WorldWideScience

Sample records for hung-fai li

  1. Li(+) solvation in glyme-Li salt solvate ionic liquids.

    Science.gov (United States)

    Ueno, Kazuhide; Tatara, Ryoichi; Tsuzuki, Seiji; Saito, Soshi; Doi, Hiroyuki; Yoshida, Kazuki; Mandai, Toshihiko; Matsugami, Masaru; Umebayashi, Yasuhiro; Dokko, Kaoru; Watanabe, Masayoshi

    2015-03-28

    Certain molten complexes of Li salts and solvents can be regarded as ionic liquids. In this study, the local structure of Li(+) ions in equimolar mixtures ([Li(glyme)]X) of glymes (G3: triglyme and G4: tetraglyme) and Li salts (LiX: lithium bis(trifluoromethanesulfonyl)amide (Li[TFSA]), lithium bis(pentafluoroethanesulfonyl)amide (Li[BETI]), lithium trifluoromethanesulfonate (Li[OTf]), LiBF4, LiClO4, LiNO3, and lithium trifluoroacetate (Li[TFA])) was investigated to discriminate between solvate ionic liquids and concentrated solutions. Raman spectra and ab initio molecular orbital calculations have shown that the glyme molecules adopt a crown-ether like conformation to form a monomeric [Li(glyme)](+) in the molten state. Further, Raman spectroscopic analysis allowed us to estimate the fraction of the free glyme in [Li(glyme)]X. The amount of free glyme was estimated to be a few percent in [Li(glyme)]X with perfluorosulfonylamide type anions, and thereby could be regarded as solvate ionic liquids. Other equimolar mixtures of [Li(glyme)]X were found to contain a considerable amount of free glyme, and they were categorized as traditional concentrated solutions. The activity of Li(+) in the glyme-Li salt mixtures was also evaluated by measuring the electrode potential of Li/Li(+) as a function of concentration, by using concentration cells against a reference electrode. At a higher concentration of Li salt, the amount of free glyme diminishes and affects the electrode reaction, leading to a drastic increase in the electrode potential. Unlike conventional electrolytes (dilute and concentrated solutions), the significantly high electrode potential found in the solvate ILs indicates that the solvation of Li(+) by the glyme forms stable and discrete solvate ions ([Li(glyme)](+)) in the molten state. This anomalous Li(+) solvation may have a great impact on the electrode reactions in Li batteries.

  2. Presence of Li Clusters in Molten LiCl-Li

    Science.gov (United States)

    Merwin, Augustus; Phillips, William C.; Williamson, Mark A.; Willit, James L.; Motsegood, Perry N.; Chidambaram, Dev

    2016-05-01

    Molten mixtures of lithium chloride and metallic lithium are of significant interest in various metal oxide reduction processes. These solutions have been reported to exhibit seemingly anomalous physical characteristics that lack a comprehensive explanation. In the current work, the physical chemistry of molten solutions of lithium chloride and metallic lithium, with and without lithium oxide, was investigated using in situ Raman spectroscopy. The Raman spectra obtained from these solutions were in agreement with the previously reported spectrum of the lithium cluster, Li8. This observation is indicative of a nanofluid type colloidal suspension of Li8 in a molten salt matrix. It is suggested that the formation and suspension of lithium clusters in lithium chloride is the cause of various phenomena exhibited by these solutions that were previously unexplainable.

  3. BARCELONA & Li-Fi

    OpenAIRE

    Verdú Leal, Adrián

    2016-01-01

    Project focused on the study of the possibility of introducing the Li-Fi technology in the city of Barcelona as a pioneering example of Smart City. Proyecto enfocado al estudio de la posibilidad de implantar la tecnología Li-Fi en la ciudad de Barcelona como ejemplo pionero de Smart City. Projecte enfocat a l'estudi de la possibilidad d'implantació la tecnologia Li-Fi a la ciudad de Barcelona com exemple innovador de Smart City.

  4. Dance Researcher Li Yayuan

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    Li Yayuan, a dance researcher with the China National Song and Dance Ensemble,choreographs African-inspired dances. Over 40 years old,she performed and taught in African countries, traveling to Senegal to learn the country’s dances in 1990,

  5. With or without "Li."

    Science.gov (United States)

    Wang, Mingquan

    1990-01-01

    Demonstrates how the important distinction between the locative and nonlocative implication of a noun is essential for the presence of the Chinese locative particle "li," identifying groups of nouns that can not take the particle, nouns that optionally use the particle, and nouns that must use the particle. (CB)

  6. LiDy(PO34

    Directory of Open Access Journals (Sweden)

    Fathia Chehimi-Moumen

    2008-07-01

    Full Text Available Single crystals of lithium dysprosium polyphosphate, LiDy(PO34, were prepared by the flux method. The atomic arrangement is built up by infinite (PO3n chains extending along the b axis. Dy3+ and Li+ cations alternate in the middle of four such chains, with Dy...Li distances of 3.54 (1 and 3.48 (1 Å. The DyO8 dodecahedra and LiO4 tetrahedra deviate significantly from the ideal geometry. Both Dy and Li occupy special positions (Wyckoff position 4e, site symmetry 2.

  7. Li-Fraumeni syndrome.

    Science.gov (United States)

    Ossa, Carlos Andrés; Molina, Gustavo; Cock-Rada, Alicia María

    2016-06-03

    The Li-Fraumeni syndrome is characterized clinically by the appearance of tumors in multiple organs generally at an early age. This hereditary condition is caused by germinal mutations in the TP53 gene, which codifies for the tumoural suppressor gene p53. We present the case of a patient aged 31 with clinical and molecular diagnosis of Li-Fraumeni syndrome who presented two synchronous tumors: a leiomyosarcoma on the forearm and a phyllodes breast tumour. She had a family history of cancer, including a son diagnosed with a cortical adrenal carcinoma when he was three years old, who died at five from the disease. Furthermore, her maternal grandmother and great-grandmother died of stomach cancer at 56 and 60 years old, respectively, while her other great-grandmother and a great aunt presented with breast cancer at the ages of 60 and 40, respectively. After genetic counseling, complete sequencing and analysis of duplications and deletions in the TP53 gene were ordered prior to diagnosis. The molecular analysis of a DNA sample taken from peripheral blood lymphocytes revealed the germinal mutation c.527G>T (p.Cys176Phe) on exon 5 of the TP53 gene, a deleterious mutation described previously in tumoural tissues. To our knowledge, this is the first published case in Colombia of Li-Fraumeni syndrome with confirmed molecular diagnosis. The diagnosis and management of Li-Fraumeni syndrome should be performed by a multidisciplinary team, and genetic counselling should be offered to patients and their relatives.

  8. Legendary Story of Li Xiaoli

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    IN a building in Fangzhuang’s residentquarters lives an old woman of Chinesedescent.Not so unusual you would thinkexcept that she holds an American passportand all her descendants have typical Westemcountenances.This American Chinese womanis called Li Xiaoli. In 1916 Li Xiaoli,originally named LiYueying,was born into a rich and influentialfamily in Lishi,Shanxi Province.Her fatherjoined the army after the Revolution of 1911.

  9. Electric dipolarizability of 7Li

    Indian Academy of Sciences (India)

    Sudhir R Jain; Arun K Jain; S Kailas

    2008-12-01

    We calculate the electric dipolarizability of 7Li nucleus within the cluster model and estimate a value of about 0.0188 fm3. We also discuss the possibility of observing this in the scattering of 7Li from a 208Pb target at energies about 30 MeV.

  10. Electronic Properties of LiFePO4 and Li doped LiFePO4

    Energy Technology Data Exchange (ETDEWEB)

    Allen, J.L.; Zhuang, G.V.; Ross, P.N.; Guo, J.-H.; Jow, T.R.

    2006-05-31

    LiFePO{sub 4} has several potential advantages in comparison to the transition metal oxide cathode materials used in commercial lithium-ion batteries. However, its low intrinsic electronic conductivity ({approx} 10{sup -9} S/cm) is problematic. We report here a study by soft x-ray absorption/emission spectroscopy of the electronic properties of undoped LiFePO{sub 4} and Li-doped LiFePO{sub 4} in which Li{sup +} ions are substituted for Fe{sup 2+} ions in an attempt to increase the intrinsic electronic conductivity. The conductivities of the Li{sub 1+x}Fe{sub 1-x}PO{sub 4} samples were, however, essentially unchanged from that of the undoped LiFePO{sub 4}. Nonetheless, evidence for changing the electronic properties of LiFePO{sub 4} by doping with excess Li+ was observed by the XAS/XES spectroscopy. New pre-edge features the O-1s XAS spectrum of Li{sub 1.05}Fe{sub 0.95}PO4 is a direct indication that the charge compensation for substitution of Fe{sup 2+} by Li{sup +} resides in the unoccupied O-2p orbitals. A charge transfer (CT) excitation was also observed in the doped material implying that the unoccupied O-2p orbitals created by doping are strongly hybridized with unoccupied Fe-3d orbitals of neighboring sites. However, the strong covalent bonding within the (PO{sub 4}){sup 3-} anions and the large separation of the Fe cations means that the charge created by doping is not delocalized in the manner of electrons or holes in a semiconductor.

  11. Enhanced Li-Ion Battery

    Directory of Open Access Journals (Sweden)

    Natasha Ross

    2015-01-01

    Full Text Available Au with Pd nanoparticles were synthesized and coated onto the spinel LiMn2O4 via a coprecipitation calcination method with the objective to improve the microstructure, conductivity, and electrochemical activities of pristine LiMn2O4. The novel LiPdAuxMn2-xO4 composite cathode had high phase purity, well crystallized particles, and more regular morphological structures with narrow size distributions. At enlarged cycling potential ranges the LiPdAuxMn2-xO4 sample delivered 90 mAh g−1 discharge capacity compared to LiMn2O4 (45 mAh g−1. It was concluded that even a small amount of the Pd and Au enhanced both the lithium diffusivity and electrochemical conductivity of the host sample due to the beneficial properties of their synergy.

  12. Electron-impact Ionization Of Li2 And Li+2

    Energy Technology Data Exchange (ETDEWEB)

    Colgan, James P [Los Alamos National Laboratory

    2008-01-01

    Electron-impact ionization cross sections for Li{sub 2} and Li{sup +}{sub 2} are calculated using a configuration-average distorted-wave method. Bound orbitals for the molecule and its ions are calculated using a single configuration self-consistent field method based on a linear combination of Slater-type orbitals. The bound orbitals are transformed onto a two-dimensional lattice ({tau}, {theta}), which is variable in the radial coordinate and constant in the angular coordinate, from which Hartree with local exchange potentials are constructed. The single particle Schrodinger equation is then solved for continuum distorted-waves with S-matrix boundary conditions. Total ionization cross sections for Li{sub 2} at an equilibrium internuclear separation of R = 5.0 and for Li{sup +}{sub 2} at an equilibrium internuclear separation of R = 5.9 are presented.

  13. Core TuLiP

    OpenAIRE

    Czenko, M.R.; Etalle, Sandro

    2007-01-01

    We propose CoreTuLiP - the core of a trust management language based on Logic Programming. CoreTuLiP is based on a subset of moded logic programming, but enjoys the features of TM languages such as RT; in particular clauses are issued by different authorities and stored in a distributed manner. We present a lookup and inference algorithm which we prove to be correct and complete w.r.t. the declarative semantics. CoreTuLiP enjoys uniform syntax and the well-established semantics and is express...

  14. Polymorphism of LiAg

    Science.gov (United States)

    Pavlyuk, V. V.; Dmytriv, G. S.; Tarasiuk, I. I.; Chumak, I. V.; Pauly, H.; Ehrenberg, H.

    2010-02-01

    A phase transition from the cubic CsCl-type structure (Pm-3m space group) into a tetragonal UPb-type structure (I4 1/amd) is observed for the LiAg binary compound at ambient conditions. The crystal structure of the tetragonal modification of the LiAg binary compound was solved by direct methods in SHELXS on the base of structure factors which were extracted from a powder diffraction pattern and refined by SHELXL and the Rietveld method ( a = 3.9605(1), c = 8.2825(2) Å, Bragg R-factor = 4.81, Rf-factor = 4.87). Elevated temperatures and/or a small Li-excess versus the equimolar composition favour the cubic structure whereas ambient and lower temperatures and/or a small Li-deficiency stabilize the tetragonal structure. This reconstructive transition is reversible but proceeds slowly.

  15. The Rise of Gong Li

    Institute of Scientific and Technical Information of China (English)

    1994-01-01

    THE advance of Chinese history and the development of the film industry have brought out a new generation of movie stars. Among them Gong Li is the most charming and most well known in the world. Gong Li was born in 1963, the youngest of five children in a family of intellectuals. Both her parents teach at a university. She liked to sing and dance since childhood and early on displayed

  16. LiFi

    Institute of Scientific and Technical Information of China (English)

    2013-01-01

    利用闪烁的灯光来传输数字信息.这个过程被称为可见光通讯(VLC),人们常把它亲切地称为“LiFi”,以示它可能给目前以WiFi为代表的无线网络传输技术带来革命性的改变。最近,复旦大学计算机科学技术学院传出消息,一种利用屋内可见光传输网络信号的国际前沿通讯技术在实验室获得验证。研究人员将网络信号接入一盏1W的LED灯珠,灯光下的四台电脑即可上网,最高速率可达3.25G,平均上网速率达到150M。

  17. Structure and properties of Li-rich Zn-doped LiNbO3 Crystal

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The Li-rich Zn-doped LiNbO3 (LN) crystals were grown by the Czochralski method. The structure of the crystals was measured by ultraviolet-visible absorption spectra. The results indicated that the Li-rich Zn-doped LN crystals had the same characteristics as the pure LN crystal. After Zn2+ entered into the lattice of Li-rich Zn-doped LN crystal, it replaced NbLi firstly. When there was no NbLi, Zn2+ replaced Li+ then. The second harmonic generation (SHG) property of Li-rich Zn-doped LiNbO3 crystal was measured. The results showed that the SHG conversation efficiency of Li-rich Zn-doped LiNbO3 crystals was higher than that of Zn-doped LiNbO3 crystals.

  18. Transport properties derived from ion-atom collisions: 6Li-6Li+ and 6Li-7Li+ Cases

    Science.gov (United States)

    Bouledroua, Moncef; Bouchelaghem, Fouzia; LPR Team

    2014-10-01

    This investigation treats quantum-mechanically the ion- atom collisions and computes the transport coefficients, such as the coefficients of mobility and diffusion. For the case of lithium, the calculations start by determining the gerade and ungerade potential curves through which ionic lithium approaches ground lithium. Then, by considering the isotopic effects and nuclear spins, the elastic and charge-transfer cross sections are calculated for the case of 6Li+and7Li+ colliding with 6Li. Finally, the temperature-dependent diffusion and mobility coefficients are analyzed, and the results are contrasted with those obtained from literature. The main results of this work have been recently published in. This work has been realized within the frames of the CNEPRU Project D01120110036 of the Algerian Ministry of Higher Education.

  19. Genetics Home Reference: Li-Fraumeni syndrome

    Science.gov (United States)

    ... Facebook Share on Twitter Your Guide to Understanding Genetic Conditions Search MENU Toggle navigation Home Page Search ... Conditions Genes Chromosomes & mtDNA Resources Help Me Understand Genetics Home Health Conditions Li-Fraumeni syndrome Li-Fraumeni ...

  20. 2002 Willapa Bay LiDAR Project

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — NOAA contracted with Spencer B. Gross, Inc. (SBG) to obtain airborne LiDAR of Willapa Bay, Washington during low tide conditions. The LiDAR data was processed to...

  1. Development of Advanced Li Rich xLi2MO3 (1 x)LiMO2 Composite Cathode for High Capacity Li Ion Batteries

    Science.gov (United States)

    2016-12-22

    powders. The XRD spectra were collected in a range of 2θ values from 10 o to 70 o at a scanning rate of 0.5 degrees per min and a step size of 0.02 o...AFRL-AFOSR-JP-TR-2017-0003 Development of Advanced Li Rich xLi2MO3-(1-x)LiMO2 Composite Cathode for High Capacity Li Ion Batteries Kuan-Zong Fung...Li Rich xLi2MO3-(1-x)LiMO2 Composite Cathode for High Capacity Li Ion Batteries 5a.  CONTRACT NUMBER 5b.  GRANT NUMBER FA2386-15-1-4115 5c.  PROGRAM

  2. Electrochemical Investigations of the Interface at Li/Li+ Ion Conducting Channel

    Science.gov (United States)

    2006-10-04

    acetone consisting of LiBF4 as the supporting electrolyte. Unlike the powdery deposits of LiPc obtained by using tetrabutyl ammonium perchlorate (TBAP...as the supporting electrolyte, the deposits are adherent to the substrates when LiBF4 is used as the supporting electrolyte. Chemical oxidation of...Li2Pc by TBAP is shown to be detrimental for the formation of powdery electrodeposits of LiPc, whereas LiBF4 does not oxidize Li2Pc and therefore

  3. Reactions of metallic Li or LiC6 with organic solvents for lithium ion battery

    Science.gov (United States)

    Nakajima, Tsuyoshi; Hirobayashi, Yuki; Takayanagi, Yuki; Ohzawa, Yoshimi

    2013-12-01

    DSC (Differential Scanning Calorimetry) study has been made on the reactions of metallic Li or LiC6 with organic solvents for lithium ion battery. Ethylene carbonate (EC) more easily reacts with metallic Li and LiC6 than propylene carbonate (PC). This may be because formation of lithium alkyl carbonate is more difficult for PC than EC. On the other hand, diethyl carbonate (DEC), ethyl methyl carbonate (EMC) and dimethyl carbonate (DMC) react with Li in the same manner. Reactions of Li and LiC6 with organic solvents have been discussed based on the results of quantum calculation.

  4. Calibration of Li-glass Detector Efficiency

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    Li-glass detector will be used to measure the flux of neutron beam in Gamma-ray Total Absorption Facility(GTAF). We have calibrated the detection efficiency of Li-glass detector in 5SDH-2 accelerator. The beam of neutron was produced by the reaction 7Li

  5. Li Shuirong and his success

    Institute of Scientific and Technical Information of China (English)

    DENG Qiwei

    2009-01-01

    @@ Li Shuirong,the CEO of Rongsheng Holding Group,was famous for his business talent.He started his business with eight shuttle weaving machines and 200 thousands Yuan assets in 1 989.In that year,all the enterprises of China faced several problems,like credit squeeze,expenditure decline and dropping rate of production.

  6. Li Na Aces French Open

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    Chinese tennis player becomes the first Asian to win a Grand Slam singles title Chinese tennis player Li Na beat defending champion Francesca Schiavone from Italy,6-4,7-6,on the clay court at Roland Garros,winning the 2011 French Open Tennis Tournament on June 4.She made history by becoming the first Chinese to win a grand slam singles title.

  7. 6Li/7Li estimates for metal-poor stars

    CERN Document Server

    Perez, A E Garcia; Inoue, S; Ryan, S G; Suzuki, T K; Chiba, M

    2009-01-01

    The presence of the lithium-6 isotope in some metal-poor stars is a matter of surprise because of the high values observed. Non-standard models of Big Bang nucleosynthesis and pre-Galactic cosmic ray fusion and spallation have been proposed to explain these values. However, the observations of this light isotope are challenging which may make some detections disputable. The goal was to determine 6Li/7Li for a sample of metal-poor stars; three of them have been previously studied and the remaining two are new for this type of study. The purpose was to increase, if possible, the number of lithium-6 detections and to confirm previously published results. Spectra of the resonance doublet line of neutral lithium Li I 670.78nm were taken with the High Dispersion Spectrograph at the Subaru 8.2m-telescope for a sample of five metal-poor stars (-3.12 < [Fe/H] < -2.19). The contribution of lithium-6 to the total observed line profile was estimated from the 1D-LTE analysis of the line asymmetry. Observed asymmetri...

  8. Neutron Transfer reactions induced by 8Li on 9Be

    CERN Document Server

    Guimarães, V; Amro, H; Assunção, M; Barioni, A; Becchetti, F D; Carmargo, O; Garcia, H; Jiang, H; Kolata, J J; Lichtenthäler, R; Lizcano, D; Martines-Quiroz, E; Jiang, Hao

    2007-01-01

    Angular distributions for the elastic scattering of 8Li on 9Be and the neutron transfer reactions 9Be(8Li,7Li)10Be and 9Be(8Li,9Li)8Be have been measured with a 27 MeV 8Li radioactive nuclear beam. Spectroscopic factors for 8Li|n=9Li and 7Li|n=8Li bound systems were obtained from the comparison between the experimental differential cross section and finite-range DWBA calculations with the code FRESCO. The spectroscopic factors obtained are compared to shell model calculations and to other experimental values from (d,p) reactions. Using the present values for the spectroscopic factor, cross sections for the direct neutron-capture reactions 7Li(n,g)8Li and 8Li(n,g)9Li were calculated in the framework of a potential model.

  9. Li-Fi (Light - Fidelity)

    OpenAIRE

    Svensson, Martin

    2016-01-01

    Dagligen blir vi ombedda att stänga av elektroniska apparater som kan sända och mottaga radiosignaler, speciellt i flygplan och sjukhusmiljöer där radiovågor kan störa viktig utrustning. Detta kan snart vara ett minne blott. En ny trådlös överförings teknik, Li-Fi, baserar sig på ljusvågor som till skillnad från radiovågor (Wi-Fi) inte stör känsliga instrument. Även om Li-Fi ännu är i sin linda kan man ana att det finns stor utvecklingspotential. I denna rapport sammanställs befintlig litterä...

  10. CASTABILITY OF Al-Li-Mg AND Al-Li-Cu-Mg ALLOYS

    OpenAIRE

    1987-01-01

    The objective of the present work is to study the casting characteristics of various Al-Li alloys, which include fluidity and strengths of the alloys and their interaction with cast molds. Materials investigated are Al-Li-Mg and Al-Li-Cu-Mg alloys with Li content of 2.5 wt%. The results show that sand molds with resin binders are good for Al-Li casting. Ceramic coatings can further reduce the metal-mold interactions. However, the permeability is also reduced by coating. The fluidity of Li-bea...

  11. Üliõpilase meelespea

    Index Scriptorium Estoniae

    2001-01-01

    16. aprill. TPÜ valitsuse otsus nr. 3 kõlab nii : alustada TPÜ lõpetanutele UNESCO, Euroopa Nõukogu ja Euroopa Komisjoni ühise töögrupi poolt välja töötatud ingliskeelse ülikooli diplomi lisa Diplome Supplement (DS) väljastamist üliõpilase soovil ; kinnitada Diploma Supplementì väljastamise kord ja vormistamise maksumus 500 krooni : [täistekst

  12. Üliõpilase meelespea

    Index Scriptorium Estoniae

    2001-01-01

    16. aprill. TPÜ valitsuse otsus nr. 3 kõlab nii : alustada TPÜ lõpetanutele UNESCO, Euroopa Nõukogu ja Euroopa Komisjoni ühise töögrupi poolt välja töötatud ingliskeelse ülikooli diplomi lisa Diplome Supplement (DS) väljastamist üliõpilase soovil ; kinnitada Diploma Supplementì väljastamise kord ja vormistamise maksumus 500 krooni : [täistekst

  13. Preparation and characterization of poly(lithium acrylate-arcylonitrile)/LiClO4-LiNO3-LiBr solid polymer electrolytes

    Institute of Scientific and Technical Information of China (English)

    PAN Chun-yue; YUAN Yun-lan; CHEN Zhen-hua; XU Xian-hua; ZHANG Jian

    2005-01-01

    Through orthogonal experiment, a new type of LiClO4-LiNO3-LiBr eutectic salt with optimum mole ratio of n(LiClO4):n(LiNO3):n(LiBr)=1.6:3.8:1.0 was prepared. The poly(lithium acrylate-acrylonitrile)/LiClO4-LiNO3-LiBr solid polymer electrolytes were prepared with poly(lithium acrylate-acrylonitrile) and LiClO4-LiNO3-LiBr eutectic salts. The effect of LiClO4-LiNO3-LiBr eutectic salts content on the conductivity of solid polymer electrolytes was studied by alternating current impedance method, and the structures of eutectic salts and solid polymer electrolytes were characterized by differential thermal analysis, infrared spectroscopy and X-ray diffractometry. The results show that the room temperature conductivity of LiClO4-LiNO3-LiBr eutectic salts reaches 3.11×10-4 S·cm-1. The poly(lithium acrylate-acrylonitrile)/LiClO4-LiNO3-LiBr solid polymer electrolytes possess the highest room temperature conductivity at 70% LiClO4-LiNO3-LiBr eutectic salts content, and exhibit lower glass transition temperature of 75 ℃ compared with that of poly(lithium acrylate-acrylonitrile) of 105 ℃. A complex may be formed in the solid polymer electrolytes from the differential thermal analysis and infrared spectroscopy analysis. X-ray diffraction results show that the poly(lithium acrylate-acrylonitrile) can suppress the crystallization of eutectic salts in this system.

  14. Ultralong Lifespan and Ultrafast Li Storage: Single-Crystal LiFePO4 Nanomeshes.

    Science.gov (United States)

    Zhang, Yan; Zhang, Hui Juan; Feng, Yang Yang; Fang, Ling; Wang, Yu

    2016-01-27

    A novel LiFePO4 material, in the shape of a nanomesh, has been rationally designed and synthesized based on the low crystal-mismatch strategy. The LiFePO4 nanomesh possesses several advantages in morphology and crystal structure, including a mesoporous structure, its crystal orientation that is along the [010] direction, and a shortened Li-ion diffusion path. These properties are favorable for their application as cathode in Li-ion batteries, as these will accelerate the Li-ion diffusion rate, improve the Li-ion exchange between the LiFePO4 nanomesh and the electrolyte, and reduce the Li-ion capacitive behavior during Li intercalation. So the LiFePO4 nanomesh exhibits a high specific capacity, enhanced rate capability, and strengthened cyclability. The method developed here can also be extended to other similar systems, for instance, LiMnPO4 , LiCoPO4 , and LiNiPO4 , and may find more applications in the designed synthesis of functional materials.

  15. Inelastic H+Li and H^-+Li^+ collisions and non-LTE Li I line formation in stellar atmospheres

    CERN Document Server

    Barklem, P S; Asplund, M

    2003-01-01

    Rate coefficients for inelastic collisions between Li and H atoms covering all transitions between the asymptotic states Li(2s,2p,3s,3p,3d,4s,4p,4d,4f)+H(1s) and Li^+ +H^- are presented for the temperature range 2000-8000 K based on recent cross-section calculations. The data are of sufficient completeness for non-LTE modelling of the Li I 670.8 nm and 610.4 nm features in late-type stellar atmospheres. Non-LTE radiative transfer calculations in both 1D and 3D model atmospheres have been carried out for test cases of particular interest. Our detailed calculations show that the classical modified Drawin-formula for collisional excitation and de-excitation (Li*+H Li*'+H) over-estimates the cross-sections by typically several orders of magnitude and consequently that these reactions are negligible for the line formation process. However, the charge transfer reactions collisional ion-pair production and mutual neutralization (Li*+H Li^+ +H^-) are of importance in thermalizing Li. In particular, 3D non-LTE calcu...

  16. First observation of $^{13}$Li ground state

    CERN Document Server

    Kohley, Z; DeYoung, P A; Volya, A; Baumann, T; Bazin, D; Christian, G; Cooper, N L; Frank, N; Gade, A; Hall, C; Hinnefeld, J; Luther, B; Mosby, S; Peters, W A; Smith, J K; Snyder, J; Spyrou, A; Thoennessen, M

    2013-01-01

    The ground state of neutron-rich unbound $^{13}$Li was observed for the first time in a one-proton removal reaction from $^{14}$Be at a beam energy of 53.6 MeV/u. The $^{13}$Li ground state was reconstructed from $^{11}$Li and two neutrons giving a resonance energy of 120$^{+60}_{-80}$ keV. All events involving single and double neutron interactions in the Modular Neutron Array (MoNA) were analyzed, simulated, and fitted self-consistently. The three-body ($^{11}$Li+$n+n$) correlations within Jacobi coordinates showed strong dineutron characteristics. The decay energy spectrum of the intermediate $^{12}$Li system ($^{11}$Li+$n$) was described with an s-wave scattering length of greater than -4 fm, which is a smaller absolute value than reported in a previous measurement.

  17. Electrical conductivity of Cu-Li alloys

    Institute of Scientific and Technical Information of China (English)

    朱达川; 宋明昭; 陈家钊; 涂铭旌; 潘海滨

    2004-01-01

    The electrical conductivity of Cu-Li alloys was studied. And the distribution of electrons near Fermi surface was detected by synchrotron radiation instrument. The results show that the electrical conductivity of Cu-Li alloys decreases from 5. 22 × 10-9 S/m to 3. 69 × 10-9 S/m with the increase of Li content. Li can decrease the oxygen, sulfur and other impurities content in commercial Cu, but Li dissolved in Cu lattice leads to distortion of Cu lattice from 0. 005 %-0. 050 %, affects the valence band of Cu, increases the binding energy of surface electron, and decreases the electron density of Fermi surface simultaneously. So the electrical conductivity decreases gradually with the increase of Li content.

  18. 2006 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Lewis County, WA

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. collected Light Detection and Ranging (LiDAR) data of Western Lewis County for the Puget Sound LiDAR Consortium. This data set covers...

  19. 2009 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Lewis County, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data for the Lewis County survey area for the Puget Sound LiDAR Consortium. This data...

  20. 2011 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Quinault River Basin

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data on the Quinault River Basin survey area for the Puget Sound LiDAR Consortium and...

  1. 2013 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Entiat

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In October 2012, WSI (Watershed Sciences, Inc.) was contracted by the Puget Sound LiDARConsortium (PSLC) to collect Light Detection and Ranging (LiDAR) data for the...

  2. 2013 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Nooksack

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In July 2012, WSI (Watershed Sciences, Inc.) was contracted by the Puget Sound LiDARConsortium (PSLC) to collect Light Detection and Ranging (LiDAR) data on a...

  3. 2015 Puget Sound LiDAR Consortium (PSLC) LiDAR: WA DNR Lands (P2)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In June 2014, WSI, a Quantum Spatial Inc. (QSI) company, was contracted by the Puget Sound LiDAR Consortium (PSLC) to collect Light Detection and Ranging (LiDAR)...

  4. 2015 Puget Sound LiDAR Consortium (PSLC) LiDAR: WA DNR Lands (P1)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In June 2014, WSI, a Quantum Spatial Inc. (QSI) company, was contracted by the Puget Sound LiDAR Consortium (PSLC) to collect Light Detection and Ranging (LiDAR)...

  5. 2013 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Tulalip Partnership

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In October 2012, WSI (Watershed Sciences, Inc.) was contracted by the Puget Sound LiDAR Consortium (PSLC)to collect Light Detection and Ranging (LiDAR) data on a...

  6. 2013 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Nooksack

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In July 2012, WSI (Watershed Sciences, Inc.) was contracted by the Puget Sound LiDAR Consortium (PSLC) to collect Light Detection and Ranging (LiDAR) data on a...

  7. 2013 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Saddle Mountain

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In October 2013, WSI, a Quantum Spatial Company (QSI), was contracted by the Puget Sound LiDAR Consortium (PSLC) to collect Light Detection and Ranging (LiDAR) data...

  8. 2014 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Willapa Valley (Delivery 1)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In January, 2014 WSI, a Quantum Spatial (QSI) company, was contracted by the Puget Sound LiDAR Consortium (PSLC) to collect Light Detection and Ranging (LiDAR) data...

  9. President Li Xiaolin Visits Saudi Arabia

    Institute of Scientific and Technical Information of China (English)

    Zhang; Min

    2016-01-01

    At the invitation of Prince Alwaleed,chairman of Kingdom Holding Company of Saudi Arabia,CPAFFC President Li Xiaolin led a delegation to visit Saudi Arabia from Feb 16 to 20.During the visit,Ms.Li met with the prince,visited Kingdom Hospital and Kingdom School and held working talks with Alwaleed Philanthropies.During the meeting with Prince Alwaleed,Ms.Li mentioned that Chi-

  10. /sup 7/Li production in Nova explosions

    Energy Technology Data Exchange (ETDEWEB)

    Starrfield, S.; Truran, J.W.; Sparks, W.M.; Arnould, M.

    1978-06-01

    Calculations of /sup 7/Li production occurring as a concomitant of thermonuclear runaways in hydrogen envelopes of white dwarfs are reported. It is found that sufficient /sup 7/Li can be produced in models displaying fast--nova-like features to suggest that the corresponding objects represent significant contributors to the /sup 7/Li enrichment of galactic matter. The sensitivities of these results to various assumptions and uncertainties are discussed.

  11. beta -delayed charged particles from /sup 9/Li and /sup 11/Li

    CERN Document Server

    Langevin, M; Détraz, C; Epherre-Rey-Campagnolle, Marcelle; Guillemaud, D; Klapisch, Robert; Mark, S K T; Naulin, F; Thibault, C; Touchard, F

    1981-01-01

    beta -delayed emission of alpha particles rom /sup 9/Li and of both alpha and /sup 6/He particles from /sup 11/Li is observed. New beta branches are reported which populate high-energy levels in the daughter nuclei. The branching ratios are measured and the beta delayed neutron emission probabilities P/sub n/ for /sup 9/Li and P /sub 3n/ for /sup 11/Li are deduced. (14 refs).

  12. Iodide substitution in lithium borohydride, LiBH{sub 4}-LiI

    Energy Technology Data Exchange (ETDEWEB)

    Rude, Line H., E-mail: line@inano.au.dk [Center for Materials Crystallography, Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Aarhus C (Denmark); Groppo, Elena, E-mail: elena.groppo@unito.it [Dipartimento di Chimica I.F.M. and NIS, Universita di Torino, Torino (Italy); Arnbjerg, Lene M., E-mail: lenem@chem.au.dk [Center for Materials Crystallography, Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Aarhus C (Denmark); Ravnsbaek, Dorthe B., E-mail: inadr@inano.au.dk [Center for Materials Crystallography, Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Aarhus C (Denmark); Malmkjaer, Regitze A., E-mail: regitze.aagaard.malmkjaer@post.au.dk [Center for Materials Crystallography, Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Aarhus C (Denmark); Filinchuk, Yaroslav, E-mail: Yaroslav.Filinchuk@uclouvain.be [Center for Materials Crystallography, Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Aarhus C (Denmark); Swiss-Norwegian Beam Lines at ESRF, BP-220, 38043 Grenoble (France); Institute of Condensed Matter and Nanosciences, Universite Catholique de Louvain, Place L. Pasteur 1, B-1348 Louvain-la-Neuve (Belgium); Baricco, Marcello, E-mail: marcello.baricco@unito.it [Dipartimento di Chimica I.F.M. and NIS, Universita di Torino, Torino (Italy); Besenbacher, Flemming, E-mail: fbe@inano.au.dk [Interdisciplinary Nanoscience Center (iNANO) and Department of Physics and Astronomy, Aarhus University, DK-8000 Aarhus C (Denmark); Jensen, Torben R., E-mail: trj@chem.au.dk [Center for Materials Crystallography, Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University, Langelandsgade 140, DK-8000 Aarhus C (Denmark)

    2011-08-18

    Graphical abstract: Highlights: > Anion substitution in LiBH{sub 4}. > Structure and properties of two LiBH{sub 4}-LiI solid solutions. > Stability upon heating and over time. > Hydrogen storage properties of LiBH{sub 4}-LiI. - Abstract: The new concept, anion substitution, is explored for possible improvement of hydrogen storage properties in the system LiBH{sub 4}-LiI. The structural chemistry and the substitution mechanism are analyzed using Rietveld refinement of in situ synchrotron radiation powder X-ray diffraction (SR-PXD) data, attenuated total reflectance infrared spectroscopy (ATR-IR), differential scanning calorimetry (DSC) and Sieverts measurements. Anion substitution is observed as formation of two solid solutions of Li(BH{sub 4}){sub 1-x}I{sub x}, which merge into one upon heating. The solid solutions have hexagonal structures (space group P6{sub 3}mc) similar to the structures of h-LiBH{sub 4} and {beta}-LiI. The solid solutions have iodide contents in the range {approx}0-62 mol% and are stable from below room temperature to the melting point at 330 deg. C. Thus the stability of the solid solutions is higher as compared to that of the orthorhombic and hexagonal polymorphs of LiBH{sub 4} and {alpha}- and {beta}-LiI. Furthermore, the rehydrogenation properties of the iodide substituted solid solution Li(BH{sub 4}){sub 1-x}I{sub x}, measured by the Sieverts method, are improved as compared to those of LiBH{sub 4}. After four cycles of hydrogen release and uptake the Li(BH{sub 4}){sub 1-x}I{sub x} solid solution maintains 68% of the calculated hydrogen storage capacity in contrast to LiBH{sub 4}, which maintains only 25% of the storage capacity after two cycles under identical conditions.

  13. Li Xiuying’s Family Planning Center

    Institute of Scientific and Technical Information of China (English)

    1996-01-01

    PEOPLE in Yinan County refer to Li Xiuying, a doctor highly respected for her gynecological and obstetrics surgical skills, as "Magic Scalpel Li." Li Xiuying assumed the post as vice director of the Department of Gynecology and Obstetrics in the People’s Hospital in Yinan County at the young age of 27. She held the post for 12 years until 1988 when she was became director of the county’s Family Planning Service Center. Li had never pursued the new position, and was unable to accept the unexpected transfer, preferring instead to continue working in the Department of Gynecology and Obstetrics throughout her career.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-08-04

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

  15. Synthesis of LiAlTiO4 and its selectivity to Li+ exchange

    Institute of Scientific and Technical Information of China (English)

    Dong Dianquan; Zhang Fengbao; Zhang Guoliang; Liu Yifan

    2006-01-01

    The ion-exchanger LiAlTiO4 of spinel type was prepared by the common precipitation/hydrothermal crystallization method,and was acid-modified.Its ion-exchange properties for alkali ions such as saturation capacity of exchange,distribution coefficient and pH titration curve were determined.LiAlTiO4 was characterized by the X-ray diffraction method.The acid treatment of LiAlTiO4 caused Li+ extraction ratio to change from 28% to 72%,while the dissolution of Al is less than 6.8%.This inorganic ion-exchanger (LiAlTiO4-700) has a higher saturation capacity of exchange for Li than for other alkali ions,the saturation capacity of exchange for Li+ reaches 4.29 mmol/g (30.03 mg/g); LiAlTiO4-700(H) has a higher selectivity of ion exchange for Li+ than for other alkali ions.These results show LiAlTiO4-700(H) has better memory and selectivity of ion exchange,and higher capacity of ion exchange for Li+.It is a kind of prospective ionic sieve for Li+.

  16. Structure of {sup 10}Li from the properties of {sup 11}Li

    Energy Technology Data Exchange (ETDEWEB)

    Garrido, E. [Inst. de Estructura de la Materia, CSIC, Madrid (Spain); Fedorov, D.V.; Jensen, A.S. [Inst. of Physics and Astronomy, Univ. of Arhus (Denmark)

    2003-07-01

    The resonances of the neutron-{sup 9}Li two-body system are decisive for the description of the {sup 11}Li three-body system. Known properties narrow down the uncertainties provided the finite spin of the {sup 9}Li are properly accounted for. The positions of two doublets of 1{sup {+-}} and 2{sup {+-}} are predicted. (orig.)

  17. Li ion diffusion in LiAlO2 investigated by Raman spectroscopy

    Science.gov (United States)

    Hu, Qiwei; Lei, Li; Jiang, Xiaodong; Feng, Zhe Chuan; Tang, Mingjun; He, Duanwei

    2014-11-01

    The temperature dependence of Li ions behavior of γ-LiAlO2 has been studied from 78 to 873 K. On heating, the Li ions underwent positional disordering along the structural channels, with the Li ions related modes at 220, 366 and 400 cm-1 broadening and weakening dramatically. An anomalous maximum in the bandwidths of the Li ions related modes is observed. It should be apparent that there are at least two distinct thermally activated processes. A model suggested by Andrade and Porto is used to describe the linewidth of a phonon.

  18. Optimized synthesis technology of LiFePO4 for Li-ion battery

    Institute of Scientific and Technical Information of China (English)

    QU Tao; TIAN Yan-wen; DING Yang; ZHONG Can-yun; ZHAI Yu-chun

    2005-01-01

    The influence of factors of the carbon black content, sintering temperature, sintering time, molar ratio of Li to Fe, as well as the electrochemical properties of LiFePO4 for lithium ion battery were studied. The only technology was obtained by using range analysis through Latin orthogonal experiment of L44 (16). The results show that the optimization synthesis technology of LiFePO4 is content of 5% doping carbon, sintering temperature of 700 ℃,molar ratio of Li to Fe of 1.03 : 1 and sintering time of 16 h. The optimized cathode synthesis techniques can make LiFePO4 have good electrochemical properties.

  19. Kinetic measurement and prediction of the hydrogen outgassing from the polycrystalline LiH/Li2O/LiOH system

    Energy Technology Data Exchange (ETDEWEB)

    Dinh, L N; Grant, D M; Schildbach, M A; Smith, R A; Siekhaus, W J; Balazs, B; Leckey, J H; Kirkpatrick, J; McLean II, W

    2005-04-06

    Due to the exothermic reaction of lithium hydride (LiH) salt with water during transportation and handling, there is always a thin film of lithium hydroxide (LiOH) present on the LiH surface. In dry or vacuum storage, this thin LiOH film slowly decomposes. We have used temperature-programmed reaction/decomposition (TPR) in combination with the isoconversion method of thermal analysis to determine the outgassing kinetics of H{sub 2}O from pure LiOH and H{sub 2} and H{sub 2}O from this thin LiOH film. H{sub 2} production via the reaction of LiH with LiOH, forming a lithium oxide (Li{sub 2}O) interlayer, is thermodynamically favored, with the rate of further reaction limited by diffusion through the Li{sub 2}O and the stability of the decomposing LiOH. Lithium hydroxide at the LiOH/vacuum interface also decomposes easily to Li{sub 2}O, releasing H{sub 2}O which subsequently reacts with LiH in a closed system to form H{sub 2}. At the onset of dry decomposition, where H{sub 2} is the predominant product, the activation energy for outgassing from a thin LiOH film is lower than that for bulk LiOH. However, as the reactions at the LiH/Li{sub 2}O/LiOH and at the LiOH/vacuum interfaces proceed, the overall activation energy barrier for the outgassing approaches that of bulk LiOH decomposition. The kinetics developed here predicts a hydrogen evolution profile in good agreement with hydrogen release observed during long term isothermal storage.

  20. Saginaw Bay, MI LiDAR

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — TASK NAME:(NRCS) Saginaw Bay, MI LiDAR LiDAR Data Acquisition and Processing Production Task USGS Contract No. G10PC00057 Task Order No. G11PD01254 Woolpert Order...

  1. Üliõpilasteatrid peavad Itaalias kongressi

    Index Scriptorium Estoniae

    2006-01-01

    Itaalia väikelinnas Urbinos lõpeb 27. juulil sealse ülikooli teatri Teatro Aenigma ja Rahvusvahelise Üliõpilasteatrite Assotsiatsiooni koostöös kuues tudengiteatrite maailmakongress. Eestist osaleb ja peab ettekande lavastaja ja Tartu Üliõpilasteatri kunstiline juht Kalev Kudu

  2. Phase evolution of Li{sub 2}ND, LiD and LiND{sub 2} in hydriding/dehydriding of Li{sub 3}N

    Energy Technology Data Exchange (ETDEWEB)

    Chien, W.-M.; Lamb, Joshua [Metallurgical Materials Engineering, MS 388, University of Nevada, Reno, NV 89557 (United States); Chandra, Dhanesh [Metallurgical Materials Engineering, MS 388, University of Nevada, Reno, NV 89557 (United States)], E-mail: dchandra@unr.edu; Huq, Ashfia [Spallation Neutron Source, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Richardson, James; Maxey, Evan [Intense Pulsed Neutron Source, Argonne National Laboratory, Argonne, IL 60439 (United States)

    2007-10-31

    Neutron and synchrotron studies have been performed on in situ hydriding of Li{sub 3}N. Commercial Li{sub 3}N is composed of {alpha} phase ({approx}70 wt.%) and {beta} phase ({approx}30 wt.%). We have performed experiments to convert {beta} {yields} {alpha}, and studied in situ deuteration using neutron diffraction experiments. We found concurrent phase evolution of Li{sub 2}ND, LiD, and LiND{sub 2}. Mass percentages of the phases evolved as a function of time and temperature have been quantified using General Structure Analysis System (GSAS) refinement of the neutron diffraction data. The problem of formation of the stable LiD is discussed in light of decreasing of the amount of LiD phase when the temperature is increased from 200 to 320 deg. C during dehydriding, and in addition the concentration of Li{sub 2}ND phase increased at this temperature. Lattice parameters, volume changes, phase evolutions in wt.% as a function of temperature and time are presented.

  3. Li-5(BH4)(3)NH

    DEFF Research Database (Denmark)

    Wolczyk, Anna; Paik, Biswajit; Sato, Toyoto

    2017-01-01

    = 7.0474(2) angstrom at 77 degrees C. The crystal structure of Lis(BH4)(3)NH has been solved in space group Pnma, and refined coupling density functional theory (DFT) and synchrotron radiation X-ray powder diffraction data have been obtained for a 3LiBH(4):2Li(2)NH ball-milled and annealed sample...

  4. Üliõpilasteatrid peavad Itaalias kongressi

    Index Scriptorium Estoniae

    2006-01-01

    Itaalia väikelinnas Urbinos lõpeb 27. juulil sealse ülikooli teatri Teatro Aenigma ja Rahvusvahelise Üliõpilasteatrite Assotsiatsiooni koostöös kuues tudengiteatrite maailmakongress. Eestist osaleb ja peab ettekande lavastaja ja Tartu Üliõpilasteatri kunstiline juht Kalev Kudu

  5. Microstructure Analysis of Synthesized LiBOB

    Directory of Open Access Journals (Sweden)

    Etty Marti Wigayati

    2015-11-01

    Full Text Available Lithium bis (oxalate borate or LiBOB is an active material used as the electrolyte for lithium battery application. LiBOB (LiB(C2O42 powder was prepared from LiOH, H2C2O4 and H3BO3. The employed method was solid state reaction. LiBOB powder produced from the reaction was then observed using SEM and TEM. Surface area was analyzed using Quantachrome Nova 4200e. From the analysis analyzed using XRD to identify the resulting phases, crystal structure, and crystallite size. The functional groups were analyzed using FT-IR. The particle morphology was result, it was seen that the resulted phases were C4LiBO8 and LiB(C2O42.H2O, the crystal structure was orthorhombic with space group Pbca and Pnma. From the particle morphology observation it was shown that micro pores were created irregularly. When the observation was deepened, nanopores with elongated round shape were seen within the micropores. The pore size was approximately 50–100 nm. The surface area, total pore volume, and average pore diameter of LiBOB powder was 88.556 m2/g, 0.4252 cm3/g, and 19.2 nm respectively.

  6. The Impact of Li Grain Size on Coulombic Efficiency in Li Batteries.

    Science.gov (United States)

    Mehdi, B Layla; Stevens, Andrew; Qian, Jiangfeng; Park, Chiwoo; Xu, Wu; Henderson, Wesley A; Zhang, Ji-Guang; Mueller, Karl T; Browning, Nigel D

    2016-10-05

    One of the most promising means to increase the energy density of state-of-the-art lithium Li-ion batteries is to replace the graphite anode with a Li metal anode. While the direct use of Li metal may be highly advantageous, at present its practical application is limited by issues related to dendrite growth and low Coulombic efficiency, CE. Here operando electrochemical scanning transmission electron microscopy (STEM) is used to directly image the deposition/stripping of Li at the anode-electrolyte interface in a Li-based battery. A non-aqueous electrolyte containing small amounts of H2O as an additive results in remarkably different deposition/stripping properties as compared to the "dry" electrolyte when operated under identical electrochemical conditions. The electrolyte with the additive deposits more Li during the first cycle, with the grain sizes of the Li deposits being significantly larger and more variable. The stripping of the Li upon discharge is also more complete, i.e., there is a higher cycling CE. This suggests that larger grain sizes are indicative of better performance by leading to more uniform Li deposition and an overall decrease in the formation of Li dendrites and side reactions with electrolyte components, thus potentially paving the way for the direct use of Li metal in battery technologies.

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

    Energy Technology Data Exchange (ETDEWEB)

    Natalie J. Gese; Batric Pesic

    2013-03-01

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

  8. The Impact of Li Grain Size on Coulombic Efficiency in Li Batteries

    Science.gov (United States)

    Mehdi, B. Layla; Stevens, Andrew; Qian, Jiangfeng; Park, Chiwoo; Xu, Wu; Henderson, Wesley A.; Zhang, Ji-Guang; Mueller, Karl T.; Browning, Nigel D.

    2016-01-01

    One of the most promising means to increase the energy density of state-of-the-art lithium Li-ion batteries is to replace the graphite anode with a Li metal anode. While the direct use of Li metal may be highly advantageous, at present its practical application is limited by issues related to dendrite growth and low Coulombic efficiency, CE. Here operando electrochemical scanning transmission electron microscopy (STEM) is used to directly image the deposition/stripping of Li at the anode-electrolyte interface in a Li-based battery. A non-aqueous electrolyte containing small amounts of H2O as an additive results in remarkably different deposition/stripping properties as compared to the “dry” electrolyte when operated under identical electrochemical conditions. The electrolyte with the additive deposits more Li during the first cycle, with the grain sizes of the Li deposits being significantly larger and more variable. The stripping of the Li upon discharge is also more complete, i.e., there is a higher cycling CE. This suggests that larger grain sizes are indicative of better performance by leading to more uniform Li deposition and an overall decrease in the formation of Li dendrites and side reactions with electrolyte components, thus potentially paving the way for the direct use of Li metal in battery technologies.

  9. The Impact of Li Grain Size on Coulombic Efficiency in Li Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Mehdi, B. Layla; Stevens, Andrew; Qian, Jiangfeng; Park, Chiwoo; Xu, Wu; Henderson, Wesley A.; Zhang, Ji-Guang; Mueller, Karl T.; Browning, Nigel D.

    2016-10-05

    One of the most promising means to increase the energy density of state-of-the-art lithium (Li)-ion batteries is to replace the graphite anode with a Li metal anode1, 2, 3. While the direct use of Li metal may be highly advantageous4,5, at present its practical application is limited by issues related to dendrite growth and low Coulombic efficiency (CE)6. Here operando electrochemical scanning transmission electron microscopy (STEM) is used to directly image the deposition/stripping of Li at the anode-electrolyte interface in a Li-based battery. A non-aqueous electrolyte containing small amounts of H2O as an additive results in remarkably different deposition/stripping properties as compared to the "dry" electrolyte when operated under identical electrochemical conditions. The electrolyte with the additive deposits more Li during the first cycle, with the grain sizes of the Li deposits being significantly larger and more variable. The stripping of the Li upon discharge is also more complete, i.e., there is a higher cycling CE. This suggests that larger grain sizes are indicative of better performance by leading to more uniform Li deposition and an overall decrease in the formation of Li dendrites and side reactions with electrolyte components, thus potentially paving the way for the direct use of Li metal in battery technologies.

  10. Theoretical and Experimental Study of LiBH4-LiCl Solid Solution

    Directory of Open Access Journals (Sweden)

    Torben R. Jensen

    2012-03-01

    Full Text Available Anion substitution is at present one of the pathways to destabilize metal borohydrides for solid state hydrogen storage. In this work, a solid solution of LiBH4 and LiCl is studied by density functional theory (DFT calculations, thermodynamic modeling, X-ray diffraction, and infrared spectroscopy. It is shown that Cl substitution has minor effects on thermodynamic stability of either the orthorhombic or the hexagonal phase of LiBH4. The transformation into the orthorhombic phase in LiBH4 shortly after annealing with LiCl is for the first time followed by infrared measurements. Our findings are in a good agreement with an experimental study of the LiBH4-LiCl solid solution structure and dynamics. This demonstrates the validity of the adopted combined theoretical (DFT calculations and experimental (vibrational spectroscopy approach, to investigate the solid solution formation of complex hydrides.

  11. Investigation of the role of 10Li resonances in the halo structure of 11Li through the Li11(p,dLi10 transfer reaction

    Directory of Open Access Journals (Sweden)

    A. Sanetullaev

    2016-04-01

    Full Text Available The first measurement of the one-neutron transfer reaction 11Li(p,d10Li performed using the IRIS facility at TRIUMF with a 5.7A MeV 11Li beam interacting with a solid H2 target is reported. The 10Li residue was populated strongly as a resonance peak with energy Er=0.62±0.04 MeV having a total width Γ=0.33±0.07 MeV. The angular distribution of this resonance is characterized by neutron occupying the 1p1/2 orbital. A DWBA analysis yields a spectroscopic factor of 0.67±0.12 for p1/2 removal strength from the ground state of 11Li to the region of the peak.

  12. Attainable gravimetric and volumetric energy density of Li-S and li ion battery cells with solid separator-protected Li metal anodes.

    Science.gov (United States)

    McCloskey, Bryan D

    2015-11-19

    As a result of sulfur's high electrochemical capacity (1675 mA h/gs), lithium-sulfur batteries have received significant attention as a potential high-specific-energy alternative to current state-of-the-art rechargeable Li ion batteries. For Li-S batteries to compete with commercially available Li ion batteries, high-capacity anodes, such as those that use Li metal, will need to be enabled to fully exploit sulfur's high capacity. The development of Li metal anodes has focused on eliminating Coulombically inefficient and dendritic Li cycling, and to this end, an interesting direction of research is to protect Li metal by employing mechanically stiff solid-state Li(+) conductors, such as garnet phase Li7La3Zr2O12 (LLZO), NASICON-type Li1+xAlxTi2-x(PO4)3 (LATP), and Li2S-P2S5 glasses (LPS), as electrode separators. Basic calculations are used to quantify useful targets for solid Li metal protective separator thickness and cost to enable Li metal batteries in general and Li-S batteries specifically. Furthermore, maximum electrolyte-to-sulfur ratios that allow Li-S batteries to compete with Li ion batteries are calculated. The results presented here suggest that controlling the complex polysulfide speciation chemistry in Li-S cells with realistic, minimal electrolyte loading presents a meaningful opportunity to develop Li-S batteries that are competitive on a specific energy basis with current state-of-the-art Li ion batteries.

  13. Effect of a pyrrolidinium zwitterion on charge/discharge cycle properties of Li/LiCoO2 and graphite/Li cells containing an ionic liquid electrolyte

    Science.gov (United States)

    Yamaguchi, Seitaro; Yoshizawa-Fujita, Masahiro; Takeoka, Yuko; Rikukawa, Masahiro

    2016-11-01

    Ionic liquids (ILs) containing zwitterions have been studied as electrolytes for lithium-ion batteries (LIBs). The effects of addition of a pyrrolidinium zwitterion in an IL electrolyte on the thermal and electrochemical stability and charge/discharge properties of Li/LiCoO2 and graphite/Li cells were investigated. The thermal decomposition temperature of the IL electrolyte composed of N-methyl-N-propylpyrrolidinium bis(fluorosulfonyl)amide ([P13][FSA])/lithium bis(trifluoromethylsulfonyl)amide (LiTFSA) with 3-(1-butylpyrrolidinium)propane-1-sulfonate (Bpyps) as the zwitterionic additive, the thermal decomposition temperature was about 300 °C. The electrochemical window of [P13][FSA]/LiTFSA/Bpyps was 0-+5.4 V vs. Li/Li+, which was almost identical to that of [P13][FSA]/LiTFSA. Li|electrolyte|LiCoO2 cells containing the IL/Bpyps electrolyte system exhibited high capacities in the cut-off voltage range of 3.0-4.6 V, even after 50 cycles. The increase in the interfacial resistance between the electrolyte and cathode with cycling was suppressed. In the cyclic voltammograms of cells employing a graphite electrode, the intercalation/deintercalation of lithium ions were observed in the range of 0 and + 0.4 V vs. Li/Li+. Further, graphite|electrolyte|Li cells containing [P13][FSA]/LiTFSA/Bpyps exhibited stable charge/discharge cycle behaviour over 50 cycles.

  14. The single electrode Peltier heats of Li{sup +}/Li, H{sub 2}/H{sup -} and Li{sup +}/Pd-Li couples in molten LiCl-KCl systems

    Energy Technology Data Exchange (ETDEWEB)

    Nakajima, Hironori; Nohira, Toshiyuki; Ito, Yasuhiko [Kyoto Univ., Dept. of Fundamental Energy Science, Kyoto (Japan)

    2004-10-30

    The thermoelectric power of the Li{sup +}/Li couple was measured in a LiCl-KCl eutectic melt at 633-773 K. The obtained value, 0.089 mV K{sup -1}, gives the single electrode Peltier heat for the reaction Li{sup +}+e{sup -} <--> Li as -5.8 kJ F{sup -1} at 673 K (endothermic cathodic reaction). The single electrode Peltier heat for the reaction 1/2H{sub 2} + e{sup -} <--> H{sup -} in a molten LiCl-KCl-LiH system has been calculated using the temperature dependence of the equilibrium potential of the H{sub 2}/H{sup -} couple measured with reference to the Li{sup +}/Li potential, which gives 5.8 kJ F{sup -l} (exothermic cathodic reaction) under the condition of hydrogen pressure of 1.0 atm, H{sup -} ion concentration of 0.01 (anion fraction) and 673 K. The single electrode Peltier heats for formation of Pd-Li alloys have been also evaluated. (Author)

  15. Li ion diffusion mechanisms in LiFePO4: an ab initio molecular dynamics study.

    Science.gov (United States)

    Yang, Jianjun; Tse, John S

    2011-11-17

    The mechanisms for thermal (self) diffusion of Li ions in fully lithiated LiFePO(4) have been investigated with spin polarized ab initio molecular dynamics calculations. The effect of electron correlation is taken into account with the GGA+U formalism. It was found that Li ion diffusion is not a continuous process but through a series of jumps from one site to another. A dominant process is the hopping between neighboring Li sites around the PO(4) groups, which results in a zigzag pathway along the crystallographic b-axis. This observation is in agreement with a recent neutron diffraction experiment. A second process involves the collaborative movements of the Fe ions leading to the formation of antisite defects and promotes Li diffusion across the Li ion channels. The finding of the second mechanism demonstrates the benefit of ab initio molecular dynamics simulation in sampling diffusion pathways that may not be anticipated.

  16. First-principles study of Li ion diffusion in LiFePO4

    Science.gov (United States)

    Ouyang, Chuying; Shi, Siqi; Wang, Zhaoxiang; Huang, Xuejie; Chen, Liquan

    2004-03-01

    The diffusion mechanism of Li ions in the olivine LiFePO4 is investigated from first-principles calculations. The energy barriers for possible spatial hopping pathways are calculated with the adiabatic trajectory method. The calculations show that the energy barriers running along the c axis are about 0.6, 1.2, and 1.5 eV for LiFePO4, FePO4, and Li0.5FePO4, respectively. However, the other migration pathways have much higher energy barriers resulting in very low probability of Li-ion migration. This means that the diffusion in LiFePO4 is one dimensional. The one-dimensional diffusion behavior has also been shown with full ab initio molecular dynamics simulation, through which the diffusion behavior is directly observed.

  17. First-principle studies on the Li-Te system

    Science.gov (United States)

    Wang, Youchun; Tian, Fubo; Li, Da; Duan, Defang; Liu, Yunxian; Liu, Bingbing; Zhou, Qiang; Cui, Tian

    2017-01-01

    First-principle evolutionary calculation was performed to search for all probable stable lithium tellurium compounds. In addition to the well-known structures of Fm-3m Li2Te and Pnma Li2Te, several novel structures, including those of P4/nmm Li2Te, Imma Li8Te2, and C2/m Li9Te2, were determined under high pressure. The transformation sequence of Li2Te induced by pressure was presented as follows. The phase transition occurred at 7.5 GPa while transforming from Fm-3m phase to Pnma structure, then transformed to P4/nmm phase at 14 GPa. P4/nmm Li2Te can remain stable at least up to 140 GPa. Li8Te2 and Li9Te2 were stable at 8-120 GPa and 80-120 GPa, respectively. Interestingly, Li8Te2 and Li9Te2 were predicted to be metallic under high pressure, Li2Te would metalize on compression. P4/nmm Li2Te is likely a super ionic conductor due to the special characteristic. Metallic P4/nmm Li2Te may be a candidate mixed conductor material under extreme pressure. Charge transfer was studied using Bader charge analysis. Charge transferred from Li to Te, and the relative debilitated ionicity between Li and Te atoms existed at high pressure.

  18. Effect of the composition of Al-Li alloys on the quantitative relation between the δ'(Al3Li), S1(Al2MgLi), and T1(Al2CuLi) phases

    Science.gov (United States)

    Betsofen, S. Ya.; Antipov, V. V.; Grushin, I. A.; Knyazev, M. I.; Khokhlatova, L. B.; Alekseev, A. A.

    2015-01-01

    Al-Li alloys are considered. A quantitative approach to the determination of the ratio of the fractions of the binary and ternary intermetallic phases in Al-Mg(Cu)-Li alloys is developed on the basis of chemical and phase composition balance equations and the experimentally measured lattice parameter of the α solid solution. The ratio of the fractions of the δ'(Al3Li) and S1(T1) phases in Al-Mg(Cu)-Li alloys is shown to be determined by the ratio of the mole fractions of Li and Mg(Cu). Equations are proposed for calculating the weight fractions of the S1(Al2MgLi), T1(Al2CuLi) and δ'(Al3Li) phases in domestic and foreign Al-Mg-Li alloys 1420, 1424, 5090 and Al-Cu-Li alloys 1440, 1460, 1461, 1441, 1469, 2090, 2095, 8090, and Weldalite 049.

  19. Strain imaging of a LiCoO2 cathode in a Li-ion battery

    Science.gov (United States)

    Matsushita, Yuki; Osaka, Ryuma; Butsugan, Kenta; Takata, Keiji

    2016-09-01

    Li-ion batteries have been recognized as promising devices for a sustainable society. Layered LiCoO2 and graphite are commonly used as electrode materials for Li-ion batteries. When charging and discharging, Li-ions are extracted or inserted into the interlayers, which causes changes in volume. Scanning probe microscopy (SPM) can allow high resolution imaging of these volume changes, which enables us to investigate Li-ion migration without destruction. We observed volume changes in the LiCoO2 cathode using SPM and successfully imaged the distribution of the volume changes corresponding to the LiCoO2 particles. Volume changes in the interspace were significantly larger than those in the particles. The large volume changes are caused by electrolyte flux induced by changes in concentration of Li ions. The volume changes were greatly reduced when the electrolyte dried out. The dry-out and infiltration of electrolyte between the LiCoO2 particles and the current collector spread out with the procedure of degradation of the batteries. The boundaries between the dry-out and infiltration regions acted as barriers of electrolyte flux.

  20. Uniform second Li ion intercalation in solid state {var_epsilon}-LiVOPO4

    Energy Technology Data Exchange (ETDEWEB)

    Wangoh, Linda W.; Sallis, Shawn; Wiaderek, Kamila M.; Lin, Yuh-Chieh; Wen, Bohua; Quackenbush, Nicholas F.; Chernova, Natasha A.; Guo, Jinghua; Ma, Lu; Wu, Tianpin; Lee, Tien-Lin; Schlueter, Christoph; Ong, Shyue Ping; Chapman, Karena W.; Whittingham, M. Stanley; Piper, Louis F. J.

    2016-08-01

    Full, reversible intercalation of two Li+ has not yet been achieved in promising VOPO4 electrodes. A pronounced Li+ gradient has been reported in the low voltage window (i.e. second lithium reaction) that is thought to originate from disrupted kinetics in the high voltage regime (i.e first lithium reaction). Here we employ a combination of hard and soft x–ray photoelectron and absorption spectroscopy techniques to depth profile solid state synthesized LiVOPO4 cycled within the low voltage window only. Analysis of the vanadium environment revealed no evidence of a Li+ gradient, which combined with almost full theoretical capacity confirms that disrupted kinetics in the high voltage window are responsible for hindering full two lithium insertion. Furthermore, we argue that the uniform Li+ intercalation is a prerequisite for the formation of intermediate phases Li1:50VOPO4 and Li1:75VOPO4. The evolution from LiVOPO4 to Li2VOPO4 via the intermediate phases is confirmed by direct comparison between O K–edge absorption spectroscopy and density functional theory.

  1. Uniform second Li ion intercalation in solid state ϵ-LiVOPO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Wangoh, Linda W.; Quackenbush, Nicholas F. [Department of Physics, Applied Physics and Astronomy, Binghamton University, Binghamton, New York 13902 (United States); Sallis, Shawn [Materials Science and Engineering, Binghamton University, Binghamton, New York 13902 (United States); Wiaderek, Kamila M.; Ma, Lu; Wu, Tianpin; Chapman, Karena W. [X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439 (United States); Lin, Yuh-Chieh; Ong, Shyue Ping [Department of NanoEngineering, University of California San Diego, 9500 Gilman Drive 0448, La Jolla, California 92093 (United States); Wen, Bohua; Chernova, Natasha A.; Whittingham, M. Stanley [NECCES, Binghamton University, Binghamton, New York 13902 (United States); Guo, Jinghua [Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States); Lee, Tien-Lin; Schlueter, Christoph [Diamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE (United Kingdom); Piper, Louis F. J., E-mail: lpiper@binghamton.edu [Department of Physics, Applied Physics and Astronomy, Binghamton University, Binghamton, New York 13902 (United States); Materials Science and Engineering, Binghamton University, Binghamton, New York 13902 (United States)

    2016-08-01

    Full, reversible intercalation of two Li{sup +} has not yet been achieved in promising VOPO{sub 4} electrodes. A pronounced Li{sup +} gradient has been reported in the low voltage window (i.e., second lithium reaction) that is thought to originate from disrupted kinetics in the high voltage regime (i.e., first lithium reaction). Here, we employ a combination of hard and soft x–ray photoelectron and absorption spectroscopy techniques to depth profile solid state synthesized LiVOPO{sub 4} cycled within the low voltage window only. Analysis of the vanadium environment revealed no evidence of a Li{sup +} gradient, which combined with almost full theoretical capacity confirms that disrupted kinetics in the high voltage window are responsible for hindering full two lithium insertion. Furthermore, we argue that the uniform Li{sup +} intercalation is a prerequisite for the formation of intermediate phases Li{sub 1.50}VOPO{sub 4} and Li{sub 1.75}VOPO{sub 4}. The evolution from LiVOPO{sub 4} to Li{sub 2}VOPO{sub 4} via the intermediate phases is confirmed by direct comparison between O K–edge absorption spectroscopy and density functional theory.

  2. [100]-Oriented LiFePO4 Nanoflakes toward High Rate Li-Ion Battery Cathode.

    Science.gov (United States)

    Li, Zhaojin; Peng, Zhenzhen; Zhang, Hui; Hu, Tao; Hu, Minmin; Zhu, Kongjun; Wang, Xiaohui

    2016-01-13

    [100] is believed to be a tough diffusion direction for Li(+) in LiFePO4, leading to the belief that the rate performance of [100]-oriented LiFePO4 is poor. Here we report the fabrication of 12 nm-thick [100]-oriented LiFePO4 nanoflakes by a simple one-pot solvothermal method. The nanoflakes exhibit unexpectedly excellent electrochemical performance, in stark contrast to what was previously believed. Such an exceptional result is attributed to a decreased thermodynamic transformation barrier height (Δμb) associated with increased active population.

  3. Synthesis and Performance of LiMnO2 as Cathodes for Li-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    ZHAO Shi-xi; LIU Han-xing; OUYANG Shi-xi; LI Qiang

    2003-01-01

    Two structure types of LiMnO2 were synthesized by sol-gel method and ion-exchange method respectively.The results indicate that orthorhombic phase LiMnO2 is more stable than layered LiMnO2,o-LiMnO2 can be synthesized directly by sol-gel methods followed by heat-treated in argon,but layered LiMnO2 was obtained only by indirect methods such as ion-exchange method.In this paper,we first synthesized layered NaMnO2 by the sol-gel method,and then obtained layered LiMnO2 by the ion-exchange method.The phase constitution,chemical composition,and images of the products were tested by XRD,AAS (atomic absorption spectroscopy) and SEM.The electrochemical performances of the two structural types of LiMnO2 are obviously different during the initial few cycles,but later they both have a good capacity-retaining ability.The capacity of layered structure LiMnO2 is higher than that of o-LiMnO2.

  4. On the {\\ss}- decay in the Li-8 and Li-9 atoms

    CERN Document Server

    Frolov, Alexei M

    2013-01-01

    The nuclear {\\ss}- decay from the ground and some excited states of the three-electron Li-8 and Li-9 atoms is considered. The final state probabilities for the arising Be+ ion are determined numerically with the use of highly accurate bound state wave functions of the Li atom and Be+ ion. The probability of electron ionization during the nuclear {\\ss}- decay of the Li atom is evaluated numerically. We also discuss a possibility to observe the double {\\ss}- decay by using the known values of the final state probabilities for the regular nuclear {\\ss}- decay.

  5. Li-ion Battery Aging Datasets

    Data.gov (United States)

    National Aeronautics and Space Administration — This data set has been collected from a custom built battery prognostics testbed at the NASA Ames Prognostics Center of Excellence (PCoE). Li-ion batteries were run...

  6. Iowa LiDAR Mapping Project

    Data.gov (United States)

    Federal Emergency Management Agency, Department of Homeland Security — This is collection level metadata for LAS and ASCII data files from the statewide Iowa Lidar Project. The Iowa Light Detection and Ranging (LiDAR) Project collects...

  7. EKA tootedisaini üliõpilane...

    Index Scriptorium Estoniae

    2005-01-01

    Eesti Kunstiakadeemia tootedisaini osakonna IV kursuse üliõpilane Riho Tiivel võitis Itaalias toimunud disainikonkursi "ReAL 13 - Eating Anywhere" peapreemia oma alumiiniumist lusikaga "Spoon Container"

  8. LiYbCl4(THF4

    Directory of Open Access Journals (Sweden)

    Lukas Richtera

    2011-06-01

    Full Text Available The title compound, di-μ-chlorido-dichlorido-1κ2Cl-tetrakis(tetrahydrofuran-1κ2O,2κ2O-lithiumytterbium(III, [LiYbCl4(C4H8O4], was prepared by the reaction of YbCl3(THF3 with LiCl in THF (THF is tetrahydrofuran. The central motif of the structure is a Yb(μ-Cl2Li ring. The Yb atom is hexacoordinated to four Cl atoms and two THF molecules oriented in a trans fashion. The Li atom has a tetrahedral environment and is coordinated to two Cl atoms and two THF molecules. No intermolecular interactions other than van der Waals forces were observed. Two of the THF molecules are disordered over two positions.

  9. Barrier Li Quantum Dots in Magnetic Fields

    Institute of Scientific and Technical Information of China (English)

    LIUYi-Min; LIXiao-Zhu; YANWen-Hong; BAOCheng-Guang

    2003-01-01

    The methods for the few-body system are introduced to investigate the states of the barrier Li quantum dots (QDs) in an arbitrary strength of magnetic field. The configuration, which consists of a positive ion located on the z-axis at a distaneed from the two-dimensional QD plane (the x-y plane) and three electrons in the dot plane bound by the positive ion, is called a barrier Li center. The system, which consists of three electrons in the dot plane bound by the ion,is called a barrier Li QD. The dependence of energy of the state of the barrier Li QD on an external magnetic field B and the distance d is obtained. The angular momentum L of the ground states is found to jump not only with the variation orB but also with d.

  10. EKA tootedisaini üliõpilane...

    Index Scriptorium Estoniae

    2005-01-01

    Eesti Kunstiakadeemia tootedisaini osakonna IV kursuse üliõpilane Riho Tiivel võitis Itaalias toimunud disainikonkursi "ReAL 13 - Eating Anywhere" peapreemia oma alumiiniumist lusikaga "Spoon Container"

  11. Li'l Red Schoolhouse workshops

    Science.gov (United States)

    1993-01-01

    Education specialists at Stennis conduct staff development workshops for elementary and secondary teachers of math, science and technology and other subjects as well as specialized workshops conducted in the NASA Li'l Red Schoolhouse.

  12. USGS Atchafalaya 2 LiDAR

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The Light Detection and Ranging (LiDAR) dataset is a survey of the Atchafalaya Basin project area. The entire survey area for Atchafalaya encompasses approximately...

  13. Specification For ST-5 Li Ion Battery

    Science.gov (United States)

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

    2000-01-01

    This Specification defines the general requirements for rechargeable Space Flight batteries intended for use in the ST-5 program. The battery chemistry chosen for this mission is lithium ion (Li-Ion).

  14. Compaction of LiBH4-LiAlH4 nanoconfined in activated carbon nanofibers

    DEFF Research Database (Denmark)

    Plerdsranoy, Praphatsorn; Javadian, Payam; Jensen, Nicholai Daugaard

    2017-01-01

    To enhance volumetric hydrogen capacity for on-board fuel cells, compaction of LiAlH4-LiBH4 nanoconfined in activated carbon nanofibers (ACNF) is for the first time proposed. Loose powders of milled and nanoconfined LiAlH4-LiBH4 samples are compacted under 976 MPa to obtain the pellet samples wit...

  15. Optical and scintillation properties of Ce3+ doped LiYF4 and LiLuF4 crystals

    NARCIS (Netherlands)

    Combes, CM; Dorenbos, P; vanEijk, CWE; Pedrini, C; DenHartog, HW; Gesland, JY; Rodnyi, PA

    1997-01-01

    Optical properties of LiYF4:Ce and LiLuF4:Ce were studied viz. optical absorption spectra and X-ray induced emission spectra. The scintillation characteristics of LiYF4:Ce and LiLuF4:Ce were investigated viz. gamma-ray induced pulse height spectra and decay time measurements. A model is presented to

  16. Unravelling Li-Ion Transport from Picoseconds to Seconds: Bulk versus Interfaces in an Argyrodite Li6PS5Cl-Li2S All-Solid-State Li-Ion Battery.

    Science.gov (United States)

    Yu, Chuang; Ganapathy, Swapna; de Klerk, Niek J J; Roslon, Irek; van Eck, Ernst R H; Kentgens, Arno P M; Wagemaker, Marnix

    2016-09-01

    One of the main challenges of all-solid-state Li-ion batteries is the restricted power density due to the poor Li-ion transport between the electrodes via the electrolyte. However, to establish what diffusional process is the bottleneck for Li-ion transport requires the ability to distinguish the various processes. The present work investigates the Li-ion diffusion in argyrodite Li6PS5Cl, a promising electrolyte based on its high Li-ion conductivity, using a combination of (7)Li NMR experiments and DFT based molecular dynamics simulations. This allows us to distinguish the local Li-ion mobility from the long-range Li-ion motional process, quantifying both and giving a coherent and consistent picture of the bulk diffusion in Li6PS5Cl. NMR exchange experiments are used to unambiguously characterize Li-ion transport over the solid electrolyte-electrode interface for the electrolyte-electrode combination Li6PS5Cl-Li2S, giving unprecedented and direct quantitative insight into the impact of the interface on Li-ion charge transport in all-solid-state batteries. The limited Li-ion transport over the Li6PS5Cl-Li2S interface, orders of magnitude smaller compared with that in the bulk Li6PS5Cl, appears to be the bottleneck for the performance of the Li6PS5Cl-Li2S battery, quantifying one of the major challenges toward improved performance of all-solid-state batteries.

  17. LiFi - Let There Be Light

    OpenAIRE

    Chauhan, Mihir; Kulai, Aditya

    2015-01-01

    The paper proclaims a summary of Li-Fi technology. It is an efficient data communication mechanism involving visible light as a medium of transmission. This monograph introduces the concept of Li-Fi and its working model. Furthermore, it discusses its benefits, shortcomings and examines ways to mitigate the drawbacks. Additionally, it analyzes its present applications and explores its future scope in the competitive wireless network market.

  18. Stan Z. Li: Rolling face recognition

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    @@ Among the galaxy of research and development organizations in northwest Beijing's Zhongguancun district, known as China's Silicon Valley, two are especially well-known to IT researchers: Microsoft Research Asia (MSRA), and, within a few blocks on the other side of the street, the CAS Institute of Automation (CASIA). While most people in Chinese scientific organizations strive to move to a large foreign counterpart, Dr. Stan Z. Li (LI Ziqing) moves against the stream.

  19. New Wedding Customs of the Li People

    Institute of Scientific and Technical Information of China (English)

    JENNIFER; LIM

    1998-01-01

    HISTORICALLY, Hainan Island has been the land of the Li people. It was only during the Western Han Dynasty (206 B.C.-A.D.25), when the centralizedgovernment established two prefectures here caned Zhuya and Dan’er, that the Han people began to come southward to this remote island. So when anthropologists study the history and local customs of Hainan, the earliest information concerns the development of the Li nationality. There is a museum which provides clues to this history, the

  20. Lithium diffusion in spinel Li4Ti5O12 and LiTi2O4 films detected with 8Liβ -NMR

    Science.gov (United States)

    Sugiyama, Jun; Umegaki, Izumi; Uyama, Takeshi; McFadden, Ryan M. L.; Shiraki, Susumu; Hitosugi, Taro; Salman, Zaher; Saadaoui, Hassan; Morris, Gerald D.; MacFarlane, W. Andrew; Kiefl, Robert F.

    2017-09-01

    Diffusion of Li+ in (111) oriented thin films of the spinels Li4Ti5O12 and LiTi2O4 has been studied with 8Liβ -detected NMR in the temperature range between 5 and 310 K. In Li4Ti5O12 , the spin-lattice relaxation rate (1 /T1 ) versus temperature shows a clear maximum around 100 K (=Tmax ) which we attribute to magnetic freezing of dilute Ti3 + local magnetic moments, consistent with the results of magnetization and muon spin relaxation (μ+SR ) measurements. The decrease in 1 /T1 with temperature above Tmax indicates that Li+ starts to diffuse with a thermal activation energy (Ea) of 0.11(1) eV. In LiTi2O4 , on the contrary, as temperature increases from 200 K, 1 /T1 increases monotonically up to 310 K. This suggests that Li also starts to diffuse above 200 K with Ea=0.16 (2 ) eV in LiTi2O4 . Comparison with conventional Li-NMR on Li4Ti5O12 implies that both β -NMR and μ+SR sense short-range Li motion, i.e., a jump diffusion of Li+ to the nearest neighboring sites.

  1. Ionic Debye Screening in Dense Liquid Plasmas Observed for Li+p,d Reactions with Liquid Li Target

    Institute of Scientific and Technical Information of China (English)

    J.Kasagi; H.Yonemura; Y.Toriyabe; A.Nakagawa; T.Sugawara; WANG Tie-shan

    2009-01-01

    Thick target yields of a particles emitted in the ~6Li(d,a)~4 He and ~7Li(p,a)~4 He reactions were measured for Li target in the solid and liquid phase.Observed reaction rates for the liquid Li are always larger than those for the solid.This suggests that the stopping power of hydrogen ion in the liquid Li metal might be smaller than in the solid.Using the empirically obtained stopping power for the liquid Li,we have deduced the screening potentials of the Li+p and Li+d reactions in both phases.The deduced screening potential for the liquid Li is about 500 eV larger than for the solid.This difference is attributed to the effect of liquefied Li~+ ions.It is concluded that the ionic screening is much stronger than the electronic screening in a low-temperature dense plasmas.

  2. Tracing Waste Water with Li isotopes

    Science.gov (United States)

    Millot, R.; Desaulty, A. M.

    2015-12-01

    The contribution of human activities such as industries, agriculture and various domestic inputs, becomes more and more significant in the chemical composition of the dissolved load of rivers. Human factors act as a supplementary key process. Therefore the mass-balance for the budget of catchments and river basins include anthropogenic disturbances. In the present study, we investigate waste water tracing by the use of Li isotopes in a small river basin near Orléans in France (l'Egoutier, 15 km² and 5 km long). It is well known that Li has strategic importance for numerous industrial applications including its use in the production of batteries for both mobile devices (computers, tablets, smartphones, etc.) and electric vehicles, but also in pharmaceutical formulations. In the present work, we collected river waters samples before and after the release from a waste water treatment plant connected to an hospital. Lithium isotopic compositions are rather homogeneous in river waters with δ7Li values around -0.5‰ ± 1 along the main course of the stream (n=7). The waste water sample is very different from the natural background of the river basin with Li concentration being twice of the values without pollution and significant heavy lithium contribution (δ7Li = +4‰). These preliminary results will be discussed in relation with factors controlling the distribution of Li and its isotopes in this specific system and compared with the release of other metals such as Pb or Zn.

  3. LiGa(OTf)(sub 4) as an Electrolyte Salt for Li-Ion Cells

    Science.gov (United States)

    Reddy, V. Prakash; Prakash, G. K. Syria; Hu, Jinbo; Yan, Ping; Smart, Marshall; Bugga, ratnakumar; Chin, Keith; Surampudi, Subarao

    2008-01-01

    Lithium tetrakis(trifluoromethane sulfo - nato)gallate [abbreviated "LiGa(OTf)4" (wherein "OTf" signifies trifluoro - methanesulfonate)] has been found to be promising as an electrolyte salt for incorporation into both liquid and polymer electrolytes in both rechargeable and non-rechargeable lithium-ion electrochemical cells. This and other ingredients have been investigated in continuing research oriented toward im proving the performances of rechargeable lithium-ion electrochemical cells, especially at low temperatures. This research at earlier stages, and the underlying physical and chemical principles, were reported in numerous previous NASA Tech Briefs articles. As described in more detail in those articles, lithiumion cells most commonly contain nonaqueous electrolyte solutions consisting of lithium hexafluorophosphate (LiPF6) dissolved in mixtures of cyclic and linear alkyl carbonates, including ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), and ethyl methyl carbonate (EMC). Although such LiPF6-based electrolyte solutions are generally highly ionically conductive and electrochemically stable, as needed for good cell performance, there is interest in identifying alternate lithium electrolyte salts that, relative to LiPF6, are more resilient at high temperature and are less expensive. Experiments have been performed on LiGa(OTf)4 as well as on several other candidate lithium salts in pursuit of this interest. As part of these experiments, LiGa(OTf)4 was synthesized by the reaction of Ga(OTf)3 with an equimolar portion of LiOTf in a solvent consisting of anhydrous acetonitrile. Evaporation of the solvent yielded LiGa(OTf)4 as a colorless crystalline solid. The LiGa(OTf)4 and the other salts were incorporated into solutions with PC and DMC. The resulting electrolyte solutions exhibited reasonably high ionic conductivities over a relatively wide temperature range down to 40 C (see figure). In cyclic

  4. Data mining of molecular dynamics data reveals Li diffusion characteristics in garnet Li7La3Zr2O12

    OpenAIRE

    Chi Chen; Ziheng Lu; Francesco Ciucci

    2017-01-01

    Understanding Li diffusion in solid conductors is essential for the next generation Li batteries. Here we show that density-based clustering of the trajectories computed using molecular dynamics simulations helps elucidate the Li diffusion mechanism within the Li7La3Zr2O12 (LLZO) crystal lattice. This unsupervised learning method recognizes lattice sites, is able to give the site type, and can identify Li hopping events. Results show that, while the cubic LLZO has a much higher hopping rate c...

  5. Li-Ion Battery with LiFePO4 Cathode and Li4Ti5O12 Anode for Stationary Energy Storage

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wei; Choi, Daiwon; Yang, Zhenguo

    2013-01-01

    i-ion batteries based on commercially available LiFePO4 cathode and Li4Ti5O12 anode were investigated for potential stationary energy storage applications. The full cell that operated at flat 1.85V demonstrated stable cycling for 200 cycles followed by a rapid fade. A significant improvement in cycling stability was achieved via Ketjen black coating of the cathode. A Li-ion full cell with Ketjen black modified LiFePO4 cathode and an unmodified Li4Ti5O12 anode exhibited negligible fade after more than 1200 cycles with a capacity of ~130mAh/g. The improved stability, along with its cost-effectiveness, environmentally benignity and safety, make the LiFePO4/ Li4Ti5O12 Li-ion battery a promising option of storing renewable energy.

  6. Synthesis and electrochemistry of cubic rocksalt Li-Ni-Ti-O compounds in the phase diagram of LiNiO 2-LiTiO 2-Li[Li 1/3Ti 2/3]O 2

    Science.gov (United States)

    Zhang, Lianqi; Noguchi, Hideyuki; Li, Decheng; Muta, Takahisa; Wang, Xiaoqing; Yoshio, Masaki; Taniguchi, Izumi

    On the basis of extreme similarity between the triangle phase diagrams of LiNiO 2-LiTiO 2-Li[Li 1/3Ti 2/3]O 2 and LiNiO 2-LiMnO 2-Li[Li 1/3Mn 2/3]O 2, new Li-Ni-Ti-O series with a nominal composition of Li 1+ z/3Ni 1/2- z/2Ti 1/2+ z/6O 2 (0 ≤ z ≤ 0.5) was designed and attempted to prepare via a spray-drying method. XRD identified that new Li-Ni-Ti-O compounds had cubic rocksalt structure, in which Li, Ni and Ti were evenly distributed on the octahedral sites in cubic closely packed lattice of oxygen ions. They can be considered as the solid solution between cubic LiNi 1/2Ti 1/2O 2 and Li[Li 1/3Ti 2/3]O 2 (high temperature form). Charge-discharge tests showed that Li-Ni-Ti-O compounds with appropriate compositions could display a considerable capacity (more than 80 mAh g -1 for 0.2 ≤ z ≤ 0.27) at room temperature in the voltage range of 4.5-2.5 V and good electrochemical properties within respect to capacity (more than 150 mAh g -1 for 0 ≤ z ≤ 0.27), cycleability and rate capability at an elevated temperature of 50 °C. These suggest that the disordered cubic structure in some cases may function as a good host structure for intercalation/deintercalation of Li +. A preliminary electrochemical comparison between Li 1+ z/3Ni 1/2- z/2Ti 1/2+ z/6O 2 (0 ≤ z ≤ 0.5) and Li 6/5Ni 2/5Ti 2/5O 2 indicated that charge-discharge mechanism based on Ni redox at the voltage of >3.0 V behaved somewhat differently, that is, Ni could be reduced to +2 in Li 1+ z/3Ni 1/2- z/2Ti 1/2+ z/6O 2 while +3 in Li 6/5Ni 2/5Ti 2/5O 2. Reduction of Ti 4+ at a plateau of around 2.3 V could be clearly detected in Li 1+ z/3Ni 1/2- z/2Ti 1/2+ z/6O 2 with 0.27 ≤ z ≤ 0.5 at 50 °C after a deep charge associated with charge compensation from oxygen ion during initial cycle.

  7. Kinetic behavior of LiFeMgPO 4 cathode material for Li-ion batteries

    Science.gov (United States)

    Hong, Jian; Wang, Chunsheng; Kasavajjula, Uday

    LiFe 0.9Mg 0.1PO 4 material was prepared by mechanical milling method, followed by heat treatment. The equilibrium potential-composition isotherm of LiFe 0.9Mg 0.1PO 4 and charge-discharge kinetics of LiFe 0.9Mg 0.1PO 4 were measured using galvanostatic intermittent titration technique (GITT), potential-step chronoamperometry (PSCA), and electrochemical impedance spectroscopy (EIS). The rate performance of the cathode is controlled by the charge-transfer kinetics, electronic conductivity, Li-ion diffusion capability, and phase transformation rate. Since LiFe 0.9Mg 0.1PO 4 has a fast charge-transfer reaction and high electronic and ionic diffusivity, the phase transformation between LiFe 0.9Mg 0.1PO 4 and Li 0.1Fe 0.9Mg 0.1PO 4 begins to play a more important role in the charge-discharge process, as is evident by an inductive loop induced by the phase transformation in the low frequency region of EIS. The phase purity and morphology of LiFe 0.9Mg 0.1PO 4 were also observed using X-ray diffraction (XRD) and scanning electron microscopy (SEM).

  8. Hyperfine structure in photoassociative spectra of 6Li2 and 7Li2

    NARCIS (Netherlands)

    Abraham, E.R.I.; McAlexander, W.I.; Stoof, H.T.C.; Hulet, R.G.

    1996-01-01

    We present spectra of hyperfine resolved vibrational levels of the A1Σu+and 1 3Σg+ states of 6Li2 and 7Li2 obtained via photoassociation of colliding ultracold atoms in a magneto-optical trap. A simple first-order perturbation theory analysis accurately accounts for the frequency splittings and rela

  9. LiSK - A C++ Library for Evaluating Classical Polylogarithms and $\\text{Li}_{22}$

    CERN Document Server

    Kirchner, Sebastian

    2016-01-01

    I present a lightweight C++ library for the evaluation of classical polylogarithms Li_n and the special function Li_{22} for arbitrary complex arguments. The evaluation is possible in arbitrary precision arithmetic and features also an explicit double precision implementation for a much faster numerical evaluation. The implementation is based on arXiv:1601.02649.

  10. A design optimization methodology for Li+ batteries

    Science.gov (United States)

    Golmon, Stephanie; Maute, Kurt; Dunn, Martin L.

    2014-05-01

    Design optimization for functionally graded battery electrodes is shown to improve the usable energy capacity of Li batteries predicted by computational simulations and numerically optimizing the electrode porosities and particle radii. A multi-scale battery model which accounts for nonlinear transient transport processes, electrochemical reactions, and mechanical deformations is used to predict the usable energy storage capacity of the battery over a range of discharge rates. A multi-objective formulation of the design problem is introduced to maximize the usable capacity over a range of discharge rates while limiting the mechanical stresses. The optimization problem is solved via a gradient based optimization. A LiMn2O4 cathode is simulated with a PEO-LiCF3SO3 electrolyte and both a Li Foil (half cell) and LiC6 anode. Studies were performed on both half and full cell configurations resulting in distinctly different optimal electrode designs. The numerical results show that the highest rate discharge drives the simulations and the optimal designs are dominated by Li+ transport rates. The results also suggest that spatially varying electrode porosities and active particle sizes provides an efficient approach to improve the power-to-energy density of Li+ batteries. For the half cell configuration, the optimal design improves the discharge capacity by 29% while for the full cell the discharge capacity was improved 61% relative to an initial design with a uniform electrode structure. Most of the improvement in capacity was due to the spatially varying porosity, with up to 5% of the gains attributed to the particle radii design variables.

  11. Coulomb excitation of {sup 8}Li

    Energy Technology Data Exchange (ETDEWEB)

    Assuncao, Marlete; Britos, Tatiane Nassar [Universidade Federal de Sao Paulo (UNIFESP), SP (Brazil). Dept. de Ciencias Exatas e da Terra; Descouvemont, Pierre [Universite Libre de Bruxelles (ULB), Brussels (Belgium). Physique Nucleaire Theorique et Physique Mathematique; Lepine-Szily, Alinka; Lichtenthaler Filho, Rubens; Barioni, Adriana; Silva, Diego Medeiros da; Pereira, Dirceu; Mendes Junior, Djalma Rosa; Pires, Kelly Cristina Cezaretto; Gasques, Leandro Romero; Morais, Maria Carmen; Added, Nemitala; Neto Faria, Pedro; Rec, Rafael [Universidade de Sao Paulo (IF/USP), SP (Brazil). Inst. de Fisica. Dept. de Fisica Nuclear

    2012-07-01

    Full text: This work shows the Coulomb Excitation of {sup 8}Li on targets that have effectively behavior of Rutherford in angles and energies of interest for determining the value of the B(E2) electromagnetic transition. Theoretical aspects involved in this type of measure, known as COULEX [1], and some results in the literature [2-3] will be presented. Some problems with the targets and measurement system while performing an experiment on Coulomb Excitation of {sup 8}Li will be discussed: the energy resolution, background, possible contributions of the primary beam and also the excited states of the target near the region of elastic and inelastic peaks. They will be illustrated by measurements of the Coulomb Excitation of {sup 8}Li on targets of {sup 197}Au and {sup 208}Pb using the system RIBRAS(Brazilian Radioactive Ion Beam). In this case, the {sup 8}Li beam(T{sub 1/2} = 838 ms)is produced by {sup 9}Be({sup 7}Li;{sup 8} Li){sup 8}Be reaction from RIBRAS system which is installed at Instituto de Fisica of the Universidade de Sao Paulo. The primary {sup 7L}i beam is provided by Pelletron Accelerator. [1] K. Alder and A. Winther, Electromagnetic Excitation, North-Holland, New York, 1975; [2] P. Descouvemont and D. Baye, Phys. Letts. B 292, 235-238, 1992; [3] J. A. Brown, F. D. Becchetti, J. W. Jaenecke, K, Ashktorab, and D. A. Roberts, J. J. Kolata, R. J. Smith, and K. Lamkin, R. E. Warner, Phys. Rev. Letts., 66, 19, 1991; [4] R. J. Smith, J. J Kolata, K. Lamkin and A. Morsard, F. D. Becchetti, J. A. Brown, W. Z. Liu, J. W. Jaenecke, and D. A. Roberts, R. E. Warner, Phys. Rev. C, 43, 5, 1991. (author)

  12. First Principles Study of Al-Li Intermetallic Compounds

    Science.gov (United States)

    Yu, Hai-li; Duan, Xiao-hui; Ma, Yong-jun; Zeng, Min

    2012-12-01

    The structural properties, heats of formation, elastic properties, and electronic structures of four compositions of binary Al-Li intermetallics, Al3Li, AlLi, Al2Li3, and Al4Li9, are analyzed in detail by using density functional theory. The calculated formation heats indicate a strong chemical interaction between Al and Li for all the Al-Li intermetallics. In particular, in the Li-rich Al-Li compounds, the thermodynamic stability of intermetallics linearly decreases with increasing concentration of Li. According to the computational single crystal elastic constants, all the four Al-Li intermetallic compounds considered here are mechanically stable. The polycrystalline elastic modulus and Poisson's ratio have been deduced by using Voigt, Reuss, and Hill approximations, and the calculated ratios of bulk modulus to shear modulus indicate that the four compositions of binary Al-Li intermetallics are brittle materials. With the increase of Li concentration, the bulk modulus of Al-Li intermetallics decreases in a linear manner.

  13. Absolute level-resolved reactive and inelastic rate constants in Li+Li2*

    Science.gov (United States)

    Coppage, Steven; Matei, Paula; Stewart, Brian

    2008-06-01

    We have used nuclear parity-changing collisions to obtain absolute level-to-level rate constants for reactive scattering in a triatomic system with identical nuclei. We have determined rate constants for the system 7Li2*(A 1Σu+)(vi=2,ji=19)+7Li-->7Li+7Li2*(A 1Σu+)(vf,jf), from laser-induced fluorescence spectra of lithium vapor in a heat pipe oven. Parity-preserving collisions yielded measurements of absolute rotationally and vibrationally inelastic rate constants as well. We compare the reactive rate constants with statistical prior distributions and the inelastic results with previously measured results on the Ne+7Li2* system.

  14. Electrochemical performance of LiFePO4 cathode material for Li-ion battery

    Institute of Scientific and Technical Information of China (English)

    LI Shuzhong; LI Chao; FAN Yanliang; XU Jiaqiang; WANG Tao; YANG Shuting

    2006-01-01

    In the search for improved materials for rechargeable lithium batteries, LiFePO4 offers interesting possibilities because of its low raw materials cost, environmental friendliness and safety. The main drawback with using the material is its poor electronic conductivity and this limitation has to be overcome. Here Al-doped LiFePO4/C composite cathode materials were prepared by a polymer-network synthesis technique. Testing of X-ray diffraction, charge-discharge, and cyclic voltammetry were carried out for its performance. Results show that Al-doped LiFePO4/C composite cathode materials have a high initial capacity, good cycle stability and excellent low temperature performance. The electrical conductivity of LiFePO4 material can be obviously improved by doping Al. The better electrochemical performances of Al-doped LiFePO4/C composite cathode materials have a connection with its conductivity.

  15. Characteristic of Absorption Heat Transfer using LiBr+LiI Solution

    Science.gov (United States)

    Tsujimori, Atsushi; Ozaki, Eiichi; Nakao, Kazushige

    LiBr-H20 absorption chiller is widely used in Japan, and many research have been made for absorption characteristic in terms of enhancing heat transfer. Another study have been performed for widening working range with higher crystallization limits, and it was reported that adding LiI salt to LiBr-H20 working fluid provide about 5 [mass%] higher crystallization limit under the condition of absorption pressure range. It is necessary to reveal absorption heat transfer performance to utilize this working fluid pair for absorption chiller. In this study absorption heat transfer characteristic was investigated for horizontal and vertical tube. As a result, it was found that heat transfer coefficient increased as mass flow rate of solution increased and mass concentration of solution decrease and that these characteristic were almost the same as LiBr solution, though this solution gave slightly less heat transfer coefficient than LiBr solution.

  16. Rate-dependent morphology of Li2O2 growth in Li-O2 batteries

    CERN Document Server

    Horstmann, B; Mitchell, R; Bessler, W G; Shao-Horn, Y; Bazant, M Z

    2013-01-01

    Compact solid discharge products enable energy storage devices with high gravimetric and volumetric energy densities, but solid deposits on active surfaces can disturb charge transport and induce mechanical stress. In this Letter we develop a nanoscale continuum model for the growth of Li2O2 crystals in lithium-oxygen batteries with organic electrolytes, based on a theory of electrochemical non-equilibrium thermodynamics originally applied to Li-ion batteries. As in the case of lithium insertion in phase-separating LiFePO4 nanoparticles, the theory predicts a transition from complex to uniform morphologies of Li2O2 with increasing current. Discrete particle growth at low discharge rates becomes suppressed at high rates, resulting in a film of electronically insulating Li2O2 that limits cell performance. We predict that the transition between these surface growth modes occurs at current densities close to the exchange current density of the cathode reaction, consistent with experimental observations.

  17. Suppressing The Growth Of Dendrites In Secondary Li Cells

    Science.gov (United States)

    Davies, Evan D.; Perrone, David E.; Shen, David H.

    1996-01-01

    Proposed technique for suppressing growth of lithium dendrites in rechargeable lithium electrochemical power cells involves periodic interruption of steady charging current with short, high-current discharge pulses. Technique applicable to lithium cells of several different types, including Li/TiS(2), Li/NbSe(3), Li/CoO(2), Li/MoS(2), Li/Vo(x), and Li/MnO(2). Cells candidates for use in spacecraft, military, communications, automotive, and other applications in which high-energy-density rechargeable batteries needed.

  18. Li-FSI Impurity Impact Study: Final CRADA Report

    Energy Technology Data Exchange (ETDEWEB)

    Pupek, Krzysztof [Argonne National Lab. (ANL), Argonne, IL (United States); Dzwiniel, Trevor [Argonne National Lab. (ANL), Argonne, IL (United States); Krumdick, Gregory [Argonne National Lab. (ANL), Argonne, IL (United States)

    2017-01-01

    There is growing interest in lithium bis(fluorosulfonyl)imide (LiFSI ) as an alternative to LiPF6 and as an additive to electrolytes used in lithium-ion cells. LiFSI has attracted attention because it is reported to have higher ionic conductivity, better high temperature stability, and enhanced stability toward hydrolysis, Also, LiFSI additive to electrolytes can bring benefits of improved storage properties and reduced gas evolution in the cells. Different levels of different electrochemically active impurities could affect the performance of LiFSI as an electrolyte salt for Li-ion batteries, generating inconsistent and conflicting interpretations of the experimental data.

  19. Anharmonicity and phase stability of antiperovskite Li3OCl

    Science.gov (United States)

    Chen, Min-Hua; Emly, Alexandra; Van der Ven, Anton

    2015-06-01

    A lattice-dynamics study of the cubic Li3OCl antiperovskite, a candidate solid electrolyte in lithium-ion batteries, reveals the presence of dynamical instabilities with respect to rotations of the Li6O octahedra. Calculated energy landscapes in the subspace of unstable octahedral rotational modes are very shallow with at most a 1 meV per formula unit reduction in energy upon breaking the cubic symmetry. While Li3OCl is not stable relative to decomposition into Li2O and LiCl at 0 K, estimates of the vibrational free energy suggest that Li3OCl antiperovskite should become entropically stabilized above approximately 480 K.

  20. 6^Li in the atmosphere of GJ 117

    CERN Document Server

    Christian, D J; Jevremovic, D; Hauschildt, P H; Baron, E

    2005-01-01

    We present high resolution VLT UVES observations of the active K dwarf GJ 117. 6^Li enhancement has been shown for energetic solar events, one chromospherically active binary, and several dwarf halo stars. Our analysis reveals the detection of 6^Li on this source with 6^Li/7^Li = 0.030+/-0.010. We found no significant contribution from other lines, including Ti I, in the Li profile of GJ 117 and a template star of similar spectral type and metallicity. We discuss the possibility for 6^Li production by spallation and find it to be consistent with the activity levels of the object.

  1. Theory of laser enhancement and suppression of cold reactions: the fermion-boson 6Li+7Li2(variant Planck's over 2pi omega0) 6Li7Li+7Li radiative collision.

    Science.gov (United States)

    Li, Xuan; Parker, Gregory A; Brumer, Paul; Thanopulos, Ioannis; Shapiro, Moshe

    2008-03-28

    We present a nonperturbative time-dependent quantum mechanical theory of the laser catalysis and control of a bifurcating A+BC(variant Planck's over 2pi omega(0))ABC*(v)(variant Planck's over 2pi omega(0) )AB+C reaction, with ABC*(v) denoting an intermediate, electronically excited, complex of ABC in the vth vibrational state. We apply this theory to the low collision energy fermion-boson light-induced exchange reaction, (6)Li((2)S)+(7)Li(2)((3)Sigma(u)(+))(variant Planck's over 2pi omega(0))((6)Li(7)Li(7)Li)*(variant Planck's over 2pi omega(0))(6)Li(7)Li((3)Sigma(+))+(7)Li((2)S). We show that at very low collision energies and energetically narrow (approximately 0.01 cm(-1)) initial reactant wave packets, it is possible to tune the yield of the exchange reaction from 0 to near-unity (yield >or=99%) values. Controllability is somewhat reduced at collisions involving energetically wider (approximately 1 cm(-1)) initial reactant wave packets. At these energetic bandwidths, the radiative reactive control, although still impressive, is limited to the 0%-76% reactive-probabilities range.

  2. Enhanced high temperature performance of LiMn2O4 coated with Li3BO3 solid electrolyte

    Indian Academy of Sciences (India)

    Liu Jinlian; Wu Xianming; Chen Shang; Liu Jianben; He Zeqiang

    2013-08-01

    Cathode material, LiMn2O4, was synthesized by solid-state reaction followed by surface coating of Li3BO3 solid electrolyte. Structure and electrochemical performance of the prepared powders were characterized by X-ray diffraction, scanning electron microscopy, cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic charge–discharge techniques, respectively. Results show that Li3BO3 coated LiMn2O4 has similar X-ray diffraction patterns as LiMn2O4. The discharge specific capacities of LiMn2O4 coated with 0.1, 0.3 and 0.6 wt% Li3BO3 are 123.3, 118.2 and 110 mAh/g, respectively, which is slightly smaller than that of 124.4 mAh/g for LiMn2O4. However, the capacity retention of Li3BO3 coated LiMn2O4 is at least 5.6 and 7.6% higher than LiMn2O4 when cycled at room temperature and 55 °C, respectively. Li3BO3 coated LiMn2O4 shows much better cycling behaviours than LiMn2O4.

  3. Quantitative analysis of Li by PIGE technique

    Science.gov (United States)

    Fonseca, M.; Mateus, R.; Santos, C.; Cruz, J.; Silva, H.; Luis, H.; Martins, L.; Jesus, A. P.

    2017-09-01

    In this work, the cross section of the reactions 7Li(p,pγ)7Li (γ - 478 keV) at the proton energy range 2.0-4.2 MeV was measured. The measurements were carried out at the 3 MV Tandem Accelerator at the CTN/IST Laboratory in Lisbon. To validate the obtained results, calculated gamma-ray yields were compared, at several proton energy values, with experimental yields for thick samples made of inorganic compounds containing lithium. In order to quantify the light elements present in the samples, we used a standard free method for PIGE in thick samples, based on a code - Emitted Radiation Yield Analysis (ERYA), which integrates the nuclear reaction excitation function along the depth of the sample. We also demonstrated the capacity of the technique for analysis of Li ores, as Spodumene, Lithium Muscovite and Holmquistite, and Li-alloys for plasma facing materials showing that this is a reliable and accurate method for PIGE analysis of Li in thick samples.

  4. Formation and reduction behaviors of zirconium oxide compounds in LiCl-Li2O melt at 923 K

    Science.gov (United States)

    Sakamura, Yoshiharu; Iizuka, Masatoshi; Kitawaki, Shinichi; Nakayoshi, Akira; Kofuji, Hirohide

    2015-11-01

    The reduction behaviors of ZrO2, Li2ZrO3 and (U,Pu,Zr)O2 in a LiCl-Li2O salt bath at 923 K were investigated. This study was conducted as part of a feasibility study on the pyrochemical treatment of damaged fuel debris generated by severe accidents at light water reactors. It was demonstrated in electrolytic reduction tests that the uranium in synthetic corium specimens of (U,Pu,Zr)O2 with various ZrO2 contents could be reduced to the metallic form and that part of the zirconium was converted to Li2ZrO3. Zirconium metal and Li2ZrO3 were obtained by the reduction of ZrO2. The reduction of Li2ZrO3 did not proceed even in LiCl containing no Li2O. Moreover, the stable chemical forms of the ZrO2-Li2O complex oxide were investigated as a function of the Li2O concentration in LiCl. ZrO2 was converted to Li2ZrO3 at a Li2O concentration of 0.018 wt%. As the Li2O concentration was increased, Li2ZrO3 was converted to Li6Zr2O7 and then to Li8ZrO6. It is suggested that the removal of Li2ZrO3 from the reduction product is a key point in the pyrochemical treatment of corium.

  5. Corrosion studies of LiH thin films

    Science.gov (United States)

    Tonks, J. P.; King, M. O.; Galloway, E. C.; Watts, J. F.

    2017-02-01

    Thin films of LiH and its corrosion products were studied using temperature programmed decomposition (TPD), x-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy (AES). Thin films were grown on Ni(100) in an ultra high vacuum system using an electron beam evaporator. Characteristic Li KLL AES peaks were identified for Li, LiH, Li2O and LiOH which facilitated identification of thin film composition. XPS of the O 1s region revealed three distinct chemical shifts which were attributed to Li2O, LiOH and chemisorbed H2O. We show that exposing LiH to very low H2O partial pressures results in formation of LiOH/Li2O domains on LiH. We also show that these XPS peaks can be linked to reaction mechanisms in the TPD profiles. TPD traces have been explicitly modelled to determine the activation energies of the reactions and compare favourably with previous measurements on bulk LiH samples.

  6. Heat capacities of polycrystalline {sup n}LiH and {sup n}LiD by differential scanning calorimetric method

    Energy Technology Data Exchange (ETDEWEB)

    Jat, Ram Avtar [Product Development Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Parida, S.C., E-mail: sureshp@barc.gov.i [Product Development Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Krishnan, K. [Fuel Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Anand, N.S.; Sawant, S.G.; Agarwal, Renu; Singh, Ziley [Product Development Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Aggarwal, S.K. [Fuel Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Venugopal, V. [RC and I Group, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India)

    2010-08-27

    The heat capacities of polycrystalline {sup n}LiH and {sup n}LiD were measured by differential scanning calorimeter in the temperature range from 125 to 800 K. The smoothed values of heat capacities were used to calculate various thermodynamic functions for {sup n}LiH and {sup n}LiD from 0 to 800 K. Isotopic effect on heat capacity of {sup n}LiH and {sup n}LiD is predominant at higher temperatures (>80 K) whereas below 80 K the isotopic effect is negligible.

  7. Photoluminescence and Optically Stimulated Luminescence Studies of LiAlO2 and LiGaO2 Crystals

    Science.gov (United States)

    2015-03-26

    PHOTOLUMINESCENCE AND OPTICALLY STIMULATED LUMINESCENCE STUDIES OF LiAlO2 AND LiGaO2 CRYSTALS THESIS Ian P. Ferguson, Second Lieutenant, USAF AFIT...STIMULATED LUMINESCENCE STUDIES OF LiAlO2 AND LiGaO2 CRYSTALS THESIS Presented to the Faculty Department of Engineering Physics Graduate School of...FOR PUBLIC RELEASE; DISTRIBUTION UNLIMITED. AFIT-ENP-MS-15-M-106 PHOTOLUMINESCENCE AND OPTICALLY STIMULATED LUMINESCENCE STUDIES OF LiAlO2 AND LiGaO2

  8. Li14P2O3N6 and Li7PN4: Computational study of two nitrogen rich crystalline LiPON electrolyte materials

    Science.gov (United States)

    Al-Qawasmeh, Ahmad; Holzwarth, N. A. W.

    2017-10-01

    Two lithium oxonitridophosphate materials are computationally examined and found to be promising solid electrolytes for possible use in all solid-state batteries having metallic Li anodes - Li14P2O3N6 and Li7PN4. The first principles simulations are in good agreement with the structural analyses reported in the literature for these materials and the computed total energies indicate that both materials are stable with respect to decomposition into binary and ternary products. The computational results suggest that both materials are likely to form metastable interfaces with Li metal. The simulations also find both materials to have Li ion migration activation energies comparable or smaller than those of related Li ion electrolyte materials. Specifically, for Li7PN4, the experimentally measured activation energy can be explained by the migration of a Li ion vacancy stabilized by a small number of O2- ions substituting for N3- ions. For Li14P2O3N6, the activation energy for Li ion migration has not yet been experimentally measured, but simulations predict it to be smaller than that measured for Li7PN4.

  9. Lattice dynamics in Bosonic 7 Li

    Science.gov (United States)

    Chen, Huiyao Y.; Jung, Minwoo; Rabinowitz, Jacob; Madjarov, Ivaylo S.; Cheung, Hil F. H.; Patil, Yogesh Sharad; Vengalattore, Mukund

    2016-05-01

    The light mass and strong spin-dependent interactions in 7 Li make it an attractive candidate to study Bosonic quantum magnetism and lattice dynamics in regimes where rapid dynamics is favored, e.g. percolative transport and entropy segregation. Such studies require large ensembles of quantum degenerate 7 Li atoms which has proved to be a technical challenge. We describe our ongoing efforts to overcome this challenge using Raman sideband cooling (RSC). In addition to enabling the rapid production of large degenerate gases, RSC is also a very powerful means of local control of lattice gas dynamics. Extending this to a spinful 7 Li Bose gas will also enable studies of transport and defect dynamics in F=1 lattice gases. This work is supported by the ARO MURI on non-equilibrium dynamics.

  10. Hydrogen diffusion in Al-Li alloys

    Science.gov (United States)

    Anyalebechi, P. N.

    1990-08-01

    The diffusion coefficients of hydrogen in binary Al-Li alloys containing 1,2, and 3 wt pct Li have been determined from desorption curves of samples saturated with hydrogen at 473 to 873 K. Within this temperature range, the diffusivity of hydrogen in the binary Al-Li alloys investigated has an Arrhenius-type temperature dependence and follows the equation of the general form D = DT) where D 0exp(-Q/R is the diffusion coefficient (m2/s), D 0 is the preexponential or frequency factor (m2/s), R is the gas constant (J/K mol), Q is the activation energy (J/mol), and T is absolute temperature (K). The rate of diffusion of hydrogen in aluminum decreases with increase in lithium additions. This is provisionally attributed to the stronger local binding energy between hydrogen and lithium atoms in the aluminum metal lattice.

  11. Solid-liquid Metastable Equilibria in Quaternary System Li_2SO_4 + Li_2CO_3 + Li_2B_4O_7 + H_2O at 288 K

    Institute of Scientific and Technical Information of China (English)

    SANG Shi-hua; ZHANG Zhen-lei; LI Ming

    2009-01-01

    Metastable equilibrium solubilities and densities of quaternary system Li_2SO_4+Li_2CO_3+Li_2B_4O_7+H_2O at 288 K were determined by isothermal evaporation method. According to the experimental data, the metastable equilibrium phase diagram was plotted. The metastable phase diagram had one invariant point F, three double saturated liquid curves E1F, E2F and E3F, and three crystallization fields corresponding to Li_2SO_4·H_2O, Li_2CO_3 and LiBO_2·8H_2O. It was found that lithium sulphate(Li_2SO_4) had the highest concentration and strong salting-out effects on the other salts. There were no solid solutions or double salts formed in the quaternary system at 288 K.

  12. Elastic and inelastic scattering of {sup 6}Li + {sup 18}O versus {sup 7}Li + {sup 18}O and {sup 6}Li + {sup 16}O

    Energy Technology Data Exchange (ETDEWEB)

    Rudchik, Adam T., E-mail: rudchik@kinr.kiev.ua [Institute for Nuclear Research, Ukrainian Academy of Sciences, Prospect Nauki 47, 03680 Kyiv (Ukraine); Kliczewski, Stanislaw [H. Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, ul. Radzikowskiego 152, PL-31-342 Cracow (Poland); Chercas, Kostyantyn A. [Institute for Nuclear Research, Ukrainian Academy of Sciences, Prospect Nauki 47, 03680 Kyiv (Ukraine); Kemper, Kirby W. [Physics Department, Florida State University, Tallahassee, FL 32306-4350 (United States); Koshchy, Evgeniy I. [Kharkiv National University, pl. Svobody 4, 61077 Kharkiv (Ukraine); Rusek, Krzysztof [National Centre for Nuclear Research, ul. Hoża 69, PL-00-681 Warsaw (Poland); Heavy Ion Laboratory of Warsaw University, ul. L. Pasteura 5A, PL-02-093 Warsaw (Poland); Rudchik, Andryi A.; Mezhevych, Sergyi Yu.; Pirnak, Valeryi M. [Institute for Nuclear Research, Ukrainian Academy of Sciences, Prospect Nauki 47, 03680 Kyiv (Ukraine); Plujko, Volodymyr A. [Taras Shevchenko Kyiv National University, vul. Volodymyrs' ka 64, 01033 Kyiv (Ukraine); Ponkratenko, Oleg A. [Institute for Nuclear Research, Ukrainian Academy of Sciences, Prospect Nauki 47, 03680 Kyiv (Ukraine); Choiński, Jaroslaw [Heavy Ion Laboratory of Warsaw University, ul. L. Pasteura 5A, PL-02-093 Warsaw (Poland); Czech, Bronislaw; Siudak, Regina; Szczurek, Antoni [H. Niewodniczański Institute of Nuclear Physics, Polish Academy of Sciences, ul. Radzikowskiego 152, PL-31-342 Cracow (Poland); Stolarz, Anna [Heavy Ion Laboratory of Warsaw University, ul. L. Pasteura 5A, PL-02-093 Warsaw (Poland); Zelinskyi, Ruslan M. [Institute for Nuclear Research, Ukrainian Academy of Sciences, Prospect Nauki 47, 03680 Kyiv (Ukraine)

    2014-02-15

    Inverse kinematics scattering of {sup 18}O on {sup 6}Li at E{sub lab}({sup 18}O) = 114 MeV was measured to obtain elastic and inelastic scattering cross sections. In this way cross sections for excited states in {sup 6}Li and {sup 18}O were determined. The data were analyzed within the optical model and coupled reaction channel method. The {sup 6}Li + {sup 18}O optical potential as well as the {sup 6}Li and {sup 18}O deformation parameters were deduced. Contributions of different nuclear processes to the {sup 6}Li + {sup 18}O elastic and inelastic scattering were explored. The isotopic differences between the {sup 6,7}Li + {sup 18}O and {sup 6}Li + {sup 16,18}O potential parameters were determined.

  13. LiFePO4/polymer/natural graphite: low cost Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zaghib, K. [Institut de Recherche d' Hydro-Quebec (IREQ), 1800 Lionel-Boulet, Varennes, QC, J3X 1S1 (Canada)]. E-mail: karimz@ireq.ca; Striebel, K. [Environmental Energy Technologies Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States); Guerfi, A. [Institut de Recherche d' Hydro-Quebec (IREQ), 1800 Lionel-Boulet, Varennes, QC, J3X 1S1 (Canada); Shim, J. [Environmental Energy Technologies Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States); Armand, M. [Joint International Lab. CNRS/UdM UMR 2289 Departement de Chimie, Universite de Montereal, P.O. Box 6128, QC, H3C 3J7 (Canada); Gauthier, M [Joint International Lab. CNRS/UdM UMR 2289 Departement de Chimie, Universite de Montereal, P.O. Box 6128, QC, H3C 3J7 (Canada)

    2004-11-30

    The aging and performance of natural graphite/PEO-based gel electrolyte/LiFePO{sub 4} cells are reported. The gel polymer electrolytes were produced by electron-beam irradiation and then soaked in a liquid electrolyte. The natural graphite anode in gel electrolyte containing LiBF4-EC/GBL exhibited high reversible capacity (345 mAh/g) and high coulombic efficiency (91%). The LiFePO{sub 4} cathode in the same gel-polymer exhibited a reversible capacity of 160 mAh/g and 93% coulombic efficiency. Better performance was obtained at high-rate discharge with 6% carbon additive in the cathode, however the graphite anode performance suffers at high rate. The Li-ion gel polymer battery shows a capacity fade of 13% after 180 cycles and has poor performance at low temperature due to low diffusion of the lithium to the graphite in the GBL system. The LiFePO{sub 4}/gel/Li system has an excellent rate capacity. LiFePO{sub 4} cathode material is suitable for HEV application.

  14. LiFePO{sub 4}/polymer/natural graphite: low cost Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zaghib, K.; Guerfi, A. [Institut de Recherche d' Hydro-Quebec, Varennes (Canada); Striebel, K.; Shim, J. [Lawrence Berkeley National Laboratory, Berkeley, CA (United States). Environmental Energy Technologies Div.; Armand, M.; Gauthier, M. [Universite de Montreal (Canada). Joint International Lab.

    2004-11-30

    The aging and performance of natural graphite/PEO-based gel electrolyte/LiFePO{sub 4} cells are reported. The gel polymer electrolytes were produced by electron-beam irradiation and then soaked in a liquid electrolyte. The natural graphite anode in gel electrolyte containing LiBF4-EC/GBL exhibited high reversible capacity (345 mAh/g) and high coulombic efficiency (91%). The LiFePO4 cathode in the same gel-polymer exhibited a reversible capacity of 160 mAh/g and 93% coulombic efficiency. Better performance was obtained at high-rate discharge with 6% carbon additive in the cathode, however the graphite anode performance suffers at high rate. The Li-ion gel polymer battery shows a capacity fade of 13% after 180 cycles and has poor performance at low temperature due to low diffusion of the lithium to the graphite in the GBL system. The LiFePO{sub 4}/gel/Li system has an excellent rate capacity. LiFePO{sub 4} cathode material is suitable for HEV application. (author)

  15. LiFePO 4 safe Li-ion polymer batteries for clean environment

    Science.gov (United States)

    Zaghib, K.; Charest, P.; Guerfi, A.; Shim, J.; Perrier, M.; Striebel, K.

    The performance of natural graphite-fibers/PEO-based gel electrolyte/LiFePO 4 cells (7 mAh, 4 cm 2) is reported. The gel polymer electrolytes were produced by electron-beam irradiation and then soaked in a liquid electrolyte. The natural graphite-fiber composite anode in gel electrolyte containing 1.5 M LiFSI-EC/GBL (1:3) exhibited high reversible capacity (361 mAh g -1) and high Coulombic efficiency (92%). The LiFePO 4 cathode in the same gel polymer exhibited a reversible capacity of 161 mAh g -1 and 93% Coulombic efficiency. A 1.5 M solution of LiFSI in ethylene carbonate (EC)/γ-butyrolactone (GBL) (1:3, v/v) mixed solvent is advantageous for use as the electrolyte in the laminated film bag because of its high flame point (135 °C), high boiling point (219 °C), low vapor pressure and high conductivity (10.2 mS cm -1 at 20 °C). The Li-ion gel polymer battery shows a very low capacity fade of 5% after 500 cycles and also has high-rate capability. The Li-ion gel polymer cell using LiFePO 4 cathodes is suitable for HEV applications.

  16. LiFePO{sub 4} safe Li-ion polymer batteries for clean environment

    Energy Technology Data Exchange (ETDEWEB)

    Zaghib, K.; Charest, P.; Guerfi, A.; Perrier, M. [Institut de Recherche d' Hydro-Quebec, 1800 Lionel-Boulet, Varennes, Que. (Canada J3X 1S1); Shim, J.; Striebel, K. [Environmental Energy Technologies Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States)

    2005-08-26

    The performance of natural graphite-fibers/PEO-based gel electrolyte/LiFePO{sub 4} cells (7mAh, 4cm{sup 2}) is reported. The gel polymer electrolytes were produced by electron-beam irradiation and then soaked in a liquid electrolyte. The natural graphite-fiber composite anode in gel electrolyte containing 1.5M LiFSI-EC/GBL (1:3) exhibited high reversible capacity (361mAhg{sup -1}) and high Coulombic efficiency (92%). The LiFePO{sub 4} cathode in the same gel polymer exhibited a reversible capacity of 161mAhg{sup -1} and 93% Coulombic efficiency. A 1.5M solution of LiFSI in ethylene carbonate (EC)/{gamma}-butyrolactone (GBL) (1:3, v/v) mixed solvent is advantageous for use as the electrolyte in the laminated film bag because of its high flame point (135{sup o}C), high boiling point (219{sup o}C), low vapor pressure and high conductivity (10.2mScm{sup -1} at 20{sup o}C). The Li-ion gel polymer battery shows a very low capacity fade of 5% after 500cycles and also has high-rate capability. The Li-ion gel polymer cell using LiFePO{sub 4} cathodes is suitable for HEV applications. (author)

  17. Preparation and Characterisation of LiFePO4/CNT Material for Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Rushanah Mohamed

    2011-01-01

    Full Text Available Li-ion battery cathode materials were synthesised via a mechanical activation and thermal treatment process and systematically studied. LiFePO4/CNT composite cathode materials were successfully prepared from LiFePO4 material. The synthesis technique involved growth of carbon nanotubes onto the LiFePO4 using a novel spray pyrolysis-modified CVD technique. The technique yielded LiFePO4/CNT composite cathode material displaying good electrochemical activity. The composite cathode exhibited excellent electrochemical performances with 163 mAh/g discharge capacity with 94% cycle efficiency at a 0.1 C discharge rate in the first cycle, with a capacity fade of approximately 10% after 30 cycles. The results indicate that carbon nanotube addition can enable LiFePO4 to display a higher discharge capacity at a fast rate with high efficiency. The research is of potential interest for the application of carbon nanotubes as a new conducting additive in cathode preparation and for the development of high-power Li-ion batteries for hybrid electric vehicles.

  18. Line shift, line asymmetry, and the 6Li/7Li isotopic ratio determination

    CERN Document Server

    Cayrel, Roger; Chand, Hum; Bonifacio, Piercarlo; Spite, Monique; Spite, François; Petitjean, Patrick; Ludwig, Hans-Günter; Caffau, Elisabetta

    2007-01-01

    Context: Line asymmetries are generated by convective Doppler shifts in stellar atmospheres, especially in metal-poor stars, where convective motions penetrate to higher atmospheric levels. Such asymmetries are usually neglected in abundance analyses. The determination of the 6Li/7Li isotopic ratio is prone to suffering from such asymmetries, as the contribution of 6Li is a slight blending reinforcement of the red wing of each component of the corresponding 7Li line, with respect to its blue wing. Aims: The present paper studies the halo star HD 74000 and estimates the impact of convection-related asymmetries on the Li isotopic ratio determination. Method: Two methods are used to meet this aim. The first, which is purely empirical, consists in deriving a template profile from another element that can be assumed to originate in the same stellar atmospheric layers as Li I, producing absorption lines of approximately the same equivalent width as individual components of the 7Li I resonance line. The second metho...

  19. NASA Goddard’s LiDAR, Hyperspectral and Thermal (G-LiHT Airborne Imager

    Directory of Open Access Journals (Sweden)

    Vuong Ly

    2013-08-01

    Full Text Available The combination of LiDAR and optical remotely sensed data provides unique information about ecosystem structure and function. Here, we describe the development, validation and application of a new airborne system that integrates commercial off the shelf LiDAR hyperspectral and thermal components in a compact, lightweight and portable system. Goddard’s LiDAR, Hyperspectral and Thermal (G-LiHT airborne imager is a unique system that permits simultaneous measurements of vegetation structure, foliar spectra and surface temperatures at very high spatial resolution (~1 m on a wide range of airborne platforms. The complementary nature of LiDAR, optical and thermal data provide an analytical framework for the development of new algorithms to map plant species composition, plant functional types, biodiversity, biomass and carbon stocks, and plant growth. In addition, G-LiHT data enhance our ability to validate data from existing satellite missions and support NASA Earth Science research. G-LiHT’s data processing and distribution system is designed to give scientists open access to both low- and high-level data products (http://gliht.gsfc.nasa.gov, which will stimulate the community development of synergistic data fusion algorithms. G-LiHT has been used to collect more than 6,500 km2 of data for NASA-sponsored studies across a broad range of ecoregions in the USA and Mexico. In this paper, we document G-LiHT design considerations, physical specifications, instrument performance and calibration and acquisition parameters. In addition, we describe the data processing system and higher-level data products that are freely distributed under NASA’s Data and Information policy.

  20. Packing Transitions in Nanosized Li Clusters

    CERN Document Server

    Sung, M W; Weare, J H; Sung, Ming Wen; Kawai, Ryoichi; Weare, John H.

    1994-01-01

    Packing transitions in the lowest energy structures of Li clusters as a function of size have been identified via simulated annealing. For N>21, the large $p$ character of Li leads to unexpected ionic structures. At N~25, a packing pattern based on interpenetrating 13-atom icosahedra and similar to that of Na and K appears. This pattern persists until at N=55, where another transition to a structure based on a Mackay icosahedron occurs. For clusters of size 55 and 147, the optimized FCC structure representative of the bulk is still slightly higher in energy than the optimal MIC. (RK-94-03)

  1. The 'LiC Detector Toy' program

    Science.gov (United States)

    Regler, M.; Mitaroff, W.; Valentan, M.; Frühwirth, R.; Höfler, R.

    2008-07-01

    LiC is a simple but powerful and flexible software tool, written in MatLab, for basic detector design studies (geometries, material budgets) by determining the resolution of reconstructed track parameters. It is based on a helix track model including multiple scattering, and consists of a simplified simulation of the detector followed by track reconstruction using the Kalman filter. After a short description of LiC's main characteristics, we demonstrate its capabilities by applying this tool in a performance study of the LDC and SiD detector concepts at the International Linear Collider (ILC).

  2. Achromatic Cooling Channel with Li Lenses

    Energy Technology Data Exchange (ETDEWEB)

    Balbekov, V. [Fermi National Accelerator Lab. (FNAL), Batavia, IL (United States)

    2002-04-29

    A linear cooling channel with Li lenses, solenoids, and 201 MHz RF cavities is considered. A special lattice design is used to minimize chromatic aberrations by suppression of several betatron resonances. Transverse emittance of muon beam decreases from 2 mm to 0.5 mm at the channel of about 110 m length. Longitudinal heating is modest, therefore transmission of the channel is rather high: 96% without decay and 90% with decay. Minimal beam emittance achievable by similar channel estimated as about 0.25 mm at surface field of Li lenses 10 T.

  3. Comment on "Cycling Li-O₂ batteries via LiOH formation and decomposition".

    Science.gov (United States)

    Viswanathan, Venkatasubramanian; Pande, Vikram; Abraham, K M; Luntz, Alan C; McCloskey, Bryan D; Addison, Dan

    2016-05-01

    Based on a simple thermodynamic analysis, we show that iodide-mediated electrochemical decomposition of lithium hydroxide (LiOH) likely occurs through a different mechanism than that proposed by Liu et al (Research Article, 30 October 2015, p. 530). The mismatch in thermodynamic potentials for iodide/triiodide (I(-)/I3 (-)) redox and O2 evolution from LiOH implies a different active iodine/oxygen electrochemistry on battery charge. It is therefore possible that the system described in Liu et al may not form the basis for a rechargeable lithium-oxygen (Li-O2) battery.

  4. Synthesis and characterization of LiZnP and LiZnAs semiconductor material

    Science.gov (United States)

    Montag, Benjamin W.; Reichenberger, Michael A.; Arpin, Kevin R.; Sunder, Madhana; Nelson, Kyle A.; Ugorowski, Philip B.; McGregor, Douglas S.

    2015-02-01

    Research for a reliable solid-state semiconductor neutron detector continues because such a device has not been developed, and would have greater efficiency, than present-day gas-filled 3He and 10BF3 neutron detectors. Further, a semiconductor neutron detector would be more compact and rugged than most gas-filled or scintillator neutron detectors. The 6Li(n,t)4He reaction yields a total Q value of 4.78 MeV, a larger yield than the 10B(n,α)7Li, and is easily identified above background radiation interactions. Hence, devices composed of either natural Li (naturally 7.5% 6Li) or enriched 6Li (approximately 95% 6Li) may provide a semiconductor material for compact high-efficiency neutron detectors. A sub-branch of the III-V semiconductors, the filled tetrahedral compounds, known as Nowotny-Juza compounds (AIBIICV), are desirable for their cubic crystal structure and semiconducting electrical properties. These compounds were originally studied for photonic applications. In the present work, Equimolar portions of Li, Zn, and P or As were sealed under vacuum (10-6 Torr) in quartz ampoules with a boron nitride lining, and loaded into a compounding furnace. The ampoule was heated to 200 °C to form the Li-Zn alloy, subsequently heated to 560 °C to form the ternary compound, LiZnP or LiZnAs, and finally annealed to promote crystallization. The chemical composition of the synthesized starting material was confirmed at Galbraith Laboratories, Inc. by Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), which showed the compounds can be reacted in equal ratios, 1-1-1, to form ternary compounds. Recent additions to the procedure have produced higher yields, and greater synthesis reliability. Synthesized powders were also characterized by x-ray diffraction, where lattice constants of 5.751±.001 Å and 5.939±.002 Å for LiZnP and LiZnAs, respectively, were determined.

  5. Charge carrier density in Li-intercalated graphene

    KAUST Repository

    Kaloni, Thaneshwor P.

    2012-05-01

    The electronic structures of bulk C 6Li, Li-intercalated free-standing bilayer graphene, and Li-intercalated bilayer and trilayer graphene on SiC(0 0 0 1) are studied using density functional theory. Our estimate of Young\\'s modulus suggests that Li-intercalation increases the intrinsic stiffness. For decreasing Li-C interaction, the Dirac point shifts to the Fermi level and the associated band splitting vanishes. For Li-intercalated bilayer graphene on SiC(0 0 0 1) the splitting at the Dirac point is tiny. It is also very small at the two Dirac points of Li-intercalated trilayer graphene on SiC(0 0 0 1). For all the systems under study, a large enhancement of the charge carrier density is achieved by Li intercalation. © 2012 Elsevier B.V. All rights reserved.

  6. Tallinnasse kogunesid üliõpilasliidrid üle Euroopa

    Index Scriptorium Estoniae

    2011-01-01

    Euroopa Üliõpilasliit korraldas Tallinnas 2.-5. mail konverentsi „Financing of higher education - financing the students future”, kus osalesid 120 üliõpilasesindajat 40-st riigist üle Euroopa

  7. Tallinnasse kogunesid üliõpilasliidrid üle Euroopa

    Index Scriptorium Estoniae

    2011-01-01

    Euroopa Üliõpilasliit korraldas Tallinnas 2.-5. mail konverentsi „Financing of higher education - financing the students future”, kus osalesid 120 üliõpilasesindajat 40-st riigist üle Euroopa

  8. LiDAR data for the Delta Area of California

    Data.gov (United States)

    California Department of Resources — LiDAR data for the Delta Area of California from the California Department of Water Resources. Bare earth grids from LiDAR.This data is in ESRI Grid format with 2...

  9. LiDAR data for the Delta Area of California

    Data.gov (United States)

    California Department of Resources — LiDAR data for the Delta Area of California from the California Department of Water Resources. Bare earth grids from LiDAR.This data is in ESRI Grid format with 2...

  10. Hydrogen storage in LiH: A first principle study

    Science.gov (United States)

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

    2014-04-01

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

  11. Hydrogen storage in LiH: A first principle study

    Energy Technology Data Exchange (ETDEWEB)

    Banger, Suman, E-mail: sumanphy28@gmail.com; Nayak, Vikas, E-mail: sumanphy28@gmail.com; Verma, U. P., E-mail: sumanphy28@gmail.com [School of Studies in Physics, Jiwaji University, Gwalior-474011 (India)

    2014-04-24

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

  12. A New Li Anode Technology for Improved Performance Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Lithium (Li) metal-based rechargeable batteries have many advantages over Li-ion systems including significantly higher energy density, lower cost, and the option of...

  13. New Li Battery Chemistry for Improved Performance Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Current state-of-the-art Lithium (Li) or Li-ion systems are unable to meet the performance goals of space-rated rechargeable batteries for many NASA's future robotic...

  14. Hydrogen Sorption in Erbium Borohydride Composite Mixtures with LiBH4 and/or LiH

    Directory of Open Access Journals (Sweden)

    Michael Heere

    2017-04-01

    Full Text Available Rare earth (RE metal borohydrides have recently been receiving attention as possible hydrogen storage materials and solid-state Li-ion conductors. In this paper, the decomposition and reabsorption of Er(BH43 in composite mixtures with LiBH4 and/or LiH were investigated. The composite of 3LiBH4 + Er(BH43 + 3LiH has a theoretical hydrogen storage capacity of 9 wt %, nevertheless, only 6 wt % hydrogen are accessible due to the formation of thermally stable LiH. Hydrogen sorption measurements in a Sieverts-type apparatus revealed that during three desorption-absorption cycles of 3LiBH4 + Er(BH43 + 3LiH, the composite desorbed 4.2, 3.7 and 3.5 wt % H for the first, second and third cycle, respectively, and thus showed good rehydrogenation behavior. In situ synchrotron radiation powder X-ray diffraction (SR-PXD after ball milling of Er(BH43 + 6LiH resulted in the formation of LiBH4, revealing that metathesis reactions occurred during milling in these systems. Impedance spectroscopy of absorbed Er(BH43 + 6LiH showed an exceptional high hysteresis of 40–60 K for the transition between the high and low temperature phases of LiBH4, indicating that the high temperature phase of LiBH4 is stabilized in the composite.

  15. Performance of new 10 kW class MCFC using Li/K and Li/Na electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Mugikura, Yoshihiro; Yoshiba, Fumihiko; Izaki, Yoshiyuki; Watanabe, Takao [Central Research Institute of Electric Power Industry, Kanagawa-ken (Japan)] [and others

    1996-12-31

    The molten carbonate fuel cell (MCFC) uses generally mixture of lithium carbonate and potassium carbonate (Li/K) as the electrolyte. NiO cathode dissolution is one of serious problems for MCFC life. The NiO cathode has been found to dissolve into the electrolyte as Ni{sup 2+} ion which is reduced to metallic Ni by H{sub 2} in the fuel gas and bridges the anode and the cathode. The bridges short circuit and degrade cell performance and shorten cell life. Since solubility of NiO in mixture of lithium carbonate and sodium carbonate (Li/Na) is lower than in Li/K, it takes longer time to take place slowing by NiO cathode dissolution in Li/Na compared with in Li/K. The ionic conductivity of Li/Na is higher than of Li/K, however, oxygen solubility in Li/Na is lower 9 than in Li/K. A new 10 kW class MCFC stack composed of Li/K cells and Li/Na cells, was tested. Basic performance of the Li/K cells and Li/Na cells of the stack was reported.

  16. Studies on the thermal decomposition kinetics of LiPF6 and LiBC4O8

    Indian Academy of Sciences (India)

    Li Shi-You; Ma Pei-Hua; Cui Xiao-Ling; Ren Qi-Du; Li Fa-Qiang

    2008-03-01

    Thermal decomposition of LiPF6 and LiBC4O8 (lithium bis(oxalate)borate, abbreviated as LiBOB) were studied using TG (thermogravimetry)-DTG (derivative thermogravimetry) method with different heating rate of 5, 10, 20 and 40°C min-1 or at different constant temperature C (109.80, 118.79, 148.41, 176.86 °C for LiPF6 and 278.51, 298.13, 317.65, 336.13 for LiBOB). From the nonisothermal kinetics we calculate that LiPF6 is 1.01, LiBOB is 1.04, LiPF6 is 91907.61 J/mol, and LiBOB is 205179.88 J/mol; from the isothermal kinetics we calculate that n for both LiPF6 and LiBOB are 1, LiPF6 is 91907.61 J/mol, LiBOB is 205179.88 J/mol, lnALiPF6 is 16.89 s-1, and lnALiBOB is 31.96 s-1. The results obtained from the two ways have minor differences and can validate each other.

  17. Structure characteristics and electrochemical properties of LiMn2O4 modified by LiCoO2

    Institute of Scientific and Technical Information of China (English)

    Zhenping Cai; Mingxun Li; Shigang Lu; Weihua Jin

    2005-01-01

    In order to improve the cycle performance of LiMn2O4, the modified LiMn2O4 was prepared by solid-state reactions using LiMn2O4 and LiCoO2 as precursors. XRD and EDS were used to study the structure properties of the modified LiMn2O4. The electrochemical properties of the modified LiMn2O4 were also investigated. The results show that Li and Co atoms could insert into the LiMn2O4 crystal lattice and a newly formed spinel phase, modified LiMn2O4 was obtained. The modified LiMn2O4 exhibits excellent cycle ability at room and elevated temperatures compared to pure LiMn2O4. The improved electrochemical stability of the modified LiMn2O4 attributes to the entrance of Li and Co ions inserted into the spinel crystal structure.

  18. Experimental studies with metal-hydrogen-systems for the development of the Li/LiH-process. Experimentelle Untersuchungen an Metall-Wasserstoff-Systemen zur Entwicklung des Li/LiH-Prozesses

    Energy Technology Data Exchange (ETDEWEB)

    Weirich, W.

    1982-01-25

    In this work an attempt is made to further develop the Li/LiH-process, which is a hybrid cyclic process, for the thermochemical splitting of water. The studies presented are related with the more critical aspects of the method, such as the development of the membrane on the basis of homogeneous alloys, and the segregation of hydrogen from Li/LiH-melts.

  19. A NOTE ON THE LI-CU-O SYSTEM

    NARCIS (Netherlands)

    Berger, R

    1991-01-01

    In the Li-Cu-O system two new ternary phases have been found, tentatively described by the stoichiometries LiCu3O3 and LiCu2O2, and both containing Cu(I) and Cu(II). They exhibit p-type "hopping" conduction owing to localized charge carriers. Their powder patterns are successfully indexed on high-sy

  20. Lithium intercalation into layered LiMnO2

    DEFF Research Database (Denmark)

    Vitins, G.; West, Keld

    1997-01-01

    Recently Armstrong and Bruce(1) reported a layered modification of lithium manganese oxide, LiMnO2, isostructural with LiCoO2. LiMnO2 obtained by ion exchange from alpha-NaMnO2 synthesized in air is characterized by x-ray diffraction and by electrochemical insertion and extraction of lithium in a...

  1. LiDAR utility for natural resource managers

    Science.gov (United States)

    Andrew Thomas Hudak; Jeffrey Scott Evans; Alistair Mattthew Stuart. Smith

    2009-01-01

    Applications of LiDAR remote sensing are exploding, while moving from the research to the operational realm. Increasingly, natural resource managers are recognizing the tremendous utility of LiDAR-derived information to make improved decisions. This review provides a cross-section of studies, many recent, that demonstrate the relevance of LiDAR across a suite of...

  2. Lattice sites of Li in CdTe

    NARCIS (Netherlands)

    Restle, M; BharuthRam, K; Quintel, H; Ronning, C; Hofsass, H; Wahl, U; Jahn, SG

    1996-01-01

    The lattice site occupation of Li in CdTe at temperatures between 40 and 500 K was investigated with the emission channeling method. Radioactive Li-8 ions were implanted at low doses into CdTe single crystals. Emission channeling patterns of alpha-particles emitted in the nuclear decay of Li-8 (t(1/

  3. 2012 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Quinault River Watershed, Washington (Delivery 1)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data on the Quinault watershed survey area for the Puget Sound LiDAR Consortium. This...

  4. 2014 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Cedar River Watershed (Delivery 1)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — In September 2013, WSI, a Quantum Spatial company (QSI), was contracted by the Puget Sound LiDAR Consortium (PSLC) to collect Light Detection and Ranging (LiDAR)...

  5. 2005 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: North Puget Sound Lowlands

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Terrapoint collected Light Detection and Ranging (LiDAR) data contributing to the Puget Sound Lowlands project of 2005. Arlington, City of Snohomish, Snohomish...

  6. 2009 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Snohomish River Estuary

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) co-acquired Light Detection and Ranging (LiDAR) data and Truecolor Orthophotographs of the Snohomish River Estuary, WA on July 20 &...

  7. 2009 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Douglas Co.

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) collected Light Detection and Ranging (LiDAR) data of the Douglas County PUD area of interest (AOI) east of Wenatchee, WA on May 2nd ?...

  8. 2003 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Snohomish County, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — TerraPoint surveyed and created this data for the Puget Sound LiDAR Consortium under contract. The area surveyed is approximately 167 square miles and covers a...

  9. 2003 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Yakima County, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — TerraPoint surveyed and created this data for the Puget Sound LiDAR Consortium under contract. The area surveyed is approximately 77 square miles and covers a...

  10. 2012 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Upper Naches River, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data of the Upper Naches River Valley and Nile Slide area of interest on September 30th,...

  11. 2005 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Lewis County

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Terrapoint collected Light Detection and Ranging (LiDAR) data for the Lewis County project of 2005. The project site covered approximately 223 square miles, divided...

  12. 2005 Puget Sound LiDAR Consortium (PSLC) Bare-Earth Topographic LiDAR: Lynnwood

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Terrapoint collected Light Detection and Ranging (LiDAR) data contributing to the Puget Sound Lowlands project of 2005. Lynnwood, Snohomish County, Washington. This...

  13. 2007 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Sumpter, OR

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) collected Light Detection and Ranging (LiDAR) data for the USDA Forest Service on September 17, 2007. The project covers an 8-mile...

  14. 2011 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Rattlesnake

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data on six days between September 15th and November 5th, and from November 6th ? 13th,...

  15. 2000 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Kitsap Peninsula, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — TerraPoint surveyed and created this data for the Puget Sound LiDAR Consortium under contract. The area surveyed is approximately 1,146 square miles and covers part...

  16. 2003 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Yakima County, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — TerraPoint surveyed and created this data for the Puget Sound LiDAR Consortium under contract. The area surveyed is approximately 77 square miles and covers a...

  17. 2005 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Yakima County

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Terrapoint collected Light Detection and Ranging (LiDAR) data to complete the 2005 project for Yakima County. This project has partial coverage of Yakima County,...

  18. Bulk and Surface Properties of Liquid Al-Li and Li-Zn Alloys

    Science.gov (United States)

    Trybula, Marcela; Gancarz, Tomasz; Gasior, Wladyslaw; Pasturel, Alain

    2014-11-01

    Physicochemical properties like density, surface tension, and viscosity of liquid binary Al-Li and Li-Zn alloys have been measured using draining crucible method. The experimentally measured surface-tension values have been compared to theoretical results based either on the Butler model or the compound formation model assuming the existence of the most favored A 1 B 2 and A 2 B 3 clusters. Several models for viscosity calculation have been also applied and discussed in confrontation with measured data. Finally, the clustering effects in the liquid Al-Li and Li-Zn alloys have been examined using two microscopic functions, i.e., the concentration fluctuation function in the long-wavelength limit and the Warren-Cowley short-range order parameter.

  19. 2005 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Olympic Peninsula

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Terrapoint collected Light Detection and Ranging (LiDAR) data for the Olympic Peninsula project of 2005, totaling approximately 114.59 sq mi: 24.5 for Clallam...

  20. Enabling High Energy Density Li-Ion Batteries through Li{sub 2}O Activation.

    Energy Technology Data Exchange (ETDEWEB)

    Abouimrane, Ali; Cui, Yanjie; Chen, Zonghai; Belharouak, Ilias; Yahia, Hamdi B.; Wu, Huiming; Assary, Rajeev; Curtiss, Larry A.; Amine, Khalil

    2016-09-01

    Lithium oxide (Li2O) is activated in the presence of a layered composite cathode material (HEM) significantly increasing the energy density of lithium-ion batteries. The degree of activation depends on the current rate, electrolyte salt, and anode type. In full-cell tests, the Li2O was used as a lithium source to counter the first-cycle irreversibility of high-capacity composite alloy anodes. When Li2O is mixed with HEM to serve as a cathode, the electrochemical performance was improved in a full cell having an SiO-SnCoC composite as an anode. The mechanism behind the Li2O activation could also explain the first charge plateau and the abnormal high capacity associated with these high energy cathode materials.

  1. 2005 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: North Puget Sound Lowlands

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Terrapoint collected Light Detection and Ranging (LiDAR) data contributing to the Puget Sound Lowlands project of 2005. Arlington, City of Snohomish, Snohomish...

  2. Electrochemical formation of Mg-Li-Ca alloys by codeposition of Mg, Li and Ca from LiCl-KCl-MgCl2-CaCl2 melts.

    Science.gov (United States)

    Yan, Yong De; Zhang, Mi Lin; Xue, Yun; Han, Wei; Cao, Dian Xue; Jing, Xiao Yan; He, Li Yi; Yuan, Yi

    2009-08-07

    This work presents electrochemical formation of Mg-Li-Ca alloys via codeposition of Mg, Li and Ca on a molybdenum electrode in KCl-LiCl-MgCl(2)-CaCl(2) melts at 943 K. Cyclic voltammograms (CVs) showed that the underpotential deposition (UPD) of calcium on pre-deposited magnesium leads to the formation of a liquid Mg-Ca alloy, and the succeeding underpotential deposition of lithium on pre-deposited Mg-Ca alloy leads to the formation of a liquid Mg-Li-Ca solution. Chronopotentiometric measurements indicated that the codepositon of Mg, Li and Ca occurs at current densities more negative than -0.31 A cm(-2) in LiCl-KCl-MgCl(2) (5 wt%) melts containing 1 wt% CaCl(2). Chronoamperograms demonstrated that the onset potential for the codeposition of Mg, Li and Ca is -2.200 V, and the codeposition of Mg, Li and Ca is formed when the applied potentials are more negative than -2.200 V. X-Ray diffraction (XRD) indicated that Mg-Li-Ca alloys with different phases were formed via galvanostatic electrolysis. The microstructures of typical alpha and beta phases of Mg-Li-Ca alloys were characterized by optical microscope (OM) and scanning electron microscopy (SEM). The analysis of energy dispersive spectrometry (EDS) showed that the element Ca mainly distributes along grain boundary in Mg-Li-Ca alloys. The results of inductively coupled plasma analysis determined that the chemical compositions of Mg-Li-Ca alloys correspond with the phase structures of XRD patterns, and the lithium and calcium contents of Mg-Li-Ca alloys depend on the concentrations of MgCl(2) and CaCl(2).

  3. Irene Väli / Ruth Alas

    Index Scriptorium Estoniae

    Alas, Ruth, 1960-

    2007-01-01

    AS Haapsalu Kuurort juhataja Irene Väli juhtimispõhimõtted, muudatuste elluviimise taktika, karjäär, väärtushinnangud, organisatsiooni arenguvõimalused, puhkus ja perekond. Eluloolised andmed, haridus, töökogemus. Kommenteerib kuurordi ilukeskuse juhataja Merle Murik

  4. Orienteerumiskaart vs. LiDAR / Marek Karm

    Index Scriptorium Estoniae

    Karm, Marek

    2012-01-01

    Bakalaureusetööst, mille eesmärk oli võrrelda orienteerumiskaardi reljeefi LiDAR-i andmete põhjal saadava reljeefimudeliga ning leida vastus küsimusele, kas o-kaart võib olla kasulik kooste- või kontrollmaterjal mistahes reljeefimudelile

  5. Grozit li Estonii energetitsheskii krizis? / Jevgenija Garanzha

    Index Scriptorium Estoniae

    Garanža, Jevgenija, 1979-

    2006-01-01

    Euroopani ulatunud Venemaa gaasitüli Ukraina ja Gruusiaga paneb mõtlema ka Eesti energeetilise julgeoleku üle. Euroopa Liidus kuulub Eesti imporditavatest energiakandjatest kõige vähem sõltuvate riikide hulka. Diagramm: Eesti põhilised energeetilised ressursid

  6. Examples for Application of Hegu (LI 4)

    Institute of Scientific and Technical Information of China (English)

    Qian Linchao

    2006-01-01

    @@ Hegu (LI 4), a source point of Large Intestine Channel for clearing intestine and regulating stomach and spleen, can be clinically used to treat stomachache, diarrhea, vomiting, hiccup and constipation caused by dysfunction of the spleen,stomach and intestine with good curative effect.Examples are taken as follows:

  7. Orienteerumiskaart vs. LiDAR / Marek Karm

    Index Scriptorium Estoniae

    Karm, Marek

    2012-01-01

    Bakalaureusetööst, mille eesmärk oli võrrelda orienteerumiskaardi reljeefi LiDAR-i andmete põhjal saadava reljeefimudeliga ning leida vastus küsimusele, kas o-kaart võib olla kasulik kooste- või kontrollmaterjal mistahes reljeefimudelile

  8. LI Ligang honored with Doornbos prize

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    @@ Together with two colleagues from Europe and US,Dr.LI Ligang from the CAS Shanghai Astronomical Observatory has been awarded the Doornbos Memorial Prize for his outstanding contributions to the studies of thermal convection inside the earth and a planet,dynamo theory,and simulation.

  9. Pakistanis Eager to Welcome Premier Li Keqiang

    Institute of Scientific and Technical Information of China (English)

    Syed; Ali; Nawaz; Gilani

    2013-01-01

    <正>"We the Pakistani Nation,are very much eager to welcome Chinese Premier Li Keqiang on his first visit to Pakistan after taking over the Premiership of the People’s Republic of China whom we are enjoying deep rooted and exemplary friendship for

  10. Gadamer em 10 lições

    Directory of Open Access Journals (Sweden)

    Claudinei Aparecido de Freitas da Silva

    2017-04-01

    Full Text Available Resenho, aqui, 10 Lições sobre Gadamer, importante trabalho introdutório sobre a gênese e o desenvolvimento do programa hermenêutico de Hans-Georg Gadamer (1900-2002, notável pensador, cuja obra impacta, decisivamente, o panorama intelectual do século passado.

  11. 6Li foil thermal neutron detector

    Energy Technology Data Exchange (ETDEWEB)

    Ianakiev, Kiril D [Los Alamos National Laboratory; Swinhoe, Martyn T [Los Alamos National Laboratory; Favalli, Andrea [Los Alamos National Laboratory; Chung, Kiwhan [Los Alamos National Laboratory; Macarthur, Duncan W [Los Alamos National Laboratory

    2010-01-01

    In this paper we report on the design of a multilayer thermal neutron detector based on {sup 6}Li reactive foil and thin film plastic scintillators. The {sup 6}Li foils have about twice the intrinsic efficiency of {sup 10}B films and about four times higher light output due to a unique combination of high energy of reaction particles, low self absorption, and low ionization density of tritons. The design configuration provides for double sided readout of the lithium foil resulting in a doubling of the efficiency relative to a classical reactive film detector and generating a pulse height distribution with a valley between neutron and gamma signals similar to {sup 3}He tubes. The tens of microns thickness of plastic scintillator limits the energy deposited by gamma rays, which provides the necessary neutron/gamma discrimination. We used MCNPX to model a multilayer Li foil detector design and compared it with the standard HLNCC-II (18 {sup 3}He tubes operated at 4 atm). The preliminary results of the {sup 6}Li configuration show higher efficiency and one third of the die-away time. These properties, combined with the very short dead time of the plastic scintillator, offer the potential of a very high performance detector.

  12. Reversible hydrogen storage in titanium-catalyzed LiAlH{sub 4}-LiBH{sub 4} system

    Energy Technology Data Exchange (ETDEWEB)

    Mao, J.F. [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); Guo, Z.P., E-mail: zguo@uow.edu.a [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); School of Mechanical, Materials and Mechatronics Engineering, University of Wollongong, NSW 2522 (Australia); CSIRO National Hydrogen Materials Alliance, CSIRO Energy Centre, 10 Murray Dwyer Circuit, Steel River Estate, Mayfield West, NSW 2304 (Australia); Liu, H.K. [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); CSIRO National Hydrogen Materials Alliance, CSIRO Energy Centre, 10 Murray Dwyer Circuit, Steel River Estate, Mayfield West, NSW 2304 (Australia); Yu, X.B., E-mail: yuxuebin@fudan.edu.c [Institute for Superconducting and Electronic Materials, University of Wollongong, NSW 2522 (Australia); CSIRO National Hydrogen Materials Alliance, CSIRO Energy Centre, 10 Murray Dwyer Circuit, Steel River Estate, Mayfield West, NSW 2304 (Australia); Department of Materials Science, Fudan University, Shanghai 200433 (China)

    2009-11-13

    We have investigated the hydrogen storage properties of the LiAlH{sub 4}-LiBH{sub 4} system, both un-doped and doped with titanium based catalysts. It was found that TiF{sub 3} exhibited the superior catalytic effects in terms of enhancing the hydriding/dehydriding kinetics and reducing the dehydrogenation temperature of the LiAlH{sub 4}-LiBH{sub 4} system. Compared to the un-doped LiAlH{sub 4}-LiBH{sub 4} system, the onset temperatures of the 5 mol% TiF{sub 3}-doped sample for the first and second dehydrogenation steps were decreased by 64 and 150 deg. C, respectively. X-ray diffraction patterns of the dehydrogenated samples revealed that the produced Al from LiAlH{sub 4} could react with B from the decomposition of LiBH{sub 4} to form AlB{sub 2} and LiAl compounds. Pressure-composition-temperature (PCT) and van't Hoff plots made it clear that the decomposition enthalpy of LiBH{sub 4} in the TiF{sub 3}-doped LiAlH{sub 4}-LiBH{sub 4} system is decreased from 74 kJ/(mol of H{sub 2}) for the pure LiBH{sub 4} to 60.4 kJ/(mol of H{sub 2}). The dehydrogenation products of the TiF{sub 3}-doped LiAlH{sub 4}-LiBH{sub 4} sample can absorb 3.76 and 4.78 wt.% of hydrogen in 1 h and 14 h, respectively, at 600 deg. C and under 4 MPa of hydrogen. The formation of LiBH{sub 4} was detected by X-ray diffraction in the rehydrogenated sample.

  13. Multi-spin-state at a Li3PO4/LiCoO2 (104) interface.

    Science.gov (United States)

    Sumita, Masato; Ohno, Takahisa

    2016-02-14

    We have found the disproportion between the intermediate spin (IS) and low spin (LS) configurations of Co atoms at a Li3PO4/LiCoO2 (104) interface through density functional molecular dynamics (DF-MD). The manifold of the spin state at the interface, however, does not affect the band alignment between the Li3PO4 and LiCoO2 regions.

  14. On the reduction of generalized polylogarithms to Li n and Li2 ,2 and on the evaluation thereof

    Science.gov (United States)

    Frellesvig, Hjalte; Tommasini, Damiano; Wever, Christopher

    2016-03-01

    We give expressions for all generalized polylogarithms up to weight four in terms of the functions log, Li n , and Li2,2, valid for arbitrary complex variables. Furthermore we provide algorithms for manipulation and numerical evaluation of Li n and Li2,2, and add codes in Mathematica and C++ implementing the results. With these results we calculate a number of previously unknown integrals, which we add in appendix C.

  15. Synthesis Of Fe Doped LiMn2O4 Cathode Materials For Li Battery By Solid State Reaction

    Directory of Open Access Journals (Sweden)

    Horata N.

    2015-06-01

    Full Text Available LiFe0.1Mn1.9O4 is expected as a cathode material for the rechargeable lithium-ion batteries. LiMn2O4 has been received attention because this has advantages such as low cost and low toxicity compared with other cathode materials of LiCoO2 and LiNiO2. However, LiMn2O4 has some problems such as small capacity and no long life. LiMn2O4 is phase transformation at around human life temperature. One of the methods to overcome this problem is to stabilize the spinel structure by substituting Mn site ion in LiMn2O4 with transition metals (Al, Mg, Ti, Ni, Fe, etc.. LiFe0.1Mn1.9O4 spinel was synthesized from Li2CO3, Fe2O3 and MnO2 powder. The purpose of this study is to report the optimal condition of Fe doped LiFe0.1Mn1.9O4. Li2CO3, Fe2O3, and MnO2 mixture powder was heated up to 1173 K by TG-DTA. Li2CO3 was thermal decomposed, and CO2 gas evolved, and formed Li2O at about 800 K. LiFe0.1Mn1.9O4 was synthesized from a consecutive reaction Li2O, Fe2O3 and MnO2 at 723 ~ 1023 K. Active energy is calculated to 178 kJmol−1 at 723 ~ 1023 K. The X-ray powder diffraction pattern of the LiFe0.1Mn1.9O4 heated mixture powder at 1023 K for 32 h in air flow was observed.

  16. Reaction mechanism study of 7Li(7Li, 6He) reaction at above Coulomb barrier energies

    Indian Academy of Sciences (India)

    V V Parkar; V Jha; S Santra; B J Roy; K Ramachandran; A Shrivastava; K Mahata; A Chatterjee; S Kailas

    2009-02-01

    The elastic scattering and the 6He angular distributions were measured in 7Li + 7Li reaction at two energies, lab = 20 and 25 MeV. FRDWBA calculations have been performed to explain the measured 6He data. The calculations were very sensitive to the choice of the optical model potentials in entrance and exit channels. The one-step proton transfer was found to be the dominant reaction mechanism in 6He production.

  17. Clay nanocomposites for use in Li batteries

    Science.gov (United States)

    Moore, Gregory John

    1999-11-01

    Nanocomposites, materials made of more than one component and combined in an ordered manner on the nanometer scale, were synthesized using clay mineral hosts with various types of guests. The guests include polymers such as polyethylene oxide (PEO) and polyaniline (PANI), large molecules such as ethylmethyl sulfone, tetramethylene sulfone, and various length alkylamines. Vanadyl groups (VO 2+) were also incorporated with the clays. The otherwise non-swellable mica clay, synthetic Na-fluorophlogopite, was expanded by intercalation of acidic ions such as Cu2+ and Fe3+. As aqueous solutions, these ions caused the stable fluoromica to go from its dehydrated interlayer spacing of 9.8 A to over 14 A. This clay became a host for many other reactions including swelling with alkylamines to over 25 A. However, despite hydrated Cu2+ ions swelling fluorophlogopite, polymeric species such as PEO or PANI could not be inserted. Another clay that was used for formation of nanocomposites came from a procedure for the synthesis of Li-taeniolite, Li(Mg2Li)Si 4O10F2. The clay was synthesized following a high temperature method that led to a non-reactive product. Instead, a novel precursor route was employed that gave a clay product with a single hydration layer. Various chemical analyses gave a formula of Li0.8(Mg 2.2Li0.8)Si4O10(F1.6O 0.4)·H2O. For the purpose of forming nanocomposite electrolytes, ethylmethyl sulfone was synthesized and incorporated into the clay. For comparison of different shaped sulfones, tetramethylene sulfone also was inserted into the layers for electrolytic studies. To make a polymer-clay electrolyte, polyethylene oxide was intercalated into the Li-taeniolite. All of these new electrolyte materials were characterized using impedance spectroscopy for measurement of their conductivity. Syntheses and analyses are thoroughly discussed for all of these materials. Special attention is placed on powder x-ray diffraction and thermogravimetric techniques to

  18. Preparation of Li-rich layered-layered type xLi2MnO3·(1-x)LiMnO2 nanorods and its electrochemical performance as cathode material for Li-ion battery

    Science.gov (United States)

    Yang, Fan; Zhang, Qinggang; Hu, Xiaohong; Peng, Tianyou; Liu, Jianqiang

    2017-06-01

    Layered-layered type xLi2MnO3·(1-x)LiMnO2 (x = 0.91, 0.78, 0.67, 0.54, 0.42, and 0.32) nanorods with a diameter of 100-200 nm and length of 400-1000 nm are prepared through a pyrolysis reduction process of monoclinic Li2MnO3 (m-Li2MnO3) nanorods. All the synthesized xLi2MnO3·(1-x)LiMnO2 nanorods exhibit the main characteristic diffraction peaks of m-Li2MnO3 in addition to some weak peaks attributable to m-LiMnO2 especially for those composites with x window of 2.0-4.8 V. The m-LiMnO2 portion in those synthesized composites can significantly enhance the reversible capacity but lower the cyclic stability, while the m-Li2MnO3 portion can improve the cyclic stability due to its retardation effect of the layered-to-spinel transformation during the charge/discharge processes, and thus xLi2MnO3·(1-x)LiMnO2 nanorods with x = 0.54 exhibits the best cyclic and rate performance since it contains appropriate m-Li2MnO3/m-LiMnO2 contents to balance the reversible capacity and Jahn-Teller effect. The present findings demonstrate an effective strategy for the development of low-cost pure Mn-based Li-rich layered cathode materials with adjustable reversible capacity, cyclic and rate performance by tailoring the composition.

  19. In-house fabrication and testing capabilities for Li and Li-ion 18650 cells

    Science.gov (United States)

    Nagasubramanian, G.

    2010-04-01

    For over 10 years Sandia Labs have been involved in an US DOE-funded program aimed at developing electric vehicle batteries for transportation applications. Currently this program is called "Advanced Battery Research (ABR)." In this effort we were preparing 18650 cells with electrodes supplied by or purchased from private companies for thermal abuse and electrical characterization studies. Lately, we are coating our own electrodes, building cells and evaluating performance. This paper describes our extensive in-house facilities for slurry making, electrode coating, cell winding etc. In addition, facilities for electrical testing and thermal abuse will be described. This facility allows us to readjust our focus quickly to the changing demands of the still evolving ABR program. Additionally, we continue to make cells for our internal use. We made several 18650 cells both primary (Li-CFx) and secondary (Li-ion) and evaluated performance. For example Li-CFx cells gave ~2.9Ahr capacity at room temperature. Our high voltage Li-ion cells consisting of carbon anode and cathode based on LiNi 0.4Mn 0.3Co 0.3O2 in organic electrolytes exhibited reproducible behavior and gave capacity on the order of 1Ahr. Performance of Li-ion cells at different temperatures and thermal abuse characteristics will be presented.

  20. Correlation of anisotropy and directional conduction in β-Li3PS4 fast Li+ conductor

    Science.gov (United States)

    Chen, Yan; Cai, Lu; Liu, Zengcai; dela Cruz, Clarina R.; Liang, Chengdu; An, Ke

    2015-07-01

    This letter reports the correlation of anisotropy and directional conduction in the fast Li+ conductor β-Li3PS4, one of the low-symmetry crystalline electrolyte candidates. The material has both high conductivity and good stability that serves well for the large-scale energy storage applications of all-solid-state lithium ion batteries. The anisotropic physical properties, demonstrated here by the thermal expansion coefficients, are crucial for compatibility in the solid-state system and battery performance. Neutron and X-ray powder diffraction measurements were done to determine the crystal structure and thermal stability. The crystallographic b-axis was revealed as a fast expansion direction, while negligible thermal expansion was observed along the a-axis around the battery operating temperatures. The anisotropic behavior has its structural origin from the Li+ conduction channels with incomplete Li occupancy and a flexible connection of LiS4 and PS4 tetrahedra within the framework. This indicates a strong correlation in the direction of the ionic transport in the low-symmetry Li+ conductor.

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

    Energy Technology Data Exchange (ETDEWEB)

    Oguchi, Hiroyuki, E-mail: oguchi@nanosys.mech.tohoku.ac.jp [Department of Nanomechanics, Tohoku University, Sendai 980-8579 (Japan); Micro System Integration Center (muSIC), Tohoku University, Sendai 980-0845 (Japan); Ikeshoji, Tamio; Orimo, Shin-ichi [Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); Advanced Institute for Materials Research (AIMR), Tohoku University, Sendai 980-8577 (Japan); Ohsawa, Takeo; Shiraki, Susumu; Hitosugi, Taro [Advanced Institute for Materials Research (AIMR), Tohoku University, Sendai 980-8577 (Japan); Kuwano, Hiroki [Department of Nanomechanics, Tohoku University, Sendai 980-8579 (Japan)

    2014-11-24

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

  2. Li-rich layer-structured cathode materials for high energy Li-ion batteries

    Science.gov (United States)

    Li, Liu; Lee, Kim Seng; Lu, Li

    2014-08-01

    Li-rich layer-structured xLi2MnO3 ṡ (1 - x)LiMO2 (M = Mn, Ni, Co, etc.) materials have attracted much attention due to their extraordinarily high reversible capacity as the cathode material in Li-ion batteries. To better understand the nature of this type of materials, this paper reviews history of development of the Li-rich cathode materials, and provides in-depth study on complicated crystal structures and reaction mechanisms during electrochemical charge/discharge cycling. Despite the fabulous capability at low rate, several drawbacks still gap this type of high-capacity cathode materials from practical applications, for instance the large irreversible capacity loss at first cycle, poor rate capability, severe voltage decay and capacity fade during electrochemical charge/discharge cycling. This review will also address mechanisms for these inferior properties and propose various possible solutions to solve above issues for future utilization of these cathode materials in commercial Li-ion batteries.

  3. Li-ion conduction in the LiBH4:LiI system from Density Functional Theory calculations and Quasi-Elastic Neutron Scattering

    DEFF Research Database (Denmark)

    Myrdal, Jon Steinar Gardarsson; Blanchard, Didier; Sveinbjörnsson, Dadi Þorsteinn

    2013-01-01

    defect sites, giving rise to high defect mobility. QENS results at 380 K show long-range diffusion of Li+, with jump lengths of one unit cell and jump rates in agreement with those obtained from DFT, and the application of the bias potential increases the diffusion constant by a factor of 2. At 300 K......The hexagonal high-temperature polymorph of LiBH4 is stabilized by solid solution with LiI to exhibit superionic Li+ ionic conductivity at room temperature. Herein, the mechanisms for the Li+ diffusion are investigated for the first time by density functional theory (DFT) calculations coupled......, the QENS data reveal jump events of shorter length (2 Å), which could correspond to a jump process of Li+ interstitials to an intermediate lattice site, in agreement with DFT calculations....

  4. Concentration dependence of Li+/Na+ diffusion in manganese hexacyanoferrates

    Science.gov (United States)

    Takachi, Masamitsu; Fukuzumi, Yuya; Moritomo, Yutaka

    2016-06-01

    Manganese hexacyanoferrates (Mn-HCFs) with a jungle-gym-type structure are promising cathode materials for Li+/Na+ secondary batteries (LIBs/SIBs). Here, we investigated the diffusion constants D Li/D Na of Li+/Na+ against the Li+/Na+ concentration x Na/x Li and temperature (T) of A 1.32Mn[Fe(CN)6]0.833.6H2O (A = Li and Na). We evaluated the activation energy E\\text{a}\\text{Li}/E\\text{a}\\text{Na} of D Li/D Na against x Na/x Li. We found that E\\text{a}\\text{Na} steeply increases with x Na from 0.41 eV at x Na = 0.69 to 0.7 eV at 1.1. The increase in E\\text{a}\\text{Na} is ascribed to the occupancy effect of the Na+ site. The increase in E\\text{a}\\text{Li} is suppressed, probably because the number of Li+ sites is three times that of Na+ sites.

  5. Revision of the Li13Si4 structure

    Directory of Open Access Journals (Sweden)

    Thomas F. Fässler

    2013-12-01

    Full Text Available Besides Li17Si4, Li16.42Si4, and Li15Si4, another lithium-rich representative in the Li–Si system is the phase Li13Si4 (tridecalithium tetrasilicide, the structure of which has been determined previously [Frank et al. (1975. Z. Naturforsch. Teil B, 30, 10–13]. A careful analysis of X-ray diffraction patterns of Li13Si4 revealed discrepancies between experimentally observed and calculated Bragg positions. Therefore, we redetermined the structure of Li13Si4 on the basis of single-crystal X-ray diffraction data. Compared to the previous structure report, decisive differences are (i the introduction of a split position for one Li site [occupancy ratio 0.838 (7:0.162 (7], (ii the anisotropic refinement of atomic displacement parameters for all atoms, and (iii a high accuracy of atom positions and unit-cell parameters. The asymmetric unit of Li13Si4 contains two Si and seven Li atoms. Except for one Li atom situated on a site with symmetry 2/m, all other atoms are on mirror planes. The structure consists of isolated Si atoms as well as Si–Si dumbbells surrounded by Li atoms. Each Si atom is either 12- or 13-coordinated. The isolated Si atoms are situated in the ab plane at z = 0 and are strictly separated from the Si–Si dumbbells at z = 0.5.

  6. Synthesis and optical characterization of LiKB4O7, Li2B6O10, and LiCsB6O10 glasses

    Energy Technology Data Exchange (ETDEWEB)

    Adamiv, V.; Teslyuk, I.; Dyachok, Ya.; Romanyuk, G.; Krupych, O.; Mys, O.; Martynyuk-Lototska, I.; Burak, Ya.; Vlokh, R.

    2010-10-01

    In the current work we report on the synthesis of LiKB4O7, Li2B6O10, and LiCsB6O10 borate glasses. The results for their piezo-optic, acousto-optic, acoustic, elastic, refractive, optical transmission, and optical resistance properties are also presented. It is shown that some of these glasses represent efficient acousto-optic materials that are transparent down to the vacuum ultraviolet range and highly resistant to laser radiation.

  7. Synthesis and optical characterization of LiKB4O7, Li2B6O10, and LiCsB6O10 glasses.

    Science.gov (United States)

    Adamiv, V; Teslyuk, I; Dyachok, Ya; Romanyuk, G; Krupych, O; Mys, O; Martynyuk-Lototska, I; Burak, Ya; Vlokh, R

    2010-10-01

    In the current work we report on the synthesis of LiKB(4)O(7), Li(2)B(6)O(10), and LiCsB(6)O(10) borate glasses. The results for their piezo-optic, acousto-optic, acoustic, elastic, refractive, optical transmission, and optical resistance properties are also presented. It is shown that some of these glasses represent efficient acousto-optic materials that are transparent down to the vacuum ultraviolet range and highly resistant to laser radiation.

  8. Exploring Half Metals in Li-based Half Heusler Alloys

    Science.gov (United States)

    Busemeyer, B.; Shaughnessy, M.; Fong, C. Y.

    2011-11-01

    We examine the electronic and magnetic properties of three Li-related half Heusler alloys, namely LiMnN, LiMnP, and LiMnSi in a structure close to the well-known zinc-blende structure in the attempt to search for new half metallic materials. If they do demonstrate half metallic properties, this will open new grounds for finding half metallic spintronic materials. Our results will furnish guidelines for future exploration of alkali-related half metals. Using the primitive cell LiMnSi is a half metal, while the pnictides are not. However when the conventional cell is used, we find that Li3Mn4P4 and Li3Mn4N4 are half metals. The physical reason for these two pnictides to be half metallic and for their magnetic moment per unit cell will be presented.

  9. Li+ ion conductivities in boro-tellurite glasses

    Indian Academy of Sciences (India)

    M Harish Bhat; M Kandavel; Munia Ganguli; K J Rao

    2004-04-01

    Lithium ion conductivity has been investigated in a boro-tellurite glass system, LiCl.LiBO$_{2}\\cdot$TeO2.In the absence of LiCl, the conductivity increases with increasing non-bridging oxygen (NBO) concentration. LiCl addition has little influence on total conductivity although the observed barriers are low. Formation of LiCl clusters appears evident. In the a.c. conductivity and dielectric studies, it is observed that the conductivity mechanism remains the same in all compositions and at all temperatures. A suggestion is made that Li+ ion transport may be driven by bridging oxygen $\\leftrightarrow$ non-bridging oxygen (BO $\\leftrightarrow$ NBO) switching, which is why the two different types of Li+ ions in the clusters and in the neighbourhood of NBOs, do not manifest in the conductivity studies.

  10. Synthesis, crystal structure, and TEM analysis of Sr19Li44 and Sr3Li2: a reinvestigation of the Sr-Li phase diagram.

    Science.gov (United States)

    Smetana, Volodymyr; Kienle, Lorenz; Duppel, Viola; Simon, Arndt

    2015-02-02

    Two intermetallic phases in the Sr-Li system have been synthesized and structurally characterized. According to single-crystal X-ray diffraction data, Sr(19)Li(44) and Sr(3)Li(2) crystallize with tetragonal unit cells (Sr(19)Li(44), I-42d, a = 15.9122(7) Å, c = 31.831(2) Å, Z = 4, V = 8059(2) Å(3); Sr(3)Li(2), P42/mnm, a = 9.803(1) Å, c = 8.784(2) Å, Z = 4, V = 844.2(2) Å(3)). The first compound is isostructural with the recently discovered Ba(19)Li(44). Sr in Sr(19)Li(44) can be fully replaced by Ba with no changes to the crystal structure, whereas the substitution of Sr by Ca is only possible within a limited concentration range. Sr(3)Li(2) can be assigned to the Al(2)Zr(3) structure type. The crystal structure determination of Sr(19)Li(44) was complicated by multiple twinning. As an experimental highlight, an electron microscopy investigation of the highly moisture- and electron-beam-sensitive crystals was performed, enabling high-resolution imaging of the defect structure.

  11. Underpotential deposition of Li in a molten LiCl-Li{sub 2}O electrolyte for the electrochemical reduction of U from uranium oxides

    Energy Technology Data Exchange (ETDEWEB)

    Hur, Jin-Mok; Jeong, Sang Mun; Lee, Hansoo [Korea Atomic Energy Research Institute, Daejeon, 305-353 (Korea)

    2010-05-15

    Reactive metal oxides are conventionally reduced to metal by metallothermic reduction. This paper presents on the efficient reduction method based on the electrochemical reaction in a molten LiCl-Li{sub 2}O electrolyte at 650 C. An underpotential deposition of Li on uranium oxides was observed that enabled the mass electrochemical reduction of U{sub 3}O{sub 8} to U. An advantage of using in-situ generated Li as a reductant is that a high-speed electrochemical reduction could be achieved with a wider operating voltage window when compared to a direct electrochemical reduction. (author)

  12. Thermophysical properties of LiCoO₂-LiMn₂O₄ blended electrode materials for Li-ion batteries.

    Science.gov (United States)

    Gotcu, Petronela; Seifert, Hans J

    2016-04-21

    Thermophysical properties of two cathode types for lithium-ion batteries were measured by dependence on temperature. The cathode materials are commercial composite thick films containing LiCoO2 and LiMn2O4 blended active materials, mixed with additives (binder and carbon black) deposited on aluminium current collector foils. The thermal diffusivities of the cathode samples were measured by laser flash analysis up to 673 K. The specific heat data was determined based on measured composite specific heat, aluminium specific heat data and their corresponding measured mass fractions. The composite specific heat data was measured using two differential scanning calorimeters over the temperature range from 298 to 573 K. For a comprehensive understanding of the blended composite thermal behaviour, measurements of the heat capacity of an additional LiMn2O4 sample were performed, and are the first experimental data up to 700 K. Thermal conductivity of each cathode type and their corresponding blended composite layers were estimated from the measured thermal diffusivity, the specific heat capacity and the estimated density based on metallographic methods and structural investigations. Such data are highly relevant for simulation studies of thermal management and thermal runaway in lithium-ion batteries, in which the bulk properties are assumed, as a common approach, to be temperature independent.

  13. Li interactions with the B40 fullerene and its application in Li-ion batteries: DFT studies

    Science.gov (United States)

    Moradi, Morteza; Bagheri, Zargham; Bodaghi, Ali

    2017-05-01

    The interaction of Li and Li+ with a B40 all-boron fullerene was theoretically investigated at the B3LYP, and Minnesota 2006 levels of theory. It was found that, unexpectedly, the interaction Li+ cation with the electron deficient B40 fullerene is stronger than the Li atom. It indicates that the B40 fullerene does not act as a conventional Lewis acid because of its highly correlated structure. Frontier molecular orbitals, partial density of states, and natural bond orbital analyses were used to discuss this unusual behavior. Our calculations indicate that this behavior makes the B40 fullerene more appropriate for application in the Li-ion batteries as anode material. The calculated cell voltage is about 530 mV. Also, it was found that Hartree Fock (HF) exchange percentage of density functionals has a reverse effect on the adsorption energies of Li and Li+. This energy is increased and decreased, respectively, for Li+ and Li adsorptions by increasing %HF exchange. Finally, a potential energy surface for Li and Li+ penetration into B40 fullerene was predicted.

  14. Data mining of molecular dynamics data reveals Li diffusion characteristics in garnet Li7La3Zr2O12

    Science.gov (United States)

    Chen, Chi; Lu, Ziheng; Ciucci, Francesco

    2017-01-01

    Understanding Li diffusion in solid conductors is essential for the next generation Li batteries. Here we show that density-based clustering of the trajectories computed using molecular dynamics simulations helps elucidate the Li diffusion mechanism within the Li7La3Zr2O12 (LLZO) crystal lattice. This unsupervised learning method recognizes lattice sites, is able to give the site type, and can identify Li hopping events. Results show that, while the cubic LLZO has a much higher hopping rate compared to its tetragonal counterpart, most of the Li hops in the cubic LLZO do not contribute to the diffusivity due to the dominance of back-and-forth type jumps. The hopping analysis and local Li configuration statistics give evidence that Li diffusivity in cubic LLZO is limited by the low vacancy concentration. The hopping statistics also shows uncorrelated Poisson-like diffusion for Li in the cubic LLZO, and correlated diffusion for Li in the tetragonal LLZO in the temporal scale. Further analysis of the spatio-temporal correlation using site-to-site mutual information confirms the weak site dependence of Li diffusion in the cubic LLZO as the origin for the uncorrelated diffusion. This work puts forward a perspective on combining machine learning and information theory to interpret results of molecular dynamics simulations.

  15. Li-Ge-H system: Hydrogenation and structural properties of LiGeHx (0

    Science.gov (United States)

    Pavlyuk, V.; Ciesielski, W.; Kulawik, D.; Prochwicz, W.; Rożdżyńska-Kiełbik, B.

    2016-11-01

    The synthesis, isothermal section at 450 °C of the Li-Ge-H system in the concentration region from 40 at.% Li to 70 at.% Li and structural characterizations of the observed phases are reported. The hydrogenation and structural properties of the LiGeHx (0 < x < 0.25) phase were studied by volumetric analysis and X-ray diffraction. The absorption of hydrogen by LiGe binary compound produce the ternary hydride phase LiGeHx (0 < x < 0.25), thus the volume tetragonal unit cell increases on 1.8 Å3. The LiGeHx solid solution is formed by means of the insertion of hydrogen atoms into tetrahedral voids of parent LiGe structure. The extension of homogeneity range of LiGeHx (0 < x < 0.25) phase and its crystal structure were more precisely refined using X-ray diffraction data. Electronic structure calculations reveal an increased occupation of electronic states at the Fermi level for LiGeHx in comparison to LiGe.

  16. Data mining of molecular dynamics data reveals Li diffusion characteristics in garnet Li7La3Zr2O12

    Science.gov (United States)

    Chen, Chi; Lu, Ziheng; Ciucci, Francesco

    2017-01-01

    Understanding Li diffusion in solid conductors is essential for the next generation Li batteries. Here we show that density-based clustering of the trajectories computed using molecular dynamics simulations helps elucidate the Li diffusion mechanism within the Li7La3Zr2O12 (LLZO) crystal lattice. This unsupervised learning method recognizes lattice sites, is able to give the site type, and can identify Li hopping events. Results show that, while the cubic LLZO has a much higher hopping rate compared to its tetragonal counterpart, most of the Li hops in the cubic LLZO do not contribute to the diffusivity due to the dominance of back-and-forth type jumps. The hopping analysis and local Li configuration statistics give evidence that Li diffusivity in cubic LLZO is limited by the low vacancy concentration. The hopping statistics also shows uncorrelated Poisson-like diffusion for Li in the cubic LLZO, and correlated diffusion for Li in the tetragonal LLZO in the temporal scale. Further analysis of the spatio-temporal correlation using site-to-site mutual information confirms the weak site dependence of Li diffusion in the cubic LLZO as the origin for the uncorrelated diffusion. This work puts forward a perspective on combining machine learning and information theory to interpret results of molecular dynamics simulations. PMID:28094317

  17. Enhanced Performance of Li|LiFePO4 Cells Using CsPF6 as an Electrolyte Additive

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Liang; Chen, Xilin; Cao, Ruiguo; Qian, Jiangfeng; Xiang, Hongfa; Zheng, Jianming; Zhang, Jiguang; Xu, Wu

    2015-10-20

    The practical application of lithium (Li) metal anode in rechargeable Li batteries is hindered by both the growth of Li dendrites and the low Coulombic efficiency (CE) during repeated charge/discharge cycles. Recently, we have discovered that CsPF6 as an electrolyte additive can significantly suppress Li dendrite growth and lead to highly compacted and well aligned Li nanorod structure during Li deposition on copper substrates. In this paper, the effect of CsPF6 additive on the performance of rechargeable Li metal batteries with lithium iron phosphate (LFP) cathode was further studied. Li|LFP coin cells with CsPF6 additive in electrolytes show well protected Li anode surface, decreased resistance, enhanced rate capability and extended cycling stability. In Li|LFP cells, the electrolyte with CsPF6 additive shows excellent long-term cycling stability (at least 500 cycles) at a charge current density of 0.5 mA cm-2 without internal short circuit. At high charge current densities, the effect of CsPF6 additive becomes less significant. Future work needs to be done to protect Li metal anode, especially at high charge current densities and for long cycle life.

  18. Li-Metal-Free Prelithiation of Si-Based Negative Electrodes for Full Li-Ion Batteries.

    Science.gov (United States)

    Zhou, Haitao; Wang, Xuehang; Chen, De

    2015-08-24

    Most of the high-capacity positive-electrode materials [for example, S, O2 (air), and MOx (M: V, Mn, Fe, etc.)] are Li-deficient and require the use of a Li-metal electrode or prelithiation. Herein, we report a novel electrolytic cell in which the Si electrode can be prelithiated in a well-controlled manner from Li-containing aqueous solution in a Li-metal-free way. MnOx/Si and S/Si Li-ion full cells were assembled by using the prelithiated Si negative electrodes, which resulted in high specific energies of 349 and 732 Wh kg(-1), respectively. The MnOx/Si full cell still retains 138 Wh kg(-1) even at a high specific power of 1710 W kg(-1). This is the first report of a whole process of making a full Li-ion battery with both Li-deficient electrodes without the use of Li metal as the Li source. This novel prelithiation process, with high controllability, no short circuiting, and an abundant Li source, is expected to contribute significantly to the development of safe, green, and powerful Li-ion batteries. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Synthesis and characterization of Carbon Nano Fiber/LiFePO{sub 4} composites for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Bhuvaneswari, M.S.; Bramnik, N.N.; Ensling, D.; Jaegermann, W. [Darmstadt University of Technology, Institute of Materials Science, Petersenstrasse 23, 64287 Darmstadt (Germany); Ehrenberg, H. [Darmstadt University of Technology, Institute of Materials Science, Petersenstrasse 23, 64287 Darmstadt (Germany); IFW Dresden, Institute for Complex Materials, Helmholtzstr, 20, 01069 Dresden (Germany)

    2008-05-15

    Carbon Nano Fibers (CNFs) coated with LiFePO{sub 4} particles have been prepared by a non-aqueous sol-gel technique. The functionalization of the CNFs by HNO{sub 3} acid treatment has been confirmed by Raman and XPS analyses. The samples pure LiFePO{sub 4} and LiFePO{sub 4}-CNF have been characterized by XRD, SEM, RAMAN, XPS and electrochemical analysis. The LiFePO{sub 4}-CNF sample shows better electrochemical performance compared to as-prepared LiFePO{sub 4}. LiFePO{sub 4}-CNF (10 wt.%) delivers a higher specific capacity ({proportional_to}140 mAh g{sup -1}) than LiFePO{sub 4} with carbon black (25 wt.%) added after synthesis ({proportional_to}120 mAh g{sup -1}) at 0.1C. (author)

  20. LiBOB基电解液在锂离子动力电池中的应用%The application of LiBOB based electrolyte in power Li-ion battery

    Institute of Scientific and Technical Information of China (English)

    连芳; 闫坤; 邢桃峰; 仇卫华

    2011-01-01

    The unique advantages of lithium bis(oxalate) borate (LiBOB) as electrolyte salt for power Li-ion battery and the key problems of LiBOB-based electrolyte were summarized. The review was especially focused on the effect of impurities,optimization of its solvents and the compatibility of LiBOB-based electrolyte with LiMn2O4, LiFePO4 electrodes.%介绍了双草酸硼酸锂(LiBOB)作为锂离子动力电池电解质锂盐的独特优势以及LiBOB基电解液应用中的关键问题.主要针对LiBOB基电解液中杂质影响和溶剂优化,以及与LiMnO、LiFePO正极材料的相容性进行了阐述.

  1. Dielectric properties of Li doped Li-Nb-O thin films

    Energy Technology Data Exchange (ETDEWEB)

    Perentzis, G.; Horopanitis, E.E.; Papadimitriou, L. [Aristotle University of Thessaloniki, Department of Physics, 54124 Thessaloniki (Greece); Durman, V.; Saly, V.; Packa, J. [Faculty of Electrical Engineering and Information Technology, Slovak University of Technology, Ilkovicova 3, 81219 Bratislava (Slovakia)

    2007-03-15

    Lithium niobate LiNbO{sub 3} was prepared as a thin film layered structure deposited on stainless steel substrate using e-gun evaporation. The Li doping was provided for by the formation of Li-Nb-O/Li/LiNb-O sandwich structure and annealing at about 250 C. AC impedance spectroscopy measurements were performed on the samples at temperatures from the interval between 28 and 165 C and in a frequency range of 10{sup -3} to 10{sup 6} Hz. Using the values Z' and Z'' at different frequencies, the dielectric parameters - parts of the complex permittivity {epsilon}' and {epsilon}'' and loss tangent tan {delta} were calculated. The results prove validity of the proposed equivalent circuit containing parallel RC elements connected in series where the first RC element represents the bulk of material and the second RC element belongs to the double layer at the metal interface. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. Thermal and Cycle-Life Behavior of Commercial Li-ion and Li-Polymer Cells

    Science.gov (United States)

    Zimmerman, Albert H.; Quinzio, M. V.

    2001-01-01

    Accelerated and real-time LEO cycle-life test data will be presented for a range of commercial Li-ion and Li-polymer (gel type) cells indicating the ranges of performance that can be obtained, and the performance screening tests that must be done to assure long life. The data show large performance variability between cells, as well as a highly variable degradation signature during non-cycling periods within the life tests. High-resolution Dynamic Calorimetry data will be presented showing the complex series of reactions occurring within these Li cells as they are cycled. Data will also be presented for cells being tested using an Adaptive Charge Control Algorithm (ACCA) that continuously adapts itself to changes in cell performance, operation, or environment to both find and maintain the optimum recharge over life. The ACCA has been used to prevent all unneeded overcharge for Li cells, NiCd cells and NiH2 cells. While this is important for all these cell types, it is most critical for Li-ion cells, which are not designed with electrochemical tolerance for overcharge.

  3. Spectroscopy of Li9Λ by electroproduction

    Science.gov (United States)

    Urciuoli, G. M.; Cusanno, F.; Marrone, S.; Acha, A.; Ambrozewicz, P.; Aniol, K. A.; Baturin, P.; Bertin, P. Y.; Benaoum, H.; Blomqvist, K. I.; Boeglin, W. U.; Breuer, H.; Brindza, P.; Bydžovský, P.; Camsonne, A.; Chang, C. C.; Chen, J.-P.; Choi, Seonho; Chudakov, E. A.; Cisbani, E.; Colilli, S.; Coman, L.; Craver, B. J.; De Cataldo, G.; de Jager, C. W.; De Leo, R.; Deur, A. P.; Ferdi, C.; Feuerbach, R. J.; Folts, E.; Fratoni, R.; Frullani, S.; Garibaldi, F.; Gayou, O.; Giuliani, F.; Gomez, J.; Gricia, M.; Hansen, J. O.; Hayes, D.; Higinbotham, D. W.; Holmstrom, T. K.; Hyde, C. E.; Ibrahim, H. F.; Iodice, M.; Jiang, X.; Kaufman, L. J.; Kino, K.; Kross, B.; Lagamba, L.; LeRose, J. J.; Lindgren, R. A.; Lucentini, M.; Margaziotis, D. J.; Markowitz, P.; Meziani, Z. E.; McCormick, K.; Michaels, R. W.; Millener, D. J.; Miyoshi, T.; Moffit, B.; Monaghan, P. A.; Moteabbed, M.; Camacho, C. Muñoz; Nanda, S.; Nappi, E.; Nelyubin, V. V.; Norum, B. E.; Okasyasu, Y.; Paschke, K. D.; Perdrisat, C. F.; Piasetzky, E.; Punjabi, V. A.; Qiang, Y.; Reimer, P. E.; Reinhold, J.; Reitz, B.; Roche, R. E.; Rodriguez, V. M.; Saha, A.; Santavenere, F.; Sarty, A. J.; Segal, J.; Shahinyan, A.; Singh, J.; Širca, S.; Snyder, R.; Solvignon, P. H.; Sotona, M.; Subedi, R.; Sulkosky, V. A.; Suzuki, T.; Ueno, H.; Ulmer, P. E.; Veneroni, P.; Voutier, E.; Wojtsekhowski, B. B.; Zheng, X.; Zorn, C.; Jefferson Lab Hall A Collaboration

    2015-03-01

    Background: In the absence of accurate data on the free two-body hyperon-nucleon interaction, the spectra of hypernuclei provides information on the details of the effective hyperon-nucleon interaction. Purpose: To obtain a high-resolution binding-energy spectrum for the 9Be (e ,e'K+) Li9Λ reaction. Method: Electroproduction of the hypernucleus Li9Λ has been studied for the first time with sub-MeV energy resolution in Hall A at Jefferson Lab on a 9Be target. In order to increase the counting rate and to provide unambiguous kaon identification, two superconducting septum magnets and a ring imaging Cherenkov detector were added to the Hall A standard equipment. Results: The cross section to low-lying states of Li9Λ is concentrated within 3 MeV of the ground state and can be fit with four peaks. The positions of the doublets agree with theory while a disagreement could exist with respect to the relative strengths of the peaks in the doublets. The Λ separation energy, BΛ, of 8.36 ±0.08 (stat.) ±0.08 (syst.) MeV was measured, in agreement with an earlier experiment.

  4. Endurance testing with Li/Na electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Ong, E.T.; Remick, R.J.; Sishtla, C.I. [Institute of Gas Technology, Des Plaines, IL (United States)

    1996-12-31

    The Institute of Gas Technology (IGT), under subcontract to M-C Power Corporation under DOE funding, has been operating bench-scale fuel cells to investigate the performance and endurance issues of the Li/Na electrolyte because it offers higher ionic conductivity, higher exchange current densities, lower vapor pressures, and lower cathode dissolution rates than the Li/K electrolyte. These cells have continued to show higher performance and lower decay rates than the Li/K cells since the publication of our two previous papers in 1994. In this paper, test results of two long-term 100-cm{sup 2} bench scale cells are discussed. One cell operated continuously at 160 mA/cm{sup 2} for 17,000 hours with reference gases (60H{sub 2}/20CO{sub 2}/20H{sub 2}O fuel at 75% utilization and 30CO{sub 2}/70 air oxidant humidified at room temperature at 50% utilization). The other cell operated at 160 mA/cm{sup 2} for 6900 hours at 3 atm with system gases (64H{sub 2}/16CO{sub 2}/20H{sub 2}O at 75% utilization and an M-C Power system-defined oxidant at 40% utilization). Both cells have shown the highest performance and longest endurance among IGT cells operated to date.

  5. CuLi2Sn and Cu2LiSn: Characterization by single crystal XRD and structural discussion towards new anode materials for Li-ion batteries

    Science.gov (United States)

    Fürtauer, Siegfried; Effenberger, Herta S.; Flandorfer, Hans

    2014-12-01

    The stannides CuLi2Sn (CSD-427095) and Cu2LiSn (CSD-427096) were synthesized by induction melting of the pure elements and annealing at 400 °C. The phases were reinvestigated by X-ray powder and single-crystal X-ray diffractometry. Within both crystal structures the ordered CuSn and Cu2Sn lattices form channels which host Cu and Li atoms at partly mixed occupied positions exhibiting extensive vacancies. For CuLi2Sn, the space group F-43m. was verified (structure type CuHg2Ti; a=6.295(2) Å; wR2(F²)=0.0355 for 78 unique reflections). The 4(c) and 4(d) positions are occupied by Cu atoms and Cu+Li atoms, respectively. For Cu2LiSn, the space group P63/mmc was confirmed (structure type InPt2Gd; a=4.3022(15) Å, c=7.618(3) Å; wR2(F²)=0.060 for 199 unique reflections). The Cu and Li atoms exhibit extensive disorder; they are distributed over the partly occupied positions 2(a), 2(b) and 4(e). Both phases seem to be interesting in terms of application of Cu-Sn alloys as anode materials for Li-ion batteries.

  6. Electrochemical Formation of Al-Li Alloys by Codeposition of Al and Li from LiCl-KCl-AlF3 Melts at 853 K

    Institute of Scientific and Technical Information of China (English)

    SUN Yi; ZHANG Mi-lin; HAN Wei; LI Mei; YANG Yu-sheng

    2013-01-01

    The electrochemical behavior of Al(Ⅲ) ions was studied in molten LiCl-KCl melts on a molybdenum electrode.Cyclic voltammetry,chronopotentiometry and chronoamperometry were used to explore the deposition mechanism of Al and Li.Cyclic voltammetry expriment indicates that under potential deposition(UPD) of lithium on pre-deposited aluminium led to the formation of liquid Al-Li alloys at 853 K.The diffusion coefficient of Al(Ⅲ) ions at 853 K in LiCl-KCl-AlF3(1%,mass fraction) melts was determined to be (2.79±0.05)× 10-5 cm2/s.Chronopotentiograms and chronoamperograms demonstrate that the codeposition of Al(Ⅲ) and Li(Ⅰ) ions formed Al-Li alloys at cathodic current densities higher than-0.28 A/cm2 or cathodic potentials more negative than-2.20 V.X-Ray diffraction(XRD) pattern indicates that Al-Li alloys with different phases formed via galvanostatic electrolysis.Inductively coupled plasma(ICP) analyses of the samples obtained by electrolysis show that lithium and aluminium contents of Al-Li alloys could be controlled by AlF3 concentration and current intensity.

  7. Nanoparticle shapes of LiMnPO4, Li+ diffusion orientation and diffusion coefficients for high volumetric energy Li+ ion cathodes

    Science.gov (United States)

    Kwon, Nam Hee; Yin, Hui; Vavrova, Tatiana; Lim, Jonathan H.-W.; Steiner, Ullrich; Grobéty, Bernard; Fromm, Katharina M.

    2017-02-01

    Nanoparticles of LiMnPO4 were fabricated in rod, elongated as well as cubic shapes. The 1D Li+ preferred diffusion direction for each shape was determined via electron diffraction spot patterns. The shape of nano-LiMnPO4 varied the diffusion coefficient of Li+ because the Li+ diffusion direction and the path length were different. The particles with the shortest dimension along the b-axis provided the highest diffusion coefficient, resulting in the highest gravimetric capacity of 135, 100 and 60 mAh g-1 at 0.05C, 1C and 10C, respectively. Using ball-milling, a higher loading of nano-LiMnPO4 in the electrode was achieved, increasing the volumetric capacity to 263 mAh cm-3, which is ca. 3.5 times higher than the one obtained by hand-mixing of electrode materials. Thus, the electrochemical performance is governed by both the diffusion coefficient of Li+, which is dependent on the shape of LiMnPO4 nanoparticles and the secondary composite structure.

  8. Characterizing Lava Flows With LiDAR

    Science.gov (United States)

    Deligne, N. I.; Cashman, K. V.; Deardorff, N.; Dietterich, H. R.; House, P. K.; Soule, S.

    2009-12-01

    Digital elevation models (DEMs) have been used in volcanology in predictive modeling of lava flow paths, both for assessment of potential hazards and specific predictions of lava flow paths. Topographic analysis of a lava flow is potentially useful for mapping and quantifying flow surface morphologies, which in turn can be used to determine flow emplacement conditions, such as effusion rate, steadiness of flow, and interactions with pre-existing topography and surface water. However, this has been limited in application because of the coarse resolution of most DEMs. In recent years, use of Light Detection and Ranging (LiDAR) airborne laser altimetry, capable of producing high resolution (≤ 1 meter) DEMs, has become increasingly common in the geomorphic and mapping community. However, volcanologists have made little use of airborne LiDAR. Here we compare information obtained using field observations and standard (10 meter) DEMs against LiDAR high resolution DEMs to assess the usefulness, capabilities, and limitations of LiDAR as applicable to lava flows. We compare morphologic characteristics of five lava flows of different compositions, tectonic settings, flow extents, slopes, and eruption duration: (1) 1984 Mauna Loa lava flow, Hawaii; (2) December 1974 Kilauea lava flow, Hawaii; (3) c. 1600 ybp Collier Cone lava flow, central Oregon Cascades; (4) Holocene lava flows from the Sand Mountain volcanic chain, central Oregon Cascades; and (5) Pleistocene lava flows along the Owyhee River, eastern Oregon basin and range. These lava flows range in composition from basalt to andesite, and have eruption durations ranging from 6 hours (observed) to years (inferred). We measure channel width, levee and flow front heights, compression ridge amplitude, wavelength and tumuli dimensions, and surface roughness. For all but the smallest scale features, LiDAR is easily used to quantify these features, which often is impossible or technically challenging to do in the field, while

  9. LiFePO 4 water-soluble binder electrode for Li-ion batteries

    Science.gov (United States)

    Guerfi, A.; Kaneko, M.; Petitclerc, M.; Mori, M.; Zaghib, K.

    A new water-soluble elastomer from ZEON Corp. was evaluated as binder with LiFePO 4 cathode material in Li-ion batteries. The mechanical characteristic of this cathode was compared to that with PVdF-based cathode binder. The elastomer-based cathode shows high flexibility with good adhesion. The electrochemical performance was also evaluated and compared to PVdF-based cathodes at 25 and at 60 °C. A lower irreversible capacity loss was obtained with the elastomer-based cathode, however, aging at 60 °C shows a comparable cycle life to that observed with PVdF-based cathodes. The LiFePO 4-WSB at high rate shows a good performance with 120 mAh g -1 at 10 C rate at 60 °C.

  10. LiFePO{sub 4} water-soluble binder electrode for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Guerfi, A.; Petitclerc, M.; Zaghib, K. [Institut de Recherche d' Hydro-Quebec, 1800 Lionel-Boulet, Varennes, Que. J3X 1S1 (Canada); Kaneko, M.; Mori, M. [ZEON Corporation, R and D Center, 1-2-1 Yako, Kawasaki, Kanagawa 210-9507 (Japan)

    2007-01-01

    A new water-soluble elastomer from ZEON Corp. was evaluated as binder with LiFePO{sub 4} cathode material in Li-ion batteries. The mechanical characteristic of this cathode was compared to that with PVdF-based cathode binder. The elastomer-based cathode shows high flexibility with good adhesion. The electrochemical performance was also evaluated and compared to PVdF-based cathodes at 25 and at 60{sup o}C. A lower irreversible capacity loss was obtained with the elastomer-based cathode, however, aging at 60{sup o}C shows a comparable cycle life to that observed with PVdF-based cathodes. The LiFePO{sub 4}-WSB at high rate shows a good performance with 120mAhg{sup -1} at 10C rate at 60{sup o}C. (author)

  11. Coincidence in the two-photon spectra of Li and Li2 at 735 nm

    Science.gov (United States)

    DeGraffenreid, W.; Sansonetti, Craig J.

    2005-02-01

    A coincidence between the 22S1/2-32S1/2 two-photon transition in the atomic spectrum of 6Li and the X 1Σ+g→ E 1Σ+g two-photon ro-vibrational series of 7Li2 was observed near 735 nm in a heat pipe oven using a tunable laser and thermionic diode detection scheme. The molecular transition obscures one component of the 6Li atomic transition. Selective detection of the atomic transition was obtained by adding an intensity-modulated laser that drives atoms from the 3S to 16P state. The coincident molecular transition and four nearby molecular lines were identified using previously determined Dunham coefficients.

  12. A Stable, Magnetic, and Metallic Li3O4 Compound as a Discharge Product in a Li-Air Battery.

    Science.gov (United States)

    Yang, Guochun; Wang, Yanchao; Ma, Yanming

    2014-08-07

    The Li-air battery with the specific energy exceeding that of a Li ion battery has been aimed as the next-generation battery. The improvement of the performance of the Li-air battery needs a full resolution of the actual discharge products. Li2O2 has been long recognized as the main discharge product, with which, however, there are obvious failures on the understanding of various experimental observations (e.g., magnetism, oxygen K-edge spectrum, etc.) on discharge products. There is a possibility of the existence of other Li-O compounds unknown thus far. Here, a hitherto unknown Li3O4 compound as a discharge product of the Li-air battery was predicted through first-principles swarm structure searching calculations. The new compound has a unique structure featuring the mixture of superoxide O2(-) and peroxide O2(2-), the first such example in the Li-O system. The existence of superoxide O2(-) creates magnetism and hole-doped metallicity. Findings of Li3O4 gave rise to direct explanations of the unresolved experimental magnetism, triple peaks of oxygen K-edge spectra, and the Raman peak at 1125 cm(-1) of the discharge products. Our work enables an opportunity for the performance of capacity, charge overpotential, and round-trip efficiency of the Li-air battery.

  13. The Spectral Properties of Zn doped LiNbO3 Crystals%掺锌LiNbO3晶体的光谱性质

    Institute of Scientific and Technical Information of China (English)

    赵业权; 徐悟生; 朱质彬; 张玥; 徐蔚青; 王继扬

    2000-01-01

    LiNbO3中掺进2 mol%,4 mol%,6 mol%,8 mol%的ZnO,生长Zn(2 mol%):LiNbO3,Zn(4 mol%):LiNbO3,Zn(6 mol%):LiNbO3和Zn(8 mol%):LiNbO3晶体,测试LiNbO3和掺锌LiNbO3晶体的透射光谱.LiNbO3和掺锌LiNbO3晶体在350-900 nm的范围内都是透明的.Zn:LiNbO3晶体的吸收边发生紫移.对Zn:LiNbO3晶体吸收边紫移的机理进行探讨.

  14. Reoxidation of uranium metal immersed in a Li2O-LiCl molten salt after electrolytic reduction of uranium oxide

    Science.gov (United States)

    Choi, Eun-Young; Jeon, Min Ku; Lee, Jeong; Kim, Sung-Wook; Lee, Sang Kwon; Lee, Sung-Jai; Heo, Dong Hyun; Kang, Hyun Woo; Jeon, Sang-Chae; Hur, Jin-Mok

    2017-03-01

    We present our findings that uranium (U) metal prepared by using the electrolytic reduction process for U oxide (UO2) in a Li2O-LiCl salt can be reoxidized into UO2 through the reaction between the U metal and Li2O in LiCl. Two salt types were used for immersion of the U metal: one was the salt used for electrolytic reduction, and the other was applied to the unused LiCl salts with various concentrations of Li2O and Li metal. Our results revealed that the degree of reoxidation increases with the increasing Li2O concentration in LiCl and that the presence of the Li metal in LiCl suppresses the reoxidation of the U metal.

  15. Diffusion of $^{6}$Li in Ta and W

    CERN Document Server

    Vacik, J

    2006-01-01

    The objective of this work was the study of 6Li diffusion in the Ta and W refractory metals. The samples were prepared by ion implantation of 380 keV 6Li+ ions into W and Ta thin foils (up to the fluence of 1016 ions/cm2) and annealed up to the temperature 1940 °C. The depth profiles of 6Li were determined using the Thermal Neutron Depth Profiling (TNDP) technique. The results showed that diffusion of 6Li in both W and Ta foils is very complex and cannot be described by simple Fick’s laws. Trapping centers (in the subsurface layers of both W and Ta metals) were supposed in a trial to explain the 6Li diffusion behaviour. However, the 6Li depth profiles were only partly explained. Other aspects are necessary to take into account for more proper quantification; such as spatially dependent diffusion coefficients, etc.

  16. Üliõpilasteatrid - teistmoodi teater / Kalev Kudu

    Index Scriptorium Estoniae

    Kudu, Kalev, 1961-

    2007-01-01

    Üliõpilasteatrite VI maailmakongressist 21. - 26. juulini Urbinos Itaalias. Autor oma ettekandest teemal "Üliõpilasteater kui mäss. Üliõpilasteatrite eriline missioon globaliseeruvas maailmas". Lühiintervjuu Liege'i ülikooli professori, üliõpilasteatri kunstilise juhi ja Rahvusvahelise Üliõpilasteatrite Liidu (AITU) esimehe Robert Germayga. Etendustest: "Shahrazad - neitsi Bagdadist" (Bologna ülikool, Itaalia"), "Mbomo-mvet" (Yaounde ülikool, Kamerun), "The Believed Dead" (Brescia Katoliiklik Ülikool, Itaalia), "Teenrid" (Teatro Verga, Milano ülikool, Itaalia), "Antigone" (Ateena ülikool, Kreeka), "Tilt!" (Teatro Aenigma, Urbino ülikool, Itaalia), "Paroodia" (Milano ja Urbino ülikoolide üliõpilased), "Erose tiivad" (Saloniki ülikool, Kreeka), "Kolmas laps" (Long Islandi ülikool, USA), "Lee-Oki lugu" (Hoseo ülikool, Lõuna-Korea), "Ülikond" (Vilniuse Tehnikaülikool, Leedu)

  17. Phase Diagrams for the PEO-LiX Electrolyte System.

    Science.gov (United States)

    1987-01-01

    rather flat, in sharp contrast to previous results. 3.2c PEO- LiBF4 System Pure PEO forms complexes with LiBF , and the subsequent phase diagram for...study; 0 ----NMR(15); 0 -DSC or DTA(7, 10,12); A ---a.c.conductivity(6,10,12); 4- optical microscopy(6). is 350 - (PEO) n- LiBF4 300 (PEO) n-LiCF 3SO 3...the PEO- LiBF4 system IS" , " ATOM RATIO O/Li 50 25 8 4 2 1 250 200 150 1 00 -50I 0 0 0.1 0.2 0.3 0.4 0.5 XLiPF6 -’+’ Figure 6. Phase diagram of the

  18. Mobilities of Li(+)-attached butanol isomers in He gas.

    Science.gov (United States)

    Takahashi, K; Saito, K; Koizumi, T; Matoba, S; Kojima, T M; Tanuma, H; Shiromaru, H

    2013-08-28

    Mobilities of Li(+)-attached butanol isomers, (n-BuOH)Li(+), (s-BuOH)Li(+), (i-BuOH)Li(+), and (t-BuOH)Li(+), in helium gas were measured over a range of reduced electric fields (E/N = 25-96 Td) at room temperature. Arrival time measurements accurately identified small differences in the measured mobilities of the isomer ions. At low E/N (≤30 Td, corresponding to a mean collision energy ε≤0.05 eV), (n-BuOH)Li(+) showed a mobility about 1.5% greater than that of the other ions, but at high E/N (≥75 Td, ε≥0.1 eV) its mobility was about 1.1% less.

  19. Elastic properties of Li+ doped lead zinc borate glasses

    Science.gov (United States)

    Rajaramakrishna, R.; Lakshmikantha, R.; Anavekar, R. V.

    2014-04-01

    Glasses in the system 0.25PbO-(0.25-x) ZnO-0.5B2O3-xLi2O have been prepared by the melt quenching technique. Elastic properties, DSC studies have been employed to study the role of Li2O in the present glass system. Elastic properties and Debye temperature have been determined using pulsed echo ultrasonic interferometer operating at 10MHz. Sound velocities Vl, Vt and elastic moduli decrease up to 5 mol% and then gradually increase with increase in Li2O concentration. Debye temperature and the glass transition temperature decreases with increase in Li2O. Densities remains almost constant up to 15 mol% Li2O concentration and increases monotonically while the molar volume decreases with the increase of Li2O concentration. The results are discussed in view of the borate structural network and dual role of Zn and Pb in these glasses.

  20. Üliõpilasteatrid - teistmoodi teater / Kalev Kudu

    Index Scriptorium Estoniae

    Kudu, Kalev, 1961-

    2007-01-01

    Üliõpilasteatrite VI maailmakongressist 21. - 26. juulini Urbinos Itaalias. Autor oma ettekandest teemal "Üliõpilasteater kui mäss. Üliõpilasteatrite eriline missioon globaliseeruvas maailmas". Lühiintervjuu Liege'i ülikooli professori, üliõpilasteatri kunstilise juhi ja Rahvusvahelise Üliõpilasteatrite Liidu (AITU) esimehe Robert Germayga. Etendustest: "Shahrazad - neitsi Bagdadist" (Bologna ülikool, Itaalia"), "Mbomo-mvet" (Yaounde ülikool, Kamerun), "The Believed Dead" (Brescia Katoliiklik Ülikool, Itaalia), "Teenrid" (Teatro Verga, Milano ülikool, Itaalia), "Antigone" (Ateena ülikool, Kreeka), "Tilt!" (Teatro Aenigma, Urbino ülikool, Itaalia), "Paroodia" (Milano ja Urbino ülikoolide üliõpilased), "Erose tiivad" (Saloniki ülikool, Kreeka), "Kolmas laps" (Long Islandi ülikool, USA), "Lee-Oki lugu" (Hoseo ülikool, Lõuna-Korea), "Ülikond" (Vilniuse Tehnikaülikool, Leedu)

  1. Li-Ion Cell Development for Low Temperature Applications

    Science.gov (United States)

    Huang, C.-K.; Sakamoto, J. S.; Surampudi, S.; Wolfenstine, J.

    2000-01-01

    JPL is involved in the development of rechargeable Li-ion cells for future Mars Exploration Missions. The specific objectives are to improve the Li-ion cell cycle life performance and rate capability at low temperature (Li-ion rate capability at low temperature has been attributed to: (1) the electrolytes becoming viscous or freezing and/or (2) reduced electrode capacity that results from decreased Li diffusivity. Our efforts focus on increasing the rate capability at low temperature for Li-ion cells. In order to improve the rate capability we evaluated the following: (1) cathode performance at low temperatures, (2) electrode active material particle size on low temperature performance and (3) Li diffusivity at room temperature and low temperatures. In this paper, we will discuss the results of our study.

  2. Li overlayer formation, oxidation and sputtering characteristics of Al-Li alloys and W/Al-Li composites for fusion applications

    Energy Technology Data Exchange (ETDEWEB)

    Krauss, A.R. (Argonne National Lab., IL (USA)); DeWald, A.B.; Scott, P.; Savage, H. (Corium Industries, Inc., Atlanta, GA (USA))

    1990-01-01

    The next generation of long pulse fusion devices will impose severe requirements on the properties of plasma-facing materials. In devices such as ITER, a divertor design is being considered, using a divertor plate which would be either tungsten or a low-Z material such as graphite or beryllium. Strongly segregating lithium alloys have been proposed as a means of producing a self-sustaining low-Z overlayer which lowers plasma Z{sub eff} and resists self-sputtering. Aluminum-lithium alloys are among the better-characterized lithium-bearing alloys, and it has been demonstrated that lithium segregates strongly in aluminum. However, aluminum has a relatively low melting point, and for low lithium concentrations, the lithium diffusion rate is too slow to replenish lithium at the rate at which it is eroded by the incoming plasma. It has been suggested previously that the superionic {beta} phase Al-Li alloy (48--54 at. % Li) should have high enough diffusivity to be able to replenish surface lithium, and that incorporation of the {beta}-phase AlLi in a composite with tungsten would provide high temperature strength and melt layer stability, along with significantly better thermal conductivity than pure tungsten. Such a composite has been fabricated, as well as a variation containing titanium as a means of controlling oxidation at grain boundaries. The Li overlayer formation, erosion, and replenishment are characterized for the {beta}-phase LiAl alloy, and W-AlLi and W-Ti-AlLi composites. It is found that if there is no oxide layer to inhibit the Li segregation, Li diffusion is extremely rapid, and an oxygen-free Li overlayer is formed which is stable under continuous ion beam sputtering. 21 refs., 7 figs.

  3. Study of vaporization of LiI, LiI/C70, LiI/LiF/C70 from the Knudsen cell located into ionization chamber of the mass spectrometer

    Directory of Open Access Journals (Sweden)

    Đustebek Jasmina

    2014-01-01

    Full Text Available The vaporization of LiI, LiI/C70 and LiI/LIF/C70 were studied using a Knudsen cell located into ionization chamber of a magnetic sector mass spectrometer in a temperature range from 350 ˚C to 850 ˚C. Аs the ion species, LinI+ (n = 2, 3, 4, and 6 were identified from a mixture LiI/C70. While the clusters LinI+ and LinF+ (n = 2 - 6 were detected from a mixture LiI/LiF/C70. The intensities of LinI+ were higher than the emission of LinF+ cluster when the ratio of LiI to LiF was 2:1. By contrast, the emission of the LinF+ is favored when the ratio of LiI to LiF was 1:2. These results show that the vaporization of a mixture LiI/LIF/C70 from the Knudsen cell located into ionization chamber of the mass spectrometer represents an efficient and simple way to obtain and investigate clusters of the type LinX, X-F, I. In this work it has also been shown that the trend of the ln (Intensity, arbit. units versus temperature for all LinI+ clusters before and after the melting point of LiI was not same. It suggested that the way of the formation of these clusters can be different due to changes in temperature. [Projekat Ministarstva nauke Republike Srbije, br. 172019

  4. The impact of nanomaterials on Li-ion rechargeable batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu, H.K.; Wang, G.X.; Guo, Z.P.; Wang, J.Z.; Konstantinov, K. [Wollongong Univ., Wollongong, NSW (Australia). Inst. for Superconducting and Electronic Materials, ARC Centre of Excellence for Electromaterials Science

    2006-07-01

    Nanotechnology is now being considered for use in lithium (Li) secondary batteries. This study investigated the impact of various nanomaterials on Li rechargeable battery performance. The study included an evaluation of carbon nanotubes (CNTs); NiO and WS{sub 2} nanotubes; Sn, si, Cu{sub 6}Sn{sub 5}, Si-C, Si mesocarbon microbeads; Si-TiC, Si-PPY and multiwalled nanotubes and Sn/SnNi nano-composites. Nanoparticles dispersed in polymer electrolytes in the Li secondary batteries were also investigated. Phase-pure compounds were prepared using sol-gel synthesis. A layer of carbon was coated on the surface of the Li crystals. Nanoparticles were dispersed in polymer electrolytes of polyethylene oxide (PEO). When NiSi was used in the Li cells, it provided a high lithium storage capacity in the initial discharge, during which Si acted as an active element to combine with Li to form Li{sub x}Si. Nano-Si-MCMB anodes showed superior performance. MCMB graphite was almost dimensionally invariable during Li insertion and extraction. The phase-pure Li compounds prepared by sol-gel fabrication methods significantly enhanced the electronic conductivity, and the Ti-doped and undoped Li iron phosphates demonstrated a stable discharge capacity. Results of the study showed that nanoparticle-dispersed polymer electrolytes that were smaller in size influenced the crystallization kinetics of the PEO polymer chains. High-energy ball milling lowered the glass transition temperature of the composite polymers, and increased the ionic conductivity by more than an order of magnitude when compared with the unmilled samples. It was concluded that the highest ionic conductivity was achieved when using LiPF{sub 6} as an added Li salt, and Al{sub 2}O{sub 3} as a dispersed particle. 8 refs., 2 figs.

  5. The interaction of 11Li with 208Pb

    CERN Document Server

    Vinodkumar, A M; Yanez, R; Leonard, M; Yao, L; Bricault, P; Dombsky, M; Kunz, P; Lassen, J; Morton, A C; Ottewell, D; Preddy, D; Trinczek, M

    2012-01-01

    Background: 11Li is one of the most studied halo nuclei. The fusion of 11Li with 208Pb has been the subject of a number of theoretical studies with widely differing predictions, ranging over four orders of magnitude, for the fusion excitation function. Purpose: To measure the excitation function for the 11Li + 208Pb reaction. Methods: A stacked foil/degrader assembly of 208Pb targets was irradiated with a 11Li beam producing center of target beam energies from above barrier to near barrier energies (40 to 29 MeV). The intensity of the 11Li beam (chopped) was 1250 p/s and the beam on-target time was 34 hours. The alpha-decay of the stopped evaporation residues was detected in a alpha-detector array at each beam energy in the beam-off period (the beam was on for <= 5 ns and then off for 170 ns). Results: The 215At evaporation residues were associated with the fusion of 11Li with 208Pb. The 213,214At evaporation residues were formed by the breakup of 11Li into 9Li + 2n, with the 9Li fusing with 208Pb. The 214...

  6. Nb-based MXenes for Li-ion battery applications

    KAUST Repository

    Zhu, Jiajie

    2015-11-16

    Li-ion batteries depend critically on the stability and capacity of the electrodes. In this respect the recently synthesized two-dimensional MXenes are promising materials, as they combine an excellent Li-ion capacity with very high charging rates. We employ density functional theory to investigate the impact of Li adsorption on the structural and electronic properties of monolayer Nb2C and Nb2CX2. The Li ions are predicted to migrate easily on the pristine MXene due to a diffusion barrier of only 36 meV, whereas larger diffusion barriers are obtained for the functionalized MXenes.

  7. Electrical conduction of LiF interlayers in organic diodes

    Energy Technology Data Exchange (ETDEWEB)

    Bory, Benjamin F.; Janssen, René A. J.; Meskers, Stefan C. J., E-mail: s.c.j.meskers@tue.nl [Molecular Materials and Nanosystems and Institute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven (Netherlands); Gomes, Henrique L. [Instituto de Telecomunicações, Av. Rovisco, Pais, 1, 1049–001, Lisboa, Portugal and Universidade do Algarve, Campus de Gambelas, 8005-139 Faro (Portugal); Leeuw, Dago M. de [Max-Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany and King Abdulaziz University, Jeddah (Saudi Arabia)

    2015-04-21

    An interlayer of LiF in between a metal and an organic semiconductor is commonly used to improve the electron injection. Here, we investigate the effect of moderate bias voltages on the electrical properties of Al/LiF/poly(spirofluorene)/Ba/Al diodes by systematically varying the thickness of the LiF layer (2-50 nm). Application of forward bias V below the bandgap of LiF (V < E{sub g} ∼ 14 V) results in reversible formation of an electrical double layer at the LiF/poly(spirofluorene) hetero-junction. Electrons are trapped on the poly(spirofluorene) side of the junction, while positively charged defects accumulate in the LiF with number densities as high as 10{sup 25}/m{sup 3}. Optoelectronic measurements confirm the built-up of aggregated, ionized F centres in the LiF as the positive trapped charges. The charged defects result in efficient transport of electrons from the polymer across the LiF, with current densities that are practically independent of the thickness of the LiF layer.

  8. Prediction of superconductivity in Li-intercalated bilayer phosphorene

    Energy Technology Data Exchange (ETDEWEB)

    Huang, G. Q. [Department of Physics, Nanjing Normal University, Nanjing 210023 (China); National Laboratory of Solid State Microstructures, Nanjing University, Nanjing 210093 (China); Xing, Z. W., E-mail: zwxing@nju.edu.cn [National Laboratory of Solid State Microstructures, Nanjing University, Nanjing 210093 (China); Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui 230026 (China); Xing, D. Y. [National Laboratory of Solid State Microstructures, Nanjing University, Nanjing 210093 (China); Collaborative Innovation Center of Advanced Microstructures and Department of Physics, Nanjing University, Nanjing 210093 (China)

    2015-03-16

    It is shown that bilayer phosphorene can be transformed from a direct-gap semiconductor to a BCS superconductor by intercalating Li atoms. For the Li-intercalated bilayer phosphorene, we find that the electron occupation of Li-derived band is small and superconductivity is intrinsic. With increasing the intercalation of Li atoms, both increased metallicity and strong electron-phonon coupling are favorable for the enhancement of superconductivity. The obtained electron-phonon coupling λ can be larger than 1 and the superconducting temperature T{sub c} can be increased up to 16.5 K, suggesting that phosphorene may be a good candidate for a nanoscale superconductor.

  9. The Role of Lithium Passivation in LiSO2

    Science.gov (United States)

    1986-12-29

    studied by mass spectrometry and scanning kuger spectroscopy. Abraham and Chaudhri (6) used IR and XPS techniques to study lithiu.i films from aged and...Lpeclfic conductivity of about 10-9 (ohm-cm)- 1 for the Li passivation layer. Peled (9) developed a model tc describe the film formation in the Li...the Li corrosion products precipitate to form the primary passivation layer. In analogy with the model put forth by Peled (9) for the Li/SOC1 2 couple

  10. Georeferenced LiDAR 3D Vine Plantation Map Generation

    OpenAIRE

    Meritxell Queraltó; Jordi Llop; Emilio Gil; Jordi Llorens

    2011-01-01

    The use of electronic devices for canopy characterization has recently been widely discussed. Among such devices, LiDAR sensors appear to be the most accurate and precise. Information obtained with LiDAR sensors during reading while driving a tractor along a crop row can be managed and transformed into canopy density maps by evaluating the frequency of LiDAR returns. This paper describes a proposed methodology to obtain a georeferenced canopy map by combining the information obtained with LiD...

  11. Synthesis and electrochemical performances of LiCoO2 recycled from the incisors bound of Li-ion batteries

    Institute of Scientific and Technical Information of China (English)

    LI Jinhui; ZHONG Shengwen; XIONG Daoling; CHEN Hao

    2009-01-01

    A new LiCoO2 recovery technology for Li-ion batteries was studied in this paper. LiCoO2 was peeled from the Al foil with dimethyl acetamide (DMAC), and then polyvinylidene fluoride (PVDF) and carbon powders in the active material were eliminated by high tempera-1.00. The new LiCoO2 was obtained by calcining the mixture at 850℃ for 12 h in air. The structure and morphology of the recycled powders and resulting samples were studied by XRD and SEM techniques, respectively. The layered structure of LiCoO2 synthesized by adding Li2CO3 is the best, and it is found to have the best characteristics as a cathode material in terms of charge-discharge capacity and cycling mAh.g-1.

  12. 基于TerraScan的LiDAR数据处理%LiDAR' Data Processing Based on TerraScan

    Institute of Scientific and Technical Information of China (English)

    黄金浪

    2007-01-01

    介绍LiDAR技术的国内外发展情况,围绕LiDAR数据后处理软件TerraScan的应用,详细论述该软件的数据处理流程,特别针对LiDAR数据特点和处理技术难点提出笔者的看法.

  13. Li/SO2 cells and Li/SOCl2 cells: Safe use and testing

    Science.gov (United States)

    Wagner, C. G.

    1992-05-01

    Most lithium/sulfur dioxide (Li/SO2) cells and lithium/thionyl chloride (Li/SOCl2)) cells have pressure relief safety devices called vents built into them. These vents are designed to open under conditions of increasing internal cell pressure. The likelihood of cell venting has been reduced to very low levels by optimizing cell designs. If fully developed Li/SO2 cells or Li/SOCl2 cells (or batteries) are discharged within the intended design limits, they are essentially nonhazardous. In addition, the consequences of cell ventings are being minimized by use of appropriate absorbant materials and protective coatings. During battery assembly and test, detection and monitoring equipment is used to sense the presence of vented gases. Tester data analysis techniques have been developed to foresee either an increasing likelihood of a vent or the presence of a vented cell. Standard cleanup procedures have been developed to safely decontaminate the assembly or test area following a cell vent.

  14. Systematic Phase Diagram of LiSi and LiAl compounds from Minima Hopping Method

    Science.gov (United States)

    Romero, Aldo; Marques, Miguel; Botti, Silvana; Sarmiento-Pérez, Rafael; Valencia-Jaime, Irais; Amsler, Max; Goedecker, Stefan

    2014-03-01

    We performed an extensive theoretical exploration of the structural phase diagram of LiSi and LiAl alloys through global structural prediction. These compounds have very interesting properties. For example, LiSi alloys have been considered for high energy density anodes for future rechargeable battery technology, while LiAl alloys are expected to have applications in the field of structural components due to its light weight and maleability. The global structural prediction was performed with the minima hopping method. In this method the low energy structures are obtained by solving a set of dynamical equations of motion that allows efficient visits to local minima on the Born Oppenheimer surface. We found very good agreement between our simulations and previously reported stoichiometries. Moreover, we were able to identify several novel thermodynamically stable compositions that have not been previously synthesized. The ground-state structures were further characterized both structurally and electronically. Our calculations show that global structural prediction is a very powerful tool to predict new thermodynamically stable materials, and that it consistently outperforms other methods commonly used. Support from ACS-PRF #54075-ND10 is recognized.

  15. Impedance Simulation of a Li-Ion Battery with Porous Electrodes and Spherical Li+ Intercalation Particles

    NARCIS (Netherlands)

    Huang, R.W.J.M.; Chung, F.; Kelder, E.M.

    2006-01-01

    We present a semimathematical model for the simulation of the impedance spectra of a rechargeable lithium batteries consisting of porous electrodes with spherical Li+ intercalation particles. The particles are considered to have two distinct homogeneous phases as a result of the intercalation and

  16. 2004 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Portland, Oregon

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The all returns ASCII files contain the X,Y,Z values of all the LiDAR returns collected during the survey mission. In addition each return also has a time stamp,...

  17. Impedance Simulation of a Li-Ion Battery with Porous Electrodes and Spherical Li+ Intercalation Particles

    NARCIS (Netherlands)

    Huang, R.W.J.M.; Chung, F.; Kelder, E.M.

    2006-01-01

    We present a semimathematical model for the simulation of the impedance spectra of a rechargeable lithium batteries consisting of porous electrodes with spherical Li+ intercalation particles. The particles are considered to have two distinct homogeneous phases as a result of the intercalation and de

  18. Formation of ultracold LiCs molecules

    CERN Document Server

    Kraft, S D; Lange, J; Vogel, L; Wester, R; Weidemüller, M; Kraft, Stephan D.; Staanum, Peter; Lange, Joerg; Vogel, Leif; Wester, Roland; Weidemueller, Matthias

    2006-01-01

    We present the first observation of ultracold LiCs molecules. The molecules are formed in a two-species magneto-optical trap and detected by two-photon ionization and time-of-flight mass spectrometry. The production rate coefficient is found to be in the range $10^{-18}\\unit{cm^3s^{-1}}$ to $10^{-16}\\unit{cm^3s^{-1}}$, at least an order of magnitude smaller than for other heteronuclear diatomic molecules directly formed in a magneto-optical trap.

  19. Practical Methods in Li-ion Batteries

    DEFF Research Database (Denmark)

    Barreras, Jorge Varela

    develops a battery system model for battery management system testing on a hardware-in-the-loop simulator • Manuscript V extends the previous work, introducing theoretical principles and presenting a practical method to develop ad hoc software and strategies for testing • Manuscript VI presents......This thesis presents, as a collection of papers, practical methods in Li-ion batteries for simplified modeling (Manuscript I and II), battery electric vehicle design (III), battery management system testing (IV and V) and balancing system control (VI and VII). • Manuscript I tackles methodologies...

  20. Raman spectrum of the solid electrolytes LiI·H2O and LiI·D2O

    DEFF Research Database (Denmark)

    Poulsen, Finn Willy

    1986-01-01

    The Raman spectra of cubic LiI·H2O and LiI·D2O have been revised. The spectra reveal only internal and librational modes of H2O (D2O). The isotopic ratios νH/νD, are in the range 1.33-1.78......The Raman spectra of cubic LiI·H2O and LiI·D2O have been revised. The spectra reveal only internal and librational modes of H2O (D2O). The isotopic ratios νH/νD, are in the range 1.33-1.78...

  1. An atomic beam of 6Li — 7Li for high resolution spectroscopy from matrix isolation sublimation

    Science.gov (United States)

    Oliveira, A. N.; Sacramento, R. L.; Silva, B. A.; Uhlmann, F. O.; Wolff, W.; Cesar, C. L.

    2016-07-01

    We propose the Matrix Isolation Sublimation (MlSu) technique for generating cold lithium atoms for the measurement of the 6Li - 7Li isotope shift in D1 and D2 transitions. The technique is capable of generating cold 6Li and 7Li beams at 4 K with forward velocity of 125 m/s. Using this beam we offer a distinguished source of lithium atoms for transitions measurements, adding a new possibility to make high resolution spectroscopy towards improving the experimental checks of the theory.

  2. Reversible superconductor-insulator transition in LiTi2O4 induced by Li-ion electrochemical reaction.

    Science.gov (United States)

    Yoshimatsu, K; Niwa, M; Mashiko, H; Oshima, T; Ohtomo, A

    2015-11-06

    Transition metal oxides display various electronic and magnetic phases such as high-temperature superconductivity. Controlling such exotic properties by applying an external field is one of the biggest continuous challenges in condensed matter physics. Here, we demonstrate clear superconductor-insulator transition of LiTi2O4 films induced by Li-ion electrochemical reaction. A compact electrochemical cell of pseudo-Li-ion battery structure is formed with a superconducting LiTi2O4 film as an anode. Li content in the film is controlled by applying a constant redox voltage. An insulating state is achieved by Li-ion intercalation to the superconducting film by applying reduction potential. In contrast, the superconducting state is reproduced by applying oxidation potential to the Li-ion intercalated film. Moreover, superconducting transition temperature is also recovered after a number of cycles of Li-ion electrochemical reactions. This complete reversible transition originates in difference in potentials required for deintercalation of initially contained and electrochemically intercalated Li(+) ions.

  3. Defect Structure of Li-Doped BPO 4: A Nanostructured Ceramic Electrolyte for Li-Ion Batteries

    Science.gov (United States)

    Jak, M. J. G.; Kelder, E. M.; Schoonman, J.

    1999-01-01

    In this paper the defect chemistry of Li-doped BPO4(BPO4-xLi2O, 0≤x≤0.1) is studied. This nanostructured ceramic electrolyte is used in all-solid-state Li-ion batteries. By changing the Li-doping level the influence on the crystal structure is studied and related to t he properties of the material. X-ray diffraction, Fourier-transformed infra-red spectroscopy (FT-IR),31P,11B, and7Li magic-angle-spinning solid state nuclear magnetic resonance, neutron diffraction, and inductively coupled plasma optical-emission spectroscopy measurements are used in order to study the structure. The electrical properties are studied with AC-impedance spectroscopy (AC-IS). The experimental data show that the defect structure of Li-doped BPO4can be described with two defect models, Li″B+2Li·iand V‴B+3Li·i, suggesting that the ionic conductivity takes place via interstitial Li ions.

  4. Li2CuVO4: A high capacity positive electrode material for Li-ion batteries

    Science.gov (United States)

    Ben Yahia, Hamdi; Shikano, Masahiro; Yamaguchi, Yoichi

    2016-07-01

    The new compound Li2CuVO4 was synthesized by a solid state reaction route, and its crystal structure was determined from single crystal X-ray diffraction data. Li2CuVO4 was characterized by galvanometric cycling, cycle voltammetry, and electrochemical impedance spectroscopy. The structure of Li2CuVO4 is isotypic to Pmn21-Li3VO4. It can be described as a disordered wurtzite structure with rows of Li1/Cu1 atoms alternating with rows of (Li2/Cu2)-V-(Li2/Cu2) atoms along [100]. All cations are tetrahedrally coordinated. The lithium and copper atoms are statistically disordered over two crystallographic sites. The electrochemical cycling between 2.0 and 4.7 V indicates that almost two lithium atoms could be extracted and re-intercalated. This delivers a maximum discharge capacity of 257 mA h g-1 at a C/50 rate (theoretical capacity = 139 mA h g-1 for one lithium). Li2CuVO4 shows also high rate capability with a capacity of 175 mA h g-1 at 1C rate. This demonstrates that Cu-based compounds can be very interesting as electrodes for Li-ion batteries if Cu-dissolution is avoided.

  5. Synthesis and electrochemical performances of spherical LiFePO4 cathode materials for Li-ion batteries

    Institute of Scientific and Technical Information of China (English)

    ZHOU Jianxin; SHEN Xiangqian; JING Maoxiang; ZHAN Yun

    2006-01-01

    Spherical LiFePO4 and LiFePO4/C composite powders for lithium ion batteries were synthesized by a novel processing route of co-precipitation and subsequent calcinations in a nitrogen and hydrogen atmosphere. The precursors of LiFePO4, LiFePO4/C composite and the resultant products were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and the electrochemical performances were investigated by galvanostatic charge and discharge tests. The precursors composed of amorphous Fe3(PO4)2·xH2O and crystalline Li3PO4 obtained in the co-precipitation processing have a sphere-like morphology. The spherical LiFePO4 derived from the calcinations of the precursor at 700 ℃ for 10 h in a reduction atmosphere shows a discharge capacity of 119 mAh·g -1 at the C/10 rate, while the LiFePO4/C composite with 10wt.% carbon addition exhibits a discharge capacity of 140 mAh·g -1.The electrochemical performances indicate that the LiFePO4/C composite has a higher specific capacity and a more stable cycling performance than the bare olivine LiFePO4 due to the carbon addition enhancing the electronic conductivity.

  6. Coulomb dissociation and momentum distributions for [sup 11]Li [yields] [sup 9]Li + n + n breakup reactions

    Energy Technology Data Exchange (ETDEWEB)

    Esbensen, H.

    1993-01-01

    Momentum distributions for the [sup 11]Li [yields] [sup 9]Li+n+n breakup reaction, generated by Coulomb dipole excitations, axe calculated in a 3-body model for [sup 11]Li. The relative momentum distribution of the two neutrons is in good agreement with recent 3-body coincidence measurements but the momentum distribution for the [sup 9]Li recoil and the decay energy spectrum are much narrower than observed. These discrepancies may be due to higher order dynamical effects which have been ignored.

  7. Coulomb dissociation and momentum distributions for {sup 11}Li {yields} {sup 9}Li + n + n breakup reactions

    Energy Technology Data Exchange (ETDEWEB)

    Esbensen, H.

    1993-03-01

    Momentum distributions for the {sup 11}Li {yields} {sup 9}Li+n+n breakup reaction, generated by Coulomb dipole excitations, axe calculated in a 3-body model for {sup 11}Li. The relative momentum distribution of the two neutrons is in good agreement with recent 3-body coincidence measurements but the momentum distribution for the {sup 9}Li recoil and the decay energy spectrum are much narrower than observed. These discrepancies may be due to higher order dynamical effects which have been ignored.

  8. Electrodeposition of Mg-Li-Al-La Alloys on Inert Cathode in Molten LiCl-KCl Eutectic Salt

    Science.gov (United States)

    Han, Wei; Chen, Qiong; Sun, Yi; Jiang, Tao; Zhang, Milin

    2011-12-01

    Electrochemical preparation of Mg-Li-Al-La alloys on inert electrodes was investigated in LiCl-KCl melt at 853 K (580 °C). Cyclic voltammograms (CVs) and square wave voltammograms (SWVs) show that the existence of AlCl3 or AlF3 could promote La deposition on an active Al substrate, which is predeposited on inert electrodes. All electrochemical tests show that the reduction of La3+ is a one-step reduction process with three electrons exchanged. The reduction of La(III)→La(0) occurred at -2.04 V, and the underpotential deposition (UPD) of La was detected at -1.55 V ( vs Ag/AgCl). The same phenomena concerning La UPD were observed on two inert cathodes, W and Mo. In addition, Mg-Li-Al-La alloys were obtained by galvanostatic electrolysis on the W cathode from La2O3 in LiCl-KCl-MgCl2-KF melts with aluminum as the anode. X-ray diffraction (XRD) measurements indicated that various phases like the Al2La, Al12Mg17, and βLi phase (LiMg/Li3Mg7) existed in the Mg-Li-Al-La alloys. The distribution of Mg, Al, and La in Mg-Li-Al-La alloys from the analysis of a scan electron micrograph (SEM) and energy dispersive spectrometry (EDS) indicated that the elements Mg, Al, and La distributed homogeneously in the alloys.

  9. Effect of borate coating on corrosion resistance of pure nickel in molten LiCl-Li2O

    Institute of Scientific and Technical Information of China (English)

    刘瑞岩; 王旭; 张俊善; 王秀敏; 祝美丽

    2004-01-01

    The pack boriding process was used to treat pure nickel at a boriding temperature of 950 ℃ for a boriding time of 5 h. A dense and continuous borided layer with 40 μm thickness was obtained on pure nickel. Corrosion behavior of the borided layer was investigated in molten LiCl-10% Li2O(mass fraction) at 750 ℃ in air. The mass lower than that of unborided pure nickel. The preferential corrosion of B in borided layer effectively prevents the corrosion of nickel, which improves the corrosion resistance of pure nickel in molten LiCl-Li2 O.

  10. LiCoO2 electrode/electrolyte interface of Li-ion batteries investigated by electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The storage behavior and the first delithiation of LiCoO2 electrode in 1 mol/L LiPF6-EC:DMC:DEC electrolyte were investigated by electrochemical impedance spectroscopy (EIS). It has found that, along with the increase of storage time, the thickness of SEI film increases, and some organic carbonate lithium compounds are formed due to spontaneous reactions occurring between the LiCoO2 electrode and the electrolyte. When electrode potential is changed from 3.8 to 3.95 V, the reversible breakdown of the resistive SEI film occurs, which is attributed to the reversible dissolution of the SEI film component. With the increase of electrode potential, the thickness of SEI film increases rapidly above 4.2 V, due to overcharge reactions. The inductive loop observed in impedance spectra of the LiCoO2 electrode in Li/LiCoO2 cells is attributed to the formation of a Li1-xCoO2/LiCoO2 concentration cell. Moreover, it has been demonstrated that the lithium-ion insertion-deinsertion in LiCoO2 hosts can be well described by both Langmuir and Frumkin insertion isotherms, and the symmetry factor of charge transfer has been evaluated at 0.5.

  11. LINE EMISSION AND ANISOTROPY EFFECTS IN C6+ ELECTRON-CAPTURE FROM LI(2S), LI-ASTERISK(2P) AND H-ASTERISK(N=2)

    NARCIS (Netherlands)

    OLSON, RE; HOEKSTRA, R

    1995-01-01

    Line emission cross sections for visible transitions after electron capture collisions of C6+ With Li(2s), Li-*(2p), and H-*(n = 2) are calculated for energies up to 50 keV/u; the values agree with available Li(2s) data. Anisotropy parameters are also given for aligned Li-*(2p). The results were obt

  12. Reversible Li-insertion in nanoscaffolds: A promising strategy to alter the hydrogen sorption properties of Li-based complex hydrides

    NARCIS (Netherlands)

    Ngene, Peter; Verkuijlen, Margriet H. W.; Barre, Charlotte; Kentgens, Arno P. M.; de Jongh, Petra E.

    Intercalation and de-intercalation of lithium into graphene layers is a well-established phenomenon in Li-ion battery technology. Here we show how this phenomenon can be exploited to destabilize, and alter the hydrogen sorption behaviour of Li-based metal hydrides (LiBH4 and LiAlH4), thereby

  13. Reversible Li-insertion in nanoscaffolds: A promising strategy to alter the hydrogen sorption properties of Li-based complex hydrides

    NARCIS (Netherlands)

    Ngene, Peter; Verkuijlen, Margriet H. W.; Barre, Charlotte; Kentgens, Arno P. M.; de Jongh, Petra E.

    2016-01-01

    Intercalation and de-intercalation of lithium into graphene layers is a well-established phenomenon in Li-ion battery technology. Here we show how this phenomenon can be exploited to destabilize, and alter the hydrogen sorption behaviour of Li-based metal hydrides (LiBH4 and LiAlH4), thereby achievi

  14. Crystal structure and magnetic properties of Li,Cr-containing molybdates Li 3Cr(MoO 4) 3, LiCr(MoO 4) 2 and Li 1.8Cr 1.2(MoO 4) 3

    Science.gov (United States)

    Sarapulova, A.; Mikhailova, D.; Senyshyn, A.; Ehrenberg, H.

    2009-12-01

    Single crystals of LiCr(MoO 4) 2, Li 3Cr(MoO 4) 3 and Li 1.8Cr 1.2(MoO 4) 3 were grown by a flux method during the phase study of the Li 2MoO 4-Cr 2(MoO 4) 3 system at 1023 K. LiCr(MoO 4) 2 and Li 3Cr(MoO 4) 3 single phases were synthesized by solid-state reactions. Li 3Cr(MoO 4) 3 adopts the same structure type as Li 3In(MoO 4) 3 despite the difference in ionic radii of Cr 3+ and In 3+ for octahedral coordination. Li 3Cr(MoO 4) 3 is paramagnetic down to 7 K and shows a weak ferromagnetic component below this temperature. LiCr(MoO 4) 2 is isostructural with LiAl(MoO 4) 2 and orders antiferromagnetically below 20 K. The magnetic structure of LiCr(MoO 4) 2 was determined from low-temperature neutron diffraction and is based on the propagation vektor k⇒=({1}/{2},{1}/{2},0). The ordered magnetic moments were refined to 2.3(1) μ B per Cr-ion with an easy axis close to the [1 1 1¯] direction. A magnetic moment of 4.37(3) μ B per Cr-ion was calculated from the Curie constant for the paramagnetic region. The crystal structures of the hitherto unknown Li 1.8Cr 1.2(MoO 4) 3 and LiCr(MoO 4) 2 are compared and reveal a high degree of similarity: In both structures MoO 4-tetrahedra are isolated from each other and connected with CrO 6 and LiO 5 via corners. In both modifications there are Cr 2O 10 fragments of edge-sharing CrO 6-octahedra.

  15. Üliõpilasesindajad võtsid vastu resolutsiooni välistudengite kaitseks / Sandra Saar

    Index Scriptorium Estoniae

    Saar, Sandra

    2016-01-01

    Eesti Üliõpilaskondade Liidu eestvedamisel toimunud Balti- ja Põhjamaade üliõpilaste kohtumisest, kus võeti vastu otsus äärmuste osas kelle tegevuse tõttu on ohustatud rahvusvaheliste üliõpilaste heaolu

  16. Nanoshell Encapsulated Li-ion Battery Anodes for Long Cycle Life Project

    Data.gov (United States)

    National Aeronautics and Space Administration — A new high capacity rechargeable Li battery anode based on Li metal alloys protected by carbon nanoshells will be developed. A reversible Li-ion capacity exceeding...

  17. Fast neutron measurements with 7Li and 6Li enriched CLYC scintillators

    Science.gov (United States)

    Giaz, A.; Blasi, N.; Boiano, C.; Brambilla, S.; Camera, F.; Cattadori, C.; Ceruti, S.; Gramegna, F.; Marchi, T.; Mattei, I.; Mentana, A.; Million, B.; Pellegri, L.; Rebai, M.; Riboldi, S.; Salamida, F.; Tardocchi, M.

    2016-07-01

    The recently developed Cs2LiYCl6:Ce (CLYC) crystals are interesting scintillation detectors not only for their gamma energy resolution (<5% at 662 keV) but also for their capability to identify and measure the energy of both gamma rays and fast/thermal neutrons. The thermal neutrons were detected by the 6Li(n,α)t reaction while for the fast neutrons the 35Cl(n,p)35S and 35Cl(n,α)32P neutron-capture reactions were exploited. The energy of the outgoing proton or α particle scales linearly with the incident neutron energy. The kinetic energy of the fast neutrons can be measured using both the Time Of Flight (TOF) technique and using the CLYC energy signal. In this work, the response to monochromatic fast neutrons (1.9-3.8 MeV) of two CLYC 1″×1″ crystals was measured using both the TOF and the energy signal. The observables were combined to identify fast neutrons, to subtract the thermal neutron background and to identify different fast neutron-capture reactions on 35Cl, in other words to understand if the detected particle is an α or a proton. We performed a dedicated measurement at the CN accelerator facility of the INFN Legnaro National Laboratories (Italy), where the fast neutrons were produced by impinging a proton beam (4.5, 5.0 and 5.5 MeV) on a 7LiF target. We tested a CLYC detector 6Li-enriched at about 95%, which is ideal for thermal neutron measurements, in parallel with another CLYC detector 7Li-enriched at more than 99%, which is suitable for fast neutron measurements.

  18. Fast neutron measurements with {sup 7}Li and {sup 6}Li enriched CLYC scintillators

    Energy Technology Data Exchange (ETDEWEB)

    Giaz, A., E-mail: agnese.giaz@mi.infn.it [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Blasi, N.; Boiano, C.; Brambilla, S. [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Camera, F. [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Università degli Studi di Milano, Physics Department, Via Celoria 16, 20133 Milano (Italy); Cattadori, C. [INFN sezione di Milano Bicocca, Piazza della Scienza 3, 20125 Milano (Italy); Ceruti, S. [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Università degli Studi di Milano, Physics Department, Via Celoria 16, 20133 Milano (Italy); Gramegna, F.; Marchi, T. [INFN Laboratori Nazionali di Legnaro, Viale dell’Università, 2, 35020 Legnaro, PD (Italy); Mattei, I. [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Mentana, A. [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Università degli Studi di Milano, Physics Department, Via Celoria 16, 20133 Milano (Italy); Million, B.; Pellegri, L. [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Rebai, M. [Università degli Studi di Milano Bicocca, Physics Department, Piazza della Scienza 3, 20126 Milano (Italy); Riboldi, S. [INFN Milano, Via Celoria 16, 20133 Milano (Italy); Università degli Studi di Milano, Physics Department, Via Celoria 16, 20133 Milano (Italy); Salamida, F. [INFN sezione di Milano Bicocca, Piazza della Scienza 3, 20125 Milano (Italy); Tardocchi, M. [Istituto di Fisica del Plasma, Associazione EURATOM-ENEA-CNR, Via R. Cozzi 53, 2015 Milano (Italy)

    2016-07-21

    The recently developed Cs{sub 2}LiYCl{sub 6}:Ce (CLYC) crystals are interesting scintillation detectors not only for their gamma energy resolution (<5% at 662 keV) but also for their capability to identify and measure the energy of both gamma rays and fast/thermal neutrons. The thermal neutrons were detected by the {sup 6}Li(n,α)t reaction while for the fast neutrons the {sup 35}Cl(n,p){sup 35}S and {sup 35}Cl(n,α){sup 32}P neutron-capture reactions were exploited. The energy of the outgoing proton or α particle scales linearly with the incident neutron energy. The kinetic energy of the fast neutrons can be measured using both the Time Of Flight (TOF) technique and using the CLYC energy signal. In this work, the response to monochromatic fast neutrons (1.9–3.8 MeV) of two CLYC 1″×1″ crystals was measured using both the TOF and the energy signal. The observables were combined to identify fast neutrons, to subtract the thermal neutron background and to identify different fast neutron-capture reactions on {sup 35}Cl, in other words to understand if the detected particle is an α or a proton. We performed a dedicated measurement at the CN accelerator facility of the INFN Legnaro National Laboratories (Italy), where the fast neutrons were produced by impinging a proton beam (4.5, 5.0 and 5.5 MeV) on a {sup 7}LiF target. We tested a CLYC detector {sup 6}Li-enriched at about 95%, which is ideal for thermal neutron measurements, in parallel with another CLYC detector {sup 7}Li-enriched at more than 99%, which is suitable for fast neutron measurements.

  19. Density functional theory study of lithium diffusion at the interface between olivine-type LiFePO4 and LiMnPO4

    Science.gov (United States)

    Shi, Jianjian; Wang, Zhiguo; Qing Fu, Yong

    2016-12-01

    Coating LiMnPO4 with a thin layer of LiFePO4 shows a better electrochemical performance than the pure LiFePO4 and LiMnPO4, thus it is critical to understand Li diffusion at their interfaces to improve the performance of electrode materials. Li diffusion at the (1 0 0)\\text{LiFeP{{\\text{O}}4}} //(1 0 0)\\text{LiMnP{{\\text{O}}4}} , (0 1 0)\\text{LiFeP{{\\text{O}}4}} //(0 1 0)\\text{LiMnP{{\\text{O}}4}} , and (0 0 1)\\text{LiFeP{{\\text{O}}4}} //(0 0 1)\\text{LiMnP{{\\text{O}}4}} interfaces between LiFePO4 and LiMnPO4 was investigated using density functional theory. The calculated diffusion energy barriers are 0.55 eV for Li to diffuse along the (0 0 1) interface, 0.44 and 0.49 eV for the Li diffusion inside the LiMnPO4 and along the (1 0 0) interface, respectively. When Li diffuses from the LiFePO4 to LiMnPO4 by passing through the (0 1 0) interfaces, the diffusion barriers are 0.45 and 0.60 eV for the Li diffusions in both sides. The diffusion barriers for Li to diffuse in LiMnPO4 near the interfaces decrease compared with those in the pure LiMnPO4. The calculated diffusion coefficient of Li along the (1 0 0) interface is in the range of 3.65  ×  10-11-5.28  ×  10-12 cm2 s-1, which is larger than that in the pure LiMnPO4 with a value of 7.5  ×  10-14 cm2 s-1. Therefore, the charging/discharging rate performance of the LiMnPO4 can be improved by surface coating with the LiFePO4.

  20. Li3PO4-added garnet-type Li6.5La3Zr1.5Ta0.5O12 for Li-dendrite suppression

    Science.gov (United States)

    Xu, Biyi; Li, Wenlong; Duan, Huanan; Wang, Haojing; Guo, Yiping; Li, Hua; Liu, Hezhou

    2017-06-01

    This paper proposes a strategy to stabilize the garnet/Li interface by introducing Li3PO4 as an additive in garnet-type Li6.5La3Zr1.5Ta0.5O12. The Li3PO4-added Li6.5La3Zr1.5Ta0.5O12 electrolyte exhibits a room-temperature Li-ion conductivity of 1.4 × 10-4 S cm-1, which is less than that of the Li3PO4-free counterparts (4.6 × 10-4 S cm-1). However, the presence of Li3PO4 improves the interfacial compatibility and suppresses Li-dendrite formation during Li-metal plating/stripping. The symmetric Li/garnet/Li cells with Li3PO4-added Li6.5La3Zr1.5Ta0.5O12 have been successfully cycled at a current density of 0.1 mA cm-2 at 60 °C for 60 h; on contrast, the control cells with Li3PO4-free Li6.5La3Zr1.5Ta0.5O12 display noisy potential with large voltage polarization and get short-circuited completely after 33-h cycling under the same operating condition. The outstanding interface stability can be attributed to the in situ reaction of the Li flux with Li3PO4 to form a self-limiting and ion-conducting interphase, Li3P, which is confirmed experimentally.

  1. Computational modeling of Li-ion batteries

    Science.gov (United States)

    Grazioli, D.; Magri, M.; Salvadori, A.

    2016-08-01

    This review focuses on energy storage materials modeling, with particular emphasis on Li-ion batteries. Theoretical and computational analyses not only provide a better understanding of the intimate behavior of actual batteries under operational and extreme conditions, but they may tailor new materials and shape new architectures in a complementary way to experimental approaches. Modeling can therefore play a very valuable role in the design and lifetime prediction of energy storage materials and devices. Batteries are inherently multi-scale, in space and time. The macro-structural characteristic lengths (the thickness of a single cell, for instance) are order of magnitudes larger than the particles that form the microstructure of the porous electrodes, which in turn are scale-separated from interface layers at which atomistic intercalations occur. Multi-physics modeling concepts, methodologies, and simulations at different scales, as well as scale transition strategies proposed in the recent literature are here revised. Finally, computational challenges toward the next generation of Li-ion batteries are discussed.

  2. Spectroscopy of Lambda-9Li by electroproduction

    CERN Document Server

    Urciuoli, G M; Marrone, S; Acha, A; Ambrozewicz, P; Aniol, K A; Baturin, P; Bertin, P Y; Benaoum, H; Blomqvist, K I; Boeglin, W U; Breuer, H; Brindza, P; Bydzovsky, P; Camsonne, A; Chang, C C; Chen, J -P; Choi, Seonho; Chudakov, E A; Cisbani, E; Colilli, S; Coman, L; Craver, B J; De Cataldo, G; de Jager, C W; De Leo, R; Deur, A P; Ferdi, C; Feuerbach, R J; Folts, E; Fratoni, R; Frullani, S; Garibaldi, F; Gayou, O; Giuliani, F; Gomez, J; Gricia, M; Hansen, J O; Hayes, D; Higinbotham, D W; Holmstrom, T K; Hyde, C E; Ibrahim, H F; Iodice, M; Jiang, X; Kaufman, L J; Kino, K; Kross, B; Lagamba, L; LeRose, J J; Lindgren, R A; Lucentini, M; Margaziotis, D J; Markowitz, P; Meziani, Z E; McCormick, K; Michaels, R W; Millener, D J; Miyoshi, T; Moffit, B; Monaghan, P A; Moteabbed, M; Camacho, C Munoz; Nanda, S; Nappi, E; Nelyubin, V V; Norum, B E; Okasyasu, Y; Paschke, K D; Perdrisat, C F; Piasetzky, E; Punjabi, V A; Qiang, Y; Reimer, P E; Reinhold, J; Reitz, B; Roche, R E; Rodriguez, V M; Saha, A; Santavenere, F; Sarty, A J; Segal, J; Shahinyan, A; Singh, J; Sirca, S; Snyder, R; Solvignon, P H; Sotona, M; Subedi, R; Sulkosky, V A; Suzuki, T; Ueno, H; Ulmer, P E; Veneroni, P; Voutier, E; Wojtsekhowski, B B; Zheng, X; Zorn, C

    2014-01-01

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

  3. Electrocatalysis in Li-S batteries

    Science.gov (United States)

    Al salem, Hesham I. A.

    Stabilizing polysulfide-shuttle process while ensuring high sulfur loading holds the key to realize high theoretical energy density (2500 Wh/kg) of lithium-sulfur (Li-S) batteries. Though several carbon based porous materials have been used as host structures for sulfur and its intermediate polysulfides, the week adsorption of polysulfides on carbon surface and its poor reaction kinetics limits them from practical application. Here, we preset a novel electcatalysis approach to stabilize polysulfide shuttle process and also enhance its red-ox kinetics. As a proof of concept, we have studied in-detail using conventional electrocatalyst (Pt/graphene composite), further the same extended to cost-effective electrocatalysts such as WS2 nanosheets and Metal carbides for viable practical applications. Nature of electrocatalyst, concentration of polysulfides and temperature of the cell on electrochemical properties will be discussed. We reveal substantial improvement in electrochemical properties such as specific capacity, rate capability, and coulombic efficiency and corroborate our findings with systematic experimental studies. Interaction between electrocatalyst and polysulfides has been evaluated by conducting X-ray photoelectron spectroscopy and electron microscopy studies at various electrochemical conditions. As a conclusion, introducing a catalyst in the Li-S system will open a new avenue for improving electrochemical performance.

  4. Computational modeling of Li-ion batteries

    Science.gov (United States)

    Grazioli, D.; Magri, M.; Salvadori, A.

    2016-12-01

    This review focuses on energy storage materials modeling, with particular emphasis on Li-ion batteries. Theoretical and computational analyses not only provide a better understanding of the intimate behavior of actual batteries under operational and extreme conditions, but they may tailor new materials and shape new architectures in a complementary way to experimental approaches. Modeling can therefore play a very valuable role in the design and lifetime prediction of energy storage materials and devices. Batteries are inherently multi-scale, in space and time. The macro-structural characteristic lengths (the thickness of a single cell, for instance) are order of magnitudes larger than the particles that form the microstructure of the porous electrodes, which in turn are scale-separated from interface layers at which atomistic intercalations occur. Multi-physics modeling concepts, methodologies, and simulations at different scales, as well as scale transition strategies proposed in the recent literature are here revised. Finally, computational challenges toward the next generation of Li-ion batteries are discussed.

  5. LiCHy: The CAF’s LiDAR, CCD and Hyperspectral Integrated Airborne Observation System

    Directory of Open Access Journals (Sweden)

    Yong Pang

    2016-05-01

    Full Text Available We describe the design, implementation and performance of a novel airborne system, which integrates commercial waveform LiDAR, CCD (Charge-Coupled Device camera and hyperspectral sensors into a common platform system. CAF’s (The Chinese Academy of Forestry LiCHy (LiDAR, CCD and Hyperspectral Airborne Observation System is a unique system that permits simultaneous measurements of vegetation vertical structure, horizontal pattern, and foliar spectra from different view angles at very high spatial resolution (~1 m on a wide range of airborne platforms. The horizontal geo-location accuracy of LiDAR and CCD is about 0.5 m, with LiDAR vertical resolution and accuracy 0.15 m and 0.3 m, respectively. The geo-location accuracy of hyperspectral image is within 2 pixels for nadir view observations and 5–7 pixels for large off-nadir observations of 55° with multi-angle modular when comparing to LiDAR product. The complementary nature of LiCHy’s sensors makes it an effective and comprehensive system for forest inventory, change detection, biodiversity monitoring, carbon accounting and ecosystem service evaluation. The LiCHy system has acquired more than 8000 km2 of data over typical forests across China. These data are being used to investigate potential LiDAR and optical remote sensing applications in forest management, forest carbon accounting, biodiversity evaluation, and to aid in the development of similar satellite configurations. This paper describes the integration of the LiCHy system, the instrument performance and data processing workflow. We also demonstrate LiCHy’s data characteristics, current coverage, and potential vegetation applications.

  6. 2006 OSIP OGRIP: Upland Counties LiDAR Survey

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The 2006 OSIP digital LiDAR data was collected during the months of March and May (leaf-off conditions). The LiDAR covers the entire land area of the northern tier...

  7. Review on Li Shiqiao’s Understanding the Chinese City

    Institute of Scientific and Technical Information of China (English)

    Martijn; de; Geus

    2015-01-01

    Understanding the Chinese City Author:Li Shiqiao Year:2014Publisher:SAGE Publications Ltd.ISBN:978-1466208830(264 pages,in English)1.Introduction Li Shiqiao’s latest book,Understanding the Chinese City,tries to create a conceptual framework for understanding the Chinese city that captures its contemporary hypermodernity and its

  8. NASA/GSFC Testing of Li-Ion Cells: Update

    Science.gov (United States)

    Vaidyanathan, Hari; Rao, Gopalakrishna M.

    2001-01-01

    This viewgraph paper presents a report on the ongoing testing of Lithium Ion (Li-Ion) cells. Characterizes cells according to capacity, self-discharge, and mid-discharge voltage. Determines the cycling performance of Li-Ion cells as batteries according to number of cycles, charge voltage, and temperature.

  9. President Li Xiaolin Meets with Apple Vice-President Jackson

    Institute of Scientific and Technical Information of China (English)

    Jiang; Yingshan

    2016-01-01

    On April 26,2016,CPAFFC President Li Xiaolin met with VicePresident Lisa Jackson of Apple Inc.She briefed Jackson on the CPAFFC’s history and major projects,including the China-US Governors Forum.Li also stressed that both China and the United States should enhance cooperation based on mutual trust.She hoped

  10. Oxygen Luminescence Centers in LiF-MeO Crystals

    Science.gov (United States)

    Lisitsyna, L. A.; Suleimen, R. N.

    2017-08-01

    Spectral-kinetic parameters of luminescence of LiF crystals doped with various polyvalent metal oxides (Li, Ti, Fe, W, U) were studied in the temperature range of 100-300 K and the absorbed doses range of 0-105 Gy. A model for describing polyvalent activation cation role in the processes of radiation energy dissipation in the crystal volume is suggested.

  11. NUCLEON POLARIZATION IN 3-BODY MODELS OF POLARIZED LI-6

    NARCIS (Netherlands)

    SCHELLINGERHOUT, NW; KOK, LP; COON, SA; ADAM, RM

    1993-01-01

    Just as He-3 --> can be approximately characterized as a polarized neutron target, polarized Li-6D has been advocated as a good isoscalar nuclear target for the extraction of the polarized gluon content of the nucleon. The original argument rests upon a presumed ''alpha + deuteron'' picture of Li-6,

  12. NUCLEON POLARIZATION IN 3-BODY MODELS OF POLARIZED LI-6

    NARCIS (Netherlands)

    SCHELLINGERHOUT, NW; KOK, LP; COON, SA; ADAM, RM

    1993-01-01

    Just as He-3 --> can be approximately characterized as a polarized neutron target, polarized Li-6D has been advocated as a good isoscalar nuclear target for the extraction of the polarized gluon content of the nucleon. The original argument rests upon a presumed ''alpha + deuteron'' picture of Li-6,

  13. Üliõpilasteater sõidab Belgiasse

    Index Scriptorium Estoniae

    2008-01-01

    Tartu Üliõpilasteater on Eugene Ionesco "Ninasarvikuga" (lavastaja Kalev Kudu) Belgias festivalil. Festivali korraldab Liege'i Kuninglik Ülikool ja sellest saab alguse Tartu Üliõplasteatri ja Liege'i Kuningliku Ülikooli teatri kolmeaastane koostööprojekt, mida rahastavad peamiselt mõlema riigi kultuuriministeeriumid

  14. THE STRUCTURE OF LIQUID LI-SI ALLOYS

    NARCIS (Netherlands)

    DEJONG, PHK; VERKERK, P; VANDERLUGT, W; DEGRAAF, LA

    1993-01-01

    The reverse Monte Carlo method is used to analyse neutron diffraction data on liquid Li65Si35. A well defined Si-Si partial pair correlation function is obtained with strong indications for covalent Si-Si bonds. It is also clear that most of the Si4 stars and Si5 rings occurring in solid Li12Si7 hav

  15. ELECTRONIC-STRUCTURE OF LI-DOPED NIO

    NARCIS (Netherlands)

    VANELP, J; ESKES, H; KUIPER, P; SAWATZKY, GA

    1992-01-01

    The electronic structure of Li(x)Ni1-xO has been investigated using x-ray photoemission spectroscopy (XPS), bremsstrahlung isochromat spectroscopy (BIS), and model-Hamiltonian cluster calculations. The measurements support the conclusion that the Li-doped holes have mainly oxygen character. The

  16. Nanostructured Materials for Li-Ion Batteries and Beyond

    Directory of Open Access Journals (Sweden)

    Xifei Li

    2016-04-01

    Full Text Available This Special Issue “Nanostructured Materials for Li-Ion Batteries and Beyond” of Nanomaterials is focused on advancements in the synthesis, optimization, and characterization of nanostructured materials, with an emphasis on the application of nanomaterials for building high performance Li-ion batteries (LIBs and future systems.[...

  17. "Fish-Scale" Boy——Li Junwei in Beijing

    Institute of Scientific and Technical Information of China (English)

    1994-01-01

    AFTER a long struggle with the rare disease, ichthy-erythroderma, 12-year-old Li Junwei was eventually able to go to school. This has been his desire for years. Li was born in Gaoxiong City in Taiwan. Since infancy he has been

  18. A Low-Li Geochemical Province in the NE Atlantic

    DEFF Research Database (Denmark)

    Bailey, J. C.; Gwozdz, R.

    1978-01-01

    Lithium was analysed in 392 basalts and related igneous rocks from the North Atlantic Tertiary-Recent province using activation analysis and Čerenkov counting. Monotonous Li values of 5.5±2 ppm in NE Atlantic basalts define a low-Li geochemical province which has persisted for 60 million years...

  19. Understanding oxygen reactions in aprotic Li-O2 batteries

    Science.gov (United States)

    Shunchao, Ma; Yelong, Zhang; Qinghua, Cui; Jing, Zhao; Zhangquan, Peng

    2016-01-01

    Although significant progress has been made in many aspects of the emerging aprotic Li-O2 battery system, an in-depth understanding of the oxygen reactions is still underway. The oxygen reactions occurring in the positive electrode distinguish Li-O2 batteries from the conventional Li-ion cells and play a crucial role in the Li-O2 cell’s performance (capacity, rate capability, and cycle life). Recent advances in fundamental studies of oxygen reactions in aprotic Li-O2 batteries are reviewed, including the reaction route, kinetics, morphological evolution of Li2O2, and charge transport within Li2O2. Prospects are also provided for future fundamental investigations of Li-O2 chemistry. Project supported by the Recruitment Program of Global Youth Experts of China, the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDA09010401), the Science and Technology Development Program of Jilin Province, China (Grant No. 20150623002TC), and the Natural Science Foundation of Jiangsu Province, China (Grant No. BK20131139).

  20. 2006 OSIP OGRIP: Upland Counties LiDAR Survey

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The 2006 OSIP digital LiDAR data was collected during the months of March and May (leaf-off conditions). The LiDAR covers the entire land area of the northern tier...

  1. Te/C nanocomposites for Li-Te Secondary Batteries

    National Research Council Canada - National Science Library

    Seo, Jeong-Uk; Seong, Gun-Kyu; Park, Cheol-Min

    2015-01-01

    ... (ca. 550 mA h cm(-3) at 5C rate). The mechanically reduced Te/C nanocomposite electrodes were found to be suitable for use as either the cathode in Li-Te secondary batteries or a high-potential anode in rechargeable Li-ion batteries...

  2. 2006 OSIP OGRIP Coastal Counties LiDAR Survey

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The 2006 OSIP digital LiDAR data was collected during the months of March and May (leaf-off conditions). The LiDAR covers the entire land area of the northern tier...

  3. LiDAR - An emerging tool for geological applications

    Science.gov (United States)

    Stoker, Jason M.

    2012-01-01

    Over the past five to ten years the use and applicability of light detection and ranging (LiDAR) technology has increased dramatically. As a result, more and more LiDAR data now are being collected across the country for a wide range of applications, and LiDAR currently is the technology of choice for high resolution terrain model creation, 3-D city and infrastructure modeling, forestry, and a wide range of scientific applications. LiDAR is a key technology for geological applications both within and outside the U.S. Geological Survey, and efforts are underway to try to collect high resolution LiDAR data for the entire United States (https://pubs.usgs.gov/fs/2012/3089/pdf/fs2012-3089.pdf).

  4. Reversible storage of hydrogen in destabilized LiBH4.

    Science.gov (United States)

    Vajo, John J; Skeith, Sky L; Mertens, Florian

    2005-03-10

    Destabilization of LiBH4 for reversible hydrogen storage has been studied using MgH2 as a destabilizing additive. Mechanically milled mixtures of LiBH4 + (1/2)MgH2 or LiH + (1/2)MgB2 including 2-3 mol % TiCl3 are shown to reversibly store 8-10 wt % hydrogen. Variation of the equilibrium pressure obtained from isotherms measured at 315-400 degrees C indicate that addition of MgH2 lowers the hydrogenation/dehydrogenation enthalpy by 25 kJ/(mol of H2) compared with pure LiBH4. Formation of MgB2 upon dehydrogenation stabilizes the dehydrogenated state and, thereby, destabilizes the LiBH4. Extrapolation of the isotherm data yields a predicted equilibrium pressure of 1 bar at approximately 225 degrees C. However, the kinetics were too slow for direct measurements at these temperatures.

  5. Four-body dynamics in 6Li elastic scattering

    CERN Document Server

    Watanabe, Shin; Ogata, Kazuyuki; Yahiro, Masanobu

    2015-01-01

    We analyze 6Li elastic scattering in a wide range of incident energies (Ein), assuming the n + p + alpha + target four-body model and solving the dynamics with the four-body version of the continuum-discretized coupled-channels method (CDCC). Four-body CDCC well reproduces the experimental data with no adjustable parameter for 6Li + 209Bi scattering at Ein = 24-50 MeV and 6Li + 208Pb scattering at Ein = 29-210 MeV. In the wide Ein range, 6Li breakup is significant and provides repulsive corrections to the folding potential. As an interesting property, d breakup is strongly suppressed in 6Li-breakup processes independently of Ein. We investigate what causes the d-breakup suppression.

  6. Preparation of Partial Spherical LiFePO4 Using Spherical Li3PO4 as Aprecursor%以球形Li3PO4制备球形LiFePO4

    Institute of Scientific and Technical Information of China (English)

    于春洋; 潘志红

    2007-01-01

    以曲拉通100作表面活性剂,用超声波法制备了球形度较好、平均粒径为10μm的球形Li3PO4.以球形Li3PO4为前驱体制备了部分球形的LiFePO4,并对其电化学性能进行了研究.由该法制备的LiFePO4振实密度为1.20 g/cm3,较其他方法制备的LiFePO4密度有所提高.

  7. The effect of vibrational entropy on the solubility and stability of ordered Al3Li phases in Al-Li alloys

    Science.gov (United States)

    Mao, Zugang; Seidman, David N.; Wolverton, C.

    2013-10-01

    The solubility and stability of three possible ordered Al3Li structures in Al-Li alloys are studied using first-principles calculations: δ'-Al3Li(L12), δ-Al3Li(DO22), and β-Al3Li(DO3). We find that δ'-Al3Li(L12) is the most stable phase and β-Al3Li(DO3) is energetically unfavorable. The vibrational formation entropy makes a significant contribution to the solubility for all three ordered Al3Li structures and yields a 1.6-fold increase in the calculated solubility of δ'-Al3Li(L12), a 1.8-fold increase for δ-Al3Li(DO22), and a 2.5-fold increase for β-Al3Li(DO3). The solubility of δ'-Al3Li(L12) is greater than those of δ-Al3Li(DO22) and β-Al3Li(DO3), and the δ'-Al3Li(L12) solvus curve is in good agreement with the experimental one.

  8. Structural characterization of slightly boron-deficient LiB, LiB0.9 and LiB0.8, under pressure.

    Science.gov (United States)

    Suarez-Alcubilla, Ainhoa; Gurtubay, Idoia G; Bergara, Aitor

    2014-11-26

    Results of computational investigations of two slightly boron-deficient lithium borides, LiB(0.9) and LiB(0.8), under pressure are reported. Structure predictions based on particle swarm optimization reveal that at low pressure both compositions adopt chain structures, as stoichiometric 1 : 1 LiB. With increasing pressure both undergo phase transitions to layered arrangements. The evolution of the structural parameters of these stoichiometries as a function of pressure and the results obtained from the enthalpies indicate that boron-deficient structures are more favoured than 1 : 1 LiB, even at zero pressure. Moreover, as pressure is increased a larger deficiency in B seems to be favoured.

  9. Fast Li ion dynamics in the solid electrolyte Li7 P3 S11 as probed by (6,7) Li NMR spin-lattice relaxation.

    Science.gov (United States)

    Wohlmuth, Dominik; Epp, Viktor; Wilkening, Martin

    2015-08-24

    The development of safe and long-lasting all-solid-state batteries with high energy density requires a thorough characterization of ion dynamics in solid electrolytes. Commonly, conductivity spectroscopy is used to study ion transport; much less frequently, however, atomic-scale methods such as nuclear magnetic resonance (NMR) are employed. Here, we studied long-range as well as short-range Li ion dynamics in the glass-ceramic Li7 P3 S11 . Li(+) diffusivity was probed by using a combination of different NMR techniques; the results are compared with those obtained from electrical conductivity measurements. Our NMR relaxometry data clearly reveal a very high Li(+) diffusivity, which is reflected in a so-called diffusion-induced (6) Li NMR spin-lattice relaxation peak showing up at temperatures as low as 313 K. At this temperature, the mean residence time between two successful Li jumps is in the order of 3×10(8) s(-1) , which corresponds to a Li(+) ion conductivity in the order of 10(-4) to 10(-3) S cm(-1) . Such a value is in perfect agreement with expectations for the crystalline but metastable glass ceramic Li7 P3 S11 . In contrast to conductivity measurements, NMR analysis reveals a range of activation energies with values ranging from 0.17 to 0.26 eV, characterizing Li diffusivity in the bulk. In our case, through-going Li ion transport, when probed by using macroscopic conductivity spectroscopy, however, seems to be influenced by blocking grain boundaries including, for example, amorphous regions surrounding the Li7 P3 S11 crystallites. As a result of this, long-range ion transport as seen by impedance spectroscopy is governed by an activation energy of approximately 0.38 eV. The findings emphasize how surface and grain boundary effects can drastically affect long-range ionic conduction. If we are to succeed in solid-state battery technology, such effects have to be brought under control by, for example, sophisticated densification or through the preparation

  10. The single-electrode Peltier heats of Li-Al alloy electrodes in LiCl-KCl eutectic system

    Energy Technology Data Exchange (ETDEWEB)

    Amezawa, Koji; Ito, Yasuhiko; Tomii, Yoichi (Kyoto Univ. (Japan))

    1994-11-01

    This paper presents the single-electrode Peltier heat of cathodic (or anodic) reaction of Li-Al alloy electrode in a coexisting phase state, or an intermetallic compound phase state estimated by thermoelectric-power measurement. The thermoelectric-power measurements of Li-Al alloys in various coexisting phase states were carried out with both potentiometric and potential-sweep methods in the LiCl-KCl eutectic system between 673 and 843 K. The values of the thermoelectric power of Li-Al alloys calculated by using thermodynamic literature data were in good agreement with those obtained by experiment. The single-electrode Peltier heat changes drastically with change of its phase state, and it was found that the formation reactions of [beta] (Li[sub 0.5]Al[sub 0.5]) and [gamma] (Li[sub 0.6]Al[sub 0.4]) phases are exothermic, and those of liquid phase from [beta] and [gamma] phase are endothermic. The single-electrode Peltier heat for the cathodic formation reaction of Li-Al alloy in intermetallic compound [gamma] phase is estimated to be exothermic by using the measured values of thermoelectric powers of Li-Al alloys in ([beta] + [gamma]) and ([gamma] + liq.) regions.

  11. 2011 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Kittitas-Colockum Study Area

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data on 6 days between September 15th and November 5th, 2010 for the Puget Sound LiDAR...

  12. Recycle and synthesis of LiCoO2 from incisors bound of Li-ion batteries

    Institute of Scientific and Technical Information of China (English)

    LIU Yun-jian; HU Qi-yang; LI Xin-hai; WANG Zhi-xing; GUO Hua-jun

    2006-01-01

    A new LiCoO2 recovery technology of Li-ion battery was studied. LiCoO2 was initially separated from the Al foil with dimethyl acetamide(DMAC), and then the polyvinylidene fluoride(PVDF) and carbon powders in the active material were eliminated by high temperature calcining. The content of the elements in the recovered powder was analyzed. The structure and morphology of the resulted samples were observed by XRD and SEM. Then the Li2CO3 was added in the recycled powder to adjust the Li/Co molar ratio to 1. The new LiCoO2 was synthesized by calcining at 850 ℃ for 12 h in air. The well-crystallized single phase LiCoO2 without Co3O4 phase was obtained. The recycle-synthesized LiCoO2 powders have good characteristics as a cathode active material in terms of charge-discharge capacity and cycling performance.

  13. Are lithium niobate (LiNbO{sub 3}) and lithium tantalate (LiTaO{sub 3}) ferroelectrics bioactive?

    Energy Technology Data Exchange (ETDEWEB)

    Vilarinho, Paula Maria, E-mail: paula.vilarinho@ua.pt; Barroca, Nathalie; Zlotnik, Sebastian; Félix, Pedro; Fernandes, Maria Helena

    2014-06-01

    The use of functional materials, such as ferroelectrics, as platforms for tissue growth in situ or ex situ, is new and holds great promise. But the usage of materials in any bioapplication requires information on biocompatibility and desirably on bioactive behavior when bone tissue engineering is envisaged. Both requirements are currently unknown for many ferroelectrics. Herein the bioactivity of LiNbO{sub 3} and LiTaO{sub 3} is reported. The formation of apatite-like structures on the surface of LiNbO{sub 3} and LiTaO{sub 3} powders after immersion in simulated body fluid (SBF) for different soaking periods indicates their bioactive potential. The mechanism of apatite formation is suggested. In addition, the significant release of lithium ions from the ferroelectric powders in the very first minutes of soaking in SBF is examined and ways to overcome this likely hurdle addressed. - Highlights: • LiNbO{sub 3} and LiTaO{sub 3} are bioactive ferroelectrics. • Cauliflower apatite type structures indicative of in-vitro bioactivity of LiNbO{sub 3} and LiTaO{sub 3.} • Negative surface charges anchor Ca{sup 2+} to which PO{sub 4}{sup 3−} attracts forming apatite structure nuclei. • Use of ferroelectrics as platforms for tissue growth in situ or ex situ is new and holds great promise.

  14. Electrochemical Performance of PEO10LiX-Li2TiO3 Composite Polymer Electrolytes

    Institute of Scientific and Technical Information of China (English)

    LU,Mi(路密); SHI,Peng-Fei(史鹏飞)

    2004-01-01

    The conductivities of polyethylene oxide (PEO)-based polymer electrolytes (PE) can be improved by the addition of inorganic inert powder. The composite polymer electrolytes (CPE) PEO10LiX (X= or )-Li2TiO3 were prepared by solution casting with inorganic solid electrolyte Li2TiO3 powder as a filler. Results showed that the conductivities of PEO10LiClO4-3wt% Li2TiO3 and PEO10LiN(CF3SO2)2-10wt% Li2TiO3 at 30 ℃ were 8.6×10-6 and 5.6×10-5 S·cm-1, respectively. The conductivities of CPE increased with the decrease of filler's particle size. The ionic conduction mechanism analysis showed that there may be three conduction routes in the CPE, i.e., PEO bulk, polymer-filler interface and Li2TiO3 crystal.

  15. Direct view on the phase evolution in individual LiFePO4 nanoparticles during Li-ion battery cycling

    NARCIS (Netherlands)

    Zhang, X.; Van Hulzen, M.; Singh, D.P.; Brownrigg, A.W.; Wright, J.P.; Van Dijk, N.H.; Wagemaker, M.

    2015-01-01

    Phase transitions in Li-ion electrode materials during (dis)charge are decisive for battery performance, limiting high-rate capabilities and playing a crucial role in the cycle life of Li-ion batteries. However, the difficulty to probe the phase nucleation and growth in individual grains is hinderin

  16. A miscibility gap in LiF-BeF₂ and LiF-BeF₂-ThF₄

    NARCIS (Netherlands)

    Meer, J.P.M. van der; Konings, R.J.M.; Jacobs, M.H.G.; Oonk, H.A.J.

    2005-01-01

    LiF BeF₂ and LiF BeF₂ ThF₄ are key systems for Molten Salt Reactor fuel. The liquid phase of these systems has been assessed using Redlich Kister polynomials. The result shows a miscibility gap on the BeF₂-rich side. This has never been proven experimentally. Nevertheless, evidence for a two liquids

  17. Experimental and computational studies on structural transitions in the LiBH4-LiI pseudobinary system

    DEFF Research Database (Denmark)

    Oguchi, H.; Matsuo, M.; Hummelshøj, Jens Strabo

    2009-01-01

    Structural transition properties of the LiBH4+xLiI (x=0–1.00) pseudobinary system were examined by powder x-ray diffraction and differential scanning calorimetry combined with periodic density functional theory calculations. We experimentally and computationally confirmed the stabilization...

  18. Optical waveguides in LiNbO3 and stoichiometric LiNbO3 crystals by proton exchange

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The formation of optical planar waveguides in LiNbO3 and stoichiometric LiNbO3 crystals by proton exchange was reported. The prism-coupling method was used to characterize the dark-line spectroscopy at the wavelength of 633 and 1539 nm, re-spectively. The mode optical near-field outputs from proton-exchanged LiNbO3 and SLN waveguides at 633 nm were presented. The mode field from stoichiometric LiNbO3 (SLN) waveguide is lighter and more uniform than that from LiNbO3 waveguide, which means the quality of the waveguide in SLN crystal is better than that of the LiNbO3 waveguide. For proton-exchanged LiNbO3 waveguides, the evo-lution of the refractive index profile with annealing was presented. The disorder profiles of Nb atoms in proton-exchanged LiNbO3 waveguides were obtained by Rutherford backscattering/channeling technique. It is shown that the longer the exchange time, the larger the displacement of Nb atoms.

  19. Mössbauer spectra as a “fingerprint” in tin lithium compounds: Applications to Li-ion batteries

    Science.gov (United States)

    Robert, F.; Lippens, P. E.; Olivier-Fourcade, J.; Jumas, J.-C.; Gillot, F.; Morcrette, M.; Tarascon, J.-M.

    2007-01-01

    Several Li-Sn crystalline phases, i.e. Li 2Sn 5, LiSn, Li 7Sn 3, Li 5Sn 2, Li 13Sn 5, Li 7Sn 2 and Li 22Sn 5 were prepared by ball-milling and characterized by X-ray powder diffraction and 119Sn Mössbauer spectroscopy. The analysis of the Mössbauer hyperfine parameters, i.e. isomer shift ( δ) and quadrupole splitting ( Δ), made it possible to define two types of Li-Sn compounds: the Sn-richest compounds (Li 2Sn 5, LiSn) and the Li-richest compounds (Li 7Sn 3, Li 5Sn 2, Li 13Sn 5, Li 7Sn 2, Li 22Sn 5). The isomer shift values ranged from 2.56 to 2.38 mm s -1 for Li 2Sn 5, LiSn and from 2.07 to 1.83 mm s -1 for Li 7Sn 3, Li 5Sn 2, Li 13Sn 5, Li 7Sn 2 and Li 22Sn 5, respectively. A Δ- δ correlation diagram is introduced in order to identify the different phases observed during the electrochemical process of new Sn-based materials. This approach is illustrated by the identification of the phases obtained at the end of the first discharge of η-Cu 6Sn 5 and SnB 0.6P 0.4O 2.9.

  20. Li vaporization property of two-phase material of Li{sub 2}TiO{sub 3} and Li{sub 2}SiO{sub 3} for tritium breeder

    Energy Technology Data Exchange (ETDEWEB)

    Ogawa, Seiya [Course of Mechanical Engineering, Graduate School of Engineering, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Masuko, Yuki; Kato, Hirokazu; Yuyama, Hayato; Sakai, Yutaro [Department of Prime Mover Engineering, School of Engineering, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Niwa, Eiki; Hashimoto, Takuya [Department of Physics, College of Humanities and Sciences, Nihon University, 3-8-1 Sakurajousui, Setagaya-ku, Tokyo 156-8550 (Japan); Mukai, Keisuke [Department of Nuclear Engineering and Management, School of Engineering, The University of Tokyo, 7-3-1 Bunkyo-ku, Tokyo 113-8656 (Japan); Hosino, Tsuyoshi [Breeding Functional Materials Development Group, Department of Blanket Systems Research, Rokkasho Fusion Institute, Sector of Fusion Research and Development, Japan Atomic Energy Agency, 2-166 Obuch, Omotedate, Rokkasho-mura, Kamikita-gun, Aomori 039-3212 (Japan); Sasaki, Kazuya, E-mail: k_sasaki@tokai-u.jp [Course of Mechanical Engineering, Graduate School of Engineering, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Department of Prime Mover Engineering, School of Engineering, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan); Course of Mechanical Engineering and Aeronautics and Astronautics, Graduate School of Science and Technology, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292 (Japan)

    2015-10-15

    Highlights: • We synthesized two phase materials based on Li{sub 2}SiO{sub 3} and Li{sub 2}TiO{sub 3}. • We investigated the Li vaporization property of the two-phase materials. • Li vaporization occurs significantly from only Li{sub 2}SiO{sub 3} grains in the vicinity of the surface of the pellets. • The Li vaporization is remarkable only for an early short time for the vaporization from Li{sub 2}SiO{sub 3} grains at the vicinity of the surface. • The second stable phase added functions effectively for inhibition of the Li vaporization. - Abstract: Li vaporization property of two-phase materials of Li{sub 2}TiO{sub 3} and Li{sub 2}SiO{sub 3} in a working condition for the solid tritium breeder used in the demonstration power plant of fusion reactor was investigated, and the suppression mechanism of the vaporization was considered. The Li vaporization rate from the specimen pellet was measured by gravimetric method, and the change of Li concentration distribution in the pellet was analyzed by time-of-flight secondary ion mass spectrometer. Li was vaporized only from the Li{sub 2}SiO{sub 3} at the vicinity of the surface of the pellet. The remarkable vaporization of Li arose only in an early short time. The inhibition of the vaporization from the Li{sub 2}SiO{sub 3} was successful by adding the small amount of the stable secondary phase of Li{sub 2}TiO{sub 3}.

  1. Improving rate performance of LiFePO{sub 4} cathode materials by hybrid coating of nano-Li{sub 3}PO{sub 4} and carbon

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Shi-Xi, E-mail: zhaosx@sz.tsinghua.edu.cn [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Ding, Hao; Wang, Yan-Chao [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Li, Bao-Hua [Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Nan, Ce-Wen [School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2013-07-25

    Highlights: •This paper reports an improved solid-state method which leads to a uniform coating. The influence of Li{sub 3}PO{sub 4} and carbon coating on the electrochemical performance of LiFePO{sub 4} was studied. •LiFePO{sub 4} coating with Li{sub 3}PO{sub 4} and carbon shows a higher capacity than pure carbon coating sample. •Results indicate that the surface structure has an important influence on the electrochemical performance of LiFePO{sub 4}. The addition of Li{sub 3}PO{sub 4} can decrease the interfacial resistance of Li FePO{sub 4}. -- Abstract: Li{sub 3}PO{sub 4} coating on the surface of LiFePO{sub 4} particles was prepared by direct dispersing LiFePO{sub 4} precursor in starch slurry with nano-Li{sub 3}PO{sub 4}. The existence of nano-Li{sub 3}PO{sub 4} was confirmed with X-ray powder diffraction (XRD). And the particle size and morphology were observed by scanning electron microscope (SEM) and transmission electron microscope analysis (TEM). The effects of the mixture coating on rate performance of LiFePO{sub 4} cathode vs Li anode at 25 °C was investigated. Li{sub 3}PO{sub 4} and carbon mixing coated LiFePO{sub 4} cathode materials exhibited markedly improved rate capability relative to bare carbon-coated LiFePO{sub 4}. Analyses on cell impedance showed that the Li{sub 3}PO{sub 4} coating decreased the interfacial impedance. Transmission electron microscope analysis, electrochemical impedance spectroscopy (EIS) and cyclic voltammograms (CV) were carried out to explain the reason of better rate performance by Li{sub 3}PO{sub 4} coating.

  2. High precision measurement of the 11Li and 9Li quadrupole moment ratio using zero-field β-NQR

    Science.gov (United States)

    Voss, A.; Pearson, M. R.; Buchinger, F.; Crawford, J. E.; Kiefl, R. F.; Levy, C. D. P.; MacFarlane, W. A.; Mané, E.; Morris, G. D.; Shelbaya, O. T. J.; Song, Q.; Wang, D.

    2014-01-01

    The ratio of electric quadrupole moments of 11Li and 9Li was measured using the zero-field β-detected nuclear quadrupole resonance technique at Triumf-Isac. The precision on the ratio Q11/Q9 = 1.0775(12) was improved by more than one order of magnitude and an absolute value for the quadrupole moment of 11Li was inferred. Systematic effects, as argued here, are not expected to contribute to the ratio on this scale. The zero-field spin-lattice relaxation time for 8Li implanted within SrTiO3 at 295 K in zero-field was found to be T1 = 1.73(2) s. A comparison of the quadrupole moments of 9, 11Li and their ratio is made with the latest models, however, no conclusion may yet be drawn owing to the size of the theoretical uncertainties.

  3. Lamb shifts and hyperfine structure in 6Li+ and 7Li+: Theory and experiment

    DEFF Research Database (Denmark)

    Riis, E.; Sinclair, A. G.; Poulsen, Ove;

    1994-01-01

    High-precision laser-resonance measurements accurate to +/-0.5 MHz, or better are reported for transitions among the 1s2s S-3(1)-1s2p P-3(J) hyperfine manifolds for each of J = 0, 1, and 2 in both Li-6(+) and Li-7(+). A detailed analysis of hyperfine structure is performed for both the S and P...... states, using newly calculated values for the magnetic dipole and electric quadrupole coupling constants, and the hyperfine shifts subtracted from the measurements. The resulting transition frequencies are then analysed on three different levels. First, the isotope shifts in the fine-structure splittings....... The accuracy of 11 parts per million is the best two-electron Lamb shift measurement in the literature, and is comparable to the accuracies achieved in hydrogen. Theoretical contributions to the two-electron Lamb shift are discussed, including terms of order (alpha Z)(4) recently obtained by Chen, Cheng...

  4. Triple α resonances in the 6Li + 6Li → 3α reaction at low energy

    Directory of Open Access Journals (Sweden)

    A. Tumino

    2015-11-01

    Full Text Available The 6Li + 6Li → 3α reaction has been measured in a kinematically complete experiment at 3.1 MeV of beam energy. The reaction mainly proceeds via intermediate 8Be states. The interaction between any two of the three α particles provides events with one, two or three 8Be interfering levels, with strong enhancement in the α–α coincidence yield. Evidence of three 8Be levels within the same 3α event suggests that one α particle is exchanged between the other two. This is a condition for Efimov states to occur in nuclei, for which no observation exists yet. The hyperspherical formalism for the low-energy three-body problem has been applied to point out the 3α particle correlation.

  5. Storage and Effective Migration of Li-Ion for Defected β-LiFePO4 Phase Nanocrystals.

    Science.gov (United States)

    Guo, Hua; Song, Xiaohe; Zhuo, Zengqing; Hu, Jiangtao; Liu, Tongchao; Duan, Yandong; Zheng, Jiaxin; Chen, Zonghai; Yang, Wanli; Amine, Khalil; Pan, Feng

    2016-01-13

    Lithium iron phosphate, a widely used cathode material, crystallizes typically in olivine-type phase, α-LiFePO4 (αLFP). However, the new phase β-LiFePO4 (βLFP), which can be transformed from αLFP under high temperature and pressure, is originally almost electrochemically inactive with no capacity for Li-ion battery, because the Li-ions are stored in the tetrahedral [LiO4] with very high activation barrier for migration and the one-dimensional (1D) migration channels for Li-ion diffusion in αLFP disappear, while the Fe ions in the β-phase are oriented similar to the 1D arrangement instead. In this work, using experimental studies combined with density functional theory calculations, we demonstrate that βLFP can be activated with creation of effective paths of Li-ion migration by optimized disordering. Thus, the new phase of βLFP cathode achieved a capacity of 128 mAh g(-1) at a rate of 0.1 C (1C = 170 mA g(-1)) with extraordinary cycling performance that 94.5% of the initial capacity retains after 1000 cycles at 1 C. The activation mechanism can be attributed to that the induced disorder (such as FeLiLiFe antisite defects, crystal distortion, and amorphous domains) creates new lithium migration passages, which free the captive stored lithium atoms and facilitate their intercalation/deintercalation from the cathode. Such materials activated by disorder are promising candidate cathodes for lithium batteries, and the related mechanism of storage and effective migration of Li-ions also provides new clues for future design of disordered-electrode materials with high capacity and high energy density.

  6. Distinguishing magnetic vs. quadrupolar relaxation in b-NMR using 8Li and 9Li

    Science.gov (United States)

    Chatzichristos, A.; McFadden, R. M. L.; Karner, V. L.; Cortie, D. L.; Fang, A.; Levy, C. D. P.; Macfarlane, W. A.; Morris, G. D.; Pearson, M. R.; Salman, Z.; Kiefl, R. F.

    2016-09-01

    Beta-detected NMR is a powerful technique in condensed matter physics. It uses the parity violation of beta decay to detect the NMR signal from a beam of highly polarized radionuclides implanted in a sample material. Spin-lattice relaxation (SLR) is studied by monitoring the rate with which the asymmetry between the beta counts in two opposing detectors is lost. Unlike classical NMR, b-NMR can study thin films and near-surface effects. The most common b-NMR isotope at TRIUMF is 8Li, which has a quadrupole moment, thus it is sensitive to both magnetic fields and electric field gradients. A challenge with 8Li b-NMR is identifying the predominant mechanism of SLR in a given sample. It is possible to distinguish between SLR mechanisms by varying the probe isotope. For two isotopes with different nuclear moments, the ratio of SLR rates should be different in the limits of either pure magnetic or quadrupolar relaxation. This method has been used in classical NMR and we report its first application to b-NMR. We measured the SLR rates for 8Li and 8Li in Pt foil and SrTiO3. Pt is a test case for pure magnetic relaxation. SrTiO3 is a non-magnetic insulator, but the source of its relaxation is not well understood. Here we show that its relaxation is mainly quadrupolar. We thank TRIUMF's CMMS for their technical support. This work was supported by: NSERC Discovery Grants to R.F.K. and W.A.M.; and IsoSiM fellowships to A.C. and R.M.L.M.

  7. High speed pulsed laser cutting of LiCoO2 Li-ion battery electrodes

    Science.gov (United States)

    Lutey, Adrian H. A.; Fortunato, Alessandro; Carmignato, Simone; Fiorini, Maurizio

    2017-09-01

    Laser cutting of Li-ion battery electrodes represents an alternative to mechanical blanking that avoids complications associated with tool wear and allows assembly of different cell geometries with a single device. In this study, laser cutting of LiCoO2 Li-ion battery electrodes is performed at up to 5m /s with a 1064nm wavelength nanosecond pulsed fiber laser with a maximum average power of 500W and a repetition rate of up to 2MHz . Minimum average cutting power for cathode and anode multi-layer films is established for 12 parameter groups with velocities over the range 1 - 5m /s , varying laser pulse fluence and overlap. Within the tested parameter range, minimum energy per unit cut length is found to decrease with increasing repetition rate and velocity. SEM analysis of the resulting cut edges reveals visible clearance widths in the range 20 - 50 μm , with cut quality found to improve with velocity due to a reduction in lateral heat conduction losses. Raman line map spectra reveal changes in the cathode at 60 μm from the cut edge, where bands at 486cm-1 and 595cm-1 , corresponding to the Eg and A1g modes of LiCoO2 , are replaced with a single wide band centered at 544cm-1 , and evidence of carbon black is no longer present. No changes in Raman spectra are observed in the anode. The obtained results suggest that further improvements in cutting efficiency and quality could be achieved by increasing the repetition rate above 2MHz , thereby improving ablation efficiency of the metallic conductor layers. The laser source utilized in the present study nonetheless represents an immediately available solution for repeatability and throughput that are superior to mechanical blanking.

  8. Pediatric cancer and Li-Fraumeni/Li-Fraumeni-like syndromes: a review for the pediatrician

    Directory of Open Access Journals (Sweden)

    Cristina Rossi Giacomazzi

    2015-06-01

    Full Text Available Summary Introduction: cancer is the second leading cause of death in children between the ages of 0 and 14 years, corresponding to approximately 3% of all cases diagnosed in Brazil. A significant percentage (5-10% of pediatric cancers are associated with hereditary cancer syndromes, including Li-Fraumeni/Li-Fraumeni-like syndromes (LFS/LFL, both of which are caused by TP53 germline mutations. Recent studies have shown that a specific TP53 mutation, known as p.R337H, is present in 1 in 300 newborns in Southern and Southeast Brazil. In addition, a significant percentage of children with LFS/LFL spectrum tumors in the region have a family history compatible with LFS/LFL. Objective: to review clinical relevant aspects of LFS/LFL by our multidisciplinary team with focus on pediatric cancer. Methods: the NCBI (PubMed and SciELO databases were consulted using the keywords Li-Fraumeni syndrome, Li-Fraumeni-like syndrome and pediatric cancer; and all manuscripts published between 1990 and 2014 using these keywords were retrieved and reviewed. Conclusion: although LFS/LFL is considered a rare disease, it appears to be substantially more common in certain geographic regions. Recognition of population- specific risks for the syndrome is important for adequate management of hereditary cancer patients and families. In Southern and Southeastern Brazil, LFS/ LFL should be considered in the differential diagnosis of children with cancer, especially if within the spectrum of the syndrome. Due to the complexities of these syndromes, a multidisciplinary approach should be sought for the counseling, diagnosis and management of patients and families affected by these disorders. Pediatricians and pediatric oncologists in areas with high prevalence of hereditary cancer syndromes have a central role in the recognition and proper referral of patients and families to genetic cancer risk evaluation and management programs.

  9. Material review of Li ion battery separators

    Science.gov (United States)

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

    2014-06-01

    Separators for Li Ion batteries have a strong impact on cell production, cell performance, life, as well as reliability and safety. The separator market volume is about 500 million m2 mainly based on consumer applications. It is expected to grow strongly over the next decade for mobile and stationary applications using large cells. At present, the market is essentially served by polyolefine membranes. Such membranes have some technological limitations, such as wettability, porosity, penetration resistance, shrinkage and meltdown. The development of a cell failure due to internal short circuit is potentially closely related to separator material properties. Consequently, advanced separators became an intense area of worldwide research and development activity in academia and industry. New separator technologies are being developed especially to address safety and reliability related property improvements.

  10. Transport measurement of Li doped monolayer graphene

    Science.gov (United States)

    Khademi, Ali; Sajadi, Ebrahim; Dosanjh, Pinder; Folk, Joshua; Stöhr, Alexander; Forti, Stiven; Starke, Ulrich

    Lithium adatoms on monolayer graphene have been predicted to induce superconductivity with a critical temperature near 8 K, and recent experimental evidence by ARPES indicates a critical temperature nearly that high. Encouraged by these results, we investigated the effects of lithium deposited at cryogenic temperatures on the electronic transport properties of epitaxial and CVD monolayer graphene down to 3 K. The change of charge carrier density due to Li deposition was monitored both by the gate voltage shift of the Dirac point and by Hall measurements, in low and high doping regimes. In the high doping regime, a saturation density of 2×1013 cm-2 was observed independent of sample type, initial carrier density and deposition conditions. No signatures of superconductivity were observed down to 3 K.

  11. Gelled membranes for Li and Li-ion batteries prepared by electrospinning

    Science.gov (United States)

    Bansal, D.; Meyer, B.; Salomon, M.

    Composite polymer gelled membranes have been prepared an electrospinning technique. Electrospinning of polymer fibers or electrospraying of particles is typically accomplished by applying a strong electric field (ca. 1-25 kV cm -1) to a polymer solution or slurry of solids in an appropriate solvent. The fibers are collected as a mat (membrane) on a grounded target such as Al, Cu, Ni, etc. Typical membranes (mats) consist of nanometer size fibers and have porosities of 65-85%. In the present paper, we describe the fabrication of electrospun membranes for use as gelled electrolytes in Li and Li-ion batteries. The electrospun polymer membranes used in this work are based on the polyimides (PIs) Matrimid and Ultem 1000. Pure PI membranes have been prepared, and blends of Matrimid and Ultem with PVdF-HFP and PAN have been studied in 250 mAh and 7 Ah Li-ion cells. Fully imidized polyimides such as Matrimid and Ultem 1000 do not form gels, and are used as a host matrix of high mechanical strength to immobilize the gelling constituents PVdF or PAN.

  12. Gelled membranes for Li and Li-ion batteries prepared by electrospinning

    Energy Technology Data Exchange (ETDEWEB)

    Bansal, D.; Meyer, B.; Salomon, M. [MaxPower, Inc., 141 Christopher Lane, Harleysville, PA 19438 (United States)

    2008-04-01

    Composite polymer gelled membranes have been prepared an electrospinning technique. Electrospinning of polymer fibers or electrospraying of particles is typically accomplished by applying a strong electric field (ca. 1-25 kV cm{sup -1}) to a polymer solution or slurry of solids in an appropriate solvent. The fibers are collected as a mat (membrane) on a grounded target such as Al, Cu, Ni, etc. Typical membranes (mats) consist of nanometer size fibers and have porosities of 65-85%. In the present paper, we describe the fabrication of electrospun membranes for use as gelled electrolytes in Li and Li-ion batteries. The electrospun polymer membranes used in this work are based on the polyimides (PIs) Matrimid and Ultem 1000. Pure PI membranes have been prepared, and blends of Matrimid and Ultem with PVdF-HFP and PAN have been studied in 250 mAh and 7 Ah Li-ion cells. Fully imidized polyimides such as Matrimid and Ultem 1000 do not form gels, and are used as a host matrix of high mechanical strength to immobilize the gelling constituents PVdF or PAN. (author)

  13. Extraction of Li and Co from Li-ion Batteries by Chemical Methods

    Science.gov (United States)

    Guzolu, Jafar Sharrivar; Gharabaghi, Mahdi; Mobin, Mohammad; Alilo, Hojat

    2016-05-01

    In this work a process involving ultrasonic washing and leaching and precipitation was used to recover Li and Co from spent Li-ion batteries. Ultrasonic washing was used to reduce energy consumption and pollution whereas hydrochloric acid was used as leaching reagent. 98 % of Li and nearly 99 % of Co were obtained under optimum condition of 5 M hydrochloric acid solution, temperature of 95 °C, reaction time of 70 min, and solid-liquid ratio of 10 g/L. In this process at first nickel, copper, iron, aluminum, cobalt, and manganese were precipitated from leaching solution using sodium hydroxide at pH f 12.5 and reaction time of 1 h and temperature was 55 °C and all metal recoveries were more than 99 %. In the precipitation experiments, lithium loss was only 18.34 %. In the next stage, white lithium carbonate was precipitated by addition of saturated sodium carbonate solution to the left filtrate from first precipitation step. The purity of the recovered powder of lithium was 95 %.

  14. Extraction of Li and Co from Li-ion Batteries by Chemical Methods

    Science.gov (United States)

    Guzolu, Jafar Sharrivar; Gharabaghi, Mahdi; Mobin, Mohammad; Alilo, Hojat

    2017-04-01

    In this work a process involving ultrasonic washing and leaching and precipitation was used to recover Li and Co from spent Li-ion batteries. Ultrasonic washing was used to reduce energy consumption and pollution whereas hydrochloric acid was used as leaching reagent. 98 % of Li and nearly 99 % of Co were obtained under optimum condition of 5 M hydrochloric acid solution, temperature of 95 °C, reaction time of 70 min, and solid-liquid ratio of 10 g/L. In this process at first nickel, copper, iron, aluminum, cobalt, and manganese were precipitated from leaching solution using sodium hydroxide at pH f 12.5 and reaction time of 1 h and temperature was 55 °C and all metal recoveries were more than 99 %. In the precipitation experiments, lithium loss was only 18.34 %. In the next stage, white lithium carbonate was precipitated by addition of saturated sodium carbonate solution to the left filtrate from first precipitation step. The purity of the recovered powder of lithium was 95 %.

  15. NMR spin-lattice relaxation study of 7Li and 93Nb nuclei in Ti- or Fe-doped LiNbO3:Mg single crystals

    Directory of Open Access Journals (Sweden)

    Tae Ho Yeom

    2016-04-01

    Full Text Available In this study, to understand the effects of paramagnetic impurities, we investigated the temperature dependent of the spin-lattice relaxation times of pure LiNbO3, LiNbO3:Mg, LiNbO3:Mg/Ti, LiNbO3:Mg/Fe, and LiNbO3:Mg/Fe (thermally treated at 500°C single crystals. The results for the LiNbO3:Mg single crystals doped with Fe3+ or Ti3+ are discussed with respect to the site distribution and atomic mobility of Li and Nb. In addition, the effects of a thermal treatment on LiNbO3:Mg/Fe single crystals were examined based on the T1 analysis of 7Li and 93Nb. It was found that the presence of impurities in the crystals induced systematic changes of activation energies concerning atomic mobility.

  16. Lição de Anatomia

    Directory of Open Access Journals (Sweden)

    João Luiz Leocadio da Nova

    2000-02-01

    Full Text Available Na formação médica, diagnosticamos a falência do modelo pedagógico/assistencial que se revela, dentre outros sintomas, na ideologia de frieza e distanciamento que perpassa a prática médica. Este modelo de relação médico-paciente reproduziria a relação estudante-cadáver. Visando modificar tal ideologia, desenvolvemos, na UFRJ, em atividade interdisciplinar com a Anatomia, grupos de reflexão com os alunos do primeiro período da Faculdade de Medicina. A partir dos resultados, de dois anos dessa pesquisa, denominada "O cadáver e a formação médica", realizamos, com o apoio da Fundação José Bonifácio, um vídeo didático, "Lição de Anatomia", por meio de equipe multidisciplinar, incluindo professores e alunos do Instituto de Artes e Comunicação Social da UFF, da Faculdade de Medicina da UFRJ e do Núcleo de Tecnologia Educacional para a Saúde da UFRJ (NUTES. Pretendemos que a utilização desse recurso audiovisual constitua mais uma ferramenta para a melhoria do ensino e da prática médica, introduzindo a discussão de questões éticas. A pesquisa e a realização do vídeo nos mostraram a possibilidade de se repensar e inovar o ensino universitário, o que foi, para todos nós, uma lição de convívio democrático.

  17. Li-ion diffusion kinetics in LiCoPO{sub 4} thin films deposited on NASICON-type glass ceramic electrolytes by magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Xie, J.; Imanishi, N.; Zhang, T.; Hirano, A.; Takeda, Y.; Yamamoto, O. [Department of Chemistry, Faculty of Engineering, Mie University, 1577 Kurimamachiya-cho, Tsu, Mie 514-8507 (Japan)

    2009-07-15

    LiCoPO{sub 4} thin films were deposited on Li{sub 1+x+y}Al{sub x}Ti{sub 2-x}Si{sub y}P{sub 3-y}O{sub 12} (LATSP) solid electrolyte by radio frequency magnetron sputtering and were characterized by X-ray diffraction and scanning electron microscope. The films show a (1 1 1) preferred orientation upon annealing and are chemically stable with LATSP up to 600 C in air. An all-solid-state Li/PEO{sub 18}-Li(CF{sub 3}SO{sub 2}){sub 2}N/LATSP/LiCoPO{sub 4}/Au cell was fabricated to investigate the electrochemical performance and Li-ion chemical diffusion coefficients, D{sub Li}, of the LiCoPO{sub 4} thin films. The potential dependence of D{sub Li} values of the LiCoPO{sub 4} thin film was investigated by potentiostatic intermittent titration technique and was compared with those of the LiFePO{sub 4} thin film. These results showed that the intercalation mechanism of Li-ion in LiCoPO{sub 4} is different from that in LiFePO{sub 4}. (author)

  18. Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-phase Li4Ti5O12/Li2TiO3 Composite in Voltage Range of 0−3 V

    KAUST Repository

    Bhatti, Humaira S

    2016-04-20

    Li4Ti5O12, Li2TiO3 and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol-gel method with average particle size of 1 µm, 0.3 µm and 0.4 µm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows good rate performance of 90 mA h g-1 at high rate of 10 C in voltage range of 1−3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers capacity retention of 88.6 % at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and capacity retention of 98.45 % at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. CV curves of Li4Ti5O12/Li2TiO3 in 0−3 V range exhibit two anodic peaks at 1.51 V and 0.7−0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/de-intercalation kinetics in 0−3 V, composite electrode delivers superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.

  19. Characteristics of LiCoO2, LiMn2O4 and LiNi0.45Co0.1Mn0.45O2 as cathodes of lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    GUO Hua-jun; LI Xin-hai; ZHANG Xin-ming; ZENG Su-ming; WANG Zhi-xing; PENG Wen-jie

    2005-01-01

    LiNi0. 45 Co0. 10 Mn0. 4sO2 was synthesized from Li2CO3 and a triple oxide of nickel, cobalt and manganese at 950 ℃ in air. The structures and characteristics of LiNi0. 45 Co0.10 Mn0. 45 O2, LiCoO2 and LiMn2 O4 were investigated by XRD, SEM and electrochemical measurements. The results show that LiNi0.4s Co0.10 Mn0. 45 O2 has a layered structure with hexagonal lattice. The commercial LicoO2 has sphere-like appearance and smooth surfaces, while the LiMn2 O4 and LiNi0.45 Co0. 10 Mn0. 45 O2 consist of cornered and uneven particles. LiNi0. 45 Co0.10 Mn0. 45 O2 has a large disLiMn2 O4 and LiCoO2, respectively. LiCoO2 and LiMn2 O4 have higher discharge voltage and better rate-capability than LiNi0. 45Co0.10 Mn0. 45 O2. All the three cathodes have excellent cycling performance with capacity retention of above 89.3 % at the 250th cycle. Batteries with LiMn2 O4 or LiNi0.45 Co0.10 Mn0. 45 O2 cathodes show better safety performance under abusive conditions than those with LiCoO2 cathodes.

  20. Lithium Ion Mobility in Lithium Phosphidosilicates: Crystal Structure, (7) Li, (29) Si, and (31) P MAS NMR Spectroscopy, and Impedance Spectroscopy of Li8 SiP4 and Li2 SiP2.

    Science.gov (United States)

    Toffoletti, Lorenzo; Kirchhain, Holger; Landesfeind, Johannes; Klein, Wilhelm; van Wüllen, Leo; Gasteiger, Hubert A; Fässler, Thomas F

    2016-12-05

    The need to improve electrodes and Li-ion conducting materials for rechargeable all-solid-state batteries has drawn enhanced attention to the investigation of lithium-rich compounds. The study of the ternary system Li-Si-P revealed a series of new compounds, two of which, Li8 SiP4 and Li2 SiP2 , are presented. Both phases represent members of a new family of Li ion conductors that display Li ion conductivity in the range from 1.15(7)×10(-6) Scm(-1) at 0 °C to 1.2(2)×10(-4) Scm(-1) at 75 °C (Li8 SiP4 ) and from 6.1(7)×10(-8) Scm(-1) at 0 °C to 6(1)×10(-6) Scm(-1) at 75 °C (Li2 SiP2 ), as determined by impedance measurements. Temperature-dependent solid-state (7) Li NMR spectroscopy revealed low activation energies of about 36 kJ mol(-1) for Li8 SiP4 and about 47 kJ mol(-1) for Li2 SiP2 . Both compounds were structurally characterized by X-ray diffraction analysis (single crystal and powder methods) and by (7) Li, (29) Si, and (31) P MAS NMR spectroscopy. Both phases consist of tetrahedral SiP4 anions and Li counterions. Li8 SiP4 contains isolated SiP4 units surrounded by Li atoms, while Li2 SiP2 comprises a three-dimensional network based on corner-sharing SiP4 tetrahedra, with the Li ions located in cavities and channels.

  1. Preparation, Thermal Stability and Electrochemical Properties of LiODFB

    Institute of Scientific and Technical Information of China (English)

    Hongming Zhou; Furong Liu; Jian Li

    2012-01-01

    Lithium oxalyldifluoroborate (LiODFB) was synthesized in dimethyl carbonate solvent and purified by the method of solvent-out crystallization. The structure characterization and thermal stability of LiODFB were performed by Fourier transform infrared (FTIR) spectrometry, nuclear magnetic resonance (NMR) spectrometry and thermogravimetric analyzer (TGA). LiODFB was exposed to 50% humid air at 25 ℃for different time, then dried at 80 ℃ for 12 h, and the electrochemical properties of the cells using 1 mol/L dried LiODFB in ethylene carbonate -I- dimethyl carbonate + ethyl(methyl)carbonate were investigated. The results showed that, pure crystallization LiODFB was obtained; it had good thermal stability with a thermal decomposition temperature of 248 ℃; when it was exposed to humid air, it was firstly converted into LiODFB.H20; with increasing exposure time, more and stronger impurity peaks in the X-ray diffraction (XRD) patterns of LiODFB were observed, and both the discharge specific capacity and the capacity retention decreased gradually.

  2. Integrated LiH Debris Shields for Warm PRS Loads

    Science.gov (United States)

    Terry, R. E.; Thornhill, J. W.; Clark, R. W.; Dasgupta, A.

    2006-10-01

    Plasma radiation sources can profitably employ thick LiH debris shields integrated into the return current surface. Shield material selection demands the highest specific enthalpy Hm to vaporization or decomposition in an attenuation length λ(Eprs) at the k-shell transmission energy of interest. As a figure of merit then, E ≡Hmρ/ M λ(Eprs) [kJcm^2] can order candidate materials. LiH is the best possible material for this purpose, offering E values of 130 for the 13 keV k-shell lines of Kr. In a level comparison, Be offers only 47 and pure Li, 77.5. For the Ti k-shell lines, a similar ordering is: LiH, 22.44; Be, 3.08; Li, 10.40. Early studies of these designs showed promise even for the more opaque Ar and Ti k-shell radiation. Here we examine the much easier problem for a Kr k-shell PRS and consider the influence of l-shell and m-shell radiation on the hydrodynamic flows developed in the LiH and its decay products. The radiation loading of the LiH shield is computed self consistently within the more generous trade space of stagnation energy, machine current, implosion time, and delivered mass for drivers capable of useful Kr k-shell yield. R.E.Terry, NRL Memo Report 6720--96-7868.

  3. Developing New Electrolytes for Advanced Li-ion Batteries

    Science.gov (United States)

    McOwen, Dennis Wayne

    The use of renewable energy sources is on the rise, as new energy generating technologies continue to become more efficient and economical. Furthermore, the advantages of an energy infrastructure which relies more on sustainable and renewable energy sources are becoming increasingly apparent. The most readily available of these renewable energy sources, wind and solar energy in particular, are naturally intermittent. Thus, to enable the continued expansion and widespread adoption of renewable energy generating technology, a cost-effective energy storage system is essential. Additionally, the market for electric/hybrid electric vehicles, which both require efficient energy storage, continues to grow as more consumers seek to reduce their consumption of gasoline. These vehicles, however, remain quite expensive, due primarily to costs associated with storing the electrical energy. High-voltage and thermally stable Li-ion battery technology is a promising solution for both grid-level and electric vehicle energy storage. Current limitations in materials, however, limit the energy density and safe operating temperature window of the battery. Specifically, the state-of-the-art electrolyte used in Li-ion batteries is not compatible with recently developed high-voltage positive electrodes, which are one of the most effectual ways of increasing the energy density. The electrolyte is also thermally unstable above 50 °C, and prone to thermal runaway reaction if exposed to prolonged heating. The lithium salt used in such electrolytes, LiPF6, is a primary contributor to both of these issues. Unfortunately, an improved lithium salt which meets the myriad property requirements for Li-ion battery electrolytes has eluded researchers for decades. In this study, a renewed effort to find such a lithium salt was begun, using a recently developed methodology to rapidly screen for desirable properties. Four new lithium salts and one relatively new but uncharacterized lithium salt were

  4. Big Bang 6Li nucleosynthesis studied deep underground (LUNA collaboration)

    Science.gov (United States)

    Trezzi, D.; Anders, M.; Aliotta, M.; Bellini, A.; Bemmerer, D.; Boeltzig, A.; Broggini, C.; Bruno, C. G.; Caciolli, A.; Cavanna, F.; Corvisiero, P.; Costantini, H.; Davinson, T.; Depalo, R.; Elekes, Z.; Erhard, M.; Ferraro, F.; Formicola, A.; Fülop, Zs.; Gervino, G.; Guglielmetti, A.; Gustavino, C.; Gyürky, Gy.; Junker, M.; Lemut, A.; Marta, M.; Mazzocchi, C.; Menegazzo, R.; Mossa, V.; Pantaleo, F.; Prati, P.; Rossi Alvarez, C.; Scott, D. A.; Somorjai, E.; Straniero, O.; Szücs, T.; Takacs, M.

    2017-03-01

    The correct prediction of the abundances of the light nuclides produced during the epoch of Big Bang Nucleosynthesis (BBN) is one of the main topics of modern cosmology. For many of the nuclear reactions that are relevant for this epoch, direct experimental cross section data are available, ushering the so-called "age of precision". The present work addresses an exception to this current status: the 2H(α,γ)6Li reaction that controls 6Li production in the Big Bang. Recent controversial observations of 6Li in metal-poor stars have heightened the interest in understanding primordial 6Li production. If confirmed, these observations would lead to a second cosmological lithium problem, in addition to the well-known 7Li problem. In the present work, the direct experimental cross section data on 2H(α,γ)6Li in the BBN energy range are reported. The measurement has been performed deep underground at the LUNA (Laboratory for Underground Nuclear Astrophysics) 400 kV accelerator in the Laboratori Nazionali del Gran Sasso, Italy. The cross section has been directly measured at the energies of interest for Big Bang Nucleosynthesis for the first time, at Ecm = 80, 93, 120, and 133 keV. Based on the new data, the 2H(α,γ)6Li thermonuclear reaction rate has been derived. Our rate is even lower than previously reported, thus increasing the discrepancy between predicted Big Bang 6Li abundance and the amount of primordial 6Li inferred from observations.

  5. Hydrogen reversibility of LiBH₄-MgH₂-Al composites.

    Science.gov (United States)

    Hansen, Bjarne R S; Ravnsbæk, Dorthe B; Skibsted, Jørgen; Jensen, Torben R

    2014-05-21

    The detailed mechanism of hydrogen release in LiBH4-MgH2-Al composites of molar ratios 4 : 1 : 1 and 4 : 1 : 5 are investigated during multiple cycles of hydrogen release and uptake. This study combines information from several methods, i.e., in situ synchrotron radiation powder X-ray diffraction, (11)B magic-angle spinning (MAS) NMR, Sievert's measurements, Fourier transform infrared spectroscopy and simultaneous thermogravimetric analysis, differential scanning calorimetry and mass spectroscopy. The composites of LiBH4-MgH2-Al are compared with the behavior of the LiBH4-Al and LiBH4-MgH2 systems. The decomposition pathway of the LiBH4-MgH2-Al system is different for the two investigated molar ratios, although it ultimately results in the formation of LiAl, Mg(x)Al(1-x)B2 and Li2B12H12 in both cases. For the 4 : 1 : 1-molar ratio, Mg(0.9)Al(0.1) and Mg17Al12 are observed as intermediates. However, only Mg is observed as an intermediate in the 4 : 1 : 5-sample, which may be due to an earlier formation of Mg(x)Al(1-x)B2, reflecting the complex chemistry of Al-Mg phases. Hydrogen release and uptake reveals a decrease in the hydrogen storage capacity upon cycling. This loss reflects the formation of Li2B12H12 as observed by (11)B NMR and infrared spectroscopy for the cycled samples. Furthermore, it is shown that the Li2B12H12 formation can be limited significantly by applying moderate hydrogen partial pressure during decomposition.

  6. Li's criterion for the Riemann hypothesis - numerical approach

    Directory of Open Access Journals (Sweden)

    Krzysztof Maślanka

    2004-01-01

    Full Text Available There has been some interest in a criterion for the Riemann hypothesis proved recently by Xian-Jin Li [Li X.-J.: The Positivity of a Sequence of Numbers and the Riemann Hypothesis. J. Number Theory 65 (1997, 325-333]. The present paper reports on a numerical computation of the first 3300 of Li's coefficients which appear in this criterion. The main empirical observation is that these coefficients can be separated in two parts. One of these grows smoothly while the other is very small and oscillatory. This apparent smallness is quite unexpected. If it persisted till infinity then the Riemann hypothesis would be true.

  7. Degradation Studies on LiFePO4 cathode

    DEFF Research Database (Denmark)

    Scipioni, Roberto; Jørgensen, Peter Stanley; Hjelm, Johan

    2015-01-01

    In this paper we examine a laboratory LiFePO4 (LFP) cathode and propose a simple model that predicts the electrode capacity as function of C-rate, number of cycles and calendar time. Microcracks were found in Li1-xFePO4 particles in a degraded LFP electrode and low-acceleration voltage (1 kV) FIB....../SEM analysis allowed us to obtain phase contrast between FePO4 and LiFePO4. The evolution of micro-cracks is expected to increase the concentration of LFP particles which are not electronically accessible and thus cause a loss in capacity....

  8. Cai-Li Communication Protocol in Noisy Quantum Channel

    Institute of Scientific and Technical Information of China (English)

    L(U) Hua; YAN Xu-Dong; ZHANG Xian-Zhou

    2004-01-01

    @@ Since the original Cai-Li protocol [Chin. Phys. Lett. 21 (2004) 601] can be used only in an ideal quantum communication, we present the modified Cai-Li protocol that can be used in the a noisy quantum channel by using Calderbank-Shor-Steane (CSS) codes to correct errors. We also give a tight bound on the connection between information Eve eavesdropped with a measurement attack in line B → A and detection probability,which shows that the Cai-Li protocol can be used as a quasisecure direct quantum communication.

  9. Tensor Modeling Based for Airborne LiDAR Data Classification

    Science.gov (United States)

    Li, N.; Liu, C.; Pfeifer, N.; Yin, J. F.; Liao, Z. Y.; Zhou, Y.

    2016-06-01

    Feature selection and description is a key factor in classification of Earth observation data. In this paper a classification method based on tensor decomposition is proposed. First, multiple features are extracted from raw LiDAR point cloud, and raster LiDAR images are derived by accumulating features or the "raw" data attributes. Then, the feature rasters of LiDAR data are stored as a tensor, and tensor decomposition is used to select component features. This tensor representation could keep the initial spatial structure and insure the consideration of the neighborhood. Based on a small number of component features a k nearest neighborhood classification is applied.

  10. Photoassociative production of ultracold heteronuclear YbLi* molecules

    Science.gov (United States)

    Roy, Richard; Shrestha, Rajendra; Green, Alaina; Gupta, Subhadeep; Li, Ming; Kotochigova, Svetlana; Petrov, Alexander; Yuen, Chi Hong

    2016-09-01

    We report on the production of ultracold heteronuclear YbLi* molecules in a dual-species magneto-optical trap by photoassociation (PA). The formation of the electronically excited molecules close to dissociation was observed by trap loss spectroscopy. We find 4 rovibrational states within a range of 250 GHz below the Yb (S10) +Li (1/2 2P) asymptote and observe isotopic PA line shifts in mixtures of 6Li with 174Yb, 172Yb, and 176Yb. We also describe our theoretical ab initio calculation for the relevant electronic potentials and utilize it to analyze and identify the lines in the experimentally observed spectrum.

  11. Photoassociative production of ultracold heteronuclear YbLi* molecules

    CERN Document Server

    Roy, Richard; Green, Alaina; Gupta, Subhadeep; Li, Ming; Kotochigova, Svetlana; Petrov, Alexander; Yuen, Chi Hong

    2016-01-01

    We report on the production of ultracold heteronuclear YbLi* molecules in a dual-species magneto-optical trap by photoassociation (PA). The formation of the electronically excited molecules close to dissociation was observed by trap loss spectroscopy. We find 4 rovibrational states within a range of $250\\,$GHz below the Yb($^1S_0$) + Li($^2P_{1/2}$) asymptote and observe isotopic PA line shifts in mixtures of $^6$Li with $^{174}$Yb, $^{172}$Yb, and $^{176}$Yb. We also describe our theoretical ab-initio calculation for the relevant electronic potentials and utilize it to analyze and identify the lines in the experimentally observed spectrum.

  12. LiFePO_4/C via fluoride doping

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    Non-stoichiometric compound fluoride-doped LiFePO4/C cathode materials were synthesized via solid-state reaction using MgF2 and AlF3 as dopant. The fluoride-doped LiFePO4/C samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical testing. The results show that the materials are well crystallized and fluoride doping cannot change the space structure of LiFePO4. Slight amounts of Fe2O3 with no fluoride impurity were ...

  13. TENSOR MODELING BASED FOR AIRBORNE LiDAR DATA CLASSIFICATION

    Directory of Open Access Journals (Sweden)

    N. Li

    2016-06-01

    Full Text Available Feature selection and description is a key factor in classification of Earth observation data. In this paper a classification method based on tensor decomposition is proposed. First, multiple features are extracted from raw LiDAR point cloud, and raster LiDAR images are derived by accumulating features or the “raw” data attributes. Then, the feature rasters of LiDAR data are stored as a tensor, and tensor decomposition is used to select component features. This tensor representation could keep the initial spatial structure and insure the consideration of the neighborhood. Based on a small number of component features a k nearest neighborhood classification is applied.

  14. Fusion around the barrier for 7Li + 12C

    Indian Academy of Sciences (India)

    A Mukherjee; M Dasgupta; D J Hinde; C R Morton; A C Berriman; R D Butt; J O Newton; H Timmers

    2001-07-01

    Fusion cross-sections for the 7Li + 12C reaction have been measured at energies above the Coulomb barrier by the direct detection of evaporation residues. The heavy evaporation residues with energies below 3 MeV could not be separated out from the -particles in the spectrum and hence their contribution was estimated using statistical model calculations. The present work indicates that suppression of fusion cross-sections due to the breakup of 7Li may not be significant for 7Li + 12C reaction at energies around the barrier.

  15. Fatigue crack growth behaviour of Al-Li alloys

    Science.gov (United States)

    Saravanakumar, R.; Ramakrishna, K. S.; Kanna, B. Avinash

    2013-06-01

    Al-Li alloys are being used in aircraft structures due to its low density and inherent mechanical properties. Fatigue Crack Growth (FCG) resistance is usually high compared to conventional Al-alloys attributed to increased modulus and crack closure. Extensive investigations concern about the FCG resistance and crack closure in Al-Li alloys. The present work reviews the FCG resistance in Al-Li alloys and the mechanisms associated with it. The alloy 8090 is taken for the consideration and sometimes compared with 2024.

  16. Electronic properties of Li-doped zigzag graphene nanoribbons

    Science.gov (United States)

    Narin, P.; Kutlu, E.; Sarikavak-Lisesivdin, B.; Lisesivdin, S. B.; Özbay, E.

    2016-10-01

    Zigzag graphene nanoribbons (ZGNRs) are known to exhibit metallic behavior. Depending on structural properties such as edge status, doping and width of nanoribbons, the electronic properties of these structures may vary. In this study, changes in electronic properties of crystal by doping Lithium (Li) atom to ZGNR structure are analyzed. In spin polarized calculations are made using Density Functional Theory (DFT) with generalized gradient approximation (GGA) as exchange correlation. As a result of calculations, it has been determined that Li atom affects electronic properties of ZGNR structure significantly. It is observed that ZGNR structure exhibiting metallic behavior in pure state shows half-metal and semiconductor behavior with Li atom.

  17. LiDAR error estimation with WAsP engineering

    DEFF Research Database (Denmark)

    Bingöl, Ferhat; Mann, Jakob; Foussekis, D.

    2008-01-01

    The LiDAR measurements, vertical wind profile in any height between 10 to 150m, are based on assumption that the measured wind is a product of a homogenous wind. In reality there are many factors affecting the wind on each measurement point which the terrain plays the main role. To model LiDAR...... measurements and predict possible error in different wind directions for a certain terrain we have analyzed two experiment data sets from Greece. In both sites LiDAR and met. mast data have been collected and the same conditions are simulated with Riso/DTU software, WAsP Engineering 2.0. Finally measurement...

  18. Structural and Electrochemical Characterization of Pure LiFePO4 and Nanocomposite C-LiFePO4 Cathodes for Lithium Ion Rechargeable Batteries

    OpenAIRE

    Arun Kumar(University of Delhi, Delhi, India); Thomas, R.; N. K. Karan; Saavedra-Arias, J. J.; M K Singh; Majumder, S. B.; Tomar, M. S.; Katiyar, R. S.

    2009-01-01

    Pure lithium iron phosphate (LiFePO4) and carbon-coated LiFePO4 (C-LiFePO4) cathode materials were synthesized for Li-ion batteries. Structural and electrochemical properties of these materials were compared. X-ray diffraction revealed orthorhombic olivine structure. Micro-Raman scattering analysis indicates amorphous carbon, and TEM micrographs show carbon coating on LiFePO4 particles. Ex situ Raman spectrum of C-LiFePO4 at various stages of charging and discharging showed reversibility upon...

  19. Synthesis and conductivities of the garnet-related Li ion conductors, Li5Ln3Sb2O12 (Ln= La, Pr, Nd, Sm, Eu)

    OpenAIRE

    Percival, Julia; Kendrick, Emma; Slater, Peter

    2008-01-01

    In this paper the synthesis and conductivities of the garnet-related Li ion conductors, Li5Ln3Sb2O12 (Ln=La, Pr, Nd, Sm, Eu), are reported. These phases show high Li ion conductivity, similar to previously reported for the related Li5La3M2O12 (M=Nb, Ta) materials. Neutron diffraction structural studies are also reported for Li5La3Sb2O12 indicating a cubic unit cell, space group Ia-3d, with Li located in two partially occupied sites.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2013-02-05

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

  1. A stabilized high-energy Li-polyiodide semi-liquid battery with a dually-protected Li anode

    Science.gov (United States)

    Ren, Y. X.; Zhao, T. S.; Jiang, H. R.; Wu, M. C.; Liu, M.

    2017-04-01

    Li-polyiodide batteries are attractive because of their high energy density and excellent rate performance. Nevertheless, the polyiodide shuttle effect and Li dendrite growth over cycling result in fast degradation of the Li anode and a short cycle life. Here we report a facile yet efficient design of high-energy membrane-free Li-polyiodide battery, in which the Li anode is shielded by a pre-deposited indium (In) layer and a graphene paper layer. The proof-of-concept semi-liquid battery with such a dual-protection strategy demonstrates a remarkably enhanced cycling stability for the reasons: (i) the In layer is capable of mitigating the Li dendrite growth and resisting the polyiodide shuttle attack; and (ii) the graphene paper physically suppresses the anode surface evolution and enables the formation of a separated passivation layer. Consequently, the battery can operate with a concentrated catholyte of 6 M I- and achieves a volumetric energy density as high as 165.3 Wh L-1 (1.5 C) for 100 cycles. The high performances achieved suggest the aprotic Li-polyiodide battery with a compact and robust architecture shows the potential for various energy storage applications.

  2. Adiponitrile-LiTFSI solution as alkylcarbonate free electrolyte for LTO/NMC Li-ion batteries.

    Science.gov (United States)

    Farhat, Douaa; Ghamouss, Fouad; Maibach, Julia; Edström, Kristina; Lemordant, Daniel

    2017-02-23

    Recently, dinitriles (NC(CH2)nCN) and especially adiponitrile (ADN, n=4) have attracted the attention as secure electrolyte solvents due to their chemical stability, high boiling points, high flash points and low vapor pressure. The good solvating properties of ADN toward lithium salts and its high electrochemical stability (~ 6V vs. Li/Li+) make it suitable for safer Li-ions cells without performances loss. In this study, ADN is used as a single electrolyte solvent with lithium bis(trimethylsulfonyl)imide (LiTFSI). This electrolyte allows the use of aluminum collectors as almost no corrosion occurs at voltages up to 4.2 V. Physico-chemical properties of ADN-LiTFSI electrolyte such as salt dissolution, conductivity and viscosity were determined. The cycling performances of batteries using Li4Ti5O12 (LTO) as anode and LiNi1/3Co1/3Mn1/3O2 (NMC) as cathode were determined. The results indicate that LTO/NMC batteries exhibit excellent rate capabilities with a columbic efficiency close to 100%. As an example, cells were able to reach a capacity of 165 mAh.g-1 at 0.1C and a capacity retention of more than 98% after 200 cycles at 0.5C. In addition, electrodes analyses by SEM, XPS and electrochemical impedance spectroscopy after cycling confirming minimal surface changes of the electrodes in the studied battery system.

  3. The B-Li System. Calorimetric and Theoretical Studies / Układ B-Li. Badania Kalorymetryczne I Teoretyczne

    Directory of Open Access Journals (Sweden)

    Dębski A.

    2015-12-01

    Full Text Available The standard enthalpy of formation of the B78Li22 alloy was measured with the use of the water reaction calorimetric method at 25 °C (298 K. An X-ray diffraction study of the prepared sample was conducted. The obtained diffraction pattern was different from the patterns for the B3Li and B14Li3 phases. The standard enthalpy of formation obtained for the B78Li22 alloy was -39.0 ± 0.7 kJ/mole of atoms. This value corresponds well with the formation enthalpies of the phases from the boron-lithium system. Theoretical calculations of the standard enthalpy of formation were conducted for the B78Li22 alloy and the phases from B-Li system, which were investigated earlier. A discussion of the deviations observed between both sets of data (experimental and calculated was performed. Additionally, DTA studies were performed for 14 alloys of the concentrations from 40 to 100 at. % of Li.

  4. Mida sa arvad üliõpilaste õppetoetuse süsteemist? / Kadri Inselberg

    Index Scriptorium Estoniae

    Inselberg, Kadri

    2008-01-01

    Küsimusele vastavad Tartu Ülikooli riigiõiguse üliõpilane Eveli Õigus, Eesti Maaülikooli veemajanduse üliõpilane Tauri Tamar, Tartu Ülikooli õigusteaduskonna üliõpilane Olavi Malla ja Tallinna Tehnikaülikooli Tartu Kolledži üliõpilane Katre Kasemägi

  5. Y-doped Li8ZrO6: A Li-Ion Battery Cathode Material with High Capacity.

    Science.gov (United States)

    Huang, Shuping; Wilson, Benjamin E; Wang, Bo; Fang, Yuan; Buffington, Keegan; Stein, Andreas; Truhlar, Donald G

    2015-09-02

    We study--experimentally and theoretically--the energetics, structural changes, and charge flows during the charging and discharging processes for a new high-capacity cathode material, Li8ZrO6 (LZO), which we study both pure and yttrium-doped. We quantum mechanically calculated the stable delithiated configurations, the delithiation energy, the charge flow during delithiation, and the stability of the delithiated materials. We find that Li atoms are easier to extract from tetrahedral sites than octahedral ones. We calculate a large average voltage of 4.04 eV vs Li/Li(+) for delithiation of the first Li atom in a primitive cell, which is confirmed by galvanostatic charge/discharge cycling data. Energy calculations indicate that topotactic delithiation is kinetically favored over decomposition into Li, ZrO2, and O2 during the charging process, although the thermodynamic energy of the topotactic reaction is less favorable. When one or two lithium atoms are extracted from a primitive cell of LZO, its volume and structure change little, whereas extraction of the third lithium greatly distorts the layered structure. The Li6ZrO6 and Li5ZrO6 delithiation products can be thermodynamically metastable to release of O2. Experimentally, materials with sufficiently small particle size for efficient delithiation and relithiation were achieved within an yttrium-doped LZO/carbon composite cathode that exhibited an initial discharge capacity of at least 200 mAh/g over the first 10 cycles, with 142 mAh/g maintained after 60 cycles. Computations predict that during the charging process, the oxygen ion near the Li vacancy is oxidized for both pure LZO and yttrium-doped LZO, which leads to a small-polaron hole.

  6. The effect of the carbon nanotube buffer layer on the performance of a Li metal battery

    Science.gov (United States)

    Zhang, Ding; Zhou, Yi; Liu, Changhong; Fan, Shoushan

    2016-05-01

    Lithium (Li) metal is one of the most promising candidates as an anode for the next-generation energy storage systems because of its high specific capacity and lowest negative electrochemical potential. But the growth of Li dendrites limits the application of the Li metal battery. In this work, a type of modified Li metal battery with a carbon nanotube (CNT) buffer layer inserted between the separator and the Li metal electrode was reported. The electrochemical results show that the modified batteries have a much better rate capability and cycling performance than the conventional Li metal batteries. The mechanism study by electrochemical impedance spectroscopy reveals that the modified battery has a smaller charge transfer resistance and larger Li ion diffusion coefficient during the deposition process on the Li electrode than the conventional Li metal batteries. Symmetric battery tests show that the interfacial behavior of the Li metal electrode with the buffer layer is more stable than the naked Li metal electrode. The morphological characterization of the CNT buffer layer and Li metal lamina reveals that the CNT buffer layer has restrained the growth of Li dendrites. The CNT buffer layer has great potential to solve the safety problem of the Li metal battery.Lithium (Li) metal is one of the most promising candidates as an anode for the next-generation energy storage systems because of its high specific capacity and lowest negative electrochemical potential. But the growth of Li dendrites limits the application of the Li metal battery. In this work, a type of modified Li metal battery with a carbon nanotube (CNT) buffer layer inserted between the separator and the Li metal electrode was reported. The electrochemical results show that the modified batteries have a much better rate capability and cycling performance than the conventional Li metal batteries. The mechanism study by electrochemical impedance spectroscopy reveals that the modified battery has a

  7. Effect of Li3PO4 coating of layered lithium-rich oxide on electrochemical performance

    Science.gov (United States)

    Chen, Dongrui; Zheng, Feng; Li, Liu; Chen, Min; Zhong, Xiaoxin; Li, Weishan; Lu, Li

    2017-02-01

    A novel composite of layered lithium-rich oxide, Li-Rich@Li3PO4, coated with Li3PO4 is synthesized through polydopamine template method. Physical characterizations reveal that Li-Rich@Li3PO4 is composed of nanoparticles of 100-200 nm that are coated with a uniform Li3PO4 layer of about 5 nm in thickness. Galvanostatic charge/discharge tests demonstrate enhanced cycling stability and largely increased rate capability of the material after Li3PO4 coating.

  8. Self-assembled LiFePO4 nanowires with high rate capability for Li-ion batteries.

    Science.gov (United States)

    Peng, Lele; Zhao, Yu; Ding, Yu; Yu, Guihua

    2014-08-28

    Controlling the dimensions in the nanometer scale of olivine-type LiFePO4 has been regarded as one of the most effective strategies to improve its electrochemical performance for Li-ion batteries. In this communication, we demonstrate a novel LiFePO4 nanoarchitecture, which is composed of self-assembled single-crystalline nanowires and exhibits good rate capability with a reversible capacity of ∼110 mA h g(-1) at a current rate of 30 C, and a stable capacity retention of ∼86% after 1000 cycles at a current rate of 10 C.

  9. Ultra LI-ideals in lattice implication algebras and MTL-algebras

    CERN Document Server

    Zhang, Xiaohong; Dudek, Wieslaw A

    2007-01-01

    A mistake concerning the ultra \\textit{LI}-ideal of a lattice implication algebra is pointed out, and some new sufficient and necessary conditions for an \\textit{LI}-ideal to be an ultra \\textit{LI}-ideal are given. Moreover, the notion of an \\textit{LI}-ideal is extended to MTL-algebras, the notions of a (prime, ultra, obstinate, Boolean) \\textit{LI}-ideal and an \\textit{ILI}-ideal of an MTL-algebra are introduced, some important examples are given, and the following notions are proved to be equivalent in MTL-algebra: (1) prime proper \\textit{LI}-ideal and Boolean \\textit{LI}-ideal, (2) prime proper \\textit{LI}-ideal and \\textit{ILI}-ideal, (3) proper obstinate \\textit{LI}-ideal, (4) ultra \\textit{LI}-ideal.

  10. Electrochemistry study on PEO-LiClO4-ZSM5 composite polymer electrolyte

    Institute of Scientific and Technical Information of China (English)

    XI Jingyu; MA Xiaomei; CUI Mengzhong; HUANG Xiaobin; ZHENG Zhen; TANG Xiaozhen

    2004-01-01

    A novel all solid-state composite polymer electrolyte, PEO-LiClO4-LiZSM5, by using "shape-selective" molecular sieves ZSM-5 as filler was obtained by the solvent casting method. The experimental results showed that the addition of LiZSM5 could enhance the ionic conductivity of the pristine PEO-LiClO4 electrolyte, the ionic conductivity of PEO10-LiClO4-10%LiZSM5 achieved 1.4×10-5 S cm-1 at 25℃. Lithium ion transference number was tested by AC impedance combined with the steady-state current method, the results showed that LiZSM5 could improve the Li+ transference number of the CPE effectively. The broad electrochemical stability window ensured the use of PEO-Li- ClO4-LiZSM5 as electrolyte materials for all solid-state rechargeable lithium ion batteries.

  11. Composited reduced graphene oxide into LiFePO4/Li2SiO3 and its electrochemical impedance spectroscopy properties

    Science.gov (United States)

    Arifin, M.; Rus, Y. B.; Aimon, A. H.; Iskandar, F.; Winata, T.; Abdullah, M.; Khairurrijal, K.

    2017-03-01

    LiFePO4 is commonly used as cathode material for Li-ion batteries due to its stable operational voltage and high specific capacity. However, it suffers from certain disadvantages such as low intrinsic electronic conductivity and low ionic diffusion. This study was conducted to analyse the effect of reduced graphene oxide (rGO) on the electrochemical properties of LiFePO4/Li2SiO3 composite. This composite was synthesized by a hydrothermal method. Fourier transform infrared spectroscopy measurement identified the O–P–O, Fe–O, P–O, and O–Si–O‑ bands in the LiFePO4/Li2SiO3 composite. X-ray diffraction measurement confirmed the formation of LiFePO4. Meanwhile, Raman spectroscopy confirmed the number of rGO layers. Further, scanning electron microscopy images showed that rGO was distributed around the LiFePO4/Li2SiO3 particles. Finally, the electrochemical impedance spectroscopy results showed that the addition of 1 wt% of rGO to the LiFePO4/Li2SiO3 composite reduced charge transfer resistance. It may be concluded that the addition of 1 wt% rGO to LiFePO4/Li2SiO3 composite can enhance its electrochemical performance as a cathode material.

  12. Rate-dependent, Li-ion insertion/deinsertion behavior of LiFePO4 cathodes in commercial 18650 LiFePO4 cells.

    Science.gov (United States)

    Liu, Qi; He, Hao; Li, Zhe-Fei; Liu, Yadong; Ren, Yang; Lu, Wenquan; Lu, Jun; Stach, Eric A; Xie, Jian

    2014-03-12

    We have performed operando synchrotron high-energy X-ray diffraction (XRD) to obtain nonintrusive, real-time monitoring of the dynamic chemical and structural changes in commercial 18650 LiFePO4/C cells under realistic cycling conditions. The results indicate a nonequilibrium lithium insertion and extraction in the LiFePO4 cathode, with neither the LiFePO4 phase nor the FePO4 phase maintaining a static composition during lithium insertion/extraction. On the basis of our observations, we propose that the LiFePO4 cathode simultaneously experiences both a two-phase reaction mechanism and a dual-phase solid-solution reaction mechanism over the entire range of the flat voltage plateau, with this dual-phase solid-solution behavior being strongly dependent on charge/discharge rates. The proposed dual-phase solid-solution mechanism may explain the remarkable rate capability of LiFePO4 in commercial cells.

  13. Gamow shell model description of radiative capture reactions $^6$Li$(p,\\gamma)$$^7$Be and $^6$Li$(n,\\gamma)$$^7$Li

    CERN Document Server

    Dong, G X; Fossez, K; Płoszajczak, M; Jaganathen, Y; Betan, R M Id

    2016-01-01

    According to standard stellar evolution, lithium abundance is believed to be a useful indicator of the stellar age. However, many evolved stars like red giants show huge fluctuations around expected theoretical abundances that are not yet fully understood. The better knowledge of nuclear reactions that contribute to the creation and destruction of lithium can help to solve this puzzle. In this work we apply the Gamow shell model (GSM) formulated in the coupled-channel representation (GSM-CC) to investigate the mirror radiative capture reactions $^6$Li$(p,\\gamma)$$^7$Be and $^6$Li$(n,\\gamma)$$^7$Li. The cross-sections are calculated using a translationally invariant Hamiltonian with the finite-range interaction which is adjusted to reproduce spectra, binding energies and one-nucleon separation energies in $^{6-7}$Li, $^7$Be. All relevant $E1$, $M1$, and $E2$ transitions from the initial continuum states to the final bound states $J={3/2}_1^-$ and $J={1/2}^-$ of $^7$Li and $^7$Be are included. We demonstrate th...

  14. Emergence of Metallic Properties at LiFePO4 Surfaces and LiFePO4/Li2S Interfaces: An Ab Initio Study.

    Science.gov (United States)

    Timoshevskii, Vladimir; Feng, Zimin; Bevan, Kirk H; Zaghib, Karim

    2015-08-26

    The atomic and electronic structures of the LiFePO4 (LFP) surface, both bare and reconstructed upon possible oxygenation, are theoretically studied by ab initio methods. On the basis of total energy calculations, the atomic structure of the oxygenated surface is proposed, and the effect of surface reconstruction on the electronic properties of the surface is clarified. While bare LFP(010) surface is insulating, adsorption of oxygen leads to the emergence of semimetallic behavior by inducing the conducting states in the band gap of the system. The physical origin of these conducting states is investigated. We further demonstrate that deposition of Li2S layers on top of oxygenated LFP(010) surface leads to the formation of additional conducting hole states in the first layer of Li2S surface because of the charge transfer from sulfur p-states to the gap states of LFP surface. This demonstrates that oxygenated LFP surface not only provides conducting layers itself, but also induces conducting channels in the top layer of Li2S. These results help to achieve further understanding of potential role of LFP particles in improving the performance of Li-S batteries through emergent interface conductivity.

  15. Elevation - LiDAR Survey Minnehaha Creek, MN Watershed

    Data.gov (United States)

    Army Corps of Engineers, Department of the Army, Department of Defense — LiDAR Bare-Earth Grid - Minnehaha Creek Watershed District. The Minnehaha Creek watershed is located primarily in Hennepin County, Minnesota. The watershed covers...

  16. 2009 PSLC-USGS Topographic LiDAR: Wenatchee

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) collected Light Detection and Ranging (LiDAR) data of the Wenatchee USGS area of interest (AOI) east of Wenatchee, WA on May 1nd - May...

  17. Safe Li-ion polymer batteries for HEV applications

    Science.gov (United States)

    Zaghib, K.; Charest, P.; Guerfi, A.; Shim, J.; Perrier, M.; Striebel, K.

    The performance of natural graphite/PEO-based gel electrolyte/LiFePO 4 cells (5 mAh, 4 cm 2) is reported. The gel polymer electrolytes were produced by electron-beam irradiation and then soaked in a liquid electrolyte. The natural graphite anode in gel electrolyte containing lithium bis(fluorosulfonyl)imide (LiFSI)-EC + PC + DMC exhibited high reversible capacity (360 mAh/g) and high coulombic efficiency (91.6%). The LiFePO 4 cathode in the same gel polymer exhibited a reversible capacity of 160 mAh/g and 92% coulombic efficiency. Better performance was obtained at high-rate discharge with 6% carbon additive (carbon and graphite) in the cathode. The Li-ion gel polymer battery shows a very low capacity fade of 1% after 100 cycles.

  18. 18650型Li4Ti5O12/LiCoO2电池失效模式分析%Degradation diagnosis of 18650 type Li4Ti5O12/LiCoO2 battery

    Institute of Scientific and Technical Information of China (English)

    2016-01-01

    采用参比电极确定18650型钛酸锂(Li4Ti5O12)/钴酸锂(LiCoO2)电池在45℃下循环失效后的限容电极,对限容电极进行形貌、结构、交流阻抗及循环伏安等分析.电池失效后,充放电限容电极均为LiCoO2正极;该电极失效的主要原因是活性物质结构被破坏,LiCoO2的晶粒细化且内部微观应变较大,导致极片的界面性能下降及嵌脱锂动力学严重降低.

  19. LiAISON: Linked, Autonomous Interplanetary Satellite Orbit Navigation Project

    Data.gov (United States)

    National Aeronautics and Space Administration — A new navigation technique known as LiAISON (Linked Autonomous Interplanetary Satellite Orbit Navigation) may be used to propel the benefits of GPS to new orbits,...

  20. Ainult kaks küsimust / Kaarel Väli

    Index Scriptorium Estoniae

    Väli, Kaarel

    2011-01-01

    Tallinnas toimunud 5. rahvusvahelise laste ja noorte moeteatrite festivali „Max Moda 2011" žürii liige Kaarel Väli põhjustest, miks osutus parimaks Moskva moeteater, Eesti võistlejate esinemisest

  1. LiDAR (Terrain), THURSTON COUNTY, WASHINGTON, USA

    Data.gov (United States)

    Federal Emergency Management Agency, Department of Homeland Security — Fugro EarthData Company furnished the collection, processing, and development of LiDAR for 825 square miles in Washington (805 square miles of Thurston County and 20...

  2. Automatic registration method for mobile LiDAR data

    Science.gov (United States)

    Wang, Ruisheng; Ferrie, Frank P.

    2015-01-01

    We present an automatic mutual information (MI) registration method for mobile LiDAR and panoramas collected from a driving vehicle. The suitability of MI for registration of aerial LiDAR and aerial oblique images has been demonstrated under an assumption that minimization of joint entropy (JE) is a sufficient approximation of maximization of MI. We show that this assumption is invalid for the ground-level data. The entropy of a LiDAR image cannot be regarded as approximately constant for small perturbations. Instead of minimizing the JE, we directly maximize MI to estimate corrections of camera poses. Our method automatically registers mobile LiDAR with spherical panoramas over an approximate 4-km drive, and is the first example we are aware of that tests MI registration in a large-scale context.

  3. Crystal structure of Li3Ga(BO32

    Directory of Open Access Journals (Sweden)

    Robert W. Smith

    2017-03-01

    Full Text Available The crystal structure of trilithium gallium bis(orthoborate, Li3Ga(BO32, is isotypic with Li3Al(BO32 in a triclinic cell in space-group type P-1. The three Li and the unique Ga atom are coordinated by four O atoms each in tetrahedra, and the two B atoms are coordinated by three O atoms in orthoborate triangles. Chains with composition [Ga2(BO34]6− extend along the a axis. The Li atoms interleave these chains in tetrahedral interstices. A comparison is made between the structure model of the title compound and that of a previously reported model for a compound with the same composition [Abdullaev & Mamedov (1972. Zh. Strukt. Khim. 13, 943–946.

  4. Characteristics of Li diffusion on silicene and zigzag nanoribbon

    Science.gov (United States)

    Yan-Hua, Guo; Jue-Xian, Cao; Bo, Xu

    2016-01-01

    We perform a density functional study on the adsorption and diffusion of Li atoms on silicene sheet and zigzag nanoribbons. Our results show that the diffusion energy barrier of Li adatoms on silicene sheet is 0.25 eV, which is much lower than on graphene and Si bulk. The diffusion barriers along the axis of zigzag silicene nanoribbon range from 0.1 to 0.25 eV due to an edge effect, while the diffusion energy barrier is about 0.5 eV for a Li adatom to enter into a silicene nanoribbon. Our calculations indicate that using silicene nanoribbons as anodes is favorable for a Li-ion battery. Project supported by the National Natural Science Foundation of China (Grant Nos. 11074212 and 11204123) and the Natural Science Foundation of Jiangsu province, China (Grant No. BK20130945).

  5. Three Typical Dermatological Cases Treated by Dr. Li Yueping

    Institute of Scientific and Technical Information of China (English)

    Xie Shaoqiong

    2005-01-01

    @@ Dr. Li Yueping has been engaged in dermatological clinic for more than 40 years, accumulating rich experience in treating dermatological diseases. The following is three typical cases she gave successful treatment.

  6. Radioactivity effects of Pb-17Li in fusion power reactors

    Energy Technology Data Exchange (ETDEWEB)

    Casini, G.; Rocco, P. (Commission of the European Communities, Joint Research Centre, Ispra (Italy)); Zucchetti, M. (Dipt. di Energetica, Politecnico Turin (Italy))

    1991-12-01

    Research on the eutectic Pb-17Li is part of the blanket studies carried out in Europe for fusion power reactors. The use of this breeder makes easier some safety problems as compared to the case of lithium as a consequence of the lower chemical reactivity of Pb-17Li. On the other hand, it increases the radioactivity problems due to the neutron activation of lead and impurities. This paper presents both short-term (accidents) and long-term (waste disposal and recycling) aspects of the Pb-17Li activation products. They include the production, mobilization, release and environmental impact. Concerning accidents, a particular attention is given to Po-210 and Hg-203. Questions related to waste management are also revised. The most attractive solution seems that of recycling the spent Pb-17Li. This will be possible about 20 y after removal from service. As an alternative to recycling, the breeder disposal as radioactive waste is discussed. (orig.).

  7. Coriolis Coupling Influence on the H+LiH Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Zhai, Hongsheng; Liu, Yufang [Henan Normal Univ., Xinxiang (China); Li, Wenliang [Key Laboratory at Universities of Education, Urumqi (China)

    2014-01-15

    We have reported the reaction probability, integral reaction cross section, and rate constant for the title system calculated with the aid of a time-dependent wave packet approach. The ab initio potential energy surface (PES) of Prudente et al. (Chem. Phys. Lett. 2009, 474, 18) is employed for the purpose. The calculations are carried out over the collision energy range of 0.05-1.4 eV for the two reaction channels of H + LiH → Li + H{sub 2} and H{sub b} + LiH{sub a} → LiH{sub b} + H{sub a}. The Coriolis coupling (CC) effect are taken into account. The importance of including the Coriolis coupling quantum scattering calculations are revealed by the comparison between the Coriolis coupling and the centrifugal sudden (CS) approximation calculations.

  8. Dynamic and kinetic properties of Al-Li melts

    Science.gov (United States)

    Kiselev, A. I.

    2008-12-01

    The dynamic and kinetic properties of Al-Li melts are calculated. The liquid phase of this system is shown to be characterized by three states with different ion distributions and different degrees of electron localization.

  9. Anisotropic lithium ion migration in LiFePO4

    Science.gov (United States)

    Park, S. B.; Park, C. K.; Hwang, J. T.; Cho, W. I.; Jang, H.

    2011-12-01

    An anisotropic behavior of lithium ion migration in LiFePO4 is investigated using the cathode particles after chemical delithiation. A phase contrast of a LiFePO4 particle validating the directional property is also found. It suggests that the lithium ion migration path is limited to the [010] direction and the phase boundary between LiFePO4 and FePO4 is perpendicular [010]. The symmetric phase boundary inside the LiFePO4 particle is contrary to the non-directional core-shell model reported by others. The molecular dynamics simulation confirms the crystallographic direction with the lowest energy for lithium ion migration.

  10. 2009 PSLC-USGS Topographic LiDAR: Wenatchee

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) collected Light Detection and Ranging (LiDAR) data of the Wenatchee USGS area of interest (AOI) east of Wenatchee, WA on May 1nd ? May...

  11. Li Ning to Sell 25% Stake to Viva

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    The founder of Li Ning Co Ltd plans to sell a 25% stake in China's best-known sportswear group to his talent management firm Viva China Holdings Ltd for $175 million as he attempts to turnaround the business.

  12. Electrolytes and Interphasial Chemistry in Li Ion Devices

    Directory of Open Access Journals (Sweden)

    Kang Xu

    2010-01-01

    Full Text Available Since its appearance in 1991, the Li ion battery has been the major power source driving the rapid digitalization of our daily life; however, much of the processes and mechanisms underpinning this newest battery chemistry remains poorly understood. As in any electrochemical device, the major challenge comes from the electrolyte/electrode interfaces, where the discontinuity in charge distribution and extreme disequality in electric forces induce diversified processes that eventually determine the kinetics of Li+ intercalation chemistry. This article will summarize the most recent efforts on the fundamental understanding of the interphases in Li ion devices. Emphasis will be placed on the formation chemistry of the so-called “SEI” on graphitic anode, the effect of solvation sheath structure of Li+ on the intercalation energy barrier, and the feasibility of tailoring a desired interphase. Biologically inspired approaches to an ideal interphase will also be briefly discussed.

  13. Hollow Nanostructured Anode Materials for Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Liu Jun

    2010-01-01

    Full Text Available Abstract Hollow nanostructured anode materials lie at the heart of research relating to Li-ion batteries, which require high capacity, high rate capability, and high safety. The higher capacity and higher rate capability for hollow nanostructured anode materials than that for the bulk counterparts can be attributed to their higher surface area, shorter path length for Li+ transport, and more freedom for volume change, which can reduce the overpotential and allow better reaction kinetics at the electrode surface. In this article, we review recent research activities on hollow nanostructured anode materials for Li-ion batteries, including carbon materials, metals, metal oxides, and their hybrid materials. The major goal of this review is to highlight some recent progresses in using these hollow nanomaterials as anode materials to develop Li-ion batteries with high capacity, high rate capability, and excellent cycling stability.

  14. Mechanochemical synthesis of Li-Mn-O spinels: positive electrode for lithium batteries

    Science.gov (United States)

    Soiron, S.; Rougier, A.; Aymard, L.; Tarascon, J.-M.

    Li-Mn-O oxides were synthesized by mechanochemistry from a stoichiometric mixture of Li 2O and MnO 2 using various grinding times (0grinding a value of 8.24 Å similar to stoichiometric LiMn 2O 4. As a matter of fact, after 8 h of milling, mechanosynthesized Li-Mn-O spinel-type oxide shows quasi-identical electrochemical performances as high temperature LiMn 2O 4 ground for 1 h.

  15. Molar conductivity calculation of Li-ion battery electrolyte based on mode coupling theory

    Science.gov (United States)

    Pu, Weihua; He, Xiangming; Lu, Jiufang; Jiang, Changyin; Wan, Chunrong

    2005-12-01

    A method is proposed to calculate molar conductivity based on mode coupling theory in which the ion transference number is introduced into the theory. The molar conductivities of LiPF6, LiClO4, LiBF4, LiAsF6 in PC (propylene carbonate) are calculated based on this method. The results fit well to the literature data. This presents a potential way to calculate the conductivities of Li-ion battery electrolytes.

  16. A Li-O2/CO2 battery.

    Science.gov (United States)

    Takechi, Kensuke; Shiga, Tohru; Asaoka, Takahiko

    2011-03-28

    A new gas-utilizing battery using mixed gas of O(2) and CO(2) was developed and proved its very high discharge capacity. The capacity reached three times as much as that of a non-aqueous Li-air (O(2)) battery. The unique point of the battery is expected to be the rapid consumption of superoxide anion radical by CO(2) as well as the slow filling property of the Li(2)CO(3) in the cathode.

  17. Shipborne LiDAR system for coastal change monitoring

    Science.gov (United States)

    Kim, chang hwan; Park, chang hong; Kim, hyun wook; hyuck Kim, won; Lee, myoung hoon; Park, hyeon yeong

    2016-04-01

    Coastal areas, used as human utilization areas like leisure space, medical care, ports and power plants, etc., are regions that are continuously changing and interconnected with oceans and land and the sea level has risen by about 8cm (1.9mm / yr) due to global warming from 1964 year to 2006 year in Korea. Coastal erosion due to sea-level rise has caused the problem of marine ecosystems and loss of tourism resources, etc. Regular monitoring of coastal erosion is essential at key locations with such volatility. But the survey method of land mobile LiDAR (light detection and ranging) system has much time consuming and many restrictions. For effective monitoring beach erosion, KIOST (Korea Institute of Ocean Science & Technology) has constructed a shipborne mobile LiDAR system. The shipborne mobile LiDAR system comprised a land mobile LiDAR (RIEGL LMS-420i), an INS (inertial navigation system, MAGUS Inertial+), a RTKGPS (LEICA GS15 GS25), and a fixed platform. The shipborne mobile LiDAR system is much more effective than a land mobile LiDAR system in the measuring of fore shore areas without shadow zone. Because the vessel with the shipborne mobile LiDAR system is continuously moved along the shoreline, it is possible to efficiently survey a large area in a relatively short time. Effective monitoring of the changes using the constructed shipborne mobile LiDAR system for seriously eroded coastal areas will be able to contribute to coastal erosion management and response.

  18. 11Li structural information from inclusive break-up measurements

    Directory of Open Access Journals (Sweden)

    Fernández-García J. P.

    2015-01-01

    Full Text Available Structure information of 11Li halo nucleus has been obtained from the inclusive break-up measurements of the 11Li+208Pb reactions at energies around the Coulomb barrier (Elab = 24.3 and 29.8 MeV. The effective break-up energy and the slope of B(E1 distribution close to the threshold have been extracted from the experimental data.

  19. {sup 8}Li + p reaction and the primordial nucleosynthesis

    Energy Technology Data Exchange (ETDEWEB)

    Mendes Junior, D.R.; Lepine-Szily, A.; Lichtenthaeler, Rubens; Guimaraes, Valdir; Faria, P.N. de; Barioni, Adriana; Camargo Junior, Orli; Pires, K.C.C.; Morcelle, Viviane; Morais, Maria Carmen; Candori, R. Pampa; Scarduelli, Valdir; Leistenschneider, Erick [Universidade de Sao Paulo (IF/USP), SP (Brazil). Inst. de Fisica. Dept. de Fisica Nuclear; Assuncao, Marlete [Universidade Federal de Sao Paulo (UNIFESP), SP (Brazil); Descouvemont, P. [Universite Libre de Bruxelles, Brussels (Belgium). Physique Theorique et Mathematique

    2011-07-01

    Full text: We present a direct measurement of the {sup 8}Li(p,{alpha}){sup 5}He cross section, using a radioactive {sup 8}Li beam impinging on target of CH{sub 2}. This target has a thickness of 6.8 mg/cm{sup 2}, that is thick enough to stop the {sup 8}Li beam in it. The {sup 8}Li beam was produced at the primary target by the reaction {sup 9}Be({sup 7}Li,{sup 8}Li){sup 8}Be and was focalized by the first superconductor solenoid of RIBRAS on a secondary CH{sub 2} target. The reaction products were measured with four silicon barrier detectors, mounted as {Delta}E-E telescopes, where the {Delta}E detectors were 20{mu}m thick and the E detectors were 1000 {mu}m thick. The measurements were performed between Ecm=0.2 and 2.5 MeV at several laboratory angles. They show a broad peak around 1.7 MeV where the cross-section is almost isotropic. At low energies the data show a clear evidence for an increase of the S-factor. This suggests the importance of subthreshold states in {sup 9}Be. An R-matrix analysis of the experimental data has been performed in order to derive spectroscopic information (such as energies, neutron and alpha widths) of some resonances and to extrapolate the data down to zero energy. This R-matrix fit is then used to determine the {sup 8}Li(p,{alpha}){sup 5}He reaction rate, which is compared to the {sup 8}Li({alpha},n){sup 11}B reaction rate. (author)

  20. Stipendiumirahastu ajalooüliõpilastele / Mati Graf

    Index Scriptorium Estoniae

    Graf, Mati, 1939-

    2002-01-01

    5.04.2002 allkirjastasid TPÜ rektor Mati Heidmets ja ajaloo õppetooli prof Mati Graf ning firma BALTECO üks omanikke Enn-Arno Sillari kokkuleppe stipendiumirahastu moodustamise kohta TPÜ ajaloo üliõpilastele. E.-A. Sillari poolt asutatud rahastu eesmärgiks on edendada ajaloouuringuid, makstes stipendiumi teadustöös silma paistnud üliõpilastele ja magistrantidele, ning katta nende teadustööga seotud kulutused

  1. Prof. Li Yueqing's Experience in Treating Male Infertility

    Institute of Scientific and Technical Information of China (English)

    Li Haisong

    2005-01-01

    @@ Prof. Li Yueqing (李曰庆), an expert in the Andriatry Department of Dongzhimen Hospital Affiliated to Beijing University of Traditional Chinese Medicine,has been engaged in medicine for 30 years, who has aprofound knowledge in TCM surgery, especially in treating andriatric diseases such as impotence,infertility, and prostatitis. The following is an introduction to Prof. Li's experience in treating male infertility.

  2. GLOBAL ENTREPRENEUR Li Ning: Gymnastic Prince, Business Giant September 5

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    @@ In 2004, Li Ning (李宁) made an auda-cious bid to become the official sports manufacturina sponsor of the 2008 Beijing Olympic Games. It ultimately lost out to Adidas. But Li Ning, founder of the self-named firm and former Olympic athlete, is not only able to perform breathtaking maneuvers on the performance mat; he is able to do so in the business arena as well.

  3. Activity on a Li-rich giant: DI Psc revisited

    CERN Document Server

    Kriskovics, Levente; Vida, Krisztián; Oláh, Katalin

    2013-01-01

    We present a new Doppler imaging study for the Li-rich single K-giant DI Psc. Surface temperature maps are reconstructed for two subsequent rotation cycles. From the time evolution of the spot distribution antisolar-type differential rotation pattern is revealed. We show marks of non-uniform Li-abundance as well. The possible connection between the current evolutionary phase of the star and its magnetic activity is briefly discussed.

  4. New Anode Material for Rechargeable Li-ION Cells

    Science.gov (United States)

    Huang, C. -K.; Smart, M.; Halpert, G.; Surampudi, S.; Wolfenstine, J.

    1995-01-01

    Carbon materials, such as graphite, cokes, pitch and PAN fibers, are being evaluated in lithium batteries as alternate anode materials with some degree of success. There is an effort to look for other non-carbon anode materials which have larger Li capacity, higher rate capability, smaller first charge capacity loss and better mechanical stability during cycling. A Li-Mg-Si material is evaluated.

  5. Õpetaja professionaalse rolli internaliseerimise hindamine õpetajakoolituse esmaõppe üliõpilaste hulgas / Äli Leijen, Katrin Kullasepp, Aivar Ots

    Index Scriptorium Estoniae

    Leijen, Äli

    2013-01-01

    Aineõpetaja magistriõppe üliõpilaste seas läbi viidud uurimusest, milles vaadeldakse, kuidas üliõpilased koordineerivad personaalset ja professionaalset mina-positsiooni erialaste ambivalentsete olukordade kontekstis

  6. Õpetaja professionaalse rolli internaliseerimise hindamine õpetajakoolituse esmaõppe üliõpilaste hulgas / Äli Leijen, Katrin Kullasepp, Aivar Ots

    Index Scriptorium Estoniae

    Leijen, Äli

    2013-01-01

    Aineõpetaja magistriõppe üliõpilaste seas läbi viidud uurimusest, milles vaadeldakse, kuidas üliõpilased koordineerivad personaalset ja professionaalset mina-positsiooni erialaste ambivalentsete olukordade kontekstis

  7. 2012-2013 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Hoh River Watershed, Washington (Deliveries 1 and 2)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data on the Hoh River watershed survey area for the Puget Sound LiDAR Consortium and...

  8. Georeferenced LiDAR 3D vine plantation map generation.

    Science.gov (United States)

    Llorens, Jordi; Gil, Emilio; Llop, Jordi; Queraltó, Meritxell

    2011-01-01

    The use of electronic devices for canopy characterization has recently been widely discussed. Among such devices, LiDAR sensors appear to be the most accurate and precise. Information obtained with LiDAR sensors during reading while driving a tractor along a crop row can be managed and transformed into canopy density maps by evaluating the frequency of LiDAR returns. This paper describes a proposed methodology to obtain a georeferenced canopy map by combining the information obtained with LiDAR with that generated using a GPS receiver installed on top of a tractor. Data regarding the velocity of LiDAR measurements and UTM coordinates of each measured point on the canopy were obtained by applying the proposed transformation process. The process allows overlap of the canopy density map generated with the image of the intended measured area using Google Earth(®), providing accurate information about the canopy distribution and/or location of damage along the rows. This methodology was applied and tested on different vine varieties and crop stages in two important vine production areas in Spain. The results indicate that the georeferenced information obtained with LiDAR sensors appears to be an interesting tool with the potential to improve crop management processes.

  9. A review of conduction phenomena in Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Park, Myounggu; Zhang, Xiangchun; Chung, Myoungdo; Less, Gregory B. [Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109 (United States); Sastry, Ann Marie [Department of Mechanical Engineering, University of Michigan, Ann Arbor, MI 48109 (United States); Department of Material Science and Engineering, University of Michigan, Ann Arbor, MI 48109 (United States); Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109 (United States)

    2010-12-15

    Conduction has been one of the main barriers to further improvements in Li-ion batteries and is expected to remain so for the foreseeable future. In an effort to gain a better understanding of the conduction phenomena in Li-ion batteries and enable breakthrough technologies, a comprehensive survey of conduction phenomena in all components of a Li-ion cell incorporating theoretical, experimental, and simulation studies, is presented here. Included are a survey of the fundamentals of electrical and ionic conduction theories; a survey of the critical results, issues and challenges with respect to ionic and electronic conduction in the cathode, anode and electrolyte; a review of the relationship between electrical and ionic conduction for three cathode materials: LiCoO{sub 2}, LiMn{sub 2}O{sub 4}, LiFePO{sub 4}; a discussion of phase change in graphitic anodes and how it relates to diffusivity and conductivity; and the key conduction issues with organic liquid, solid-state and ionic liquid electrolytes. (author)

  10. Nuclear Magnetic Resonance Imaging of Li-ion Battery

    Directory of Open Access Journals (Sweden)

    D. Ohno

    2010-12-01

    Full Text Available Nuclear magnetic resonance (NMR imaging has high sensitivity to proton (1H and lithium (7Li. It is a useful measurement for electrolyte in Li-ion battery. 1H NMR images of lithium ion battery which is composed of LiMn2O4 / LiClO4 + propylene carbonate (PC / Li-metal have been studied. 1H NMR images of electrolyte near cathode material (LiMn2O4 showed anomalous intensity distribution, which was quite inhomogeneous. From NMR images as a function of repetition time (TR, it was concluded that the anomalous intensity distribution was not due to change of relaxation time but an indirect (spatial para-magnetization effect from cathode material. The paramagnetization induced by high magnetic field distorts linearity of magnetic gradient field, leading to apparent intensity variance. This functional image is an easy diagnostic measurement for magnetization of cathode material, which allows the possibility to check uniformity of cathode material and change of magnetization under electrochemical process.

  11. Li mobility in fast ion conductors followed by NMR spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sanz, J.

    2010-07-01

    Structural features that enhance Li mobility in fast ion conductors with perovskite (Li{sub 3}xLa{sub 2}/3-xTiO{sub 3} series) and Nasicon structure (Li{sub 1}+xTi{sub 2}-xAl{sub x} (PO{sub 4}){sub 3} series) have been investigated. From the analysis of quadrupolar interactions, the local symmetry and exchange processes between structural sites occupied by lithium have been deduced to investigate local motions of lithium in conduction paths of analyzed compounds. The study of spin-lattice (T{sub 1}) and spin-spin (T{sub 2}) relaxation times made possible the analysis of the temperature dependence of Li residence times at structural sites. The comparison of these values with those deduced from conductivity (ac and dc-measurements) allowed the study of Li-motion mechanisms. The onset of long range motions requires the analysis of low frequency measurements (T{sub 2} relaxation and dc-conductivity). The non- Arrhenius behaviour, often observed in fast ion conductors, has been ascribed to order/disorder transitions. At increasing temperatures, Li motions become less correlated, producing the decrement of activation energy. In analyzed compounds, a direct measurement of diffusion coefficients has been obtained from NMR experiments performed with the pulse field gradient (PFG) technique. Finally, it is emphasized the importance of the vacancy percolation in conductivity processes. (Author)

  12. Georeferenced LiDAR 3D Vine Plantation Map Generation

    Directory of Open Access Journals (Sweden)

    Meritxell Queraltó

    2011-06-01

    Full Text Available The use of electronic devices for canopy characterization has recently been widely discussed. Among such devices, LiDAR sensors appear to be the most accurate and precise. Information obtained with LiDAR sensors during reading while driving a tractor along a crop row can be managed and transformed into canopy density maps by evaluating the frequency of LiDAR returns. This paper describes a proposed methodology to obtain a georeferenced canopy map by combining the information obtained with LiDAR with that generated using a GPS receiver installed on top of a tractor. Data regarding the velocity of LiDAR measurements and UTM coordinates of each measured point on the canopy were obtained by applying the proposed transformation process. The process allows overlap of the canopy density map generated with the image of the intended measured area using Google Earth®, providing accurate information about the canopy distribution and/or location of damage along the rows. This methodology was applied and tested on different vine varieties and crop stages in two important vine production areas in Spain. The results indicate that the georeferenced information obtained with LiDAR sensors appears to be an interesting tool with the potential to improve crop management processes.

  13. Ab initio evaluations of the He solubility in liquid Li

    Energy Technology Data Exchange (ETDEWEB)

    Sedano, Luis A. [EURATOM-CIEMAT Assoc., Materials for Fusion Program, Bd. 43 P0.04, Avda. Complutense 22, 28040 Madrid (Spain)]. E-mail: luis.sedano@ciemat.es; Hassanein, Ahmed [Argonne Nat. Lab, 9700 South Class Av., Argonne, IL (United States)]. E-mail: hassanein@anl.gov; Sanz, Javier [ETSII-UNED, c/Juan del Rosal, 12, 28040 Madrid (E) (Spain)]. E-mail: jsanz@ind.UNED.es

    2005-11-15

    Modified embedding atom methods (MEAM) are developed to have predictions of the partial molar heat of solution (-H{sub s}) by direct simulation of metal cohesion, He-metal and He-He interaction. Transitions from crystalline Li to configurations, having the liquid Li structure's factors (h-bar (q)), are simulated ab initio. Once h-bar (q) reproduced, He atoms are added, one by one, to the Li system. Parallel lines for each case, with slopes clearly independent on the number of He atoms in the system, are obtained for energy versus pressure at given temperatures. Average differences between two adjacent parallels at zero pressure, once kinetic energy of the system discounted, represents the energy gained by an He atom when added to the Li system, related to the solution energy -H{sub s}. The molar excess entropy of gas in solution (S-bar {sub l}{sup ex}) is previously evaluated following diverse fundamental approaches: a 'thermodynamic liquid-hole' (TL-H) model for alkali liquids and a statistical-mechanics (Neff and McQuarrie's) model (SMM). Between 600 and 900 deg. C, a typical range of interest for the use of Li in fusion technology, the computed values for the (He) Henry's constant in Li range from 8x10{sup -14} to 10{sup -13} at. fr. Pa{sup -1}.

  14. Te/C nanocomposites for Li-Te Secondary Batteries.

    Science.gov (United States)

    Seo, Jeong-Uk; Seong, Gun-Kyu; Park, Cheol-Min

    2015-01-22

    New battery systems having high energy density are actively being researched in order to satisfy the rapidly developing market for longer-lasting mobile electronics and hybrid electric vehicles. Here, we report a new Li-Te secondary battery system with a redox potential of ~1.7 V (vs. Li(+)/Li) adapted on a Li metal anode and an advanced Te/C nanocomposite cathode. Using a simple concept of transforming TeO2 into nanocrystalline Te by mechanical reduction, we designed an advanced, mechanically reduced Te/C nanocomposite electrode material with high energy density (initial discharge/charge: 1088/740 mA h cm(-3)), excellent cyclability (ca. 705 mA h cm(-3) over 100 cycles), and fast rate capability (ca. 550 mA h cm(-3) at 5C rate). The mechanically reduced Te/C nanocomposite electrodes were found to be suitable for use as either the cathode in Li-Te secondary batteries or a high-potential anode in rechargeable Li-ion batteries. We firmly believe that the mechanically reduced Te/C nanocomposite constitutes a breakthrough for the realization and mass production of excellent energy storage systems.

  15. The Introduction of a Domestic Airborne LiDAR System SW-LiDAR%国产SW-LiDAR系统的简介

    Institute of Scientific and Technical Information of China (English)

    李志杰; 施昆; 关艳玲; 蒋凤保

    2013-01-01

    This paper introduced the structure, characteristics of a domestic airborne LiDAR systems SW-LiDAR and USES. This paper also provided highlights of inertial navigation principle, the principle of differential GPS and conformation equation, which is integrate theory. The workflow was introduced. Finally, the development trend of the system were prospected.%本文介绍国产机载SW-LiDAR系统的构成、特点和用途。重点阐述了该系统的三个集成原理:惯性导航原理、差分GPS原理和构象方程。介绍了该系统的工作流程。最后展望了该系统的应用前景。

  16. Mg2Si As Li-Intercalation Host For Li Cells

    Science.gov (United States)

    Huang, Chen-Kuo; Surampudi, Subbarao; Attia, Alan; Halpert, Gerald

    1993-01-01

    Compound Mg2Si shows promise as lithium-intercalation host for ambient-temperature rechargeable lithium electrochemical cells. As anode reactant material, LiXMg2Si chemically stable in presence of organic electrolyte used in such cells and stores large amounts of lithium. Intercalation reactions highly reversible at room temperature. Also retains sufficient mechanical strength during charge/discharge cycling. Lithium cells containing LixMg2Si anodes prove useful in spacecraft, military, communications, automotive, and other applications in which high energy-storage densities of lithium cells in general and rechargeability of cells needed.

  17. 2001-2002 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Clallam County, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — TerraPoint surveyed and created this data for the Puget Sound LiDAR Consortium under contract with Clallam County. The data covers an area of approximately 524...

  18. 2012 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Chehalis River Watershed Area, Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WSI) collected Light Detection and Ranging (LiDAR) data for the Chehalis River Watershed study area on January 28th, February 2nd-7th,...

  19. 2006 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Eastern Washington and River Corridors

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) collected Light Detection and Ranging (LiDAR) data in eastern Washington, eastern Oregon, and southern Canada in October and November,...

  20. 2002 Puget Sound LiDAR Consortium (PSLC) Unclassified Topographic LiDAR: Puget Sound Lowlands Washington

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — TerraPoint surveyed and created this data for the Puget Sound LiDAR Consortium under contract. The area surveyed is approximately 730 square miles and covers the...

  1. Identity of Passive Film Formed on Aluminum in Li-ion BatteryElectrolytes with LiPF6

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Xueyuan; Devine, T.M.

    2006-09-01

    The passive film that forms on aluminum in 1:1 ethylene carbonate + ethylmethyl carbonate with 1.2M LiPF{sub 6} and 1:1 ethylene carbonate + dimethyl carbonate with 1.0M LiPF{sub 6} was investigated by a combination of electrochemical quartz crystal microbalance measurements (EQCM), electrochemical impedance spectroscopy (EIS), and x-ray photoelectron spectroscopy. During anodic polarization of aluminum a film of AlF{sub 3} forms on top of the air-formed oxide, creating a duplex, or two-layered film. The thickness of the AlF{sub 3} increases with the applied potential. Independent measurements of film thickness by EQCM and EIS indicate that at a potential of 5.5V vs. Li/Li{sup +}, the thickness of the AlF{sub 3} is approximately 1 nm.

  2. Controllable synthesis, morphology evolution and electrochemical properties of LiFePO4 cathode materials for Li-ion batteries.

    Science.gov (United States)

    Song, Jianjun; Wang, Lin; Shao, Guangjie; Shi, Meiwu; Ma, Zhipeng; Wang, Guiling; Song, Wei; Liu, Shuang; Wang, Caixia

    2014-05-07

    Monodispersed LiFePO4 nanocrystals with diverse morphologies were successfully synthesized via a mild and controllable solvothermal approach with a mixture of ethylene glycol and oleic acid as the solvent. Morphology evolution of LiFePO4 nanoparticles from nanoplates to nanorods can be simply realized by varying the volume ratio of oleic acid to ethylene glycol. Moreover, the mechanism of competitive adsorption between ethylene glycol and oleic acid was proposed for the formation of different morphologies. Electrochemical measurements show that the LiFePO4/C nanorods have an initial discharge capacity of 155 mA h g(-1) at 0.5 C with a capacity retention of 80% at a high rate of 5 C, which confirms that LiFePO4/C nanorods exhibit excellent rate capability and cycling stability.

  3. Surface Modification of LiMn2O4 for Lithium Batteries by Nanostructured LiFePO4 Phosphate

    Directory of Open Access Journals (Sweden)

    B. Sadeghi

    2012-01-01

    Full Text Available LiMn2O4 spinel cathode materials have been successfully synthesized by solid-state reaction. Surface of these particles was modified by nanostructured LiFePO4 via sol gel dip coating method. Synthesized products were characterized by thermally analyzed thermogravimetric and differential thermal analysis (TG/DTA, X-ray diffraction (XRD, scanning electron microscopy (SEM, transmission electron microscopy (TEM, and energy dispersive X-ray spectroscopy (EDX. The results of electrochemical tests showed that the charge/discharge capacities improved and charge retention of battery enhanced. This improved electrochemical performance is caused by LiFePO4 phosphate layer on surfaces of LiMn2O4 cathode particles.

  4. Single-crystalline LiFePO4 nanosheets for high-rate Li-ion batteries.

    Science.gov (United States)

    Zhao, Yu; Peng, Lele; Liu, Borui; Yu, Guihua

    2014-05-14

    The lithiation/delithiation in LiFePO4 is highly anisotropic with lithium-ion diffusion being mainly confined to channels along the b-axis. Controlling the orientation of LiFePO4 crystals therefore plays an important role for efficient mass transport within this material. We report here the preparation of single crystalline LiFePO4 nanosheets with a large percentage of highly oriented {010} facets, which provide the highest pore density for lithium-ion insertion/extraction. The LiFePO4 nanosheets show a high specific capacity at low charge/discharge rates and retain significant capacities at high C-rates, which may benefit the development of lithium batteries with both favorable energy and power density.

  5. Structural phase transition and Li-ion diffusion in Li7La3Zr2O12

    Science.gov (United States)

    Hoang, Khang; Bernstein, Noam; Johannes, Michelle

    2013-03-01

    Garnet-type Li7La3Zr2O12 (LLZO) is a promising candidate for solid electrolytes in Li-ion battery applications because of its high ionic conductivity and electrochemical and chemical stability. The material has a low-conductivity tetragonal phase and a high-conductivity cubic phase. It has been reported that the cubic phase can be stabilized at ambient conditions, usually with the incorporation of a certain amount of supervalent impurities. In this talk, we present results from density-functional theory and variable cell shape molecular dynamics simulations, and discuss the origin of structural phase transition, effects of extrinsic impurities, and diffusion of Li ions in LLZO. By identifying relevant mechanisms and critical concentrations of the impurities (Li vacancies) for achieving the high-conductivity phase, this work shows how controlled synthesis could be used to improve the material's electrolytic performance.

  6. 2007 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Eastern Washington and River Corridors

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) collected Light Detection and Ranging (LiDAR) data in eastern Washington, eastern Oregon, and southern Canada in October and November,...

  7. Muusikaüliõpilaste refleksiooni toetamine pilliõppes / Tuulike Kivestu, Äli Leijen, Kadri Steinbach

    Index Scriptorium Estoniae

    Kivestu, Tuulike

    2014-01-01

    Uurimusest, mille eesmärgiks oli selgitada välja, millised on üliõpilaste kogemused refleksioonimudeli rakendamisel ja nende hinnangud refleksiooniülesannete kasulikkusele pillimängu oskuste arendamisel

  8. 2007 Puget Sound LiDAR Consortium (PSLC) Topographic LiDAR: Eastern Washington and River Corridors

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Watershed Sciences, Inc. (WS) collected Light Detection and Ranging (LiDAR) data in eastern Washington, eastern Oregon, and southern Canada in October and November,...

  9. Monoclinic β-Li2TiO3: Neutron diffraction study and estimation of Li diffusion pathways

    Science.gov (United States)

    Monchak, M.; Dolotko, O.; Mühlbauer, M. J.; Baran, V.; Senyshyn, A.; Ehrenberg, H.

    2016-11-01

    A neutron powder diffraction study on lithium titanate Li2TiO3 was performed at low temperatures. The monoclinic β-phase has been found to be stable over the whole investigated range of temperatures (4 K-300 K). A smooth and nonlinear increase of the lattice parameters has been observed upon heating and correlated to the behavior of interatomic distances. Lithium diffusion pathways in Li2TiO3 were estimated theoretically on the basis of the obtained structural data using bond-valence modeling. Experimentally diffusion pathways were evaluated by analysis of the negative nuclear scattering densities at 1073 K, which were reconstructed using a maximum entropy method. Although the bond-valence mismatch map indicated a possible Li diffusion either in ab plane or along c direction, analysis of the experimental data revealed that Li migration is thermodynamically less feasible in latter case.

  10. Are lithium niobate (LiNbO3) and lithium tantalate (LiTaO3) ferroelectrics bioactive?

    Science.gov (United States)

    Vilarinho, Paula Maria; Barroca, Nathalie; Zlotnik, Sebastian; Félix, Pedro; Fernandes, Maria Helena

    2014-06-01

    The use of functional materials, such as ferroelectrics, as platforms for tissue growth in situ or ex situ, is new and holds great promise. But the usage of materials in any bioapplication requires information on biocompatibility and desirably on bioactive behavior when bone tissue engineering is envisaged. Both requirements are currently unknown for many ferroelectrics. Herein the bioactivity of LiNbO3 and LiTaO3 is reported. The formation of apatite-like structures on the surface of LiNbO3 and LiTaO3 powders after immersion in simulated body fluid (SBF) for different soaking periods indicates their bioactive potential. The mechanism of apatite formation is suggested. In addition, the significant release of lithium ions from the ferroelectric powders in the very first minutes of soaking in SBF is examined and ways to overcome this likely hurdle addressed.

  11. THE HIGH TEMPERATURE CHEMICAL REACTIVITY OF LI2O

    Energy Technology Data Exchange (ETDEWEB)

    Kessinger, G.; Missimer, D.

    2009-11-13

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

  12. Electrochemical Codeposition of Al-Li-Mg Alloys at Solid Aluminum Electrode from LiCl-KCl-MgCl2 Molten Salt System

    Science.gov (United States)

    Ye, Ke; Zhang, Mi Lin; Chen, Ye; Han, Wei; de Yan, Yong; Cao, Peng

    2010-06-01

    The electrochemical codeposition of Mg and Li at an aluminium electrode in LiCl-KCl (50:50 wt pct) melts containing different concentrations of MgCl2 at 893 K (620 °C) to form Al-Li-Mg alloys was investigated. Cyclic voltammograms showed that the potential of Li metal deposition at an Al electrode, before the addition of MgCl2, is more positive than that of Li metal deposition at an Mo electrode, which indicated the formation of an Al-Li alloy. The underpotential deposition of magnesium at an aluminium electrode leads to the formation of Al-Mg alloys, and the succeeding underpotential deposition of lithium on predeposited Al-Mg alloys leads to the formation of Al-Li-Mg alloys. Chronopotentiometric measurements indicated that the codeposition of Mg and Li occurs at current densities lower than -0.668 A cm-2 in LiCl-KCl-MgCl2 (8 wt pct) melts at an aluminium electrode. The chronoamperometric studies indicated that the onset potential for the codeposition of Mg and Li is -2.000 V, and the codeposition of Mg and Li at an aluminium electrode is formed into Al-Li-Mg alloys when the applied potentials are more negative than -2.000 V. X-ray diffraction and inductively coupled plasma analysis indicated that Al-Li-Mg alloys with different lithium and magnesium contents were prepared via potentiostatic and galvanostatic electrolysis. The microstructure of typical dual phases of the Al-Li-Mg alloy was characterized by an optical microscope and by scanning electron microscopy. The analysis of energy dispersive spectrometry showed that the elements of Al and Mg distribute homogeneously in the Al-Li-Mg alloy. The lithium and magnesium contents of Al-Li-Mg alloys can be controlled by MgCl2 concentrations and by electrolytic parameters.

  13. Toward garnet electrolyte–based Li metal batteries: An ultrathin, highly effective, artificial solid-state electrolyte/metallic Li interface

    Science.gov (United States)

    Fu, Kun (Kelvin); Gong, Yunhui; Liu, Boyang; Zhu, Yizhou; Xu, Shaomao; Yao, Yonggang; Luo, Wei; Wang, Chengwei; Lacey, Steven D.; Dai, Jiaqi; Chen, Yanan; Mo, Yifei; Wachsman, Eric; Hu, Liangbing

    2017-01-01

    Solid-state batteries are a promising option toward high energy and power densities due to the use of lithium (Li) metal as an anode. Among all solid electrolyte materials ranging from sulfides to oxides and oxynitrides, cubic garnet–type Li7La3Zr2O12 (LLZO) ceramic electrolytes are superior candidates because of their high ionic conductivity (10−3 to 10−4 S/cm) and good stability against Li metal. However, garnet solid electrolytes generally have poor contact with Li metal, which causes high resistance and uneven current distribution at the interface. To address this challenge, we demonstrate a strategy to engineer the garnet solid electrolyte and the Li metal interface by forming an intermediary Li-metal alloy, which changes the wettability of the garnet surface (lithiophobic to lithiophilic) and reduces the interface resistance by more than an order of magnitude: 950 ohm·cm2 for the pristine garnet/Li and 75 ohm·cm2 for the surface-engineered garnet/Li. Li7La2.75Ca0.25Zr1.75Nb0.25O12 (LLCZN) was selected as the solid-state electrolyte (SSE) in this work because of its low sintering temperature, stabilized cubic garnet phase, and high ionic conductivity. This low area-specific resistance enables a solid-state garnet SSE/Li metal configuration and promotes the development of a hybrid electrolyte system. The hybrid system uses the improved solid-state garnet SSE Li metal anode and a thin liquid electrolyte cathode interfacial layer. This work provides new ways to address the garnet SSE wetting issue against Li and get more stable cell performances based on the hybrid electrolyte system for Li-ion, Li-sulfur, and Li-oxygen batteries toward the next generation of Li metal batteries. PMID:28435874

  14. Toward garnet electrolyte-based Li metal batteries: An ultrathin, highly effective, artificial solid-state electrolyte/metallic Li interface.

    Science.gov (United States)

    Fu, Kun Kelvin; Gong, Yunhui; Liu, Boyang; Zhu, Yizhou; Xu, Shaomao; Yao, Yonggang; Luo, Wei; Wang, Chengwei; Lacey, Steven D; Dai, Jiaqi; Chen, Yanan; Mo, Yifei; Wachsman, Eric; Hu, Liangbing

    2017-04-01

    Solid-state batteries are a promising option toward high energy and power densities due to the use of lithium (Li) metal as an anode. Among all solid electrolyte materials ranging from sulfides to oxides and oxynitrides, cubic garnet-type Li7La3Zr2O12 (LLZO) ceramic electrolytes are superior candidates because of their high ionic conductivity (10(-3) to 10(-4) S/cm) and good stability against Li metal. However, garnet solid electrolytes generally have poor contact with Li metal, which causes high resistance and uneven current distribution at the interface. To address this challenge, we demonstrate a strategy to engineer the garnet solid electrolyte and the Li metal interface by forming an intermediary Li-metal alloy, which changes the wettability of the garnet surface (lithiophobic to lithiophilic) and reduces the interface resistance by more than an order of magnitude: 950 ohm·cm(2) for the pristine garnet/Li and 75 ohm·cm(2) for the surface-engineered garnet/Li. Li7La2.75Ca0.25Zr1.75Nb0.25O12 (LLCZN) was selected as the solid-state electrolyte (SSE) in this work because of its low sintering temperature, stabilized cubic garnet phase, and high ionic conductivity. This low area-specific resistance enables a solid-state garnet SSE/Li metal configuration and promotes the development of a hybrid electrolyte system. The hybrid system uses the improved solid-state garnet SSE Li metal anode and a thin liquid electrolyte cathode interfacial layer. This work provides new ways to address the garnet SSE wetting issue against Li and get more stable cell performances based on the hybrid electrolyte system for Li-ion, Li-sulfur, and Li-oxygen batteries toward the next generation of Li metal batteries.

  15. On the reduction of generalized polylogarithms to $\\text{Li}_n$ and $\\text{Li}_{2,2}$ and on the evaluation thereof

    CERN Document Server

    Frellesvig, Hjalte; Wever, Christopher

    2016-01-01

    We give expressions for all generalized polylogarithms up to weight four in terms of the functions log, $\\text{Li}_n$, and $\\text{Li}_{2,2}$, valid for arbitrary complex variables. Furthermore we provide algorithms for manipulation and numerical evaluation of $\\text{Li}_n$ and $\\text{Li}_{2,2}$, and add codes in Mathematica and C++ implementing the results. With these results we calculate a number of previously unknown integrals, which we add in App. C.

  16. Measuring the ratio of aqueous diffusion coefficients between 6Li +Cl - and 7Li +Cr - by osmometry

    Science.gov (United States)

    Fritz, Steven J.

    1992-10-01

    Osmotic equilibrium is a singular occurrence in the evolution of an osmotic cell because at this event the net solution flux is zero such that -J w · V¯w = J s · V¯s. At this juncture, the diffusion coefficient of the solute through the membrane (ω) equals the solute flux ( Js) divided by the osmotic pressure (ΔΠ). Because the solute permeability coefficient (ω) is related to the Fickian diffusion coefficient ( D) through the gas constant, temperature, and the membrane's thickness and tortuosity, the ratio of ω values for individual isotopic species equals the ratio of D values for the same isotopic components. A 0.9450 molal LiCl solution was placed within sealed dialysis tubing and osmoted against a kilogram of deionized water at 22°C. Osmotic equilibrium occurred at 164 ± 10 min. The ratio of ω6Li +Cl -/ω7Li +Cl - was measured to be 1.011 ± 0.003 - a value close to the square root of the mass ratio between 7LiCl and 6LiCl (= 1.012) as calculated by Graham's Law. The measured diffusion coefficient ratio was used to predict the degree of hyperfiltration-induced fractionation of Li isotopes as a function of membrane ideality. When a membrane's σ exceeds 0.95 (as is likely for low-porosity shales) the 6Li /7Li ratio on the high-pressure side of the membrane can theoretically vary by more than 0.0017.

  17. Investigation of gas concentration cell based on LiSiPO electrolyte and Li2CO3, Au electrode

    Institute of Scientific and Technical Information of China (English)

    ZHU YongMing; CHU WingFong; WEPPNER Werner

    2009-01-01

    Solid lithium ion conducting electrochemical cells using LiSiPO as solid electrolyte and Li2CO3 mixed with Au as electrodes were prepared and employed as chemical sensors for the detection of CO2 gas.The EMF of the cell depends on the concentration of CO2 in air according to the partial pressure de-pendence of Nernst's law in the investigated range from 100 to 2000 ppm over the temperature range from 473 K to 673 K.

  18. The Origin of Capacity Fade in the Li2MnO3·LiMO2 (M = Li, Ni, Co, Mn) Microsphere Positive Electrode: An Operando Neutron Diffraction and Transmission X-ray Microscopy Study.

    Science.gov (United States)

    Chen, Chih-Jung; Pang, Wei Kong; Mori, Tatsuhiro; Peterson, Vanessa K; Sharma, Neeraj; Lee, Po-Han; Wu, She-Huang; Wang, Chun-Chieh; Song, Yen-Fang; Liu, Ru-Shi

    2016-07-20

    The mechanism of capacity fade of the Li2MnO3·LiMO2 (M = Li, Ni, Co, Mn) composite positive electrode within a full cell was investigated using a combination of operando neutron powder diffraction and transmission X-ray microscopy methods, enabling the phase, crystallographic, and morphological evolution of the material during electrochemical cycling to be understood. The electrode was shown to initially consist of 73(1) wt % R3̅m LiMO2 with the remaining 27(1) wt % C2/m Li2MnO3 likely existing as an intergrowth. Cracking in the Li2MnO3·LiMO2 electrode particle under operando microscopy observation was revealed to be initiated by the solid-solution reaction of the LiMO2 phase on charge to 4.55 V vs Li(+)/Li and intensified during further charge to 4.7 V vs Li(+)/Li during the concurrent two-phase reaction of the LiMO2 phase, involving the largest lattice change of any phase, and oxygen evolution from the Li2MnO3 phase. Notably, significant healing of the generated cracks in the Li2MnO3·LiMO2 electrode particle occurred during subsequent lithiation on discharge, with this rehealing being principally associated with the solid-solution reaction of the LiMO2 phase. This work reveals that while it is the reduction of lattice size of electrode phases during charge that results in cracking of the Li2MnO3·LiMO2 electrode particle, with the extent of cracking correlated to the magnitude of the size change, crack healing is possible in the reverse solid-solution reaction occurring during discharge. Importantly, it is the phase separation during the two-phase reaction of the LiMO2 phase that prevents the complete healing of the electrode particle, leading to pulverization over extended cycling. This work points to the minimization of behavior leading to phase separation, such as two-phase and oxygen evolution, as a key strategy in preventing capacity fade of the electrode.

  19. Li Metal Anodes and Rechargeable Lithium Metal Batteries. Springer Series in Materials Science

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jiguang; Xu, Wu; Henderson, Wesley A.

    2017-01-03

    Lithium (Li) metal is an ideal anode material for rechargeable batteries. With the urgent need for the “next generation” rechargeable batteries, such as Li-S, Li-air batteries as well as rechargeable Li metal batteries using Li intercalation compounds as the cathode, the use of Li metal anode has attracted significant interests in recent years. Unfortunately, rechargeable batteries based on Li metal anode have not yet been commercialized mainly due to two barriers: one is the growth of Li dendrites and associated safety hazard, and another is the low Coulombic efficiency (CE) of Li cycling and associated early battery failure due to Li powdering and increasing cell impedance. To have a high CE, minimum side reactions between freshly/native deposited Li and electrolyte has to be minimized. These reactions are proportional to the chemical and electrochemical activity of native Li when they are in direct contact with surrounding electrolyte. They are also proportional to the surface area of deposited Li. This means that high CE of Li deposition/stripping always related to a low surface area Li deposition and suppressed Li dendrite growth. Therefore, the enhancement of CE is a more fundamental factors controlling long term, stable cycling of Li metal anode. In this book, we will first review the general models of the dendrite growth mechanism. The effect of SEI layer on the modeling of Li dendrite growth will also be discussed. Then we will discuss various instruments/tools that are critical for the investigation of Li dendrite growth. In the Chapter 3, various factors which affect CE of Li cycling and dendrite growth will be discussed together with an emphasize on enhancement of CE. Chapter 4 of the book will discuss the specific application of Li metal anode in several key rechargeable Li metal batteries, including Li-air batteries, Li-S batteries and Li metal batteries using intercalation compounds as cathode. At last, the perspective on the future development

  20. Evaluation of the relative thermoluminescence efficiency of LiF:Mg,Ti and LiF:Mg,Cu,P TL detectors to low-energy heavy ions

    DEFF Research Database (Denmark)

    Gieszczyk, W.; Bilski, P.; Olko, P.

    2013-01-01

    The most popular types of LiF-based thermoluminescent (TL) detectors, LiF:Mg,Ti (MTS-N) and LiF:Mg,Cu,P (MCP-N), have been investigated, with respect to their dose (fluence) response and relative TL efficiency to different ion species. The detectors were irradiated using the nitrogen, iron, krypt...

  1. Synthesis and electrochemical properties of nanocrystalline Li[Li1/3Ti5/3O4] by complex sol-gel method

    Institute of Scientific and Technical Information of China (English)

    杨建文; 钟晖; 钟海云; 戴艳阳; 李荐; 赵绚

    2004-01-01

    Li[Li1/3 Ti5/3 O4] spinel-framework structure material is a kind of great interest for negative electrodes in energy storage cell. The synthesis of nanocrystalline Li[Li1/3 Ti5/3 O4] by sol-gel method using inorganic compounds and citric acid is developed, and single phase powder is obtained above 700 ℃. The electrochemical performances of Li[Li1/3Ti5/3O4] cathodes in lithium cell are studied. Special capacities are 131 mA · h · g-1 at 0.5C rate and 154 mA · h · g-1 at 0.1C in cycle test. No passivation layer is formed on Li[Li1/3Ti5/3O4] anode in lithium ion battery, and it is much safer than lithium metal and carbonaceous anodes. Faradic impedance in the charged cell is remarkably higher than that in discharged state, which is caused by distinct conductivities of Li [ Li1/3 Ti5/3 O4 ] and Li2 [Li1/3 Ti5/3 O4 ].

  2. Characterization of Li4Ti5O12 and LiMn2O4 spinel materials treated with aqueous acidic solutions

    NARCIS (Netherlands)

    Simon, D.R.

    2007-01-01

    In this thesis an investigation of two spinel materials, Li4Ti5O12 and LiMn2O4 used for Li-ion battery applications is performed interms of formation and reactivity towards acidic solutions. Subsequent characterizations such as structural, magnetic, chemical, and electrochemical characterizations ar

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

    Science.gov (United States)

    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.

  4. Pebble fabrication of super advanced tritium breeders using a solid solution of Li2+xTiO3+y with Li2ZrO3

    Directory of Open Access Journals (Sweden)

    Tsuyoshi Hoshino

    2016-12-01

    Full Text Available Lithium titanate with excess lithium (Li2+xTiO3+y is one of the most promising candidates among advanced tritium breeders for demonstration power plant reactors because of its good tritium release characteristics. However, the tritium breeding ratio (TBR of Li2+xTiO3+y is smaller than that of e.g., Li2O or Li8TiO6 because of its lower Li density. Therefore, new Li-containing ceramic composites with both high stability and high Li density have been developed. Thus, this study focused on the development of a solid solution with a new characteristic. The solid-solution pebbles of Li2+xTiO3+y with Li2ZrO3 (Li2+x(Ti,ZrO3+y, designated as LTZO, were fabricated by an emulsion method. The X-ray diffraction patterns of sintered LTZO pebbles are approximately the same as those of Li2+xTiO3+y pebbles, and no peaks attributable to Li2ZrO3 are observed. These results demonstrate that LTZO pebbles are not a two-phase material but rather a solid solution. Furthermore, LTZO pebbles were easily sintered under air. Thus, the LTZO solid solution is a candidate breeder material for super advanced (SA tritium breeders.

  5. (p,px) reaction on /sup 6/Li and /sup 7/Li nuclei at incident proton energy of 70 MeV

    Energy Technology Data Exchange (ETDEWEB)

    Gorpinich, O.K.; Kadkin, E.P.; Kondrat' ev, S.N.; Lobach, Yu.M.; Pasechnik, M.V.; Saltykov, L.S.; Tokarevskij, V.V. (AN Ukrainskoj SSR, Kiev. Inst. Yadernykh Issledovanij)

    1983-01-01

    Measurements of two-dimensional coincidence spectra of charged particles from the /sup 6/Li(p, 2p)/sup 5/He, /sup 6/Li(p, p..cap alpha..)/sup 2/H, /sup 7/Li(p, pt)/sup 4/He, /sup 7/Li(p, p..cap alpha..)/sup 3/H reactions has been carried out using the equipment for simultaneous investigation of correlation of charged particles of different types. The /sup 6/Li(p, pd) reaction probability reaches the maximum value when the residual nucleus momentum is close to zero. This fact may confirm an existance of strong /sup 6/Li ..cap alpha..d-clusterization. The /sup 7/Li(p, pt) reaction occurs with the minimum probability in a quasi-free region that confirms /sup 7/Li ..cap alpha..t-structure. A direct comparison of particle two-dimensional spectra projections of (p, px) type reactions reveals that a probability of quasi-free scattering of proton on deuteron (triton) /sup 6/Li(/sup 7/Li) cluster is higher than quasi-free scattering on intranuclear protons. This fact is also confirmed by an assumption on ..cap alpha..d(..cap alpha..t)-cluster /sup 6/Li(/sup 7/Li) nucleus structure.

  6. Structural and Electrochemical Characterization of Pure LiFePO4 and Nanocomposite C-LiFePO4 Cathodes for Lithium Ion Rechargeable Batteries

    Directory of Open Access Journals (Sweden)

    Arun Kumar

    2009-01-01

    Full Text Available Pure lithium iron phosphate (LiFePO4 and carbon-coated LiFePO4 (C-LiFePO4 cathode materials were synthesized for Li-ion batteries. Structural and electrochemical properties of these materials were compared. X-ray diffraction revealed orthorhombic olivine structure. Micro-Raman scattering analysis indicates amorphous carbon, and TEM micrographs show carbon coating on LiFePO4 particles. Ex situ Raman spectrum of C-LiFePO4 at various stages of charging and discharging showed reversibility upon electrochemical cycling. The cyclic voltammograms of LiFePO4 and C-LiFePO4 showed only a pair of peaks corresponding to the anodic and cathodic reactions. The first discharge capacities were 63, 43, and 13 mAh/g for C/5, C/3, and C/2, respectively for LiFePO4 where as in case of C-LiFePO4 that were 163, 144, 118, and 70 mAh/g for C/5, C/3, C/2, and 1C, respectively. The capacity retention of pure LiFePO4 was 69% after 25 cycles where as that of C-LiFePO4 was around 97% after 50 cycles. These results indicate that the capacity and the rate capability improved significantly upon carbon coating.

  7. Preparation, structure, and electrochemistry of layered polyanionic hydroxysulfates: LiMSO4OH (M = Fe, Co, Mn) electrodes for Li-ion batteries.

    Science.gov (United States)

    Subban, Chinmayee V; Ati, Mohamed; Rousse, Gwenaëlle; Abakumov, Artem M; Van Tendeloo, Gustaaf; Janot, Raphaël; Tarascon, Jean-Marie

    2013-03-01

    The Li-ion rechargeable battery, due to its high energy density, has driven remarkable advances in portable electronics. Moving toward more sustainable electrodes could make this technology even more attractive to large-volume applications. We present here a new family of 3d-metal hydroxysulfates of general formula LiMSO4OH (M = Fe, Co, and Mn) among which (i) LiFeSO4OH reversibly releases 0.7 Li(+) at an average potential of 3.6 V vs Li(+)/Li(0), slightly higher than the potential of currently lauded LiFePO4 (3.45 V) electrode material, and (ii) LiCoSO4OH shows a redox activity at 4.7 V vs Li(+)/Li(0). Besides, these compounds can be easily made at temperatures near 200 °C via a synthesis process that enlists a new intermediate phase of composition M3(SO4)2(OH)2 (M = Fe, Co, Mn, and Ni), related to the mineral caminite. Structurally, we found that LiFeSO4OH is a layered phase unlike the previously reported 3.2 V tavorite LiFeSO4OH. This work should provide an impetus to experimentalists for designing better electrolytes to fully tap the capacity of high-voltage Co-based hydroxysulfates, and to theorists for providing a means to predict the electrochemical redox activity of two polymorphs.

  8. Polyethylene separator activated by hybrid coating improving Li+ ion transference number and ionic conductivity for Li-metal battery

    Science.gov (United States)

    Mao, Xufeng; Shi, Liyi; Zhang, Haijiao; Wang, Zhuyi; Zhu, Jiefang; Qiu, Zhengfu; Zhao, Yin; Zhang, Meihong; Yuan, Shuai

    2017-02-01

    Low Li+ ion transference number is one fatal defect of the liquid LiPF6 electrolyte for Li-metal anode based batteries. This work aims to improve Li+ ion transference number and ionic conductivity polyethylene (PE) separators. By a simple dip-coating method, the water-borne nanosized molecular sieve with 3D porous structure (ZSM-5) can be coated on PE separators. Especially, the Li+ ion transference number is greatly enhanced from 0.28 to 0.44, which should be attributed to the specific pore structure and channel environment of ZSM-5 as well as the interaction between ZSM-5 and electrolyte. Compared with the pristine PE separator, the ionic conductivity of modified separators is remarkably improved from 0.30 to 0.54 mS cm-1. As results, the C-rate capability and cycling stability are both improved. The Li-metal battery using the ZSM-5-modified PE separator keeps 94.2% capacity after 100 cycles. In contrast, the discharge capacity retention of the battery using pristine PE is only 74.7%.

  9. The Light Source Requirements of LiFi (Ⅱ)%LiFi的光源要求(下)

    Institute of Scientific and Technical Information of China (English)

    王伟; 陈超中

    2015-01-01

    从光源的选择、光源颜色和光源布局3个方面阐述了LiFi的光源要求.首先,通过分析LED载流子浓度对调制带宽的影响和激光二极管(LD)的调制带宽来比较PC-LED(荧光粉转换LED)、RGB-LED(红绿蓝LED)和LD作为LiFi光源的优缺点.其次,从光谱功率分布(SPD)模型和色漂键控(CSK)调节的角度阐述了LiFi光源的颜色质量.最后,对要同时满足照明和通信需求的LiFi光源室内布局进行了说明.随着对LiFi光源器件的持续深入研发,必定会给人类带来照明优质和通信良好的LiFi产品.

  10. The Light Source Requirements of LiFi (Ⅰ)%LiFi的光源要求(上)

    Institute of Scientific and Technical Information of China (English)

    王伟; 陈超中

    2015-01-01

    从光源的选择、光源颜色和光源布局3个方面阐述了LiFi的光源要求.首先,通过分析LED载流子浓度对调制带宽的影响和激光二极管(LD)的调制带宽来比较PC-LED(荧光粉转换LED)、RGB-LED(红绿蓝LED)和LD作为LiFi光源的优缺点.其次,从光谱功率分布(SPD)模型和色漂键控(CSK)调节的角度阐述了LiFi光源的颜色质量.最后,对要同时满足照明和通信需求的LiFi光源室内布局进行了说明.随着对LiFi光源器件的持续深入研发,必定会给人类带来照明优质和通信良好的LiFi产品.

  11. Relating the 3D electrode morphology to Li-ion battery performance; a case for LiFePO4

    Science.gov (United States)

    Liu, Zhao; Verhallen, Tomas W.; Singh, Deepak P.; Wang, Hongqian; Wagemaker, Marnix; Barnett, Scott

    2016-08-01

    One of the main goals in lithium ion battery electrode design is to increase the power density. This requires insight in the relation between the complex heterogeneous microstructure existing of active material, conductive additive and electrolyte providing the required electronic and Li-ion transport. FIB-SEM is used to determine the three phase 3D morphology, and Li-ion concentration profiles obtained with Neutron Depth Profiling (NDP) are compared for two cases, conventional LiFePO4 electrodes and better performing carbonate templated LiFePO4 electrodes. This provides detailed understanding of the impact of key parameters such as the tortuosity for electron and Li-ion transport though the electrodes. The created hierarchical pore network of the templated electrodes, containing micron sized pores, appears to be effective only at high rate charge where electrolyte depletion is hindering fast discharge. Surprisingly the carbonate templating method results in a better electronic conductive CB network, enhancing the activity of LiFePO4 near the electrolyte-electrode interface as directly observed with NDP, which in a large part is responsible for the improved rate performance both during charge and discharge. The results demonstrate that standard electrodes have a far from optimal charge transport network and that significantly improved electrode performance should be possible by engineering the microstructure.

  12. Electrochemical performance of carbon nanotube-modified LiFePO_4 cathodes for Li-ion batteries

    Institute of Scientific and Technical Information of China (English)

    陈召勇; 朱华丽; 朱伟; 张建利; 李奇峰

    2010-01-01

    Carbon nanotubes (CNTs) and acetylene black (AB) were dispersed synchronously or separately between LiFePO4 (LFP) particles as conducting agents during the course of manufacture of LiFePO4 cathodes. The morphology and electrochemical performances of as-prepared LiFePO4 were evaluated by means of transmission electron microscopy (TEM), charge-discharge test, electrochemical impedance spectroscope (EIS) and cyclic voltammetry (CV). CNTs contribute to the interconnection of the isolated LiFePO4 or carbon particles. For the CNTs-modified LiFePO4, it exhibits excellent performance in terms of both specific capacity and cycle life. The initial discharge capacity is 147.9 mA·h/g at 0.2C rate and 134.2 mA·h/g at 1C rate, keeping a capacity retention ratio of 97% after 50 cycles. The results from EIS indicate that the impedance value of the solid electrolyte interface decreases. The cyclic voltammetric peak profiles is more symmetric and spiculate and there are fewer peaks. CNTs are promising conductive additives candidate for high-power Li-ion batteries.

  13. Facile Solution Route to Synthesize Nanostructure Li4Ti5O12 for High Rate Li-Ion Battery

    Directory of Open Access Journals (Sweden)

    M. V. Tran

    2016-01-01

    Full Text Available High rate Li-ion batteries have been given great attention during the last decade as a power source for hybrid electric vehicles (HEVs, EVs, etc. due to the highest energy and power density. These lithium batteries required a new design of material structure as well as innovative electrode materials. Among the promising candidates, spinel Li4Ti5O12 has been proposed as a high rate anode to replace graphite anode because of high capacity and a negligible structure change during intercalation of lithium. In this work, we synthesized a spinel Li4Ti5O12 in nanosize by a solution route using LiOH and Ti(OBu4 as precursor. An evaluation of structure and morphology by XRD and SEM exhibited pure spinel phase Li4Ti5O12 and homogenous nanoparticles around 100 nm. In the charge-discharge test, nanospinel Li4Ti5O12 presents excellent discharge capacity 160 mAh/g at rate C/10, as well as good specific capacities of 120, 110, and 100 mAh/g at high rates C, 5C and 10C, respectively.

  14. ON INFRARED EXCESSES ASSOCIATED WITH Li-RICH K GIANTS

    Energy Technology Data Exchange (ETDEWEB)

    Rebull, Luisa M. [Spitzer Science Center (SSC) and Infrared Science Archive (IRSA), Infrared Processing and Analysis Center - IPAC, 1200 E. California Blvd., California Institute of Technology, Pasadena, CA 91125 (United States); Carlberg, Joleen K. [NASA Goddard Space Flight Center, Code 667, Greenbelt, MD 20771 (United States); Gibbs, John C.; Cashen, Sarah; Datta, Ashwin; Hodgson, Emily; Lince, Megan [Glencoe High School, 2700 NW Glencoe Rd., Hillsboro, OR 97124 (United States); Deeb, J. Elin [Bear Creek High School, 9800 W. Dartmouth Pl., Lakewood, CO 80227 (United States); Larsen, Estefania; Altepeter, Shailyn; Bucksbee, Ethan; Clarke, Matthew [Millard South High School, 14905 Q St., Omaha, NE 68137 (United States); Black, David V., E-mail: rebull@ipac.caltech.edu [Walden School of Liberal Arts, 4230 N. University Ave., Provo, UT 84604 (United States)

    2015-10-15

    Infrared (IR) excesses around K-type red giants (RGs) have previously been discovered using Infrared Astronomy Satellite (IRAS) data, and past studies have suggested a link between RGs with overabundant Li and IR excesses, implying the ejection of circumstellar shells or disks. We revisit the question of IR excesses around RGs using higher spatial resolution IR data, primarily from the Wide-field Infrared Survey Explorer. Our goal was to elucidate the link between three unusual RG properties: fast rotation, enriched Li, and IR excess. Our sample of RGs includes those with previous IR detections, a sample with well-defined rotation and Li abundance measurements with no previous IR measurements, and a large sample of RGs asserted to be Li-rich in the literature; we have 316 targets thought to be K giants, about 40% of which we take to be Li-rich. In 24 cases with previous detections of IR excess at low spatial resolution, we believe that source confusion is playing a role, in that either (a) the source that is bright in the optical is not responsible for the IR flux, or (b) there is more than one source responsible for the IR flux as measured in IRAS. We looked for IR excesses in the remaining sources, identifying 28 that have significant IR excesses by ∼20 μm (with possible excesses for 2 additional sources). There appears to be an intriguing correlation in that the largest IR excesses are all in Li-rich K giants, though very few Li-rich K giants have IR excesses (large or small). These largest IR excesses also tend to be found in the fastest rotators. There is no correlation of IR excess with the carbon isotopic ratio, {sup 12}C/{sup 13}C. IR excesses by 20 μm, though relatively rare, are at least twice as common among our sample of Li-rich K giants. If dust shell production is a common by-product of Li enrichment mechanisms, these observations suggest that the IR excess stage is very short-lived, which is supported by theoretical calculations. Conversely, the

  15. Research progress in cathode material Li2MSiO4 for Li-ion battery%锂离子电池正极材料Li2MSiO4的研究进展

    Institute of Scientific and Technical Information of China (English)

    兰建云; 赵敏寿

    2012-01-01

    The research status quo of structure and synthesizing methods of polyanionic cathode material Li2MSiO4( M = Fe, Mn, Co and Ni) for Li-ion battery was reviewed. The research of doping modification of Li2FeSiO4,Li2MnSiO4 and Li2CoSiO4 was summarized. The development trend of Li2MSiO4 was prospected.%综述了聚阴离子锂离子电池正极材料Li2MSiO4(M=Fe、Mn、Co及Ni)结构及合成方法的研究现状;对Li2FeSiO4、Li2MnSiO4和Li2CoSiO4掺杂改性的研究进行了综述;对Li2MSiO4的发展趋势进行了预测.

  16. Electrochemical Li Topotactic Reaction in Layered SnP3 for Superior Li-Ion Batteries

    Science.gov (United States)

    Park, Jae-Wan; Park, Cheol-Min

    2016-10-01

    The development of new anode materials having high electrochemical performances and interesting reaction mechanisms is highly required to satisfy the need for long-lasting mobile electronic devices and electric vehicles. Here, we report a layer crystalline structured SnP3 and its unique electrochemical behaviors with Li. The SnP3 was simply synthesized through modification of Sn crystallography by combination with P and its potential as an anode material for LIBs was investigated. During Li insertion reaction, the SnP3 anode showed an interesting two-step electrochemical reaction mechanism comprised of a topotactic transition (0.7–2.0 V) and a conversion (0.0–2.0 V) reaction. When the SnP3-based composite electrode was tested within the topotactic reaction region (0.7–2.0 V) between SnP3 and LixSnP3 (x ≤ 4), it showed excellent electrochemical properties, such as a high volumetric capacity (1st discharge/charge capacity was 840/663 mA h cm‑3) with a high initial coulombic efficiency, stable cycle behavior (636 mA h cm‑3 over 100 cycles), and fast rate capability (550 mA h cm‑3 at 3C). This layered SnP3 anode will be applicable to a new anode material for rechargeable LIBs.

  17. Systematics of the breakup probability function for {sup 6}Li and {sup 7}Li projectiles

    Energy Technology Data Exchange (ETDEWEB)

    Capurro, O.A., E-mail: capurro@tandar.cnea.gov.ar [Laboratorio TANDAR, Comisión Nacional de Energía Atómica, Av. General Paz 1499, B1650KNA San Martín, Buenos Aires (Argentina); Pacheco, A.J.; Arazi, A. [Laboratorio TANDAR, Comisión Nacional de Energía Atómica, Av. General Paz 1499, B1650KNA San Martín, Buenos Aires (Argentina); CONICET, Av. Rivadavia 1917, C1033AAJ Buenos Aires (Argentina); Carnelli, P.F.F. [CONICET, Av. Rivadavia 1917, C1033AAJ Buenos Aires (Argentina); Instituto de Investigación e Ingeniería Ambiental, Universidad Nacional de San Martín, 25 de Mayo y Francia, B1650BWA San Martín, Buenos Aires (Argentina); Fernández Niello, J.O. [Laboratorio TANDAR, Comisión Nacional de Energía Atómica, Av. General Paz 1499, B1650KNA San Martín, Buenos Aires (Argentina); CONICET, Av. Rivadavia 1917, C1033AAJ Buenos Aires (Argentina); Instituto de Investigación e Ingeniería Ambiental, Universidad Nacional de San Martín, 25 de Mayo y Francia, B1650BWA San Martín, Buenos Aires (Argentina); and others

    2016-01-15

    Experimental non-capture breakup cross sections can be used to determine the probability of projectile and ejectile fragmentation in nuclear reactions involving weakly bound nuclei. Recently, the probability of both type of dissociations has been analyzed in nuclear reactions involving {sup 9}Be projectiles onto various heavy targets at sub-barrier energies. In the present work we extend this kind of systematic analysis to the case of {sup 6}Li and {sup 7}Li projectiles with the purpose of investigating general features of projectile-like breakup probabilities for reactions induced by stable weakly bound nuclei. For that purpose we have obtained the probabilities of projectile and ejectile breakup for a large number of systems, starting from a compilation of the corresponding reported non-capture breakup cross sections. We parametrize the results in accordance with the previous studies for the case of beryllium projectiles, and we discuss their systematic behavior as a function of the projectile, the target mass and the reaction Q-value.

  18. Effect of Acupuncture Manipulations at LI4 or LI11 on Blood Flow and Skin Temperature.

    Science.gov (United States)

    Li, Weihui; Ahn, Andrew

    2016-06-01

    Acupuncture induces physiological changes, and patients have reported warm or cool sensations with "Burning Fire" (BF) or "Penetrating Cool" (PC) manipulations. This study aimed to evaluate whether these techniques had distinct effects on skin temperature and blood flow and to examine whether skin temperature correlated with blood flow. The participants were 25 healthy volunteers, each receiving acupuncture manipulations on points LI4 and LI11 bilaterally. Skin temperatures and blood flow were recorded continuously on both arms. The study found that acupuncture significantly increased skin temperature on the needling arm by 0.3514°C on average, but decreased it on the contralateral arm by 0.2201°C on average. Blood flow decreased significantly in both arms during needling (-3.4% and -5.97% for the ipsilateral and the contralateral sides, respectively), but the changes in skin temperature did not correlate with the changes in blood flow. Furthermore, these changes were not significantly different between acupuncture techniques and acupuncture points. In conclusion, acupuncture changes local skin temperature and blood flow independent of the manipulation technique. Moreover, blood flow may not be affected by the increased temperature on the needling arm. These results help to verify traditional Chinese medicine concepts and may help in establishing standards for acupuncture treatments.

  19. Unsupported claims of ultrafast charging of LiFePO 4 Li-ion batteries

    Science.gov (United States)

    Zaghib, K.; Goodenough, J. B.; Mauger, A.; Julien, C.

    Energy storage by batteries has become an issue of strategic importance. A scientific breakthrough in this context is the lithium-ion battery. Indeed, lithium-ion batteries can store up to three times more electricity and generate twice the power of nickel-metal-hydride batteries now in use, making possible great improvements in energy storage for electric vehicles and portable electronics. Major investments are being made for the commercial development of Li-ion batteries and there are government funds available offering billions in grants for research, development, and manufacturing. In this context, we wish to call attention to a deceptive paper that recently appeared in Nature [1], which has received much publicity since it announced an impossibly high recharging rate capability for a Li-ion battery of 9 s! Close examination of the work [1] shows that the authors have no direct evidence in support of such a high recharging rate, but imply their dramatic conclusion only from the high discharge rate. Experienced battery materials scientists would understand that the charge and discharge processes of batteries are basically asymmetric, resulting in rates of discharge that are generally much higher than rates suitable for recharge! The ability of a battery to be recharged in a few seconds, as the authors claim, would indeed be of great benefit, but this goal remains unmet despite the claims of Kang and Ceder [1] as we will explain herein.

  20. Solid state NMR investigation of a novel Li ion ceramic electrolyte. Li doped BPO sub 4

    CERN Document Server

    Dodd, A J

    2002-01-01

    Over the last decade lithium ion conducting batteries have emerged as the leading technology in battery materials. Their performance, however, is limited to applications below around 50 deg C by the liquid nature of the electrolytes used. In the quest for a solid state electrolyte for use in high temperature applications the nano-crystalline ceramic lithium doped boron phosphate material was developed. Solid state nuclear magnetic resonance (NMR) has been employed to investigate some of the fundamental properties of this material including ionic mobility, defect structure, sample purity and ionic distribution. The findings of this work show that when synthesised at a reaction temperature above 600 deg C the loss of boron from the structure results in the incorporation of vacancy sites about which the Li ions gather in small clusters. Multiple-pulse multiple-quantum spin counting techniques are employed in an effort to count the number of quadrupolar sup 7 Li nuclei interacting in a cluster though it is ultima...

  1. Electrochemical Li Topotactic Reaction in Layered SnP3 for Superior Li-Ion Batteries

    Science.gov (United States)

    Park, Jae-Wan; Park, Cheol-Min

    2016-01-01

    The development of new anode materials having high electrochemical performances and interesting reaction mechanisms is highly required to satisfy the need for long-lasting mobile electronic devices and electric vehicles. Here, we report a layer crystalline structured SnP3 and its unique electrochemical behaviors with Li. The SnP3 was simply synthesized through modification of Sn crystallography by combination with P and its potential as an anode material for LIBs was investigated. During Li insertion reaction, the SnP3 anode showed an interesting two-step electrochemical reaction mechanism comprised of a topotactic transition (0.7–2.0 V) and a conversion (0.0–2.0 V) reaction. When the SnP3-based composite electrode was tested within the topotactic reaction region (0.7–2.0 V) between SnP3 and LixSnP3 (x ≤ 4), it showed excellent electrochemical properties, such as a high volumetric capacity (1st discharge/charge capacity was 840/663 mA h cm−3) with a high initial coulombic efficiency, stable cycle behavior (636 mA h cm−3 over 100 cycles), and fast rate capability (550 mA h cm−3 at 3C). This layered SnP3 anode will be applicable to a new anode material for rechargeable LIBs. PMID:27775090

  2. Effect of Cr doping on structure of LiMnO2

    Institute of Scientific and Technical Information of China (English)

    谷亦杰; 周恒辉; 陈继涛; 常文保

    2003-01-01

    The monoclinic and orthorhombic ordered-rocksalt polymorphs of LiMnO2 are of interest as high-capacity cathode materials for rechargeable Li batteries. LiMnO2 and LiMn1-xCrxO2 were prepared by a high temperature solid-state route. In comparison with undoping Cr orthorhombic LiMnO2, monoclinic LiMnO2 was preserved with Cr doping. The volume of m-LiMnO2 decreasing with increasing Cr confirms that the length of bond around Cr ion decreases with Mn substituted by Cr ion. A phase transformation mechanism was proposed for understanding the structure relationship between the LiMnO2 and chromium-substituted LiMnO2 oxides.

  3. Ionic Transport in Polyethylene Oxide (PEO)-LiX Polymeric Solid Electrolyte.

    Science.gov (United States)

    1988-03-01

    the temperatures specified below; LiCF3SO3 (3M) at 50 0C for several days, LiAsF6 (Alfa) used as received, LiBF4 (Alfa) 50°C for 24 hours, LiAlCl4...converge at about 0.9eV. The trend is as follows: LiBF4 >LiCF 3 S03>LiPF6>LiAICl4>LiASF6 The general dependence of activation energy on salt composition...mole fraction of LIBF4 in the electrolyte 1.0 > 0.8- C LU C 0 0.6- 0.4 0 0.1 0.2 0.3 0.4 0.5 [X(salt)] Figure 6. Variation in the activation energy vs

  4. Uas Topographic Mapping with Velodyne LiDAR Sensor

    Science.gov (United States)

    Jozkow, G.; Toth, C.; Grejner-Brzezinska, D.

    2016-06-01

    Unmanned Aerial System (UAS) technology is nowadays willingly used in small area topographic mapping due to low costs and good quality of derived products. Since cameras typically used with UAS have some limitations, e.g. cannot penetrate the vegetation, LiDAR sensors are increasingly getting attention in UAS mapping. Sensor developments reached the point when their costs and size suit the UAS platform, though, LiDAR UAS is still an emerging technology. One issue related to using LiDAR sensors on UAS is the limited performance of the navigation sensors used on UAS platforms. Therefore, various hardware and software solutions are investigated to increase the quality of UAS LiDAR point clouds. This work analyses several aspects of the UAS LiDAR point cloud generation performance based on UAS flights conducted with the Velodyne laser scanner and cameras. The attention was primarily paid to the trajectory reconstruction performance that is essential for accurate point cloud georeferencing. Since the navigation sensors, especially Inertial Measurement Units (IMUs), may not be of sufficient performance, the estimated camera poses could allow to increase the robustness of the estimated trajectory, and subsequently, the accuracy of the point cloud. The accuracy of the final UAS LiDAR point cloud was evaluated on the basis of the generated DSM, including comparison with point clouds obtained from dense image matching. The results showed the need for more investigation on MEMS IMU sensors used for UAS trajectory reconstruction. The accuracy of the UAS LiDAR point cloud, though lower than for point cloud obtained from images, may be still sufficient for certain mapping applications where the optical imagery is not useful.

  5. Visual-LiDAR Odometry Aided by Reduced IMU

    Directory of Open Access Journals (Sweden)

    Yashar Balazadegan Sarvrood

    2016-01-01

    Full Text Available This paper proposes a method for combining stereo visual odometry, Light Detection And Ranging (LiDAR odometry and reduced Inertial Measurement Unit (IMU including two horizontal accelerometers and one vertical gyro. The proposed method starts with stereo visual odometry to estimate six Degree of Freedom (DoF ego motion to register the point clouds from previous epoch to the current epoch. Then, Generalized Iterative Closest Point (GICP algorithm refines the motion estimation. Afterwards, forward velocity and Azimuth obtained by visual-LiDAR odometer are integrated with reduced IMU outputs in an Extended Kalman Filter (EKF to provide final navigation solution. In this paper, datasets from KITTI (Karlsruhe Institute of Technology and Toyota technological Institute were used to compare stereo visual odometry, integrated stereo visual odometry and reduced IMU, stereo visual-LiDAR odometry and integrated stereo visual-LiDAR odometry and reduced IMU. Integrated stereo visual-LiDAR odometry and reduced IMU outperforms other methods in urban areas with buildings around. Moreover, this method outperforms simulated Reduced Inertial Sensor System (RISS, which uses simulated wheel odometer and reduced IMU. KITTI datasets do not include wheel odometry data. Integrated RTK (Real Time Kinematic GPS (Global Positioning System and IMU was replaced by wheel odometer to simulate the response of RISS method. Visual Odometry (VO-LiDAR is not only more accurate than wheel odometer, but it also provides azimuth aiding to vertical gyro resulting in a more reliable and accurate system. To develop low-cost systems, it would be a good option to use two cameras plus reduced IMU. The cost of such a system will be reduced than using full tactical MEMS (Micro-Electro-Mechanical Sensor based IMUs because two cameras are cheaper than full tactical MEMS based IMUs. The results indicate that integrated stereo visual-LiDAR odometry and reduced IMU can achieve accuracy at the

  6. UAS TOPOGRAPHIC MAPPING WITH VELODYNE LiDAR SENSOR

    Directory of Open Access Journals (Sweden)

    G. Jozkow

    2016-06-01

    Full Text Available Unmanned Aerial System (UAS technology is nowadays willingly used in small area topographic mapping due to low costs and good quality of derived products. Since cameras typically used with UAS have some limitations, e.g. cannot penetrate the vegetation, LiDAR sensors are increasingly getting attention in UAS mapping. Sensor developments reached the point when their costs and size suit the UAS platform, though, LiDAR UAS is still an emerging technology. One issue related to using LiDAR sensors on UAS is the limited performance of the navigation sensors used on UAS platforms. Therefore, various hardware and software solutions are investigated to increase the quality of UAS LiDAR point clouds. This work analyses several aspects of the UAS LiDAR point cloud generation performance based on UAS flights conducted with the Velodyne laser scanner and cameras. The attention was primarily paid to the trajectory reconstruction performance that is essential for accurate point cloud georeferencing. Since the navigation sensors, especially Inertial Measurement Units (IMUs, may not be of sufficient performance, the estimated camera poses could allow to increase the robustness of the estimated trajectory, and subsequently, the accuracy of the point cloud. The accuracy of the final UAS LiDAR point cloud was evaluated on the basis of the generated DSM, including comparison with point clouds obtained from dense image matching. The results showed the need for more investigation on MEMS IMU sensors used for UAS trajectory reconstruction. The accuracy of the UAS LiDAR point cloud, though lower than for point cloud obtained from images, may be still sufficient for certain mapping applications where the optical imagery is not useful.

  7. Synthesis of LiBOB Fine Powder to Increase Solubility

    Directory of Open Access Journals (Sweden)

    Etty Marti Wigayati

    2017-04-01

    Full Text Available Lithium bis (oxalate borate or LiBOB compound has captured interest of researchers, because it is potentially viable to be used as electrolyte salt in lithium-ion battery system. This compound is easy to synthesize and considered to be more environmentally friendly compared to conventional electrolyte salt because LiBOB does not contain halogen element. This research focused on the synthesis of LiBOB fine powder, which main purpose is improving LiBOB salt solubility in liquid electrolyte solution. This will aid the ion transfer between electrodes which in turn will increase the electrolyte performance. Solid state reaction was employed in this experiment. Synthesis of LiBOB compound was performed by reacting oxalic acid dihydrate, lithium hydroxide monohydrate, and boric acid. The resulting powder was then processed into fine powder using ball milling technique with varying milling time (0, 6, 10, and 13 hour. Microstructure of the sample was then analyzed to obtain information regarding phase formation, functional groups, grain surface morphology, surface area, pore volume, solubility, and ionic conductivity. The analysis shown that LiBOB and LiBOB hydrate phase was formed during the reaction, there was no changed in existing phase during milling process, crystallinity index was shifted to lower value but there was no difference in functional groups. Highest value in surface area was found to be 83.11 m2/g, with pore volume of 1.21311e+02 A at 10 hours milling. Smaller powder size resulted in higher solubility, unfortunately the ionic conductivity was found to be decreased.

  8. Long term stability of Li-S batteries using high concentration lithium nitrate electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Adams, Brian DG; Carino, Emily V.; Connell, Justin G.; Han, Kee Sung; Cao, Ruiguo; Chen, Junzheng; Zheng, Jianming; Li, Qiuyan; Mueller, Karl T.; Henderson, Wesley A.; Zhang, Jiguang

    2017-09-08

    Lithium-sulfur (Li-S) battery is a very promising candidate for the next generation of energy storage systems required for electrical vehicles and grid energy storage applications due to its very high theoretical specific energy (2500 W h kg-1). However, the low coulombic efficiency (CE) during repeated Li plating/stripping of these processes have limited practical application of rechargeable Li-S batteries. In this work, a new electrolyte system based on high concentration of LiNO3 in diglyme solvent is developed which enables high CE of Li metal plating/stripping and high stability of Li anode in the sulfur containing electrolyte. Tailoring of electrolyte properties for the Li negative electrode has proven to be a successful strategy for improving the capacity retention and cycle life of Li-S batteries. This electrolyte provides a CE for Li plating/stripping of greater than 99% for over 200 cycles. In contrast, Li metal cycles for only less than 35 cycles at high CE in the standard 1 M LiTFSI + 2wt% LiNO3 in DOL:DME electrolyte under the same conditions. The stable Li metal anode enabled by the new electrolyte may accelerate the applications of high energy density Li-S batteries in both electrical vehicles and large-scale grid energy storage markets.

  9. The effect of the carbon nanotube buffer layer on the performance of a Li metal battery.

    Science.gov (United States)

    Zhang, Ding; Zhou, Yi; Liu, Changhong; Fan, Shoushan

    2016-06-07

    Lithium (Li) metal is one of the most promising candidates as an anode for the next-generation energy storage systems because of its high specific capacity and lowest negative electrochemical potential. But the growth of Li dendrites limits the application of the Li metal battery. In this work, a type of modified Li metal battery with a carbon nanotube (CNT) buffer layer inserted between the separator and the Li metal electrode was reported. The electrochemical results show that the modified batteries have a much better rate capability and cycling performance than the conventional Li metal batteries. The mechanism study by electrochemical impedance spectroscopy reveals that the modified battery has a smaller charge transfer resistance and larger Li ion diffusion coefficient during the deposition process on the Li electrode than the conventional Li metal batteries. Symmetric battery tests show that the interfacial behavior of the Li metal electrode with the buffer layer is more stable than the naked Li metal electrode. The morphological characterization of the CNT buffer layer and Li metal lamina reveals that the CNT buffer layer has restrained the growth of Li dendrites. The CNT buffer layer has great potential to solve the safety problem of the Li metal battery.

  10. Solution and computed structure of O-lithium N,N-diisopropyl-P,P-diphenylphosphinic amide. Unprecedented Li-O-Li-O self-assembly of an aryllithium.

    Science.gov (United States)

    Fernández, Ignacio; Oña-Burgos, Pascual; Oliva, Josep M; Ortiz, Fernando López

    2010-04-14

    The structural characterization of an ortho-lithiated diphenylphosphinic amide is described for the first time. Multinuclear magnetic resonance ((1)H, (7)Li, (13)C, (31)P) studies as a function of temperature and concentration employing 1D and 2D methods showed that the anion exists as a mixture of one monomer and two diastereomeric dimers. In the dimers the chiral monomer units are assembled in a like and unlike manner through oxygen-lithium bonds, leading to fluxional ladder structures. This self-assembling mode leads to the formation of Li(2)O(2) four-membered rings, a structural motif unprecedented in aryllithium compounds. DFT computations of representative model compounds of ortho-lithiated phosphinic amide monomer and Li(2)C(2) and Li(2)O(2) dimers with different degrees of solvation by THF molecules showed that Li(2)O(2) dimers are thermodynamically favored with respect to the alternative Li(2)C(2) structures by 4.3 kcal mol(-1) in solvent-free species and by 2.3 kcal mol(-1) when each lithium atom is coordinated to one THF molecule. Topological analysis of the electron density distribution revealed that the Li(2)O(2) four-membered ring is characterized by four carbon-lithium bond paths and one oxygen-oxygen bond path. The latter divides the Li-O-Li-O ring into two Li-O-Li three-sided rings, giving rise to two ring critical points. On the contrary, the bond path network in the Li(2)C(2) core includes a catastrophe point, suggesting that this molecular system can be envisaged as an intermediate in the formation of Li(2)O(2) dimers. The computed (13)C chemical shifts of the C-Li carbons support the existence of monomeric and dimeric species containing only one C-Li bond and are consistent with the existence of tricoordinated lithium atoms in all species in solution.

  11. High performance anode for advanced Li batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lake, Carla [Applied Sciences, Inc., Cedarville, OH (United States)

    2015-11-02

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

  12. Compounds of 6Li and natural Li for EPR dosimetry in photon/neutron mixed radiation fields.

    Science.gov (United States)

    Lund, E; Gustafsson, H; Danilczuk, M; Sastry, M D; Lund, A

    2004-05-01

    Formates and dithionates of 6Li, enriched and 7Li in natural composition of Li offer a possibility to measure the absorbed dose from photons and thermal neutrons in a mixed radiation field for instance at a boron neutron capture therapy (BNCT) facility. Tests with formates and dithionates of enriched 6Li and lithium compounds with natural composition have been performed at the BNCT facility at Studsvik, Sweden. Irradiations have been performed at 3 cm depth in a Perspex phantom in a fluence rate of thermal neutrons 1.8 x 10(9) n cm(-2) s(-1). The compounds were also irradiated in a pure X-ray field from a 4MV linear accelerator at 5 cm depth in a phantom with accurately determined absorbed doses. The signal intensity and shape was investigated within 3 h after the irradiation. A single line spectrum attributed to the CO2- radical was observed after irradiation of lithium formate. An increase in line width occurring after neutron irradiation in comparison with photon irradiation of the 6Li sample was attributed to dipolar broadening between CO2- radicals trapped in the tracks of the alpha particles. A spectrum due to the SO3- radical anion was observed after irradiation of lithium dithionate. The signal amplitude increased using the 6Li in place of the Li with natural composition of isotopes, in studies with low energy X-ray irradiation. Due to the decreased line width, caused by the difference in g(N) and I between the isotopes, the sensitivity with 6Li dithionate may be enhanced by an order of magnitude compared to alanine dosimetry. After comprehensive examination of the different combinations of compounds with different amounts of 6Li and 7Li regarding dosimetry, radiation chemistry and EPR properties these dosimeter material might be used for dose determinations at BNCT treatments and for biomedical experiments. Interesting properties of the radical formation might be visible due to the large difference in ionization density of neutrons compared to photons.

  13. Microstructure, cold rolling, heat treatment, and mechanical properties of Mg-Li alloys

    Institute of Scientific and Technical Information of China (English)

    Haibin Ji; Guangchun Yao; Hongbin Li

    2008-01-01

    The magnesium-lithium (Mg-Li) alloy exhibits two phase structures between 5.7wt% and 10.3wt% Li contents, consisting of the a (hcp) Mg-rich and the β (bee) Li-rich phases, at room temperature. In the experiment, Mg-5Li-2Zn, Mg-9Li-2Zn,Mg-16Li-2Zn, Mg-22Li-2Zn, Mg-5Li-2Zn-2Ca, Mg-9Li-2Zn-2Ca, Mg-16Li-2Zn-2Ca, and Mg-22Li-2Zn-2Ca (wt%) were melted.During the melting process, the flux, which was composed of lithium chloride (LiCI) and lithium fluoride (LiF) in the proportion of 3:1 (mass ratio) and argon gas were used to protect the alloys from oxidation. The mierostructure, mechanical properties, and cold-rolling workability of the wrought alloys were studied. The crystal grain of the alloys (adding Ga) is fine. The hardness of the studied alloys decreases with an increase in element Li. The density of the studied alloys is in the range of 1.187 to 1.617 g/cm3 The reduction of the Mg-16Li-2Zn and Mg-22Li-2Zn alloys can exceed 85% at room temperature. The Mg-9Li-2Zn-2Ca alloy was heat treated at 300℃ for 8, 12, 16, and 24 h, respectively. The optimum heat treatment of the Mg-9Li-2Zn-2Ca alloy is 300~Cx12h by metallographic observation and by studying the mechanical properties of the alloys.

  14. LiFAP-based PVdF-HFP microporous membranes by phase-inversion technique with Li/LiFePO{sub 4} cell

    Energy Technology Data Exchange (ETDEWEB)

    Aravindan, V.; Vickraman, P. [Gandhigram Rural University, Department of Physics, Gandhigram (India); Sivashanmugam, A.; Thirunakaran, R.; Gopukumar, S. [Central Electrochemical Research Institute, Electrochemical Energy Systems Division, Karaikudi (India)

    2009-12-15

    Polyvinylidenefluoride-hexafluoropropylene-based (PVdF-HFP-based) gel and composite microporous membranes (GPMs and CPMs) were prepared by phase-inversion technique in the presence 10 wt% of AlO(OH){sub n} nanoparticles. The prepared membranes were gelled with 0.5-M LiPF{sub 3}(CF{sub 2}CF{sub 3}){sub 3} (lithium fluoroalkylphosphate, LiFAP) in EC:DEC (1:1 v/v) and subjected to various characterizations; the AC impedance study shows that CPMs exhibit higher conductivity than GPMs. Mechanical stability measurements on these systems reveal that CPMs exhibit Young's modulus higher than that of bare and GPMs and addition of nanoparticles drastically improves the elongation break was also noted. Transition of the host from {alpha} to {beta} phase after the loading of nanosized filler was confirmed by XRD and Raman studies. Physico-chemical properties, like liquid uptake, porosity, surface area, and activation energy, of the membranes were calculated and results are summarized. Cycling performance of Li/CPM/LiFePO{sub 4} coin cell was fabricated and evaluated at C/10 rate and delivered a discharge capacity of 157 and 148 mAh g {sup -1} respectively for first and tenth cycles. (orig.)

  15. LiFAP-based PVdF-HFP microporous membranes by phase-inversion technique with Li/LiFePO4 cell

    Science.gov (United States)

    Aravindan, V.; Vickraman, P.; Sivashanmugam, A.; Thirunakaran, R.; Gopukumar, S.

    2009-12-01

    Polyvinylidenefluoride-hexafluoropropylene-based (PVdF-HFP-based) gel and composite microporous membranes (GPMs and CPMs) were prepared by phase-inversion technique in the presence 10 wt% of AlO(OH) n nanoparticles. The prepared membranes were gelled with 0.5-M LiPF3(CF2CF3)3 (lithium fluoroalkylphosphate, LiFAP) in EC:DEC (1:1 v/v) and subjected to various characterizations; the AC impedance study shows that CPMs exhibit higher conductivity than GPMs. Mechanical stability measurements on these systems reveal that CPMs exhibit Young’s modulus higher than that of bare and GPMs and addition of nanoparticles drastically improves the elongation break was also noted. Transition of the host from α to β phase after the loading of nanosized filler was confirmed by XRD and Raman studies. Physico-chemical properties, like liquid uptake, porosity, surface area, and activation energy, of the membranes were calculated and results are summarized. Cycling performance of Li/CPM/LiFePO4 coin cell was fabricated and evaluated at C/10 rate and delivered a discharge capacity of 157 and 148 mAh g-1 respectively for first and tenth cycles.

  16. Preparing different phases of Mg-Li-Sm alloys by molten salt electrolysis in LiCl-KCl-MgCl_2-SmCl_3 melts

    Institute of Scientific and Technical Information of China (English)

    韩伟; 田阳; 张密林; 叶克; 赵全友; 魏树权

    2010-01-01

    Different phases of Mg-Li-Sm alloys were prepared by galvanostatic electrolysis in LiCl-KCl-MgCl2-SmCl3 melts at 670 °C.The electrolysis process and phase control of Mg-Li-Sm alloys were studied.The microstructures of α,α+β,β phases of Mg-Li-Sm alloys were characterized by X-ray diffraction(XRD) and optical microscope(OM).Analysis of scanning electron microscopy(SEM) and EDS mapping analysis showed that Mg distributed homogeneously in Mg-Li-Sm alloys.EDS result showed that the distribution of Sm was more at...

  17. A TECHNIQUE FOR IMPROVING THE TOUGHNESS OF Al-Li POWDER METALLURGY ALLOYS

    OpenAIRE

    1987-01-01

    A technique has been developed for increasing the toughness of Al-Li products made by powder metallurgy. The technique which involves the addition of unalloyed aluminum powder to Al-Li powder before compaction was evaluated with Al-Li-Cu-Mg-Zr alloys (Al 8090), and Al-Li-Zn-Cu-Mg-Zr and Al-Li-Mg-Si-Cr alloys . The addition of 15% aluminum to Al 8090 aged at 422K for 40 h produced an increase in impact toughness of 215% at the expense of a drop in yield strength of 11%. The Al-Li-Mg-Si-Cr allo...

  18. Device fabrication, characterization, and thermal neutron detection response of LiZnP and LiZnAs semiconductor devices

    Science.gov (United States)

    Montag, Benjamin W.; Ugorowski, Philip B.; Nelson, Kyle A.; Edwards, Nathaniel S.; McGregor, Douglas S.

    2016-11-01

    Nowotny-Juza compounds continue to be explored as candidates for solid-state neutron detectors. Such a device would have greater efficiency, in a compact form, than present day gas-filled 3He and 10BF3 detectors. The 6Li(n,t)4He reaction yields a total Q-value of 4.78 MeV, larger than 10B, an energy easily identified above background radiations. Hence, devices fabricated from semiconductor compounds having either natural Li (nominally 7.5% 6Li) or enriched 6Li (usually 95% 6Li) as constituent atoms may provide a material for compact high efficiency neutron detectors. Starting material was synthesized by preparing equimolar portions of Li, Zn, and As sealed under vacuum (10-6 Torr) in quartz ampoules lined with boron nitride and subsequently reacted in a compounding furnace [1]. The raw synthesized material indicated the presence high impurity levels (material and electrical property characterizations). A static vacuum sublimation in quartz was performed to help purify the synthesized material [2,3]. Bulk crystalline samples were grown from the purified material [4,5]. Samples were cut using a diamond wire saw, and processed into devices. Bulk resistivity was determined from I-V curve measurements, ranging from 106-1011 Ω cm. Devices were characterized for sensitivity to 5.48 MeV alpha particles, 337 nm laser light, and neutron sensitivity in a thermal neutron diffracted beam at the Kansas State University TRIGA Mark II nuclear reactor. Thermal neutron reaction product charge induction was measured with a LiZnP device, and the reaction product spectral response was observed.

  19. Spectroscopy of ultracold LiRb molecules using ionization detection

    Science.gov (United States)

    Altaf, Adeel

    We present spectroscopic studies of ultracold LiRb molecules using ionization detection. The molecules are created by cooling and trapping Li and Rb atoms in overlapping magneto-optical traps (MOTs) and using light resonant with a free-bound transition to create weakly bound excited state molecules in a process known as photoassociation (PA). We explore weakly bound vibrational levels of LiRb with PA spectroscopy using ionization detection and, where possible, compare our results with earlier measurements performed in our lab using trap-loss spectroscopy. In addition, we also probe vibrational levels of the ground triplet electronic state and excited electronic states using resonantly enhanced multiphoton ionization (REMPI) spectroscopy. We identify several vibrational levels of the alpha3Sigma+, (3)3piO and (4)3Sigma + states and compare our observations with theoretical calculations. As LiRb is one of the least studied heteronuclear diatomic molecules, these studies are aimed towards exploring the molecular structure. The spectroscopic work is also in line with the long-term project goals of transferring ultracold LiRb molecules into the lowest rotational and vibrational levels of the ground singlet electronic state. Molecules in this rovibronic ground state possess a large electric dipole moment, which is essential for application of ultracold molecules in various quantum computation schemes. The rovibronic ground state will also be an ideal starting point for investigating molecular entangled states.

  20. Mathematical modelling applied to LiDAR data

    Directory of Open Access Journals (Sweden)

    Javier Estornell

    2013-06-01

    Full Text Available The aim of this article is to explain the application of several mathematic calculations to LiDAR (Light Detection And Ranging data to estimate vegetation parameters and modelling the relief of a forest area in the town of Chiva (Valencia. To represent the surface that describes the topography of the area, firstly, morphological filters were applied iteratively to select LiDAR ground points. From these data, the Triangulated Irregular Network (TIN structure was applied to model the relief of the area. From LiDAR data the canopy height model (CHM was also calculated. This model allowed obtaining bare soil, shrub and tree vegetation mapping in the study area. In addition, biomass was estimated from measurements taken in the field in 39 circular plots of radius 0.5 m and the 95th percentile of the LiDAR height datanincluded in each plot. The results indicated a high relationship between the two variables (measurednbiomass and 95th percentile with a coeficient of determination (R2 of 0:73. These results reveal the importance of using mathematical modelling to obtain information of the vegetation and land relief from LiDAR data.

  1. Mechanism of reaction synthesis of Li-B alloys

    Institute of Scientific and Technical Information of China (English)

    LIU; Zhijian; (刘志坚); QU; Xuanhui; (曲选辉); LI; Zhiyou; (李志友); HUANG; Baiyun; (黄伯云)

    2003-01-01

    A model for reaction synthesis of Li-B alloys has been presented. Results show that the first exothermal reaction can be divided into three stages. The first stage is an instantaneous reaction on the boundary between boron particles and lithium melting, in which the caloric released is inversely proportional to the particle size of the boron powder. The second stage is a reaction between the unreacted boron and the lithium that diffuses through the product LiB3 on the surface of the boron particle. This process can be described by Johnston model. The third stage is dissolution of the product LiB3 to Li liquid, which takes place at temperature up to 420℃. At the same time, the second exothermal reaction begins, which consists of nucleation and growth of the last Li-B compound. It can be divided into two substages, i.e. the nucleation pregnant stage and the exploded reaction stage. When the concentration of the particle nucleated is high enough, an exploding reaction takes place. The lower the temperature, the longer the time needed for the exploding reaction. By the model presented, the experimental phenomena in the synthesis are explained.

  2. High Performance Cathodes for Li-Air Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Xing, Yangchuan

    2013-08-22

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

  3. Li I and K I Scatter in Cool Pleiades Dwarfs

    CERN Document Server

    King, J R; Hobbs, L M; Pinsonneault, M H

    2010-01-01

    We utilize high-resolution (R~60,000), high S/N (~100) spectroscopy of 17 cool Pleiades dwarfs to examine the confounding star-to-star scatter in the 6707 Li I line strengths in this young cluster. Our Pleiads, selected for their small projected rotational velocity and modest chromospheric emission, evince substantial scatter in the linestrengths of 6707 Li I feature that is absent in the 7699 K I resonance line. The Li I scatter is not correlated with that in the high-excitation 7774 O I feature, and the magnitude of the former is greater than the latter despite the larger temperature sensitivity of the O I feature. These results suggest that systematic errors in linestrength measurements due to blending, color (or color-based T_eff) errors, or line formation effects related to an overlying chromosphere are not the principal source of Li I scatter in our stars. There do exist analytic spot models that can produce the observed Li scatter without introducing scatter in the K I line strengths or the color-magni...

  4. Extraction of building by airborne LiDAR point cloud with support of ENVI LiDAR%ENVI LiDAR 支持下利用机载 LiDAR 点云提取建筑物

    Institute of Scientific and Technical Information of China (English)

    张杰; 贺清清; 王飞

    2016-01-01

    对机载激光雷达测量技术、ENVI LiDAR 软件、建筑物提取流程进行了介绍,以 ISPRS 第三委员会提供的机载激光雷达点云数据为基础,基于 ENVI LiDAR 5.1对实验区的建筑物进行了提取,并通过 ArcGIS 结合同地区影像对其质量进行评价,实验流程及结果有一定的参考意义。%Technology of Airborne LiDAR(Light Detection And Ranging),the ENVI LiDAR and the process of building extraction are intro-duced briefly in this paper. Then,based on the International Society for Photogrammetry and Remote Sensing(ISPRS)commission Ⅲ and ENVI LiDAR 5. 1,the buildings in testing area were extracted. The evaluation results of quality was learned by overlaying the buildings onto the image in same place through ArcGIS,and the process and results thereof have certain reference significance.

  5. Biomass Estimation for Individual Trees using Waveform LiDAR

    Science.gov (United States)

    Wang, K.; Kumar, P.; Dutta, D.

    2015-12-01

    Vegetation biomass information is important for many ecological models that include terrestrial vegetation in their simulations. Biomass has strong influences on carbon, water, and nutrient cycles. Traditionally biomass estimation requires intensive, and often destructive, field measurements. However, with advances in technology, airborne LiDAR has become a convenient tool for acquiring such information on a large scale. In this study, we use infrared full waveform LiDAR to estimate biomass information for individual trees in the Sangamon River basin in Illinois, USA. During this process, we also develop automated geolocation calibration algorithms for raw waveform LiDAR data. In the summer of 2014, discrete and waveform LiDAR data were collected over the Sangamon River basin. Field measurements commonly used in biomass equations such as diameter at breast height and total tree height were also taken for four sites across the basin. Using discrete LiDAR data, individual trees are delineated. For each tree, a voxelization methods is applied to all waveforms associated with the tree to result in a pseudo-waveform. By relating biomass extrapolated using field measurements from a training set of trees to waveform metrics for each corresponding tree, we are able to estimate biomass on an individual tree basis. The results can be especially useful as current models increase in resolution.

  6. Forest Road Detection Using LiDAR Data

    Institute of Scientific and Technical Information of China (English)

    Zahra Azizi; Akbar Najafi; Saeed Sadeghian

    2014-01-01

    We developed a three-step classification approach for forest road extraction utilizing LiDAR data. The first step employed the IDW method to interpolate LiDAR point data (first and last pulses) to achieve DSM, DTM and DNTM layers (at 1 m resolution). For this interpolation RMSE was 0.19 m. In the second step, the Support Vector Machine (SVM) was employed to classify the LiDAR data into two classes, road and non-road. For this classification, SVM indicated the merged distance layer with intensity data and yielded better identification of the road position. Assessments of the obtained results showed 63% correctness, 75% completeness and 52% quality of classification. In the next step, road edges were defined in the LiDAR-extracted layers, enabling accu-rate digitizing of the centerline location. More than 95% of the Li-DAR-derived road was digitized within 1.3 m to the field surveyed nor-mal. The proposed approach can provide thorough and accurate road inventory data to support forest management.

  7. A Study on Factors Affecting Airborne LiDAR Penetration

    Directory of Open Access Journals (Sweden)

    Wei-Chen Hsu

    2015-01-01

    Full Text Available This study uses data from different periods, areas and parameters of airborne LiDAR (light detection and ranging surveys to understand the factors that influence airborne LiDAR penetration rate. A discussion is presented on the relationships between these factors and LiDAR penetration rate. The results show that the flight height above ground level (AGL does not have any relationship with the penetration rate. There are some factors that should have larger influence. For example, the laser is affected by a wet ground surface by reducing the number of return echoes. The field of view (FOV has a slightly negative correlation with the penetration rate, which indicates that the laser incidence angle close to zero should achieve the best penetration. The vegetation cover rate also shows a negative correlation with the penetration rate, thus bare ground and reduced vegetation in the aftermath of a typhoon also cause high penetration rate. More return echoes could be extracted from the full-waveform system, thereby effectively improving the penetration rate. This study shows that full-waveform LiDAR is an effective method for increasing the number of surface reflected echoes. This study suggests avoiding LiDAR survey employment directly following precipitation to prevent laser echo reduction.

  8. The Li Overabundance of J37: Diffusion or Accretion?

    CERN Document Server

    Ashwell, J F; Smalley, B; Deliyannis, C P; Steinhauer, A; King, J R

    2004-01-01

    In September 2002 the discovery of a super Li-rich F-dwarf (J37) in NGC 6633, an iron poor analogue of the better studied Hyades and Praecepe open clusters, was announced. This unique star was thought to be the smoking gun for the action of diffusion, models of which predict a narrow "Li-peak" at approximately the correct temperature. However, with more detailed studies into J37s abundance pattern this star provides firm evidence for the accretion of planetesimals or other material from the circumstellar environment of new born stars. Thanks to the specific predictions made about the behaviour of Be abundances, (the most striking of which being no Be in super-Li-rich dwarfs subject to diffusion) the opposing diffusion/accretion predictions can be tested. Initial modelling of the Be line indicates that J37 is as Be rich as it is Li rich; log N(Be) = 2.25 +/- 0.25, and so is broadly consistent with an accretion-fuelled enhancement. However, that both Li and Be are enhanced by much more than the iron-peak elemen...

  9. Cr and Si Substituted-LiCo0.9Fe0.1PO4: Structure, full and half Li-ion cell performance

    Science.gov (United States)

    Allen, Jan L.; Allen, Joshua L.; Thompson, Travis; Delp, Samuel A.; Wolfenstine, Jeff; Jow, T. Richard

    2016-09-01

    The use of LiCoPO4 as a Li-ion cathode material can enable high energy 5 V batteries. However, LiCoPO4 shows limited cycle life and much less than theoretical energy density. In order to address these shortcomings, Fe, Cr and Si substituted-LiCoPO4(Cr,Si-LiCo0.9Fe0.1PO4) was investigated as an improved LiCoPO4 based cathode material. Fe substitution greatly improves the cycle life and increases the energy density. Cr substitution further increases the energy density, cycle life and rate capability. Si substitution reduces the reactivity of the cathode with electrolyte thereby increasing cycle life. In combination, the substituents lead to a LiCoPO4 based cathode material with no capacity fade over 250 cycles in Li/Cr,Si-LiCo0.9Fe0.1PO4 half cells, a discharge capacity of 140 mAh g-1 at C/3 at an average discharge voltage of 4.78 V giving an energy density of 670 Wh per kg of cathode. In graphite/Cr,Si-LiCo0.9Fe0.1PO4 full Li-ion cells, the cathode material shows an energy density of 550 Wh per kg of cathode material at 1C rate for the initial cycles and 510 Wh per kg of cathode material at the 250th cycle.

  10. Li3AlB2O6:Synthesis, Crystal Structure, and Its Luminescence Property Compared with LiSrBO3

    Institute of Scientific and Technical Information of China (English)

    WANG, Hai-Xia(王海侠); CHENG, Wen-Dan(程文旦); CHEN, Da-Gui(陈达贵); ZHANG, Hao(张浩); WU, Dong-Sheng(吴东升); GONG, Ya-Jin(龚亚京)

    2004-01-01

    The synthesis and crystal structure of Li3AlB2O6 with different cell parameters are reported and these cells are transformed each other from the confirmation of crystallographic structural analyses. The absorption spectrum, luminescence and lifetimes of the Li3AlB2O6 and LiSrBO3 solid compounds are measured and the comparisons are made between them. It is shown that the absorption edges are at about 400 nm (or band gap 3.1 eV) and there is one of absorption peaks at about 350 nm for the Li3AlB2O6 and LiSrBO3. The emission band (530 nm) makes a red shift and fluorescence decay time (24.39 ns) of the Li3AlB2O6 becomes smaller compared with the emission band (480 nm) and lifetime (93.16 ns) of the LiSrBO3 at the visible region. The transition energies and oscillator strengths of the clusters (Li3AlB2O6)2 and (LiSrBO3)2 lying at low excited states are calculated by the time-dependent Hartree-Fock method. The obtained results are used to model the photophysical properties and discuss the origin of spectral bands of the Li3AlB2O6 and LiSrBO3.

  11. Synthesis of LiFePO4/Li2SiO3/reduced Graphene Oxide (rGO) Composite via Hydrothermal Method

    Science.gov (United States)

    Arifin, M.; Iskandar, F.; Aimon, A. H.; Munir, M. M.; Nuryadin, B. W.

    2016-08-01

    LiFePO4 is a type of cathode active material used for lithium ion batteries. It has a high electrochemical performance. However, it suffers from certain disadvantages such as a very low intrinsic electronic conductivity and low ionic diffusion. This study was conducted to increase the conductivity of LiFePO4. We have investigated the addition of Li2SiO3 and reduced graphene oxide (rGO) to LiFePO4. The objective of this research was to synthesize LiFePO4/Li2SiO3/rGO via hydrothermal method. Fourier transform infrared spectroscopy (FTIR) measurement showed that the peaks corresponded to the vibration of LiFePO4/Li2SiO3. Further, X-ray diffraction (XRD) measurement confirmed a single phase of LiFePO4. Finally, scanning electron microscopy (SEM) images showed that rGO was distributed on the LiFePO4/Li2SiO3 structure.

  12. Dopant occupancy and exposure energy in Hf:Nd:LiNbO3 crystal as a function of [Li]/[Nb] ratios

    Science.gov (United States)

    Dai, Li; Liu, Chunrui; Han, Xianbo; Yan, Zhehua; Tan, Chao; Wang, Luping; Xu, Yuheng

    2017-09-01

    A series of Hf: Nd: LiNbO3 crystals with various [Li]/[Nb] ratios ([Li]/[Nb] = 0.94, 1.05, 1.20, 1.38) in the melt were grown by conventional Czochralski technique. The distribution coefficients of Hf4+ and Nd3+ ions were recorded by an inductively coupled plasma-atomic emission spectrometer (ICP-AES). The effective distribution coefficient of Hf4+ is reduced and that of Nd3+ is increased with the increase of [Li]/[Nb] ratio in the melts. In all cases, the effective distribution coefficients is less than 1. The IR transmission spectroscopy of the Hf: Nd: LiNbO3 crystals were measured, getting the results that Hf: Yb: Ho: LiNbO3 crystals with 1.05 [Li]/[Nb] ratios was the stoichiometric. The optical damage resistance ability of Hf:Nd:LiNbO3 crystals were studied by light-induced scattering exposure energy flux threshold method and it increases with the increasing of [Li]/[Nb] ratios. When the [Li]/[Nb] ratio is 1.38 in the melt (the sample 4#), the exposure energy achieves 687.35 J/cm2, approximately 441 folds than that of the sample 1# ([Li]/[Nb] = 0.94) in magnitude.

  13. High-Performance Li-O2 Batteries with Controlled Li2O2 Growth in Graphene/Au-Nanoparticles/Au-Nanosheets Sandwich.

    Science.gov (United States)

    Wang, Guoqing; Tu, Fangfang; Xie, Jian; Du, Gaohui; Zhang, Shichao; Cao, Gaoshao; Zhao, Xinbing

    2016-10-01

    The working of nonaqueous Li-O2 batteries relies on the reversible formation/decomposition of Li2O2 which is electrically insulating and reactive with carbon and electrolyte. Realizing controlled growth of Li2O2 is a prerequisite for high performance of Li-O2 batteries. In this work, a sandwich-structured catalytic cathode is designed: graphene/Au-nanoparticles/Au-nanosheets (G/Au-NP/Au-NS) that enables controlled growth of Li2O2 spatially and structurally. It is found that thin-layer Li2O2 (below 10 nm) can grow conformally on the surface of Au NPs confined in between graphene and Au NSs. This unique crystalline behavior of Li2O2 effectively relieves or defers the electrode deactivation with Li2O2 accumulation and largely reduces the contact of Li2O2 with graphene and electrolyte. As a result, Li-O2 batteries with the G/Au-NP/Au-NS cathode exhibit superior electrochemical performance. A stable cycling of battery can last 300 times at 400 mA g(-1) when the capacity is limited at 500 mAh g(-1). This work provides a practical design of catalytic cathodes capable of controlling Li2O2 growth.

  14. Phase equilibria in the Li-Ti-O system and physical properties of Li sub 2 TiO sub 3

    CERN Document Server

    Kleykamp, H

    2002-01-01

    The phase equilibria of the pseudo-binary Li sub 2 O-TiO sub 2 system and the stoichiometry shift of Li sub 2 TiO sub 3 during the Li transmutation process are investigated. The structural properties, the thermal expansion, enthalpy, heat capacity, enthalpy of transformation and melting, thermal conductivity and the vapourisation behaviour of Li sub 2 TiO sub 3 are assessed. The ternary Li-Ti-O system is treated with emphasis to the characteristic of Li sub 2 TiO sub 3 under reducing conditions. The phase is reduced to LiTiO sub 2 with the Ti valence +3 due to its transition metal character.

  15. Novel Organic-Inorganic Hybrid Electrolyte to Enable LiFePO4 Quasi-Solid-State Li-Ion Batteries Performed Highly around Room Temperature.

    Science.gov (United States)

    Tan, Rui; Gao, Rongtan; Zhao, Yan; Zhang, Mingjian; Xu, Junyi; Yang, Jinlong; Pan, Feng

    2016-11-16

    A novel type of organic-inorganic hybrid polymer electrolytes with high electrochemical performances around room temperature is formed by hybrid of nanofillers, Y-type oligomer, polyoxyethylene and Li-salt (PBA-Li), of which the Tg and Tm are significantly lowered by blended heterogeneous polyethers and embedded nanofillers with benefit of the dipole modification to achieve the high Li-ion migration due to more free-volume space. The quasi-solid-state Li-ion batteries based on the LiFePO4/15PBA-Li/Li-metal cells present remarkable reversible capacities (133 and 165 mAh g(-1) @0.2 C at 30 and 45 °C, respectively), good rate ability and stable cycle performance (141.9 mAh g(-1) @0.2 C at 30 °C after 150 cycles).

  16. Enhanced electrochemical properties of LiFePO4 (LFP) cathode using the carboxymethyl cellulose lithium (CMC-Li) as novel binder in lithium-ion battery.

    Science.gov (United States)

    Qiu, Lei; Shao, Ziqiang; Wang, Daxiong; Wang, Wenjun; Wang, Feijun; Wang, Jianquan

    2014-10-13

    Novel water-based binder CMC-Li is synthesized using cotton as raw material. The mechanism of the CMC-Li as a binder is reported. Electrochemical properties of batteries cathodes based on commercially available lithium iron phosphate (LiFePO4, LFP) and CMC-Li as a water-soluble binder are investigated. CMC-Li is a novel lithium-ion binder. Compare with conventional poly(vinylidene fluoride) (PVDF) binder, and the battery with CMC-Li as the binder retained 97.8% of initial reversible capacity after 200 cycles at 176 mAh g(-1), which is beyond the theoretical specific capacity of LFP. Constant current charge-discharge test results demonstrate that the LFP electrode using CMC-Li as the binder has the highest rate capability, follow closely by that using PVDF binder. The batteries have good electrochemical property, outstanding pollution-free and excellent stability.

  17. Li6La3SnMO12 (M = Sb, Nb, Ta), a Family of Lithium Garnets with High Li-Ion Conductivity

    Energy Technology Data Exchange (ETDEWEB)

    Bridges, Craig A [ORNL; Goodenough, J. B. [University of Texas, Austin; Gupta, Dr Asha [University of Texas, Austin; Nakanishi, Masahiro [ORNL; Paranthaman, Mariappan Parans [ORNL; Sokolov, Alexei P [ORNL; Bi, Zhonghe [ORNL; Li, Yutao [University of Texas, Austin; Han, Jiantao [University of Texas, Austin; Dong, Youzhong [South China University of Technology, Guangzhou, PR China; Wang, Long [University of Texas, Austin; Xu, Maowen [University of Texas, Austin

    2012-01-01

    In order to investigate the influence of covalent bonding within the garnet framework on the conductivity of Li+ in the interstitial space, the Li+ conductivities in the family of Sn-based compounds Li6La3 SnMO12 (M = Sb, Nb, Ta) have been obtained and are compared with those of Li6La3ZrMO12. Refinement of the neutron diffraction pattern of Li6La3 SnNbO12shows that the interstitial tetrahedral sites (24d ) are about half-occupied and most of the Li in the interstitial bridging octahedral sites are displaced from the center position (48g ). The Sb-based compound has the largest lattice parameter while the Ta-based compound has the highest Li+-ion conductivity of 0.42 10 4 Scm 1.

  18. Effect of [Li]/[Nb] ratios on the absorption and up-conversion emission spectra in In:Yb:Ho:LiNbO{sub 3} crystal

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Li, E-mail: daili198108@126.com [Applied Science College, Harbin University of Science and Technology, Harbin 150080 (China); State Key Laboratory of Crystal Material, Shandong University, Jinan 250100 (China); Yan, Zhehua; Jiao, Shanshan [Applied Science College, Harbin University of Science and Technology, Harbin 150080 (China); Xu, Chao; Xu, Yuheng [Department of the Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)

    2015-09-25

    Highlights: • In:Yb:Ho:LiNbO{sub 3} crystals were grown with various [Li]/[Nb] ratios. • The influence of [Li]/[Nb] ratios on the UV–VIS–NIR is investigated. • This UC process is three-photon process. • In:Yb:Ho:LiNbO{sub 3} crystals (Li/Nb = 1.38) is a promising material for 2 μm wavelength radiation. - Abstract: In:Yb:Ho:LiNbO{sub 3} crystals with high optical quality were grown by the Czochralski method with various ratios of [Li]/[Nb], that is 0.94, 1.05, 1.20 and 1.38 in the melt. The UV–VIS–NIR absorption spectra of In:Yb:Ho:LiNbO{sub 3} crystals were measured. The transition intensity parameters Ω{sub t} (t = 2, 4 and 6), spectroscopic quality factor (X) and the lifetimes of Ho{sup 3+} in In:Yb:Ho:LiNbO{sub 3} crystals were all evaluated by the Judd–Ofelt theory. The spectroscopic quality factor Ω{sub 4}/Ω{sub 6} of In:Yb:Ho:LiNbO{sub 3} crystals with the [Li]/[Nb] ratio of 1.38 was found to be 1.69, which is comparable with those found in widely used Ho{sup 3+} doped crystals. Furthermore, up-conversion emission spectra were determined and analyzed under 980 nm LD excitation in the In:Yb:Ho:LiNbO{sub 3} crystals. The results revealed that In:Yb:Ho:LiNbO{sub 3} crystal with the [Li]/[Nb] ratio of 1.38 is a promising material for 2 μm wavelength radiation.

  19. Influence of different substrates on the ionic conduction in LiCoO{sub 2}/LiNbO{sub 3} thin-film bi-layers

    Energy Technology Data Exchange (ETDEWEB)

    Horopanitis, E.E.; Perentzis, G.; Papadimitriou, L. [Aristotle University of Thessaloniki, Department of Physics, Section of Solid State Physics, Thessaloniki (Greece)

    2008-07-01

    LiNbO{sub 3} thin films, deposited by e-gun evaporation, show lithium deficiency, which is cured by ''Li doping''. The ''Li doping'' of the films was achieved by preparing a structure of Li-Nb-O/Li/Li-Nb-O, which after annealing forms a homogenized LiNbO{sub 3} layer because of diffusion of Li in the two Li-Nb-O layers. The LiCoO{sub 2}/LiNbO{sub 3} bi-layers were prepared either on Stainless Steel/TiN or on Al{sub 2}O{sub 3}/Co/Pt substrates/ohmic-contacts by depositing first either the cathode LiCoO{sub 2} or the electrolyte LiNbO{sub 3}. The Nyquist plots of the AC impedance measurements of all structures showed that the interfaces prepared on Stainless-Steel/TiN consisted of two semicircles. The structures deposited on Al{sub 2}O{sub 3}/Co/Pt showed a third semicircle, which is probably due to the roughness of the substrate. It is important that the ionic properties of the bi-layers with the cathode material deposited first, a usual structure in a microbattery, are improved compared to the other structures. The quality of the LiNbO{sub 3} layer depends very much on the substrate. It can be evaluated from Arrhenius plots that the activation energy of this layer is considerably lower when the whole structure is deposited on Stainless Steel/TiN. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  20. Üliõpilasnõustaja: õppejõud peaks ideaalis juba enne esimest loengut teadma oma tudengite vajadustest / Sven Kõlamets

    Index Scriptorium Estoniae

    Kõlamets, Sven

    2010-01-01

    Küsimustele erivajadustega tudengite hetkeolukorrast vastab Tallinna Tehnikaülikooli üliõpilane ja üliõpilasesinduse liige Sven Kõlamets, kes tegutseb üliõpilasnõustajana erivajadustega tudengitele