. Such large increases in volume limit the practical use of lithium-tin electrodes in electrochemical cells. It is generally recognized that metal oxide electrodes, MO{sub y}, in lithium-ion cells operate during charge and discharge by means of a reversible lithium insertion/extraction process, and that the cells offer excellent cycling behavior when the crystallographic changes to the unit cell parameters and unit cell volume of the Li{sub x}MO{sub y} electrode are kept to a minimum. An excellent example of such an electrode is the spinel Li{sub 4}Ti{sub 5}O{sub 12}, which maintains its cubic symmetry without any significant change to the lattice parameter (and hence unit cell volume) during lithium insertion to the rock-salt composition Li{sub 7}Ti{sub 5}O{sub 12}. This spinel electrode is an example of a ternary Li{sub x}MO{sub y} system in which a binary MO{sub y} framework provides a stable host structure for lithium. With this approach, the authors have turned their attention to exploring ternary intermetallic systems Li{sub x}MM{prime} in the hope of finding a system that is not subject to the high volumetric expansion that typifies many binary systems. In this paper, the authors present recent data of their investigations of lithium-copper-tin and lithium-indium-antimonide electrodes in lithium cells. The data show that lithium can be inserted reversibly into selected intermetallic compounds with relatively small expansion of the lithiated intermetallic structures.

  15. Truncated octahedral LiNi0.5Mn1.5O4 cathode material for ultralong-life lithium-ion battery: Positive (100) surfaces in high-voltage spinel system

    NASA Astrophysics Data System (ADS)

    Liu, Haidong; Kloepsch, Richard; Wang, Jun; Winter, Martin; Li, Jie

    2015-12-01

    So far, it has not yet reached an agreement that (111) surfaces or (100) surfaces are more positive to electrochemical performance in the spinel system. Herein, we present the synthesis of regular truncated octahedral high-voltage spinel LiNi0.5Mn1.5O4 single crystals with preferred growth of (100) surfaces, which incredibly exhibit the best long-term cycling stability compared with the state-of-art spinel material. The capacity retention is about 90% after 2000 cycles at 1 C. The extraordinary performance is mostly attributed to the highly regular truncated octahedral microstructure with large portions of stable (100) facets, which can stabilize the spinel structure to effectively suppress the side reactions with the electrolyte at high operating voltage and are also orientated to support Li+ transport kinetics. Therefore, our work further promotes the practical application of LiNi0.5Mn1.5O4 cathode material in next generation Lithium-ion batteries with high energy density and power performance.

  16. High rate performance of the carbon encapsulated Li4Ti5O12 for lithium ion battery

    NASA Astrophysics Data System (ADS)

    Cheng, Qi; Tang, Shun; Liang, Jiyuan; Zhao, Jinxing; Lan, Qian; Liu, Chang; Cao, Yuan-Cheng

    Li4Ti5O12 (LTO) is attractive alternative anode material with excellent cyclic performance and high rate after coating modifications of the conductive materials. Anatase TiO2 and glucose were applied of the synthesis of the carbon coated LTO (C@LTO). XRD results showed that all the major diffractions from the spinel structure of LTO can be found in the C@LTO such as (1 1 1), (3 1 1), (4 0 0) but there are no observations of the Carbon diffraction peaks. Electrochemical Impedance Spectroscopy (EIS) data shows C@LTO resistance was nearly half of the LTO value. Rate performance showed that capacity of C@LTO was higher than that of the pure LTO from 0.1 C, 0.2 C, 1 C, 2 C, 5 C and 10 C, which indicates that this is a promising approach to prepare the high performance LTO anode.

  17. Heavily Cr3+-modified Li4Ti5O12: An advanced anode material for rechargeable lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Lin, Chunfu; Liang, Guisheng; Gao, Jinxiang; Deng, Shengjue; Lin, Shiwei; Li, Jianbao

    2016-11-01

    Heavily Cr3+-modified Li4Ti5O12 powders with a designed nominal composition of Li3Cr7Ti2O16 have been prepared by one-step solid-state reaction. X-ray diffraction (XRD) combined with Rietveld refinement indicates that these powders contain 96.5wt.% spinel Li0.759Cr1.724Ti0.517O4 and 3.5wt.% Cr2O3. Due to the combination of Ti3+/Ti4+ and Cr2+/Cr3+ redox couples in Li0.759Cr1.724Ti0.517O4 and the existence of Cr2O3, the composite exhibits a large first-cycle discharge capacity of 315mAhṡg-1 at a small current density of 62.5mAṡg-1. Li0.759Cr1.724Ti0.517O4 shows an improved Li+ ion diffusion coefficient and electronic conductivity, respectively arising from the small O2- ion fractional coefficient and unpaired 3d electrons in Cr3+ ions. The majority of Cr2O3 is reduced to Cr after the first two lithiation processes, which benefits the electrical conduction between the Li0.759Cr1.724Ti0.517O4 particles. Consequently, the composite exhibits a good rate performance and cyclability. Its capacity at 1000mAṡg-1 is as large as 141mAhṡg-1 with large retention of 90.1% after 100 cycles.

  18. STUDY ON LITHIUM FAST ION CONDUCTORS OF Li2O SiO2 V2O5 SYSTEM

    NASA Astrophysics Data System (ADS)

    Huang, Geng; Wang, Wenji

    Fast ion conductors of Li2O SiO2 V2O5 system have been prepared by using Li2O, SiO2 and V2O5 as starting materials. The optimal ratio of starting materials was designed by Uniform Design. The conductivities of both electric and ionic were investigated. The highest ion conductivity is 1.5 × 10-4S/cm at ambient temperature for the above lithium fast ion conductor system, the electronic conductivity is 4 orders of magnitude lower than the ionic conductivity.

  19. Review of lithium effects on brain and blood.

    PubMed

    Young, Wise

    2009-01-01

    Clinicians have long used lithium to treat manic depression. They have also observed that lithium causes granulocytosis and lymphopenia while it enhances immunological activities of monocytes and lymphocytes. In fact, clinicians have long used lithium to treat granulocytopenia resulting from radiation and chemotherapy, to boost immunoglobulins after vaccination, and to enhance natural killer activity. Recent studies revealed a mechanism that ties together these disparate effects of lithium. Lithium acts through multiple pathways to inhibit glycogen synthetase kinase-3beta (GSK3 beta). This enzyme phosphorylates and inhibits nuclear factors that turn on cell growth and protection programs, including the nuclear factor of activated T cells (NFAT) and WNT/beta-catenin. In animals, lithium upregulates neurotrophins, including brain-derived neurotrophic factor (BDNF), nerve growth factor, neurotrophin-3 (NT3), as well as receptors to these growth factors in brain. Lithium also stimulates proliferation of stem cells, including bone marrow and neural stem cells in the subventricular zone, striatum, and forebrain. The stimulation of endogenous neural stem cells may explain why lithium increases brain cell density and volume in patients with bipolar disorders. Lithium also increases brain concentrations of the neuronal markers n-acetyl-aspartate and myoinositol. Lithium also remarkably protects neurons against glutamate, seizures, and apoptosis due to a wide variety of neurotoxins. The effective dose range for lithium is 0.6-1.0 mM in serum and >1.5 mM may be toxic. Serum lithium levels of 1.5-2.0 mM may have mild and reversible toxic effects on kidney, liver, heart, and glands. Serum levels of >2 mM may be associated with neurological symptoms, including cerebellar dysfunction. Prolonged lithium intoxication >2 mM can cause permanent brain damage. Lithium has low mutagenic and carcinogenic risk. Lithium is still the most effective therapy for depression. It "cures" a third

  20. Lithium toxicity in a neonate owing to false elevation of blood lithium levels caused by contamination in a lithium heparin container: case report and review of the literature.

    PubMed

    Arslan, Zainab; Athiraman, Naveen K; Clark, Simon J

    2016-08-01

    Lithium toxicity in a neonate can occur owing to antenatal exposure as a result of maternal treatment for psychiatric illnesses. False elevation of lithium levels has been reported in the paediatric population when the sample was mistakenly collected in a lithium heparin container. A term, male infant was born to a mother who was on lithium treatment for a psychiatric illness. On day 1, the infant was jittery, had a poor suck with difficulties in establishing feeds. Blood taken from the infant approximately 8 hours after birth demonstrated a lithium level of 4.9 mmol/L (adult toxic level w1.5 mmol/L). However, the sample for lithium levels was sent in a lithium heparin container and the probability of false elevation was considered. He was closely monitored in the neonatal intensive care unit and his hydration was optimised with intravenous fluids. Clinically, he remained well and commenced feeding, and his jitteriness had decreased the following day. A repeat blood lithium level, collected in a gel container, was only 0.4 mmol/L. The initially raised lithium level was owing to contamination from the lithium heparin container.

  1. Lithium-ion capacitors using carbide-derived carbon as the positive electrode - A comparison of cells with graphite and Li4Ti5O12 as the negative electrode

    NASA Astrophysics Data System (ADS)

    Rauhala, Taina; Leis, Jaan; Kallio, Tanja; Vuorilehto, Kai

    2016-11-01

    The use of carbide-derived carbon (CDC) as the positive electrode material for lithium-ion capacitors (LICs) is investigated. CDC based LIC cells are studied utilizing two different negative electrode materials: graphite and lithium titanate Li4Ti5O12 (LTO). The graphite electrodes are prelithiated before assembling the LICs, and LTO containing cells are studied with and without prelithiation. The rate capability and cycle life stability during 1000 cycles are evaluated by galvanostatic cycling at current densities of 0.4-4 mA cm-2. The CDC shows a specific capacitance of 120 F g-1 in the organic lithium-containing electrolyte, and the LICs demonstrate a good stability over 1000 charge-discharge cycles. The choice of the negative electrode is found to have an effect on the utilization of the CDC positive electrode during cycling and on the specific energy of the device. The graphite/CDC cell delivers a maximum specific discharge energy of 90 Wh kg-1 based on the total mass of active material in the cell. Both the prelithiated and non-prelithiated LTO/CDC cells show a specific energy of around 30 Wh kg-1.

  2. Quercetin as electrolyte additive for LiNi0.5Mn1.5O4 cathode for lithium-ion secondary battery at elevated temperature

    NASA Astrophysics Data System (ADS)

    Kim, Sungkyung; Kim, Myeongho; Choi, Insoo; Kim, Jae Jeong

    2016-12-01

    In an attempt to ameliorate the poor cyclability of LiNi0.5Mn1.5O4 at elevated temperature, quercetin is applied as an additive. The irreversible oxidative behavior of quercetin is thoroughly investigated by electrochemical method. The improved cyclability of the quercetin-containing cell at high temperature implies that by forming robust and less-resistive SEI, quercetin is preferentially oxidized and passivates the LiNi0.5Mn1.5O4 electrode. EIS result coherently suggests that the quercetin-added electrolyte forms a more compact and Li-ion conducting interface. The surface sensitive XPS analysis confirms that the presence of quercetin restrains the formation of LiF, suppresses the reaction of PF5, and alleviates Mn dissolution. Meanwhile, ICP-MS analysis affirms the effectiveness of quercetin against Mn dissolution. The self-discharge experiment which exhibits the retained charged state of LiNi0.5Mn1.5O4 at high temperature, gives convincing evidence of the effect of quercetin. Intensive analyses confirm that quercetin can effectively prolong the cycle-life of LiNi0.5Mn1.5O4 at elevated temperature. We envision its potential and practical usage as an electrolyte additive for high-voltage cathode.

  3. The synergetic effect of lithium polysulfide and lithium nitrate to prevent lithium dendrite growth

    NASA Astrophysics Data System (ADS)

    Li, Weiyang; Yao, Hongbin; Yan, Kai; Zheng, Guangyuan; Liang, Zheng; Chiang, Yet-Ming; Cui, Yi

    2015-06-01

    Lithium metal has shown great promise as an anode material for high-energy storage systems, owing to its high theoretical specific capacity and low negative electrochemical potential. Unfortunately, uncontrolled dendritic and mossy lithium growth, as well as electrolyte decomposition inherent in lithium metal-based batteries, cause safety issues and low Coulombic efficiency. Here we demonstrate that the growth of lithium dendrites can be suppressed by exploiting the reaction between lithium and lithium polysulfide, which has long been considered as a critical flaw in lithium-sulfur batteries. We show that a stable and uniform solid electrolyte interphase layer is formed due to a synergetic effect of both lithium polysulfide and lithium nitrate as additives in ether-based electrolyte, preventing dendrite growth and minimizing electrolyte decomposition. Our findings allow for re-evaluation of the reactions regarding lithium polysulfide, lithium nitrate and lithium metal, and provide insights into solving the problems associated with lithium metal anodes.

  4. Method of recycling lithium borate to lithium borohydride through diborane

    DOEpatents

    Filby, Evan E.

    1976-01-01

    This invention provides a method for the recycling of lithium borate to lithium borohydride which can be reacted with water to generate hydrogen for utilization as a fuel. The lithium borate by-product of the hydrogen generation reaction is reacted with hydrogen chloride and water to produce boric acid and lithium chloride. The boric acid and lithium chloride are converted to lithium borohydride through a diborane intermediate to complete the recycle scheme.

  5. Lithium in Stellar Atmospheres: Observations and Theory

    NASA Astrophysics Data System (ADS)

    Lyubimkov, L. S.

    2016-09-01

    Of all the light elements, lithium is the most sensitive indicator of stellar evolution. This review discusses current data on the abundance of lithium in the atmospheres of A-, F-, G-, and K-stars of different types, as well as the consistency of these data with theoretical predictions. The variety of observed Li abundances is illustrated by the following objects in different stages of evolution: (1) Old stars in the galactic halo, which have a lithium abundance logɛ(Li)=2.2 (the "lithium plateau") that appears to be 0.5 dex lower than the primordial abundance predicted by cosmological models. (2) Young stars in the galactic disk, which have been used to estimate the contemporary initial lithium abundance logɛ(Li)=3.2±0.1 for stars in the Main sequence. Possible sources of lithium enrichment in the interstellar medium during evolution of the galaxy are discussed. (3) Evolving FGK dwarfs in the galactic disk, which have lower logɛ(Li) for lower effective temperature T eff and mass M. The "lithium dip" near T eff ~6600 K in the distribution of logɛ(Li) with respect to T eff in old clusters is discussed. (4) FGK giants and supergiants, of which most have no lithium at all. This phenomenon is consistent with rotating star model calculations. (5) Lithium rich cold giants with logɛ(Li) ≥ 2.0, which form a small, enigmatic group. Theoretical models with rotation can explain the existence of these stars only in the case of low initial rotation velocities V 0 <50 km/s. In all other cases it is necessary to assume recent synthesis of lithium (capture of a giant planet is an alternative). (6) Magnetic Ap-stars, where lithium is concentrated in spots located at the magnetic poles. There the lithium abundance reaches logɛ(Li)=6. Discrepancies between observations and theory are noted for almost all the stars discussed in this review.

  6. Characterizations and electrochemical performance of pure and metal-doped Li{sub 4}Ti{sub 5}O{sub 12} for anode materials of lithium-ion batteries

    SciTech Connect

    Jeong, Euh Duck; Han, Hyun Ju; Jung, Ok Sang; Ha, Myoung Gyu; Doh, Chil Hoon; Hwang, Min Ji; Yang, Ho-Soon; Hong, K.S.

    2012-10-15

    Pure and metal (Cu, Al, Sn, and V)-doped Li{sub 4}Ti{sub 5}O{sub 12} powders are prepared with solid-state reaction method. The effects of dopants on the physical and electrochemical properties are characterized by using TGA, XRD, and SEM. Compared with pure Li{sub 4}Ti{sub 5}O{sub 12}, metal-doped Li{sub 4}Ti{sub 5}O{sub 12} powders show structural stability and enhanced lithium ion diffusivity brought by doped metal ions. Voltage characteristics and initial charge–discharge characteristics according to the C rates in pure and metal-doped Li{sub 4}Ti{sub 5}O{sub 12} electrode materials are studied. Pure Li{sub 4}Ti{sub 5}O{sub 12} powder shows a relatively good discharge capacity of 164 mAh/g at a rate 0.2C, and some of metal-doped Li{sub 4}Ti{sub 5}O{sub 12} powders show higher discharge capacities. Metal-doped Li{sub 4}Ti{sub 5}O{sub 12} powders are promising candidates as anode materials for lithium-ion batteries.

  7. Improving the rate capability of high voltage lithium-ion battery cathode material LiNi0.5Mn1.5O4 by ruthenium doping

    NASA Astrophysics Data System (ADS)

    Kiziltas-Yavuz, Nilüfer; Bhaskar, Aiswarya; Dixon, Ditty; Yavuz, Murat; Nikolowski, Kristian; Lu, Li; Eichel, Rüdiger-A.; Ehrenberg, Helmut

    2014-12-01

    The citric acid-assisted sol-gel method was used to produce the high-voltage cathodes LiNi0.5Mn1.5O4 and LiNi0.4Ru0.05Mn1.5O4 at 800 °C and 1000 °C final calcination temperatures. High resolution powder diffraction using synchrotron radiation, inductively coupled plasma - optical emission spectroscopy and scanning electron microscopy analyses were carried out to characterize the structure, chemical composition and morphology. X-ray absorption spectroscopy studies were conducted to confirm Ru doping inside the spinel as well as to compare the oxidation states of transition metals. The formation of an impurity LixNi1-xO in LiNi0.5Mn1.5O4 powders annealed at high temperatures (T ≥ 800 °C) can be suppressed by partial substitution of Ni2+ by Ru4+ ion. The LiNi0.4Ru0.05Mn1.5O4 powder synthesized at 1000 °C shows the highest performance regarding the rate capability and cycling stability. It has an initial capacity of ∼139 mAh g-1 and capacity retention of 84% after 300 cycles at C/2 charging-discharging rate between 3.5 and 5.0 V. The achievable discharge capacity at 20 C for a charging rate of C/2 is ∼136 mAh g-1 (∼98% of the capacity delivered at C/2). Since the electrode preparation plays a crucial role on parameters like the rate capability, the influence of the mass loading of active materials in the cathode mixture is discussed.

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

    SciTech Connect

    Wan, Shun; Jiang, Xueguang; Guo, Bingkun; Dai, Sheng; Goodenough, John B.; Sun, Xiao-Guang

    2015-01-01

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

  9. A Polymer Lithium-Oxygen Battery

    PubMed Central

    Elia, Giuseppe Antonio; Hassoun, Jusef

    2015-01-01

    Herein we report the characteristics of a lithium-oxygen battery using a solid polymer membrane as the electrolyte separator. The polymer electrolyte, fully characterized in terms of electrochemical properties, shows suitable conductivity at room temperature allowing the reversible cycling of the Li-O2 battery with a specific capacity as high as 25,000 mAh gC−1 reflected in a surface capacity of 12.5 mAh cm−2. The electrochemical formation and dissolution of the lithium peroxide during Li-O2 polymer cell operation is investigated by electrochemical techniques combined with X-ray diffraction study, demonstrating the process reversibility. The excellent cell performances in terms of delivered capacity, in addition to its solid configuration allowing the safe use of lithium metal as high capacity anode, demonstrate the suitability of the polymer lithium-oxygen as high-energy storage system. PMID:26238552

  10. A Polymer Lithium-Oxygen Battery.

    PubMed

    Elia, Giuseppe Antonio; Hassoun, Jusef

    2015-08-04

    Herein we report the characteristics of a lithium-oxygen battery using a solid polymer membrane as the electrolyte separator. The polymer electrolyte, fully characterized in terms of electrochemical properties, shows suitable conductivity at room temperature allowing the reversible cycling of the Li-O2 battery with a specific capacity as high as 25,000 mAh gC(-1) reflected in a surface capacity of 12.5 mAh cm(-2). The electrochemical formation and dissolution of the lithium peroxide during Li-O2 polymer cell operation is investigated by electrochemical techniques combined with X-ray diffraction study, demonstrating the process reversibility. The excellent cell performances in terms of delivered capacity, in addition to its solid configuration allowing the safe use of lithium metal as high capacity anode, demonstrate the suitability of the polymer lithium-oxygen as high-energy storage system.

  11. Structural properties and application in lithium cells of Li(Ni0.5Co0.5)1-yFeyO2 (0 ≤ y ≤ 0.25) prepared by sol-gel route: Doping optimization

    NASA Astrophysics Data System (ADS)

    Abdel-Ghany, A. E.; Hashem, A. M.; Elzahany, E. A.; Abuzeid, H. A.; Indris, S.; Nikolowski, K.; Ehrenberg, H.; Zaghib, K.; Mauger, A.; Julien, C. M.

    2016-07-01

    Layered Li(Co0.5Ni0.5)1-yFeyO2 (0.0 ≤ y ≤ 0.25) oxides were prepared by citric-acid assisted sol-gel method. Elemental and structural properties were investigated by energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Raman scattering (RS) and Mössbauer spectroscopy, and magnetometry. EDX images show a homogeneous distribution of Fe ions. XRD and RS spectroscopy reveal that the materials crystallize as a LiNiO2sbnd LiCoO2sbnd LiFeO2 solid solution with the typical rhombohedral α-NaFeO2 structure (R 3 bar m S.G.) up to y = 0.2 at which composition a secondary phase was observed. For y > 0.2 the XRD results show the appearance of the α-LiFeO2 phase with the cubic structure (Fm3m S.G.). The degree of cation mixing investigated by XRD analysis and magnetic measurements is z < 0.04, for y < 0.2. Electrochemical tests of Li(Co0.5Ni0.5)1-yFeyO2 (0.0 ≤ y ≤ 0.1) oxides in lithium cells show the influence of iron substitution. The best results have been obtained for the composition y(Fe) = 0.05, where the electrical conductivity is maximum. A specific capacity 32 mAh g-1 is maintained at 8C rate.

  12. Lithium Surface Coatings and Improved Plasma Performance in NSTX

    NASA Astrophysics Data System (ADS)

    Kugel, H. W.

    2007-11-01

    NSTX research on lithium-coated plasma facing components is the latest step in a decade-long, multi-institutional research program to develop lithium as a plasma-facing system that can withstand the high heat and neutron fluxes in a DT reactor. The NSTX research is also aimed towards sustaining the current non- inductively in H-mode plasmas which requires control of both wall recycling and impurity influxes. Employing several techniques to coat the plasma facing components (PFCs) with lithium, NSTX experiments have shown, for the first time, significant benefits in high-power divertor plasmas. Lithium pellet injection (LPI) uses the plasma itself to distribute lithium on the divertor or limiter surfaces. The multi-barrel LPI on NSTX can introduce either lithium pellets with masses 1 - 5 mg or powder during a discharge. This significantly lowered recycling and reduced the density in a subsequent NBI-heated, divertor plasma. Lithium coatings have also been applied with a LIThium EvaporatoR (LITER) that was installed on an upper vacuum vessel port to direct a collimated stream of lithium vapor toward the graphite tiles of the lower center stack and divertor. The lithium was evaporated either before tokamak discharges, or continuously between and during them. By evaporating lithium into the helium glow discharge that typically precedes each tokamak discharge, a coating of the entire PFC area was achieved. Lithium depositions from a few mg to 1 g have been applied between discharges. Among the effects observed in subsequent neutral-beam heated plasmas were decreases in oxygen impurities, plasma density, and the inductive flux consumption, and increases in electron temperature, ion temperature, energy confinement and DD neutron rate. In addition, a reduction in the ELM frequency, including their complete suppression, was achieved in H-mode plasmas. Additional observations, such as, the duration of the lithium coatings, increases in core metal impurity radiation, and

  13. Lithium purification technique

    DOEpatents

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

    1984-01-10

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

  14. Lithium purification technique

    DOEpatents

    Keough, Robert F.; Meadows, George E.

    1985-01-01

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

  15. Lithium and hematopoiesis.

    PubMed Central

    Barr, R. D.; Galbraith, P. R.

    1983-01-01

    Some of lithium's effects on blood cell formation suggest that the element may be of value in treating hematologic disorders. Lithium enhances granulopoiesis and thereby induces neutrophilia. Two possible mechanisms of action are suggested: a direct action on the pluripotent stem cells, or an inhibition of the suppressor cells (thymus-dependent lymphocytes) that limit hematopoiesis. Lithium also inhibits erythropoiesis. Although most studies use concentrations at or above pharmacologic levels there is evidence that lithium plays a role in normal cell metabolism. PMID:6336655

  16. Lithium nephrotoxicity revisited.

    PubMed

    Grünfeld, Jean-Pierre; Rossier, Bernard C

    2009-05-01

    Lithium is widely used to treat bipolar disorder. Nephrogenic diabetes insipidus (NDI) is the most common adverse effect of lithium and occurs in up to 40% of patients. Renal lithium toxicity is characterized by increased water and sodium diuresis, which can result in mild dehydration, hyperchloremic metabolic acidosis and renal tubular acidosis. The concentrating defect and natriuretic effect develop within weeks of lithium initiation. After years of lithium exposure, full-blown nephropathy can develop, which is characterized by decreased glomerular filtration rate and chronic kidney disease. Here, we review the clinical and experimental evidence that the principal cell of the collecting duct is the primary target for the nephrotoxic effects of lithium, and that these effects are characterized by dysregulation of aquaporin 2. This dysregulation is believed to occur as a result of the accumulation of cytotoxic concentrations of lithium, which enters via the epithelial sodium channel (ENaC) on the apical membrane and leads to the inhibition of signaling pathways that involve glycogen synthase kinase type 3beta. Experimental and clinical evidence demonstrates the efficacy of the ENaC inhibitor amiloride for the treatment of lithium-induced NDI; however, whether this agent can prevent the long-term adverse effects of lithium is not yet known.

  17. [Parkinsonism during lithium use].

    PubMed

    Walrave, T R W M; Bulens, C

    2009-01-01

    Two patients with bipolar disorder had been treated for years with lithium without any complications but began to develop symptoms of rigidity and an altered gait, namely symptoms compatible with a diagnosis of Parkinsonism with an action tremor. In both patients lithium levels were within the therapeutic range. Medication-induced Parkinsonism occurs frequently in patients using antipsychotic medication, but is a rare complication in patients receiving long term treatment with lithium. The lithium dosage was reduced gradually and within a few months all neurological symptoms subsided completely.

  18. Rechargeable Thin-film Lithium Batteries

    DOE R&D Accomplishments Database

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

    1993-08-01

    Rechargeable thin film batteries consisting of lithium metal anodes, an amorphous inorganic electrolyte, and cathodes of lithium intercalation compounds have recently been developed. The batteries, which are typically less than 6 {mu}m thick, can be fabricated to any specified size, large or small, onto a variety of substrates including ceramics, semiconductors, and plastics. The cells that have been investigated include Li TiS{sub 2}, Li V{sub 2}O{sub 5}, and Li Li{sub x}Mn{sub 2}O{sub 4}, with open circuit voltages at full charge of about 2.5, 3.6, and 4.2, respectively. The development of these batteries would not have been possible without the discovery of a new thin film lithium electrolyte, lithium phosphorus oxynitride, that is stable in contact with metallic lithium at these potentials. Deposited by rf magnetron sputtering of Li{sub 3}PO{sub 4} in N{sub 2}, this material has a typical composition of Li{sub 2.9}PO{sub 3.3}N{sub 0.46} and a conductivity at 25{degrees}C of 2 {mu}S/cm. The maximum practical current density obtained from the thin film cells is limited to about 100 {mu}A/cm{sup 2} due to a low diffusivity of Li{sup +} ions in the cathodes. In this work, the authors present a short review of their work on rechargeable thin film lithium batteries.

  19. The electrochemistry of molten lithium chlorate and its possible use with lithium in a battery

    SciTech Connect

    Su-Chee Simon Wang; Bennion, D.N.

    1983-04-01

    Lithium chlorate, LiClO/sub 3/, has reported melting points of 127.6/sup 0/ and 129/sup 0/C. The specific conductance of molten lithium chlorate at 130/sup 0/C is relatively high compared to common aqueous electrolytic solutions at room temperature. Therefore, lithium chlorate offers the chance to operate a new lithium battery system at a temperature betwee 130/sup 0/ and 150/sup 0/C. It was found experimentally that lithium chlorate is stable in the potential range between 3.2 and 4.6V relative to an Li reference electrode. An Li-Cl/sub 2/ secondary battery system was observed to have an open-circuit potential of 3.97V, making an Li-Cl/sub 2/ secondary battery in molten lithium chlorate possible, in principle. A lithium-lithium chlorate primary battery system is also possible. Lithium negative electrode performance was found to be hindered by corrosion and possible runaway reactions with LiClO/sub 3/. Dendrite formation on charging was observed. The solubility of Li/sub 2/O and LiCl in LiClO/sub 3/ at 145/sup 0/C is 7.5 X 10/sup -5/ and 1.78 X 10/sup -3/ mol/cm/sup 3/, respectively. The diffusion coefficients are 1.5 X 10/sup -7/ for Li/sub 2/O and 3.4 X 10/sup -7/ cm/sup 2//sec for LiCl. Platinum appeared to be an inert positive electrode for chlorate, chlorine, or oxygen reactions fo runs on the order of several hours. Nickel shows an active-passive behavior which is complex. Nickel appears suitable for use in a primary cell for the cathodic discharge of LiClO/sub 3/, but it does not appear suitable for a Cl/sub 2/ or O/sub 2/ electrode.

  20. Use of copper powder extinguishers on lithium fires

    NASA Astrophysics Data System (ADS)

    Leonard, Joseph T.; Burns, R.; Beither, J.; Ouelette, R.; Darwin, R.

    1994-07-01

    The suitability of using copper powder extinguishers for controlling lithium fires resulting from a damaged Mark 50 Torpedo boiler assembly was evaluated. The results indicated that under ideal conditions, i.e., unobstructed access to the fire, copper powder will extinguish burning lithium when applied at the recommended rate of 4.5 kg (10 lb) of copper per 0.45 kg (1 lb) of lithium. However, the presence of obstructions or of high spots on the surface of the burning lithium increases the quantity of copper powder required for extinguishment.

  1. Lithium brines: A global perspective: Chapter 14

    USGS Publications Warehouse

    Munk, LeeAnn; Hynek, Scott; Bradley, Dwight C.; Boutt, David; Labay, Keith A.; Jochens, Hillary; Verplanck, Philip L.; Hitzman, Murray W.

    2016-01-01

    Lithium is a critical and technologically important element that has widespread use, particularly in batteries for hybrid cars and portable electronic devices. Global demand for lithium has been on the rise since the mid-1900s and is projected to continue to increase. Lithium is found in three main deposit types: (1) pegmatites, (2) continental brines, and (3) hydrothermally altered clays. Continental brines provide approximately three-fourths of the world’s Li production due to their relatively low production cost. The Li-rich brine systems addressed here share six common characteristics that provide clues to deposit genesis while also serving as exploration guidelines. These are as follows: (1) arid climate; (2) closed basin containing a salar (salt crust), a salt lake, or both; (3) associated igneous and/or geothermal activity; (4) tectonically driven subsidence; (5) suitable lithium sources; and (6) sufficient time to concentrate brine. Two detailed case studies of Li-rich brines are presented; one on the longest produced lithium brine at Clayton Valley, Nevada, and the other on the world’s largest producing lithium brine at the Salar de Atacama, Chile.

  2. Electroactive compositions with poly(arylene oxide) and stabilized lithium metal particles

    DOEpatents

    Zhang, Zhengcheng; Yuan, Shengwen; Amine, Khalil

    2015-05-12

    An electroactive composition includes an anodic material; a poly(arylene oxide); and stabilized lithium metal particles; where the stabilized lithium metal particles have a size less than about 200 .mu.m in diameter, are coated with a lithium salt, are present in an amount of about 0.1 wt % to about 5 wt %, and are dispersed throughout the composition. Lithium secondary batteries including the electroactive composition along with methods of making the electroactive composition are also discussed.

  3. LITHIUM AND RENAL FUNCTIONS

    PubMed Central

    Sethi, N.; Trivedi, J.K.; Sethi, B.B.

    1987-01-01

    SUMMARY Thirty patients of affective disorder who were on lithium for a year and thirty patients on antidepressant were studied in detail for renal functions. Our observation is that lithium therapy does not lead to any deterioration in kidney functions. The results are discussed. PMID:21927211

  4. Improving electrolytes for lithium-ion and lithium oxygen

    NASA Astrophysics Data System (ADS)

    Chalasani, Dinesh

    There is an ever increasing demand for fossil fuels. Lithium ion batteries (LIBs) can effectively reduce the production of greenhouse gases and lessen the need for fossil fuels. LIBs also have great potential in electric vehicle applications as an alternative to petroleum modes of transportation. Understanding the chemical reactions between the electrolyte and electrodes in LIBs is very crucial in developing batteries which can work over a wide temperature range and also give a wide potential window. The Solid Electrolyte Interface (SEI), formed by the reduction of solvent molecules on the surface of electrodes, is an important component of LIBs. The SEI is very essential to the performance of LIBs. One electron reduction pathway products of solvent molecules was investigated using lithium-naphthalenide. Methylene ethylene carbonate, a high temperature additive has been synthesized and its performance has been tested at 60°C. Lithium-Oxygen batteries have an energy density ten times greater than that of LIBs. However, lithium-oxygen batteries have rechargability problems associated with them. The most common electrolyte used in this type of batteries is LiPF6 in carbonate or ether based solvents. LiPF6 inherently decreases electrolyte stability, since LiPF 6 can undergo thermal dissociation into PF5 and LiF. PF 5 being a strong Lewis acid, can react with electron rich species. The thermal decomposition reactions of LiPF6 based electrolytes are studied in detail with regard to LIBs. The comprehensive study has been conducted on the thermal degradation of several electrolyte systems in the presence of Li2O2.

  5. Cathode material for lithium batteries

    DOEpatents

    Park, Sang-Ho; Amine, Khalil

    2013-07-23

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

  6. Cathode material for lithium batteries

    DOEpatents

    Park, Sang-Ho; Amine, Khalil

    2015-01-13

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

  7. Electrochemistry of molten lithium chlorate and its possible use with lithium in a battery

    SciTech Connect

    Wang, S.S.; Bennion, D.N.

    1980-12-01

    Lithium chlorate, LiClO/sub 3/, has a reported melting point of 127.6 C or 129 C. The specific conductance of molten lithium chlorate is relatively high compared to most electrolytic solutions used at room temperature. Therefore, lithium chlorate offers the chance to operate a new lithium battery system at a temperature between 130 C and 150 C. It is found from experiments that lithium chlorate is stable in the potential range between 3.2 V and 4.6 V relative to a Li reference electrode. A Li-Cl/sub 2/ secondary battery system has an open circuit potential of 3.97 V, making a Li-Cl/sub 2/ secondary battery in molten lithium chlorate, in principle, possible. A lithium-lithium chlorate primary battery system is also possible. Lithium negative electrode performance is hindered by corrosion and possible runaway reactions with LiClO/sub 3/ and dendrite formation on charging. The solubility of Li/sub 2/O and LiCl in LiClO/sub 3/ at 145 C is .000075 mol/cubic cm and .00178 mol/cubic cm, respectively. The diffusion coefficients are 1.5 x 10/sup -7/ cm/sup 2//s for Li/sub 2/O and 3.4 x 10/sup -7/ cm/sup 2//s for LiCl. Platinum appeared to be an inert positive electrode for chlorate, chlorine, or oxygen reactions for short term runs, order of several hours. Nickel shows active-passive behavior which is complex. Nickel appears suitable for primary cell, cathodic discharge of LiClO/sub 3/, but it does not appear suitable for a Cl/sub 2/ or O/sub 2/ electrode.

  8. Cation Miscibility and Lithium Mobility in NASICON Li1+xTi2-xScx(PO4)3 (0 ≤ x ≤ 0.5) Series: A Combined NMR and Impedance Study.

    PubMed

    Kahlaoui, Radhouene; Arbi, Kamel; Sobrados, Isabel; Jimenez, Ricardo; Sanz, Jesus; Ternane, Riadh

    2017-02-06

    Rhombohedral NASICON compounds with general formula Li1+xTi2-xScx(PO4)3 (0 ≤ x ≤ 0.5) have been prepared using a conventional solid-state reaction and characterized by X-ray diffraction (XRD), nuclear magnetic resonance (NMR), and impedance spectroscopy. The partial substitution of Ti(4+) by Sc(3+) and Li(+) in pristine LiTi2(PO4)3 increases unit-cell dimensions and the number of charge carriers. In Sc-rich samples, the analysis of XRD data and (6)Li/(7)Li, (31)P, and (45)Sc MAS NMR spectra confirms the presence of secondary LiScO2 and LiScP2O7 phases that reduce the amount of lithium incorporated in the NASICON phase. In samples with x < 0.3, electrostatic repulsions between Li ions located at M1 and M3 sites increase Li mobility. For x ≥ 0.3, ionic conductivity decreases because of secondary nonconducting phases formed at grain boundaries of the NASICON particles (core-shell structures). For x = 0.2, high bulk conductivity (2.5 × 10(-3) S·cm(-1)) and low activation energy (Ea = 0.25 eV) measured at room temperature make Li1.2Ti1.8Sc0.2(PO4)3 one of the best lithium ionic conductors reported in the literature. In this material, the vacancy arrangement enhances Li conductivity.

  9. Three-volt lithium-ion battery with Li[Ni 1/2Mn 3/2]O 4 and the zero-strain insertion material of Li[Li 1/3Ti 5/3]O 4

    NASA Astrophysics Data System (ADS)

    Ariyoshi, Kingo; Yamamoto, Satoshi; Ohzuku, Tsutomu

    A 3 V lithium-ion cell with Li[Ni 1/2Mn 3/2]O 4 ( Fd 3¯m ; a=8.17 Å) and the zero-strain insertion material of Li[Li 1/3Ti 5/3]O 4 ( Fd 3¯m ; a=8.36 Å) was examined with an emphasis on rate-capability and cycle life. This cell showed a quite flat operating voltage of 3.2 V with excellent cycleability. Accelerated cycle tests indicated that 83% of the initial capacity was delivered and stored even after 1100 cycles. Although the calculated energy density of a Li[Li 1/3Ti 5/3]O 4/Li[Ni 1/2Mn 3/2]O 4 cell was about 250 Wh kg -1 or 1000 Wh dm -3 based on the active material weight or volume, the 3 V lithium-ion battery exhibited positive characteristic features, such as flatness in operating voltage, high rate capability, and cycle life.

  10. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

    Thackeray, Michael M.; Kim, Jeom-Soo; Johnson, Christopher S.

    2008-01-01

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

  11. Lithium-coated polymeric matrix as a minimum volume-change and dendrite-free lithium metal anode

    PubMed Central

    Liu, Yayuan; Lin, Dingchang; Liang, Zheng; Zhao, Jie; Yan, Kai; Cui, Yi

    2016-01-01

    Lithium metal is the ideal anode for the next generation of high-energy-density batteries. Nevertheless, dendrite growth, side reactions and infinite relative volume change have prevented it from practical applications. Here, we demonstrate a promising metallic lithium anode design by infusing molten lithium into a polymeric matrix. The electrospun polyimide employed is stable against highly reactive molten lithium and, via a conformal layer of zinc oxide coating to render the surface lithiophilic, molten lithium can be drawn into the matrix, affording a nano-porous lithium electrode. Importantly, the polymeric backbone enables uniform lithium stripping/plating, which successfully confines lithium within the matrix, realizing minimum volume change and effective dendrite suppression. The porous electrode reduces the effective current density; thus, flat voltage profiles and stable cycling of more than 100 cycles is achieved even at a high current density of 5 mA cm−2 in both carbonate and ether electrolyte. The advantages of the porous, polymeric matrix provide important insights into the design principles of lithium metal anodes. PMID:26987481

  12. Lithium-coated polymeric matrix as a minimum volume-change and dendrite-free lithium metal anode

    SciTech Connect

    Liu, Yayuan; Lin, Dingchang; Liang, Zheng; Zhao, Jie; Yan, Kai; Cui, Yi

    2016-03-18

    Lithium metal is the ideal anode for the next generation of high-energy-density batteries. Nevertheless, dendrite growth, side reactions and infinite relative volume change have prevented it from practical applications. Here, we demonstrate a promising metallic lithium anode design by infusing molten lithium into a polymeric matrix. The electrospun polyimide employed is stable against highly reactive molten lithium and, via a conformal layer of zinc oxide coating to render the surface lithiophilic, molten lithium can be drawn into the matrix, affording a nano-porous lithium electrode. Importantly, the polymeric backbone enables uniform lithium stripping/plating, which successfully confines lithium within the matrix, realizing minimum volume change and effective dendrite suppression. The porous electrode reduces the effective current density; thus, flat voltage profiles and stable cycling of more than 100 cycles is achieved even at a high current density of 5 mA cm-2 in both carbonate and ether electrolyte. Furthermore, the advantages of the porous, polymeric matrix provide important insights into the design principles of lithium metal anodes.

  13. Lithium-coated polymeric matrix as a minimum volume-change and dendrite-free lithium metal anode

    DOE PAGES

    Liu, Yayuan; Lin, Dingchang; Liang, Zheng; ...

    2016-03-18

    Lithium metal is the ideal anode for the next generation of high-energy-density batteries. Nevertheless, dendrite growth, side reactions and infinite relative volume change have prevented it from practical applications. Here, we demonstrate a promising metallic lithium anode design by infusing molten lithium into a polymeric matrix. The electrospun polyimide employed is stable against highly reactive molten lithium and, via a conformal layer of zinc oxide coating to render the surface lithiophilic, molten lithium can be drawn into the matrix, affording a nano-porous lithium electrode. Importantly, the polymeric backbone enables uniform lithium stripping/plating, which successfully confines lithium within the matrix, realizingmore » minimum volume change and effective dendrite suppression. The porous electrode reduces the effective current density; thus, flat voltage profiles and stable cycling of more than 100 cycles is achieved even at a high current density of 5 mA cm-2 in both carbonate and ether electrolyte. Furthermore, the advantages of the porous, polymeric matrix provide important insights into the design principles of lithium metal anodes.« less

  14. Lithium-coated polymeric matrix as a minimum volume-change and dendrite-free lithium metal anode

    NASA Astrophysics Data System (ADS)

    Liu, Yayuan; Lin, Dingchang; Liang, Zheng; Zhao, Jie; Yan, Kai; Cui, Yi

    2016-03-01

    Lithium metal is the ideal anode for the next generation of high-energy-density batteries. Nevertheless, dendrite growth, side reactions and infinite relative volume change have prevented it from practical applications. Here, we demonstrate a promising metallic lithium anode design by infusing molten lithium into a polymeric matrix. The electrospun polyimide employed is stable against highly reactive molten lithium and, via a conformal layer of zinc oxide coating to render the surface lithiophilic, molten lithium can be drawn into the matrix, affording a nano-porous lithium electrode. Importantly, the polymeric backbone enables uniform lithium stripping/plating, which successfully confines lithium within the matrix, realizing minimum volume change and effective dendrite suppression. The porous electrode reduces the effective current density; thus, flat voltage profiles and stable cycling of more than 100 cycles is achieved even at a high current density of 5 mA cm-2 in both carbonate and ether electrolyte. The advantages of the porous, polymeric matrix provide important insights into the design principles of lithium metal anodes.

  15. Towards understanding the effects of carbon and nitrogen-doped carbon coating on the electrochemical performance of Li4Ti5O12 in lithium ion batteries: a combined experimental and theoretical study.

    PubMed

    Ding, Zijing; Zhao, Liang; Suo, Liumin; Jiao, Yang; Meng, Sheng; Hu, Yong-Sheng; Wang, Zhaoxiang; Chen, Liquan

    2011-09-07

    We investigate the effects of carbon coating, with and without nitrogen-dopants, on the electrochemical performance of a promising anode material Li(4)Ti(5)O(12) (LTO) in lithium ion battery applications. The comparative experimental results show that LTO samples coated with nitrogen-doped carbon derived from pyridine and an ionic liquid exhibit significant improvements in rate capability and cycling performance compared with a LTO sample coated by carbon derived from toluene and the pristine LTO sample. For the first time, we construct an atomistic model for the interface between the lithium transition metal oxide and carbon coating layers. Our first-principles calculations based on density functional theory reveal that at this interface there is strong binding between the graphene coating layer and the Ti-terminated LTO surface, which significantly reduces the chemical activity of LTO surfaces and stabilizes the electrode/electrolyte interface, providing a clue to solve the swelling problem for LTO-based batteries. More importantly, electron transfer from the LTO surface to graphene greatly improves the electric conductivity of the interface. Nitrogen-dopants in graphene coatings further increase the interfacial stability and electric conductivity, which is beneficial to the electrochemical performance in energy storage applications.

  16. Sealed Lithium Inorganic Battery

    DTIC Science & Technology

    1976-08-01

    MuWrn , 1,ad iw..am m4 IdM.D to We"L406W) Inorganic Electrolyte lattery Carbon Cathode Evaluation Thionyl Chloride Gas Generation Lithium C ell sign...hardware surface to carry the reductIon of thionyl chloride when in contact with lithium (self discharge) and the corro,’ion of hardware materials... Lithium - Aluminum Chloride 10) AOSTSAC? (Cmawl/e o ade H .m.eewr W MWO, AV 600 nwe w) Stdies were continued of the effects of hardware materials on the

  17. Lithium Dendrite Formation

    SciTech Connect

    2015-03-06

    Scientists at the Department of Energy’s Oak Ridge National Laboratory have captured the first real-time nanoscale images of lithium dendrite structures known to degrade lithium-ion batteries. The ORNL team’s electron microscopy could help researchers address long-standing issues related to battery performance and safety. Video shows annular dark-field scanning transmission electron microscopy imaging (ADF STEM) of lithium dendrite nucleation and growth from a glassy carbon working electrode and within a 1.2M LiPF6 EC:DM battery electrolyte.

  18. Solid composite electrolytes for lithium batteries

    DOEpatents

    Kumar, Binod; Scanlon, Jr., Lawrence G.

    2001-01-01

    Solid composite electrolytes are provided for use in lithium batteries which exhibit moderate to high ionic conductivity at ambient temperatures and low activation energies. In one embodiment, a polymer-ceramic composite electrolyte containing poly(ethylene oxide), lithium tetrafluoroborate and titanium dioxide is provided in the form of an annealed film having a room temperature conductivity of from 10.sup.-5 S cm.sup.-1 to 10.sup.-3 S cm.sup.-1 and an activation energy of about 0.5 eV.

  19. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

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

    2010-06-08

    An uncycled preconditioned electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula xLi.sub.2-yH.sub.yO.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 in which 0lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. The xLi.sub.2-yH.sub.y.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 material is prepared by preconditioning a precursor lithium metal oxide (i.e., xLi.sub.2M'O.sub.3.(1-x)LiMO.sub.2) with a proton-containing medium with a pH<7.0 containing an inorganic acid. Methods of preparing the electrodes are disclosed, as are electrochemical cells and batteries containing the electrodes.

  20. European Scientific Notes. Volume 35, Number 5,

    DTIC Science & Technology

    1981-05-31

    included £1.5 million (S3.S million) it seems lithium / thionyl chloride and lithium /sul- likely that more studies, especially fur dioxide batteries, sea... lithium thionyl chloride systems, the cell conductivity. The cell perform- was still the major concern. ance remains essentially unchanged, Lithium ...button-type batteries the chemistry and products produced during annually for use in calculators, etc., the discharge of lithium - thionyl chloride and

  1. APPARATUS FOR THE PRODUCTION OF LITHIUM METAL

    DOEpatents

    Baker, P.S.; Duncan, F.R.; Greene, H.B.

    1961-08-22

    Methods and apparatus for the production of high-purity lithium from lithium halides are described. The apparatus is provided for continuously contacting a molten lithium halide with molten barium, thereby forming lithium metal and a barium halide, establishing separate layers of these reaction products and unreacted barium and lithium halide, and continuously withdrawing lithium and barium halide from the reaction zone. (AEC)

  2. Simultaneous Extraction of Lithium and Hydrogen from Seawater

    DTIC Science & Technology

    2011-08-22

    lithium adsorbing ion-sieve LiMg0.5Mn1.5O4 was prepared by solid state reaction. 6.1g of Li2CO3 , 8.9g of Mg(CH3COO)2.4H2O and 5.6g of MnCO3 were mixed...from 1 ppm lithium model solution Nafion was used as the electrolyte and carbon felt was used as the electrode or current collector. Anolyte is 1...of time. Figure 14. Concentration of lithium ions in the extractant solution with time (anode: carbon , cathode: carbon , anolyte: 1

  3. Simultaneous Extraction of Lithium and Hydrogen from Seawater

    DTIC Science & Technology

    2011-01-26

    Experimental: Synthesis of Li+ adsorbents: Lithium adsorbing ion-sieve LiMg0.5Mn1.5O4 was prepared by solid state reaction. 6.1g of Li2CO3 , 8.9g of...E7(/(3+21(180%(5 ,QFOXGHDUHDFRGH 01/26/2011 Quarterly Progress Report 10/26/2010-01/25/2011 Simultaneous Extraction of Lithium and Hydrogen...of electrolytic process and to develop effective membranes for the diffusion of lithium ion from natural seawater to an extractant. Process variables

  4. Lithium Sulfuryl Chloride Battery.

    DTIC Science & Technology

    Primary batteries , Electrochemistry, Ionic current, Electrolytes, Cathodes(Electrolytic cell), Anodes(Electrolytic cell), Thionyl chloride ...Phosphorus compounds, Electrical conductivity, Calibration, Solutions(Mixtures), Electrical resistance, Performance tests, Solvents, Lithium compounds

  5. Lithium drifted germanium system

    NASA Technical Reports Server (NTRS)

    Fjarlie, E. J.

    1969-01-01

    General characteristics of the lithium-drifted germanium photodiode-Dewar-preamplifier system and particular operating instructions for the device are given. Information is included on solving operational problems.

  6. Performance of SONY 18650-HC Lithium-Ion Cells for Various Cycling Rates

    DTIC Science & Technology

    2010-01-15

    AEROSPACE REPORT NO. TR-2010(8550)-5 Performance of SONY 18650 -HC Lithium-Ion Cells for Various Cycling Rates 15 January 2010 Albert H...SONY 18650 -HC Lithium-Ion Cells for Various Cycling Rates 5a. CONTRACT NUMBER FA8802-09-C-0001 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6...Approved for public release; distribution unlimited. 13. SUPPLEMENTARY NOTES 20100310195 14. ABSTRACT Five different life tests of SONY 18650 -HC lithium

  7. Solid-state lithium battery

    SciTech Connect

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

    2014-11-04

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

  8. Lithium battery management system

    DOEpatents

    Dougherty, Thomas J [Waukesha, WI

    2012-05-08

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

  9. Layered P3-NaxCo1/3Ni1/3Mn1/3O2 versus Spinel Li4Ti5O12 as a Positive and a Negative Electrode in a Full Sodium-Lithium Cell.

    PubMed

    Ivanova, Svetlana; Zhecheva, Ekaterina; Kukeva, Rositsa; Nihtianova, Diana; Mihaylov, Lyuben; Atanasova, Genoveva; Stoyanova, Radostina

    2016-07-13

    The development of lithium and sodium ion batteries without using lithium and sodium metal as anodes gives the impetus for elaboration of low-cost and environmentally friendly energy storage devices. In this contribution we demonstrate the design and construction of a new type of hybrid sodium-lithium ion cell by using unique electrode combination (Li4Ti5O12 spinel as a negative electrode and layered Na3/4Co1/3Ni1/3Mn1/3O2 as a positive electrode) and conventional lithium electrolyte (LiPF6 salt dissolved in EC/DMC). The cell operates at an average potential of 2.35 V by delivering a reversible capacity of about 100 mAh/g. The mechanism of the electrochemical reaction in the full sodium-lithium ion cell is studied by means of postmortem analysis, as well as ex situ X-ray diffraction analysis, HR-TEM, and electron paramagnetic resonance spectroscopy (EPR). The changes in the surface composition of electrodes are examined by ex situ X-ray photoelectron spectroscopy (XPS).

  10. Transparent lithium loaded plastic scintillators for thermal neutron detection

    NASA Astrophysics Data System (ADS)

    Breukers, R. D.; Bartle, C. M.; Edgar, A.

    2013-02-01

    The fabrication of a series of novel, optically transparent, bulk plastic scintillators loaded with lithium methacrylate, and incorporating 2,5-diphenyloxazole and 5-phenyl-2-[4-(5-phenyl-1,3-oxazol-2-yl)phenyl]-1,3-oxazole fluorescent centres, is described. The attenuation length, photoluminescence, and both gamma ray and thermal neutron scintillation responses were compared over a range of lithium methacrylate concentrations. The maximum concentration corresponded to a weight percentage of lithium-6 of 0.63%. The photoluminescence shows a composite 2,5-diphenyloxazole and 5-phenyl-2-[4-(5-phenyl-1,3-oxazol-2-yl)phenyl]-1,3-oxazole broad band with vibronic features in the range 350-500 nm, and lifetimes in the range 0.9-2.7 ns. An increasing luminescence in a thermal neutron beam with increasing lithium-6 content is demonstrated.

  11. New MALDI matrices based on lithium salts for the analysis of hydrocarbons and wax esters.

    PubMed

    Horká, Petra; Vrkoslav, Vladimír; Hanus, Robert; Pecková, Karolina; Cvačka, Josef

    2014-07-01

    Lithium salts of organic aromatic acids (lithium benzoate, lithium salicylate, lithium vanillate, lithium 2,5-dimethoxybenzoate, lithium 2,5-dihydroxyterephthalate, lithium α-cyano-4-hydroxycinnamate and lithium sinapate) were synthesized and tested as potential matrices for the matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry analysis of hydrocarbons and wax esters. The analytes were desorbed using nitrogen laser (337.1 nm) and ionized via the attachment of a lithium cation, yielding [M + Li](+) adducts. The sample preparation and the experimental conditions were optimized for each matrix using stearyl behenate and n-triacontane standards. The performance of the new matrices in terms of signal intensity and reproducibility, the mass range occupied by matrix ions and the laser power threshold were studied and compared with a previously recommended lithium 2,5-dihydroxybenzoate matrix (LiDHB) (Cvačka and Svatoš, Rapid Commun. Mass Spectrom. 2003, 17, 2203). Several of the new matrices performed better than LiDHB. Lithium vanillate offered a 2-3 times and 7-9 times higher signal for wax esters and hydrocarbons, respectively. Also, the signal reproducibility improved substantially, making this matrix a suitable candidate for imaging applications. In addition, the diffuse reflectance spectra and solubility of the synthesized compounds were investigated and discussed with respect to the compound's ability to serve as MALDI matrices. The applicability of selected matrices was tested on natural samples of wax esters and hydrocarbons.

  12. Sorption of atmospheric gases by bulk lithium metal

    NASA Astrophysics Data System (ADS)

    Hart, C. A.; Skinner, C. H.; Capece, A. M.; Koel, B. E.

    2016-01-01

    Lithium conditioning of plasma facing components has enhanced the performance of several fusion devices. Elemental lithium will react with air during maintenance activities and with residual gases (H2O, CO, CO2) in the vacuum vessel during operations. We have used a mass balance (microgram sensitivity) to measure the mass gain of lithium samples during exposure of a ˜1 cm2 surface to ambient and dry synthetic air. For ambient air, we found an initial mass gain of several mg/h declining to less than 1 mg/h after an hour and decreasing by an order of magnitude after 24 h. A 9 mg sample achieved a final mass gain corresponding to complete conversion to Li2CO3 after 5 days. Exposure to dry air resulted in a 30 times lower initial rate of mass gain. The results have implications for the chemical state of lithium plasma facing surfaces and for safe handling of lithium coated components.

  13. Lithium storage mechanism in nongraphitizable carbon

    SciTech Connect

    Nagai, Aisaku; Ishikawa, Minoru; Masuko, Jiro; Sonobe, Naohiro; Iwasaki, Takao; Chuman, Hiroshi

    1995-12-31

    A nongraphitizable carbon prepared from the cross-linked petroleum pitch and carbonized at 1,473 K was found to have a unique structure and a charge capacity of more than 600 Ah/kg. A main peak of the {sup 7}Li Nuclear Magnetic Resonance spectra of the charged carbon shifted downfield with an increase of charge capacity. A Knight shift of lithium in the carbon charged to 600 Ah/kg reached 110 ppm when LiCl was used as the reference of 0 ppm. This shift was clearly distinguished from that of the lithium state in the first stage of the graphite intercalation compound, because the latter was observed at 45 ppm. A modified extended Huekel molecular orbital calculation showed that the average net electron density on lithium atoms drastically increased with increasing concentration of lithium atoms if the aromatic molecular planes are more than 0.5 nm apart. Both the experimental and theoretical results suggest that lithium atoms form clusters in this nongraphitizable carbon.

  14. Hydrogen Outgassing from Lithium Hydride

    SciTech Connect

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

    2006-04-20

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

  15. Determination of lithium in rocks by distillation

    USGS Publications Warehouse

    Fletcher, M.H.

    1949-01-01

    A method for the quantitative extraction and recovery of lithium from rocks is based on a high temperature volatilization procedure. The sample is sintered with a calcium carbonate-calcium chloride mixture at 1200?? C. for 30 minutes in a platinum ignition tube, and the volatilization product is collected in a plug of Pyrex glass wool in a connecting Pyrex tube. The distillate, which consists of the alkali chlorides with a maximum of 5 to 20 mg. of calcium oxide and traces of a few other elements, is removed from the apparatus by dissolving in dilute hydrochloric acid and subjected to standard analytiaal procedures. The sinter residues contained less than 0.0005% lithium oxide. Lithium oxide was recovered from synthetic samples with an average error of 1.1%.

  16. Polyfluorinated boron cluster-based salts: A new electrolyte for application in Li 4Ti 5O 12/LiMn 2O 4 rechargeable lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Ionica-Bousquet, C. M.; Muñoz-Rojas, D.; Casteel, W. J.; Pearlstein, R. M.; GirishKumar, G.; Pez, G. P.; Palacín, M. R.

    The cycling performance of Li 4Ti 5O 12 and LiMn 2O 4 electrode materials has been studied in half and complete Li-ion cells with two new polyfluorinated boron cluster lithium salts (Li 2B 12F xH 12- x) as the electrolytes. The results were compared with those obtained for the standard electrolyte, 1 M LiPF 6 dissolved in ethylene carbonate and dimethyl carbonate (EC:DMC; 1:1, v/v). Three different technologies were employed for electrode fabrication: powder mixture, self-standing films and films deposited on the current collector. The latter exhibit the most interesting behavior and best performance. Cells assembled using the new electrolyte salts show excellent reversibility, coulombic efficiency, rate capability and cyclability comparable with the standard electrolyte. These features confirm the feasibility of using these polyfluorinated boron cluster-based salts as new stable Li-ion battery electrolytes.

  17. Possible resonance in positron-lithium scattering

    NASA Astrophysics Data System (ADS)

    Abdel-Raouf, M. A.; Wood, R. F.

    1990-09-01

    The possible appearance of resonances in the partial cross sections of the inelastic collisions of positrons with lithium atoms at energies below 5 eV is investigated. It is assumed that only elastic and rearrangement channels are open, while excitation channels are closed. A coupled static formalism, in which the polarization potentials of the lithium and positronium are switched on, is employed. The basis set of Clementi and Roetti [At. Data Nucl. Data Tables 14, 177 (1974)] is used for describing the target model. Comparison between the resulting total cross sections and those obtained by other authors is presented.

  18. Advanced Rechargeable Lithium Sulfur Dioxide Cell

    DTIC Science & Technology

    1991-11-01

    electrolyte. Surface treatments were carried out at 2406C using water (Cell 15) and thionyl chloride (Cell 16). 3 Cathodes were placed in a Parr Bomb...Pawcatuck, CT 06379 94-02298 1425 Best Available Copy I ADVANCED RECHARGEABLE LITHIUM SULFUR DIOXIDE CELL I R.C. McDonald, P. Harris, F. Goebel, S. Hossain...Test Group 3 13 Test Group 4 22 Test Group 5 22 Test Group 6 24 Test Group 7 46 Test Group 8 52 Test Group 9 65 I CHEMICAL ANALYSIS 65 LITHIUM CYCLING

  19. New promising lithium malonatoborate salts for high voltage lithium ion batteries

    DOE PAGES

    Sun, Xiao -Guang; Wan, Shun; Guang, Hong Yu; ...

    2016-12-01

    Here, three new lithium salts, lithium difluoro-2-methyl-2-fluoromalonaoborate (LiDFMFMB), lithium difluoro-2-ethyl-2-fluoromalonaoborate (LiDFEFMB), and lithium difluoro-2-propyl-2-fluoro malonaoborate (LiDFPFMB), have been synthesized and evaluated for application in lithium ion batteries. These new salts are soluble in a mixture of ethylene carbonate (EC) and ethyl methyl carbonate (EMC) (1:2 by wt.) and 1.0 M salt solutions can be easily prepared. The ionic conductivities of these new salts are close to those of LiBF4 and LiPF6. Cyclic voltammograms reveal that these new salt based electrolytes can passivate both natural graphite and high voltage spinel LiNi0.5Mn1.5O4 (LNMO) to form effective solid electrolyte interphases (SEIs). In addition,more » these new salts based electrolytes exhibit good cycling stability with high coulombic efficiencies in both LiNi0.5Mn1.5O4 and graphite based half-cells and full cells.« less

  20. New promising lithium malonatoborate salts for high voltage lithium ion batteries

    SciTech Connect

    Sun, Xiao -Guang; Wan, Shun; Guang, Hong Yu; Fang, Youxing; Reeves, Kimberly Shawn; Chi, Miaofang; Dai, Sheng

    2016-12-01

    Here, three new lithium salts, lithium difluoro-2-methyl-2-fluoromalonaoborate (LiDFMFMB), lithium difluoro-2-ethyl-2-fluoromalonaoborate (LiDFEFMB), and lithium difluoro-2-propyl-2-fluoro malonaoborate (LiDFPFMB), have been synthesized and evaluated for application in lithium ion batteries. These new salts are soluble in a mixture of ethylene carbonate (EC) and ethyl methyl carbonate (EMC) (1:2 by wt.) and 1.0 M salt solutions can be easily prepared. The ionic conductivities of these new salts are close to those of LiBF4 and LiPF6. Cyclic voltammograms reveal that these new salt based electrolytes can passivate both natural graphite and high voltage spinel LiNi0.5Mn1.5O4 (LNMO) to form effective solid electrolyte interphases (SEIs). In addition, these new salts based electrolytes exhibit good cycling stability with high coulombic efficiencies in both LiNi0.5Mn1.5O4 and graphite based half-cells and full cells.

  1. Lithium: for harnessing renewable energy

    USGS Publications Warehouse

    Bradley, Dwight; Jaskula, Brian W.

    2014-01-01

    Lithium, which has the chemical symbol Li and an atomic number of 3, is the first metal in the periodic table. Lithium has many uses, the most prominent being in batteries for cell phones, laptops, and electric and hybrid vehicles. Worldwide sources of lithium are broken down by ore-deposit type as follows: closed-basin brines, 58%; pegmatites and related granites, 26%; lithium-enriched clays, 7%; oilfield brines, 3%; geothermal brines, 3%; and lithium-enriched zeolites, 3% (2013 statistics). There are over 39 million tons of lithium resources worldwide. Of this resource, the USGS estimates there to be approximately 13 million tons of current economically recoverable lithium reserves. To help predict where future lithium supplies might be located, USGS scientists study how and where identified resources are concentrated in the Earth’s crust, and they use that knowledge to assess the likelihood that undiscovered resources also exist.

  2. US Navy lithium cell applications

    NASA Technical Reports Server (NTRS)

    Bowers, F. M.

    1978-01-01

    Applications of lithium systems that are already in the fleet are discussed. The approach that the Navy is taking in the control of the introduction of lithium batteries into the fleet is also discussed.

  3. Glass for sealing lithium cells

    DOEpatents

    Leedecke, C.J.

    1981-08-28

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

  4. Crystal growth of a series of lithium garnets Ln3Li 5Ta 2O 12 ( Ln=La, Pr, Nd): Structural properties, Alexandrite effect and unusual ionic conductivity

    NASA Astrophysics Data System (ADS)

    Roof, Irina P.; Smith, Mark D.; Cussen, Edmund J.; zur Loye, Hans-Conrad

    2009-02-01

    We report the single crystal structures of a series of lanthanide containing tantalates, Ln3Li 5Ta 2O 12 ( Ln=La, Pr, Nd) that were obtained out of a reactive lithium hydroxide flux. The structures of Ln3Li 5Ta 2O 12 were determined by single crystal X-ray diffraction, where the Li + positions and Li + site occupancies were fixed based on previously reported neutron diffraction data for isostructural compounds. All three oxides crystallize in the cubic space group Ia3¯d (No. 230) with lattice parameters a=12.7735(1), 12.6527(1), and 12.5967(1) Å for La 3Li 5Ta 2O 12, Pr 3Li 5Ta 2O 12, and Nd 3Li 5Ta 2O 12, respectively. A UV-Vis diffuse reflectance spectrum of Nd 3Li 5Ta 2O 12 was collected to explain its unusual Alexandrite-like optical behavior. To evaluate the transport properties of Nd 3Li 5Ta 2O 12, the impedance data were collected in air in the temperature range 300⩽ T(°C)⩽500.

  5. Dual Phase Li4Ti5O12–TiO2 Nanowire Arrays As Integrated Anodes For High-rate Lithium-ion Batteries

    SciTech Connect

    Liao, Jin; Chabot, Victor; Gu, Meng; Wang, Chong M.; Xiao, Xingcheng; Chen, Zhongwei

    2014-08-19

    Lithium titanate (Li4Ti5O12) is well known as a zero strain material inherently, which provides excellent long cycle stability as a negative electrode for lithium ion batteries. However, the low specific capacity (175 mA h g-1) limits it to power batteries although the low electrical conductivity is another intrinsic issue need to be solved. In this work, we developed a facile hydrothermal and ion-exchange route to synthesize the self-supported dual-phase Li4Ti5O12–TiO2 nanowire arrays to further improve its capacity as well as rate capability. The ratio of Li4Ti5O12 to TiO2 in the dual phase Li4Ti5O12–TiO2 nanowire is around 2:1. The introduction of TiO2 into Li4Ti5O12 increases the specific capacity. More importantly, by interface design, it creates a dual-phase nanostructure with high grain boundary density that facilitates both electron and Li ion transport. Compared with phase-pure nanowire Li4Ti5O12 and TiO2 nanaowire arrays, the dual-phase nanowire electrode yielded superior rate capability (135.5 at 5 C, 129.4 at 10 C, 120.2 at 20 C and 115.5 mA h g-1 at 30 C). In-situ transmission electron microscope clearly shows the near zero deformation of the dual phase structure, which explains its excellent cycle stability.

  6. Particle Control and Plasma Performance in the Lithium Tokamak Experiment (LTX)

    SciTech Connect

    Richard Majeski, et. al.

    2013-02-21

    The Lithium Tokamak eXperiment (LTX) is a small, low aspect ratio tokamak, which is fitted with a stainless steel-clad copper liner, conformal to the last closed flux surface. The liner can be heated to 350{degree}C. Several gas fueling systems, including supersonic gas injection, and molecular cluster injection have been studied, and produce fueling efficiencies up to 35%. Discharges are strongly affected by wall conditioning. Discharges without lithium wall coatings are limited to plasma currents of order 10 kA, and discharge durations of order 5 msec. With solid lithium coatings discharge currents exceed 70 kA, and discharge durations exceed 30 msec. Heating the lithium wall coating, however, results in a prompt degradation of the discharge, at the melting point of lithium. These results suggest that the simplest approach to implementing liquid lithium walls in a tokamak - thin, evaporated, liquefied coatings of lithium - does not produce an adequately clean surface.

  7. Lithiated vanadium oxide (LVO), gamma-lithium vanadium bronze (gamma-LiV2O5) and vanadium dioxide (Vo2) as thermal-battery cathode materials. Technical report

    SciTech Connect

    Richie, A.G.; Warner, K.

    1991-05-01

    Thermal batteries are high temperature reserve batteries, predominantly used in missiles. Modern designs use a lithium (or lithium alloy) anode, an immobilized molten salt electrolyte and an iron-disulphide cathode. These batteries have many advantages: high reliability, long storage life without maintenance, wide temperature range of operation and, sometimes, high power. However, the energy density is rather low and this could be improved if the individual cell voltage could be raised above the present 2.2 V/cell open circuit-voltage for the lithium iron-disulphide couple. A new cathode material, lithiated vanadium oxide (LVO), been invented at RAE with the advantage of the much higher open-circuit voltage of 2.6 V/cell versus lithium. The properties of LVO have been investigated and it has been shown that LVO consists of vanadium dioxide as the major component. Some lithium bromide is also present.

  8. Er{sup 3+}-doped strontium lithium bismuth borate glasses for broadband 1.5 {mu}m emission - optical properties

    SciTech Connect

    Rajesh, D.; Balakrishna, A.; Ratnakaram, Y. C.

    2013-02-05

    Strontium lithium bismuth borate glasses (SLBiB) doped with various concentrations of Er{sup 3+} were prepared using conventional melt quench technique and investigated their optical properties. The amorphous nature of the prepared glass samples was confirmed by X-ray diffraction and SEM analysis. Optical properties were studied by measuring the optical absorption and near infrared luminescence spectra at room temperature. Judd-Ofelt (J-O) theory has been applied for the f.f transitions of Er{sup 3+} ions to evaluate J-O intensity parameters, {Omega}{lambda} ({lambda} = 2, 4 and 6). Using the J-O intensity parameters, radiative properties such as transition probabilities (A{sub R}), branching ratios ({beta}) and radiative lifetimes ({tau}) are estimated for certain transitions. From the emission spectra, peak emission-cross sections ({sigma}{sub p}) and products of stimulated emission cross-section and full width at half maximum ({sigma}{sub p} Multiplication-Sign FWHM) were calculated for the observed emission transition, {sup 4}I{sub 13/2}{yields}{sup 4}I{sub 15/2}.

  9. Reversibility of anodic lithium in rechargeable lithium-oxygen batteries.

    PubMed

    Shui, Jiang-Lan; Okasinski, John S; Kenesei, Peter; Dobbs, Howard A; Zhao, Dan; Almer, Jonathan D; Liu, Di-Jia

    2013-01-01

    Non-aqueous lithium-air batteries represent the next-generation energy storage devices with very high theoretical capacity. The benefit of lithium-air batteries is based on the assumption that the anodic lithium is completely reversible during the discharge-charge process. Here we report our investigation on the reversibility of the anodic lithium inside of an operating lithium-air battery using spatially and temporally resolved synchrotron X-ray diffraction and three-dimensional micro-tomography technique. A combined electrochemical process is found, consisting of a partial recovery of lithium metal during the charging cycle and a constant accumulation of lithium hydroxide under both charging and discharging conditions. A lithium hydroxide layer forms on the anode separating the lithium metal from the separator. However, numerous microscopic 'tunnels' are also found within the hydroxide layer that provide a pathway to connect the metallic lithium with the electrolyte, enabling sustained ion-transport and battery operation until the total consumption of lithium.

  10. Heart Attack in the Course of Lithium Overdose

    PubMed Central

    Asim, Kalkan; Selman, Yeniocak; Suleyman, Yazici; Ozgur, Karcioglu; Ozlem, Bilir; Gokhan, Ersunan

    2016-01-01

    Introduction Lithium overdose can be associated with cardiac toxicity, especially in those with underlying heart disease. Toxic levels of serum lithium are associated with cardiotoxic effects ranging from simple ECG disorders to dysrhythmias, cardiomyopathy and even acute myocardial infarction (AMI). This report describes a patient with AMI accompanied by high blood levels of lithium. Case Presentation A 62-year-old woman was admitted to the emergency department due to weakness and acute chest pain. Her ECG revealed ST elevation in leads DI, aVL and V5-6, with a ventricular rate of 80 bpm. Blood chemistry and complete blood count were within normal limits. The patient’s blood lithium level was measured as 2.3 mmol/L (N: 0.5 - 0.8 mmol/L), and her troponin I level was 0.892 ng/mL (N: 0 - 0.01 ng/mL). Coronary angiography produced normal findings, concurrent with the resolution of electrocardiographic abnormalities following elimination of lithium. The clinical course in the intensive care unit was uneventful and the patient was discharged on the seventh day. Conclusions Lithium intoxication should be considered in the differential diagnosis, especially in elderly patients on lithium therapy who are admitted to the emergency department with chest pain. PMID:27703795

  11. Improved lithium-ion battery performance of LiNi0.5Mn1.5-xTixO4 high voltage spinel in full-cells paired with graphite and Li4Ti5O12 negative electrodes

    NASA Astrophysics Data System (ADS)

    Kim, Jung-Hyun; Pieczonka, Nicholas P. W.; Sun, Yang-Kook; Powell, Bob R.

    2014-09-01

    The effect of Ti-substitution on the electrochemical properties of LiNi0.5Mn1.5-xTixO4 was investigated by using half-cells paired with lithium metal, and full-cells paired with either graphite or Li4Ti5O12 (LTO) negative electrodes. In half-cells, Ti-substitution increased the operation voltage, but reduced the specific capacity. While some improvements in performance, such as higher operation voltage and less self-discharge, could be measured in the half-cells, the critical advantages of the Ti-substitution were readily observed in full-cell cycling. Compared with Ti-free LiNi0.5Mn1.5O4, the LiNi0.5Mn1.5-xTixO4 electrodes delivered improved full-cell performance whether paired with graphite or LTO negative electrodes; greater cycle life, higher cell operating voltage, and lower voltage polarization on charging/discharging. Based on relatively low self-discharge and high Coulombic efficiency, it is suggested that the Ti-substitution in LiNi0.5Mn1.5-xTixO4 retards electrolyte oxidation. In addition, scanning electron microscopy (SEM) images revealed that cycle-aged LiNi0.5Mn1.2Ti0.3O4 particle surfaces remained relatively clean compared with those of LiNi0.5Mn1.5O4 particles. These results are consistent with the hypothesis that Ti-substitution reduces electrolyte oxidation and retards or prevents some of the degradative parasitic reactions at the electrode/electrolyte interfaces during battery cell operation.

  12. Lithium Depletion in the Beta Pictoris Moving Group

    NASA Astrophysics Data System (ADS)

    Yee, Jennifer C.; Jensen, E. L.; Reaser, B. E.

    2006-12-01

    We present a study of lithium depletion in twelve late-type pre-main-sequence stars in the coeval Beta Pictoris Moving Group (BPMG). The age of this group ( 12 Myr) is well constrained because all of the stars in the sample have Hipparcos distances. We have determined Li abundances for these K and M stars using equivalent width measurements of the 6707.8 Angstrom Li I line from new high-resolution, high-S/N echelle spectra, and we compare these abundances to models of pre-main-sequence Li depletion by Baraffe et al. (1998), D'Antona & Mazzitelli (1997, 1998), and Siess, Dufour, & Forestini (2000). Significantly more lithium depletion is observed in the sample than is predicted for a group of this age. In particular, the discrepancy between the predicted and the observed lithium abundances increases with decreasing effective temperature, suggesting a problem with theories describing pre-main-sequence lithium depletion. Our data indicate that M stars deplete lithium more rapidly than predicted, which could make M-type post-T-Tauri stars difficult to identify. In addition, we compare our results to the work of Song, Bessell, & Zuckerman (2002) on HIP 112312. In contrast to that work, we did not observe the lithium depletion boundary of the BPMG; none of the three M4.5 stars in the sample showed evidence of lithium (log N(Li) < -0.5), indicating a lithium depletion boundary later than M4.5, further underscoring the gap between age estimates from lithium depletion and those from theoretical evolutionary tracks. We gratefully acknowledge the support of the National Science Foundation through grant AST-0307830.

  13. Lithium Dinitramide as an Additive in Lithium Power Cells

    NASA Technical Reports Server (NTRS)

    Gorkovenko, Alexander A.

    2007-01-01

    Lithium dinitramide, LiN(NO2)2 has shown promise as an additive to nonaqueous electrolytes in rechargeable and non-rechargeable lithium-ion-based electrochemical power cells. Such non-aqueous electrolytes consist of lithium salts dissolved in mixtures of organic ethers, esters, carbonates, or acetals. The benefits of adding lithium dinitramide (which is also a lithium salt) include lower irreversible loss of capacity on the first charge/discharge cycle, higher cycle life, lower self-discharge, greater flexibility in selection of electrolyte solvents, and greater charge capacity. The need for a suitable electrolyte additive arises as follows: The metallic lithium in the anode of a lithium-ion-based power cell is so highly reactive that in addition to the desired main electrochemical reaction, it engages in side reactions that cause formation of resistive films and dendrites, which degrade performance as quantified in terms of charge capacity, cycle life, shelf life, first-cycle irreversible capacity loss, specific power, and specific energy. The incidence of side reactions can be reduced through the formation of a solid-electrolyte interface (SEI) a thin film that prevents direct contact between the lithium anode material and the electrolyte. Ideally, an SEI should chemically protect the anode and the electrolyte from each other while exhibiting high conductivity for lithium ions and little or no conductivity for electrons. A suitable additive can act as an SEI promoter. Heretofore, most SEI promotion was thought to derive from organic molecules in electrolyte solutions. In contrast, lithium dinitramide is inorganic. Dinitramide compounds are known as oxidizers in rocket-fuel chemistry and until now, were not known as SEI promoters in battery chemistry. Although the exact reason for the improvement afforded by the addition of lithium dinitramide is not clear, it has been hypothesized that lithium dinitramide competes with other electrolyte constituents to react with

  14. Poly[dithio-2,5-(1,3,4-thiadiazole)] (PDMcT)-poly(3,4-ethylenedioxythiophene) (PEDOT) composite cathode for high-energy lithium/lithium-ion rechargeable batteries

    NASA Astrophysics Data System (ADS)

    Kiya, Yasuyuki; Iwata, Asao; Sarukawa, Tomoo; Henderson, Jay C.; Abruña, Héctor D.

    We present a characterization of the redox behavior of organosulfur-based composite cathodes composed of poly[dithio-2,5-(1,3,4-thiadiazole)] (PDMcT), which is a polymer derived from 2,5-dimercapto-1,3,4-thiadiazole (DMcT), and poly(3,4-ethylenedioxythiophene) (PEDOT) in a carbonate-based mixed solvent containing 1.0 M LiBF 4. We have previously shown that PEDOT films, electrochemically generated at glassy carbon electrode surfaces, gave rise to a dramatic enhancement of the interfacial charge transfer kinetics of DMcT in solution. In a similar fashion, chemically prepared PEDOT films exhibited dramatic electrocatalytic activity towards the redox reactions of PDMcT in the composite cathodes. While the composite cathode exhibited a very high capacity of 205 mAh g -1 (based on the electroactive mass) at the first discharge, in subsequent charge/discharge tests, the capacity of the PDMcT-PEDOT composite cathode (1:1 mole ratio) decreased significantly because of dissolution of the reduction products of PDMcT into the electrolyte solution. We also found that an ionic polymer, consisting of a mixture of PEDOT and polystyrene sulfonate (PEDOT-PSS) could electrostatically, but not physically, prevent, at least in part, leaching of the DMcT species into the electrolyte solution, thus improving the coulomb efficiency for the redox reactions of DMcT in a PDMcT-PEDOT composite film during charge/discharge cycles.

  15. Lithium Ion Batteries

    NASA Technical Reports Server (NTRS)

    1997-01-01

    Lithium ion batteries, which use a new battery chemistry, are being developed under cooperative agreements between Lockheed Martin, Ultralife Battery, and the NASA Lewis Research Center. The unit cells are made in flat (prismatic) shapes that can be connected in series and parallel to achieve desired voltages and capacities. These batteries will soon be marketed to commercial original-equipment manufacturers and thereafter will be available for military and space use. Current NiCd batteries offer about 35 W-hr/kg compared with 110 W-hr/kg for current lithium ion batteries. Our ultimate target for these batteries is 200 W-hr/kg.

  16. Lithium tetraborate transducer cuts

    NASA Astrophysics Data System (ADS)

    Kosinski, John; Ballato, Arthur; Lukaszek, Theodore

    1990-03-01

    Lithium tetraborate is a tetragonal material of considerable promise for frequency control and signal processing applications. It exhibits piezoelectric coupling values that fall between those of lithium niobate and quartz, but possesses orientations for which the temperature coefficient of frequency and delay time is zero for bulk and surface acoustic waves. In this report, we discuss the properties of two doubly rotated bulk wave resonator orientations having both first- and second-order temperature coefficients equal to zero. These are suitable for shear and compressional wave transducers in applications where very low temperature sensitivity is required simultaneously with moderately strong piezocoupling coefficients.

  17. Lithium tetraborate transducers

    NASA Astrophysics Data System (ADS)

    Ballato, Arthur; Kosinski, John A.; Lukaszek, Ted J.

    1991-01-01

    Lithium tetraborate is a tetragonal material of considerable promise for frequency control and signal processing applications. It exhibits piezoelectric coupling values that fall between those of lithium niobate and quartz, but possesses orientations for which the temperature coefficient of frequency and delay time is zero for bulk and surface acoustic waves. The properties of two doubly rotated bulk wave resonator orientations having first- and second-order temperature coefficients equal to zero are discussed. These are suitable for shear and compressional wave transducers in applications where very low temperature sensitivity is required simultaneously with moderately strong piezocoupling coefficients.

  18. The lithium abundances of a large sample of red giants

    SciTech Connect

    Liu, Y. J.; Tan, K. F.; Wang, L.; Zhao, G.; Li, H. N.; Sato, Bun'ei; Takeda, Y. E-mail: gzhao@nao.cas.cn

    2014-04-20

    The lithium abundances for 378 G/K giants are derived with non-local thermodynamic equilibrium correction considered. Among these are 23 stars that host planetary systems. The lithium abundance is investigated, as a function of metallicity, effective temperature, and rotational velocity, as well as the impact of a giant planet on G/K giants. The results show that the lithium abundance is a function of metallicity and effective temperature. The lithium abundance has no correlation with rotational velocity at v sin i < 10 km s{sup –1}. Giants with planets present lower lithium abundance and slow rotational velocity (v sin i < 4 km s{sup –1}). Our sample includes three Li-rich G/K giants, 36 Li-normal stars, and 339 Li-depleted stars. The fraction of Li-rich stars in this sample agrees with the general rate of less than 1% in the literature, and the stars that show normal amounts of Li are supposed to possess the same abundance at the current interstellar medium. For the Li-depleted giants, Li-deficiency may have already taken place at the main sequence stage for many intermediate mass (1.5-5 M {sub ☉}) G/K giants. Finally, we present the lithium abundance and kinematic parameters for an enlarged sample of 565 giants using a compilation of the literature, and confirm that the lithium abundance is a function of metallicity and effective temperature. With the enlarged sample, we investigate the differences between the lithium abundance in thin-/thick-disk giants, which indicate that the lithium abundance in thick-disk giants is more depleted than that in thin-disk giants.

  19. Anisotropic Tuning of Graphite Thermal Conductivity by Lithium Intercalation.

    PubMed

    Qian, Xin; Gu, Xiaokun; Dresselhaus, Mildred S; Yang, Ronggui

    2016-11-17

    Understanding thermal transport in lithium intercalated layered materials is not only important for managing heat generation and dissipation in lithium ion batteries but also the understanding potentially provides a novel way to design materials with reversibly tunable thermal conductivity. In this work, the thermal conductivity of lithium-graphite intercalation compounds (LixC6) is calculated using molecular dynamics simulations as a function of the amount of lithium intercalated. We found that intercalation of lithium has an anisotropic effect on tuning the thermal conductivity: the thermal conductivity in the basal plane decreases monotonically from 1232 W/m·K of pristine graphite to 444 W/m·K of the fully lithiated LiC6, while the thermal conductivity along the c-axis decreases first from 6.5 W/m·K for graphite to 1.3 W/m·K for LiC18 and then increases to 5.0 W/m·K for LiC6 as the lithium composition increases. More importantly, we provide the very first atomic-scale insight into the effect of lithium intercalation on the spectral phonon properties of graphite. The intercalated lithium ions are found to suppress the phonon lifetime and to reduce the group velocity of phonons parallel to the basal plane but significantly to increase the phonon group velocity along the c-axis, which anisotropically tunes the thermal conductivity of lithiated graphite compounds. This work could shed some light on the search for tunable thermal conductivity materials and might have strong impacts on the thermal management of lithium ion batteries.

  20. Thin-film Rechargeable Lithium Batteries

    DOE R&D Accomplishments Database

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

    1993-11-01

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

  1. Electronic and Electrochemical Properties of Li 1–x Mn 1.5 Ni 0.5 O 4 Spinel Cathodes As a Function of Lithium Content and Cation Ordering

    SciTech Connect

    Moorhead-Rosenberg, Zach; Huq, Ashfia; Goodenough, John B.; Manthiram, Arumugam

    2015-10-05

    The electronic and electrochemical properties of the high-voltage spinel LiMn1.5Ni0.5O4 as a function of cation ordering and lithium content have been investigated. Conductivity and activation energy measurements confirm that charge transfer occurs by small polaron hopping and the charge carrier conduction is easier in the Ni:3d band than in the in Mn:3d band. Seebeck coefficient data reveal that the Ni2+/3+. and Ni3+/4+ redox couples are combined in a single,3d band, and that maximum charge carrier concentration occurs where the average Ni oxidation state is close to 3+, corresponding to x = 0.5 in Li Li1-xMn1.5Ni0.5O4. Furthermore, maximum electronic conductivity is found at x = 0.5, regardless of cation ordering. The thermodynamically stable phases formed during cycling were investigated by recording the X-ray diffraction (XRD) of chemically delithiated powders. The more ordered spinels maintained two separate two-phase regions upon lithium extraction, while the more disordered samples exhibited a solid-solubility region from LiMn1.5Ni0.5O4 to Li0.5Mn1.5Ni0.5O4. The conductivity and phase-transformation data of four samples with varying degrees of cation ordering were compared to the electrochemical data collected with lithium cells. Only the most ordered spinel showed inferior rate performance, while the sample annealed for a shorter time performed comparable to the unannealed or disordered samples. Our results challenge the most common beliefs about high-voltage spinel: (i) low Mn3+ content is responsible for poor rate performance and (ii) thermodynamically stable solid-solubility is critical for fast kinetics.

  2. 77 FR 28259 - Mailings of Lithium Batteries

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-14

    ... for mailpieces containing lithium metal or lithium-ion cells or batteries and applies regardless of...'' instead of ``lithium content'' for secondary lithium-ion batteries when describing maximum quantity limits...-ion (Rechargeable) Cells and Batteries Small consumer-type lithium-ion cells and batteries like...

  3. A high-rate long-life Li4Ti5O12/Li[Ni0.45Co0.1Mn1.45]O4 lithium-ion battery.

    PubMed

    Jung, Hun-Gi; Jang, Min Woo; Hassoun, Jusef; Sun, Yang-Kook; Scrosati, Bruno

    2011-11-01

    Lithium batteries are receiving considerable attention as storage devices in the renewable energy and sustainable road transport fields. However, low-cost, long-life lithium batteries with higher energy densities are required to facilitate practical application. Here we report a lithium-ion battery that can be cycled at rates as high as 10 C has a life exceeding 500 cycles and an operating temperature range extending from -20 to 55 °C. The estimated energy density is 260 W h kg(-1), which is considerably higher than densities delivered by the presently available Li-ion batteries.

  4. Application potential of rechargeable lithium batteries

    SciTech Connect

    Hunger, H.F.; Bramhall, P.J.

    1983-10-01

    Rechargeable lithium cells with Cr /SUB 0.5/ V/sub 0/ /sub 5/S/sub 2/ and MoO/sub 3/ cathodes were investigated in the temperature range of -30/sup 0/C to +25/sup 0/C. The electrolyte was 1.5M LiAsF/sub 6/ in 2-methyl tetrahydrofuran with tetrahydrofuran (50:50 V percent). Current densities and capacities as a function of temperature, cathode utilization efficiencies versus cycle life, and shelf lives were determined. The state of charge could be related to open circuit voltages after partial discharge. The potential of the system for communication applications is discussed. Recent advances in rechargeable lithium batteries were mainly due to the discovery of stable, cyclic ether electrolyte solvents (1) and to the use of rechargeable cathode materials (2). The practical usefulness of rechargeable lithium cells with Cr /SUB 0.5/ V /SUB 0.5/ S/sub 2/ and MoO/sub 3/ cathodes was investigated in the temperature range of -30/sup 0/C to +25/sup 0/C. The electrolyte was mainly 1.5M LiAsF/sub 6/ in 2-methyl tetrahydrofuran with tetrahydrofuran (50:50 V percent). The two cathode materials were chosen because Cr /SUB 0.5/ V /SUB 0.5/ S/sub 2/ resembles TiS/sub 2/ in capacity and cycling behavior and MoO/sub 3/ is a low cost cathode material of interest.

  5. Facile Synthesis of Carbon-Coated Spinel Li4Ti5O12/Rutile-TiO2 Composites as an Improved Anode Material in Full Lithium-Ion Batteries with LiFePO4@N-Doped Carbon Cathode.

    PubMed

    Wang, Ping; Zhang, Geng; Cheng, Jian; You, Ya; Li, Yong-Ke; Ding, Cong; Gu, Jiang-Jiang; Zheng, Xin-Sheng; Zhang, Chao-Feng; Cao, Fei-Fei

    2017-02-22

    The spinel Li4Ti5O12/rutile-TiO2@carbon (LTO-RTO@C) composites were fabricated via a hydrothermal method combined with calcination treatment employing glucose as carbon source. The carbon coating layer and the in situ formed rutile-TiO2 can effectively enhance the electric conductivity and provide quick Li(+) diffusion pathways for Li4Ti5O12. When used as an anode material for lithium-ion batteries, the rate capability and cycling stability of LTO-RTO@C composites were improved in comparison with those of pure Li4Ti5O12 or Li4Ti5O12/rutile-TiO2. Moreover, the potential of approximately 1.8 V rechargeable full lithium-ion batteries has been achieved by utilizing an LTO-RTO@C anode and a LiFePO4@N-doped carbon cathode.

  6. Crystal growth of a series of lithium garnets Ln{sub 3}Li{sub 5}Ta{sub 2}O{sub 12} (Ln=La, Pr, Nd): Structural properties, Alexandrite effect and unusual ionic conductivity

    SciTech Connect

    Roof, Irina P.; Smith, Mark D.; Cussen, Edmund J.; Loye, Hans-Conrad zur

    2009-02-15

    We report the single crystal structures of a series of lanthanide containing tantalates, Ln{sub 3}Li{sub 5}Ta{sub 2}O{sub 12} (Ln=La, Pr, Nd) that were obtained out of a reactive lithium hydroxide flux. The structures of Ln{sub 3}Li{sub 5}Ta{sub 2}O{sub 12} were determined by single crystal X-ray diffraction, where the Li{sup +} positions and Li{sup +} site occupancies were fixed based on previously reported neutron diffraction data for isostructural compounds. All three oxides crystallize in the cubic space group Ia3-bard (No. 230) with lattice parameters a=12.7735(1), 12.6527(1), and 12.5967(1) A for La{sub 3}Li{sub 5}Ta{sub 2}O{sub 12}, Pr{sub 3}Li{sub 5}Ta{sub 2}O{sub 12}, and Nd{sub 3}Li{sub 5}Ta{sub 2}O{sub 12}, respectively. A UV-Vis diffuse reflectance spectrum of Nd{sub 3}Li{sub 5}Ta{sub 2}O{sub 12} was collected to explain its unusual Alexandrite-like optical behavior. To evaluate the transport properties of Nd{sub 3}Li{sub 5}Ta{sub 2}O{sub 12}, the impedance data were collected in air in the temperature range 300{<=}T(deg. C){<=}500. - Graphical abstract: Crystal structure of garnets Ln{sub 3}Li{sub 5}Ta{sub 2}O{sub 12} (Ln=La, Pr, Nd). TaO{sub 6} polyhedra are shown in yellow and Ln{sup 3+} are shown as light blue spheres. Octahedrally and tetrahedrally coordinated Li{sup +} ions are shown in green and brown, respectively. Oxygen atoms are omitted for clarity.

  7. Copper-doped dual phase Li4Ti5O12-TiO2 nanosheets as high-rate and long cycle life anodes for high-power lithium-ion batteries.

    PubMed

    Chen, Chengcheng; Huang, Yanan; An, Cuihua; Zhang, Hao; Wang, Yijing; Jiao, Lifang; Yuan, Huatang

    2015-01-01

    Cu-doped Li4 Ti5 O12 -TiO2 nanosheets were synthesized by a facile, cheap, and environmentally friendly solution-based method. These nanostructures were investigated as an anode material for lithium-ion batteries. Cu doping was found to enhance the electron conductivity of the materials, and the amount of Cu doped controlled the crystal structure and content of TiO2 . In addition, the samples, which benefit from multiphases and doping, exhibited much improved capacity, cycle performance, and high rate capability over Cu-free Li4 Ti5 O12 -TiO2 . The discharge capacity of the 0.05 Cu-doped sample was 190 mAh g(-1) at 1C, and even 144 mAh g(-1) was obtained at 30C after 100 cycles. Moreover, after 500 cycles at 30C, the discharge capacity remained at approximately 130 mAh g(-1) . The excellent electrochemical performance of the cell demonstrated that Cu-doping was able to adjust and control the Li4 Ti5 O12 -TiO2 system appropriately.

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

    PubMed

    Jha, Manis Kumar; Kumari, Anjan; Jha, Amrita Kumari; Kumar, Vinay; Hait, Jhumki; Pandey, Banshi Dhar

    2013-09-01

    In view of the stringent environmental regulations, availability of limited natural resources and ever increasing need of alternative energy critical elements, an environmental eco-friendly leaching process is reported for the recovery of lithium and cobalt from the cathode active materials of spent lithium-ion batteries of mobile phones. The experiments were carried out to optimize the process parameters for the recovery of lithium and cobalt by varying the concentration of leachant, pulp density, reductant volume and temperature. Leaching with 2M sulfuric acid with the addition of 5% H(2)O(2) (v/v) at a pulp density of 100 g/L and 75°C resulted in the recovery of 99.1% lithium and 70.0% cobalt in 60 min. H(2)O(2) in sulfuric acid solution acts as an effective reducing agent, which enhance the percentage leaching of metals. Leaching kinetics of lithium in sulfuric acid fitted well to the chemical controlled reaction model i.e. 1-(1-X)(1/3)=k(c)t. Leaching kinetics of cobalt fitted well to the model 'ash diffusion control dense constant sizes spherical particles' i.e. 1-3(1-X)(2/3)+2(1-X)=k(c)t. Metals could subsequently be separated selectively from the leach liquor by solvent extraction process to produce their salts by crystallization process from the purified solution.

  9. Monitoring and toxicity evaluation of phytoplankton on lithium manganese oxide adsorbents at lithium recovery pilot plant field.

    NASA Astrophysics Data System (ADS)

    Yoon, H. O.; Kim, J. A.; Kim, J. C.; Chung, K. S.; Ryu, J. H.

    2015-12-01

    For recovery of rare mineral resources such as lithium or boron from seawater, the lithium adsorbent material have been made by Korea Institute of Geoscience and Mineral Resources (KIGAM) and pilot plant was conducted in Okgye Harbor, Gangneung, Korea. The application of lithium adsorbent in pilot plant, it is important to consider the impact on the marine environment. Especially phytoplankton communities are important marine microorganism to represent marine primary product. At the same time, phytoplankton is possible to induce the decrease of lithium recovery rate due to cause of biofouling to surfaces of lithium adsorbents. Therefore long-term and periodic monitoring of phytoplankton is necessary to understand the environmental impact and biofouling problems near the lithium pilot plant. The abundance and biomass of phytoplankton have been evaluated through monthly interval sampling from February 2013 to May 2015. Abundance and species diversity of phytoplankton went up to summer from winter. When lithium adsorbents were immersing to seawater, eco-toxicities of released substances were determined using Microtox with bioluminescence bacteria Vibrio fischeri. The adsorbents were soaked in sterilized seawater and aeration for 1, 3, 5, 7, 10 and 14 days intervals under controlled temperature. Maximum EC50 concentration was 61.4% and this toxicity was showed in more than 10 days exposure.

  10. Lithium disulfide battery

    DOEpatents

    Kaun, Thomas D.

    1988-01-01

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

  11. Lithium ion conducting electrolytes

    DOEpatents

    Angell, C.A.; Liu, C.

    1996-04-09

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

  12. Lithium ion conducting electrolytes

    DOEpatents

    Angell, C. Austen; Liu, Changle

    1996-01-01

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

  13. Lithium battery discharge tests

    NASA Technical Reports Server (NTRS)

    Johnson, C. J.

    1980-01-01

    The long term discharge of a variety of lithium cells was characterized and the susceptibility of the cells to chemical variation during the slow discharge was tested. A shunt resistor was set across the terminals to monitor the voltage as a function of time. Failures were identified by premature voltage drops.

  14. Hectorite-based nanocomposite electrolytes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Riley, Michael William

    Hectorite clay is presented in this work as a promising component for electrolytes for lithium-ion batteries. This negatively-charged, plate-shaped (250 nm diameter by 1 nm thickness) clay has exchangeable cations for which lithium may be substituted. When properly dispersed in high-dielectric solvents such as the carbonates (ethylene carbonate and propylene carbonate) typically used in lithium-ion cells, a shear-thinning physical gel is created possessing a good conductivity (as high as 2 x 10-4 S/cm at room temperature has been measured) with near unity lithium-ion transference numbers. As a result, hectorite-based electrolytes could drastically reduce concentration polarization and present an inherently safer electrolyte as toxic salts such as LiPF6 that are typically used could be eliminated. Hectorite clay dispersions in aqueous and non-aqueous (1:1 (v:v) ethylene carbonate: poly(ethylene)glycol dimethyl ether 250 MW) solvents have been studied using rheology (dynamic and steady) and conductivity. The aqueous dispersions show a highly-exfoliated microstructure (fractal dimension, Df ≈ 1.6) created primarily through electrostatic repulsive forces which recovers after shear deformation by reorientation of the clay platelets. The non-aqueous dispersions form gel structures with a much higher degree of aggregation (Df ≈ 2.5), and recovery after shear deformation appears to be an aggregation controlled process as well. TEM imaging of non-aqueous clay dispersions shows the clay to be uniformly distributed, with the platelets existing in aggregates of 3 to 5 layers. Use of the hectorite-based electrolytes in lithium-ion cells requires electrodes that contain a single-ion conductor in the typically porous structures. Cathodes based on LiCoO2 that contain various lithium-conducting species (lithium hectorite, lithium LaponiteRTM, and lithium-exchanged NAFIONRTM) have been studied. AC impedance spectroscopy was used to probe the cells and equivalent circuits were

  15. Lithium D-cell study

    NASA Technical Reports Server (NTRS)

    Size, P.; Takeuchi, Esther S.

    1993-01-01

    The purpose of this contract is to evaluate parametrically the effects of various factors including the electrolyte type, electrolyte concentration, depolarizer type, and cell configuration on lithium cell electrical performance and safety. This effort shall allow for the selection and optimization of cell design for future NASA applications while maintaining close ties with WGL's continuous improvements in manufacturing processes and lithium cell design. Taguchi experimental design techniques are employed in this task, and allow for a maximum amount of information to be obtained while requiring significantly less cells than if a full factorial design were employed. Acceptance testing for this task is modeled after the NASA Document EP5-83-025, Revision C, for cell weights, OCV's and load voltages. The performance attributes that are studied in this effort are fresh capacity and start-up characteristics evaluated at two rates and two temperatures, shelf-life characteristics including start-up and capacity retention, and iterative microcalorimetry measurements. Abuse testing includes forced over discharge at two rates with and without diode protection, temperature tolerance testing, and shorting tests at three rates with the measurement of heat generated during shorting conditions.

  16. Lithium ionic mobility study in xLi2CO3-yLiI (x = 95-70, y = 5-30 wt.%) solid electrolyte by impedance spectroscopy technique

    NASA Astrophysics Data System (ADS)

    Omar, Mohd Khari; Ahmad, Azizah Hanom

    2015-08-01

    A detailed systematic study on the effects of different amount (wt.%) of LiI addition on the electrical conductivity and dielectric behavior of the xLi2CO3-xLiI (x = 95-70, y = 5-30 wt.%) electrolyte system was carried out. The samples with different compositions were prepared and ground by mechanical milling method. The electrical and dielectric properties of the samples over a range of frequency (50Hz - 1MHz) were investigated by deploying electrical impedance spectroscopy (EIS) technique in a series of temperature set (298-373K). Normally, Li2CO3 itself shows a very low electrical conductivity (10-5 Scm-1). However, the electrical conductivity of the system was found to be increased (10-3 Scm-1) as the lithium salt (LiI) were introduced to the system. The dielectric analysis displayed that the activation energy was inversely proportional to the increment of LiI (wt.%). As the electrical conductivity reached their maximum value (4.63 × 10-3 Scm-1) at the 20 wt.% of LiI, the activation energy was dropped to the minimum (0.1 eV). The electrical conductivity increases with the temperature (298 - 373K) indicate that the system obeys Arrhenius law.

  17. Lithium ionic mobility study in xLi{sub 2}CO{sub 3}-yLiI (x = 95-70, y = 5-30 wt.%) solid electrolyte by impedance spectroscopy technique

    SciTech Connect

    Omar, Mohd Khari; Ahmad, Azizah Hanom

    2015-08-28

    A detailed systematic study on the effects of different amount (wt.%) of LiI addition on the electrical conductivity and dielectric behavior of the xLi{sub 2}CO{sub 3}-xLiI (x = 95-70, y = 5-30 wt.%) electrolyte system was carried out. The samples with different compositions were prepared and ground by mechanical milling method. The electrical and dielectric properties of the samples over a range of frequency (50Hz – 1MHz) were investigated by deploying electrical impedance spectroscopy (EIS) technique in a series of temperature set (298–373K). Normally, Li{sub 2}CO{sub 3} itself shows a very low electrical conductivity (10{sup −5} Scm{sup −1}). However, the electrical conductivity of the system was found to be increased (10{sup −3} Scm{sup −1}) as the lithium salt (LiI) were introduced to the system. The dielectric analysis displayed that the activation energy was inversely proportional to the increment of LiI (wt.%). As the electrical conductivity reached their maximum value (4.63 × 10{sup −3} Scm{sup −1}) at the 20 wt.% of LiI, the activation energy was dropped to the minimum (0.1 eV). The electrical conductivity increases with the temperature (298 – 373K) indicate that the system obeys Arrhenius law.

  18. A Strategy for Synthesis of Nanosheets Consisting of Alternating Spinel Li4Ti5O12 and Rutile TiO2 Lamellas for High-Rate Anodes of Lithium-Ion Batteries.

    PubMed

    Wu, Libo; Leng, Xuning; Liu, Yan; Wei, Sufeng; Li, Chunlin; Wang, Guoyong; Lian, Jianshe; Jiang, Qing; Nie, Anmin; Zhang, Tong-Yi

    2017-02-08

    Ultrathin dual phase nanosheets consisting of alternating spinel Li4Ti5O12 (LTO) and rutile TiO2 (RT) lamellas are synthesized through a facile and scalable hydrothermal method, and the formation mechanism is explored. The thickness of constituent lamellas can be controlled exactly by adjusting the mole ratio of Li:Ti in the original reactants. Alternating insertion of the RT lamellas significantly improves the electrochemical performance of LTO nanosheets, especially at high charge/discharge rates. As anodes in lithium-ion batteries (LIBs), the dual phase nanosheet electrode with the optimized phase ratio can deliver stable discharge capacities of 178.5, 154.9, 148.4, 142.3, 138.2, and 131.4 mA h g(-1) at current densities of 1, 10, 20, 30, 40, and 50 C, respectively. Meanwhile, they inherit the excellent cyclic stability of pure spinel LTO and exhibit a capacity retention of 93.1% even after 500 cycles at 50 C. Our results indicate that the alternating nanoscaled lamella structure is a good alternative to facilitate the transfer of both the Li ions and electrons into the spinel LTO, giving rise to an excellent cyclability and fast rate performance. Therefore, the newly prepared carbon-free LTO-RT nanosheets with high safety provide a new opportunity to develop high-power anodes for LIBs.

  19. Cross state-dependent retrieval between histamine and lithium.

    PubMed

    Zarrindast, Mohammad-Reza; Fazli-Tabaei, Soheila; Khalilzadeh, Azita; Farahmanfar, Maryam; Yahyavi, Seyed-Hossein

    2005-09-15

    Histamine and lithium state-dependent (StD) retrieval of passive avoidance task and their interactions was examined in mice. The pre-training or pre-test intracerebroventricular (i.c.v.) injection of histamine (20 microg/mouse) impaired retrieval when it was tested 24 h later. In the animals, in which retrieval was impaired due to histamine pre-training administration, pre-test administration of histamine, with the same dose, restored retrieval. The H1 blocker, pyrilamine (20 microg/mouse, i.c.v.), but not the H(2) blocker; ranitidine prevented the restoration of retrieval by pre-test histamine. The pre-training (5 and 10 mg/kg) or pre-test (5 mg/kg) injection of lithium also impaired retrieval, when it was tested 24 h later. In the animals that received lithium (5 mg/kg) or histamine (20 microg/mouse) as pre-training treatment, administration of histamine, clobenpropit or lithium, respectively, resulted in restoration of memory retrieval. Neither pyrilamine nor ranitidine prevented the restoration of retrieval by pre-test lithium. In conclusion, histamine or lithium can induce state-dependent retrieval and a cross-StD exists between these drugs, which may be mediated through the inositol pathway.

  20. Hydrogel-forming microneedle arrays: Potential for use in minimally-invasive lithium monitoring.

    PubMed

    Eltayib, Eyman; Brady, Aaron J; Caffarel-Salvador, Ester; Gonzalez-Vazquez, Patricia; Zaid Alkilani, Ahlam; McCarthy, Helen O; McElnay, James C; Donnelly, Ryan F

    2016-05-01

    We describe, for the first time, hydrogel-forming microneedle (s) (MN) arrays for minimally-invasive extraction and quantification of lithium in vitro and in vivo. MN arrays, prepared from aqueous blends of hydrolysed poly(methyl-vinylether-co-maleic anhydride) and crosslinked by poly(ethyleneglycol), imbibed interstitial fluid (ISF) upon skin insertion. Such MN were always removed intact. In vitro, mean detected lithium concentrations showed no significant difference following 30min MN application to excised neonatal porcine skin for lithium citrate concentrations of 0.9 and 2mmol/l. However, after 1h application, the mean lithium concentrations extracted were significantly different, being appropriately concentration-dependent. In vivo, rats were orally dosed with lithium citrate equivalent to 15mg/kg and 30mg/kg lithium carbonate, respectively. MN arrays were applied 1h after dosing and removed 1h later. The two groups, having received different doses, showed no significant difference between lithium concentrations in serum or MN. However, the higher dosed rats demonstrated a lithium concentration extracted from MN arrays equivalent to a mean increase of 22.5% compared to rats which received the lower dose. Hydrogel-forming MN clearly have potential as a minimally-invasive tool for lithium monitoring in outpatient settings. We will now focus on correlation between serum and MN lithium concentrations.

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

    SciTech Connect

    Dudney, N.J.; Bates, J.B.; Luck, C.F. ); Robertson, J.D. . Dept. of Chemistry)

    1991-01-01

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

  2. Stoichiometric Lithium Niobate (SLN) Based Linearized Electro-Optic (EO) Modulator

    DTIC Science & Technology

    2006-01-01

    AFRL-SN-RS-TR-2006-15 Final Technical Report January 2006 STOICHIOMETRIC LITHIUM NIOBATE (SLN) BASED LINEARIZED ELECTRO - OPTIC (EO...LITHIUM NIOBATE (SLN) BASED LINEARIZED ELECTRO - OPTIC (EO) MODULATOR 6. AUTHOR(S) Dr Stuart Kingsley, Dr Sri Sriram 5. FUNDING NUMBERS C...SUBJECT TERMS electro - optic modulator, linearization, directional coupler, variable coupling, optical waveguide, Mach-Zehnder, photonic link, lithium

  3. Antiviral effect of lithium chloride.

    PubMed

    Cernescu, C; Popescu, L; Constantinescu, S; Cernescu, S

    1988-01-01

    Studies in human embryo fibroblasts infected with measles or herpes simplex virus showed a reduction in virus yield when cultures were pretreated with 1-10 mM lithium chloride doses. Maximum effect was obtained by a 1 h treatment with 10 mM lithium chloride, preceding viral infection by 19-24 hours. A specific antiviral effect against measles virus was manifest immediately after culture pretreatment. Intermittent treatment with 10 mM lithium chloride of cultures persistently infected with measles or herpes virus obtained from human myeloid K-562 cell line shows a reduction in the extracellular virus yield. In the K-562/herpes virus system, the culture treatment with lithium chloride and acyclovir (10 microM) has an additive inhibitory effect on virus production. The paper is focused on the mechanism of lithium chloride antiviral action and the expediency of lithium therapy in SSPE (subacute sclerosing panencephalitis).

  4. Experimental lithium system. Final report

    SciTech Connect

    Kolowith, R.; Berg, J.D.; Miller, W.C.

    1985-04-01

    A full-scale mockup of the Fusion Materials Irradiation Test (FMIT) Facility lithium system was built at the Hanford Engineering Development Laboratory (HEDL). This isothermal mockup, called the Experimental Lithium System (ELS), was prototypic of FMIT, excluding the accelerator and dump heat exchanger. This 3.8 m/sup 3/ lithium test loop achieved over 16,000 hours of safe and reliable operation. An extensive test program demonstrated satisfactory performance of the system components, including the HEDL-supplied electromagnetic lithium pump, the lithium jet target, the purification and characterization hardware, as well as the auxiliary argon and vacuum systems. Experience with the test loop provided important information on system operation, performance, and reliability. This report presents a complete overview of the entire Experimental Lithium System test program and also includes a summary of such areas as instrumentation, coolant chemistry, vapor/aerosol transport, and corrosion.

  5. Benzimidazole-derived anion for lithium-conducting electrolytes

    NASA Astrophysics Data System (ADS)

    Niedzicki, Leszek; Oledzki, Piotr; Bitner, Anna; Bukowska, Maria; Szczecinski, Przemyslaw

    2016-02-01

    In this work we announce new lithium salt of 5,6-dicyano-2-(trifluoromethyl)benzimidazolide (LiTDBI) designed for application in lithium conductive electrolytes. It was synthesized and completely characterized by NMR techniques. Studies show salt's thermal stability up to 270 °C and electrochemical stability in liquid solvents up to +4.7 V vs. metallic lithium anode. Basic characterization of electrolytes made with this salt show conductivity over 1 mS cm-1 and unusually high transference number at high concentrations (0.74 in EC:DMC 1:2 ratio mixture) along with low onset of conductivity peak. As a final proof of concept, cycling in half-cell was performed and electrolyte based on LiTDBI showed perfect capacity retention. Such properties show remarkable progress in creating efficient lithium-conducting electrolytes with use of weakly-coordinating anions.

  6. Membranes in lithium ion batteries.

    PubMed

    Yang, Min; Hou, Junbo

    2012-07-04

    Lithium ion batteries have proven themselves the main choice of power sources for portable electronics. Besides consumer electronics, lithium ion batteries are also growing in popularity for military, electric vehicle, and aerospace applications. The present review attempts to summarize the knowledge about some selected membranes in lithium ion batteries. Based on the type of electrolyte used, literature concerning ceramic-glass and polymer solid ion conductors, microporous filter type separators and polymer gel based membranes is reviewed.

  7. Sealed Lithium Inorganic Electrolyte Cell

    DTIC Science & Technology

    1976-03-01

    revere side it necoeery and idM,1117 "~ bfoh numiber) Inorganic Electrolyte Battery Carbon Cathode Evaluation Thionyl Chloride Gas Generation Lithium ...hardware corrosion in cold rolled steel cans, due to cathodic protection of the cans by the lithium . Recent data 4 showed that thionyl chloride is reduced...very slowly on the surface of nickel and stainless steel, when these materials were in contact with a lithium anode in the thionyl chloride

  8. Advanced lithium ion battery charger

    SciTech Connect

    Teofilo, V.L.; Merritt, L.V.; Hollandsworth, R.P.

    1997-12-01

    A lithium ion battery charger has been developed for four and eight cell batteries or multiples thereof. This charger has the advantage over those using commercial lithium ion charging chips in that the individual cells are allowed to be taper charged at their upper charging voltage rather than be cutoff when all cells of the string have reached the upper charging voltage limit. Since 30--60% of the capacity of lithium ion cells maybe restored during the taper charge, this charger has a distinct benefit of fully charging lithium ion batteries by restoring all of the available capacity to all of its cells.

  9. Lithium-Inorganic Electrolyte Batteries.

    DTIC Science & Technology

    PRIMARY BATTERIES , TEMPERATURE, LITHIUM , CATHODES, ELECTRODES, PROTECTIVE COATINGS, PLATINUM, NICKEL, SULFUR, STORAGE, GOLD, RELIABILITY(ELECTRONICS...CHEMICAL ANALYSIS, CARBON BLACK, GAS CHROMATOGRAPHY, THIONYL CHLORIDE , REDUCTION(CHEMISTRY).

  10. Enhancement of lithium ion conductivity by doping Li3BO3 in Li2S-P2S5 glass-ceramics electrolytes for all-solid-state batteries

    NASA Astrophysics Data System (ADS)

    Eom, Minyong; Choi, Sunho; Son, Seunghyeon; Choi, Lakyoung; Park, Chanhwi; Shin, Dongwook

    2016-11-01

    (100-x) (0.78Li2S·0.22P2S5)·xLi3BO3 (0 ≤ x ≤ 5) solid electrolytes are prepared via mechanical milling and a post heat-treatment process, and the resulting electrochemical properties are investigated in conjunction with structural analysis. Adding of Li3BO3 into the (100-x) (0.78Li2S·0.22P2S5)·xLi3BO3 solid electrolyte is expected to enhance the conductivity and lower the activation energy as a consequence of changing the structural unit in the glass network. It turned out that the doping of Li3BO3 enhances the conductivity by enlarging the glass forming region and promoting precipitation of high lithium ion conductive thio-LISICON II analog. 97 (0.78Li2S·0.22P2S5)·3Li3BO3 (x = 3) glass-ceramics exhibits the highest conductivity (1.03 × 10-3 S cm-1). Structural analysis shows that the samples with Li3BO3 added to the electrolyte are composed of the main structural unit of PS43- with partially-modified structural unit of PO43-, which are believed to effectively enhance the conductivity and decrease the activation energy. In glass-ceramics produced from these materials, the thio-LISICON II phase with higher ionic conductivity tends to be stabilized by the addition of Li3BO3. Additionally, the formation of space-charge layer is relaxed by Li3BO3 doping. As a result, the all-solid-state cell shows high initial discharge capacity of 156 mAh g-1, and the capacity is retained to be 149 mAh g-1 for 40 cycles.

  11. Synthesis and electrochemical properties of Li2/3Ni1/3Mn2/3O2 as a novel 5 V class positive electrode material for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Chiba, Kazuki; Shikano, Masahiro; Sakaebe, Hikari

    2016-02-01

    A lithium nickel manganese oxide, O3-Li2/3Ni1/3Mn2/3O2, is synthesized from the precursor, P3-Na2/3Ni1/3Mn2/3O2, by a Na+/Li+ ion exchange reaction using molten salt. Post-heating at 300, 400, 500, 600, and 700 °C is carried out for 5 h in air. The products are characterized by powder XRD, inductively coupled plasma-atomic emission spectroscopy (ICP-AES), SEM, 6Li-magic-angle-spinning-NMR, and electrochemical measurements. The charge/discharge profiles of O3-Li2/3Ni1/3Mn2/3O2, thermally treated at 500 °C, show a high-potential plateau region at 4.8 V. Furthermore, sloping voltage profiles are observed at an average voltage of 3.21 V. An initial discharge capacity of 257 mA h g-1 is obtained between 2.0 and 4.8 V with a current density of 15 mA g-1 at 25 °C. This capacity corresponds to 0.90 electron transfers per formula unit. This study shows that Post-heating of O3-Li2/3Ni1/3Mn2/3O2 is effective to improve its electrochemical properties.

  12. Optimization of operation conditions for extracting lithium ions from calcium chloride-type oil field brine

    NASA Astrophysics Data System (ADS)

    Yang, Hong-jun; Li, Qing-hai; Li, Bing; Guo, Feng-qin; Meng, Qing-fen; Li, Wu

    2012-04-01

    Al(OH)3 was prepared to extract lithium ions from calcium chloride-type oil field brine. The influences of four factors, namely temperature, Al3+/Li+ molar ratio, OH-/Al3+ molar ratio, and contact time between Al(OH)3 and the brine, on the yield of lithium ions were investigated. It is found that their optimal values are 35°C, 4.5, 2.6, and 6 h, respectively. In the course of the experiment, the apparent pH value was observed. The results reveal that the apparent pH value has no remarkable influence on the yield of lithium ions. Meanwhile, the effects of the concentrations of calcium ions and magnesium ions in the brine on lithium recovery were studied. The results indicate that calcium ions have minor negative influence on the yield of lithium ions under optimal conditions, and magnesium ions slightly influence the yield of lithium ions.

  13. Optimized lithium oxyhalide cells

    NASA Astrophysics Data System (ADS)

    Kilroy, W. P.; Schlaikjer, C.; Polsonetti, P.; Jones, M.

    1993-04-01

    Lithium thionyl chloride cells were optimized with respect to electrolyte and carbon cathode composition. Wound 'C-size' cells with various mixtures of Chevron acetylene black with Ketjenblack EC-300J and containing various concentrations of LiAlCl4 and derivatives, LiGaCl4, and mixtures of SOCl2 and SO2Cl2 were evaluated as a function of discharge rate, temperature, and storage condition.

  14. Exposure to lithium through drinking water and calcium homeostasis during pregnancy: A longitudinal study.

    PubMed

    Harari, Florencia; Åkesson, Agneta; Casimiro, Esperanza; Lu, Ying; Vahter, Marie

    2016-05-01

    There is increasing evidence of adverse health effects due to elevated lithium exposure through drinking water but the impact on calcium homeostasis is unknown. This study aimed at elucidating if lithium exposure through drinking water during pregnancy may impair the maternal calcium homeostasis. In a population-based mother-child cohort in the Argentinean Andes (n=178), with elevated lithium concentrations in the drinking water (5-1660μg/L), blood lithium concentrations (correlating significantly with lithium in water, urine and plasma) were measured repeatedly during pregnancy by inductively coupled plasma mass spectrometry and used as exposure biomarker. Markers of calcium homeostasis included: plasma 25-hydroxyvitamin D3, serum parathyroid hormone (PTH), and calcium, phosphorus and magnesium concentrations in serum and urine. The median maternal blood lithium concentration was 25μg/L (range 1.9-145). In multivariable-adjusted mixed-effects linear regression models, blood lithium was inversely associated with 25-hydroxyvitamin D3 (-6.1nmol/L [95%CI -9.5; -2.6] for a 25μg/L increment in blood lithium). The estimate increased markedly with increasing percentiles of 25-hydroxyvitamin D3. In multivariable-adjusted mixed-effects logistic regression models, the odds ratio of having 25-hydroxyvitamin D3<30nmol/L (19% of the women) was 4.6 (95%CI 1.1; 19.3) for a 25μg/L increment in blood lithium. Blood lithium was also positively associated with serum magnesium, but not with serum calcium and PTH, and inversely associated with urinary calcium and magnesium. In conclusion, our study suggests that lithium exposure through drinking water during pregnancy may impair the calcium homeostasis, particularly vitamin D. The results reinforce the need for better control of lithium in drinking water, including bottled water.

  15. Effects of 10 to 30 years of lithium treatment on kidney function.

    PubMed

    Aiff, Harald; Attman, Per-Ola; Aurell, Mattias; Bendz, Hans; Ramsauer, Bernd; Schön, Staffan; Svedlund, Jan

    2015-05-01

    Long-term lithium treatment is associated with end-stage renal disease, but there is little evidence of a clinically significant reduction in renal function in most patients. We previously found that 1.5% of people who took lithium from the 1960s and 1970s developed end-stage renal disease; however, none of the patients who started after 1980 had end-stage renal disease. Here we aimed to study the prevalence and extent of kidney damage during the course of long-term lithium treatment since 1980. We retrieved serum lithium and creatinine levels from 4879 patients examined between 1 January 1981 and 31 December 2010. Only patients who started their lithium treatment during the study period and had at least 10 years of cumulative treatment were included. The study group comprised 630 adult patients (402 women and 228 men) with normal creatinine levels at the start of lithium treatment. There was a yearly increase in median serum creatinine levels already from the first year of treatment. About one-third of the patients who had taken lithium for 10-29 years had evidence of chronic renal failure but only 5% were in the severe or very severe category. The results indicate that a substantial proportion of adult patients who are treated with lithium for more than a decade develop signs of renal functional impairment, also when treated according to modern therapeutic principles. Our results emphasise that lithium treatment requires continuous monitoring of kidney function.

  16. A lithium-sensitive and sodium-tolerant 3'-phosphoadenosine-5'-phosphatase encoded by halA from the cyanobacterium Arthrospira platensis is closely related to its counterparts from yeasts and plants.

    PubMed

    Zhang, Ju-Yuan; Zou, Jie; Bao, Qiyu; Chen, Wen-Li; Wang, Li; Yang, Huanming; Zhang, Cheng-Cai

    2006-01-01

    3'-Phosphoadenosine-5'-phosphatase (PAPase) is required for the removal of toxic 3'-phosphoadenosine-5'-phosphate (PAP) produced during sulfur assimilation in various eukaryotic organisms. This enzyme is a well-known target of lithium and sodium toxicity and has been used for the production of salt-resistant transgenic plants. In addition, PAPase has also been proposed as a target in the treatment of manic-depressive patients. One gene, halA, which could encode a protein closely related to the PAPases of yeasts and plants, was identified from the cyanobacterium Arthrospira (Spirulina) platensis. Phylogenic analysis indicated that proteins related to PAPases from several cyanobacteria were found in different clades, suggesting multiple origins of PAPases in cyanobacteria. The HalA polypeptide from A. platensis was overproduced in Escherichia coli and used for the characterization of its biochemical properties. HalA was dependent on Mg2+ for its activity and could use PAP or 3'-phosphoadenosine-5'-phosphosulfate as a substrate. HalA is sensitive to Li+ (50% inhibitory concentration [IC50] = 3.6 mM) but only slightly sensitive to Na+ (IC50 = 600 mM). The salt sensitivity of HalA was thus different from that of most of its eukaryotic counterparts, which are much more sensitive to both Li+ and Na+, but was comparable to the PAPase AtAHL (Hal2p-like protein) from Arabidopsis thaliana. The properties of HalA could help us to understand the structure-function relationship underlying the salt sensitivity of PAPases. The expression of halA improved the Li+ tolerance of E. coli, suggesting that the sulfur-assimilating pathway is a likely target of salt toxicity in bacteria as well.

  17. Advanced High Energy Lithium Polymer Electrolyte Battery

    DTIC Science & Technology

    2007-11-02

    of the two phase nature of the latter materials.5,6 These materials are also always intrinsically ’ wet ’ in physical appearance. The above...into polymeric matrix of respectively PVC or PAN and radiation polymerized polyethers (so called gel or " wet " electrolytes). In spite of rather...The most widely studied material was polyethylene oxide ) (PEO), incorporating lithium salts such as LiC104 and LiCF3S03. This material however

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

    SciTech Connect

    Jha, Manis Kumar Kumari, Anjan; Jha, Amrita Kumari; Kumar, Vinay; Hait, Jhumki; Pandey, Banshi Dhar

    2013-09-15

    Graphical abstract: Recovery of valuable metals from scrap batteries of mobile phone. - Highlights: • Recovery of Co and Li from spent LIBs was performed by hydrometallurgical route. • Under the optimum condition, 99.1% of lithium and 70.0% of cobalt were leached. • The mechanism of the dissolution of lithium and cobalt was studied. • Activation energy for lithium and cobalt were found to be 32.4 kJ/mol and 59.81 kJ/mol, respectively. • After metal recovery, residue was washed before disposal to the environment. - Abstract: In view of the stringent environmental regulations, availability of limited natural resources and ever increasing need of alternative energy critical elements, an environmental eco-friendly leaching process is reported for the recovery of lithium and cobalt from the cathode active materials of spent lithium-ion batteries of mobile phones. The experiments were carried out to optimize the process parameters for the recovery of lithium and cobalt by varying the concentration of leachant, pulp density, reductant volume and temperature. Leaching with 2 M sulfuric acid with the addition of 5% H{sub 2}O{sub 2} (v/v) at a pulp density of 100 g/L and 75 °C resulted in the recovery of 99.1% lithium and 70.0% cobalt in 60 min. H{sub 2}O{sub 2} in sulfuric acid solution acts as an effective reducing agent, which enhance the percentage leaching of metals. Leaching kinetics of lithium in sulfuric acid fitted well to the chemical controlled reaction model i.e. 1 − (1 − X){sup 1/3} = k{sub c}t. Leaching kinetics of cobalt fitted well to the model ‘ash diffusion control dense constant sizes spherical particles’ i.e. 1 − 3(1 − X){sup 2/3} + 2(1 − X) = k{sub c}t. Metals could subsequently be separated selectively from the leach liquor by solvent extraction process to produce their salts by crystallization process from the purified solution.

  19. Porous V2O5/RGO/CNT hierarchical architecture as a cathode material: Emphasis on the contribution of surface lithium storage.

    PubMed

    Palanisamy, Kowsalya; Um, Ji Hyun; Jeong, Mihee; Yoon, Won-Sub

    2016-08-11

    A three dimensional vanadium pentoxide/reduced graphene oxide/carbon nanotube (3D V2O5/RGO/CNT) composite is synthesized by microwave-assisted hydrothermal method. The combination of 2D RGO and 1D CNT establishes continuous 3D conductive network, and most notably, the 1D CNT is designed to form hierarchically porous structure by penetrating into V2O5 microsphere assembly constituted of numerous V2O5 nanoparticles. The highly porous V2O5 microsphere enhances electrolyte contact and shortens Li(+) diffusion path as a consequence of its developed surface area and mesoporosity. The successive phase transformations of 3D V2O5/RGO/CNT from α-phase to ε-, δ-, γ-, and ω-phase and its structural reversibility upon Li(+) intercalation/de-intercalation are investigated by in situ XRD analysis, and the electronic and local structure reversibility around vanadium atom in 3D V2O5/RGO/CNT is observed by in situ XANES analysis. The 3D V2O5/RGO/CNT achieves a high capacity of 220 mAh g(-1) at 1 C after 80 cycles and an excellent rate capability of 100 mAh g(-1) even at a considerably high rate of 20 C. The porous 3D V2O5/RGO/CNT structure not only provides facile Li(+) diffusion into bulk but contributes to surface Li(+) storage as well, which enables the design of 3D V2O5/RGO/CNT composite to become a promising cathode architecture for high performance LIBs.

  20. Porous V2O5/RGO/CNT hierarchical architecture as a cathode material: Emphasis on the contribution of surface lithium storage

    NASA Astrophysics Data System (ADS)

    Palanisamy, Kowsalya; Um, Ji Hyun; Jeong, Mihee; Yoon, Won-Sub

    2016-08-01

    A three dimensional vanadium pentoxide/reduced graphene oxide/carbon nanotube (3D V2O5/RGO/CNT) composite is synthesized by microwave-assisted hydrothermal method. The combination of 2D RGO and 1D CNT establishes continuous 3D conductive network, and most notably, the 1D CNT is designed to form hierarchically porous structure by penetrating into V2O5 microsphere assembly constituted of numerous V2O5 nanoparticles. The highly porous V2O5 microsphere enhances electrolyte contact and shortens Li+ diffusion path as a consequence of its developed surface area and mesoporosity. The successive phase transformations of 3D V2O5/RGO/CNT from α-phase to ε-, δ-, γ-, and ω-phase and its structural reversibility upon Li+ intercalation/de-intercalation are investigated by in situ XRD analysis, and the electronic and local structure reversibility around vanadium atom in 3D V2O5/RGO/CNT is observed by in situ XANES analysis. The 3D V2O5/RGO/CNT achieves a high capacity of 220 mAh g‑1 at 1 C after 80 cycles and an excellent rate capability of 100 mAh g‑1 even at a considerably high rate of 20 C. The porous 3D V2O5/RGO/CNT structure not only provides facile Li+ diffusion into bulk but contributes to surface Li+ storage as well, which enables the design of 3D V2O5/RGO/CNT composite to become a promising cathode architecture for high performance LIBs.

  1. Porous V2O5/RGO/CNT hierarchical architecture as a cathode material: Emphasis on the contribution of surface lithium storage

    PubMed Central

    Palanisamy, Kowsalya; Um, Ji Hyun; Jeong, Mihee; Yoon, Won-Sub

    2016-01-01

    A three dimensional vanadium pentoxide/reduced graphene oxide/carbon nanotube (3D V2O5/RGO/CNT) composite is synthesized by microwave-assisted hydrothermal method. The combination of 2D RGO and 1D CNT establishes continuous 3D conductive network, and most notably, the 1D CNT is designed to form hierarchically porous structure by penetrating into V2O5 microsphere assembly constituted of numerous V2O5 nanoparticles. The highly porous V2O5 microsphere enhances electrolyte contact and shortens Li+ diffusion path as a consequence of its developed surface area and mesoporosity. The successive phase transformations of 3D V2O5/RGO/CNT from α-phase to ε-, δ-, γ-, and ω-phase and its structural reversibility upon Li+ intercalation/de-intercalation are investigated by in situ XRD analysis, and the electronic and local structure reversibility around vanadium atom in 3D V2O5/RGO/CNT is observed by in situ XANES analysis. The 3D V2O5/RGO/CNT achieves a high capacity of 220 mAh g−1 at 1 C after 80 cycles and an excellent rate capability of 100 mAh g−1 even at a considerably high rate of 20 C. The porous 3D V2O5/RGO/CNT structure not only provides facile Li+ diffusion into bulk but contributes to surface Li+ storage as well, which enables the design of 3D V2O5/RGO/CNT composite to become a promising cathode architecture for high performance LIBs. PMID:27511434

  2. Flashover lithium ion source development for large pulsed power accelerators

    SciTech Connect

    Bieg, K.W.; Burns, E.J.T.; Gerber, R.A.; Olsen, J.N.; Lamppa, K.P.

    1985-01-01

    PBFA II, a light-ion pulsed power accelerator intended for inertial confinement fusion (ICF) applications, is currently under construction at Sandia National Laboratories. The accelerator will deliver a 30 MV, 5 MA lithium beam from an Applied-B diode to drive an ICF target. The ion source for this diode will require a thin (approx.1 mm), dense (10 W cm S) anode plasma layer of singly-ionized lithium over an anode area of 10T cmS. One type of source being investigated is the flashover ion source, which generates the anode plasma via vacuum flashover of a lithium-bearing dielectric material. Experiments with a LiF flashover source on the 0.03 TW Nereus accelerator have shown that contaminant ions account for as much as 70% of the extracted ion beam current. To overcome this, we have explored in-diode cleaning of the externally-prepared anode surface by glow discharge cleaning and vacuum baking as well as in-diode preparation of the anode surface by vacuum evaporation of the lithium dielectric. Lithium-bearing dielectric materials which have been investigated include LiF, LiI, LiNO3, and Li3N. These techniques have resulted in a two- to three-fold improvement in the extracted lithium ion purity. As a result, a glow-discharge cleaned LiF flashover source will be used for initial pulsed-power testing on PBFA II.

  3. Lithium stimulates the release of human parathyroid hormone in vitro.

    PubMed

    Birnbaum, J; Klandorf, H; Giuliano, A; Van Herle, A

    1988-06-01

    The effect of lithium on PTH release from human parathyroid tissue was studied using a perifusion system and an immunoradiometric assay for intact human PTH. Tissue was obtained from three patients undergoing surgery for thyroid disease, three patients with secondary hyperparathyroidism due to chronic renal insufficiency, and four patients with primary hyperparathyroidism due to a parathyroid adenoma. Addition of lithium in concentrations equivalent to the therapeutic serum levels normally attained in man (1.3 mmol/L) resulted in a significant (P less than 0.05) increase in PTH release under normocalcemic (1.15 mmol/L) conditions from normal and hyperplastic tissues. The magnitude of the lithium-induced response of PTH release ranged from a 1.4- to 5.3-fold increase above basal levels (perifusion with 1.15 mmol/L calcium alone) and was comparable to the response during a low calcium (0.42 mmol/L) perifusion. Although the response to lithium was delayed compared to that of hypocalcemia, PTH returned to basal levels immediately after removal of either stimulator. In contrast, parathyroid adenomas did not respond to either lithium or hypocalcemia in a characteristic manner, but, rather, functioned in an autonomous fashion with repeated pulsatile bursts of PTH release that were not suppressible even under hypercalcemic (1.70 mmol/L) conditions. These in vitro studies suggest that lithium therapy may elevate serum PTH levels in some patients and could, thus, be responsible for hypercalcemia in them.

  4. Effects of dopant on the electrochemical performance of Li 4Ti 5O 12 as electrode material for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Huang, Shahua; Wen, Zhaoyin; Zhu, Xiujian; Lin, Zuxiang

    The effects of dopant on the electrochemical properties of spinel-type Li 3.95M 0.15Ti 4.9O 12 (M = Al, Ga, Co) and Li 3.9Mg 0.1Al 0.15Ti 4.85O 12 were systematically investigated. Charge-discharge cycling were performed at a constant current density of 0.15 mA cm -2 between the cut-off voltages of 2.3 and 0.5 V, the experimental results showed that Al 3+ dopant greatly improved the reversible capacity and cycling stability over the pristine Li 4Ti 5O 12. The substitution of the Ga 3+ slightly increased the capacity of the Li 4Ti 5O 12, but did not essentially alleviate the degradation of cycling stability. Dopants such as Co 3+ and Mg 2+ to some extent worsened the electrochemical performance of the Li 4Ti 5O 12.

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

    SciTech Connect

    Voronin, V.I.; Sherstobitova, E.A.; Blatov, V.A.; Shekhtman, G.Sh.

    2014-03-15

    The electrical conductivity of lithium diphosphate Li{sub 4}P{sub 2}O{sub 7} has been measured and jump-like increasing of ionic conductivity at 913 K has been found. The crystal structure of Li{sub 4}P{sub 2}O{sub 7} has been refined using high temperature neutron diffraction at 300–1050 K. At 913 K low temperature triclinic form of Li{sub 4}P{sub 2}O{sub 7} transforms into high temperature monoclinic one, space group P2{sub 1}/n, a=8.8261(4) Å, b=5.2028(4) Å, c=13.3119(2) Å, β=104.372(6)°. The migration maps of Li{sup +} cations based on experimental data implemented into program package TOPOS have been explored. It was found that lithium cations in both low- and high temperature forms of Li{sub 4}P{sub 2}O{sub 7} migrate in three dimensions. Cross sections of the migrations channels extend as the temperature rises, but at the phase transition point have a sharp growth showing a strong “crystal structure – ion conductivity” correlation. -- Graphical abstract: Crystal structure of Li{sub 4}P{sub 2}O{sub 7} at 950 K. Red balls represent oxygen atoms; black lines show Li{sup +} ion migration channels in the layers perpendicular to [001] direction. Highlights: • Structure of Li{sub 4}P{sub 2}O{sub 7} has been refined using high temperature neutron diffraction. • At 913 K triclinic form of Li{sub 4}P{sub 2}O{sub 7} transforms into high temperature monoclinic one. • The migration maps of Li{sup +} implemented into program package TOPOS have been explored. • Cross sections of the migrations channels at the phase transition have a sharp growth.

  6. Novel synthesis process and structure refinements of Li{sub 4}Mn{sub 5}O{sub 12} for rechargeable lithium batteries

    SciTech Connect

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

    1996-12-31

    Well crystallized Li4Mn5O12 was prepared from LiOAc-Mn(NO3)2 under flowing oxygen. Rietveld refinement with XRD and neutron powder diffraction indicated that Li4Mn5O12 has cubic spinel structure in which the Li ions occupy both the tetrahedral sites 8a and part of the octahedral sites 16d but not the 16c sites, while all the Mn ions occupy the 16d sites of the space group Fd{bar 3}m. The lattice parameter was found to be sensitive to synthesis temperature owing to variation in Mn valence. Sample prepared at 500 C showed better electrode performance: a rechargeable capacity of 135 mAh/g for the cell Li/Li4Mn5O12 at cell voltages 2.5-3.6 V. It is found that Mn oxidation state in Li4Mn5O12 has a strong effect on electrode performance of Li/Li4Mn5O12 cell.

  7. Solid lithium-ion electrolyte

    DOEpatents

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

    1998-02-10

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

  8. Solid lithium-ion electrolyte

    DOEpatents

    Zhang, Ji-Guang; Benson, David K.; Tracy, C. Edwin

    1998-01-01

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

  9. Structural and kinetic characterization of lithium intercalation into carbon anodes for secondary lithium batteries

    SciTech Connect

    Takami, Norio; Satoh, Asako; Hara, Michikazu; Ohsaki, Takahisa

    1995-02-01

    Electrochemical intercalation of lithium into carbons has been studied using mesophase-pitch-based carbon fibers with different heat-treatment temperatures, coke, and graphites as anodes for secondary lithium batteries. The variations in the average layer spacing and the voltage profile for the carbons with intercalating depend on the degree of graphitization. The intercalation into a more disordered carbon fiber heated at 900 C has been characterized as intercalation into the layer structure for 0 < x < 0.5 in Li{sub x}C{sub 6}, but additional lithium insertion into an unorganized carbon loses the layer structure. The polarization resistance (R{sub p}) estimated from the impedance spectrum decreased by increasing degree of graphitization. The variation in R{sub p} with intercalation revealed the intercalation processes in various disordered carbons to be single-phase reactions with different stoichiometries of lithium intercalation. The chemical diffusion coefficient D{sub Li} of lithium ions in carbons decreased by increasing the composition x in Li{sub x}C{sub 6} up to x = 0.5. The chemical diffusion coefficient was considerably affected by the texture and the degree of graphitization of the carbons. The graphitized carbon fiber heated at 3,000 C for 0.1 < x < 0.5 in Li{sub x}C{sub 6} exhibited one order magnitude larger values of D{sub Li} than those of graphites. The rapid diffusion in the graphitized carbon fiber has been attributed to the radial texture in the cross section. It has been found that the activation energy for the diffusion process decreased by increasing the degree of graphitization.

  10. The preparation and role of Li2ZrO3 surface coating LiNi0.5Co0.2Mn0.3O2 as cathode for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Xu, Yue; Liu, Yang; Lu, Zhongpei; Wang, Haiying; Sun, Deqin; Yang, Gang

    2016-01-01

    Li2ZrO3-coated LiNi0.5Co0.2Mn0.3O2 (LZO-LMO) is successful synthesized by using a wet chemical method. Li2ZrO3 coating formed a uniform layer on LiNi0.5Co0.2Mn0.3O2 particles (LMO) without changing the crystal structure. Cyclic voltammetry (CV) and charge-discharge tests show that the Li2ZrO3-modified layer can improve the cyclic and rate performance. In the cut-off voltage of 2.7-4.6 V, LZO-LMO maintains 86% of the initial capacity at the 50th cycle, which is much higher than LMO with the retention of 66% of the initial capacity. The coating layer of LZO plays the positive role in conductivity of lithium diffusion and improves rate performance of LMO. At 10 C rates, LZO-LMO delivers the initial capacity of 95 mAh g-1 which is much higher than 40 mAh g-1 delivered by LMO. At the environmental temperature of 55 °C, LZO-LMO delivers the initial capacity of 194 mAh g-1 at 0.2 C rate and presents an improved cyclic performance in comparison with LMO. The elemental analysis of electrodes carried out after 50 charge/discharge cycles shows minor Ni content deviation in LMO, but LZO-LMO still remains the stoichiometric ratio, because the Li2ZrO3 coating efficiently hinders the metal dissolution during charge/discharge.

  11. Electrochemical characterization and post-mortem analysis of aged LiMn2O4-Li(Ni0.5Mn0.3Co0.2)O2/graphite lithium ion batteries. Part I: Cycle aging

    NASA Astrophysics Data System (ADS)

    Stiaszny, Barbara; Ziegler, Jörg C.; Krauß, Elke E.; Schmidt, Jan P.; Ivers-Tiffée, Ellen

    2014-04-01

    A detailed capacity fade analysis was carried out for a commercial lithium ion battery with a mixed LiMn2O4/NMC cathode, cycled at room temperature with a continuous discharge rate of 1C. Complementary electrochemical and physical-analytical investigations revealed that the most significant aging processes was loss of cycleable lithium due to SEI-layer formation on the anode. The layer formation is accelerated by transition metals coming from the cathode. Impedance spectroscopy proved a significant increase of the cathode charge transfer resistance and of the serial resistance due to electrolyte decomposition and the formation of a surface layer on the anode. The changing of the impedance spectra of the lithium ion battery with aging could be interpreted with the help of impedance spectra of symmetric cells. From DRT analysis equivalent circuits for anode and cathode were derived, which were used for fitting of the impedance spectra.

  12. Synthesis and electrochemical performance of hole-rich Li4Ti5O12 anode material for lithium-ion secondary batteries

    NASA Astrophysics Data System (ADS)

    Zhu, Weibo; Zhuang, Zhenyuan; Yang, Yanmin; Zhang, Ruidan; Lin, Zhiya; Lin, Yingbin; Huang, Zhigao

    2016-06-01

    Hole-rich Li4Ti5O12 composites are synthesized by spray drying using carbon nanotubes as additives in precursor solution, subsequently followed calcinated at high temperature in air. The structure, morphology, and texture of the as-prepared composites are characterized with XRD, Raman, BET and SEM techniques. The electrochemical properties of the as-prepared composites are investigated systematically by charge/discharge testing, cyclic voltammograms and AC impedance spectroscopy, respectively. In comparison with the pristine Li4Ti5O12, the hole-rich Li4Ti5O12 induced by carbon nanotubes exhibits superior electrochemical performance, especially at high rates. The obtained excellent electrochemical performances of should be attributed to the hole-rich structure of the materials, which offers more connection-area with the electrolyte, shorter diffusion-path length as well faster migration rate for both Li ions and electrons during the charge/discharge process.

  13. Li3Mo4P5O24: A two-electron cathode for lithium-ion batteries with three-dimensional diffusion pathways

    DOE PAGES

    Wen, Bohua; Khalifah, Peter G.; Liu, Jue; ...

    2016-04-12

    The structure of the novel compound Li3Mo4P5O24 has been solved from single crystal X-ray diffraction data. The Mo cations in Li3Mo4P5O24 are present in four distinct types of MoO6 octahedra, each of which has one open vertex at the corner participating in a Mo=O double bond and whose other five corners are shared with PO4 tetrahedra. On the basis of a bond valence sum difference map (BVS-DM) analysis, this framework is predicted to support the facile diffusion of Li+ ions, a hypothesis that is confirmed by electrochemical testing data, which show that Li3Mo4P5O24 can be utilized as a rechargeable batterymore » cathode material. It is found that Li can both be removed from and inserted into Li3Mo4P5O24. The involvement of multiple redox processes occurring at the same Mo site is reflected in electrochemical plateaus around 3.8 V associated with the Mo6+/Mo5+ redox couple and 2.2 V associated with the Mo5+/Mo4+ redox couple. The two-electron redox properties of Mo cations in this structure lead to a theoretical capacity of 198 mAh/g. When cycled between 2.0 and 4.3 V versus Li+/Li, an initial capacity of 113 mAh/g is observed with 80% of this capacity retained over the first 20 cycles. Lastly, this compound therefore represents a rare example of a solid state cathode able to support two-electron redox capacity and provides important general insights about pathways for designing next-generation cathodes with enhanced specific capacities.« less

  14. Lithium/bromine cell systems

    SciTech Connect

    Howard, W.G.; Skarstad, P.M.; Hayes, T.G.; Owens, B.B.

    1980-01-01

    Bromine is attractive as a cathode material because cells with a high energy density and high cell voltage are theoretically possible. The addition of small amounts of certain salts or organic compounds results in bromine solutions of sufficient conductivity for cathode applications. However, given these highly conductive bromine cathodes, lithium/bromine cells are limited in rate and practical available capacity by the high resistivity of the discharge product. The rate of resistance increase for the best bromine cells in this study is more than one order of magnitude greater than that observed for corresponding lithium/iodine cells. Lithium/bromine cells can function at pacemaker rates and they may be superior to cells used in early pacemakers. However, the authors have not found the lithium/bromine cells described to be superior to existing lithium/iodine cells available for cardiac pacemakers. 17 refs.

  15. Toward understanding the lithiation/delithiation process in Fe0.5TiOPO4/C electrode material for lithium-ion batteries

    DOE PAGES

    Lasri, Karima; Mahmoud, Abdelfattah; Saadoune, Ismael; ...

    2015-11-28

    We used Fe0.5TiOPO4/C composite as anode material for LIB and exhibits excellent cycling performance when the electrode is cycled in two different voltage ranges [3.0-1.3V] and [3.0- 0.02V] where different insertion mechanisms were involved. Based on in situ X-ray diffraction, in situ XANES spectroscopy results, and various electrochemical analyses at high and low voltage cut-off, we found that Fe0.5TiOPO4/C electrode materials still maintains its structure crystallinity after cycling between [3.0-1.3V] showing formation of new phase at the end of first discharge, with a reversible capacity of 100 mAhg-1 after 50 cycles at C/5 rate. Moreover, at highly lithiated states, [3.0-0.02V]more » voltage range, a reduction decomposition reaction highlights the Li-insertion/extraction behaviors, and low phase crystallinity is observed during cycling, in addition an excellent rate behavior and a reversible capacity of 250 mAhg- 1 can still be maintained after 50 cycles at high cycling rate 5C.« less

  16. Conference Report on the 3rd International Symposium on Lithium Application for Fusion Devices

    NASA Astrophysics Data System (ADS)

    Mazzitelli, G.; Hirooka, Y.; Hu, J. S.; Mirnov, S. V.; Nygren, R.; Shimada, M.; Ono, M.; Tabares, F. L.

    2015-02-01

    The third International Symposium on Lithium Application for Fusion Device (ISLA-2013) was held on 9-11 October 2013 at ENEA Frascati Centre with growing participation and interest from the community working on more general aspect of liquid metal research for fusion energy development. ISLA-2013 has been confirmed to be the largest and the most important meeting dedicated to liquid metal application for the magnetic fusion research. Overall, 45 presentation plus 5 posters were given, representing 28 institutions from 11 countries. The latest experimental results from nine magnetic fusion devices were presented in 16 presentations from NSTX (PPPL, USA), FTU (ENEA, Italy), T-11M (Trinity, RF), T-10 (Kurchatov Institute, RF), TJ-II (CIEMAT, Spain), EAST(ASIPP, China), HT-7 (ASIPP, China), RFX (Padova, Italy), KTM (NNC RK, Kazakhstan). Sessions were devoted to the following: (I) lithium in magnetic confinement experiments (facility overviews), (II) lithium in magnetic confinement experiments (topical issues), (III) special session on liquid lithium technology, (IV) lithium laboratory test stands, (V) Lithium theory/modelling/comments, (VI) innovative lithium applications and (VII) special Session on lithium-safety and lithium handling. There was a wide participation from the fusion technology communities, including IFMIF and TBM communities providing productive exchange with the physics oriented magnetic confinement liquid metal research groups. This international workshop will continue on a biennial basis (alternating with the Plasma-Surface Interactions (PSI) Conference) and the next workshop will be held at CIEMAT, Madrid, Spain, in 2015.

  17. Lithium sorption properties of HMnO in seawater and wastewater.

    PubMed

    Park, HyunJu; Singhal, Naresh; Jho, Eun Hea

    2015-12-15

    The lithium concentration in seawater is 0.17 mg/L, which is very low, but the overall quantity is approximately 2.5 × 10(14) kg. Therefore, seawater, which contains a vast amount of lithium, could be a major alternative source that might supply the rising demand for lithium. This research was undertaken to evaluate the feasibility of a manganese oxide (HMnO) adsorbent, which was produced after leaching lithium from lithium manganese oxide, for lithium collection from seawater. The HMnO was synthesized and deformed to a plastic after wet blending of manganese oxide and lithium hydroxide, and subsequently, the influence of pH, sorption isotherms, sorption rates, sorption energies, and effects of the co-ions were measured. Thermodynamic parameters such as ΔG°, ΔH°, and ΔS° indicated that the nature of the lithium sorption was both spontaneous and endothermic. The used HMnO could be regenerated by washing it with an HCl solution. The results demonstrated that HMnO could be effectively used for the collection of lithium from seawater with good selectivity.

  18. Conference report on the 3rd International Symposium on Lithium Application for Fusion Devices

    SciTech Connect

    Mazzitelli, Guiseppe; Hirooka, Y.; Hu, J. S.; Mirnov, S. V.; Nygren, R.; Shimada, M.; Ono, M.; Tabares, F. L.

    2015-01-14

    The third International Symposium on Lithium Application for Fusion Device (ISLA-2013) was held on 9-11 October 2013 at ENEA Frascati Centre with growing participation and interest from the community working on more general aspect of liquid metal research for fusion energy development. ISLA-2013 has been confirmed to be the largest and the most important meeting dedicated to liquid metal application for the magnetic fusion research. Overall, 45 presentation plus 5 posters were given, representing 28 institutions from 11 countries. The latest experimental results from nine magnetic fusion devices were presented in 16 presentations from NSTX (PPPL, USA), FTU (ENEA, Italy), T-11M (Trinity, RF), T-10 (Kurchatov Institute, RF), TJ-II (CIEMAT, Spain), EAST(ASIPP, China), HT-7 (ASIPP, China), RFX (Padova, Italy), KTM (NNC RK, Kazakhstan). Sessions were devoted to the following: (I) lithium in magnetic confinement experiments (facility overviews), (II) lithium in magnetic confinement experiments (topical issues), (III) special session on liquid lithium technology, (IV) lithium laboratory test stands, (V) Lithium theory/modelling/comments, (VI) innovative lithium applications and (VII) special Session on lithium-safety and lithium handling. There was a wide participation from the fusion technology communities, including IFMIF and TBM communities providing productive exchange with the physics oriented magnetic confinement liquid metal research groups. Furthermore, this international workshop will continue on a biennial basis (alternating with the Plasma-Surface Interactions (PSI) Conference) and the next workshop will be held at CIEMAT, Madrid, Spain, in 2015.

  19. Lithium Abundance in M3 Red Giant

    NASA Astrophysics Data System (ADS)

    Givens, Rashad; Pilachowski, Catherine A.

    2015-01-01

    We present the abundance of lithium in the red giant star vZ 1050 (SK 291) in the globular cluster M3. A previous survey of giants in the cluster showed that like IV-101, vZ 1050 displays a prominent Li I 6707 Å feature. vZ 1050 lies on the blue side of the red giant branch about 1.3 magnitudes above the level of the horizontal branch, and may be an asymptotic giant branch star. A high resolution spectrum of M3 vZ1050 was obtained with the ARC 3.5m telescope and the ARC Echelle Spectrograph (ARCES). Atmospheric parameters were determined using Fe I and Fe II lines from the spectrum using the MOOG spectral analysis program, and the lithium abundance was determined using spectrum synthesis.

  20. Manganese oxide composite electrodes for lithium batteries

    DOEpatents

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

    2009-12-22

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

  1. Elevated Thyrotropin in Bipolar Youths Prescribed Both Lithium and Divalproex Sodium

    ERIC Educational Resources Information Center

    Gracious, Barbara L.; Findling, Robert L.; Seman, Christopher; Youngstrom, Eric A.; Demeter, Christine A.; Calabrese, Joseph R.

    2004-01-01

    Objective: To examine the effect of combined lithium and divalproex sodium on thyroid-stimulating hormone (TSH) levels in children and adolescents with bipolar disorders and to identify risk factors for lithium-induced hypothyroidism. Method: Bipolar youths aged 5 to 17 years participating in an open-label clinical trial received treatment with…

  2. Mesoporous Nitrogen Doped Carbon-Glass Ceramic Cathode for High Performance Lithium-Oxygen Battery

    DTIC Science & Technology

    2012-06-01

    3 . DATES COVERED (From - To) June 2012 Conference Proceedings Postprint 01 June 2012 – 01 June 2012 4 . TITLE AND SUBTITLE MESOPOROUS NITROGEN... 3 , a solid-state lithium-oxygen cell with a 2 cm2 area was fabricated (Figure 4 ). Figure 4 . Photograph of a Solid-State lithium-oxygen...0.5 1 1.5 2 2.5 3 3.5 0 2 4 6 8 10 12 Vo lta ge (V ) Cell Capacity (mA.h) 1 2 3 Figure 5. Discharge profiles for a lithium-oxygen cell at 75 C

  3. Lithium-methomyl induced seizures in rats: A new model of status epilepticus?

    SciTech Connect

    Kaminski, Rafal M. . E-mail: kaminskr@mail.nih.gov; Blaszczak, Piotr; Dekundy, Andrzej; Parada-Turska, Jolanta; Calderazzo, Lineu; Cavalheiro, Esper A.; Turski, Waldemar A.

    2007-03-15

    Behavioral, electroencephalographic (EEG) and neuropathological effects of methomyl, a carbamate insecticide reversibly inhibiting acetylcholinesterase activity, were studied in naive or lithium chloride (24 h, 3 mEq/kg, s.c.) pretreated male Wistar rats. In naive animals, methomyl with equal potency produced motor limbic seizures and fatal status epilepticus. Thus, the CD50 values (50% convulsant dose) for these seizure endpoints were almost equal to the LD50 (50% lethal dose) of methomyl (13 mg/kg). Lithium pretreated rats were much more susceptible to convulsant, but not lethal effect of methomyl. CD50 values of methomyl for motor limbic seizures and status epilepticus were reduced by lithium pretreatment to 3.7 mg/kg (a 3.5-fold decrease) and 5.2 mg/kg (a 2.5-fold decrease), respectively. In contrast, lithium pretreatment resulted in only 1.3-fold decrease of LD50 value of methomyl (9.9 mg/kg). Moreover, lithium-methomyl treated animals developed a long-lasting status epilepticus, which was not associated with imminent lethality observed in methomyl-only treated rats. Scopolamine (10 mg/kg) or diazepam (10 mg/kg) protected all lithium-methomyl treated rats from convulsions and lethality. Cortical and hippocampal EEG recordings revealed typical epileptic discharges that were consistent with behavioral seizures observed in lithium-methomyl treated rats. In addition, convulsions induced by lithium-methomyl treatment were associated with widespread neurodegeneration of limbic structures. Our observations indicate that lithium pretreatment results in separation between convulsant and lethal effects of methomyl in rats. As such, seizures induced by lithium-methomyl administration may be an alternative to lithium-pilocarpine model of status epilepticus, which is associated with high lethality.

  4. Lithium-methomyl induced seizures in rats: a new model of status epilepticus?

    PubMed

    Kaminski, Rafal M; Blaszczak, Piotr; Dekundy, Andrzej; Parada-Turska, Jolanta; Calderazzo, Lineu; Cavalheiro, Esper A; Turski, Waldemar A

    2007-03-01

    Behavioral, electroencephalographic (EEG) and neuropathological effects of methomyl, a carbamate insecticide reversibly inhibiting acetylcholinesterase activity, were studied in naive or lithium chloride (24 h, 3 mEq/kg, s.c.) pretreated male Wistar rats. In naive animals, methomyl with equal potency produced motor limbic seizures and fatal status epilepticus. Thus, the CD50 values (50% convulsant dose) for these seizure endpoints were almost equal to the LD50 (50% lethal dose) of methomyl (13 mg/kg). Lithium pretreated rats were much more susceptible to convulsant, but not lethal effect of methomyl. CD50 values of methomyl for motor limbic seizures and status epilepticus were reduced by lithium pretreatment to 3.7 mg/kg (a 3.5-fold decrease) and 5.2 mg/kg (a 2.5-fold decrease), respectively. In contrast, lithium pretreatment resulted in only 1.3-fold decrease of LD50 value of methomyl (9.9 mg/kg). Moreover, lithium-methomyl treated animals developed a long-lasting status epilepticus, which was not associated with imminent lethality observed in methomyl-only treated rats. Scopolamine (10 mg/kg) or diazepam (10 mg/kg) protected all lithium-methomyl treated rats from convulsions and lethality. Cortical and hippocampal EEG recordings revealed typical epileptic discharges that were consistent with behavioral seizures observed in lithium-methomyl treated rats. In addition, convulsions induced by lithium-methomyl treatment were associated with widespread neurodegeneration of limbic structures. Our observations indicate that lithium pretreatment results in separation between convulsant and lethal effects of methomyl in rats. As such, seizures induced by lithium-methomyl administration may be an alternative to lithium-pilocarpine model of status epilepticus, which is associated with high lethality.

  5. Impact of lithium alone and in combination with antidepressants on cytokine production in vitro.

    PubMed

    Petersein, Charlotte; Sack, Ulrich; Mergl, Roland; Schönherr, Jeremias; Schmidt, Frank M; Lichtblau, Nicole; Kirkby, Kenneth C; Bauer, Katrin; Himmerich, Hubertus

    2015-01-01

    Lithium is an important psychopharmacological agent for the treatment of unipolar as well as bipolar affective disorders. Lithium has a number of side effects such as hypothyroidism and aggravation of psoriasis. On the other hand, lithium has pro-inflammatory effects, which appear beneficial in some disorders associated with immunological deficits, such as human immunodeficiency virus (HIV) infection and systemic lupus erythematosus (SLE). Therefore, immunological characteristics of lithium may be an important consideration in individualized therapeutic decisions. We measured the levels of the cytokines interleukin (IL)-1ß, IL-2, IL-4, IL-6, IL-22, IL-17 and tumour necrosis factor (TNF)-α in the stimulated blood of thirty healthy subjects supplemented with lithium alone, the antidepressants citalopram, escitalopram or mirtazapine alone, the combination of each antidepressant with lithium, and a no drug control. These drugs were tested under three blood stimulant conditions: murine anti-human CD3 monoclonal antibody OKT3 and the 5C3 monoclonal antibody (OKT3/5C3), phytohemagglutinin (PHA), and unstimulated blood. Lithium, alone and in combination with any of the tested antidepressants, led to a consistent increase of IL-1ß, IL-6 and TNF-α levels in the unstimulated as well as the stimulated blood. In the OKT3/5C3- and PHA-stimulated blood, IL-17 production was significantly enhanced by lithium. Lithium additionally increased IL-2 concentrations significantly in PHA-stimulated blood. The data support the view that lithium has pro-inflammatory properties. These immunological characteristics may contribute to side effects of lithium, but may also explain its beneficial effects in patients suffering from HIV infection or SLE.

  6. Absence of PKC-alpha attenuates lithium-induced nephrogenic diabetes insipidus.

    PubMed

    Sim, Jae H; Himmel, Nathaniel J; Redd, Sara K; Pulous, Fadi E; Rogers, Richard T; Black, Lauren N; Hong, Seongun M; von Bergen, Tobias N; Blount, Mitsi A

    2014-01-01

    Lithium, an effective antipsychotic, induces nephrogenic diabetes insipidus (NDI) in ∼40% of patients. The decreased capacity to concentrate urine is likely due to lithium acutely disrupting the cAMP pathway and chronically reducing urea transporter (UT-A1) and water channel (AQP2) expression in the inner medulla. Targeting an alternative signaling pathway, such as PKC-mediated signaling, may be an effective method of treating lithium-induced polyuria. PKC-alpha null mice (PKCα KO) and strain-matched wild type (WT) controls were treated with lithium for 0, 3 or 5 days. WT mice had increased urine output and lowered urine osmolality after 3 and 5 days of treatment whereas PKCα KO mice had no change in urine output or concentration. Western blot analysis revealed that AQP2 expression in medullary tissues was lowered after 3 and 5 days in WT mice; however, AQP2 was unchanged in PKCα KO. Similar results were observed with UT-A1 expression. Animals were also treated with lithium for 6 weeks. Lithium-treated WT mice had 19-fold increased urine output whereas treated PKCα KO animals had a 4-fold increase in output. AQP2 and UT-A1 expression was lowered in 6 week lithium-treated WT animals whereas in treated PKCα KO mice, AQP2 was only reduced by 2-fold and UT-A1 expression was unaffected. Urinary sodium, potassium and calcium were elevated in lithium-fed WT but not in lithium-fed PKCα KO mice. Our data show that ablation of PKCα preserves AQP2 and UT-A1 protein expression and localization in lithium-induced NDI, and prevents the development of the severe polyuria associated with lithium therapy.

  7. A Shuttle mechanism for molten-electrolyte lithium batteries

    NASA Astrophysics Data System (ADS)

    Kaun, T. D.; Nelson, P. A.

    1993-12-01

    The lithium-transport rates arising from a lithium shuttle mechanism (LSM) were examined by potentiometric control of a lithium-alloy electrode in a temperature range of 400 to 515 C in three electrolytes: LiCl-KCl, LiCl-LiBr-KBr, and LiF-LiCl-LiBr. Lithium transport in Li/FeS(x) cells by LSM was found to occur by diffusion of reduced lithium species across the separator layer, which was controlled by the Li-activity of the Li-alloy electrode. Solubility of lithium was strongly affected by electrolyte composition, especially K(+) content, which in turn regulated the lithium transport rate. As evidenced by LSM rates, the solubilized lithium would appear to form dimers (e.g. Li2(+) or LiK(+)). The half-cell self-discharge rates, which were measured, correlate well with self-discharge rates in developmental cells ranging from 0.1 to 10 mA/sq cm. Innovative application of the LSM has led to the development of overcharge tolerant Li/FeS(x) cells. A bimodal self-discharge characteristic (a 20-fold increase toward the end of charge) results from a 150-250 mV step increase in lithium activity of a two-phase Li-alloy electrode (Li-Al plus Li-Al 5Fe2). Three versions of the battery cell (100 sq cm separator area) have been demonstrated: LiAl+Li5Al5Fe2 (10% of capacity) /LiCl-LiBr-KBr(MgO)/FeS2, as well as a FeS-type, (both operated at 400 C) and LiAl+Li5Al5Fe2 (10% of capacity) /LiF-LiCl-LiBr(MgO)/FeS (operated at 475C). These cells exhibit a unique combination of overcharge capacity and extended trickle-charge tolerance at 2-5 mA/sq cm. Additionally, Li/FeS2 cells having overcharge tolerance have operated with stable performance for greater than 500 cycles. The overcharge tolerance rates are sufficient for battery cells to exhibit built-in charge/equalization capability by way of full-battery trickle charging.

  8. Improving the electrochemical performance of the li4 ti5 o12 electrode in a rechargeable magnesium battery by lithium-magnesium co-intercalation.

    PubMed

    Wu, Na; Yang, Zhen-Zhong; Yao, Hu-Rong; Yin, Ya-Xia; Gu, Lin; Guo, Yu-Guo

    2015-05-04

    Rechargeable magnesium batteries have attracted recent research attention because of abundant raw materials and their relatively low-price and high-safety characteristics. However, the sluggish kinetics of the intercalated Mg(2+) ions in the electrode materials originates from the high polarizing ability of the Mg(2+) ion and hinders its electrochemical properties. Here we report a facile approach to improve the electrochemical energy storage capability of the Li4 Ti5 O12 electrode in a Mg battery system by the synergy between Mg(2+) and Li(+) ions. By tuning the hybrid electrolyte of Mg(2+) and Li(+) ions, both the reversible capacity and the kinetic properties of large Li4 Ti5 O12 nanoparticles attain remarkable improvement.

  9. Positive electrode for a lithium battery

    DOEpatents

    Park, Sang-Ho; Amine, Khalil

    2015-04-07

    A method for producing a lithium alkali transition metal oxide for use as a positive electrode material for lithium secondary batteries by a precipitation method. The positive electrode material is a lithium alkali transition metal composite oxide and is prepared by mixing a solid state mixed with alkali and transition metal carbonate and a lithium source. The mixture is thermally treated to obtain a small amount of alkali metal residual in the lithium transition metal composite oxide cathode material.

  10. Li-Rich Li-Si Alloy As A Lithium-Containing Negative Electrode Material Towards High Energy Lithium-Ion Batteries

    PubMed Central

    Iwamura, Shinichiroh; Nishihara, Hirotomo; Ono, Yoshitaka; Morito, Haruhiko; Yamane, Hisanori; Nara, Hiroki; Osaka, Tetsuya; Kyotani, Takashi

    2015-01-01

    Lithium-ion batteries (LIBs) are generally constructed by lithium-including positive electrode materials, such as LiCoO2, and lithium-free negative electrode materials, such as graphite. Recently, lithium-free positive electrode materials, such as sulfur, are gathering great attention from their very high capacities, thereby significantly increasing the energy density of LIBs. Though the lithium-free materials need to be combined with lithium-containing negative electrode materials, the latter has not been well developed yet. In this work, the feasibility of Li-rich Li-Si alloy is examined as a lithium-containing negative electrode material. Li-rich Li-Si alloy is prepared by the melt-solidification of Li and Si metals with the composition of Li21Si5. By repeating delithiation/lithiation cycles, Li-Si particles turn into porous structure, whereas the original particle size remains unchanged. Since Li-Si is free from severe constriction/expansion upon delithiation/lithiation, it shows much better cyclability than Si. The feasibility of the Li-Si alloy is further examined by constructing a full-cell together with a lithium-free positive electrode. Though Li-Si alloy is too active to be mixed with binder polymers, the coating with carbon-black powder by physical mixing is found to prevent the undesirable reactions of Li-Si alloy with binder polymers, and thus enables the construction of a more practical electrochemical cell. PMID:25626879

  11. Li-rich Li-Si alloy as a lithium-containing negative electrode material towards high energy lithium-ion batteries.

    PubMed

    Iwamura, Shinichiroh; Nishihara, Hirotomo; Ono, Yoshitaka; Morito, Haruhiko; Yamane, Hisanori; Nara, Hiroki; Osaka, Tetsuya; Kyotani, Takashi

    2015-01-28

    Lithium-ion batteries (LIBs) are generally constructed by lithium-including positive electrode materials, such as LiCoO2, and lithium-free negative electrode materials, such as graphite. Recently, lithium-free positive electrode materials, such as sulfur, are gathering great attention from their very high capacities, thereby significantly increasing the energy density of LIBs. Though the lithium-free materials need to be combined with lithium-containing negative electrode materials, the latter has not been well developed yet. In this work, the feasibility of Li-rich Li-Si alloy is examined as a lithium-containing negative electrode material. Li-rich Li-Si alloy is prepared by the melt-solidification of Li and Si metals with the composition of Li21Si5. By repeating delithiation/lithiation cycles, Li-Si particles turn into porous structure, whereas the original particle size remains unchanged. Since Li-Si is free from severe constriction/expansion upon delithiation/lithiation, it shows much better cyclability than Si. The feasibility of the Li-Si alloy is further examined by constructing a full-cell together with a lithium-free positive electrode. Though Li-Si alloy is too active to be mixed with binder polymers, the coating with carbon-black powder by physical mixing is found to prevent the undesirable reactions of Li-Si alloy with binder polymers, and thus enables the construction of a more practical electrochemical cell.

  12. Electrochemical behavior of [(Mn(Bpy))(VO{sub 3}){sub 2}]≈(H{sub 2}O){sub 1.24} and [(Mn(Bpy){sub 0.5})(VO{sub 3}){sub 2}]≈(H{sub 2}O){sub 0.62} inorganic–organic Brannerites in lithium and sodium cells

    SciTech Connect

    Fernández de Luis, Roberto; Rosa Palacín, M.; Karmele Urtiaga, M.

    2014-04-01

    The performance of MnV{sub 2}O{sub 6} (MnV) and its [(Mn(Bpy))(VO{sub 3}){sub 2}]≈(H{sub 2}O){sub 1.16} (MnBpy) and [(Mn(Bpy){sub 0.5})(VO{sub 3}){sub 2}]≈(H{sub 2}O){sub 0.62}(MnBpy0.5) hybrid derivative compounds was investigated against sodium and lithium counter electrodes. For MnV{sub 2}O{sub 6} stable capacities of 850 mAh/g were achieved in lithium cells, the best value reported so far. The whole capacity is ascribed to a conversion reaction in which the amorphization of the compounds takes place. No significant differences in the capacities for the inorganic compound and the hybrid ones were observed. Interestingly, the potential hysteresis decreases in the hybrid compounds. The difference between Li and Na cell capacity most probably comes from the difference of standard potential of the two redox couples Li{sup +}/Li and Na{sup +}/Na of about ca. 0.3 V leading to an incomplete conversion reaction and thus lowers capacity in the case of Na cells. The Raman and IR ex-situ experiments after cycling indicate that the bipyridine organic ligands are completely decomposed during the electrochemical testing. The IR studies in MnV inorganic and MnBpy and MnBpy0.5 hybrid electrodes after the electrochemical cycling, suggest that the SEI formation and bipyridine degradation give rise to different aliphatic compounds. - Graphical abstract: The electrochemical performance of [(Mn(Bpy))(VO{sub 3}){sub 2}]≈(H{sub 2}O){sub 1.16} and [(Mn(Bpy){sub 0.5})(VO{sub 3}){sub 2}]≈(H{sub 2}O){sub 0.62} against sodium and lithium counter electrodes give rise to the structural collapse of the initial compounds. The IR and Raman studies show that the Bpy organic ligand is completely decomposed during the during the electrochemical testing. However, after the amorphization stable capacities as high as 850 mAh/g for lithium cells were achieved. - Highlights: • We test the lithium and sodium insertion in hybrid brannerites. • Capacities as large as 850 mAh/g were obtained

  13. Lithium niobate explosion monitor

    DOEpatents

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

    1990-01-09

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

  14. Lithium niobate explosion monitor

    DOEpatents

    Bundy, Charles H.; Graham, Robert A.; Kuehn, Stephen F.; Precit, Richard R.; Rogers, Michael S.

    1990-01-01

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

  15. Halo Star Lithium Depletion

    SciTech Connect

    Pinsonneault, M. H.; Walker, T. P.; Steigman, G.; Narayanan, Vijay K.

    1999-12-10

    The depletion of lithium during the pre-main-sequence and main-sequence phases of stellar evolution plays a crucial role in the comparison of the predictions of big bang nucleosynthesis with the abundances observed in halo stars. Previous work has indicated a wide range of possible depletion factors, ranging from minimal in standard (nonrotating) stellar models to as much as an order of magnitude in models that include rotational mixing. Recent progress in the study of the angular momentum evolution of low-mass stars permits the construction of theoretical models capable of reproducing the angular momentum evolution of low-mass open cluster stars. The distribution of initial angular momenta can be inferred from stellar rotation data in young open clusters. In this paper we report on the application of these models to the study of lithium depletion in main-sequence halo stars. A range of initial angular momenta produces a range of lithium depletion factors on the main sequence. Using the distribution of initial conditions inferred from young open clusters leads to a well-defined halo lithium plateau with modest scatter and a small population of outliers. The mass-dependent angular momentum loss law inferred from open cluster studies produces a nearly flat plateau, unlike previous models that exhibited a downward curvature for hotter temperatures in the 7Li-Teff plane. The overall depletion factor for the plateau stars is sensitive primarily to the solar initial angular momentum used in the calibration for the mixing diffusion coefficients. Uncertainties remain in the treatment of the internal angular momentum transport in the models, and the potential impact of these uncertainties on our results is discussed. The 6Li/7Li depletion ratio is also examined. We find that the dispersion in the plateau and the 6Li/7Li depletion ratio scale with the absolute 7Li depletion in the plateau, and we use observational data to set bounds on the 7Li depletion in main-sequence halo

  16. Method of recycling lithium borate to lithium borohydride through methyl borate

    DOEpatents

    Filby, Evan E.

    1977-01-01

    This invention provides a method for the recycling of lithium borate to lithium borohydride which can be reacted with water to generate hydrogen for utilization as a fuel. The lithium borate by-product of the hydrogen generation reaction is reacted with hydrogen chloride and water to produce boric acid and lithium chloride. The boric acid and lithium chloride are converted to lithium borohydride through a methyl borate intermediate to complete the recycle scheme.

  17. Prototype Rechargeable Lithium Batteries. Phase 1

    DTIC Science & Technology

    1987-06-01

    pentoxide [ V2o5 ], titanium disulfide [TiS ], vanadium V) sulfide [V2S 5 ], and lithium cobalt oxide [Li Co02]) witi high conductivity, ester-Eased...contaminated with lower oxides of vanadium. Best results are achieved using thin layers of ammonium metavanadate and forced air flow. Synthesis of V 205...b = 3.559A. c = 4.371A, orthorhombic. 3-59 NSWC TR 86-108 TABLE 3-16. X-RAY DIFFRACTION DATA FOR V2O5 STORED IN 2M LiAsF6 /MA AT 71 0 C d-spacing, A

  18. Post mortem analysis of fatigue mechanisms in LiNi0.8Co0.15Al0.05O2 - LiNi0.5Co0.2Mn0.3O2 - LiMn2O4/graphite lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Lang, Michael; Darma, Mariyam Susana Dewi; Kleiner, Karin; Riekehr, Lars; Mereacre, Liuda; Ávila Pérez, Marta; Liebau, Verena; Ehrenberg, Helmut

    2016-09-01

    The fatigue of commercial lithium ion batteries after long-term cycling at two different temperatures and cycling rates is investigated. The cells are opened after cycling and post-mortem analysis are conducted. Two main contributions to the capacity loss of the batteries are revealed. The loss of active lithium leads to a relative shift between anodes and cathodes potentials. A growth of the solid electrolyte interface (SEI) on the anode is determined as well as the formation of lithium fluoride species as an electrolyte decomposition product. Those effects are reinforced by increasing cycling rates from 1C/2C (charge/discharge) to 2C/3C as well as by increasing cycling temperatures from 25 °C to 40 °C. The other contribution to the capacity loss originates from a fatigue of the blended cathodes consisting of LiNi0.5Co0.2Mn0.3O2 (NCM), LiNi0.8Co0.15Al0.05O2 (NCA) and LiMn2O4 (LMO). Phase-specific capacity losses and fatigue mechanisms are identified. The layered oxides tend to form microcracks and reveal changes of the surface structure leading to a worsening of the lithium kinetics. The cathode exhibits a loss of manganese at 40 °C cycling temperature. Cycling at 40 °C instead of 25 °C has the major impact on cathodes capacity loss, while cycling at 2C/3C rates barely influences it.

  19. Sinus node dysfunction during long-term lithium treatment.

    PubMed Central

    Rosenqvist, M; Bergfeldt, L; Aili, H; Mathé, A A

    1993-01-01

    BACKGROUND AND OBJECTIVE--Lithium has occasionally been reported to cause symptomatic sinus node bradyarrhythmias. The prevalence and mechanism of these arrhythmias during long-term treatment are unknown. The aims of this study were (a) to evaluate the systemic effects of lithium treatment on cardiac conduction in individuals who were free from cardiovascular disorders; (b) to assess the prevalence of lithium treatment in a group of patients with pacemakers; and (c) to evaluate the interaction between the parasympathetic limb of the autonomous nervous system and the sinus node cells during long-term lithium treatment. PATIENTS AND METHODS--45 patients who had been treated with lithium for > 12 months were investigated in a long-term electrocardiography study. Only patients without cardiovascular disease, or concomitant chronotropic medication, or metabolic disorders known to cause rhythm disturbances were included. An age-stratified population was used as a reference group. 21 patients also underwent analysis of carotid sinus pressure and sinus cycle length before and after atropine to clarify whether neural mechanisms were involved. The prevalence of lithium treated patients was determined in 650 patients with pacemakers. RESULTS--(a) Signs of moderate sinus node dysfunction (sinus arrest > 1.5 s, minimum heart rate < 50 beats/min) were found in 56% and 78% respectively in the lithium-treated group compared with 30% and 30% respectively in the reference group (p < 0.01). Severe sinus node dysfunction was equally common in both groups. (b) The prevalence of chronic lithium treatment in the pacemaker population was 0.46%. (c) Sinus cycle variations were abnormal in the basal state in three (14%) patients and in 11 (52%) patients after atropine despite signs of intact and normal parasympathetic innervation. CONCLUSIONS--Depressed sinus node function was significantly more common in a lithium-treated population than in an age-stratified reference group. Clinically

  20. Safer Electrolytes for Lithium-Ion Cells

    NASA Technical Reports Server (NTRS)

    Kejha, Joe; Smith, Novis; McCloseky, Joel

    2004-01-01

    A number of nonvolatile, low-flammability liquid oligomers and polymers based on aliphatic organic carbonate molecular structures have been found to be suitable to be blended with ethylene carbonate to make electrolytes for lithium-ion electrochemical cells. Heretofore, such electrolytes have often been made by blending ethylene carbonate with volatile, flammable organic carbonates. The present nonvolatile electrolytes have been found to have adequate conductivity (about 2 mS/cm) for lithium ions and to remain liquid at temperatures down to -5 C. At normal charge and discharge rates, lithiumion cells containing these nonvolatile electrolytes but otherwise of standard design have been found to operate at current and energy densities comparable to those of cells now in common use. They do not perform well at high charge and discharge rates -- an effect probably attributable to electrolyte viscosity. Cells containing the nonvolatile electrolytes have also been found to be, variously, nonflammable or at least self-extinguishing. Hence, there appears to be a basis for the development of safer high-performance lithium-ion cells.

  1. A lithium superionic conductor

    NASA Astrophysics Data System (ADS)

    Kamaya, Noriaki; Homma, Kenji; Yamakawa, Yuichiro; Hirayama, Masaaki; Kanno, Ryoji; Yonemura, Masao; Kamiyama, Takashi; Kato, Yuki; Hama, Shigenori; Kawamoto, Koji; Mitsui, Akio

    2011-09-01

    Batteries are a key technology in modern society. They are used to power electric and hybrid electric vehicles and to store wind and solar energy in smart grids. Electrochemical devices with high energy and power densities can currently be powered only by batteries with organic liquid electrolytes. However, such batteries require relatively stringent safety precautions, making large-scale systems very complicated and expensive. The application of solid electrolytes is currently limited because they attain practically useful conductivities (10-2 S cm-1) only at 50-80 °C, which is one order of magnitude lower than those of organic liquid electrolytes. Here, we report a lithium superionic conductor, Li10GeP2S12 that has a new three-dimensional framework structure. It exhibits an extremely high lithium ionic conductivity of 12 mS cm-1 at room temperature. This represents the highest conductivity achieved in a solid electrolyte, exceeding even those of liquid organic electrolytes. This new solid-state battery electrolyte has many advantages in terms of device fabrication (facile shaping, patterning and integration), stability (non-volatile), safety (non-explosive) and excellent electrochemical properties (high conductivity and wide potential window).

  2. 5L-Scale Magnesio-Milling Reduction of Nanostructured SiO2 for High Capacity Silicon Anodes in Lithium-Ion Batteries.

    PubMed

    Cho, Won Chul; Kim, Hye Jin; Lee, Hae In; Seo, Myung Won; Ra, Ho Won; Yoon, Sang Jun; Mun, Tae Young; Kim, Yong Ku; Kim, Jae Ho; Kim, Bo Hwa; Kook, Jin Woo; Yoo, Chung-Yul; Lee, Jae Goo; Choi, Jang Wook

    2016-11-09

    Nanostructured silicon (Si) is useful in many applications and has typically been synthesized by bottom-up colloid-based solution processes or top-down gas phase reactions at high temperatures. These methods, however, suffer from toxic precursors, low yields, and impractical processing conditions (i.e., high pressure). The magnesiothermic reduction of silicon oxide (SiO2) has also been introduced as an alternative method. Here, we demonstrate the reduction of SiO2 by a simple milling process using a lab-scale planetary-ball mill and industry-scale attrition-mill. Moreover, an ignition point where the reduction begins was consistently observed for the milling processes, which could be used to accurately monitor and control the reaction. The complete conversion of rice husk SiO2 to high purity Si was demonstrated, taking advantage of the rice husk's uniform nanoporosity and global availability, using a 5L-scale attrition-mill. The resulting porous Si showed excellent performance as a Li-ion battery anode, retaining 82.8% of the initial capacity of 1466 mAh g(-1) after 200 cycles.

  3. Insight into the electrochemical behaviors of 5V-class high-voltage batteries composed of lithium-rich layered oxide with multifunctional additive

    NASA Astrophysics Data System (ADS)

    Lim, Sang Hoo; Cho, Woosuk; Kim, Young-Jun; Yim, Taeeun

    2016-12-01

    (Trimethylsilyl)methanesulfonate (TMSOMs), functionalized with task-specific chemical moieties, is proposed as an interface-stabilizing additive to improve the electrochemical performance of 5V-class layered over-lithiated oxides (OLOs). TMSOMs offers a great opportunity to enhance the interfacial stability of an OLO material by providing an effective protective layer composed of sbnd SO3sbnd and sbnd Osbnd Sisbnd functional groups after its electrochemical oxidation over 4.0 V (vs. Li/Li+), which remarkably reduces the internal pressure of the cell associated with electrolyte decomposition. As a result, the cell employing TMSOMs affords excellent capacity retention (92.8% at 100 cycles) together with considerable rate performance, negligible transition metal dissolution, and stable high temperature performance based on its enhanced interfacial stability. These results are attributed to the synergistic effects of the sbnd SO3sbnd and sbnd Osbnd Sisbnd functional groups that once the sulfonic ester-based protective layer is developed on the electrode surface, it effectively mitigates decomposition of the electrolyte, while the sbnd Osbnd Sisbnd functional groups readily scavenge fluoride species in the electrolyte, leading to outstanding interfacial stability for the OLO material. On the basis of spectroscopic evidence, a comprehensive mechanism for the action of TMSOMs is suggested considering the specific role of each functional group.

  4. Anodes for rechargeable lithium batteries

    DOEpatents

    Thackeray, Michael M.; Kepler, Keith D.; Vaughey, John T.

    2003-01-01

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

  5. Lithium-Thionyl Chloride Battery.

    DTIC Science & Technology

    1981-04-01

    EEEElhIhEEEEEE 1111 1 - MI(CRO( fy Hl ff1Sf UIIIUN Ift I IA I~t Research and Development Technical Report DELET - TR - 78 - 0563 - F Cq LITHIUM - THIONYL CHLORIDE ...2b(1110) S. TYPE OF REPORT & PERIOD COVERED Lithium - Thionyl Chloride Battery -10/1/78 - 11/30/80 6. PNING ORG. REPORT NUMBER Z %A a.~as B.,OWRACT OR...block number) Inorganic Electrolyte battery, Thionyl Chloride , lithium , high rate D cell, high rate flat cylindrical cell, laser designator battery. C//i

  6. Lithium ion conducting ionic electrolytes

    DOEpatents

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

    1996-01-16

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

  7. Lithium ion conducting ionic electrolytes

    DOEpatents

    Angell, C. Austen; Xu, Kang; Liu, Changle

    1996-01-01

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

  8. Plasticized Polymer Composite Single-Ion Conductors for Lithium Batteries.

    PubMed

    Zhao, Hui; Asfour, Fadi; Fu, Yanbao; Jia, Zhe; Yuan, Wen; Bai, Ying; Ling, Min; Hu, Heyi; Baker, Gregory; Liu, Gao

    2015-09-02

    Lithium bis(trifluoromethane) sulfonamide (TFSI) is a promising electrolyte salt in lithium batteries, due to its good conductivity and high dissociation between the lithium cation and its anion. By tethering N-pentane trifluoromethane sulfonamide (C5NHTf), a TFSI analogue molecule, onto the surface of silica nanoparticle as a monolayer coverage should increase the Li(+) transference number to unity since anions bound to particles have reduced mobilities. Silica polymer composite has better mechanical property than that of the pure PEO. Analogously trifluoromethane sulfonic aminoethyl methacrylate (TfMA), a TFSI analogue vinyl monomer, was polymerized on silica nanoparticle surface as a multilayer coverage. Anchored polyelectrolytes to particle surfaces offer multiple sites for anions, and in principle the carrier concentration would increase arbitrarily and approach the carrier concentration of the bulk polyelectrolyte. Monolayer grafted nanoparticles have a lithium content of 1.2 × 10(-3) g Li/g, and multilayer grafted nanoparticles have a lithium content over an order higher at 2 × 10(-2) g Li/g. Electrolytes made from monolayer grafted particles exhibit a weak conductivity dependence on temperature, exhibiting an ionic conductivity in the range of 10(-6) S/cm when temperatures increase to 80 °C. While electrolytes made from multilayer grafted particles show a steep increase in conductivity with temperature with an ionic conductivity increase to 3 × 10(-5) S/cm at 80 °C, with an O/Li ratio of 32.

  9. A randomized controlled pilot trial of lithium in spinocerebellar ataxia type 2.

    PubMed

    Saccà, Francesco; Puorro, Giorgia; Brunetti, Arturo; Capasso, Giovambattista; Cervo, Amedeo; Cocozza, Sirio; de Leva, Mariafulvia; Marsili, Angela; Pane, Chiara; Quarantelli, Mario; Russo, Cinzia Valeria; Trepiccione, Francesco; De Michele, Giuseppe; Filla, Alessandro; Morra, Vincenzo Brescia

    2015-01-01

    Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder. Lithium is able to stimulate autophagy, and to reduce Ca(2+) efflux from the inositol-1,4,5-triphosphate receptor. We designed a phase II, randomized, placebo-controlled, double-blind, 48-week trial with lithium carbonate in 20 patients with SCA2. The primary objective was to determine safety and tolerability of lithium. The secondary objectives were to determine disease progression, quality of life, mood, and brain volume change. Sixteen patients completed the trial, 8 randomized to lithium, 8 to placebo. Forty adverse events (AEs) were reported during the trial, twenty-eight in the lithium and 12 in the placebo group (p = 0.11). Mean AE duration was 57.4 ± 60.8 and 77.4 ± 68.5 days (p = 0.37). Non-significant differences were observed for the SARA and for brain volume change, whereas a significant reduction in the BDI-II was observed for lithium group (p < 0.05). Lithium was well tolerated and reported AEs were similar to those previously described for bipolar disorder patients. A correctly powered phase III trial is needed to assess if lithium may slow disease progression in SCA2.

  10. Lithium metal doped electrodes for lithium-ion rechargeable chemistry

    DOEpatents

    Liu, Gao; Battaglia, Vince; Wang, Lei

    2016-09-13

    An embodiment of the invention combines the superior performance of a polyvinylidene difluoride (PVDF) or polyethyleneoxide (POE) binder, the strong binding force of a styrene-butadiene (SBR) binder, and a source of lithium ions in the form of solid lithium metal powder (SLMP) to form an electrode system that has improved performance as compared to PVDF/SBR binder based electrodes. This invention will provide a new way to achieve improved results at a much reduced cost.

  11. Cyanoethylated compounds as additives in lithium/lithium batteries

    DOEpatents

    Nagasubramanian, Ganesan

    1999-01-01

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

  12. Population pharmacokinetic model of lithium and drug compliance assessment.

    PubMed

    Pérez-Castelló, Isabel; Mangas-Sanjuan, Víctor; González-García, Ignacio; Gonzalez-Alvarez, Isabel; Bermejo, Marival; Marco-Garbayo, Jose Luis; Trocóniz, Iñaki F

    2016-12-01

    Population pharmacokinetic analysis of lithium during therapeutic drug monitoring and drug compliance assessment was performed in 54 patients and 246 plasma concentrations levels were included in this study. Patients received several treatment cycles (1-9) and one plasma concentration measurement for each patient was obtained always before starting next cycle (pre-dose) at steady state. Data were analysed using the population approach with NONMEM version 7.2. Lithium measurements were described using a two-compartment model (CL/F=0.41Lh(-1), V1/F=15.3L, Q/F=0.61Lh(-1), and V2/F = 15.8L) and the most significant covariate on lithium CL was found to be creatinine clearance (reference model). Lithium compliance was analysed using inter-occasion variability or Markovian features (previous lithium measurement as ordered categorical covariate) on bioavailability parameter. Markov-type model predicted the lithium compliance in the next cycle with higher success rate (79.8%) compared to IOV model (65.2%) and reference model (43.2%). This model becomes an efficient tool, not only being able to adequately describe the observed outcome, but also to predict the individual drug compliance in the next cycle. Therefore, Bipolar disorder patients can be classified regarding their probability to become extensive or poor compliers in the next cycle and then, individual probabilities lower than 0.5 highlight the need of intensive monitoring, as well as other pharmaceutical care measurements that might be applied to enhance drug compliance for a better and safer lithium treatment.

  13. Evolution of lithium abundance in the Sun and solar twins

    NASA Astrophysics Data System (ADS)

    Thévenin, F.; Oreshina, A. V.; Baturin, V. A.; Gorshkov, A. B.; Morel, P.; Provost, J.

    2017-02-01

    Evolution of the 7Li abundance in the convection zone of the Sun during different stages of its life time is considered to explain its low photospheric value in comparison with that of the solar system meteorites. Lithium is intensively and transiently burned in the early stages of evolution (pre-main sequence, pMS) when the radiative core arises, and then the Li abundance only slowly decreases during the main sequence (MS). We study the rates of lithium burning during these two stages. In a model of the Sun, computed ignoring pMS and without extra-convective mixing (overshooting) at the base of the convection zone, the lithium abundance does not decrease significantly during the MS life time of 4.6 Gyr. Analysis of helioseismic inversions together with post-model computations of chemical composition indicates the presence of the overshooting region and restricts its thickness. It is estimated to be approximately half of the local pressure scale height (0.5HP) which corresponds to 3.8% of the solar radius. Introducing this extra region does not noticeably deplete lithium during the MS stage. In contrast, at the pMS stage, an overshooting region with a value of approximately 0.18HP is enough to produce the observed lithium depletion. If we conclude that the dominant lithium burning takes place during the pMS stage, the dispersion of the lithium abundance in solar twins is explained by different physical conditions, primarily during the early stage of evolution before the MS.

  14. 21 CFR 862.3560 - Lithium test system.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Lithium test system. 862.3560 Section 862.3560....3560 Lithium test system. (a) Identification. A lithium test system is a device intended to measure lithium (from the drug lithium carbonate) in serum or plasma. Measurements of lithium are used to...

  15. 21 CFR 862.3560 - Lithium test system.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Lithium test system. 862.3560 Section 862.3560....3560 Lithium test system. (a) Identification. A lithium test system is a device intended to measure lithium (from the drug lithium carbonate) in serum or plasma. Measurements of lithium are used to...

  16. 21 CFR 862.3560 - Lithium test system.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Lithium test system. 862.3560 Section 862.3560....3560 Lithium test system. (a) Identification. A lithium test system is a device intended to measure lithium (from the drug lithium carbonate) in serum or plasma. Measurements of lithium are used to...

  17. 21 CFR 862.3560 - Lithium test system.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Lithium test system. 862.3560 Section 862.3560....3560 Lithium test system. (a) Identification. A lithium test system is a device intended to measure lithium (from the drug lithium carbonate) in serum or plasma. Measurements of lithium are used to...

  18. 21 CFR 862.3560 - Lithium test system.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Lithium test system. 862.3560 Section 862.3560....3560 Lithium test system. (a) Identification. A lithium test system is a device intended to measure lithium (from the drug lithium carbonate) in serum or plasma. Measurements of lithium are used to...

  19. 49 CFR 173.185 - Lithium cells and batteries.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 20 Wh for a lithium ion cell or 100 Wh for a lithium ion battery. After December 31, 2015, each lithium ion battery subject to this provision must be marked with the Watt-hour rating on the outside case... cell and 25 g for a lithium metal battery and 60 Wh for a lithium ion cell or 300 Wh for a lithium......

  20. Grain Boundary Engineering of Lithium-Ion-Conducting Lithium Lanthanum Titanate for Lithium-Air Batteries

    DTIC Science & Technology

    2015-01-01

    Tojo T, Sakurai Y. Synthesis and lithium - ion conductivity for perovskite-type Li3/8Sr7/16Ta3/4Zr1/4O3 solid electrolyte by powder-bed sintering...battery performance is limited by the electrolytic membrane, which needs high Li-ionic conductivity. Lithium lanthanum titanate (Li3xLa(2/3)-xTiO3, or...of the A-site ions and lithium ion conductivity in the perovskite solid solution La0.67-xLi3xTiO3 (x=0.11). Journal of Solid State Ionics. 1999;121

  1. Silica Precipitation and Lithium Sorption

    SciTech Connect

    Jay Renew

    2015-09-20

    This file contains silica precipitation and lithium sorption data from the project. The silica removal data is corrected from the previous submission. The previous submission did not take into account the limit of detection of the ICP-MS procedure.

  2. Differential display RT-PCR reveals genes associated with lithium-induced neuritogenesis in SK-N-MC cells.

    PubMed

    Italia, Jennifer; Mukhopadhyaya, Rita; Rajadhyaksha, Medha S

    2011-10-01

    Lithium is shown to be neurotrophic and protective against variety of environmental stresses both in vitro as well as in vivo. In view of the wider clinical applications, it is necessary to examine alterations in levels of expression of genes affected by lithium. Lithium induces neuritogenesis in human neuroblastoma cell line SK-N-MC. Our aim was to elucidate genes involved in lithium-induced neuritogenesis using SK-N-MC cells. The differential display reverse transcriptase polymerase chain reaction (DD-RT-PCR) technique was used to study gene expression profiles in SK-N-MC cells undergoing lithium-induced neuritogenesis. Differential expression of genes in control and lithium (2.5 mM, 24 h)-treated cells was compared by display of cDNAs generated by reverse transcription of mRNA followed by PCR using arbitrary primers. Expression of four genes was altered in lithium-treated cells. Real-time PCR was done to confirm the levels of expression of each of these genes using specific primers. Lithium significantly up-regulated NCAM, a molecule known to stimulate neuritogenesis, occludin, a molecule participating in tight junctions and PKD2, a molecule known to modulate calcium transport. ANP 32c, a gene whose function is not fully known yet, was found to be down-regulated by lithium. This is the first report demonstrating altered levels of expression of these genes in lithium-induced neuritogenesis and contributes four hitherto unreported candidates possibly involved in the process.

  3. Lithium Coatings on NSTX Plasma Facing Components and Its Effects On Boundary Control, Core Plasma Performance, and Operation

    SciTech Connect

    H.W.Kugel, M.G.Bell, H.Schneider, J.P.Allain, R.E.Bell, R Kaita, J.Kallman, S. Kaye, B.P. LeBlanc, D. Mansfield, R.E. Nygen, R. Maingi, J. Menard, D. Mueller, M. Ono, S. Paul, S.Gerhardt, R.Raman, S.Sabbagh, C.H.Skinner, V.Soukhanovskii, J.Timberlake, L.E.Zakharov, and the NSTX Research Team

    2010-01-25

    NSTX high-power divertor plasma experiments have used in succession lithium pellet injection (LPI), evaporated lithium, and injected lithium powder to apply lithium coatings to graphite plasma facing components. In 2005, following wall conditioning and LPI, discharges exhibited edge density reduction and performance improvements. Since 2006, first one, and now two lithium evaporators have been used routinely to evaporate lithium onto the lower divertor region at total rates of 10-70 mg/min for periods 5-10 min between discharges. Prior to each discharge, the evaporators are withdrawn behind shutters. Significant improvements in the performance of NBI heated divertor discharges resulting from these lithium depositions were observed. These evaporators are now used for more than 80% of NSTX discharges. Initial work with injecting fine lithium powder into the edge of NBI heated deuterium discharges yielded comparable changes in performance. Several operational issues encountered with lithium wall conditions, and the special procedures needed for vessel entry are discussed. The next step in this work is installation of a Liquid Lithium Divertor surface on the outer part of the lower divertor.

  4. Compatibility of lithium plasma-facing surfaces with high edge temperatures in the Lithium Tokamak Experiment (LTX)

    NASA Astrophysics Data System (ADS)

    Majeski, Dick

    2016-10-01

    High edge electron temperatures (200 eV or greater) have been measured at the wall-limited plasma boundary in the Lithium Tokamak eXperiment (LTX). High edge temperatures, with flat electron temperature profiles, are a long-predicted consequence of low recycling boundary conditions. The temperature profile in LTX, measured by Thomson scattering, varies by as little as 10% from the plasma axis to the boundary, determined by the lithium-coated high field-side wall. The hydrogen plasma density in the outer scrape-off layer is very low, 2-3 x 1017 m-3 , consistent with a low recycling metallic lithium boundary. The plasma surface interaction in LTX is characterized by a low flux of high energy protons to the lithium PFC, with an estimated Debye sheath potential approaching 1 kV. Plasma-material interactions in LTX are consequently in a novel regime, where the impacting proton energy exceeds the peak in the sputtering yield for the lithium wall. In this regime, further increases in the edge temperature will decrease, rather than increase, the sputtering yield. Despite the high edge temperature, the core impurity content is low. Zeff is 1.2 - 1.5, with a very modest contribution (<0.1) from lithium. So far experiments are transient. Gas puffing is used to increase the plasma density. After gas injection stops, the discharge density is allowed to drop, and the edge is pumped by the low recycling lithium wall. An upgrade to LTX which includes a 35A, 20 kV neutral beam injector to provide core fueling to maintain constant density, as well as auxiliary heating, is underway. Two beam systems have been loaned to LTX by Tri Alpha Energy. Additional results from LTX, as well as progress on the upgrade - LTX- β - will be discussed. Work supported by US DOE contracts DE-AC02-09CH11466 and DE-AC05-00OR22725.

  5. Secondary lithium batteries for space applications

    NASA Technical Reports Server (NTRS)

    Carter, B.; Khanna, S. K.; Yen, S. P. S.; Shen, D.; Somoano, R. B.

    1981-01-01

    Secondary lithium cells which use a LiAsF6-2-Me-THF electrolyte and a TiS2 intercalatable cathode exhibit encouraging cycle life at ambient temperature. Electrochemical and surface analytical studies indicate that the electrolyte is unstable in the presence of metallic lithium, leading to the formation of a lithium passivating film composed of lithium arsenic oxyfluorides and lithium fluorsilicates. The lithium cyclability remains as the most important problem to solve. Different electrolyte solvents, such as sulfolane, exhibit promising characteristics but lead to new compatibility problems with the other cell component materials.

  6. Lithium compensation for full cell operation

    DOEpatents

    Xiao, Jie; Zheng, Jianming; Chen, Xilin; Lu, Dongping; Liu, Jun; Jiguang, Jiguang

    2016-05-17

    Disclosed herein are embodiments of a lithium-ion battery system comprising an anode, an anode current collector, and a layer of lithium metal in contact with the current collector, but not in contact with the anode. The lithium compensation layer dissolves into the electrolyte to compensate for the loss of lithium ions during usage of the full cell. The specific placement of the lithium compensation layer, such that there is no direct physical contact between the lithium compensation layer and the anode, provides certain advantages.

  7. Dendrite preventing separator for secondary lithium batteries

    NASA Technical Reports Server (NTRS)

    Shen, David H. (Inventor); Surampudi, Subbarao (Inventor); Huang, Chen-Kuo (Inventor); Halpert, Gerald (Inventor)

    1993-01-01

    Dendrites are prevented from shorting a secondary lithium battery by use of a first porous separator, such as porous polypropylene, adjacent to the lithium anode that is unreactive with lithium and a second porous fluoropolymer separator between the cathode and the first separator, such as polytetrafluoroethylene, that is reactive with lithium. As the tip of a lithium dendrite contacts the second separator, an exothermic reaction occurs locally between the lithium dendrite and the fluoropolymer separator. This results in the prevention of the dendrite propagation to the cathode.

  8. Dendrite preventing separator for secondary lithium batteries

    NASA Technical Reports Server (NTRS)

    Shen, David H. (Inventor); Surampudi, Subbarao (Inventor); Huang, Chen-Kuo (Inventor); Halpert, Gerald (Inventor)

    1995-01-01

    Dendrites are prevented from shorting a secondary lithium battery by use of a first porous separator such as porous polypropylene adjacent the lithium anode that is unreactive with lithium and a second porous fluoropolymer separator between the cathode and the first separator such as polytetrafluoroethylene that is reactive with lithium. As the tip of a lithium dendrite contacts the second separator, an exothermic reaction occurs locally between the lithium dendrite and the fluoropolymer separator. This results in the prevention of the dendrite propagation to the cathode.

  9. Air breathing lithium power cells

    SciTech Connect

    Farmer, Joseph C.

    2014-07-15

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

  10. Modeling the Lithium Ion Battery

    ERIC Educational Resources Information Center

    Summerfield, John

    2013-01-01

    The lithium ion battery will be a reliable electrical resource for many years to come. A simple model of the lithium ions motion due to changes in concentration and voltage is presented. The battery chosen has LiCoO[subscript 2] as the cathode, LiPF[subscript 6] as the electrolyte, and LiC[subscript 6] as the anode. The concentration gradient and…

  11. Erosive effects in liquid lithium

    SciTech Connect

    Down, M.G.; Bagnall, C.; Keeton, A.R.; Tsu, T.C.

    1982-09-01

    Results are reported of experimental testing to investigate the potential erosive effect of liquid lithium at 270/sup 0/C and velocities up to 24 ms/sup -1/, on type 304 stainless steel. Two experiments were performed in order to compare data from a conventional flow-through isothermal test leg with those from specimens attached to the circumference of a rotating disc in static lithium.

  12. Lithium-iodine pacemaker cell

    SciTech Connect

    Schneider, A.A.; Snyder, S.E.; DeVan, T.; Harney, M.J.; Harney, D.E.

    1980-01-01

    The lithium-iodine pacemaker cell is described as supplied by several manufacturers. The features of each design are discussed along with their effect on energy density, self-discharge and shape of the discharge curve. Differences in performance characteristics are related to morphology of the lithium iodine electrolyte and to the form of the cathode. A new, high-drain cell is mentioned which can supply 60 /mu/a/cm/sup 2/. 10 refs.

  13. Synergistic and diminutive effects between halogen bond and lithium bond in complexes involving aromatic compounds.

    PubMed

    Liu, Mingxiu; Cai, Mengyang; Li, Qingzhong; Li, Wenzuo; Cheng, Jianbo

    2015-10-01

    Quantum chemical calculations have been performed to study the interplay between halogen bond and lithium bond in the ternary systems FX-C6H5CN-LiF, FLi-C6H5CN-XF, and FLi-C6H5X-NH3 (X = Cl, Br, and I) involving aromatic compounds. This effect was studied in terms of interaction energy, electron density, charge transfer, and orbital interaction. The results showed that both FX-C6H5CN-LiF and FLi-C6H5CN-XF exhibit diminutive effects with the weakening of halogen bond and lithium bond, while FLi-C6H5X-NH3 displays synergistic effects with the strengthening of halogen bond and lithium bond. The nature of halogen bond and lithium bond in the corresponding binary complexes has been unveiled by the quantum theory of atoms in molecules methodology and energy decomposition analysis.

  14. Possible sources of the Population I lithium abundance and light-element evolution

    NASA Technical Reports Server (NTRS)

    Brown, Lawrence E.

    1992-01-01

    One-zone numerical models of Galactic chemical evolution of the light elements (lithium, beryllium, boron, and deuterium) with a broad sample of possible stellar lithium production sites and star formation histories, including the multiple merger model of Mathews and Schramm (1992), are examined. Models with high primordial lithium are constrained by observations of lithium and potassium in the interstellar medium of the LMC to have Li abundances close to the Population I value of about 10 exp -9. Li-7 production in intermediate- or high-mass stars (greater than 4 solar masses) is found to fit observations somewhat better than production in low-mass (1-5 solar masses) stars. Since elevated levels of lithium are commonly observed in intermediate-mass stars in the LMC, it is argued that this is indeed the major source of the Population I Li-7 abundance.

  15. A stable graphite negative electrode for the lithium-sulfur battery.

    PubMed

    Jeschull, Fabian; Brandell, Daniel; Edström, Kristina; Lacey, Matthew J

    2015-12-14

    Efficient, reversible lithium intercalation into graphite in ether-based electrolytes is enabled through a protective electrode binder, polyacrylic acid sodium salt (PAA-Na). In turn, this enables the creation of a stable "lithium-ion-sulfur" cell, using a lithiated graphite negative electrode with a sulfur positive electrode, using the common DME:DOL solvent system suited to the electrochemistry of the lithium-sulfur battery. Graphite-sulfur lithium-ion cells show average coulombic efficiencies of ∼99.5%, compared with <95% for lithium-sulfur cells, and significantly better capacity retention, taking into account cell balancing considerations. The high efficiency derives from the considerably better interfacial stability of the graphite electrode, which suppresses the polysulfide redox shuttle and self-discharge.

  16. Lithium-Ion Electrolytes with Improved Safety Tolerance to High Voltage Systems

    NASA Technical Reports Server (NTRS)

    Smart, Marshall C. (Inventor); Bugga, Ratnakumar V. (Inventor); Prakash, Surya G. (Inventor); Krause, Frederick C. (Inventor)

    2015-01-01

    The invention discloses various embodiments of electrolytes for use in lithium-ion batteries, the electrolytes having improved safety and the ability to operate with high capacity anodes and high voltage cathodes. In one embodiment there is provided an electrolyte for use in a lithium-ion battery comprising an anode and a high voltage cathode. The electrolyte has a mixture of a cyclic carbonate of ethylene carbonate (EC) or mono-fluoroethylene carbonate (FEC) co-solvent, ethyl methyl carbonate (EMC), a flame retardant additive, a lithium salt, and an electrolyte additive that improves compatibility and performance of the lithium-ion battery with a high voltage cathode. The lithium-ion battery is charged to a voltage in a range of from about 2.0 V (Volts) to about 5.0 V (Volts).

  17. Possible use of non-flammable phosphonate ethers as pure electrolyte solvent for lithium batteries

    NASA Astrophysics Data System (ADS)

    Feng, J. K.; Ai, X. P.; Cao, Y. L.; Yang, H. X.

    Dimethyl methyl phosphonate (DMMP) was selected and tested as a non-flammable solvent for primary and secondary lithium batteries, because of its non-flammability, good solvency of lithium salts and appropriate liquidus properties. Experimental results demonstrated that DMMP can solvate considerable amount of commonly used lithium salts to form non-flammable and Li +-conducting electrolyte, which has very wide electrochemical window (>5 V vs. Li) and excellent electrochemical compatibility with metallic lithium anode and oxide cathodes. Primary Li-MnO 2 cells using DMMP-based electrolyte showed almost the same discharge performances as those using organic carbonate electrolytes, and also, Li-LiMn 2O 4 cells using DMMP electrolyte exhibited greatly improved cycleability and dischargeability, suggesting a feasible application of this new electrolyte for constructing high performance and non-flammable lithium batteries.

  18. Sorption of atmospheric gases by bulk lithium metal

    SciTech Connect

    Hart, C. A.; Skinner, C. H.; Capece, A. M.; Koel, B. E.

    2016-01-01

    Lithium conditioning of plasma facing components has enhanced the performance of several fusion devices. Elemental lithium will react with air during maintenance activities and with residual gases (H2O, CO, CO2) in the vacuum vessel during operations. We have used a mass balance (microgram sensitivity) to measure the mass gain of lithium samples during exposure of a ~1 cm2 surface to ambient and dry synthetic air. For ambient air, we found an initial mass gain of several mg/h declining to less than 1 mg/h after an hour and decreasing by an order of magnitude after 24 h. A 9 mg sample achieved a final mass gain corresponding to complete conversion to Li2CO3 after 5 days. Exposure to dry air resulted in a 30 times lower initial rate of mass gain. The results have implications for the chemical state of lithium plasma facing surfaces and for safe handling of lithium coated components.

  19. Precision lifetime measurements of the 2p levels in lithium

    SciTech Connect

    Berry, H.G.; Kurtz, C.; Tanner, C.E.

    1995-08-01

    These measurements are motivated by the theoretical challenges posed by lithium. The three-electron lithium atom is one of the simplest atomic systems with which to test atomic structure calculations. Recently, there were several ab initio calculations of the lithium 2s-2p oscillator strengths, which agree to 0.15%. However, the theoretical results differ by 5 sigma from the precise fast-beam-laser lifetime measurement of Gaupp and Andra (Berlin). Hence the need for a new independent and precise measurement. Improvements were added to the fast beam laser techniques developed for cesium in order to measure the lithium 2p state lifetime. Although the technique is similar to that of cesium, the lithium atom presents a few new complications. Since the atom is lighter, it travels more quickly through the interaction and detection regions. Therefore, the 670 nm wavelength requires a dye laser to produce sufficient intensity to populate the excited state. Unfortunately, the intensity of the dye laser is inherently less stable than that of a diode laser. Another complication is that the ion-beam intensity is much more sensitive to fluctuations in the accelerating voltage. Two detectors were added: one to monitor the ion-beam intensity, and the other to monitor the laser power. With the information from the additional detectors, a new data analysis scheme was developed. Sufficient data were taken to evaluate the benefits of the new detectors. No additional work is planned at Argonne for this experiment.

  20. An improved high-performance lithium-air battery.

    PubMed

    Jung, Hun-Gi; Hassoun, Jusef; Park, Jin-Bum; Sun, Yang-Kook; Scrosati, Bruno

    2012-06-10

    Although dominating the consumer electronics markets as the power source of choice for popular portable devices, the common lithium battery is not yet suited for use in sustainable electrified road transport. The development of advanced, higher-energy lithium batteries is essential in the rapid establishment of the electric car market. Owing to its exceptionally high energy potentiality, the lithium-air battery is a very appealing candidate for fulfilling this role. However, the performance of such batteries has been limited to only a few charge-discharge cycles with low rate capability. Here, by choosing a suitable stable electrolyte and appropriate cell design, we demonstrate a lithium-air battery capable of operating over many cycles with capacity and rate values as high as 5,000 mAh g(carbon)(-1) and 3 A g(carbon)(-1), respectively. For this battery we estimate an energy density value that is much higher than those offered by the currently available lithium-ion battery technology.

  1. Sorption of atmospheric gases by bulk lithium metal

    DOE PAGES

    Hart, C. A.; Skinner, C. H.; Capece, A. M.; ...

    2016-01-01

    Lithium conditioning of plasma facing components has enhanced the performance of several fusion devices. Elemental lithium will react with air during maintenance activities and with residual gases (H2O, CO, CO2) in the vacuum vessel during operations. We have used a mass balance (microgram sensitivity) to measure the mass gain of lithium samples during exposure of a ~1 cm2 surface to ambient and dry synthetic air. For ambient air, we found an initial mass gain of several mg/h declining to less than 1 mg/h after an hour and decreasing by an order of magnitude after 24 h. A 9 mg samplemore » achieved a final mass gain corresponding to complete conversion to Li2CO3 after 5 days. Exposure to dry air resulted in a 30 times lower initial rate of mass gain. The results have implications for the chemical state of lithium plasma facing surfaces and for safe handling of lithium coated components.« less

  2. An improved high-performance lithium-air battery

    NASA Astrophysics Data System (ADS)

    Jung, Hun-Gi; Hassoun, Jusef; Park, Jin-Bum; Sun, Yang-Kook; Scrosati, Bruno

    2012-07-01

    Although dominating the consumer electronics markets as the power source of choice for popular portable devices, the common lithium battery is not yet suited for use in sustainable electrified road transport. The development of advanced, higher-energy lithium batteries is essential in the rapid establishment of the electric car market. Owing to its exceptionally high energy potentiality, the lithium-air battery is a very appealing candidate for fulfilling this role. However, the performance of such batteries has been limited to only a few charge-discharge cycles with low rate capability. Here, by choosing a suitable stable electrolyte and appropriate cell design, we demonstrate a lithium-air battery capable of operating over many cycles with capacity and rate values as high as 5,000 mAh gcarbon-1 and 3 A gcarbon-1, respectively. For this battery we estimate an energy density value that is much higher than those offered by the currently available lithium-ion battery technology.

  3. A Novel Optical Diagnostic for In Situ Measurements of Lithium Polysulfides in Battery Electrolytes.

    PubMed

    Saqib, Najmus; Silva, Cody J; Maupin, C Mark; Porter, Jason M

    2017-01-01

    An optical diagnostic technique to determine the order and concentration of lithium polysulfides in lithium-sulfur (Li-S) battery electrolytes has been developed. One of the major challenges of lithium-sulfur batteries is the problem of polysulfide shuttling between the electrodes, which leads to self-discharge and loss of active material. Here we present an optical diagnostic for quantitative in situ measurements of lithium polysulfides using attenuated total reflection Fourier transform infrared (FT-IR) spectroscopy. Simulated infrared spectra of lithium polysulfide molecules were generated using computational quantum chemistry routines implemented in Gaussian 09. The theoretical spectra served as a starting point for experimental characterization of lithium polysulfide solutions synthesized by the direct reaction of lithium sulfide and sulfur. Attenuated total reflection FT-IR spectroscopy was used to measure absorption spectra. The lower limit of detection with this technique is 0.05 M. Measured spectra revealed trends with respect to polysulfide order and concentration, consistent with theoretical predictions, which were used to develop a set of equations relating the order and concentration of lithium polysulfides in a sample to the position and area of a characteristic infrared absorption band. The diagnostic routine can measure the order and concentration to within 5% and 0.1 M, respectively.

  4. Fewer metabolites of dietary choline reach the blood of rats after treatment with lithium

    SciTech Connect

    Pomfret, E.A.; O'Connor, S.C.; Zola, T.H.; Zeisel, S.H.

    1988-01-01

    The authors studies the effect of lithium treatment upon the appearance in blood, liver and intestine of metabolites formed from dietary choline. Rats were treated for 9 days with 2 mEq/kg lithium carbonate or water. Animals were fasted overnight, and on the 10th day were fed with a solution containing radiolabeled choline chloride. The lithium treated groups also received 2.0 mEq/kg lithium as part of this solution. After an oral dose of 1 ml of a 1 mM choline solution, the lithium-treated animals had significantly lower levels of choline derived radiolabel in blood than did controls at 30, 60, 120, and 180 minutes (47%, 51%, 59% and 74%, respectively). They observed similar decreases of the accumulation in blood, at 180 minutes after the dose, of choline-derived radiolabel when choline was administered at lower or higher concentrations. After an oral treatment containing 0.1, 1 or 10 mM choline, lithium treated animals accumulated 69%, 66% and 72% as much radiolabel in serum as did controls. Most of the radiolabel found in blood at 180 minutes was in metabolites of choline which are formed within liver. The diminished accumulation of radiolabel in serum after lithium treatment was not due to increased accumulation of label by erythrocytes, liver or gut wall. They suggest that lithium influences the release by liver of betaine and phosphatidylcholine. 36 references, 5 figures.

  5. Lithium-based surfaces controlling fusion plasma behavior at the plasma-material interfacea)

    NASA Astrophysics Data System (ADS)

    Allain, Jean Paul; Taylor, Chase N.

    2012-05-01

    The plasma-material interface and its impact on the performance of magnetically confined thermonuclear fusion plasmas are considered to be one of the key scientific gaps in the realization of nuclear fusion power. At this interface, high particle and heat flux from the fusion plasma can limit the material's lifetime and reliability and therefore hinder operation of the fusion device. Lithium-based surfaces are now being used in major magnetic confinement fusion devices and have observed profound effects on plasma performance including enhanced confinement, suppression and control of edge localized modes (ELM), lower hydrogen recycling and impurity suppression. The critical spatial scale length of deuterium and helium particle interactions in lithium ranges between 5-100 nm depending on the incident particle energies at the edge and magnetic configuration. Lithium-based surfaces also range from liquid state to solid lithium coatings on a variety of substrates (e.g., graphite, stainless steel, refractory metal W/Mo/etc., or porous metal structures). Temperature-dependent effects from lithium-based surfaces as plasma facing components (PFC) include magnetohydrodynamic (MHD) instability issues related to liquid lithium, surface impurity, and deuterium retention issues, and anomalous physical sputtering increase at temperatures above lithium's melting point. The paper discusses the viability of lithium-based surfaces in future burning-plasma environments such as those found in ITER and DEMO-like fusion reactor devices.

  6. Mixed solvent electrolytes for ambient temperature secondary lithium cells

    NASA Technical Reports Server (NTRS)

    Shen, David H. (Inventor); Surampudi, Subbarao (Inventor); Deligiannis, Fotios (Inventor); Halpert, Gerald (Inventor)

    1991-01-01

    The present invention comprises an improved electrolyte for secondary lithium-based cells as well as batteries fabricated using this electrolyte. The electrolyte is a lithium containing salt dissolved in a non-aqueous solvent, which is made from a mixture of ethylene carbonate, ethylene propylene diene terpolymer, 2-methylfuran, and 2-methyltetrahydrofuran. This improved, mixed solvent electrolyte is more conductive than prior electrolytes and much less corrosive to lithium anodes. Batteries constructed with this improved electrolyte utilize lithium or lithium alloy anodes and cathodes made of metal chalcogenides or oxides, such as TiS.sub.2, NbSe.sub.3, V.sub.6 O.sub.13, V.sub.2 O.sub.5, MoS.sub.2, MoS.sub.3, CoO.sub.2, or CrO.sub.2, dissolved in a supporting polymer matrix, like EPDM. The preferred non-aqueous solvent mixture comprises approximately 5 to 30 volume percent ethylene carbonate, approximately 0.01 to 0.1 weight percent ethylene propylene diene terpolymer, and approximately 0.2 to 2 percent 2-methylfuran, with the balance being 2-methyltetrahydrofuran. The most preferred solvent comprises approximately 10 to 20 volume percent ethylene carbonate, about 0.05 weight percent ethylene propylene diene terpolymer, and about 1.0 percent 2-methylfuran, with the balance being 2-methyltetrahydrofuran. The concentration of lithium arsenic hexafluoride can range from about 1.0 to 1.8 M; a concentration 1.5 M is most preferred. Secondary batteries made with the improved electrolyte of this invention have lower internal impedance, longer cycle life, higher energy density, low self-discharge, and longer shelf life.

  7. Parameter estimation for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Santhanagopalan, Shriram

    road conditions is important. An algorithm to predict the SOC in time intervals as small as 5 ms is of critical demand. In such cases, the conventional non-linear estimation procedure is not time-effective. There exist methodologies in the literature, such as those based on fuzzy logic; however, these techniques require a lot of computational storage space. Consequently, it is not possible to implement such techniques on a micro-chip for integration as a part of a real-time device. The Extended Kalman Filter (EKF) based approach presented in this work is a first step towards developing an efficient method to predict online, the State of Charge of a lithium ion cell based on an electrochemical model. The final part of the dissertation focuses on incorporating uncertainty in parameter values into electrochemical models using the polynomial chaos theory (PCT).

  8. High-G Verification of Lithium-Polymer (Li-Po) Pouch Cells

    DTIC Science & Technology

    2016-05-19

    UNCLASSIFIED UNCLASSIFIED AD-E403 766 Technical Report ARMET-TR-15067 HIGH-G VERIFICATION OF LITHIUM- POLYMER (LI-PO) POUCH...TITLE AND SUBTITLE HIGH-G VERIFICATION OF LITHIUM- POLYMER (LI-PO) POUCH CELLS 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT... ORGANIZATION NAME(S) AND ADDRESS(ES) U.S. Army ARDEC, METC Fuze & Precision Armaments Technology Directorate (RDAR-MEF-I) Picatinny Arsenal, NJ 07806

  9. Fabrication of densely packed LiNi0.5Mn1.5O4 cathode material with excellent long-term cycleability for high-voltage lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Fang, Jun-Chuan; Xu, Yue-Feng; Xu, Gui-Liang; Shen, Shou-Yu; Li, Jun-Tao; Huang, Ling; Sun, Shi-Gang

    2016-02-01

    Densely packed submicron polyhedral LiNi0.5Mn1.5O4 material with disordered Fd 3 barm structure was synthesized via a modified sol-gel method. The as-synthesized material has a high tap density of 2.15 g cm-3, guaranteeing a high volumetric energy density for high power batteries. Electrochemical properties were investigated in both a LiNi0.5Mn1.5O4/Li half-cell and a LiNi0.5Mn1.5O4/graphite full-cell. The LiNi0.5Mn1.5O4/Li half-cell exhibits a superior cycle stability and rate capability. Here the LiNi0.5Mn1.5O4 material can deliver capacity retentions of 86% at 25 °C and 75% at 55 °C within 1000 cycles for a charge-discharge rate of 1 C. At a much higher rate of 10 C, a discharge capacity of 95 mAh g-1 can be still obtained. The LiNi0.5Mn1.5O4/graphite full-cell delivers a stable discharge capacity of 130.2 mAh g-1 at 0.2 C, corresponding to a discharge energy density as high as 576.2 Wh kg-1. After 100 cycles, the full cell can maintain a working voltage of 4.55 V and capacity retention of 84.6%. The excellent cycle stability is attributed to the dense structure, large particle size, low specific surface area and less exposed (110) facets, which dramatically reduce irreversible surface chemical reactions and manganese dissolution.

  10. The AMBRE project: Constraining the lithium evolution in the Milky Way

    NASA Astrophysics Data System (ADS)

    Guiglion, G.; de Laverny, P.; Recio-Blanco, A.; Worley, C. C.; De Pascale, M.; Masseron, T.; Prantzos, N.; Mikolaitis, Š.

    2016-10-01

    Context. The chemical evolution of lithium in the Milky Way represents a major problem in modern astrophysics. Indeed, lithium is, on the one hand, easily destroyed in stellar interiors, and, on the other hand, produced at some specific stellar evolutionary stages that are still not well constrained. Aims: The goal of this paper is to investigate the lithium stellar content of Milky Way stars in order to put constraints on the lithium chemical enrichment in our Galaxy, in particular in both the thin and thick discs. Methods: Thanks to high-resolution spectra from the ESO archive and high quality atmospheric parameters, we were able to build a massive and homogeneous catalogue of lithium abundances for 7300 stars derived with an automatic method coupling, a synthetic spectra grid, and a Gauss-Newton algorithm. We validated these lithium abundances with literature values, including those of the Gaia benchmark stars. Results: In terms of lithium galactic evolution, we show that the interstellar lithium abundance increases with metallicity by 1 dex from [M/H] = -1 dex to + 0.0 dex. Moreover, we find that this lithium ISM abundance decreases by about 0.5 dex at super-solar metalllicity. Based on a chemical separation, we also observed that the stellar lithium content in the thick disc increases rather slightly with metallicity, while the thin disc shows a steeper increase. The lithium abundance distribution of α-rich, metal-rich stars has a peak at ALi ~ 3 dex. Conclusions: We conclude that the thick disc stars suffered of a low lithium chemical enrichment, showing lithium abundances rather close to the Spite plateau while the thin disc stars clearly show an increasing lithium chemical enrichment with the metallicity, probably thanks to the contribution of low-mass stars. Full Table 2 is only available at the CDS via anonymous ftp to http://cdsarc.u-strasbg.fr (http://130.79.128.5) or via http://cdsarc.u-strasbg.fr/viz-bin/qcat?J/A+A/595/A18

  11. A large format in operando wound cell for analysing the structural dynamics of lithium insertion materials

    NASA Astrophysics Data System (ADS)

    Brant, William R.; Roberts, Matthew; Gustafsson, Torbjörn; Biendicho, Jordi Jacas; Hull, Stephen; Ehrenberg, Helmut; Edström, Kristina; Schmid, Siegbert

    2016-12-01

    This paper presents a large wound cell for in operando neutron diffraction (ND) from which high quality diffraction patterns are collected every 15 min while maintaining conventional electrochemical performance. Under in operando data collection conditions the oxygen atomic displacement parameters (ADPs) and cell parameters were extracted for Li0.18Sr0.66Ti0.5Nb0.5O3. Analysis of diffraction data collected under in situ conditions revealed that the lithium is located on the (0.5 0.5 0) site, corresponding to the 3c Wyckoff position in the cubic perovskite unit cell, after the cell is discharged to 1 V. When the cell is discharged under potentiostatic conditions the quantity of lithium on this site increases, indicating a potential position where lithium becomes pinned in the thermodynamically stable phase. During this potentiostatic step the oxygen ADPs reduce significantly. On discharge, however, the oxygen ADPs were observed to increase gradually as more lithium is inserted into the structure. Finally, the rate of unit cell expansion changed by ∼44% once the lithium content approached ∼0.17 Li per formula unit. A link between lithium content and degree of mobility, disorder of the oxygen positions and changing rate of unit cell expansion at various stages during lithium insertion and extraction is thus presented.

  12. Performance Evaluation of a 4.5 kW (1.3 Refrigeration Tons) Air-Cooled Lithium Bromide/Water Solar Powered (Hot-Water-Fired) Absorption Unit

    SciTech Connect

    Zaltash, Abdolreza; Petrov, Andrei Y; Linkous, Randall Lee; Vineyard, Edward Allan

    2007-01-01

    During the summer months, air-conditioning (cooling) is the single largest use of electricity in both residential and commercial buildings with the major impact on peak electric demand. Improved air-conditioning technology has by far the greatest potential impact on the electric industry compared to any other technology that uses electricity. Thermally activated absorption air-conditioning (absorption chillers) can provide overall peak load reduction and electric grid relief for summer peak demand. This innovative absorption technology is based on integrated rotating heat exchangers to enhance heat and mass transfer resulting in a potential reduction of size, cost, and weight of the "next generation" absorption units. Rotartica Absorption Chiller (RAC) is a 4.5 kW (1.3 refrigeration tons or RT) air-cooled lithium bromide (LiBr)/water unit powered by hot water generated using the solar energy and/or waste heat. Typically LiBr/water absorption chillers are water-cooled units which use a cooling tower to reject heat. Cooling towers require a large amount of space, increase start-up and maintenance costs. However, RAC is an air-cooled absorption chiller (no cooling tower). The purpose of this evaluation is to verify RAC performance by comparing the Coefficient of Performance (COP or ratio of cooling capacity to energy input) and the cooling capacity results with those of the manufacturer. The performance of the RAC was tested at Oak Ridge National Laboratory (ORNL) in a controlled environment at various hot and chilled water flow rates, air handler flow rates, and ambient temperatures. Temperature probes, mass flow meters, rotational speed measuring device, pressure transducers, and a web camera mounted inside the unit were used to monitor the RAC via a web control-based data acquisition system using Automated Logic Controller (ALC). Results showed a COP and cooling capacity of approximately 0.58 and 3.7 kW respectively at 35 C (95 F) design condition for ambient

  13. Time-dependent effects of lithium on the agonist-stimulated accumulation of second messenger inositol 1,4,5-trisphosphate in SH-SY5Y human neuroblastoma cells.

    PubMed

    Los, G V; Artemenko, I P; Hokin, L E

    1995-10-01

    In order to approach the molecular mechanism of Li+'s mood-stabilizing action, the effect of Li+ (LiCl) on inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] mass was investigated in human neuroblastoma SH-SY5Y cells, which express muscarinic M3 receptors, coupled to PtdIns hydrolysis. Stimulation of these cells, with the cholinergic agonist acetylcholine, resulted in a rapid and transient increase in Ins(1,4,5)P3 with a maximum at 10 s. This was followed by a rapid decline in Ins(1,4,5)P3 within 30 s to a plateau level above baseline, which gradually declined to reach a new steady state, which was significantly higher than resting Ins(1,4,5)P3 at 30 min. Li+ had no effect on Ins(1,4,5)P3 in resting cells, as well as on the acetylcholine-dependent peak of Ins(1,4,5)P3. However, Li+ caused a transient reduction (at 45 s), followed by a long lasting increase in the Ins(1,4,5)P3 (30 min), as compared with controls. The Li+ effects were dose-dependent and were observed at concentrations used in the treatment of bipolar disorders. Supplementation with inositol had no effect on the level of Ins(1,4,5)P3, at least over the time periods studied. Stimulation of muscarinic receptors with consequent activation of phospholipase C were necessary for the manifestation of Li+ effects in SH-SY5Y cells, Li+ did not interfere with degradation of Ins(1,4,5)P3 after receptor-blockade with atropine, suggesting that Li+ has no direct effect on the Ins(1,4,5)P3-metabolizing enzymes. A direct effect of Li+ on the phospholipase C also is unlikely. Blockade of Ca2+ entry into the cells by Ni2+, or incubation with EGTA, which reduces agonist-stimulated accumulation of Ins(1,4,5)P3, had no effect on the Li(+)-dependent increase in Ins(1,4,5)P3.

  14. Micro-channel-based high specific power lithium target

    NASA Astrophysics Data System (ADS)

    Mastinu, P.; Martın-Hernández, G.; Praena, J.; Gramegna, F.; Prete, G.; Agostini, P.; Aiello, A.; Phoenix, B.

    2016-11-01

    A micro-channel-based heat sink has been produced and tested. The device has been developed to be used as a Lithium target for the LENOS (Legnaro Neutron Source) facility and for the production of radioisotope. Nevertheless, applications of such device can span on many areas: cooling of electronic devices, diode laser array, automotive applications etc. The target has been tested using a proton beam of 2.8MeV energy and delivering total power shots from 100W to 1500W with beam spots varying from 5mm2 to 19mm2. Since the target has been designed to be used with a thin deposit of lithium and since lithium is a low-melting-point material, we have measured that, for such application, a specific power of about 3kW/cm2 can be delivered to the target, keeping the maximum surface temperature not exceeding 150° C.

  15. Lithium effects: protection against nitrogen narcosis, potentiation of HPNS.

    PubMed

    Bennett, P B; Leventhal, B L; Coggin, R; Roby, J; Racanska, L

    1980-03-01

    The effect of either 10, 8, or 6 meq/kg of intraperitoneal lithium chloride or sodium chloride on the loss of righting response (RR50) produced by 18.2 ATA N2-ATA O2 was examined in rats. Results were compared to the effects of 10, 8, 6, or 4 meq/kg of intraperitoneal lithium chloride given 24 h before determination of the convulsion pressure (PC) in 40 rats compressed with He-O2 at 160 atm/h at 37 +/- 0.5 degrees C. Lithium (10 meq/kg) prevented the nitrogen-narcosis-induced loss of righting response but significantly potentiated the pressure (depth) at which convulsions and tremors occurred.

  16. Lithium rich cathode/graphite anode combination for lithium ion cells with high tolerance to near zero volt storage

    NASA Astrophysics Data System (ADS)

    Crompton, K. R.; Staub, J. W.; Hladky, M. P.; Landi, B. J.

    2017-03-01

    Management of reversible lithium is an advantageous approach to design lithium ion cells that are tolerant to near zero volt (NZV) storage under fixed resistive load towards highly controllable, enhanced user-inactive safety. Presently, the first cycle loss from a high energy density Li-rich HE5050 cathode is used to provide excess reversible lithium when paired with an appropriately capacity matched mesocarbon microbead (MCMB) anode. Cells utilizing 1.2 M LiPF6 3:7 v/v ethylene carbonate:ethyl methyl carbonate electrolyte and a lithium reference were used for 3-electrode testing. After conditioning, a fixed resistive load was applied to 3-electrode cells for 72 or 168-h during which the anode potential and electrode asymptotic potential (EAP) remained less than the copper dissolution potential. After multiple storage cycles (room temperature or 40 °C), the NZV coulombic efficiency (cell reversibility) exceeded 97% and the discharge capacity retention was >98%. Conventional 2-electrode HE5050/MCMB pouch cells stored at NZV or open circuit for 3 days had nearly identical rate capability (up to 5C) and discharge performance stability (for 500 cycles under a 30% depth of discharge low-earth-orbit regime). Thus, lithium ion cells with appropriately capacity matched HE5050/MCMB electrodes have excellent tolerance to prolonged NZV storage, which can lead to enhanced user-inactive safety.

  17. Lithium intercalation reaction into the Keggin type polyoxomolybdates

    NASA Astrophysics Data System (ADS)

    Sonoyama, Noriyuki; Suganuma, Yoshiaki; Kume, Tomohiro; Quan, Zhen

    The electrochemical property of Keggin type hetero polyoxomolybdate K 3[PMo 12O 40] (KPM) as the cathode electrode material for lithium battery was examined. KPM showed charge-discharge performance in the potential region from 4.2 V to 1.5 V with capacity of over 200 mAh g -1. From the result of the ex situ XRD measurement, it is presumed that the electrochemical reaction of KPM proceeds via the lithium (de-)intercalation. The cycle performance of KPM is largely dependent on the charge-discharge potential range. The capacity fade caused by deep discharging seems to be concerned to the < to ® isomerization of KPM.

  18. FIRE EXTINGUISHERS CONTAINING INHIBITED LITHIUM CHLORIDE SOLUTION FOR POLAR USE

    DTIC Science & Technology

    Previous experiments under this task using small metal test panels resulted in the selection of a sodium dichromate- oxalic acid inhibitor for use in...of drawn brass or silicon bronze and lined with a lead alloys, were tested with the lithium chloride solution using either sodium dichromate- oxalic ... acid or sodium dichromate alone as an inhibitor. It was determined that 0.5 percent sodium dichromate satisfactorily inhibits corrosion by the water solution of lithium chloride when contained in an extinguisher of drawn brass.

  19. High Performance Batteries Based on Hybrid Magnesium and Lithium Chemistry

    SciTech Connect

    Cheng, Yingwen; Shao, Yuyan; Zhang, Jiguang; Sprenkle, Vincent L.; Liu, Jun; Li, Guosheng

    2014-01-01

    Magnesium and lithium (Mg/Li) hybrid batteries that combine Mg and Li electrochemistry, consisting of a Mg anode, a lithium-intercalation cathode and a dual-salt electrolyte with both Mg2+ and Li+ ions, were constructed and examined in this work. Our results show that hybrid (Mg/Li) batteries were able to combine the advantages of Li-ion and Mg batteries, and delivered outstanding rate performance (83% for capacities at 15C and 0.1C) and superior cyclic stability (~5% fade after 3000 cycles).

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

    DOEpatents

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

    2006-05-23

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

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

    DOEpatents

    Bates, John B.

    1994-01-01

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

  2. High performance discharges in the Lithium Tokamak eXperiment with liquid lithium walls

    SciTech Connect

    Schmitt, J. C.; Bell, R. E.; Boyle, D. P.; Esposti, B.; Kaita, R.; Kozub, T.; LeBlanc, B. P.; Lucia, M.; Maingi, R.; Majeski, R.; Merino, E.; Punjabi-Vinoth, S.; Tchilingurian, G.; Capece, A.; Koel, B.; Roszell, J.; Biewer, T. M.; Gray, T. K.; Kubota, S.; Beiersdorfer, P.; and others

    2015-05-15

    The first-ever successful operation of a tokamak with a large area (40% of the total plasma surface area) liquid lithium wall has been achieved in the Lithium Tokamak eXperiment (LTX). These results were obtained with a new, electron beam-based lithium evaporation system, which can deposit a lithium coating on the limiting wall of LTX in a five-minute period. Preliminary analyses of diamagnetic and other data for discharges operated with a liquid lithium wall indicate that confinement times increased by 10× compared to discharges with helium-dispersed solid lithium coatings. Ohmic energy confinement times with fresh lithium walls, solid and liquid, exceed several relevant empirical scaling expressions. Spectroscopic analysis of the discharges indicates that oxygen levels in the discharges limited on liquid lithium walls were significantly reduced compared to discharges limited on solid lithium walls. Tokamak operations with a full liquid lithium wall (85% of the total plasma surface area) have recently started.

  3. Recent advances in lithium ion technology

    SciTech Connect

    Levy, S.C.

    1995-01-01

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

  4. Two-Dimensional Wavelike Spinel Lithium Titanate for Fast Lithium Storage

    PubMed Central

    Liu, Jiehua; Wei, Xiangfeng; Liu, Xue-Wei

    2015-01-01

    Safe fast-charging lithium-ion batteries (LIBs) have huge potential market size on demand according to their shortened charging time for high-power devices. Zero-strain spinel Li4Ti5O12 is one of ideal candidates for safe high-power batteries owing to its good cycling performance, low cost and safety. However, the inherent insulating characteristic of LTO seriously limits its high-rate capability. In this work, we successfully synthesize novel wavelike spinel LTO nanosheets using a facile ‘co-hydrolysis’ method, which is superior to molten-salt approach and traditional solvothermal method in some respects. The unique 2D structures have single-crystal framework with shortened path for Li ion transport. As a result, the N-doped 2D wavelike LTO with 0.6 wt.% of ‘carbon joint’ not only exhibits exciting capacity of ~180 and ~150 mA h g−1 for fast lithium storage at high discharge/charge rates of 1.7 and 8.5 A g−1 (10C and 50C) respectively, but also shows excellent low-temperature performance at −20°C. In addition, the cost may be further decreased due to recycled functional reagents. This novel nanostructured 2D LTO anode material makes it possible to develop safe fast-charging high-power lithium ion batteries. PMID:25985465

  5. Reduced Dimensionality Lithium Niobate Microsystems

    SciTech Connect

    Eichenfield, Matt

    2017-01-01

    The following report describes work performed under the LDRD program at Sandia National Laboratories October 2014 and September 2016. The work presented demonstrates the ability of Sandia Labs to develop state-of-the-art photonic devices based on thin film lithium niobate (LiNbO3 ). Section 1 provides an introduction to integrated LiNbO3 devices and motivation for developing thin film nonlinear optical systems. Section 2 describes the design, fabrication, and photonic performance of thin film optical microdisks fabricated from bulk LiNbO3 using a bulk implantation method developed at Sandia. Sections 3 and 4 describe the development of similar thin film LiNbO3 structures fabricated from LiNbO3 on insulator (LNOI) substrates and our demonstration of optical frequency conversion with state-of-the-art efficiency. Finally, Section 5 describes similar microdisk resonators fabricated from LNOI wafers with a buried metal layer, in which we demonstrate electro-optic modulation.

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

    DOEpatents

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

    2014-05-13

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

  7. Lithium in Medicine: Mechanisms of Action.

    PubMed

    Mota de Freitas, Duarte; Leverson, Brian D; Goossens, Jesse L

    2016-01-01

    In this chapter, we review the mechanism of action of lithium salts from a chemical perspective. A description on how lithium salts are used to treat mental illnesses, in particular bipolar disorder, and other disease states is provided. Emphasis is not placed on the genetics and the psychopharmacology of the ailments for which lithium salts have proven to be beneficial. Rather we highlight the application of chemical methodologies for the characterization of the cellular targets of lithium salts and their distribution in tissues.

  8. Sealed Primary Lithium-Inorganic Electrolyte Cell

    DTIC Science & Technology

    1977-02-01

    Battery , Thionyl Chloride , Lithium , Lithium Aluminum Chloride , Hermetic Lithium Battery , D Cell, Voltage-Delay, Shelf Life, High Energy Density Battery ... lithium - thionyl chloride , inorganic electrclyte system is one of the highest energy density systems known to date (1-4). The cells contain an Li anoae, a...However, this is not tne case with te thionyl chloride system. A completely discharged battery , while sitting on

  9. Rechargeable lithium battery technology - A survey

    NASA Technical Reports Server (NTRS)

    Halpert, Gerald; Surampudi, Subbarao

    1990-01-01

    The technology of the rechargeable lithium battery is discussed with special attention given to the types of rechargeable lithium cells and to their expected performance and advantages. Consideration is also given to the organic-electrolyte and polymeric-electrolyte cells and to molten salt lithium cells, as well as to technical issues, such as the cycle life, charge control, rate capability, cell size, and safety. The role of the rechargeable lithium cell in future NASA applications is discussed.

  10. Novel Electrolytes for Lithium Ion Batteries

    SciTech Connect

    Lucht, Brett L.

    2014-12-12

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

  11. Primary lithium batteries, some consumer considerations

    NASA Technical Reports Server (NTRS)

    Bro, P.

    1983-01-01

    In order to determine whether larger size lithium batteries would be commercially marketable, the performance of several D size lithium batteries was compared with that of an equivalent alkaline manganese battery, and the relative costs of the different systems were compared. It is concluded that opportunities exist in the consumer market for the larger sizes of the low rate and moderate rate lithium batteries, and that the high rate lithium batteries need further improvements before they can be recommended for consumer applications.

  12. New Liquid Cathodes for Lithium Batteries. Part A. Halocarbons,

    DTIC Science & Technology

    1984-05-01

    difluoroethane , 99 percent; PCR Inc. thionyl chloride, doubly-distilled, Apache Chemicals, Seward, Ill. l.5M LiAlCI4 in SOC1 2 , ɝppm Fe, Lithium Corp. of...tetrachloroethane, and 1,2-dichloro-l,1- difluoroethane appeared stable towards Li during the study. When in contact with electrolyte solutions of 50

  13. Study of multiple hologram recording in lithium niobate

    NASA Technical Reports Server (NTRS)

    Gaylord, T. K.; Callen, W. R.

    1974-01-01

    The results of detailed experimental and theoretical considerations relating to multiple hologram recording in lithium niobate are reported. The following problem areas are identified and discussed: (1) the angular selectivity of the stored holograms, (2) interference effects due to the crystal surfaces, (3) beam divergence effects, (4) material recording sensitivity, and (5) scattered light from material inhomogeneities.

  14. Solid electrolyte: The key for high-voltage lithium batteries

    DOE PAGES

    Li, Juchuan; Ma, Cheng; Chi, Miaofang; ...

    2014-10-14

    A solid-state high-voltage (5 V) lithium battery is demonstrated to deliver a cycle life of 10 000 with 90% capacity retention. Furthermore, the solid electrolyte enables the use of high-voltage cathodes and Li anodes with minimum side reactions, leading to a high Coulombic efficiency of 99.98+%.

  15. Solid composite electrolytes for lithium batteries

    DOEpatents

    Kumar, Binod; Scanlon, Jr., Lawrence G.

    2000-01-01

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

  16. Anode materials for lithium-ion batteries

    DOEpatents

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

    2014-12-30

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

  17. Magnetism in lithium-oxygen discharge product.

    PubMed

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

    2013-07-01

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

  18. Lithium toxicity: the importance of clinical signs.

    PubMed

    Dunne, Francis J

    2010-04-01

    Although there appears to be a decline in its use, lithium is still used extensively in the UK to treat bipolar disorder. However, lithium can be quite toxic and lead to long-term problems, rarely death. Therefore, doctors need to carefully monitor patients taking lithium and seek appropriate advice whenever concerns are raised.

  19. Lithium Battery Fire Tests and Mitigation

    DTIC Science & Technology

    2014-08-25

    referred to as a separator. An electrolyte composed of an organic solvent and dissolved lithium salt provides the medium for lithium ion transport. A...inorganic solvents containing dissolved ionic lithium salts. Where the electrolytes are not organic esters/carbonate mixtures, they are inorganic

  20. Preparation of LiNi0.5Mn1.5O4 for Lithium Batteries Via Solid-State Redox Method using Nitrate and Acetate Based Reactants

    NASA Astrophysics Data System (ADS)

    Mat, A.; Sulaiman, K. S.; Sulaiman, M. A.; Hasim, M. F.

    2010-03-01

    LiNi0.5Mn1.5O4 is a potential cathode material for 5 V batteries. This material was prepared by the solid-state redox method using nitrate and acetate based reactants. The precursor material was obtained when the mixture reactants was heated at 500° C for 10 hours and calcined at different temperatures in the range between 650 and 950° C for 12 hours. The structures of the synthesized materials were verified with X- ray diffraction (XRD) measurement and Scanning Electron Microscope (SEM). The charge-discharge technique was determined using Solartron 1470. As calcination temperature increases, the well-ordered crystal growth oriented to [1 1 1] direction shows a clear octahedral morphology, which is the characteristic of the typical cubic spinel. The Li/LiNi0.5Mn1.5O4 prepared from acetate based reactants calcined at 750° C for 12 h delivered the discharge capacity of 140 mAh/g.

  1. Morphology controlled Si-modified LiNi0.5Mn1.5O4 microspheres as high performance high voltage cathode materials in lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Nageswaran, Shubha; Keppeler, Miriam; Kim, Sung-Jin; Srinivasan, Madhavi

    2017-04-01

    Well-crystallized, microspherical LiNi0.5Mn1.5-nSinO4 (0.05 < n < 0.2) is successfully synthesized by a template directed approach in combination with the partial substitution of manganese by silicon. Structural and electrochemical characteristics are investigated through FE-SEM, XRD, EDX, cyclic voltammetry and galvanostatic charge/discharge testing. Spherical shape and incorporation of silicon into the crystal leads to higher proportion of the disordered Fd-3m phase, and electrochemical performance is significantly improved. High capacity retention of 99.4% after 100 cycles at 1 C rate for LiNi0.5Mn1.45Si0.05O4 microspheres is achieved, which is superior compared to 93.1% capacity retention of the pristine LiNi0.5Mn1.5O4 microspheres. Since the Sisbnd O bond exhibits higher dissociation energy compared to the dissociation energies of the Mnsbnd O or Nisbnd O bonds, the excellent electrochemical performance might be associated with an increased structural and chemical stability caused by incorporation of silicon into the oxygen rich crystal lattice.

  2. Conductive lithium storage electrode

    DOEpatents

    Chiang, Yet-Ming; Chung, Sung-Yoon; Bloking, Jason T.; Andersson, Anna M.

    2008-03-18

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

  3. Conductive lithium storage electrode

    DOEpatents

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

    2012-04-03

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

  4. Space-charge at the lithium-lithium chloride interface

    NASA Astrophysics Data System (ADS)

    Jamnik, J.; Gaberscek, M.; Meden, A.; Pejovnik, S.

    1991-06-01

    The electrical properties of the passive layer formed on lithium as the product of the corrosion reaction in thionyl chloride are discussed. The passive layer is regarded as a thin layer of an ionic crystal placed between two party blocking electrodes (i.e., lithium and liquid electrolyte). After a short review of thermodynamic properties of the system, a model for description of the electric properties of the static space-charge regions is presented. On this basis, a comment on and partial reinterpretation of impedance measurements of the passive layer is given. The suggested approach leads to the conclusion that the quality of Li/SOCl2 batteries decisively depends on the properties of the lithium passive layer interface. Finally, experiments to confirm the model are suggested.

  5. The lithium vapor box divertor

    NASA Astrophysics Data System (ADS)

    Goldston, R. J.; Myers, R.; Schwartz, J.

    2016-02-01

    It has long been recognized that volumetric dissipation of the plasma heat flux from a fusion power system is preferable to its localized impingement on a material surface. Volumetric dissipation mitigates both the anticipated very high heat flux and intense particle-induced damage due to sputtering. Recent projections to a tokamak demonstration power plant suggest an immense upstream parallel heat flux, of order 20 GW m-2, implying that fully detached operation may be a requirement for the success of fusion power. Building on pioneering work on the use of lithium by Nagayama et al and by Ono et al as well as earlier work on the gas box divertor by Watkins and Rebut, we present here a concept for a lithium vapor box divertor, in which lithium vapor extracts momentum and energy from a fusion-power-plant divertor plasma, using fully volumetric processes. At the high powers and pressures that are projected this requires a high density of lithium vapor, which must be isolated from the main plasma in order to avoid lithium build-up on the chamber walls or in the plasma. Isolation is achieved through a powerful multi-box differential pumping scheme available only for condensable vapors. The preliminary box-wise calculations are encouraging, but much more work is required to demonstrate the practical viability of this scheme, taking into account at least 2D plasma and vapor flows within and between the vapor boxes and out of the vapor boxes to the main plasma.

  6. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

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

    2006-11-14

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

  7. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

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

    2004-01-13

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

  8. Flashover lithium ion source development for large pulsed power accelerators

    SciTech Connect

    Bieg, K.W.; Burns, E.J.T.; Gerber, R.A.; Olsen, J.N.; Lamppa, K.P.

    1986-05-01

    The Particle Beam Fusion Accelerator II (PBFA II), a light-ion pulsed power accelerator intended for inertial confinement fusion (ICF) applications, is currently under construction at Sandia National Laboratories. The accelerator will deliver a 30 MV, 5 MA lithium beam from an Applied-B diode to drive an ICF target. The ion source for this diode will require a thin (approx.1 mm), dense (10/sup 16/ cm/sup -2/) anode plasma layer of singly ionized lithium over an anode area of 10/sup 3/ cm/sup 2/. One type of source being investigated is the flashover ion source, which generates the anode plasma via vacuum flashover of a lithium-bearing dielectric material. Experiments with a LiF flashover source on the 0.03 TW Nereus accelerator have shown that contaminant ions account for as much as 70% of the extracted ion beam current. To overcome this, we have explored in-diode cleaning of the externally prepared anode surface by glow discharge cleaning and vacuum baking as well as in-diode preparation of the anode surface by vacuum evaporation of the lithium dielectric. Lithium-bearing dielectric materials which have been investigated include LiF, LiI, LiNO/sub 3/, and Li/sub 3/N. These techniques have resulted in a two to threefold improvement in the extracted lithium ion purity. As a result, a glow-discharge cleaned LiF flashover source will be used for initial pulsed-power testing on PBFA II.

  9. The protective influence of selenium on oxidant disturbances in brain of rats exposed to lithium.

    PubMed

    Kiełczykowska, M; Kocot, J; Lewandowska, A; Żelazowska, R; Musik, I

    2015-01-01

    For more than sixty years lithium carbonate has been used in medicine. However, during its administration different side effects including oxidative stress can occur. Selenium belongs to essential elements possessing antioxidant properties. This study aimed at evaluating if selenium could be used as a protective adjuvant in lithium therapy. The experiment was performed on four groups of Wistar rats: I (control), II (Li), III (Se), IV (Li + Se) treated with saline, lithium carbonate (2.7 mg Li/kg b.w.), sodium selenite (0.5 mg Se/kg b.w.) and lithium carbonate (2.7 mg Li/kg b.w.) + sodium selenite (0.5 mg Se/kg b.w.), respectively. All substances were administered as water solutions by stomach tube for 3 or 6 weeks. Catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPx) as well as malonyldialdehyde (MDA) were determined in brain homogenates. Lithium slightly enhanced MDA and depressed CAT and SOD after 6 weeks as well as GPx after 3 weeks. Selenium co-administration showed tendency to restore the disturbed parameters. Selenium alone and given with lithium significantly increased GPx vs. Li-treated group after 3 weeks. Having regarded the outcomes of this study, the research on application of selenium during lithium treatment seems to be worth continuation.

  10. [The acute renal and cerebral toxicity of lithium: a cerebro-renal syndrome? A case report].

    PubMed

    Prencipe, M; Cicchella, A; Del Giudice, A; Di Giorgio, A; Scarlatella, A; Vergura, M; Aucella, F

    2013-01-01

    This descriptive report describes the case of a 50 year-old woman with bipolar disorder, whose maintenance therapy comprised risperidone, sodium valproato and lithium carbonate without any past occurrence of toxicity. Her past medical history was significant for hypertension, cardiopathy and obesity. She presented with a 1-week history of fever, increasing confusion and slurred speech. At presentation, the patient was somnolent. Laboratory investigations revealed a serum creatinine of 3,6 mg/dl, BUN 45 mg/dl serum lithium 3,0 mEq/L with polyuria defined as more than 3 litres a day. EEG and ECG were abnormal. CT brain scanning and lumbar puncture were negative for brain haemorrage or infection. Lithium toxicity causes impairment of renal concentration and encephalopathy due to lithium recirculation, a mechanism responsible for the so-called cerebro-renal syndrome, where dialysis plays an important role in treatment.The patient was treated with continous veno-venous haemodiafiltration (CVVHDF) over 35 hours with gradual improvement of her general condition and efficacy of renal concentration. Our case highlights a few important points. Lithium nefrotoxicity and neurotoxicity can cause a cerebro-renal syndrome even when serum lithium levels are not particularly raised (2,5-3,5 mEq/L). Haemodialysis is the treatment of choice to reduce the molecular mechanisms of lithium-related changes in urinary concentration and reinstate dopaminergic activity in the brain.

  11. Quantitative analysis of the hydration of lithium salts in water using multivariate curve resolution of near-infrared spectra.

    PubMed

    Barba, M Isabel; Larrechi, M Soledad; Coronas, Alberto

    2016-05-05

    The hydration process of lithium iodide, lithium bromide, lithium chloride and lithium nitrate in water was analyzed quantitatively by applying multivariate curve resolution alternating least squares (MCR-ALS) to their near infrared spectra recorded between 850 nm and 1100 nm. The experiments were carried out using solutions with a salt mass fraction between 0% and 72% for lithium bromide, between 0% and 67% for lithium nitrate and between 0% and 62% for lithium chloride and lithium iodide at 323.15 K, 333.15 K, 343.15 K and 353.15 K, respectively. Three factors were determined for lithium bromide and lithium iodide and two factors for the lithium chloride and lithium nitrate by singular value decomposition (SVD) of their spectral data matrices. These factors are associated with various chemical environments in which there are aqueous clusters containing the ions of the salts and non-coordinated water molecules. Spectra and concentration profiles of non-coordinated water and cluster aqueous were retrieved by MCR-ALS. The amount of water involved in the process of hydration of the various salts was quantified. The results show that the water absorption capacity increases in the following order LiI < LiBr < LiNO3 < LiCl. The salt concentration at which there is no free water in the medium was calculated at each one of the temperatures considered. The values ranged between 62.6 and 65.1% for LiBr, 45.5-48.3% for LiCl, 60.4-61.2% for LiI and 60.3-63.7% for LiNO3. These values are an initial approach to determining the concentration as from which crystal formation is favored.

  12. On the "gluing" effect of lithium: the lithium-driven assembly of circum-arranged, edge-fused cyclopentadienyl lithium compounds and aza analogues.

    PubMed

    Saá, José M; Yañez, Manuel

    2009-01-01

    Predictions (DFT/B3LYP calculations) are that cyclopentadienyl lithium edge-fused to [n]circulenes in a circum-like manner should self-assemble as rod-like, nanometer long, supersandwich compounds (see figure). On the contrary, triazolyl lithium analogues prefer to dimerize thereby giving rise to shell-like dimers of variable curvatures.This study is aimed at exploring M. Etter's (T. W. Panunto, Z. Urbanczyk-Lipkowska, R. Jonhson, M. Etter, J. Am. Chem. Soc. 1987, 109, 7786-7797) bottom-up approach towards the design of organic-solid sate materials. Guided by the electrostatic paste ("gluing") effect of lithium, we examined the self-assembly modes of a series of cyclopentadienyl lithium edge-fused to benzene, as well as to [n]circulenes, arranged in a circum-like manner by means of DFT/B3 LYP calculations. We have also examined the self-assembly modes of the analogous triazolyl derivatives. Generally, well defined trends have been found. Thus, whereas cylcopentadienyl derivatives 1, 3 and 5 tend to aggregate as rod-like, nanometer-long, supersandwich compounds, the corresponding triazolyl analogues 2, 4 and 6 tend to dimerize thus giving rise to shell-like dimers of variable curvatures. In our view, M. Etter's bottom-up approach combined with high level calculations appears to have great potential for designing complex molecular architectures and nanostructures. Hopefully, these studies will spur the activity of synthetic and materials chemists.

  13. Research on lithium batteries

    NASA Astrophysics Data System (ADS)

    Hill, I. R.; Goledzinowski, M.; Dore, R.

    1993-12-01

    Research was conducted on two types of lithium batteries. The first is a rechargeable Li-SO2 system using an all-inorganic electrolyte. A Li/liquid cathode system was chosen to obtain a relatively high discharge rate capability over the +20 to -30 C range. The fabrication and cycling performance of research cells are described, including the preparation and physical properties of porous polytetra fluoroethylene bonded carbon electrodes. Since the low temperature performance of the standard electrolyte was unsatisfactory, studies of electrolytes containing mixed salts were made. Raman spectroscopy was used to study the species present in these electrolytes and to identify discharge products. Infrared spectroscopy was used to measure electrolyte impurities. Film growth on the LiCl was also monitored. The second battery is a Li-thionyl chloride nonrechargeable system. Research cells were fabricated containing cobalt phthalo cyanine in the carbon cathode. The cathode was heat treated at different temperatures and the effect on cell discharge rate and capacity evaluated. Commercially obtained cells were used in an investigation of a way to identify substandard cells. The study also involved electrochemical impedance spectroscopy and cell discharging at various rates. The results are discussed in terms of LiCl passivation.

  14. Epitaxial growth and lithium ion conductivity of lithium-oxide garnet for an all solid-state battery electrolyte.

    PubMed

    Kim, Sangryun; Hirayama, Masaaki; Taminato, Sou; Kanno, Ryoji

    2013-09-28

    Epitaxial thin films of Al-doped Li7La3Zr2O12 (LLZO) with a cubic garnet-type structure were successfully synthesized using pulsed laser deposition to investigate the lithium ion conduction in grains. Two orientations of the films were obtained depending on the Gd3Ga5O12 (GGG) substrate orientation, LLZO(001)/GGG(001) and LLZO(111)/GGG(111). The ionic conductivities in the grains of the (001) and (111) films were 2.5 × 10(-6) and 1.0 × 10(-5) S cm(-1) at 298 K, respectively, which were lower than those of polycrystalline LLZO of over 10(-4) S cm(-1). X-ray reflectometry and inductively coupled plasma mass spectrometry revealed a large amount of Al(3+) of over 0.6 moles substituted for Li(+). These results indicate that the Al(3+) substitution in the LLZO lattice decreases the number of movable lithium ions and blocks the three-dimensional lithium migration pathway. The lattice mismatch between the film and the substrate induced the lattice distortion of the LLZO, resulting in different conductivities between the (001) and (111) films. The epitaxial-film model system directly clarified a substantial impact of the Al substitution and the lattice distortion on the lithium ion conductivity in the LLZO.

  15. Lithium iron phosphates as cathode materials in lithium ion batteries for electric vehicles

    NASA Astrophysics Data System (ADS)

    Wang, Gaojun; Chen, Linfeng; Mathur, Gyanesh N.; Varadan, Vijay K.

    2012-04-01

    Olivine-structured lithium iron phosphates are promising cathode materials in the development of high power lithium ion batteries for electric vehicles. However, the low electronic conductivity and ionic conductivity of lithium iron phosphates hinder their commercialization pace. This work aims to verify the approaches for improving the electrochemical properties of lithium iron phosphates. In this work, sol-gel method was used to synthesize carbon coated lithium iron phosphates and nickel doped lithium iron phosphates, and their particle sizes were controlled in the nanometer to sub-micrometer range. The crystalline structures of the synthesized lithium iron phosphates were characterized by X-ray diffraction, and their morphologies were analyzed by scanning electron microscopy. To study their electrochemical properties, prototype lithium ion batteries were assembled with the synthesized lithium iron phosphates as cathode active materials, and with lithium metal discs as the anodes, and the discharge / charge properties and cycling behaviors of the prototype batteries were tested at different rates. The synthesized lithium iron phosphate materials exhibited high capacity and high cycling stability. It was confirmed that particle size reduction, carbon coating and metal doping are three effective approaches for increasing the conductivity of lithium iron phosphates, and thus improving their electrochemical properties. Experimental results show that by combing the three approaches for improving the electrochemical properties, lithium iron phosphate composites with characteristics favorable for their applications in lithium ion batteries for electric vehicles can be developed, including high specific capacity, high rate capacity, flat discharge voltage plateau and high retention ratio.

  16. Lithium insertion in graphite from ternary ionic liquid-lithium salt electrolytes: II. Evaluation of specific capacity and cycling efficiency and stability at room temperature

    NASA Astrophysics Data System (ADS)

    Lux, Simon F.; Schmuck, Martin; Appetecchi, Giovanni B.; Passerini, Stefano; Winter, Martin; Balducci, Andrea

    In this paper we report the results about the use of ternary room temperature ionic liquid-lithium salt mixtures as electrolytes for lithium-ion battery systems. Mixtures of N-methyl- N-propyl pyrrolidinium bis(fluorosulfonyl) imide, PYR 13FSI, and N-butyl- N-methylpyrrolidinium bis(trifluoromethansulfonyl) imide, PYR 14TFSI, with lithium hexafluorophosphate, LiPF 6 and lithium bis(trifluoromethansulfonyl) imide, LiTFSI, containing 5 wt.% of vinylene carbonate (VC) as additive, have been used in combination with a commercial graphite, KS6 TIMCAL. The performance of the graphite electrodes has been considered in term of specific capacity, cycling efficiency and cycling stability. The results clearly show the advantage of the use of ternary mixtures on the performance of the graphite electrode.

  17. Protected Sulfur Cathode with Mixed Conductive Coating Layer for Lithium Sulfur Battery

    NASA Astrophysics Data System (ADS)

    Jin, Jun; Wen, Zhaoyin; Wang, Qingsong; Gu, Sui; Huang, Xiao; Chen, Chunhua

    2016-10-01

    A mixed conductive coating layer composed of lithium ion conductive ceramic powder, carbon and binder was introduced on the surface of a sulfur electrode. This coating layer is designed to suppress the migration of lithium polysulfides from the sulfur electrode, and improve the cycling capacity of a lithium sulfur battery. The protected sulfur cathode with a mixed conductive coating layer delivered an initial specific capacity of 1236 mAh g-1 at 0.5C and maintained a capacity of 842 mAh g-1 after 100 cycles. In particular, a soft package battery with protected cathode exhibits improved cycling capacity and excellent rate performance.

  18. Primary Results of Lithium Coating for the Improvement of Plasma Performance in EAST

    NASA Astrophysics Data System (ADS)

    Zuo, Guizhong; Hu, Jiansheng; Li, Jiangang; Luo, Nanchang; Hu, Liqun; Fu, Jia; Chen, Kaiyun; Ti, Ang; Zhang, Lili

    2010-12-01

    First lithium coating associated with ion cyclotron range of frequency (ICRF) plasma was performed successfully in EAST. Results in reduction of both residual impurity and deuterium in the vacuum vessel were obtained. Particularly the partial pressure of deuterium after the lithium coating was reduced by about a factor of 5. Impurity radiation in the plasma was reduced and electron temperature increased by about 50%. Moreover, reproducible plasma discharges with high parameters, such as higher plasma current and density, could be easily obtained. These results showed that plasma performance was improved. Even though only 2 g of lithium were injected, the effective lifetime of the Li film was raised up to 40 shots.

  19. Key strategies for enhancing the cycling stability and rate capacity of LiNi0.5Mn1.5O4 as high-voltage cathode materials for high power lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Yi, Ting-Feng; Mei, Jie; Zhu, Yan-Rong

    2016-06-01

    Spinel LiNi0.5Mn1.5O4 (LNMO) is one of the most promising high voltage cathode materials for future application due to its advantages of large reversible capacity, high thermal stability, low cost, environmental friendliness, and high energy density. LNMO can provide 20% and 30% higher energy density than traditional cathode materials LiCoO2 and LiFePO4, respectively. Unfortunately, LNMO-based batteries with LiPF6-based carbonate electrolytes always suffer from severe capacity deterioration and poor thermostability because of the oxidization of organic carbonate solvents and decomposition of LiPF6, especially at elevated temperatures and water-containing environment. Hence, it is necessary to systematically and comprehensively summarize the progress in understanding and modifying LNMO cathode from various aspects. In this review, the structure, transport properties and different reported possible fading mechanisms of LNMO cathode are first discussed detailedly. And then, the major goal of this review is to highlight new progress in using proposed strategies to improve the cycling stability and rate capacity of LNMO-based batteries, including synthesis, control of special morphologies, element doping and surface coating etc., especially at elevated temperatures. Finally, an insight into the future research and further development of LNMO cathode is discussed.

  20. Hierarchical Mesoporous/Macroporous Perovskite La0.5Sr0.5CoO3-x Nanotubes: A Bifunctional Catalyst with Enhanced Activity and Cycle Stability for Rechargeable Lithium Oxygen Batteries.

    PubMed

    Liu, Guoxue; Chen, Hongbin; Xia, Lu; Wang, Suqing; Ding, Liang-Xin; Li, Dongdong; Xiao, Kang; Dai, Sheng; Wang, Haihui

    2015-10-14

    Perovskites show excellent specific catalytic activity toward both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in alkaline solutions; however, small surface areas of the perovskites synthesized by traditional sol-gel methods lead to low utilization of catalytic sites, which gives rise to poor Li-O2 batteries performance and restricts their application. Herein, a hierarchical mesporous/macroporous perovskite La0.5Sr0.5CoO3-x (HPN-LSC) nanotube is developed to promote its application in Li-O2 batteries. The HPN-LSC nanotubes were synthesized via electrospinning technique followed by postannealing. The as-prepared HPN-LSC catalyst exhibits outstanding intrinsic ORR and OER catalytic activity. The HPN-LSC/KB electrode displays excellent performance toward both discharge and charge processes for Li-O2 batteries, which enhances the reversibility, the round-trip efficiency, and the capacity of resultant batteries. The synergy of high catalytic activity and hierarchical mesoporous/macroporous nanotubular structure results in the Li-O2 batteries with good rate capability and excellent cycle stability of sustaining 50 cycles at a current density of 0.1 mA cm(-2) with an upper-limit capacity of 500 mAh g(-1). The results will benefit for the future development of high-performance Li-O2 batteries using hierarchical mesoporous/macroporous nanostructured perovskite-type catalysts.

  1. Lithium-cupric sulfide cell

    SciTech Connect

    Cuesta, A.J.; Bump, D.D.

    1980-01-01

    Lithium cells have become the primary power source for cardiac pacemakers due to their reliability and longevity at low current drain rates. A lithium-cupric sulfide cell was developed which makes maximum use of the shape of a pacemaker's battery compartment. The cell has a stable voltage throughout 90% of its lifetime. It then drops to a second stable voltage before depletion. The voltage drop creates a small decrease in pacemaker rate, which alerts the physician to replace the pacemaker. No loss of capacity due to self-discharge as been seen to date, and cells have proven to be safe under extreme conditions. 2 refs.

  2. Solid solution lithium alloy cermet anodes

    SciTech Connect

    Richardson, Thomas J.

    2013-07-09

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

  3. Surface protected lithium-metal-oxide electrodes

    DOEpatents

    Thackeray, Michael M.; Kang, Sun-Ho

    2016-04-05

    A lithium-metal-oxide positive electrode having a layered or spinel structure for a non-aqueous lithium electrochemical cell and battery is disclosed comprising electrode particles that are protected at the surface from undesirable effects, such as electrolyte oxidation, oxygen loss or dissolution by one or more lithium-metal-polyanionic compounds, such as a lithium-metal-phosphate or a lithium-metal-silicate material that can act as a solid electrolyte at or above the operating potential of the lithium-metal-oxide electrode. The surface protection significantly enhances the surface stability, rate capability and cycling stability of the lithium-metal-oxide electrodes, particularly when charged to high potentials.

  4. Lithium-Ion Batteries for Aerospace Applications

    NASA Technical Reports Server (NTRS)

    Surampudi, S.; Halpert, G.; Marsh, R. A.; James, R.

    1999-01-01

    This presentation reviews: (1) the goals and objectives, (2) the NASA and Airforce requirements, (3) the potential near term missions, (4) management approach, (5) the technical approach and (6) the program road map. The objectives of the program include: (1) develop high specific energy and long life lithium ion cells and smart batteries for aerospace and defense applications, (2) establish domestic production sources, and to demonstrate technological readiness for various missions. The management approach is to encourage the teaming of universities, R&D organizations, and battery manufacturing companies, to build on existing commercial and government technology, and to develop two sources for manufacturing cells and batteries. The technological approach includes: (1) develop advanced electrode materials and electrolytes to achieve improved low temperature performance and long cycle life, (2) optimize cell design to improve specific energy, cycle life and safety, (3) establish manufacturing processes to ensure predictable performance, (4) establish manufacturing processes to ensure predictable performance, (5) develop aerospace lithium ion cells in various AH sizes and voltages, (6) develop electronics for smart battery management, (7) develop a performance database required for various applications, and (8) demonstrate technology readiness for the various missions. Charts which review the requirements for the Li-ion battery development program are presented.

  5. Spectrophotometric determination of lithium ion using a water-soluble octabromoporphyrin in aqueous solution.

    PubMed

    Tabata, M; Nishimoto, J; Kusano, T

    1998-08-01

    A water-soluble porphyrin, (2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin; H(2)obtpps(4-)) was synthesized and developed for the determination of lithium ion in aqueous solution. The octabromo groups lower the basicity of the porphyrin by their electron-withdrawing effect, and enable the porphyrin to react with the lithium ion in alkaline solution to form the lithium complex along with a shift of absorption maximum: lambda max/nm (logepsilon/mol(-1) dm(3) cm(-1)) of the lithium porphyrin are 490.5 nm (5.31) and 734 nm (4.36). Sodium and potassium ions did not react with the porphyrin. The equilibrium constant for the reaction Li(+)+Hobtpps(5-)right harpoon over left harpoon[Li(obtpps)](5-)+H(+) was found to be 10(-8.80) and the conditional formation constant of the [Li(obtpps)](5-) at pH 13 is 10(4.21). The above results were applied to the determination of lithium ion in aqueous solution. The interference from transition and heavy metal ions was masked by using N,N'-1,2-ethanediylbis[N(carboxylmethy)glycinato]magnesium(II) ([Mg(edta)](2-)) solution. Absorbance at 490 nm was measured against a blank solution. A calibration graph was linear over the range of 0.007-0.7 mug cm(-3) (1x10(-6)-1x10(-4) mol dm(-3)) of lithium(I) with a correlation factor of 0.967. Lithium ion less than ppm level was determined spectrophtometrically in aqueous solution. The proposed method was applied to the determination of lithium in human serum and sea water samples.

  6. Fatigue in 0.5Li2MnO3:0.5Li(Ni1/3Co1/3Mn1/3)O2 positive electrodes for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Riekehr, Lars; Liu, Jinlong; Schwarz, Björn; Sigel, Florian; Kerkamm, Ingo; Xia, Yongyao; Ehrenberg, Helmut

    2016-09-01

    Two different Li-rich nickel-cobalt-manganese-oxide (Li-rich NCM) active materials with the same nominal composition 0.5Li2MnO3:0.5Li(Ni1/3Co1/3Mn1/3)O2 but different pristine nano structure have been analyzed structurally and electrochemically in different cycling states. For structural characterization, transmission electron microscopy (TEM) and high resolution synchrotron powder diffraction (S-XRD) experiments were conducted. The changes in structure with increasing cycle number are correlated with characteristic features in the corresponding electrochemical dQ/dV-profiles that were obtained by galvanostatically cycling the two different active materials. The presented data demonstrates that structural changes upon cycling, e.g. LiMnO2 and spinel formation, strongly depend on the degree oxygen is involved in the reversible charge compensation for delithiation/lithiation. According to our data, firstly a twin-like environment with nanometer dimensions is formed within the R-3m matrix during the initial cycle, which then gradually transforms into a spinel-like structure with increasing cycle number. As another result, we can show that Li2MnO3 to LiMnO2 transformation is not directly dependent in the irreversible oxygen loss in the first cycle but more importantly on transition metal migration. A model is presented explaining the dependency of LiMnO2 and spinel formation on the ability of Li-rich active materials to include oxygen in the charge compensation process.

  7. Lithium vanadium bronze thin films for electrochromic applications

    SciTech Connect

    Green, M.; Pita, K.

    1997-04-01

    Thin films of fine grained polycrystalline stoichiometric vanadium pentoxide (85{percent} of bulk density) have been prepared by vacuum evaporation. These films have been made into lithium vanadium bronze, Li{sub x}V{sub 2}O{sub 5}, by inserting lithium, either electrochemically or chemically. In addition, lithium vanadium bronze thin films have been prepared by co-evaporation of Li and V{sub 2}O{sub 5}. The optical properties, absorption and refractive index, have been measured from 2000 to about 200 nm. Strong absorption arises from indirect transitions across the main gap and is {approx}2.2 eV for x=0. The variation of the energy gap up to an x value of 2 has been obtained from the absorption data and the importance of irreversible phase changes noted. High x value bronze is useful as a counter electrode material in glazings, having an energy gap of about 3 eV. There is a considerable, technologically significant, band tail in the absorption spectrum thought to arise from polaronic-type states, perhaps modified by the presence of guest species ions. The optical behavior upon lithium electrochemical insertion has also been examined. It is found that nonstoichiometry gives rise to an overall reduction in optical change per guest atom inserted. These effects are fast compared with electrochemical insertion times. {copyright} {ital 1997 American Institute of Physics.}

  8. 49 CFR 173.185 - Lithium cells and batteries.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 49 Transportation 2 2013-10-01 2013-10-01 false Lithium cells and batteries. 173.185 Section 173... Class 7 § 173.185 Lithium cells and batteries. (a) Cells and batteries. A lithium cell or battery, including a lithium polymer cell or battery and a lithium-ion cell or battery, must conform to all of...

  9. 49 CFR 173.185 - Lithium cells and batteries.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 49 Transportation 2 2012-10-01 2012-10-01 false Lithium cells and batteries. 173.185 Section 173... Class 7 § 173.185 Lithium cells and batteries. (a) Cells and batteries. A lithium cell or battery, including a lithium polymer cell or battery and a lithium-ion cell or battery, must conform to all of...

  10. 49 CFR 173.185 - Lithium cells and batteries.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Lithium cells and batteries. 173.185 Section 173... Class 7 § 173.185 Lithium cells and batteries. (a) Cells and batteries. A lithium cell or battery, including a lithium polymer cell or battery and a lithium-ion cell or battery, must conform to all of...

  11. 49 CFR 173.185 - Lithium cells and batteries.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 2 2011-10-01 2011-10-01 false Lithium cells and batteries. 173.185 Section 173... Class 7 § 173.185 Lithium cells and batteries. (a) Cells and batteries. A lithium cell or battery, including a lithium polymer cell or battery and a lithium-ion cell or battery, must conform to all of...

  12. Role of lithium augmentation in the management of major depressive disorder.

    PubMed

    Bauer, Michael; Adli, Mazda; Ricken, Roland; Severus, Emanuel; Pilhatsch, Maximilian

    2014-04-01

    The high rate of non-responders to initial treatment with antidepressants requires subsequent treatment strategies such as augmentation of antidepressants. Clinical guidelines recommend lithium augmentation as a first-line treatment strategy for non-responding depressed patients. The objectives of this review were to discuss the current place of lithium augmentation in the management of treatment-resistant depression and to review novel findings concerning lithium's mechanisms of action. We conducted a comprehensive and critical review of randomized, placebo-controlled trials, controlled and naturalistic comparator studies, and continuation-phase and discontinuation studies of lithium augmentation in major depression. The outcomes of interest were efficacy, factors allowing outcome prediction and results from preclinical studies investigating molecular mechanisms of lithium action. Substantial efficacy of lithium augmentation in the acute treatment of major depression has been demonstrated in more than 30 open-label studies and 10 placebo-controlled trials. In a meta-analysis addressing the efficacy of lithium in 10 randomized, controlled trials, it had a significant positive effect versus placebo, with an odds ratio of 3.11 corresponding to a number-needed-to-treat (NNT) of 5 and a mean response rate of 41.2% (versus 14.4% in the placebo group). The main limitations of these studies were the relatively small numbers of study participants and the fact that most studies included augmentation of tricyclic antidepressants, which are not in widespread use anymore. Evidence from continuation-phase studies is sparse but suggests that lithium augmentation should be maintained in the lithium-antidepressant combination for at least 1 year to prevent early relapses. Concerning outcome prediction, single studies have reported associations of better outcome rates with more severe depressive symptomatology, significant weight loss, psychomotor retardation, a history of more

  13. Efficiently photo-charging lithium-ion battery by perovskite solar cell.

    PubMed

    Xu, Jiantie; Chen, Yonghua; Dai, Liming

    2015-08-27

    Electric vehicles using lithium-ion battery pack(s) for propulsion have recently attracted a great deal of interest. The large-scale practical application of battery electric vehicles may not be realized unless lithium-ion batteries with self-charging suppliers will be developed. Solar cells offer an attractive option for directly photo-charging lithium-ion batteries. Here we demonstrate the use of perovskite solar cell packs with four single CH3NH3PbI3 based solar cells connected in series for directly photo-charging lithium-ion batteries assembled with a LiFePO4 cathode and a Li4Ti5O12 anode. Our device shows a high overall photo-electric conversion and storage efficiency of 7.80% and excellent cycling stability, which outperforms other reported lithium-ion batteries, lithium-air batteries, flow batteries and super-capacitors integrated with a photo-charging component. The newly developed self-chargeable units based on integrated perovskite solar cells and lithium-ion batteries hold promise for various potential applications.

  14. Hydrothermal synthesis and characterization of titanium dioxide nanotubes as novel lithium adsorbents

    SciTech Connect

    Moazeni, Maryam; Hajipour, Hengameh; Askari, Masoud; Nusheh, Mohammad

    2015-01-15

    The ion exchange process is a promising method for lithium extraction from brine and seawater having low concentrations of this element. To achieve this goal, it is vital to use an effective adsorbent with maximum lithium adsorption potential together with a stable structure during extraction and insertion of the ions. In this study, titanium dioxide and then lithium titanate spinel with nanotube morphology was synthesized via a simple two-step hydrothermal process. The produced Li{sub 4}Ti{sub 5}O{sub 12} spinel ternary oxide nanotube with about 70 nm diameter was then treated with dilute acidic solution in order to prepare an adsorbent suitable for lithium adsorption from local brine. Morphological and phase analysis of the obtained nanostructured samples were done by using transmission and scanning electron microscopes along with X-ray diffraction. Lithium ion exchange capacity of this adsorbent was finally evaluated by means of adsorption isotherm. The results showed titanium dioxide adsorbent could recover 39.43 mg/g of the lithium present in 120 mg/L of lithium solution.

  15. [Elevated serum lithium concentration due to switch from parenteral nutrition alone to parenteral with enteral nutrition].

    PubMed

    Goto, Hidekazu; Tomita, Takashi; Doki, Shotaro; Nakanishi, Rie; Kojima, Chikako; Yoneshima, Mihoko; Yoshida, Tadashi; Tanaka, Katsuya; Kohda, Yukinao

    2015-01-01

    We report a patient with elevated serum lithium concentration caused by switching from parenteral nutrition alone to parenteral with enteral nutrition. A 73-year-old female inpatient was treated with lithium carbonate 600 mg/d for manic episodes of bipolar disorder. Her serum lithium level was maintained at 0.57-0.79 mEq/L. She was administered total parenteral nutrition owing to difficulty in oral intake. Her diet contained 4.8-5.8 g/d of sodium chloride. After this, parenteral with enteral nutrition was initiated. The total sodium chloride intake decreased from 6.3 to 3.0-4.0 g/d following this change. On day 15 after initiation of parenteral with enteral nutrition, her serum lithium level increased to 1.17 mEq/L, which is closer to the upper therapeutic range limit. Therefore enteral nutrition was stopped immediately, and an electrolyte solution was administered instead of enteral nutrition. An antibiotic agent was also simultaneously administered because of infection. The total amount of sodium chloride administered was increased to 7.0 g/d during this treatment. Four days after treatment, the serum lithium level returned to 0.57 mEq/L. This case suggests that administration of appropriate sodium chloride nutrition is important during treatment with lithium carbonate, because disposition of lithium ion is paralleled to that of sodium.

  16. Early-life exposure to lithium and boron from drinking water.

    PubMed

    Harari, Florencia; Ronco, Ana María; Concha, Gabriela; Llanos, Miguel; Grandér, Margaretha; Castro, Francisca; Palm, Brita; Nermell, Barbro; Vahter, Marie

    2012-12-01

    The transfer of lithium and boron from exposed mothers to fetuses and breast-fed infants was investigated in areas in northern Argentina and Chile with up to 700 μg lithium/L and 5-10 mg boron/L in drinking water. Maternal and cord blood concentrations were strongly correlated and similar in size for both lithium (47 and 70 μg/L, respectively) and boron (220 and 145 μg/L, respectively). The first infant urine produced after birth contained the highest concentrations (up to 1700 μg lithium/L and 14,000 μg boron/L). Breast-milk contained 40 and 60% of maternal blood concentrations of lithium and boron, respectively (i.e. about 30 and 250 μg/L, respectively, in high exposure areas), and infant urine concentrations decreased immediately after birth (120 μg lithium/L and 920 μg boron/L). We conclude that lithium and boron easily passed the placenta to the fetus, and that exclusively breast-fed infants seemed to have lower exposure than formula-fed infants.

  17. Lithium Decreases Glial Fibrillary Acidic Protein in a Mouse Model of Alexander Disease.

    PubMed

    LaPash Daniels, Christine M; Paffenroth, Elizabeth; Austin, Elizabeth V; Glebov, Konstantin; Lewis, Diana; Walter, Jochen; Messing, Albee

    2015-01-01

    Alexander disease is a fatal neurodegenerative disease caused by mutations in the astrocyte intermediate filament glial fibrillary acidic protein (GFAP). The disease is characterized by elevated levels of GFAP and the formation of protein aggregates, known as Rosenthal fibers, within astrocytes. Lithium has previously been shown to decrease protein aggregates by increasing the autophagy pathway for protein degradation. In addition, lithium has also been reported to decrease activation of the transcription factor STAT3, which is a regulator of GFAP transcription and astrogliogenesis. Here we tested whether lithium treatment would decrease levels of GFAP in a mouse model of Alexander disease. Mice with the Gfap-R236H point mutation were fed lithium food pellets for 4 to 8 weeks. Four weeks of treatment with LiCl at 0.5% in food pellets decreased GFAP protein and transcripts in several brain regions, although with mild side effects and some mortality. Extending the duration of treatment to 8 weeks resulted in higher mortality, and again with a decrease in GFAP in the surviving animals. Indicators of autophagy, such as LC3, were not increased, suggesting that lithium may decrease levels of GFAP through other pathways. Lithium reduced the levels of phosphorylated STAT3, suggesting this as one pathway mediating the effects on GFAP. In conclusion, lithium has the potential to decrease GFAP levels in Alexander disease, but with a narrow therapeutic window separating efficacy and toxicity.

  18. Stabilizing lithium metal using ionic liquids for long-lived batteries

    PubMed Central

    Basile, A.; Bhatt, A. I.; O'Mullane, A. P.

    2016-01-01

    Suppressing dendrite formation at lithium metal anodes during cycling is critical for the implementation of future lithium metal-based battery technology. Here we report that it can be achieved via the facile process of immersing the electrodes in ionic liquid electrolytes for a period of time before battery assembly. This creates a durable and lithium ion-permeable solid–electrolyte interphase that allows safe charge–discharge cycling of commercially applicable Li|electrolyte|LiFePO4 batteries for 1,000 cycles with Coulombic efficiencies >99.5%. The tailored solid–electrolyte interphase is prepared using a variety of electrolytes based on the N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide room temperature ionic liquid containing lithium salts. The formation is both time- and lithium salt-dependant, showing dynamic morphology changes, which when optimized prevent dendrite formation and consumption of electrolyte during cycling. This work illustrates that a simple, effective and industrially applicable lithium metal pretreatment process results in a commercially viable cycle life for a lithium metal battery. PMID:27292652

  19. Efficiently photo-charging lithium-ion battery by perovskite solar cell

    NASA Astrophysics Data System (ADS)

    Xu, Jiantie; Chen, Yonghua; Dai, Liming

    2015-08-01

    Electric vehicles using lithium-ion battery pack(s) for propulsion have recently attracted a great deal of interest. The large-scale practical application of battery electric vehicles may not be realized unless lithium-ion batteries with self-charging suppliers will be developed. Solar cells offer an attractive option for directly photo-charging lithium-ion batteries. Here we demonstrate the use of perovskite solar cell packs with four single CH3NH3PbI3 based solar cells connected in series for directly photo-charging lithium-ion batteries assembled with a LiFePO4 cathode and a Li4Ti5O12 anode. Our device shows a high overall photo-electric conversion and storage efficiency of 7.80% and excellent cycling stability, which outperforms other reported lithium-ion batteries, lithium-air batteries, flow batteries and super-capacitors integrated with a photo-charging component. The newly developed self-chargeable units based on integrated perovskite solar cells and lithium-ion batteries hold promise for various potential applications.

  20. Stabilizing lithium metal using ionic liquids for long-lived batteries.

    PubMed

    Basile, A; Bhatt, A I; O'Mullane, A P

    2016-06-13

    Suppressing dendrite formation at lithium metal anodes during cycling is critical for the implementation of future lithium metal-based battery technology. Here we report that it can be achieved via the facile process of immersing the electrodes in ionic liquid electrolytes for a period of time before battery assembly. This creates a durable and lithium ion-permeable solid-electrolyte interphase that allows safe charge-discharge cycling of commercially applicable Li|electrolyte|LiFePO4 batteries for 1,000 cycles with Coulombic efficiencies >99.5%. The tailored solid-electrolyte interphase is prepared using a variety of electrolytes based on the N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide room temperature ionic liquid containing lithium salts. The formation is both time- and lithium salt-dependant, showing dynamic morphology changes, which when optimized prevent dendrite formation and consumption of electrolyte during cycling. This work illustrates that a simple, effective and industrially applicable lithium metal pretreatment process results in a commercially viable cycle life for a lithium metal battery.

  1. Quantum Monte Carlo methods and lithium cluster properties

    SciTech Connect

    Owen, R.K.

    1990-12-01

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

  2. Quantum Monte Carlo methods and lithium cluster properties. [Atomic clusters

    SciTech Connect

    Owen, R.K.

    1990-12-01

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

  3. Protective Effects of Lithium on Sumatriptan-Induced Memory Impairment in Mice.

    PubMed

    Nikoui, Vahid; Javadi-Paydar, Mehrak; Salehi, Mahtab; Behestani, Selda; Dehpour, Ahmad-Reza

    2016-04-01

    Lithium is a drug used for the treatment of bipolar disorder. It has several mechanisms of action, and recently it is shown that lithium can antagonize the 5-HT1B/1D serotonin receptors. Sumatriptan is a 5-HT1B/1D receptor agonist used for the treatment of cluster headaches and migraine which might cause memory impairment as a potential side effect. In this study, effects of lithium on sumatriptan-induced memory impairment have been determined in a two-trial recognition Y-maze and passive avoidance tests. Male mice weighing 25-30 g were divided into several groups randomly. In Y-maze test, effects of lithium (1,5,10,20,40,80 mg/kg) and sumatriptan (1,5,10 mg/kg) were assessed on memory acquisition, then lithium (0.1,1,10 mg/kg) and sumatriptan (1,10 mg/kg) were studied in passive avoidance test. Effects of lithium (1mg/kg) on sumatriptan (10 mg/kg)-induced memory impairment were studied in both of tests. The present study demonstrated that sumatriptan impaired memory in Y-maze and passive avoidance tests (P<0.05, P<0.01, respectively). Lithium did not show any significant effect on memory function compared to saline-treated control group in both tests (P>0.05), but significantly reversed sumatriptan-induced memory impairment in Y-maze and passive avoidance tests (P<0.001, P<0.05, respectively). It is concluded that lithium reverses the sumatriptan-induced memory impairment probably through 5-HT1B/1D receptors antagonism.

  4. Heat capacities of the water + lithium bromide + ethanolamine and water + lithium bromide + 1,3-propanediol systems

    SciTech Connect

    Kim, J.S.; Park, Y.; Lee, H.; Yu, S.I.

    1997-03-01

    Heat capacities of the water + lithium bromide + ethanolamine (LiBr/H{sub 2}N(CH{sub 2}){sub 2}OH mass ratio = 3.5) and water + lithium bromide + 1,3-propanediol (LiBr/HO(CH{sub 2}){sub 3}OH mass ratio = 3.5) systems were measured by using an isoperibol solution calorimeter at four temperatures (283.15, 298.15, 313.15, and 333.15 K) and absorbent (LiBr + H{sub 2}N(CH{sub 2}){sub 2}OH and LiBr + HO(CH{sub 2}){sub 3}OH) concentration ranges of (29.2 to 70.7)% and (30.7 to 68.3)%, respectively. The measured values were fitted with a simple equation by a least-squares method and the average absolute deviations between experimental and calculated values were 0.21% for the water + lithium bromide + ethanolamine system and 0.15% for the water + lithium bromide + 1,3-propanediol system, respectively.

  5. Method for producing a secondary lithium cell comprising a heat-sensitive protective mechanism

    DOEpatents

    Ullrich, Matthias; Bechtold, Dieter; Rabenstein, Heinrich; Brohm, Thomas

    2003-01-01

    A method for producing a secondary lithium cell which has at least one lithium-cycling negative electrode, at least one lithium-intercalating positive electrode, at least one separator disposed between the positive and the negative electrode, and a nonaqueous lithium ion-conducting electrolyte. The method is carried out by the electrodes and/or the separator being coated, by means of electrostatic powder coating, with wax particles which are insoluble in the electrolyte and have a melting temperature of from about 50 to about 150 .degree. C. and a mean particle size of from about 6 to about 20 .mu.m, the amount of wax being between about 0.5 and about 2.5 mg/cm.sup.2 of electrode area.

  6. Evaluation of tantalum-alloy-clad uranium mononitride fuel specimens from 7500-hour, 1040 C pumped-lithium-loop test

    NASA Technical Reports Server (NTRS)

    Watson, G. K.

    1974-01-01

    Simulated nuclear fuel element specimens, consisting of uranium mononitride (UN) fuel cylinders clad with tungsten-lined T-111, were exposed for up to 7500 hr at 1040 C (1900 F) in a pumped-lithium loop. The lithium flow velocity was 1.5 m/sec (5 ft/sec) in the specimen test section. No evidence of any compatibility problems between the specimens and the flowing lithium was found based on appearance, weight change, chemistry, and metallography. Direct exposure of the UN to the lithium through a simulated cladding crack resulted in some erosion of the UN in the area of the defect. The T-111 cladding was ductile after lithium exposure, but it was sensitive to hydrogen embrittlement during post-test handling.

  7. Analysis of the Galvanostatic Intermittent Titration Technique (GITT) as applied to a lithium-ion porous electrode

    NASA Astrophysics Data System (ADS)

    Dees, Dennis W.; Kawauchi, Shigehiro; Abraham, Daniel P.; Prakash, Jai

    Galvanostatic Intermittent Titration Technique (GITT) experiments were conducted to determine the lithium diffusion coefficient of LiNi 0.8Co 0.15Al 0.05O 2, used as the active material in a lithium-ion battery porous composite positive electrode. An electrochemical model, based on concentrated solution porous electrode theory, was developed to analyze the GITT experimental results and compare to the original GITT analytical theory. The GITT experimental studies on the oxide active material were conducted between 3.5 and 4.5 V vs. lithium, with the maximum lithium diffusion coefficient value being 10 -10 cm 2 s -1 at 3.85 V. The lithium diffusion coefficient values obtained from this study agree favorably with the values obtained from an earlier electrochemical impedance spectroscopy study.

  8. Analysis of the Galvanostatic Intermittent Titration Technique (GITT) as applied to a lithium-Ion porous electrode.

    SciTech Connect

    Dees, D. W.; Kawauchi, S.; Abraham, D. P.; Prakash, J.; Chemical Sciences and Engineering Division; Toyota Central R&D Labs Inc.; Illinois Inst. of Tech.

    2009-04-01

    Galvanostatic Intermittent Titration Technique (GITT) experiments were conducted to determine the lithium diffusion coefficient of LiNi{sub 0.8}Co{sub 0.15}Al{sub 0.05}O{sub 2}, used as the active material in a lithium-ion battery porous composite positive electrode. An electrochemical model, based on concentrated solution porous electrode theory, was developed to analyze the GITT experimental results and compare to the original GITT analytical theory. The GITT experimental studies on the oxide active material were conducted between 3.5 and 4.5 V vs. lithium, with the maximum lithium diffusion coefficient value being 10{sup -10} cm{sup 2} s{sup -1} at 3.85 V. The lithium diffusion coefficient values obtained from this study agree favorably with the values obtained from an earlier electrochemical impedance spectroscopy study.

  9. Lithium-free transition metal monoxides for positive electrodes in lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Jung, Sung-Kyun; Kim, Hyunchul; Cho, Min Gee; Cho, Sung-Pyo; Lee, Byungju; Kim, Hyungsub; Park, Young-Uk; Hong, Jihyun; Park, Kyu-Young; Yoon, Gabin; Seong, Won Mo; Cho, Yongbeom; Oh, Myoung Hwan; Kim, Haegyeom; Gwon, Hyeokjo; Hwang, Insang; Hyeon, Taeghwan; Yoon, Won-Sub; Kang, Kisuk

    2017-01-01

    Lithium-ion batteries based on intercalation compounds have dominated the advanced portable energy storage market. The positive electrode materials in these batteries belong to a material group of lithium-conducting crystals that contain redox-active transition metal and lithium. Materials without lithium-conducting paths or lithium-free compounds could be rarely used as positive electrodes due to the incapability of reversible lithium intercalation or the necessity of using metallic lithium as negative electrodes. These constraints have significantly limited the choice of materials and retarded the development of new positive electrodes in lithium-ion batteries. Here, we demonstrate that lithium-free transition metal monoxides that do not contain lithium-conducting paths in their crystal structure can be converted into high-capacity positive electrodes in the electrochemical cell by initially decorating the monoxide surface with nanosized lithium fluoride. This unusual electrochemical behaviour is attributed to a surface conversion reaction mechanism in contrast with the classic lithium intercalation reaction. Our findings will offer a potential new path in the design of positive electrode materials in lithium-ion batteries.

  10. Anode material for lithium batteries

    DOEpatents

    Belharouak, Ilias; Amine, Khalil

    2011-04-05

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

  11. Anode material for lithium batteries

    DOEpatents

    Belharouak, Ilias [Westmont, IL; Amine, Khalil [Downers Grove, IL

    2012-01-31

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

  12. Anode material for lithium batteries

    DOEpatents

    Belharouak, Ilias; Amine, Khalil

    2008-06-24

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

  13. Lithium equation-of-state

    SciTech Connect

    Blink, J.A.

    1983-09-01

    In 1977, Dave Young published an equation-of-state (EOS) for lithium. This EOS was used by Lew Glenn in his AFTON calculations of the HYLIFE inertial-fusion-reactor hydrodynamics. In this paper, I summarize Young's development of the EOS and demonstrate a computer program (MATHSY) that plots isotherms, isentropes and constant energy lines on a P-V diagram.

  14. New electrolytes and electrolyte additives to improve the low temperature performance of lithium-ion batteries

    SciTech Connect

    Yang, Xiao-Qing

    2008-08-31

    In this program, two different approaches were undertaken to improve the role of electrolyte at low temperature performance - through the improvement in (i) ionic conductivity and (ii) interfacial behavior. Several different types of electrolytes were prepared to examine the feasibil.ity of using these new electrolytes in rechargeable lithium-ion cells in the temperature range of +40°C to -40°C. The feasibility studies include (a) conductivity measurements of the electrolytes, (b) impedance measurements of lithium-ion cells using the screened electrolytes with di.fferent electrochemical history such as [(i) fresh cells prior to formation cycles, (ii) after first charge, and (iii) after first discharge], (c) electrical performance of the cells at room temperatures, and (d) charge discharge behavior at various low temperatures. Among the different types of electrolytes investigated in Phase I and Phase II of this SBIR project, carbonate-based LiPF6 electrolytes with the proposed additives and the low viscous ester as a third component to the carbonate-based LiPF6 electrolytes show promising results at low temperatures. The latter electrolytes deliver over 80% of room temperature capacity at -20{degrees}C when the lithium-ion cells containing these electrolytes were charged at -20 °C. Also, there was no lithium plating when the lithium­-ion cells using C-C composite anode and LiPF{sub 6} in EC/EMC/MP electrolyte were charged at -20{degrees}C at C/5 rate. The studies of ionic conductivity and AC impedance of these new electrolytes, as well as the charge discharge characteristics of lithium-ion cells using these new electrolytes at various low temperatures provide new findings: The reduced capacity and power capability, as well as the problem of lithium plating at low temperatures charging of lithium-ion cells are primarily due to slow the lithium-ion intercalation/de-intercalation kinetics in the carbon structure.

  15. Conference report on the 3rd International Symposium on Lithium Application for Fusion Devices

    DOE PAGES

    Mazzitelli, Guiseppe; Hirooka, Y.; Hu, J. S.; ...

    2015-01-14

    The third International Symposium on Lithium Application for Fusion Device (ISLA-2013) was held on 9-11 October 2013 at ENEA Frascati Centre with growing participation and interest from the community working on more general aspect of liquid metal research for fusion energy development. ISLA-2013 has been confirmed to be the largest and the most important meeting dedicated to liquid metal application for the magnetic fusion research. Overall, 45 presentation plus 5 posters were given, representing 28 institutions from 11 countries. The latest experimental results from nine magnetic fusion devices were presented in 16 presentations from NSTX (PPPL, USA), FTU (ENEA, Italy),more » T-11M (Trinity, RF), T-10 (Kurchatov Institute, RF), TJ-II (CIEMAT, Spain), EAST(ASIPP, China), HT-7 (ASIPP, China), RFX (Padova, Italy), KTM (NNC RK, Kazakhstan). Sessions were devoted to the following: (I) lithium in magnetic confinement experiments (facility overviews), (II) lithium in magnetic confinement experiments (topical issues), (III) special session on liquid lithium technology, (IV) lithium laboratory test stands, (V) Lithium theory/modelling/comments, (VI) innovative lithium applications and (VII) special Session on lithium-safety and lithium handling. There was a wide participation from the fusion technology communities, including IFMIF and TBM communities providing productive exchange with the physics oriented magnetic confinement liquid metal research groups. Furthermore, this international workshop will continue on a biennial basis (alternating with the Plasma-Surface Interactions (PSI) Conference) and the next workshop will be held at CIEMAT, Madrid, Spain, in 2015.« less

  16. Novel carbonaceous materials for lithium secondary batteries

    SciTech Connect

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

    1997-07-01

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

  17. Status of lithium-filled specimen subcapsules for the HFIR-MFE-RB10J experiment

    SciTech Connect

    Robertson, J.P.; Howell, M.; Lenox, K.E.

    1998-09-01

    The HFIR-MFE-RB-10J experiment will be irradiated in a Removable Beryllium position in the HFIR for 10 reactor cycles, accumulating approximately 5 dpa in steel. The upper region of the capsule contains two lithium-filled subcapsules containing vanadium specimens. This report describes the techniques developed to achieve a satisfactory lithium fill with a specimen occupancy of 26% in each subcapsule.

  18. Determination of the heat capacities of Lithium/BCX (bromide chloride in thionyl chloride) batteries

    NASA Astrophysics Data System (ADS)

    Kubow, Stephen A.; Takeuchi, Kenneth J.; Takeuchi, Esther S.

    1989-12-01

    Heat capacities of twelve different Lithium/BCX (BrCl in thionyl chloride) batteries in sizes AA, C, D, and DD were determined. Procedures and measurement results are reported. The procedure allowed simple, reproducible, and precise determinations of heat capacities of industrially important Lithium/BCX cells, without interfering with performance of the cells. Use of aluminum standards allowed the accuracy of the measurements to be maintained. The measured heat capacities were within 5 percent of calculated heat capacity values.

  19. Determination of the heat capacities of Lithium/BCX (bromide chloride in thionyl chloride) batteries

    NASA Technical Reports Server (NTRS)

    Kubow, Stephen A.; Takeuchi, Kenneth J.; Takeuchi, Esther S.

    1989-01-01

    Heat capacities of twelve different Lithium/BCX (BrCl in thionyl chloride) batteries in sizes AA, C, D, and DD were determined. Procedures and measurement results are reported. The procedure allowed simple, reproducible, and precise determinations of heat capacities of industrially important Lithium/BCX cells, without interfering with performance of the cells. Use of aluminum standards allowed the accuracy of the measurements to be maintained. The measured heat capacities were within 5 percent of calculated heat capacity values.

  20. Chemical Shuttle Additives in Lithium Ion Batteries

    SciTech Connect

    Patterson, Mary

    2013-03-31

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

  1. Lithium and the kidney: an updated review.

    PubMed

    Gitlin, M

    1999-03-01

    Despite the availability of alternative agents, lithium continues to be the standard against which all mood stabilisers, prescribed for acute and maintenance treatment of bipolar (and, to a lesser extent, unipolar) mood disorders, are compared. As a medication often used on a maintenance basis for a lifelong disorder, the potential for lithium to cause long term organ toxicity has generated appropriate concern. Foremost among these concerns are its renal effects. Lithium adversely affects renal tubular function, causing polyuria secondary to a deficit in urine concentrating ability. This effect is probably progressive for the first decade of lithium therapy, i.e. it correlates with duration of lithium therapy. Although this effect of lithium is probably functional and reversible early in treatment, it may become structural and irreversible over time. In contrast, the effect of lithium on glomerular function is not progressive. Conclusions in this area are hampered by the evidence that patients with psychiatric disorders who are not receiving lithium also show defects in certain aspects of renal function. Despite the generally sanguine data on glomerular function, a very small group of patients may develop renal insufficiency due to lithium (possibly in conjunction with other somatic factors) in the form of interstitial nephritis. However, for the vast majority of patients, the renal effects of lithium are benign. Current strategies for minimising the renal effects of lithium include: (i) assiduously avoiding episodes of renal toxicity; (ii) monitoring serum lithium concentrations in order to achieve optimal efficacy at the lowest possible concentration; (iii) monitoring serum creatinine levels on a yearly basis, getting further medical evaluation when the serum creatinine level consistently rises above 140 mmol/L (1.6 mg/dl); and (iv) possibly administering lithium once a day.

  2. Velocity Measurements of Thermoelectric Driven Flowing Liquid Lithium

    NASA Astrophysics Data System (ADS)

    Szott, Matthew; Xu, Wenyu; Fiflis, Peter; Haehnlein, Ian; Kapat, Aveek; Kalathiparambil, Kishor; Ruzic, David N.

    2014-10-01

    Liquid lithium has garnered additional attention as a PFC due to its several advantages over solid PFCs, including reduced erosion and thermal fatigue, increased heat transfer, higher device lifetime, and enhanced plasma performance due to the establishment of low recycling regimes at the wall. The Lithium Metal Infused Trenches concept (LiMIT) has demonstrated thermoelectric magnetohydrodynamic flow of liquid lithium through horizontal open-faced metal trenches with measured velocities varying from 3.7+/-0.5 cm/s in the 1.76 T field of HT-7 to 22+/-3 cm/s in the SLiDE facility at UIUC at 0.059 T. To demonstrate the versatility of the concept, a new LiMIT design using narrower trenches shows steady state, thermoelectric-driven flow at an arbitrary angle from horizontal. Velocity characteristics are measured and discussed. Based on this LiMIT concept, a new limiter design has been developed to be tested on the mid-plane of the EAST plasma. Preliminary modelling suggests lithium flow of 6 cm/s in this device. Additionally, recent testing at the Magnum-PSI facility has given encouraging results, and velocity measurements in relation to magnetic field strength and plasma flux are also presented.

  3. Electrochemical Intercalation of Lithium Ions into Carbon Nanotube Bundles

    NASA Astrophysics Data System (ADS)

    Allen, J. L.; Sumanasekera, G. U.; Rao, A. M.; Fang, S.; Eklund, P. C.

    1998-03-01

    We have investigated the electrochemical intercalation of lithium ions into ropes of single-walled carbon nanotubes (SWNTs) in a standard three electrode cell. The SWNT mat pressed onto a Pt plate was the working electrode. Lithium was used at both the counter and reference electrodes, and 1M LiAsF6 in ethylene carbonate:diethyl carbonate (1:1 by volume) served as the electrolyte. Raman spectra of the SWNTs were recorded in situ as a function of electrochemical charge using 514.5 nm excitation. During galvanostatic intercalation, we observed a relatively steep decrease in voltage until a plateau at around 1.2 V is reached. We attribute this initial decrease to the intercalation of lithium into SWNT and a concurrent electron doping of the SWNT π band. In the Raman spectrum, as the voltage reaches 1.2 V, the tangential mode frequency down shifted from 1593 cm-1 to 1591 cm-1 consistent with electron addition to the π^* band. We speculate that surface reactions of the lithium doped SWNT and the electrolyte are occuring during the plateau. During the evolution of the plateau, the Raman signal of the tangential mode gradually diminishes without further downshift of the its frequency and eventually disappears completely. Cyclic voltammograms show a minimum at around 1.2 V and peaks at around 0.7 V and 1.7 V. The origin of this structure is not presently understood.

  4. Lithium-Sulfur Batteries: from Liquid to Solid Cells?

    SciTech Connect

    Lin, Zhan; Liang, Chengdu

    2015-01-01

    Lithium-sulfur (Li-S) batteries supply a theoretical specific energy 5 times higher than that of lithium-ion batteries (2,500 vs. ~500 Wh kg-1). However, the insulating properties and polysulfide shuttle effects of the sulfur cathode and the safety concerns of the lithium anode in liquid electrolytes are still key limitations to practical use of traditional Li-S batteries. In this review, we start with a brief discussion on fundamentals of Li-S batteries and key challenges associated with the conventional liquid cells. Then, we introduce the most recent progresses in the liquid systems, including the sulfur positive electrodes, the lithium negative electrodes, and the electrolytes and binders. We discuss the significance of investigating electrode reaction mechanisms in liquid cells using in-situ techniques to monitor the compositional and morphological changes. By moving from the traditional liquid cells to recent solid cells, we discuss the importance of this game-changing shift with positive advances in both solid electrolytes and electrode materials. Finally, the opportunities and perspectives for future research on Li-S batteries are presented.

  5. Lithium-Sulfur Batteries: from Liquid to Solid Cells?

    DOE PAGES

    Lin, Zhan; Liang, Chengdu

    2015-01-01

    Lithium-sulfur (Li-S) batteries supply a theoretical specific energy 5 times higher than that of lithium-ion batteries (2,500 vs. ~500 Wh kg-1). However, the insulating properties and polysulfide shuttle effects of the sulfur cathode and the safety concerns of the lithium anode in liquid electrolytes are still key limitations to practical use of traditional Li-S batteries. In this review, we start with a brief discussion on fundamentals of Li-S batteries and key challenges associated with the conventional liquid cells. Then, we introduce the most recent progresses in the liquid systems, including the sulfur positive electrodes, the lithium negative electrodes, and themore » electrolytes and binders. We discuss the significance of investigating electrode reaction mechanisms in liquid cells using in-situ techniques to monitor the compositional and morphological changes. By moving from the traditional liquid cells to recent solid cells, we discuss the importance of this game-changing shift with positive advances in both solid electrolytes and electrode materials. Finally, the opportunities and perspectives for future research on Li-S batteries are presented.« less

  6. Characterization of Lithium Borohydride using Neutron Scattering Techniques

    NASA Astrophysics Data System (ADS)

    Hartman, Michael; Rush, Jack; Udovic, Terry

    2006-03-01

    Lithium borohydride, LiBH4, is a complex metal hydride that shows great promise as a hydrogen storage medium with a volumetric hydrogen density of 122 kg H/m^3 and a gravimetric hydrogen density of 18.5 wt. %. While numerous NMR, Raman, and infrared investigations have been reported in the literature, neutron scattering investigations of LiBH4 have been limited due to the large neutron absorption cross-section of naturally occurring lithium and boron. We have recently synthesized an isotopically-enriched lithium borohydride, containing ^7Li and ^11B, which eliminates the large neutron absorption cross-section that arises from the presence of ^6Li and ^10B. The results of powder neutron diffraction, inelastic neutron scattering, and quasi-elastic neutron scattering investigations on the ^7Li^11BH4 material are presented. These measurements provide a fundamental understanding of the behavior of hydrogen within lithium borohydride, and they provide a basis to understand changes concomitant with the introduction of catalytic or destabilizing compounds.

  7. Fast lithium-ion conducting thin-film electrolytes integrated directly on flexible substrates for high-power solid-state batteries.

    PubMed

    Ihlefeld, Jon F; Clem, Paul G; Doyle, Barney L; Kotula, Paul G; Fenton, Kyle R; Apblett, Christopher A

    2011-12-15

    By utilizing an equilibrium processing strategy that enables co-firing of oxides and base metals, a means to integrate the lithium-stable fast lithium-ion conductor lanthanum lithium tantalate directly with a thin copper foil current collector appropriate for a solid-state battery is presented. This resulting thin-film electrolyte possesses a room temperature lithium-ion conductivity of 1.5 × 10(-5) S cm(-1) , which has the potential to increase the power of a solid-state battery over current state of the art.

  8. Primary lithium cell life studies

    NASA Technical Reports Server (NTRS)

    Capulli, John; Donley, Sam; Deligiannis, Frank; Shen, David

    1990-01-01

    One solution for providing a truly independent power source is to package, within the critical subsystem element, a primary battery that can remain dormant for time periods as long as the mission life, which can be 10-15 years, maximum. When primary power from the spacecraft solar array/battery system is interrupted, the backup battery system, which is connected through a diode to the power input line, would automatically support the load to avoid a power interruption to the critical load for a time period long enough to ensure that ground control could access the satellite and correct the anomaly by sending appropriate commands to the spacecraft. Critical subsystems identified for the application are telemetry and command circuits, volatile computer memory, attitude control circuits, and some critical payloads. Due to volume packaging and weight restrictions that exist on most spacecraft, coupled with the long storage periods required, lithium cell technology was selected for the backup power source. Because of the high energy density (200-400 Wh/kg), long shelf life, and load capability, soluble cathode primary lithium technology was chosen. The most important lithium cell properties that require detail characterization for this application are capacity loss, shelf life, and the voltage delay mechanism. These are functions of storage time and temperature. During storage, a passive film builds up on the lithium electrode. The film protects the lithium electrode from progressive capacity decay but requires time to break down when a load is applied. This phenomenon results in a depressed voltage during the period of film breakdown which can last from fractions of a second to minutes.

  9. The lithium vapor box divertor

    DOE PAGES

    Goldston, R. J.; Myers, R.; Schwartz, J.

    2016-01-13

    It has long been recognized that volumetric dissipation of the plasma heat flux from a fusion power system is preferable to its localized impingement on a material surface. Volumetric dissipation mitigates both the anticipated very high heat flux and intense particle-induced damage due to sputtering. Our recent projections to a tokamak demonstration power plant suggest an immense upstream parallel heat flux, of order 20 GW m-2, implying that fully detached operation may be a requirement for the success of fusion power. Building on pioneering work on the use of lithium by Nagayama et al and by Ono et al asmore » well as earlier work on the gas box divertor by Watkins and Rebut, we present here a concept for a lithium vapor box divertor, in which lithium vapor extracts momentum and energy from a fusion-power-plant divertor plasma, using fully volumetric processes. Furthermore, at the high powers and pressures that are projected this requires a high density of lithium vapor, which must be isolated from the main plasma in order to avoid lithium build-up on the chamber walls or in the plasma. Isolation is achieved through a powerful multi-box differential pumping scheme available only for condensable vapors. The preliminary box-wise calculations are encouraging, but much more work is required in order to demonstrate the practical viability of this scheme, taking into account at least 2D plasma and vapor flows within and between the vapor boxes and out of the vapor boxes to the main plasma.« less

  10. The lithium vapor box divertor

    SciTech Connect

    Goldston, R. J.; Myers, R.; Schwartz, J.

    2016-01-13

    It has long been recognized that volumetric dissipation of the plasma heat flux from a fusion power system is preferable to its localized impingement on a material surface. Volumetric dissipation mitigates both the anticipated very high heat flux and intense particle-induced damage due to sputtering. Our recent projections to a tokamak demonstration power plant suggest an immense upstream parallel heat flux, of order 20 GW m-2, implying that fully detached operation may be a requirement for the success of fusion power. Building on pioneering work on the use of lithium by Nagayama et al and by Ono et al as well as earlier work on the gas box divertor by Watkins and Rebut, we present here a concept for a lithium vapor box divertor, in which lithium vapor extracts momentum and energy from a fusion-power-plant divertor plasma, using fully volumetric processes. Furthermore, at the high powers and pressures that are projected this requires a high density of lithium vapor, which must be isolated from the main plasma in order to avoid lithium build-up on the chamber walls or in the plasma. Isolation is achieved through a powerful multi-box differential pumping scheme available only for condensable vapors. The preliminary box-wise calculations are encouraging, but much more work is required in order to demonstrate the practical viability of this scheme, taking into account at least 2D plasma and vapor flows within and between the vapor boxes and out of the vapor boxes to the main plasma.

  11. What do patients in a lithium outpatient clinic know about lithium therapy?

    PubMed Central

    Schaub, Rainer T.; Berghoefer, Anne; Müller-Oerlinghausen, Bruno

    2001-01-01

    Objective To determine how much patients know about lithium therapy and to examine factors that might influence this knowledge. Setting Lithium outpatient clinic. Patients Patients (n = 123) affiliated with a lithium outpatient clinic (mean treatment duration of 12 years). Diagnoses, according to the Diagnostic and Statistical Manual of Mental Disorders, 3rd edition, revised, included bipolar disorder, recurrent unipolar depression and schizoaffective disorder. Outcome measures Quantitative assessment of lithium-related knowledge, obtained by responses to a questionnaire adapted from the Lithium Knowledge Test, and factors affecting this knowledge. Results Age was negatively correlated with lithium therapy knowledge scores, whereas duration of treatment, sex, education and diagnosis appeared to be unrelated to knowledge. Conclusion Patient education about lithium treatment should be intensified, especially for older patients taking lithium because adverse drug reactions pose a greater risk to the elderly. PMID:11590971

  12. Lithium cell technology and safety report of the Tri-Service Lithium Safety Committee

    NASA Technical Reports Server (NTRS)

    Reiss, E.

    1980-01-01

    The organization of the Tri-Service Lithium Safety Committee is described. The following areas concerning lithium batteries are discussed: transportation--DOT Exemption 7052, FAA; disposal; storage; individual testing/test results; and battery design and usage.

  13. Light-assisted delithiation of lithium iron phosphate nanocrystals towards photo-rechargeable lithium ion batteries.

    PubMed

    Paolella, Andrea; Faure, Cyril; Bertoni, Giovanni; Marras, Sergio; Guerfi, Abdelbast; Darwiche, Ali; Hovington, Pierre; Commarieu, Basile; Wang, Zhuoran; Prato, Mirko; Colombo, Massimo; Monaco, Simone; Zhu, Wen; Feng, Zimin; Vijh, Ashok; George, Chandramohan; Demopoulos, George P; Armand, Michel; Zaghib, Karim

    2017-04-10

    Recently, intensive efforts are dedicated to convert and store the solar energy in a single device. Herein, dye-synthesized solar cell technology is combined with lithium-ion materials to investigate light-assisted battery charging. In particular we report the direct photo-oxidation of lithium iron phosphate nanocrystals in the presence of a dye as a hybrid photo-cathode in a two-electrode system, with lithium metal as anode and lithium hexafluorophosphate in carbonate-based electrolyte; a configuration corresponding to lithium ion battery charging. Dye-sensitization generates electron-hole pairs with the holes aiding the delithiation of lithium iron phosphate at the cathode and electrons utilized in the formation of a solid electrolyte interface at the anode via oxygen reduction. Lithium iron phosphate acts effectively as a reversible redox agent for the regeneration of the dye. Our findings provide possibilities in advancing the design principles for photo-rechargeable lithium ion batteries.

  14. Repeated administration of histamine improves memory retrieval of inhibitory avoidance by lithium in mice.

    PubMed

    Zarrindast, Mohammad Reza; Parsaei, Leila; Ahmadi, Shamseddin

    2008-01-01

    The influence of repeated administration of histamine on lithium-induced state dependency has been investigated. A single-trial step-down inhibitory avoidance task was used to assess memory in adult male NMRI mice. Intraperitoneal (i.p.) administration of lithium (10 mg/kg), immediately after training (post-training), impaired inhibitory avoidance memory on the test day. Pre-test administration of lithium reversed amnesia induced by the drug given after training, with the maximum response at a dose of 10 mg/kg. Repeated intracerebroventricular (i.c.v.) administration of histamine (20 microg/mouse) for 3 consecutive days followed by 5 days of no drug treatment improved memory retrieval of inhibitory avoidance by a pre-test lower dose (5 mg/kg i.p.) of lithium. In contrast, 3 days of i.c.v. injections of both the histamine H1 receptor antagonist pyrilamine (40 microg/mouse) and the histamine H2 receptor antagonist ranitidine (6.25 and 12.5 microg/mouse) prevented the improving effect of pre-test lithium (10 mg/kg i.p.) on memory retrieval. The results suggest that the repeated administration of histaminergic agents may induce a sensitization which affects the memory impairment induced by lithium.

  15. [Lithium can be given to patients on haemodialysis treatment].

    PubMed

    Kancir, Anne Sophie Pinholt; Viftrup, Jens Emil; Pedersen, Erling Bjerregaard

    2015-01-26

    Lithium-induced nephropathy is a known complication of lithium treatment in bipolar disorder. Treatment with lithium should be discontinued, if there is evidence of lithium-induced nephropathy. However, lithium can be given to patients with end-stage-renal-disease on haemodialysis treatment, if there is no other way to control the bipolar disorder. We report one patient who was successfully treated with lithium in parallel with haemodialysis.

  16. Lithium-Excess Research of Cathode Material Li2MnTiO4 for Lithium-Ion Batteries

    PubMed Central

    Zhang, Xinyi; Yang, Le; Hao, Feng; Chen, Haosen; Yang, Meng; Fang, Daining

    2015-01-01

    Lithium-excess and nano-sized Li2+xMn1−x/2TiO4 (x = 0, 0.2, 0.4) cathode materials were synthesized via a sol-gel method. The X-ray diffraction (XRD) experiments indicate that the obtained main phases of Li2.0MnTiO4 and the lithium-excess materials are monoclinic and cubic, respectively. The scanning electron microscope (SEM) images show that the as-prepared particles are well distributed and the primary particles have an average size of about 20–30 nm. The further electrochemical tests reveal that the charge-discharge performance of the material improves remarkably with the lithium content increasing. Particularly, the first discharging capacity at the current of 30 mA g−1 increases from 112.2 mAh g−1 of Li2.0MnTiO4 to 187.5 mAh g−1 of Li2.4Mn0.8TiO4. In addition, the ex situ XRD experiments indicate that the monoclinic Li2MnTiO4 tends to transform to an amorphous state with the extraction of lithium ions, while the cubic Li2MnTiO4 phase shows better structural reversibility and stability.

  17. Mesoporous Nitrogen-Doped Carbon-LiSICON Glass Ceramics as High Performance Cathodes in Solid-State Lithium Oxygen Batteries

    DTIC Science & Technology

    2013-03-18

    SUBTITLE MESOPOROUS NITROGEN-DOPED CARBON-LiSICON GLASS CERAMICS AS HIGH PERFORMANCE CATHODES IN SOLID-STATE LITHIUM -OXYGEN BATTERIES (POSTPRINT) 5a...AFRL-RQ-WP-TP-2015-0054 MESOPOROUS NITROGEN-DOPED CARBON-LiSICON GLASS CERAMICS AS HIGH PERFORMANCE CATHODES IN SOLID-STATE LITHIUM -OXYGEN...superior electrochemical activity of composite 3 for the reduction of oxygen and the higher ionic conductivity of LAGP to transport lithium ions in the

  18. Hydrogen storage properties of lithium silicon alloy synthesized by mechanical alloying

    NASA Astrophysics Data System (ADS)

    Doi, Koichi; Hino, Satoshi; Miyaoka, Hiroki; Ichikawa, Takayuki; Kojima, Yoshitsugu

    A lithium silicon alloy was synthesized by mechanical alloying method. Hydrogen storage properties of this Li-Si-H system were studied. During hydrogenation of the lithium silicon alloy, lithium atom was extracted from the alloy and lithium hydride was generated. Equilibrium hydrogen pressures for desorption and absorption reactions were measured in a temperature range from 400 to 500 °C to investigate the thermodynamic characteristics of the system, which can reversibly store 5.4 mass% hydrogen with smaller reaction enthalpy than simple metal Li. Li absorbing alloys, which have been widely studied as a negative electrode material for Li ion rechargeable batteries, can be used as hydrogen storage materials with high hydrogen capacity.

  19. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

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

    2008-12-23

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

  20. Prismatic cell lithium-ion battery using lithium manganese oxide

    SciTech Connect

    Ehrlich, G.M.; Hellen, R.M.; Reddy, T.B.

    1997-12-01

    Lithium-ion (Li-ion) batteries have demonstrated the ability to fulfill the energy storage needs of many new technologies. The most significant drawbacks of currently available technologies, such as LiCoO{sub 2} based Li-ion cells, is their high cost and significant environmental hazards. Li-ion cells which use a lithium manganese oxide (LiMn{sub 2}O{sub 4}) spinel based cathode material should be much less costly and safer than LiCoO{sub 2} based cells. Performance data from prismatic design cells which use a LiMn{sub 2}O{sub 4} based cathode material is presented and shown to meet many military performance criteria. The most significant drawback of this technology, at the present time, is the short cycle life.