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Sample records for liquid lithium thin

  1. Research proposal for development of an electron stripper using a thin liquid lithium film for rare isotope accelerator.

    Energy Technology Data Exchange (ETDEWEB)

    Momozaki, Y.; Nuclear Engineering Division

    2006-03-06

    Hydrodynamic instability phenomena in a thin liquid lithium film, which has been proposed for the first stripper in the driver linac of Rare Isotope Accelerator (RIA), were discussed. Since it was considered that film instability could significantly impair the feasibility of the liquid lithium film stripper concept, potential issues and research tasks in the RIA project due to these instability phenomena were raised. In order to investigate these instability phenomena, a research proposal plan was developed. In the theoretical part of this research proposal, a use of the linear stability theory was suggested. In the experimental part, it was pointed out that the concept of Reynolds number and Weber number scaling may allow conducting a preliminary experiment using inert simulants, hence reducing technical difficulty, complexity, and cost of the experiments. After confirming the thin film formation in the preliminary experiment using simulants, demonstration experiments using liquid lithium were proposed.

  2. Rechargeable Thin-film Lithium Batteries

    Science.gov (United States)

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

    1993-08-01

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

  3. Rechargeable thin-film lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

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

    1993-08-01

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

  4. Wetting properties of liquid lithium on lithium compounds

    Energy Technology Data Exchange (ETDEWEB)

    Krat, S.A., E-mail: stepan.krat@gmail.com [Center for Plasma Material Interactions, Department of Nuclear, Plasma, and Radiological Engineering, University Illinois at Urbana-Champaign, Urbana (United States); National Research Nuclear University MEPhI, Moscow (Russian Federation); Popkov, A.S. [Center for Plasma Material Interactions, Department of Nuclear, Plasma, and Radiological Engineering, University Illinois at Urbana-Champaign, Urbana (United States); National Research Nuclear University MEPhI, Moscow (Russian Federation); Gasparyan, Yu. M.; Pisarev, A.A. [National Research Nuclear University MEPhI, Moscow (Russian Federation); Fiflis, Peter; Szott, Matthew; Christenson, Michael; Kalathiparambil, Kishor; Ruzic, David N. [Center for Plasma Material Interactions, Department of Nuclear, Plasma, and Radiological Engineering, University Illinois at Urbana-Champaign, Urbana (United States)

    2017-04-15

    Highlights: • Contact angles of liquid lithium and Li{sub 3}N, Li{sub 2}O, Li{sub 2}CO{sub 3} were measured. • Liquid lithium wets lithium compounds at relatively low temperatures: Li{sub 3}N at 257 °C, Li{sub 2}O at 259 °C, Li{sub 2}CO{sub 3} at 323 °C. • Li wets Li{sub 2}O and Li{sub 3}N better than previously measured fusion-relevant materials (W, Mo, Ta, TZM, stainless steel). • Li wets Li{sub 2}CO{sub 3} better than most previously measured fusion-relevant materials (W, Mo, Ta). - Abstract: Liquid metal plasma facing components (LMPFC) have shown a potential to supplant solid plasma facing components materials in the high heat flux regions of magnetic confinement fusion reactors due to the reduction or elimination of concerns over melting, wall damage, and erosion. To design a workable LMPFC, one must understand how liquid metal interacts with solid underlying structures. Wetting is an important factor in such interaction, several designs of LMPFC require liquid metal to wet the underlying solid structures. The wetting of lithium compounds (lithium nitride, oxide, and carbonate) by 200 °C liquid lithium at various surface temperature from 230 to 330 °C was studied by means of contact angle measurements. Wetting temperatures, defined as the temperature above which the contact angle is less than 90°, were measured. The wetting temperature was 257 °C for nitride, 259 °C for oxide, and 323 °C for carbonate. Surface tensions of solid lithium compounds were calculated from the contact angle measurements.

  5. Ionic Liquids in Lithium-Ion Batteries.

    Science.gov (United States)

    Balducci, Andrea

    2017-04-01

    Lithium-ion batteries are among the most widespread energy storage devices in our society. In order to introduce these devices in new key applications such as transportation, however, their safety and their operative temperature range need to be significantly improved. These improvements can be obtained only by developing new electrolytes. Ionic liquids are presently considered among the most attractive electrolytes for the development of advanced and safer lithium-ion batteries. In this manuscript, the use of various types of ionic liquids, e.g. aprotic and protic, in lithium-ion batteries is considered. The advantages and the limits associated to the use of these innovative electrolytes are critically analysed.

  6. Characterization of lithium phosphorous oxynitride thin films

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Xiaohua; Bates, J.B.; Jellison, G.E. Jr.

    1996-01-01

    Electrical and electrochemical properties of an amorphous thin-film lithium electrolyte, lithium phosphorous oxynitride (Lipon), have been studied with emphasis on the stability window vs Li metal and the behavior of the Li/Lipon interface. Ion conductivity of Lipon exhibits Arrhenius behavior at {minus}26 to +140 C, with a conductivity of 1.7 {times} 10{sup {minus}6}S/cm at 25 C and an activity energy of 0.50 {plus_minus} 0.01 eV. A stability window of 5.5 V was observed with respect to a Li{sup +}/Li reference, and no detectable reaction or degradation was evident at the Li/Lipon interface upon lithium cycling.

  7. Rechargeable thin-film lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

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

    1993-09-01

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

  8. The liquid lithium limiter control system on FTU

    Energy Technology Data Exchange (ETDEWEB)

    Bertocchi, A. [EURATOM-ENEA Association, Frascati Research Center, Via E. Fermi 45, 00044 Frascati (Rome) (Italy)], E-mail: bertocchi@frascati.enea.it; Di Donna, M. [Department of Informatics, Systems and Productions, University of Rome Tor Vergata, Rome (Italy); Panella, M.; Vitale, V. [EURATOM-ENEA Association, Frascati Research Center, Via E. Fermi 45, 00044 Frascati (Rome) (Italy)

    2007-10-15

    In the second half of 2005, a liquid lithium limiter (LLL) with capillary porous system (CPS) configuration was installed to test on Tokamak FTU. The liquid lithium flows through capillaries from a reservoir to the side faced to the plasma to form a thin lithium film as wall coating. The system includes three stainless steel cases, which contain two thermocouples each one. A heating system brings the Li temperature about 200 deg. C to allow the liquid to flow. This temperature, monitored by thermocouples, needs to be controlled. To carry out this experimental procedure, some new features have been introduced in the existent control system based on Opto22{sup TM} modules and a CORBA/PHP/MySQL software architecture. The historical data storage to keep the lithium temperature evolution has been added. Two graphical tools - developed in MATLAB{sup TM} and Java environments, respectively, to monitor the lithium temperature coming from thermocouples - have been also implemented. The LLL control system allows to regulate the heater temperature in each unit to reach operational conditions, where the temperature adjustment can be performed either automatically through a specific control law or manually by the operator. During the plasma shot the system switches off the limiter power supply to prevent instruments damage. Moreover, in the same experimental context, a first approach to automatically obtain executable code - starting from control laws designed by Simulink{sup TM} tool - has been realized.

  9. Triboelectric Nanogenerator Using Lithium Niobate Thin Film

    Science.gov (United States)

    Geng, Juan; Zhang, Xinzheng; Kong, Yongfa; Xu, Jingjun

    2017-06-01

    We present a triboelectric nanogenerator (TENG) using a lithium niobate thin film, as one of the triboelectric pairs which was grown on a silicon substrate by laser molecule beam epitaxy (LMBE). The designed TENG has the advantages of simple structure, easy fabrication, small size (1.1*1.0*0.15 cm3). An open-circuit voltage of 136 V and a short-circuit current of 8.40 μA have been achieved. The maximum output power is 307.5μW under the load resistance of 10MΩ. This is the first time to use lithium niobate thin film as one of the friction pair, which may make it possible to expand the application of triboelectric nanogenerator to optical field.

  10. High performance discharges in the Lithium Tokamak eXperiment with liquid lithium wallsa)

    Science.gov (United States)

    Schmitt, J. C.; Bell, R. E.; Boyle, D. P.; Esposti, B.; Kaita, R.; Kozub, T.; LeBlanc, B. P.; Lucia, M.; Maingi, R.; Majeski, R.; Merino, E.; Punjabi-Vinoth, S.; Tchilingurian, G.; Capece, A.; Koel, B.; Roszell, J.; Biewer, T. M.; Gray, T. K.; Kubota, S.; Beiersdorfer, P.; Widmann, K.; Tritz, K.

    2015-05-01

    The first-ever successful operation of a tokamak with a large area (40% of the total plasma surface area) liquid lithium wall has been achieved in the Lithium Tokamak eXperiment (LTX). These results were obtained with a new, electron beam-based lithium evaporation system, which can deposit a lithium coating on the limiting wall of LTX in a five-minute period. Preliminary analyses of diamagnetic and other data for discharges operated with a liquid lithium wall indicate that confinement times increased by 10× compared to discharges with helium-dispersed solid lithium coatings. Ohmic energy confinement times with fresh lithium walls, solid and liquid, exceed several relevant empirical scaling expressions. Spectroscopic analysis of the discharges indicates that oxygen levels in the discharges limited on liquid lithium walls were significantly reduced compared to discharges limited on solid lithium walls. Tokamak operations with a full liquid lithium wall (85% of the total plasma surface area) have recently started.

  11. Ionic liquids for rechargeable lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

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

    2005-09-29

    We have investigated possible anticipated advantages of ionic-liquid electrolytes for use in lithium-ion batteries. Thermal stabilities and phase behavior were studied by thermal gravimetric analysis and differential scanning calorimetry. The ionic liquids studied include various imidazoliumTFSI systems, pyrrolidiniumTFSI, BMIMPF{sub 6}, BMIMBF{sub 4}, and BMIMTf. Thermal stabilities were measured for neat ionic liquids and for BMIMBF{sub 4}-LiBF{sub 4}, BMIMTf-LiTf, BMIMTFSI-LiTFSI mixtures. Conductivities have been measured for various ionic-liquid lithium-salt systems. We show the development of interfacial impedance in a Li|BMIMBF{sub 4} + LiBF{sub 4}|Li cell and we report results from cycling experiments for a Li|BMIMBF{sub 4} + 1 mol/kg LIBF{sub 4}|C cell. The interfacial resistance increases with time and the ionic liquid reacts with the lithium electrode. As expected, imidazolium-based ionic liquids react with lithium electrodes. We seek new ionic liquids that have better chemical stabilities.

  12. Liquid electrolytes for lithium and lithium-ion batteries

    Science.gov (United States)

    Blomgren, George E.

    A number of advances in electrolytes have occurred in the past 4 years, which have contributed to increased safety, wider temperature range of operation, better cycling and other enhancements to lithium-ion batteries. The changes to basic electrolyte solutions that have occurred to accomplish these advances are discussed in detail. The solvent components that have led to better low-temperature operation are also considered. Also, additives that have resulted in better structure of the solid electrolyte interphase (SEI) are presented as well as proposed methods of operation of these additives. Other additives that have lessened the flammability of the electrolyte when exposed to air and also caused lowering of the heat of reaction with the oxidized positive electrode are discussed. Finally, additives that act to open current-interrupter devices by releasing a gas under overcharge conditions and those that act to cycle between electrodes to alleviate overcharging are presented. As a class, these new electrolytes are often called "functional electrolytes". Possibilities for further progress in this most important area are presented. Another area of active work in the recent past has been the reemergence of ambient-temperature molten salt electrolytes applied to alkali metal and lithium-ion batteries. This revival of an older field is due to the discovery of new salt types that have a higher voltage window (particularly to positive potentials) and also have greatly increased hydrolytic stability compared to previous ionic liquids. While practical batteries have not yet emerged from these studies, the increase in the number of active researchers and publications in the area demonstrates the interest and potentialities of the field. Progress in the field is briefly reviewed. Finally, recent results on the mechanisms for capacity loss on shelf and cycling in lithium-ion cells are reviewed. Progress towards further market penetration by lithium-ion cells hinges on improved

  13. Preliminary experimental study of liquid lithium water interaction

    Energy Technology Data Exchange (ETDEWEB)

    You, X.M.; Tong, L.L.; Cao, X.W., E-mail: caoxuewu@sjtu.edu.cn

    2015-10-15

    Highlights: • Explosive reaction occurs when lithium temperature is over 300 °C. • The violence of liquid lithium water interaction increases with the initial temperature of liquid lithium. • The interaction is suppressed when the initial water temperature is above 70 °C. • Steam explosion is not ignorable in the risk assessment of liquid lithium water interaction. • Explosion strength of liquid lithium water interaction is evaluated by explosive yield. - Abstract: Liquid lithium is the best candidate for a material with low Z and low activation, and is one of the important choices for plasma facing materials in magnetic fusion devices. However, liquid lithium reacts violently with water under the conditions of loss of coolant accidents. The release of large heats and hydrogen could result in the dramatic increase of temperature and pressure. The lithium–water explosion has large effect on the safety of fusion devices, which is an important content for the safety assessment of fusion devices. As a preliminary investigation of liquid lithium water interaction, the test facility has been built and experiments have been conducted under different conditions. The initial temperature of lithium droplet ranged from 200 °C to 600 °C and water temperature was varied between 20 °C and 90 °C. Lithium droplets were released into the test section with excess water. The shape of lithium droplet and steam generated around the lithium were observed by the high speed camera. At the same time, the pressure and temperature in the test section were recorded during the violent interactions. The preliminary experimental results indicate that the initial temperature of lithium and water has an effect on the violence of liquid lithium water interaction.

  14. Wetting Properties of Liquid Lithium on Stainless Steel and Enhanced Stainless Steel Surfaces

    Science.gov (United States)

    Fiflis, P.; Xu, W.; Raman, P.; Andruczyk, D.; Ruzic, D. N.; Curreli, D.

    2012-10-01

    Research into lithium as a first wall material has proven its ability to effectively getter impurities and reduce recycling of hydrogen ions at the wall. Current schemes for introducing lithium into a fusion device consist of lithium evaporators, however, as these devices evolve from pulsed to steady state, new methods will need to be employed such as the LIMIT concept of UIUC, or thin flowing film lithium walls. Critical to their implementation is understanding the interactions of liquid lithium with various surfaces. One such interaction is the wetting of materials by lithium, which may be characterized by the contact angle between the lithium and the surface. Experiments have been performed at UIUC into the contact angle of liquid lithium with a given surface, as well as methods to increase it. To reduce the oxidation rate of the droplets, the experiments were performed in vacuum, using a lithium injector to deposit drops on each surface. Among the materials investigated are stainless steel, both untreated and coated with a diamond like carbon (DLC) layer, molybdenum, and boronized molybdenum. The contact angle and its dependence on temperature is measured.

  15. Visualization of Surface Acoustic Waves in Thin Liquid Films

    OpenAIRE

    Rambach, R. W.; Taiber, J.; Scheck, C. M. L.; Meyer, C.; Reboud, J.; Cooper, Jonathan M.; Franke, T.

    2016-01-01

    We demonstrate that the propagation path of a surface acoustic wave (SAW), excited with anWe demonstrate that the propagation path of a surface acoustic wave (SAW), excited with an interdigitated transducer (IDT), can be visualized using a thin liquid film dispensed onto a lithium niobate (LiNbO3) substrate. The practical advantages of this visualization method are its rapid and simple implementation, with many potential applications including in characterising acoustic pumping within microfl...

  16. Lithium conducting ionic liquids based on lithium borate salts

    Energy Technology Data Exchange (ETDEWEB)

    Zygadlo-Monikowska, E.; Florjanczyk, Z.; Sluzewska, K.; Ostrowska, J.; Langwald, N.; Tomaszewska, A. [Warsaw University of Technology, Faculty of Chemistry, ul. Noakowskiego 3, 00-664 Warsaw (Poland)

    2010-09-15

    The simple reaction of trialkoxyborates with butyllithium resulted in the obtaining of new lithium borate salts: Li{l_brace}[CH{sub 3}(OCH{sub 2}CH{sub 2}){sub n}O]{sub 3}BC{sub 4}H{sub 9}{r_brace}, containing oxyethylene substituents (EO) of n=1, 2, 3 and 7. Salts of n {>=} 2 show properties of room temperature ionic liquid (RTIL) of low glass transition temperature, T{sub g} of the order from -70 to -80 C. The ionic conductivity of the salts depends on the number of EO units, the highest conductivity is shown by the salt with n = 3; in bulk its ambient temperature conductivity is 2 x 10{sup -5} S cm{sup -1} and in solution in cyclic propylene sulfite or EC/PC mixture, conductivity increases by an order of magnitude. Solid polymer electrolytes with borate salts over a wide concentration range, from 10 to 90 mol.% were obtained and characterized. Three types of polymeric matrices: poly(ethylene oxide) (PEO), poly(trimethylene carbonate) (PTMC) and two copolymers of acrylonitrile and butyl acrylate p(AN-BuA) were used in them as polymer matrices. It has been found that for systems of low salt concentration (10 mol.%) the best conducting properties were shown by solid polymer electrolytes with PEO, whereas for systems of high salt concentration, of the polymer-in-salt type, good results were achieved for PTMC as polymer matrix. (author)

  17. Advances in primary lithium liquid cathode batteries

    Science.gov (United States)

    Blomgren, George E.

    1989-05-01

    Recent work on cell development and various aspects of cell chemistry and cell development of lithium/thionyl chloride liquid cathode batteries is reviewed. As a result of safety studies, a number of cell sizes can now be considered satisfactory for many applications and the energy densities of these cells is higher than any other developed battery system. Primary batteries operate with low to moderate currents and the anode delay effect appears to be under reasonable control. Reserve cells are in the design stage and operate at high to very high power densities as well as very high energy densities. The nature of the anode film and the operation of the lithium anode has been studied with substantial success and understanding has grown accordingly. Also, studies of the structure of the electrolyte and the effects on the electrolyte of impurities and additives have led to improved understanding in this area as well. Work in progress on new electrolytes is reviewed. The state of the art of mathematical modeling is also discussed and it is expected that this work will continue to develop.

  18. Lithium titanium oxynitride thin film with enhanced lithium storage and rate capability

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Zhaozhe, E-mail: yuzhaozhe@126.com [School of Microelectronics and Solid-State Electronics, University of Electronic Science and Technology of China, Chengdu 610054 (China); Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); Xu, Huarui, E-mail: huaruixu@guet.edu.cn [School of Microelectronics and Solid-State Electronics, University of Electronic Science and Technology of China, Chengdu 610054 (China); Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); Zhu, Guisheng; Yan, Dongliang [Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); Yu, Aibing [Department of Chemical Engineering, Monash University, Clayton, 3800, VIC (Australia)

    2016-04-15

    Graphical abstract: - Highlights: • LTON thin films are deposited by RF magnetron sputtering with powder target. • The substitution of nitrogen for oxygen can make more abundant cross-linking structures and favor the higher mobility of lithium ions. • The LTON had a high capacity of 290 mAh g{sup −1} at 0.1C, excellent rate capability of 160 mAh g{sup −1} at 5C and only ≈7% capacity loss after 100 cycles at 5C charge and discharge rate. - Abstract: The lithium titanium oxynitride (LTON) thin film electrode was prepared by radio frequency (RF) magnetron sputtering deposition using a cubic spinel structure Li{sub 4}Ti{sub 5}O{sub 12} (LTO) powder target in a N{sub 2} atmosphere for lithium ion batteries. XRD and SEM test results showed that the thin film was composed of weak crystal or amorphous structure and that its surface was homogeneous. XPS analyses indicated that nitrogen atoms were actually incorporated into the LTO matrix framework. The substitution of nitrogen for oxygen in the thin film created more abundant cross-linking structures, which favored the higher mobility of lithium ions. The LTON had a high capacity of 290 mAh g{sup −1} at 0.1C, excellent rate capability of 160 mAh g{sup −1} at 5C and only ≈7% capacity loss after 100 cycles at 5C charge and discharge rate. These properties make this thin film electrode a promising candidate material for use in thin film lithium ion batteries.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-02-04

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

  20. Stable lithium electrodeposition in liquid and nanoporous solid electrolytes

    KAUST Repository

    Lu, Yingying

    2014-08-10

    Rechargeable lithium, sodium and aluminium metal-based batteries are among the most versatile platforms for high-energy, cost-effective electrochemical energy storage. Non-uniform metal deposition and dendrite formation on the negative electrode during repeated cycles of charge and discharge are major hurdles to commercialization of energy-storage devices based on each of these chemistries. A long-held view is that unstable electrodeposition is a consequence of inherent characteristics of these metals and their inability to form uniform electrodeposits on surfaces with inevitable defects. We report on electrodeposition of lithium in simple liquid electrolytes and in nanoporous solids infused with liquid electrolytes. We find that simple liquid electrolytes reinforced with halogenated salt blends exhibit stable long-term cycling at room temperature, often with no signs of deposition instabilities over hundreds of cycles of charge and discharge and thousands of operating hours. We rationalize these observations with the help of surface energy data for the electrolyte/lithium interface and impedance analysis of the interface during different stages of cell operation. Our findings provide support for an important recent theoretical prediction that the surface mobility of lithium is significantly enhanced in the presence of lithium halide salts. Our results also show that a high electrolyte modulus is unnecessary for stable electrodeposition of lithium.

  1. Diagnostics for liquid lithium experiments in CDX-U

    Energy Technology Data Exchange (ETDEWEB)

    R. Kaita; P. Efthimion; D. Hoffman; B. Jones; H. Kugel; R. Majeski; T. Munsat; S. Raftopoulos; G. Taylor; J. Timberlake; V. Soukhanovskii; D. Stutman; M. Iovea; M. Finkenthal; R. Doerner; S. Luckhardt; R. Maingi; R. Causey

    2000-06-21

    A flowing liquid lithium first wall or diverter target could virtually eliminate the concerns with power density and erosion, tritium retention, and cooling associated with solid walls in fusion reactors. To investigate the interaction of a spherical torus plasma with liquid lithium limiters, large area diverter targets, and walls, discharges will be established in the Current Drive Experiment-Upgrade (CDX-U) where the plasma-wall interactions are dominated by liquid lithium surfaces. Among the unique CDX-U lithium diagnostics is a multi-layer mirror (MLM) array, which will monitor the 135 {angstrom} LiIII line for core lithium concentrations. Additional spectroscopic diagnostics include a grazing incidence XUV spectrometer (STRS) and a filterscope system to monitor D{sub {alpha}} and various impurity lines local to the lithium limiter. Profile data will be obtained with a multichannel tangential bolometer and a multipoint Thomson scattering system configured to give enhanced edge resolution. Coupons on th e inner wall of the CDX-U vacuum vessel will be used for surface analysis. A 10,000 frame per second fast visible camera and an IR camera will also be available.

  2. Stable lithium electrodeposition in liquid and nanoporous solid electrolytes

    Science.gov (United States)

    Lu, Yingying; Tu, Zhengyuan; Archer, Lynden A.

    2014-10-01

    Rechargeable lithium, sodium and aluminium metal-based batteries are among the most versatile platforms for high-energy, cost-effective electrochemical energy storage. Non-uniform metal deposition and dendrite formation on the negative electrode during repeated cycles of charge and discharge are major hurdles to commercialization of energy-storage devices based on each of these chemistries. A long-held view is that unstable electrodeposition is a consequence of inherent characteristics of these metals and their inability to form uniform electrodeposits on surfaces with inevitable defects. We report on electrodeposition of lithium in simple liquid electrolytes and in nanoporous solids infused with liquid electrolytes. We find that simple liquid electrolytes reinforced with halogenated salt blends exhibit stable long-term cycling at room temperature, often with no signs of deposition instabilities over hundreds of cycles of charge and discharge and thousands of operating hours. We rationalize these observations with the help of surface energy data for the electrolyte/lithium interface and impedance analysis of the interface during different stages of cell operation. Our findings provide support for an important recent theoretical prediction that the surface mobility of lithium is significantly enhanced in the presence of lithium halide salts. Our results also show that a high electrolyte modulus is unnecessary for stable electrodeposition of lithium.

  3. Liquid lithium for high power density fragmentation targets

    Science.gov (United States)

    Nolen, J. A.; Reed, C. B.; Hassanein, A.; Morrissey, D. J.; Ottarson, J. H.; Sherrill, B. M.

    2001-10-01

    Windowless liquid lithium targets for in-flight fragmentation or fission of high power heavy ion beams are being developed for the U.S. RIA project. With uranium beam power of 100 kW and a beam spot diameter of 1 mm the power density in the target is over 1 MW/cm3. Thermal analysis for this example indicates a very low peak temperature for the lithium when flowing at a linear velocity of 10 m/s. A vacuum test chamber is under construction at Argonne at an existing liquid lithium facility to demonstrate a 2 cm thick windowless target. As a first step towards using liquid lithium target technology at a nuclear physics fragmentation facility, a lower power target is being constructed for use at the NSCL. This target will use beryllium windows with flowing lithium. It is designed for beams between oxygen and calcium with beam power above 3 kW. The tapered beryllium windows are each 1 mm thick for the calcium beams and 7 mm thick for the oxygen beams. The lithium is 5 mm thick. This gives an overall target thickness ranging from about 1 g/cm2 to 3 g/cm2 which is adjusted by moving the target vertically. The designs of these targets and the status of the prototypes will be discussed.

  4. Different roles of ionic liquids in lithium batteries

    Science.gov (United States)

    Eftekhari, Ali; Liu, Yang; Chen, Pu

    2016-12-01

    Ionic liquids are often named solvents of the future because of flexibility in design. This statement has given credence that ionic liquids should simply replace the problematic electrolytes of lithium batteries. As a result, the promising potentials of ionic liquids in electrochemical systems are somehow obscured by inappropriate expectations. We summarize recent advancements in this field, especially, ionic liquids as standalone electrolytes, additives, plasticizers in gel polymer electrolytes, and binders; and attempt to shed light on the future pathway of this area of research. Ionic liquids are not dilute media to serve as pure solvents in electrochemical systems where mobility of ions is the priority; instead, they can contribute to the ionic conductivity of various components in a battery system. Owing to the enormous possibilities of ionic liquids, it is not merely a matter of choice. Ionic liquids can be used to design novel types of electrolytes for a new generation of lithium batteries. A promising possibility, which is still at a very early stage, is supercooled ionic liquid crystals for fast ion diffusion through the guided channels of a liquid-like medium. This, of course, will be a breakthrough in the realm of electrochemistry, far beyond lithium battery field, when materialized.

  5. Silver: high performance anode for thin film lithium ion batteries

    Science.gov (United States)

    Taillades, G.; Sarradin, J.

    Among metals and intermetallic compounds, silver exhibits a high specific capacity according to the formation of different Ag-Li alloys (up to AgLi 12) in a very low voltage range versus lithium (0.250-0 V). Electrochemical results including Galvanostatic Intermittent Titration Technique (GITT) as well as cycling behaviour experiments confirmed the interesting characteristics of silver thin film electrodes prepared by radio frequency (r.f.) sputtering. XRD patterns recorded at different electrochemical stages of the alloying/de-alloying processes showed the complexity of the silver-lithium system under dynamic conditions. Cycling life depends on several parameters and particularly of the careful choice of cut-off voltages. In very well monitored conditions, galvanostatic cycles exhibited flat reversible plateaus with a minimal voltage value (0.050 V) between charge and discharge, a feature of great interest in the use of an electrode. The first results of a lithium ion battery with both silver and LiMn 1.5Ni 0.5O 4 thin films are presented.

  6. Ultra-thin lithium micro-batteries. Performances and applications; Microaccumulateurs ultra minces au lithium. Performances et applications

    Energy Technology Data Exchange (ETDEWEB)

    Martin, M.; Terrat, J.P. [Hydromecanique et frottement (HEF), 42 - Andrezieux Boutheon (France); Levasseur, A.; Vinatier, P.; Meunier, G. [Centre National de la Recherche Scientifique (CNRS), 33 - Talence (France). Institut de Chimie de la Matiere Condensee et Physique de Bordeaux

    1996-12-31

    This short paper (abstract) describes the characteristics and performances of prototypes of ultra-thin lithium micro-batteries (thickness < 0.2 mm) which can be incorporated into microelectronic circuits. (J.S.)

  7. TECXY study of a liquid lithium divertor for DEMO

    Energy Technology Data Exchange (ETDEWEB)

    Pelka, G.; Chmielewski, P.; Zagorski, R. [Institute of Plasma Physics and Laser Microfusion, Warsaw (Poland); Pericoli-Ridolfini, V.; Viola, B. [ENEA C.R. Frascati, Roma (Italy)

    2016-08-15

    Divertor targets made out of a capillary porous system (CPS) filled with liquid lithium, have been proposed as an alternative to standard, solid state plates. In the current work we simulate the DEMO edge plasma in either a standard single-null or snowflake divertor configuration. Our tool is the 2D code TECXY. Lithium ablated from the target plate surface and released into the plasma is shown here to partially screen the incoming heat flux. Lithium's moderate SOL radiation levels suggest additional seeding to be beneficial. Very high heat fluxes to the divertor need to be avoided, as intensive lithium evaporation might unacceptably pollute the plasma. (copyright 2016 The Authors. Contributions to Plasma Physics published by Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  8. Visualization of Surface Acoustic Waves in Thin Liquid Films

    Science.gov (United States)

    Rambach, R. W.; Taiber, J.; Scheck, C. M. L.; Meyer, C.; Reboud, J.; Cooper, J. M.; Franke, T.

    2016-02-01

    We demonstrate that the propagation path of a surface acoustic wave (SAW), excited with an interdigitated transducer (IDT), can be visualized using a thin liquid film dispensed onto a lithium niobate (LiNbO3) substrate. The practical advantages of this visualization method are its rapid and simple implementation, with many potential applications including in characterising acoustic pumping within microfluidic channels. It also enables low-cost characterisation of IDT designs thereby allowing the determination of anisotropy and orientation of the piezoelectric substrate without the requirement for sophisticated and expensive equipment. Here, we show that the optical visibility of the sound path critically depends on the physical properties of the liquid film and identify heptane and methanol as most contrast rich solvents for visualization of SAW. We also provide a detailed theoretical description of this effect.

  9. Time-of-flight secondary ion mass spectrometry study of lithium intercalation process in LiCoO2 thin film

    Science.gov (United States)

    Dellen, C.; Gehrke, H.-G.; Möller, S.; Tsai, C.-L.; Breuer, U.; Uhlenbruck, S.; Guillon, O.; Finsterbusch, M.; Bram, M.

    2016-07-01

    A detailed time-of-flight secondary ion mass spectrometry (ToF-SIMS) analysis of the lithium de-/intercalation in thin films of the insertion cathode material lithium cobalt oxide is presented. The LiCoO2 (LCO) thin films are deposited by radio frequency magnetron sputtering at 600 °C, having a (003) preferred orientation after the deposition. The thin electrode films are cycled with liquid electrolyte against lithium metal, showing 80-86% extractable capacities. After disassembling the cells, the depth resolved elemental distribution in the LCO is investigated by ToF-SIMS and glow discharge optical emission spectroscopy. Both techniques show a stepwise lithium distribution in charged state, leading to a lithium depleted layer close to the surface. In combination with the electrochemical results, the qualitative comparison of the different lithium depth profiles yields a reversible lithium extraction in the depleted area below the stability limit for bulk materials of LCO. For bulk LCO, a phase change normally occurs when the lithium concentration in LixCoO2 is lower than x = 0.5. As a possible cause for the inhibition of the phase change, the preferred orientation and thus pinning of the crystal structure of the film by the substrate is proposed.

  10. Nano-sponge ionic liquid-polymer composite electrolytes for solid-state lithium power sources

    Energy Technology Data Exchange (ETDEWEB)

    Liao, Kang-Shyang; Andreoli, Enrico; Curran, Seamus A. [Department of Physics, University of Houston, Houston, TX 77004 (United States); Sutto, Thomas E. [Naval Research Labs-DC, Materials Science and Technology Division, Washington, DC 20375 (United States); Ajayan, Pulickel [Department of Materials Engineering, Rice University, Houston, TX 77005 (United States); McGrady, Karen A. [Marine Corps System Command, 50 Tech Parkway, Garrisonville, VA 22463 (United States)

    2010-02-01

    Solid polymer gel electrolytes composed of 75 wt.% of the ionic liquid, 1-n-butyl-2,3-dimethylimidazolium bis-trifluoromethanesulfonylimide with 1.0 M lithium bis-trifluoromethanesulfonylimide and 25 wt.% poly(vinylidenedifluoro-hexafluoropropene) are characterized as the electrolyte/separator in solid-state lithium batteries. The ionic conductivity of these gels ranges from 1.5 to 2.0 mS cm{sup -1}, which is several orders of magnitude more conductive than any of the more commonly used solid polymers, and comparable to the best solid gel electrolytes currently used in industry. TGA indicates that these polymer gel electrolytes are thermally stable to over 280 C, and do not begin to thermally decompose until over 300 C; exhibiting a significant advancement in the safety of lithium batteries. Atomic force microscopy images of these solid thin films indicate that these polymer gel electrolytes have the structure of nano-sponges, with a sub-micron pore size. For these thin film batteries, 150 charge-discharge cycles are run for Li{sub x}CoO{sub 2} where x is cycled between 0.95 down to 0.55. Minimal internal resistance effects are observed over the charging cycles, indicating the high ionic conductivity of the ionic liquid solid polymer gel electrolyte. The overall cell efficiency is approximately 98%, and no significant loss in battery efficiency is observed over the 150 cycles. (author)

  11. Thin film passivation of laser generated 3D micro patterns in lithium manganese oxide cathodes

    Science.gov (United States)

    Pröll, J.; Kohler, R.; Bruns, M.; Oberst, V.; Weidler, P. G.; Heißler, S.; Kübel, C.; Scherer, T.; Prang, R.; Seifert, H. J.; Pfleging, W.

    2013-03-01

    The increasing need for long-life lithium-ion batteries requires the further development of electrode materials. Especially on the cathode side new materials or material composites are needed to increase the cycle lifetime. On the one hand, spinel-type lithium manganese oxide is a promising candidate to be used as cathode material due to its non-toxicity, low cost and good thermal stability. On the other hand, the spinel structure suffers from change in the oxidation state of manganese during cycling which is also accompanied by loss of active material into the liquid electrolyte. The general trend is to enhance the active surface area of the cathode in order to increase lithium-ion mobility through the electrode/electrolyte interface, while an enhanced surface area will also promote chemical degradation. In this work, laser microstructuring of lithium manganese oxide thin films was applied in a first step to increase the active surface area. This was done by using 248 nm excimer laser radiation and chromium/quartz mask imaging techniques. In a second step, high power diode laser-annealing operating at a wavelength of 940 nm was used for forming a cubic spinel-like battery phase. This was verified by means of Raman spectroscopy and cyclic voltammetric measurements. In a last step, the laser patterned thin films were coated with indium tin oxide (ITO) layers with a thickness of 10 nm to 50 nm. The influence of the 3D surface topography as well as the ITO thickness on the electrochemical performance was studied by cyclic voltammetry. Post-mortem studies were carried out by using scanning electron microscopy and focused ion beam analysis.

  12. Thin liquid films dewetting and polymer flow

    CERN Document Server

    Blossey, Ralf

    2012-01-01

    This book is a treatise on the thermodynamic and dynamic properties of thin liquid films at solid surfaces and, in particular, their rupture instabilities. For the quantitative study of these phenomena, polymer thin films haven proven to be an invaluable experimental model system.   What is it that makes thin film instabilities special and interesting, warranting a whole book? There are several answers to this. Firstly, thin polymeric films have an important range of applications, and with the increase in the number of technologies available to produce and to study them, this range is likely to expand. An understanding of their instabilities is therefore of practical relevance for the design of such films.   Secondly, thin liquid films are an interdisciplinary research topic. Interdisciplinary research is surely not an end to itself, but in this case it leads to a fairly heterogeneous community of theoretical and experimental physicists, engineers, physical chemists, mathematicians and others working on the...

  13. Electrical detection of liquid lithium leaks from pipe jointsa)

    Science.gov (United States)

    Schwartz, J. A.; Jaworski, M. A.; Mehl, J.; Kaita, R.; Mozulay, R.

    2014-11-01

    A test stand for flowing liquid lithium is under construction at Princeton Plasma Physics Laboratory. As liquid lithium reacts with atmospheric gases and water, an electrical interlock system for detecting leaks and safely shutting down the apparatus has been constructed. A defense in depth strategy is taken to minimize the risk and impact of potential leaks. Each demountable joint is diagnosed with a cylindrical copper shell electrically isolated from the loop. By monitoring the electrical resistance between the pipe and the copper shell, a leak of (conductive) liquid lithium can be detected. Any resistance of less than 2 kΩ trips a relay, shutting off power to the heaters and pump. The system has been successfully tested with liquid gallium as a surrogate liquid metal. The circuit features an extensible number of channels to allow for future expansion of the loop. To ease diagnosis of faults, the status of each channel is shown with an analog front panel LED, and monitored and logged digitally by LabVIEW.

  14. Homogeneous lithium electrodeposition with pyrrolidinium-based ionic liquid electrolytes.

    Science.gov (United States)

    Grande, Lorenzo; von Zamory, Jan; Koch, Stephan L; Kalhoff, Julian; Paillard, Elie; Passerini, Stefano

    2015-03-18

    In this study, we report on the electroplating and stripping of lithium in two ionic liquid (IL) based electrolytes, namely N-butyl-N-methylpyrrolidinium bis(fluorosulfonyl) imide (Pyr14FSI) and N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (Pyr14TFSI), and mixtures thereof, both on nickel and lithium electrodes. An improved method to evaluate the Li cycling efficiency confirmed that homogeneous electroplating (and stripping) of Li is possible with TFSI-based ILs. Moreover, the presence of native surface features on lithium, directly observable via scanning electron microscope imaging, was used to demonstrate the enhanced electrolyte interphase (SEI)-forming ability, that is, fast cathodic reactivity of this class of electrolytes and the suppressed dendrite growth. Finally, the induced inhomogeneous deposition enabled us to witness the SEI cracking and revealed previously unreported bundled Li fibers below the pre-existing SEI and nonrod-shaped protuberances resulting from Li extrusion.

  15. Liquid electrolytes based on new lithium conductive imidazole salts

    Energy Technology Data Exchange (ETDEWEB)

    Niedzicki, L.; Kasprzyk, M.; Kuziak, K.; Zukowska, G.Z.; Marcinek, M.; Wieczorek, W. [Department of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warsaw (Poland); Armand, M. [LRCS, University de Picardie Jules Verne, UMR 6007 CNRS, 33 rue de Saint-Leu, 80039 Amiens (France)

    2011-02-01

    In the present paper new generation of imidazole-derived lithium salts (LiTDI - lithium 4,5-dicyano-2-(trifluoromethyl)imidazolide, LiPDI - lithium 4,5-dicyano-2-(pentafluoroethyl)imidazolide and LiHDI - lithium 4,5-dicyano-2-(n-heptafluoropropyl)imidazolide) applied in a model liquid electrolyte, with propylene carbonate used as a solvent, is described. Room temperature ionic conductivities measured by Impedance Spectroscopy are as high as 10{sup -2} to 10{sup -3} S cm{sup -1} for the 0.1-1 mol dm{sup -3} salt concentration range. Lithium cation transference numbers calculated using the Bruce-Vincent method exceed 0.4 at salt concentration equal to 1 mol dm{sup -3}. Interface resistance measurements showed good stability at high - 0.5 mol dm{sup -3} or low - 0.01 mol dm{sup -3} salt concentrations. Ionic associations were estimated using Fuoss-Kraus semiempirical method revealing relatively low association rates. The effect of anion structure on ionic interactions and electrochemical characteristics of the studied electrolytes is discussed. (author)

  16. Velocity Measurements of Thermoelectric Driven Flowing Liquid Lithium

    Science.gov (United States)

    Szott, Matthew; Xu, Wenyu; Fiflis, Peter; Haehnlein, Ian; Kapat, Aveek; Kalathiparambil, Kishor; Ruzic, David N.

    2014-10-01

    Liquid lithium has garnered additional attention as a PFC due to its several advantages over solid PFCs, including reduced erosion and thermal fatigue, increased heat transfer, higher device lifetime, and enhanced plasma performance due to the establishment of low recycling regimes at the wall. The Lithium Metal Infused Trenches concept (LiMIT) has demonstrated thermoelectric magnetohydrodynamic flow of liquid lithium through horizontal open-faced metal trenches with measured velocities varying from 3.7+/-0.5 cm/s in the 1.76 T field of HT-7 to 22+/-3 cm/s in the SLiDE facility at UIUC at 0.059 T. To demonstrate the versatility of the concept, a new LiMIT design using narrower trenches shows steady state, thermoelectric-driven flow at an arbitrary angle from horizontal. Velocity characteristics are measured and discussed. Based on this LiMIT concept, a new limiter design has been developed to be tested on the mid-plane of the EAST plasma. Preliminary modelling suggests lithium flow of 6 cm/s in this device. Additionally, recent testing at the Magnum-PSI facility has given encouraging results, and velocity measurements in relation to magnetic field strength and plasma flux are also presented.

  17. Effect of Energetic Plasma Flux on Flowing Liquid Lithium Surfaces

    Science.gov (United States)

    Kalathiparambil, Kishor; Jung, Soonwook; Christenson, Michael; Fiflis, Peter; Xu, Wenyu; Szott, Mathew; Ruzic, David

    2014-10-01

    An operational liquid lithium system with steady state flow driven by thermo-electric magneto-hydrodynamic force and capable of constantly refreshing the plasma exposed surface have been demonstrated at U of I. To evaluate the system performance in reactor relevant conditions, specifically to understand the effect of disruptive plasma events on the performance of the liquid metal PFCs, the setup was integrated to a pulsed plasma generator. A coaxial plasma generator drives the plasma towards a theta pinch which preferentially heats the ions, simulating ELM like flux, and the plasma is further guided towards the target chamber which houses the flowing lithium system. The effect of the incident flux is examined using diagnostic tools including triple Langmuir probe, calorimeter, rogowski coils, Ion energy analyzers, and fast frame spectral image acquisition with specific optical filters. The plasma have been well characterized and a density of ~1021 m-3, with electron temperature ~10 - 20 eV is measured, and final plasma velocities of 34 - 74 kms-1 have been observed. Calorimetric measurements using planar molybdenum targets indicate a maximum plasma energy (with 6 kV plasma gun and 20 kV theta pinch) of 0.08 MJm-2 with plasma divergence effects resulting in marginal reduction of 40 +/- 23 J in plasma energy. Further results from the other diagnostic tools, using the flowing lithium targets and the planar targets coated with lithium will be presented. DOE DE-SC0008587.

  18. New, ionic liquid-based membranes for lithium battery application

    Energy Technology Data Exchange (ETDEWEB)

    Sirisopanaporn, C.; Fernicola, A.; Scrosati, B. [Department of Chemistry, University of Rome La Sapienza, 00185 Rome (Italy)

    2009-01-15

    New types of dimensionally stable, flexible gel-type electrolyte membranes with a relatively wide electrochemical stability, high lithium ion conductivity and other desirable properties have been prepared by immobilizing N-n-butyl-N-ethylpyrrolidinium N,N-bis(trifluoromethane)sulfonimide-lithium N,N-bis(trifluoromethane)sulfonimide (Py{sub 24}TFSI-LiTFSI), ionic liquid, IL, solutions in a poly(vinylidene fluoride)-hexafluoropropylene copolymer (PVdF-HFP) matrix. The addition of a discrete amount of ethylene and propylene carbonate (EC-PC), solvent mixture to the membranes resulted in an improvement of the ionic conductivity and in a stabilization of the interface with the lithium electrode. These IL-based gel type membranes can operate without degradation up to a temperature of 110 C where they reach conductivity values of the order of 10{sup -2} S cm{sup -1}. All these properties make these polymer electrolyte membranes of interest for applications as separators in advanced lithium batteries. (author)

  19. Investigation of parameters of interaction of hydrogen isotopes with liquid lithium and lithium capillary-porous system under reactor irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Tazhibayeva, I. L., E-mail: tazhibayeva@ntsc.kz; Kulsartov, T. V.; Gordienko, Yu. N.; Zaurbekova, Zh. A.; Ponkratov, Yu. V.; Barsukov, N. I.; Tulubayev, Ye. Yu.; Baklanov, V. V.; Gnyrya, V. S. [Institute of Atomic Energy NNC RK (Kazakhstan); Kenzhin, Ye. A. [Institute of Nuclear Physics (Kazakhstan)

    2015-12-15

    In this study, the effect of reactor irradiation on the processes of interaction of hydrogen with liquid lithium and a lithium capillary-porous system (CPS) is considered. The experiments are carried out by the gas-absorption method with use of a specially designed ampoule device. The results of investigation of the interaction of hydrogen with liquid lithium and a lithium CPS under conditions of reactor irradiation are described; namely, these are the temperature dependences of the rate constant for the interaction of hydrogen with liquid lithium at different reactor powers, the activation energies of the processes, and the pre-exponential factor in the Arrhenius dependence. The effect of increasing absorption of hydrogen by the samples under investigation as a result of the reactor irradiation is fixed. The effect can be explained by increasing mobility of hydrogen in liquid lithium due to hot spots in lithium bulk and the interaction of helium and tritium ions (formed as a result of the nuclear reaction of {sup 6}Li with neutron) with a surface hydride film.

  20. Preparation of the liquid lithium divertor plates for NSTX

    Science.gov (United States)

    Nygren, R. E.; McKee, G. R.; Fordham, J. A.; Lewis, S. A.; Kugel, H.; Ellis, R. A.; Viola, M. E.; O'Dell, J. S.

    2011-10-01

    Each of the four toroidal panels of the liquid lithium divertor being installed in NSTX for operation in the 2010 campaign is a conical section inclined at 22° like the previous graphite divertor tiles. Each panel is a copper plate clad with stainless steel and a surface layer of porous plasma sprayed molybdenum (Mo) that will host lithium deposited from an evaporator. This paper describes the processes in fabrication; these include cutting to rough shape, die pressing into conical sections, machining to near final shape with holes for electrical heaters, thermocouples and a groove for a cooling tube, brazing of the 0.25-mm cladding and vacuum plasma spraying of the Mo coating.

  1. Tunable Bloch surface waves in anisotropic photonic crystals based on lithium niobate thin films.

    Science.gov (United States)

    Kovalevich, Tatiana; Ndao, Abdoulaye; Suarez, Miguel; Tumenas, Saulius; Balevicius, Zigmas; Ramanavicius, Arunas; Baleviciute, Ieva; Häyrinen, Markus; Roussey, Matthieu; Kuittinen, Markku; Grosjean, Thierry; Bernal, Maria-Pilar

    2016-12-01

    We present an original type of one-dimensional photonic crystal that includes one anisotropic layer made of a lithium niobate thin film. We demonstrate the versatility of such a device sustaining different Bloch surface waves (BSWs), depending on the orientation of the incident wave. By varying the orientation of the illumination of the multilayer, we measured an angle variation of 7° between the BSWs corresponding to the extraordinary and the ordinary index of the lithium niobate thin film. The potential of such a platform opens the way to novel tunable and active planar optics based on the electro- and thermo-optical properties of lithium niobate.

  2. Sputter deposition and characterization of lithium cobalt oxide thin films and their applications in thin-film rechargeable lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang, B.; Bates, J.B.; Luck, C.F.; Sales, B.C.; Zuhr, R.A. [Oak Ridge National Lab., TN (United States); Robertson, J.D. [Kentucky Univ., Lexington, KY (United States). Dept. of Chemistry

    1996-01-01

    Li Co oxide thin films were deposited by rf magnetron sputtering of a LiCoO{sub 2} target in a 3:1 Ar/O{sub 2} mixture gas. From proton-induced gamma-ray emission analysis and Rutherford backscattering spectrometry, the average composition of these films was determined to be Li{sub 1.15}CoO{sub 2.16}. X-ray powder diffraction patterns of films annealed in air at 500-700 C were consistent with regular rhombohedral structure of crystalline LiCoO{sub 2}. Discharge curves of thin film lithium cells with amoprohous LiCoO{sub 2} showed no obvious structural transition between 4.2 and 1.5 V. Shape of discharge curves of cells with polycrystalline cathodes were consistent with a two-phase voltage plateau at {similar_to}3.9 V with a relatively large capacity and two additional smaller plateaus at higher voltages. Cells with the 700 C annealed cathodes showed a capacity loss of {similar_to} after 1000 cycles between 4.2 and 3.0 V.

  3. Response of NSTX liquid lithium divertor to high heat loads

    Energy Technology Data Exchange (ETDEWEB)

    Abrams, T., E-mail: tabrams@pppl.gov [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Jaworski, M.A. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Kallman, J. [Lawrence Livermore National Laboratory, Livermore, CA 94550 (United States); Kaita, R. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Foley, E.L. [Nova Photonics, Inc., Princeton, NJ 08543 (United States); Gray, T.K. [Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Kugel, H. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Levinton, F. [Nova Photonics, Inc., Princeton, NJ 08543 (United States); McLean, A.G. [Lawrence Livermore National Laboratory, Livermore, CA 94550 (United States); Skinner, C.H. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States)

    2013-07-15

    Samples of the NSTX Liquid Lithium Divertor (LLD) with and without an evaporative Li coating were directly exposed to a neutral beam ex-situ at a power of ∼1.5 MW/m{sup 2} for 1–3 s. Measurements of front face and bulk sample temperature were obtained. Predictions of temperature evolution were derived from a 1D heat flux model. No macroscopic damage occurred when the “bare” sample was exposed to the beam but microscopic changes to the surface were observed. The Li-coated sample developed a lithium hydroxide (LiOH) coating, which did not change even when the front face temperature exceeded the pure Li melting point. These results are consistent with the lack of damage to the LLD surface and imply that heating alone may not expose pure liquid Li if the melting point of surface impurities is not exceeded. This suggests that flow and heat are needed for future PFCs requiring a liquid Li surface.

  4. 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.

  5. Effects of a liquid lithium curtain as the first wall in a fusion reactor plasma

    Institute of Scientific and Technical Information of China (English)

    Li Cheng-Yue; J.P. Allain; Deng Bai-Quan

    2007-01-01

    This paper explores the effect of a liquid lithium curtain on fusion reactor plasma, such curtain is utilized as the first wall for the engineering outline design of the Fusion Experimental Breeder (FEB-E). The relationships between the surface temperature of a liquid lithium curtain and the effective plasma charge, fuel dilution and fusion power production have been derived. Results indicate that under normal operation, the evaporation of liquid lithium does not seriously affect the effective plasma charge, but effects on fuel dilution and fusion power are more sensitive. As an example, it has investigated the relationships between the liquid lithium curtain flow velocity and the rise of surface temperature based on operation scenario Ⅱ of the FEB-E design with reversed shear configuration and high power density. Results show that even if the liquid lithium curtain flow velocity is as low as 0.5 m/s, the effects of evaporation from the liquid lithium curtain on plasma are negligible. In the present design, the sputtering of liquid lithium curtain and the particle removal effects of the divertor are not yet considered in detail. Further studies are in progress, and in this work implication of lithium erosion and divertor physics on fusion reactor operation are discussed.

  6. Thin Flexible Lithium Ion Battery Featuring Graphite Paper Based Current Collectors with Enhanced Conductivity

    CERN Document Server

    Qu, Hang; Tang, Yufeng; Semenikihin, Oleg; Skorobogatiy, Maksim

    2015-01-01

    A flexible, light weight and high conductivity current collector is the key element that enables fabrication of high performance flexible lithium ion battery. Here we report a thin, light weight and flexible lithium ion battery that uses graphite paper enhanced with a nano-sized metallic layers as the current collector, LiFePO4 and Li4Ti5O12 as the cathode and anode materials, and PE membrane soaked in LiPF6 as a separator. Using thin and flexible graphite paper as a substrate for the current collector instead of a rigid and heavy metal foil enables us to demonstrate a very thin Lithium-Ion Battery into ultra-thin (total thickness including encapsulation layers of less than 250 {\\mu}m) that is also light weight and highly flexible.

  7. Liquid lithium self-cooled breeding blanket design for ITER

    Energy Technology Data Exchange (ETDEWEB)

    Kirillov, I.R.; Sidorenkov, S.I. [Research Inst. of Electrophysical Apparatus, St. Petersburg (Russian Federation); Danilov, I.V.; Strebkov, Yu.S. [Research and Development Institute of Power Engineering, 101100 Moscow (Russian Federation); Mattas, R.F.; Hua, T.Q.; Smith, D.L. [Fusion Power Program, Argonne National Laboratory, Chicago, IL 60439 (United States); Gohard, Y. [ITER Garching Joint Work Site, Max-Planck-Institut fur Plasmaphysik, D-85748 Garching bei Munchen (Germany)

    1998-09-01

    To meet the technical objectives of the ITER extended performance phase (EPP) an advanced tritium breeding lithium/vanadium (Li/V) blanket was developed by two home teams (US and RF). The design is based on the use of liquid Li as coolant and breeder and vanadium alloy (V-Cr-Ti) as structural material. The first wall is coated with a beryllium protection layer. Beryllium is also integrated in the blanket for neutron multiplication and improved shielding. The use of tungsten carbide in the primary shield and in vacuum vessel provides adequate protection for toroidal field coils. A self-healing electrical insulator in the form of CaO or AlN coating layer is utilized to reduce MHD pressure drop in the system. To have a self-consistent ITER design, liquid metal cooling of the divertor and vacuum vessel is considered as well. (orig.) 16 refs.

  8. Thin liquid sample fabrication for neutron resonance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Noguere, G. [CEA Cadarache, F-13108 Saint Paul les Durance (France)], E-mail: gilles.noguere@cea.fr; Brusegan, A. [EC-JRC-IRMM, B-2440 Geel (Belgium); Lepretre, A. [CEA Saclay, F-91191 Gif sur Yvette (France); Lombard, T.; Lupo, J. [EC-JRC-IRMM, B-2440 Geel (Belgium)

    2008-03-11

    In neutron resonance spectroscopy, preparation of thin cylindrical samples of large diameter containing 10{sup -4}-10{sup -5} atoms per barn of raw materials in powder form make pressing a uniform thickness sample difficult. The use of liquid samples is a suitable alternative to overcome the technical limits inherent to the fabrication of pressed solid samples by compaction methods. This paper presents the fabrication of a 2 mm thick cylindrical sample, with a inner diameter of 65 mm, filled with an aqueous solution of lithium iodide. The sample was designed to measure the low neutron energy range of the {sup 127}I total cross-section by means of the neutron resonance transmission technique. The resonance shape analysis provided results consistent with those obtained by measuring a 17.5 mm thick lead iodine sample under the same experimental conditions as for LiI sample. Such liquid sample could be used to repeat similar measurements on a large variety of stable isotopes and low radioactive materials.

  9. Effects of Large Area Liquid Lithium Limiters on Spherical Torus Plasmas

    Energy Technology Data Exchange (ETDEWEB)

    R. Kaita; R. Majeski; M. Boaz; P. Efthimion; G. Gettelfinger; T. Gray; D. Hoffman; S. Jardin; H. Kugel; P. Marfuta; T. Munsat; C. Neumeyer; S. Raftopoulos; V. Soukhanovskii; J. Spaleta; G. Taylor; J. Timberlake; R. Woolley; L. Zakharov; M. Finkenthal; D. Stutman; L. Delgado-Aparicio; R.P. Seraydarian; G. Antar; R. Doerner; S. Luckhardt; M. Baldwin; R.W. Conn; R. Maingi; M. Menon; R. Causey; D. Buchenauer; M. Ulrickson; B. Jones; D. Rodgers

    2004-06-07

    Use of a large-area liquid lithium surface as a first wall has significantly improved the plasma performance in the Current Drive Experiment-Upgrade (CDX-U) at the Princeton Plasma Physics Laboratory. Previous CDX-U experiments with a partially-covered toroidal lithium limiter tray have shown a decrease in impurities and the recycling of hydrogenic species. Improvements in loading techniques have permitted nearly full coverage of the tray surface with liquid lithium. Under these conditions, there was a large drop in the loop voltage needed to sustain the plasma current. The data are consistent with simulations that indicate more stable plasmas having broader current profiles, higher temperatures, and lowered impurities with liquid lithium walls. As further evidence for reduced recycling with a liquid lithium limiter, the gas puffing had to be increased by up to a factor of eight for the same plasma density achieved with an empty toroidal tray limiter.

  10. Effects of Large Area Liquid Lithium Limiters on Spherical Torus Plasmas

    Energy Technology Data Exchange (ETDEWEB)

    Kaita, R; Jajeski, R; Boaz, M; Efthimion, P; Gettelfinger, G; Gray, T; Hoffman, D; Jardin, S; Kugel, H; Marfuta, P; Munsat, T; Neumeyer, C; Raftopoulos, S; Soukhanovskii, V; Spaleta, J; Taylor, G; Timberlake, J; Woolley, R; Zakharov, L; Finkenthal, M; Stutman, D; Delgado-Aparicio, L; Seraydarian, R; Antar, G; Doerner, R; Luckhardt, S; Baldwin, M; Conn, R; Maingi, R; Menon, M; Causey, R; Buchenauer, D; Ulrickson, M; Jones, B; Rodgers, D

    2004-06-03

    Use of a large-area liquid lithium surface as a first wall has significantly improved the plasma performance in the Current Drive Experiment-Upgrade (CDX-U) at the Princeton Plasma Physics Laboratory. Previous CDX-U experiments with a partially-covered toroidal lithium limiter tray have shown a decrease in impurities and the recycling of hydrogenic species. Improvements in loading techniques have permitted nearly full coverage of the tray surface with liquid lithium. Under these conditions, there was a large drop in the loop voltage needed to sustain the plasma current. The data are consistent with simulations that indicate more stable plasmas having broader current profiles, higher temperatures, and lowered impurities with liquid lithium walls. As further evidence for reduced recycling with a liquid lithium limiter, the gas puffing had to be increased by up to a factor of eight for the same plasma density achieved with an empty toroidal tray limiter.

  11. Effects of large area liquid lithium limiters on spherical torus plasmas

    Energy Technology Data Exchange (ETDEWEB)

    Kaita, R. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States)]. E-mail: kaita@pppl.gov; Majeski, R. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Boaz, M. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Efthimion, P. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Gettelfinger, G. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Gray, T. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Hoffman, D. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Jardin, S. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Kugel, H. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Marfuta, P. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Soukhanovskii, V. [Lawrence Livermore National Laboratory, Livermore, CA (United States); Munsat, T.; Neumeyer, C.; Raftopoulos, S.; Spaleta, J.; Taylor, G.; Timberlake, J.; Woolley, R.; Zakharov, L. [Princeton Plasma Physics Laboratory, P.O. Box 451, Princeton, NJ 08543 (United States); Finkenthal, M.; Stutman, D.; Delgado-Aparicio, L. [Johns Hopkins University, Baltimore, MD (United States); Seraydarian, R.P.; Antar, G.; Doerner, R.; Luckhardt, S.; Baldwin, M.; Conn, R.W. [University of California at San Diego, La Jolla, CA (United States); Maingi, R.; Menon, M. [Oak Ridge National Laboratory, Oak Ridge, TN (United States); Causey, R.; Buchenauer, D.; Ulrickson, M.; Jones, B. [Sandia National Laboratories, Albuquerque, NM (United States); Rodgers, D. [Drexel University, Philadelphia, PA (United States)

    2005-03-01

    Use of a large-area liquid lithium surface as a limiter has significantly improved the plasma performance in the Current Drive Experiment-Upgrade (CDX-U) at the Princeton Plasma Physics Laboratory. Previous CDX-U experiments with a partially-covered toroidal lithium limiter tray have shown a decrease in impurities and the recycling of hydrogenic species. Improvements in loading techniques have permitted nearly full coverage of the tray surface with liquid lithium. Under these conditions, there was a large drop in the loop voltage needed to sustain the plasma current. The data are consistent with simulations that indicate more stable plasmas having broader current profiles, higher temperatures, and lowered impurities with liquid lithium walls. As further evidence for reduced recycling with a liquid lithium limiter, the gas puffing had to be increased by up to a factor of eight for the same plasma density achieved with an empty toroidal tray limiter.

  12. Novel intercore-cladding lithium niobate thin film coated MOEMS fiber sensor/modulator

    Science.gov (United States)

    Jamlson, Tracee L.; Konreich, Phillip; Yu, Chung

    2005-01-01

    A MOEMS fiber modulator/sensor is fabricated by depositing a lithium niobate sol-gel thin film between the core and cladding of a fiber preform. The preform is then drawn into 125-micron fibers. Such a MOEMS modulator design is expected to enhance existing lithium niobate undersea acousto-optic sound wave detectors. In our proposed version, the lithium niobate thin film alters the ordinary silica core/cladding boundary conditions such that, when a stress or strain is applied to the fiber, the core light confinement factor changes, leading to modulation of fiber light transmission. Test results of the lithium niobate embedded fiber with a 1550-nm, 4-mW laser source revealed a reduction in light transmission with applied tension. As a comparison, using the same laser source, an ordinary silica core/cladding fiber did not exhibit any reduction in transmitted light when the same strain was applied. Further experimental work and theoretical analysis is ongoing.

  13. Novel intercore-cladding lithium niobate thin film coated MOEMS fiber sensor/modulator

    Science.gov (United States)

    Jamlson, Tracee L.; Konreich, Phillip; Yu, Chung

    2005-01-01

    A MOEMS fiber modulator/sensor is fabricated by depositing a lithium niobate sol-gel thin film between the core and cladding of a fiber preform. The preform is then drawn into 125-micron fibers. Such a MOEMS modulator design is expected to enhance existing lithium niobate undersea acousto-optic sound wave detectors. In our proposed version, the lithium niobate thin film alters the ordinary silica core/cladding boundary conditions such that, when a stress or strain is applied to the fiber, the core light confinement factor changes, leading to modulation of fiber light transmission. Test results of the lithium niobate embedded fiber with a 1550-nm, 4-mW laser source revealed a reduction in light transmission with applied tension. As a comparison, using the same laser source, an ordinary silica core/cladding fiber did not exhibit any reduction in transmitted light when the same strain was applied. Further experimental work and theoretical analysis is ongoing.

  14. A Novel Inter Core-Cladding Lithium Niobate Thin Film Coated Fiber Modulator/Sensor

    Science.gov (United States)

    Jamison, Tracee L.; Komriech, Phillip; Yu, Chung

    2004-01-01

    A fiber modulator/sensor has been fabricated by depositing a lithium niobate sol-gel thin film between the core and cladding of a fiber preform. The preform is then drawn into 125 micron fiber. The proposed design of lithium niobate cylinder fibers can enhance the existing methodology for detecting sound waves under water utilizing the acoustooptic properties of lithium niobate. Upon application of a stress or strain, light propagating inside the core, according to the principle of total internal reflection, escapes, into the cladding because of the photoelastic boundary layer of lithium niobate. Test results of the lithium niobate fiber reveal a reduction in the 1550 nm, 4mW source with applied tension. The source power from an ordinary quartz fiber under the same stress condition remained invariant to applied tension.

  15. Synthesis and Characterization of Thin Film Lithium-Ion Batteries Using Polymer Electrolytes

    Science.gov (United States)

    Maranchi, Jeffrey P.; Kumta, Prashant N.; Hepp, Aloysius F.; Raffaelle, Ryne P.

    2002-01-01

    The present paper describes the integration of thin film electrodes with polymer electrolytes to form a complete thin film lithium-ion battery. Thin film batteries of the type, LiCoO2 [PAN, EC, PC, LiN(CF3SO2)2] SnO2 have been fabricated. The results of the synthesis and characterization studies will be presented and discussed.

  16. Lithium ion conductive behavior of TiO2 nanotube/ionic liquid matrices

    OpenAIRE

    2014-01-01

    A series of TiO_2 nanotube (TNT)/ionic liquid matrices were prepared, and their lithium ion conductive properties were studied. SEM images implied that ionic liquid was dispersed on the whole surface of TNT. Addition of TNT to ionic liquid (1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide (BMImTFSA)) resulted in significant increase of ionic conductivity. Furthermore, lithium transference number was also largely enhanced due to the interaction of anion with TNT. Vogel-Fulcher-Tam...

  17. Study of electrical resistivity of lithium-indium thin films

    Science.gov (United States)

    Chandra, Gyanesh; Katyal, O. P.

    1984-12-01

    Experimental results are presented on the electrical resistivity of lithium-indium films. The resistivity has been studied as a function of temperature (150-300 K), thickness of the films (570-3300 Å) and concentration of Li (11.0-58.7 at. %). The resistivity is observed to be minimum for samples having a Li concentration of 25 and 50 at. %. In general, resistivity varies linearly with temperature but resistivity versus temperature plot shows two distinct regions which have different slopes, i.e., dρ/dT. The role of lithium in indium-lithium films is discussed.

  18. VUV/XUV measurements of impurity emission in plasmas with liquid lithium surfaces on LTX

    Science.gov (United States)

    Tritz, Kevin; Bell, Ronald E.; Beiersdorfer, Peter; Boyle, Dennis; Clementson, Joel; Finkenthal, Michael; Kaita, Robert; Kozub, Tom; Kubota, Shigeyuki; Lucia, Matthew; Majeski, Richard; Merino, Enrique; Schmitt, John; Stutman, Dan

    2014-12-01

    The VUV/XUV spectrum has been measured on the Lithium Tokamak eXperiment (LTX) using a transmission grating imaging spectrometer (TGIS) coupled to a direct-detection x-ray charge-coupled device camera. TGIS data show significant changes in the ratios between the lithium and oxygen impurity line emission during discharges with varying lithium wall conditions. Lithium coatings that have been passivated by lengthy exposure to significant levels of impurities contribute to a large O/Li ratio measured during LTX plasma discharges. Furthermore, previous results have indicated that a passivated lithium film on the plasma facing components will function as a stronger impurity source when in the form of a hot liquid layer compared to a solid lithium layer. However, recent TGIS measurements of plasma discharges in LTX with hot stainless steel boundary shells and a fresh liquid lithium coating show lower O/Li impurity line ratios when compared to discharges with a solid lithium film on cool shells. These new measurements help elucidate the somewhat contradictory results of the effects of solid and liquid lithium on plasma confinement observed in previous experiments.

  19. Cathode limited charge transport and performance of thin-film rechargeable lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Bates, J.B.; Hart, F.X.; Lubben, D.; Kwak, B.S.; van Zomeren, A.

    1994-11-01

    Several types of thin-film rechargeable batteries based on lithium metal anodes and amorphous V{sub 2}O{sub 5} (aV{sub 2}O{sub 5}), LiMn{sub 2}O{sub 4}, and LiCoO{sub 2} cathodes have been investigated in this laboratory. In all cases, the current density of these cells is limited by lithium ion transport in the cathodes. This paper, discusses sources of this impedance in Li-aV{sub 2}O{sub 5} and Li-LiMn{sub 2}O{sub 4} thin-film cells and their effect on cell performance.

  20. Tailoring the dispersion behavior of optical nanowires with intercore-cladding lithium niobate thin film.

    Science.gov (United States)

    He, Hairong; Miao, Lili; Jiang, Guobao; Zhao, Chujun; Wen, Shuangchun

    2015-10-19

    The dispersion properties of silica and silicon subwavelength-diameter wires with intercore-cladding uniaxial dielectric lithium niobate thin film has been studied numerically in detail. The waveguide dispersion shifts centered around 1550-nm wavelength have been investigated. It shows that the dispersion of optical nanowires with intercore-cladding lithium niobate thin film is highly sensitive to fiber geometry. Moreover, with applied electric field, considerable dispersion shifts without changing its geometric structure can be obtained. Our work may provide an inroad for developing miniaturized functional optoelectronic devices.

  1. Efficient second harmonic generation in χ(2) profile reconfigured lithium niobate thin film

    Science.gov (United States)

    Cai, Lutong; Wang, Yiwen; Hu, Hui

    2017-03-01

    Second harmonic wave was efficiently generated in proton exchanged lithium niobate thin film channel waveguides. Modal dispersion phase matching was achieved between two guided modes at pump and second-harmonic wavelengths with the same polarization, enabling using the largest second-order nonlinear component d33. The χ(2) profile in the lithium niobate thin film was reconfigured by proton exchange, leading to significantly enhanced modal overlap integral between the interacting modes. Normalized conversion efficiency up to 48% W-1 cm-2 was achieved in experiments.

  2. Mixed ionic liquid as electrolyte for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Diaw, M. [Universite Cheikh Anta Diop, Dakar (Senegal); Chagnes, A.; Carre, B.; Lemordant, D. [Laboratoire de Chimie-physique des Interfaces et des Milieux Reactionnels, (EA2098), Universite F. Rabelais, Faculte des Sciences et Techniques, Parc de Grandmont, 37200 Tours (France); Willmann, P. [CNES, 18 Avenue E. Belin, 31055 Toulouse Cedex (France)

    2005-08-26

    Ionic liquids like 1-butyl-3-methylimidazolium tetrafluoroborate (IMIBF{sub 4}) or hexafluorophosphate (IMIPF{sub 6}) and 1-butyl-4-methylpyridinium tetrafluoroborate (PyBF{sub 4}) were mixed with organic solvents such as butyrolactone (BL) and acetonitrile (ACN). A lithium salt (LiBF{sub 4} or LiPF{sub 6}) was added to these mixtures for possible application in the field of energy storage (batteries or supercapacitors). Viscosities, conductivities and electrochemical windows at a Pt electrode of these electrolytes were investigated. All studied electrolytes are stable toward oxidation and exhibit a vitreous phase transition, which has been determined by application of the VTF theory to conductivity measurements. Mixtures containing the BF{sub 4}{sup -} anion exhibit the lowest viscosity and the highest conductivity. Two mixtures have been optimized in terms of conductivity: BL/IMIBF{sub 4} (60/40, v/v) and ACN/IMIBF{sub 4} (70/30, v/v). (author)

  3. Flexible lithium-ion planer thin-film battery

    KAUST Repository

    Kutbee, Arwa T.

    2016-02-03

    Commercialization of wearable electronics requires miniaturized, flexible power sources. Lithium ion battery is a strong candidate as the next generation high performance flexible battery. The development of flexible materials for battery electrodes suffers from the limited material choices. In this work, we present a flexible inorganic lithium-ion battery with no restrictions on the materials used. The battery showed an enhanced normalized capacity of 146 ??Ah/cm2.

  4. Commentary on the Liquid Metallic Hydrogen Model of the Sun III. Insight into Solar Lithium Abundances

    Directory of Open Access Journals (Sweden)

    Robitaille P.-M.

    2013-04-01

    Full Text Available The apparent depletion of lithium represents one of the grea test challenges to modern gaseous solar models. As a result, lithium has been hypothes ized to undergo nuclear burning deep within the Sun. Conversely, extremely low lith ium abundances can be easily accounted for within the liquid metallic hydrogen mo del, as lithium has been hypothesized to greatly stabilize the formation of metalli c hydrogen (E. Zurek et al. A little bit of lithium does a lot for hydrogen. Proc. Nat. Acad. Sci. USA , 2009, v. 106, no. 42, 17640–17643. Hence, the abundances of lithium on th e solar surface can be explained, not by requiring the nuclear burning of this elem ent, but rather, by suggesting that the Sun is retaining lithium within the solar body in ord er to help stabilize its liquid metallic hydrogen lattice. Unlike lithium, many of t he other elements synthesized within the Sun should experience powerful lattice exclusio nary forces as they are driven out of the intercalate regions between the layered liquid me tallic hydrogen hexagonal planes (Robitaille J.C. and Robitaille P.M. Liquid Metalli c Hydrogen III. Intercalation and Lattice Exclusion Versus Gravitational Settling and Th eir Consequences Relative to Internal Structure, Surface Activity, and Solar Winds in the Sun. Progr. Phys ., 2013, v. 2, in press. As for lithium, its stabilizing role within t he solar interior helps to account for the lack of this element on the surface of the Sun.

  5. Hydrogen, lithium, and lithium hydride production

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-06-20

    A method is provided for extracting hydrogen from lithium hydride. The method includes (a) heating lithium hydride to form liquid-phase lithium hydride; (b) extracting hydrogen from the liquid-phase lithium hydride, leaving residual liquid-phase lithium metal; (c) hydriding the residual liquid-phase lithium metal to form refined lithium hydride; and repeating steps (a) and (b) on the refined lithium hydride.

  6. Conductive lithium nickel oxide thin film patterns via inkjet printing technology

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Chun-Chih, E-mail: r00524055@ntu.edu.tw [Department of Chemical Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan (China); Su, Pei-Chen, E-mail: peichensu@ntu.edu.sg [School of Mechanical and Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Liao, Ying-Chih, E-mail: liaoy@ntu.edu.tw [Department of Chemical Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan (China)

    2013-10-01

    In this research, a simple direct-writing method by inkjet printing to create conductive lithium nickel oxide thin film patterns at micrometer-scale is presented. Nickel/lithium hydroxides dissolved in acetic acid were inkjet-printed on quartz plates to create micro patterns, including lines and meshes, and converted into oxides by thermal pyrolysis. The synthesized thin films were composed of nanoparticles with 60 nm diameter after the sintering process. Thermogravimetric analysis results showed that the precursor inks decomposed into oxides at temperatures higher than 420 °C. The X-ray diffractograms showed that Ni{sub 2}O{sub 3} was synthesized with lithium oxides after sintered at 500 °C for an hour. The existence of Ni{sub 2}O{sub 3} in the prepared thin films leads to better electrical conductivity, which follows the Arrhenius relation with activation energy of 0.38 eV. - Highlights: • Conductive lithium nickel oxide patterns are fabricated via inkjet printing method. • The precursor inks decompose into oxides at temperatures higher than 420 °C. • Surface morphology and crystal structures of the sintered thin films are examined. • Electrical resistivity of the oxide thin films obeys the Arrhenius relation. • An activation energy of 0.38 eV is found in the Arrhenius relation.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2006-06-01

    In this work, thermal and electrochemical properties of neat and mixed ionic liquid - lithium salt systems have been studied. The presence of a lithium salt causes both thermal and phase-behavior changes. Differential scanning calorimeter DSC and thermal gravimetric analysis TGA were used for thermal analysis for several imidazolium bis(trifluoromethylsulfonyl)imide, trifluoromethansulfonate, BF{sub 4}, and PF{sub 6} systems. Conductivities and diffusion coefficient have been measured for some selected systems. Chemical reactions in electrode - ionic liquid electrolyte interfaces were studied by interfacial impedance measurements. Lithium-lithium and lithium-carbon cells were studied at open circuit and a charged system. The ionic liquids studied include various imidazolium systems that are already known to be electrochemically unstable in the presence of lithium metal. In this work the development of interfacial resistance is shown in a Li|BMIMBF{sub 4} + LiBF{sub 4}|Li cell as well as results from some cycling experiments. As the ionic liquid reacts with the lithium electrode the interfacial resistance increases. The results show the magnitude of reactivity due to reduction of the ionic liquid electrolyte that eventually has a detrimental effect on battery performance.

  8. Ionic Liquid-Nanoparticle Hybrid Electrolytes and their Application in Secondary Lithium-Metal Batteries

    KAUST Repository

    Lu, Yingying

    2012-07-12

    Ionic liquid-tethered nanoparticle hybrid electrolytes comprised of silica nanoparticles densely grafted with imidazolium-based ionic liquid chains are shown to retard lithium dendrite growth in rechargeable batteries with metallic lithium anodes. The electrolytes are demonstrated in full cell studies using both high-energy Li/MoS2 and high-power Li/TiO2 secondary batteries. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Magnetowetting of Ferrofluidic Thin Liquid Films

    Science.gov (United States)

    Tenneti, Srinivas; Subramanian, Sri Ganesh; Chakraborty, Monojit; Soni, Gaurav; Dasgupta, Sunando

    2017-03-01

    An extended meniscus of a ferrofluid solution on a silicon surface is subjected to axisymmetric, non-uniform magnetic field resulting in significant forward movement of the thin liquid film. Image analyzing interferometry is used for accurate measurement of the film thickness profile, which in turn, is used to determine the instantaneous slope and the curvature of the moving film. The recorded video, depicting the motion of the film in the Lagrangian frame of reference, is analyzed frame by frame, eliciting accurate information about the velocity and acceleration of the film at any instant of time. The application of the magnetic field has resulted in unique changes of the film profile in terms of significant non-uniform increase in the local film curvature. This was further analyzed by developing a model, taking into account the effect of changes in the magnetic and shape-dependent interfacial force fields.

  10. A silicon-containing nanocomposite for a thin-film lithium-ion battery

    Science.gov (United States)

    Berdnikov, A. E.; Gerashchenko, V. N.; Gusev, V. N.; Kulova, T. L.; Metlitskaya, A. V.; Mironenko, A. A.; Rudyi, A. S.; Skundin, A. M.

    2013-04-01

    A technological basis for manufacturing of a thin-film anode based on a silicon-containing nano-composite for lithium-ion batteries is developed. The results of experimental studies of charge-discharge characteristics, morphology and phase composition for the silicon-containing nanocomposite are presented, confirming the promising character of its application as an anodic material.

  11. Thin-liquid-film evaporation at contact line

    Institute of Scientific and Technical Information of China (English)

    Hao WANG; Zhenai PAN; Zhao CHEN

    2009-01-01

    When a liquid wets a solid wall, the extended meniscus near the contact line may be divided into three regions: a nonevaporating region, where the liquid is adsorbed on the wall; a transition region or thin-film region, where effects of long-range molecular forces (disjoining pressure) are felt; and an intrinsic meniscus region, where capillary forces dominate. The thin liquid film, with thickness from nanometers up to micrometers, covering the transition region and part of intrinsic meniscus, is gaining interest due to its high heat transfer rates. In this paper, a review was made of the researches on thin-liquid-film evaporation. The major characteristics of thin film, thin-film modeling based on continuum theory, simulations based on molecular dynamics, and thin-film profile and temperature measurements were summarized.

  12. Liquid Cooling of Tractive Lithium Ion Batteries Pack with Nanofluids Coolant.

    Science.gov (United States)

    Li, Yang; Xie, Huaqing; Yu, Wei; Li, Jing

    2015-04-01

    The heat generated from tractive lithium ion batteries during discharge-charge process has great impacts on the performances of tractive lithium ion batteries pack. How to solve the thermal abuse in tractive lithium ion batteries pack becomes more and more urgent and important for future development of electrical vehicles. In this work, TiO2, ZnO and diamond nanofluids are prepared and utilized as coolants in indirect liquid cooling of tractive lithium ion batteries pack. The results show that nanofluids present superior cooling performance to that of pure fluids and the diamond nanofluid presents relatively excellent cooling abilities than that of TiO2 and ZnO nanofluids. During discharge process, the temperature distribution of batteries in batteries pack is uniform and stable, due to steady heat dissipation by indirect liquid cooling. It is expected that nanofluids could be considered as a potential alternative for indirect liquid cooling in electrical vehicles.

  13. Lithium

    Science.gov (United States)

    Jaskula, B.W.

    2012-01-01

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

  14. Investigation of tin-lithium eutectic as a liquid plasma facing material

    Science.gov (United States)

    Ruzic, David; Szott, Matthew; Christenson, Michael; Shchelkanov, Ivan; Kalathiparambil, Kishor Kumar

    2016-10-01

    Innovative materials and techniques need to be utilized to address the high heat and particle flux incident on plasma facing components in fusion reactors. A liquid metal diverter module developed at UIUC with self circulating lithium has been successfully demonstrated to be capable of handling the relevant heat flux in plasma gun based tests and on operational tokamaks. The proper geometry of the liquid lithium trenches to minimize droplet ejection during transient plasma events have also been identified. Although lithium has proven to be effective in improved plasma performance and contributes to other advantageous factors like reduction in the fuel recycling, impurity gettering and, owing to the low Z, a significantly reduced impact on plasma as compared to the solid wall materials, it still poses several drawbacks related to its high reactivity and high vapor pressure at the relevant tokamak wall temperatures. The evaporation properties of a new eutectic mixture of tin and lithium (20% Sn) shows that lithium segregates to the surface at melting temperatures and hence is an effective replacement for pure lithium. Also, the vapor from the eutectic is dominated by lithium, minimizing the entry of high Z Sn into the plasma. At UIUC experiments for the synthesis and characterization of the eutectic - measurement of the critical wetting parameters and Seebeck coefficients with respect to the trench materials have been performed to ensure lithium wetting and flow in the trenches. The results will be presented. DOE project DEFG02- 99ER54515.

  15. Mechanical measurements on lithium phosphorous oxynitride coated silicon thin film electrodes for lithium-ion batteries during lithiation and delithiation

    Science.gov (United States)

    Al-Obeidi, Ahmed; Kramer, Dominik; Boles, Steven T.; Mönig, Reiner; Thompson, Carl V.

    2016-08-01

    The development of large stresses during lithiation and delithiation drives mechanical and chemical degradation processes (cracking and electrolyte decomposition) in thin film silicon anodes that complicate the study of normal electrochemical and mechanical processes. To reduce these effects, lithium phosphorous oxynitride (LiPON) coatings were applied to silicon thin film electrodes. Applying a LiPON coating has two purposes. First, the coating acts as a stable artificial solid electrolyte interphase. Second, it limits mechanical degradation by retaining the electrode's planar morphology during cycling. The development of stress in LiPON-coated electrodes was monitored using substrate curvature measurements. LiPON-coated electrodes displayed highly reproducible cycle-to-cycle behavior, unlike uncoated electrodes which had poorer coulombic efficiency and exhibited a continual loss in stress magnitude with continued cycling due to film fracture. The improved mechanical stability of the coated silicon electrodes allowed for a better investigation of rate effects and variations of mechanical properties during electrochemical cycling.

  16. Solution behavior of hydrogen isotopes and other non-metallic elements in liquid lithium

    Energy Technology Data Exchange (ETDEWEB)

    Maroni, V.A.; Calaway, W.F.; Veleckis, E.; Yonco, R.M.

    1976-01-01

    Results of experimental studies to measure selected thermodynamic properties for systems of lithium with non-metallic elements are reported. Investigations of the Li-H, Li-D, and Li-T systems have led to the elucidation of the dilute solution behavior and the H/D/T isotope effects. In the case of the Li-H and Li-D systems, the principal features of the respective phase diagrams have been delineated. The solubility of Li-D in liquid lithium has been measured down to 200/sup 0/C. The solubility of Li/sub 3/N in liquid lithium and the thermal decomposition of Li/sub 3/N have also been studied. From these data, the free energy of formation of Li/sub 3/N and the Sieverts' constant for dissolution of nitrogen in lithium have been determined. Based on studies of the distribution of non-metallic elements between liquid lithium and selected molten salts, it appears that molten salt extraction offers promise as a means of removing these impurity elements (e.g., H, D, T, O, N, C) from liquid lithium.

  17. Ionic Liquid-Doped Gel Polymer Electrolyte for Flexible Lithium-Ion Polymer Batteries

    Science.gov (United States)

    Zhang, Ruisi; Chen, Yuanfen; Montazami, Reza

    2015-01-01

    Application of gel polymer electrolytes (GPE) in lithium-ion polymer batteries can address many shortcomings associated with liquid electrolyte lithium-ion batteries. Due to their physical structure, GPEs exhibit lower ion conductivity compared to their liquid counterparts. In this work, we have investigated and report improved ion conductivity in GPEs doped with ionic liquid. Samples containing ionic liquid at a variety of volume percentages (vol %) were characterized for their electrochemical and ionic properties. It is concluded that excess ionic liquid can damage internal structure of the batteries and result in unwanted electrochemical reactions; however, samples containing 40–50 vol % ionic liquid exhibit superior ionic properties and lower internal resistance compared to those containing less or more ionic liquids.

  18. Second harmonic generation in nano-structured thin-film lithium niobate waveguides

    CERN Document Server

    Wang, Cheng; Andrade, Nicolas; Venkataraman, Vivek; Ren, Xi-Feng; Guo, Guang-Can; Lončar, Marko

    2016-01-01

    Lithium niobate is the most well-known optical material with a second-order \\c{hi}(2) nonlinearity that is widely employed in modern optical technology. Integrated lithium niobate platform has recently emerged as a promising candidate for next-generation, high-efficiency wavelength conversion systems that allow dense packaging and mass-production. Here we demonstrate efficient, phase-matched second harmonic generation in lithographically-defined thin-film lithium niobate waveguides with sub-micron dimensions. Both natural phase matching in fixed-width waveguides and quasi-phase matching in periodically-grooved waveguides are theoretically proposed and experimentally demonstrated. Our low-loss (~2.52 dB/cm) nanowaveguides possess normalized conversion efficiencies as high as 41% W-1cm-2, promising for future on-chip quantum wavelength conversion.

  19. Experiments with Liquid Metal Walls: Status of the Lithium Tokamak Experiment

    Energy Technology Data Exchange (ETDEWEB)

    Kaita, Robert; Boyle, Dennis; Gray, Timothy; Granstedt, Erik; Hammett, Gregory; Jacobson, Craig M; Jones, Andrew; Kozub, Thomas; Kugel, Henry; Leblanc, Benoit; Logan, Nicholas; Lucia, Matthew; Lundberg, Daniel; Majeski, Richard; Mansfield, Dennis; Menard, Jonathan; Spaleta, Jeffrey; Strickler, Trevor

    2010-02-16

    Liquid metal walls have been proposed to address the first wall challenge for fusion reactors. The Lithium Tokamak Experiment (LTX) at the Princeton Plasma Physics Laboratory (PPPL) is the first magnetic confinement device to have liquid metal plasma-facing components (PFC's) that encloses virtually the entire plasma. In the Current Drive Experiment-Upgrade (CDX-U), a predecessor to LTX at PPPL, the highest improvement in energy confinement ever observed in Ohmically-heated tokamak plasmas was achieved with a toroidal liquid lithium limiter. The LTX extends this liquid lithium PFC by using a conducting conformal shell that almost completely surrounds the plasma. By heating the shell, a lithium coating on the plasma-facing side can be kept liquefied. A consequence of the low-recycling conditions from liquid lithium walls is the need for efficient plasma fueling. For this purpose, a molecular cluster injector is being developed. Future plans include the installation of a neutral beam for core plasma fueling, and also ion temperature measurements using charge-exchange recombination spectroscopy. Low edge recycling is also predicted to reduce temperature gradients that drive drift wave turbulence. Gyrokinetic simulations are in progress to calculate fluctuation levels and transport for LTX plasmas, and new fluctuation diagnostics are under development to test these predictions. __________________________________________________

  20. Experiments with liquid metal walls: Status of the lithium tokamak experiment

    Energy Technology Data Exchange (ETDEWEB)

    Kaita, Robert, E-mail: kaita@pppl.gov [Princeton Plasma Physics Laboratory, Princeton, NJ (United States); Berzak, Laura; Boyle, Dennis; Gray, Timothy; Granstedt, Erik; Hammett, Gregory; Jacobson, Craig M.; Jones, Andrew; Kozub, Thomas; Kugel, Henry; Leblanc, Benoit; Logan, Nicholas; Lucia, Matthew; Lundberg, Daniel; Majeski, Richard; Mansfield, Dennis; Menard, Jonathan; Spaleta, Jeffrey; Strickler, Trevor; Timberlake, John [Princeton Plasma Physics Laboratory, Princeton, NJ (United States)

    2010-11-15

    Abstarct: Liquid metal walls have been proposed to address the first wall challenge for fusion reactors. The lithium tokamak experiment (LTX) at the Princeton Plasma Physics Laboratory (PPPL) is the first magnetic confinement device to have liquid metal plasma-facing components (PFC's) that encloses virtually the entire plasma. In the current drive experiment-upgrade (CDX-U), a predecessor to LTX at PPPL, the highest improvement in energy confinement ever observed in ohmically heated tokamak plasmas was achieved with a toroidal liquid lithium limiter. The LTX extends this liquid lithium PFC by using a conducting conformal shell that almost completely surrounds the plasma. By heating the shell, a lithium coating on the plasma-facing side can be kept liquefied. A consequence of the low-recycling conditions from liquid lithium walls is the need for efficient plasma fueling. For this purpose, a molecular cluster injector is being developed. Future plans include the installation of a neutral beam for core plasma fueling, and also ion temperature measurements using charge-exchange recombination spectroscopy (CHERS). Low edge recycling is also predicted to reduce temperature gradients that drive drift wave turbulence. Gyrokinetic simulations are in progress to calculate fluctuation levels and transport for LTX plasmas, and new fluctuation diagnostics are under development to test these predictions.

  1. High-flux neutron source based on a liquid-lithium target

    Science.gov (United States)

    Halfon, S.; Feinberg, G.; Paul, M.; Arenshtam, A.; Berkovits, D.; Kijel, D.; Nagler, A.; Eliyahu, I.; Silverman, I.

    2013-04-01

    A prototype compact Liquid Lithium Target (LiLiT), able to constitute an accelerator-based intense neutron source, was built. The neutron source is intended for nuclear astrophysical research, boron neutron capture therapy (BNCT) in hospitals and material studies for fusion reactors. The LiLiT setup is presently being commissioned at Soreq Nuclear research Center (SNRC). The lithium target will produce neutrons through the 7Li(p,n)7Be reaction and it will overcome the major problem of removing the thermal power generated by a high-intensity proton beam, necessary for intense neutron flux for the above applications. The liquid-lithium loop of LiLiT is designed to generate a stable lithium jet at high velocity on a concave supporting wall with free surface toward the incident proton beam (up to 10 kW). During off-line tests, liquid lithium was flown through the loop and generated a stable jet at velocity higher than 5 m/s on the concave supporting wall. The target is now under extensive test program using a high-power electron-gun. Up to 2 kW electron beam was applied on the lithium flow at velocity of 4 m/s without any flow instabilities or excessive evaporation. High-intensity proton beam irradiation will take place at SARAF (Soreq Applied Research Accelerator Facility) superconducting linear accelerator currently in commissioning at SNRC.

  2. Solid-State Thin-Film Lithium Batteries for Integration in Microsystems

    Science.gov (United States)

    Ribeiro, J. F.; Silva, M. F.; Carmo, J. P.; Gonçalves, L. M.; Silva, M. M.; Correia, J. H.

    The increasing miniaturization of electronic devices requires the miniaturization of devices that provide energy to them. Autonomous devices of reduced energy consumption are increasingly common and they have benefited from energy harvesting techniques. However, these devices often have peak power consumption, requiring storage of energy.This chapter presents the fabrication and characterization of thin-films for solid-state lithium battery. The solid-state batteries stand out for the possibility of all materials being solid and therefore ideal for microelectronics fabrication techniques. Lithium batteries are composed primarily of three materials, the cathode, the electrolyte and the anode. The positive electrode (cathode) and negative (anode) have high electrical conductivity and capacity for extraction and insertion of lithium ions. The electrolyte's main features are the high ionic conductivity and high electrical resistivity. The materials chosen for the battery are lithium cobalt oxide (cathode), lithium phosphorus oxynitride (electrolyte), and metallic lithium (anode).The lithium cobalt oxide cathode (LiCoO2) was deposited by RF sputtering and characterized using the XRD, EDX, SEM techniques, and electrical resistivity. Fully crystalline {LiCoO}2 was achieved with an annealing of 65{0}° in vacuum for 2 h. Electrical resistivity of 3.7 Ω \\cdot mm was achieved.The lithium phosphorus oxynitride electrolyte (LIPON) was deposited by RF sputtering and characterized using the techniques EDX, SEM, ionic conductivity, DSC, and TGA. Ionic conductivity of 6.3 × 1{0}^{-7} S \\cdot {cm}^{-1} for a temperature of 2{6}°C was measured. The thermal stability of LIPON up to 40{0}°C was also proved.The metallic lithium anode (Li) was deposited by thermal evaporation and its electrical resistance measured at four points during the deposition. Resistance of about 3. 5 Ω was measured for a thickness of 3 μm. The oxidation rate of the lithium in contact with the ambient

  3. Preparation of room temperature terahertz detector with lithium tantalate crystal and thin film

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jun, E-mail: ueoewj@gmail.com; Gou, Jun; Li, Weizhi [State Key Lab of Electronic Thin Films and Integrated Devices, School of Optoelectronic Information, University of Electronic Science and Technology of China, Chengdu 610054 (China)

    2014-02-15

    Research on room temperature terahertz (THz) detector is essential for promoting the application of THz science and technology. Both lithium tantalate crystal (LiTaO{sub 3}) and lithium tantalate thin film were used to fabricate the THz detector in this paper. Polishing process were used to reduce the thickness of LiTaO{sub 3} crystal slice by chemical mechanical polishing techniques and an improved sol-gel process was used to obtain high concentration LiTaO{sub 3} precursor solution to fabricate LiTaO{sub 3} thin film. Three dimension models of two THz detectors were set up and the temperature increasing map of two devices were simulated using finite element method. The lowest noise equivalent power value for terahertz detector using pyroelectric material reaches 6.8 × 10{sup −9} W at 30 Hz operating frequency, which is suitable for THz imaging application.

  4. Preparation of room temperature terahertz detector with lithium tantalate crystal and thin film

    Directory of Open Access Journals (Sweden)

    Jun Wang

    2014-02-01

    Full Text Available Research on room temperature terahertz (THz detector is essential for promoting the application of THz science and technology. Both lithium tantalate crystal (LiTaO3 and lithium tantalate thin film were used to fabricate the THz detector in this paper. Polishing process were used to reduce the thickness of LiTaO3 crystal slice by chemical mechanical polishing techniques and an improved sol-gel process was used to obtain high concentration LiTaO3 precursor solution to fabricate LiTaO3 thin film. Three dimension models of two THz detectors were set up and the temperature increasing map of two devices were simulated using finite element method. The lowest noise equivalent power value for terahertz detector using pyroelectric material reaches 6.8 × 10−9 W at 30 Hz operating frequency, which is suitable for THz imaging application.

  5. Free-standing high quality factor thin-film lithium niobate micro-photonic disk resonators

    CERN Document Server

    Wang, Renyuan

    2014-01-01

    Lithium Niobate (LN or just niobate) thin-film micro-photonic resonators have promising prospects in many applications including high efficiency electro-optic modulators, optomechanics and nonlinear optics. This paper presents free-standing thin-film lithium niobate photonic resonators on a silicon platform using MEMS fabrication technology. We fabricated a 35um radius niobate disk resonator that exhibits high intrinsic optical quality factor (Q) of 484,000. Exploiting the optomechanical interaction from the released free-standing structure and high optical Q, we were able to demonstrate acousto-optic modulation from these devices by exciting a 56MHz radial breathing mechanical mode (mechanical Q of 2700) using a probe.

  6. Laser annealing of textured thin film cathode material for lithium ion batteries

    Science.gov (United States)

    Kohler, R.; Bruns, M.; Smyrek, P.; Ulrich, S.; Przybylski, M.; Pfleging, W.

    2010-02-01

    The material development for advanced lithium ion batteries plays an important role in future mobile applications and energy storage systems. It is assumed that electrode materials made of nano-composited materials will improve battery lifetime and will lead to an enhancement of lithium diffusion and thus improve battery capacity and cyclability. Lithium cobalt oxide (LiCoO2) is commonly used as a cathode material. Thin films of this electrode material were synthesized by non-reactive r.f. magnetron sputtering of LiCoO2 targets on silicon or stainless steel substrates. For the formation of the high temperature phase of LiCoO2 (HT-LiCoO2), which exhibits good electrochemical performance with a specific capacity of 140 mAh/g and high capacity retention, a subsequent annealing treatment is necessary. For this purpose laser annealing of thin film LiCoO2 was investigated in detail and compared to conventional furnace annealing. A high power diode laser system operating at a wavelength of 940 nm with an integrated pyrometer for temperature control was used. Different temperatures (between 200°C and 700°C) for the laser structured and unstructured thin films were applied. The effects of laser treatment on the LiCoO2 thin films studied with Raman spectroscopy, X-ray photoelectron spectroscopy and X-ray diffraction to determine their stoichiometry and crystallinity. The development of HT-LiCoO2 and also the formation of a Co3O4 phase were discussed. The electrochemical properties of the manufactured films were investigated via electrochemical cycling against a lithium anode.

  7. Structural and Electrochemical Properties of Lithium Nickel Oxide Thin Films

    Directory of Open Access Journals (Sweden)

    Gyu-bong Cho

    2014-01-01

    Full Text Available LiNiO2 thin films were fabricated by RF magnetron sputtering. The microstructure of the films was determined by X-ray diffraction and field-emission scanning electron microscopy. The electrochemical properties were investigated with a battery cycler using coin-type half-cells. The LiNiO2 thin films annealed below 500°C had the surface carbonate. The results suggest that surface carbonate interrupted the Li intercalation and deintercalation during charge/discharge. Although the annealing process enhanced the crystallization of LiNiO2, the capacity did not increase. When the annealing temperature was increased to 600°C, the FeCrNiO4 oxide phase was generated and the discharge capacity decreased due to an oxygen deficiency in the LiNiO2 thin film. The ZrO2-coated LiNiO2 thin film provided an improved discharge capacity compared to bare LiNiO2 thin film suggesting that the improved electrochemical characteristic may be attributed to the inhibition of surface carbonate by ZrO2 coating layer.

  8. High-power liquid-lithium jet target for neutron production

    CERN Document Server

    Halfon, S; Kijel, D; Paul, M; Berkovits, D; Eliyahu, I; Feinberg, G; Friedman, M; Hazenshprung, N; Mardor, I; Nagler, A; Shimel, G; Tessler, M; Silverman, I

    2013-01-01

    A compact Liquid-Lithium Target (LiLiT) was built and tested with a high-power electron gun at Soreq Nuclear Research Center. The lithium target, to be bombarded by the high-intensity proton beam of the Soreq Applied Research Accelerator Facility (SARAF), will constitute an intense source of neutrons produced by the 7Li(p,n)7Be reaction for nuclear astrophysics research and as a pilot setup for accelerator-based Boron Neutron Capture Therapy (BNCT). The liquid-lithium jet target acts both as neutron-producing target and beam dump by removing the beam thermal power (>5 kW, >1 MW/cm3) with fast transport. The target was designed based on a thermal model, accompanied by a detailed calculation of the 7Li(p,n) neutron yield, energy distribution and angular distribution. Liquid lithium is circulated through the target loop at ~200oC and generates a stable 1.5 mm-thick film flowing at a velocity up to 7 m/s onto a concave supporting wall. Electron beam irradiation demonstrated that the liquid-lithium target can diss...

  9. Thin-film Rechargeable Lithium Batteries for Implantable Devices

    Science.gov (United States)

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

    1997-05-01

    Thin films of LiCoO{sub 2} have been synthesized in which the strongest x ray reflection is either weak or missing, indicating a high degree of preferred orientation. Thin film solid state batteries with these textured cathode films can deliver practical capacities at high current densities. For example, for one of the cells 70% of the maximum capacity between 4.2 V and 3 V ({approximately}0.2 mAh/cm{sup 2}) was delivered at a current of 2 mA/cm{sup 2}. When cycled at rates of 0.1 mA/cm{sup 2}, the capacity loss was 0.001%/cycle or less. The reliability and performance of Li LiCoO{sub 2} thin film batteries make them attractive for application in implantable devices such as neural stimulators, pacemakers, and defibrillators.

  10. Thin-film rechargeable lithium batteries for implantable devices

    Energy Technology Data Exchange (ETDEWEB)

    Bates, J.b.; Dudney, N.J.

    1997-05-01

    Thin films of LiCoO{sub 2} have been synthesized in which the strongest x-ray reflection is either weak or missing, indicating a high degree of preferred orientation. Thin-film solid state batteries with these textured cathode films can deliver practical capacities at high current densities. For example, for one of the cells 70% of the maximum capacity between 4.2 V and 3 V ({approximately}0.2 mAh/cm{sup 2}) was delivered at a current of 2 mA/cm{sup 2}. When cycled at rates of 0.1 mA/cm{sup 2}, the capacity loss was 0.001 %/cycle or less. The reliability and performance of Li-LiCoO{sub 2} thin-film batteries make them attractive for application in implantable devices such as neural stimulators, pacemakers, and defibrillators.

  11. Flexible thin-film battery based on solid-like ionic liquid-polymer electrolyte

    Science.gov (United States)

    Li, Qin; Ardebili, Haleh

    2016-01-01

    The development of high-performance flexible batteries is imperative for several contemporary applications including flexible electronics, wearable sensors and implantable medical devices. However, traditional organic liquid-based electrolytes are not ideal for flexible batteries due to their inherent safety and stability issues. In this study, a non-volatile, non-flammable and safe ionic liquid (IL)-based polymer electrolyte film with solid-like feature is fabricated and incorporated in a flexible lithium ion battery. The ionic liquid is 1-Ethyl-3-methylimidazolium dicyanamide (EMIMDCA) and the polymer is composed of poly(vinylidene fluoride-co-hexafluoropropene) (PVDF-HFP). The electrolyte exhibits good thermal stability (i.e. no weight loss up to 300 °C) and relatively high ionic conductivity (6 × 10-4 S cm-1). The flexible thin-film lithium ion battery based on solid-like electrolyte film is encapsulated using a thermal-lamination process and demonstrates excellent electrochemical performance, in both flat and bent configurations.

  12. Quantized friction across ionic liquid thin films

    Science.gov (United States)

    Smith, Alexander M.; Lovelock, Kevin R. J.; Gosvami, Nitya Nand; Welton, Tom; Perkin, Susan

    Ionic liquids, salts in the liquid state under ambient conditions, are of great interest as precision lubricants. Ionic liquids form layered structures at surfaces, yet it is not clear how this nano-structure relates to their lubrication properties. We measured the friction force between atomically smooth solid surfaces across ionic liquid films of controlled thickness in terms of the number of ion layers. Multiple friction-load regimes emerge, each corresponding to a different number of ion layers in the film. In contrast to molecular liquids, the friction coefficients differ for each layer due to their varying composition.

  13. Quantized friction across ionic liquid thin films.

    Science.gov (United States)

    Smith, Alexander M; Lovelock, Kevin R J; Gosvami, Nitya Nand; Welton, Tom; Perkin, Susan

    2013-10-07

    Ionic liquids - salts in the liquid state under ambient conditions - are of great interest as precision lubricants. Ionic liquids form layered structures at surfaces, yet it is not clear how this nano-structure relates to their lubrication properties. We measured the friction force between atomically smooth solid surfaces across ionic liquid films of controlled thickness in terms of the number of ion layers. Multiple friction-load regimes emerge, each corresponding to a different number of ion layers in the film. In contrast to molecular liquids, the friction coefficients differ for each layer due to their varying composition.

  14. Study on hydrogen isotopes permeation in fluidized state of liquid lithium-lead

    Energy Technology Data Exchange (ETDEWEB)

    Yoshimura, S.; Yoshimura, R.; Okada, M.; Fukada, S.; Edao, Y. [Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, Kasuga-shi, Fukuoka (Japan)

    2015-03-15

    Lithium-lead (Li-Pb) is one of the most promising candidate materials for the liquid blanket of fusion reactors. Hydrogen transfer under a fluidized condition of Li-Pb is investigated experimentally to design a Li-Pb blanket system. Li-Pb eutectic alloy flows inside a Ni tube in the experimental system, where H{sub 2} permeates into and out of the forced Li-Pb flow. The overall H{sub 2} permeation rate is analyzed using a mass balance model. Hydrogen atoms diffuse in Ni and Li-Pb. The steady-state H{sub 2} permeation rate obtained by this experiment is smaller than the result of the calculation model. A resistance factor is introduced to the present analysis in order to evaluate the influence of other H{sub 2} transfer mechanisms, such as diffusion in Li-Pb and dissolution reaction between Ni and Li-Pb. The contribution of the resistance to the overall H{sub 2} permeation rate becomes large when the flow rate of Li-Pb is low. This is because the boundary layer thickness between Ni and Li-Pb affects the overall H{sub 2} permeation rate. When the flow velocity of Li-Pb increases, the thickness of the boundary layer becomes thin, and the driving force of H{sub 2} permeation through the Ni wall becomes bigger. (authors)

  15. Ionic liquid-based membranes as electrolytes for advanced lithium polymer batteries.

    Science.gov (United States)

    Navarra, M A; Manzi, J; Lombardo, L; Panero, S; Scrosati, Bruno

    2011-01-17

    Gel-type polymer electrolytes are formed by immobilizing a solution of lithium N,N-bis(trifluoromethanesulfonyl)imide (LiTFSI) in N-n-butyl-N-ethylpyrrolidinium N,N-bis(trifluoromethanesulfonyl)imide (Py₂₄TFSI) ionic liquid (IL) with added mixtures of organic solvents, such as ethylene, propylene and dimethyl carbonates (EC, PC, and DMC, respectively), into a poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-HFP) matrix, and their properties investigated. The addition of the organic solvent mixtures results in an improvement of the ionic conductivity and in the stabilization of the interface with the lithium electrode. Conductivity values in the range of 10⁻³-10⁻²  S cm⁻¹ are obtained in a wide temperature range. These unique properties allow the effective use of these membranes as electrolytes for the development of advanced polymer batteries based on a lithium metal anode and an olivine-type lithium iron phosphate cathode.

  16. Analysis of carbonated thin liquids in pediatric neurogenic dysphagia.

    Science.gov (United States)

    Lundine, Jennifer P; Bates, D Gregory; Bates, David G; Yin, Han

    2015-08-01

    Aspiration of liquids is a serious complication of neurological impairments such as traumatic brain injury or stroke. Carbonated liquids have been examined as a possible alternative to thickened liquids to help reduce aspiration in cases of dysphagia in adults, but no published literature to the best of our knowledge has evaluated this technique in children. If carbonated liquids result in safer swallowing in children, they could provide a preferred alternative to thickened liquids. This pilot study examined whether carbonated thin liquids (CARB) improved swallowing compared to non-carbonated thin liquids (NOCARB) for children with neurogenic dysphagia. Twenty-four children admitted to a level I trauma center for acute neurological injury/disease were evaluated via videofluoroscopic swallow studies. Four descriptive outcome measures were contrasted. CARB significantly decreased pooling (P = 0.0006), laryngeal penetration/aspiration (P = 0.0044) and Penetration-Aspiration Scale scores (P = 0.0127) when compared to NOCARB. On average, CARB improved scores on the Penetration-Aspiration Scale by 3.7 points for participants who aspirated NOCARB. There was no significant difference in pharyngeal residue noted between CARB and NOCARB (P = 0.0625). These findings support the hypothesis that carbonated thin liquids may provide an alternative to thickened liquids for children with neurogenic dysphagia. Implications for future research and clinical practice are discussed.

  17. High-power liquid-lithium target prototype for accelerator-based boron neutron capture therapy.

    Science.gov (United States)

    Halfon, S; Paul, M; Arenshtam, A; Berkovits, D; Bisyakoev, M; Eliyahu, I; Feinberg, G; Hazenshprung, N; Kijel, D; Nagler, A; Silverman, I

    2011-12-01

    A prototype of a compact Liquid-Lithium Target (LiLiT), which will possibly constitute an accelerator-based intense neutron source for Boron Neutron Capture Therapy (BNCT) in hospitals, was built. The LiLiT setup is presently being commissioned at Soreq Nuclear Research Center (SNRC). The liquid-lithium target will produce neutrons through the (7)Li(p,n)(7)Be reaction and it will overcome the major problem of removing the thermal power generated using a high-intensity proton beam (>10 kW), necessary for sufficient neutron flux. In off-line circulation tests, the liquid-lithium loop generated a stable lithium jet at high velocity, on a concave supporting wall; the concept will first be tested using a high-power electron beam impinging on the lithium jet. High intensity proton beam irradiation (1.91-2.5 MeV, 2-4 mA) will take place at Soreq Applied Research Accelerator Facility (SARAF) superconducting linear accelerator currently in construction at SNRC. Radiological risks due to the (7)Be produced in the reaction were studied and will be handled through a proper design, including a cold trap and appropriate shielding. A moderator/reflector assembly is planned according to a Monte Carlo simulation, to create a neutron spectrum and intensity maximally effective to the treatment and to reduce prompt gamma radiation dose risks.

  18. Periodic domain inversion in x-cut single-crystal lithium niobate thin film

    Science.gov (United States)

    Mackwitz, P.; Rüsing, M.; Berth, G.; Widhalm, A.; Müller, K.; Zrenner, A.

    2016-04-01

    We report the fabrication of periodically poled domain patterns in x-cut lithium niobate thin-film. Here, thin films on insulator have drawn particular attention due to their intrinsic waveguiding properties offering high mode confinement and smaller devices compared to in-diffused waveguides in bulk material. In contrast to z-cut thin film lithium niobate, the x-cut geometry does not require back electrodes for poling. Further, the x-cut geometry grants direct access to the largest nonlinear and electro-optical tensor element, which overall promises smaller devices. The domain inversion was realized via electric field poling utilizing deposited aluminum top electrodes on a stack of LN thin film/SiO2 layer/Bulk LN, which were patterned by optical lithography. The periodic domain inversion was verified by non-invasive confocal second harmonic microscopy. Our results show domain patterns in accordance to the electrode mask layout. The second harmonic signatures can be interpreted in terms of spatially, overlapping domain filaments which start their growth on the +z side.

  19. Intrinsic instability of thin liquid films on nanostructured surfaces

    Science.gov (United States)

    Rokoni, Arif; Hu, Han; Sun, Liyong; Sun, Ying

    2016-11-01

    The instability of a thin liquid film on nanostructures is not well understood but is important in liquid-vapor two-phase heat transfer (e.g., thin film evaporation and boiling), lubrication, and nanomanufacturing. In thin film evaporation, the comparison between the non-evaporating film thickness and the critical film breakup thickness determines the stability of the film: the film becomes unstable when the critical film breakup thickness is larger than the non-evaporating film thickness. In this study, a closed-form model is developed to predict the critical breakup thickness of a thin liquid film on 2D periodic nanostructures based on minimization of system free energy in the limit of a liquid monolayer. Molecular dynamics simulations are performed for water thin films on square nanostructures of varying depth and wettability and the simulations agree with the model predictions. The results show that the critical film breakup thickness increases with the nanostructure depth and the surface wettability. The model developed here enables the prediction of the minimum film thickness for stable thin film evaporation on a given nanostructure.

  20. Properties and Structure of the LiCl-films on Lithium Anodes in Liquid Cathodes

    DEFF Research Database (Denmark)

    Mogensen, Mogens Bjerg; Hennesø, Erik

    2016-01-01

    Lithium anodes passivated by LiCl layers in different types of liquid cathodes (catholytes) based on LiAlCl4 in SOCl2 or SO2 have been studied by means of impedance spectroscopy. The impedance spectra have been fitted with two equivalent circuits using a nonlinear least squares fit program...

  1. Lithium diffusion in sputter-deposited Li4Ti5O12 thin films

    Science.gov (United States)

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

    2012-10-01

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

  2. Foldable interpenetrated metal-organic frameworks/carbon nanotubes thin film for lithium-sulfur batteries

    Science.gov (United States)

    Mao, Yiyin; Li, Gaoran; Guo, Yi; Li, Zhoupeng; Liang, Chengdu; Peng, Xinsheng; Lin, Zhan

    2017-03-01

    Lithium-sulfur batteries are promising technologies for powering flexible devices due to their high energy density, low cost and environmental friendliness, when the insulating nature, shuttle effect and volume expansion of sulfur electrodes are well addressed. Here, we report a strategy of using foldable interpenetrated metal-organic frameworks/carbon nanotubes thin film for binder-free advanced lithium-sulfur batteries through a facile confinement conversion. The carbon nanotubes interpenetrate through the metal-organic frameworks crystal and interweave the electrode into a stratified structure to provide both conductivity and structural integrity, while the highly porous metal-organic frameworks endow the electrode with strong sulfur confinement to achieve good cyclability. These hierarchical porous interpenetrated three-dimensional conductive networks with well confined S8 lead to high sulfur loading and utilization, as well as high volumetric energy density.

  3. Foldable interpenetrated metal-organic frameworks/carbon nanotubes thin film for lithium-sulfur batteries.

    Science.gov (United States)

    Mao, Yiyin; Li, Gaoran; Guo, Yi; Li, Zhoupeng; Liang, Chengdu; Peng, Xinsheng; Lin, Zhan

    2017-03-06

    Lithium-sulfur batteries are promising technologies for powering flexible devices due to their high energy density, low cost and environmental friendliness, when the insulating nature, shuttle effect and volume expansion of sulfur electrodes are well addressed. Here, we report a strategy of using foldable interpenetrated metal-organic frameworks/carbon nanotubes thin film for binder-free advanced lithium-sulfur batteries through a facile confinement conversion. The carbon nanotubes interpenetrate through the metal-organic frameworks crystal and interweave the electrode into a stratified structure to provide both conductivity and structural integrity, while the highly porous metal-organic frameworks endow the electrode with strong sulfur confinement to achieve good cyclability. These hierarchical porous interpenetrated three-dimensional conductive networks with well confined S8 lead to high sulfur loading and utilization, as well as high volumetric energy density.

  4. Fano resonance-based highly sensitive, compact temperature sensor on thin film lithium niobate.

    Science.gov (United States)

    Qiu, Wentao; Ndao, Abdoulaye; Vila, Venancio Calero; Salut, Roland; Courjal, Nadège; Baida, Fadi Issam; Bernal, Maria-Pilar

    2016-03-15

    In this Letter, we report a Fano resonance-based highly sensitive and compact temperature sensor fabricated on thin film lithium niobate (TFLN) Suzuki phase lattice (SPL) photonic crystal. The experimental sensitivity is estimated to be 0.77 nm/°C with a photonic crystal size of only 25  μm × 24  μm. This sensitivity is 38 times larger than the intrinsic one of lithium niobate which is 0.02 nm/°C. The demonstrated sharp and high extinction ratio characteristics of the Fano lineshape resonance could be an excellent candidate in developing a high sensitivity temperature sensor, electric field sensor, etc.

  5. Mechanical measurements on lithium phosphorous oxynitride coated silicon thin film electrodes for lithium-ion batteries during lithiation and delithiation

    Energy Technology Data Exchange (ETDEWEB)

    Al-Obeidi, Ahmed, E-mail: alobeidi@mit.edu; Thompson, Carl V., E-mail: reiner.moenig@kit.edu, E-mail: cthomp@mit.edu [Department of Materials Science and Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139 (United States); Kramer, Dominik, E-mail: dominik.kramer@kit.edu; Mönig, Reiner, E-mail: reiner.moenig@kit.edu, E-mail: cthomp@mit.edu [Institute for Applied Materials, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Helmholtz Institute Ulm for Electrochemical Energy Storage (HIU), Helmholtzstraße 11, 89081 Ulm (Germany); Boles, Steven T., E-mail: steven.t.boles@polyu.edu.hk [Institute for Applied Materials, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Hong Kong Polytechnic University, 11 Yuk Choi Rd, Hung Hom (Hong Kong)

    2016-08-15

    The development of large stresses during lithiation and delithiation drives mechanical and chemical degradation processes (cracking and electrolyte decomposition) in thin film silicon anodes that complicate the study of normal electrochemical and mechanical processes. To reduce these effects, lithium phosphorous oxynitride (LiPON) coatings were applied to silicon thin film electrodes. Applying a LiPON coating has two purposes. First, the coating acts as a stable artificial solid electrolyte interphase. Second, it limits mechanical degradation by retaining the electrode's planar morphology during cycling. The development of stress in LiPON-coated electrodes was monitored using substrate curvature measurements. LiPON-coated electrodes displayed highly reproducible cycle-to-cycle behavior, unlike uncoated electrodes which had poorer coulombic efficiency and exhibited a continual loss in stress magnitude with continued cycling due to film fracture. The improved mechanical stability of the coated silicon electrodes allowed for a better investigation of rate effects and variations of mechanical properties during electrochemical cycling.

  6. Experimental research conception of thin liquid film boiling and evaporation

    Directory of Open Access Journals (Sweden)

    Feoktistov Dmitry V.

    2015-01-01

    Full Text Available The concept of conducting the experiments for studying thin liquid film boiling and evaporation was developed. Implementing this conception on developed experimental setup, we will obtain the data on the change of liquid film thickness in thermosiphon and temperature distribution in the liquid film, also the evaporation rate of liquid film and heat transfer coefficient change will be calculated using the measured values in the experiment. Three series of preliminary experiment were conducted. As a result, the main influencing factors and their values were defined.

  7. Use of Ionic Liquids in Rod-Coil Block Copolyimides for Improved Lithium Ion Conduction

    Science.gov (United States)

    Meador, Mary Ann B.; Tigelaar, Dean M.; Chapin, Kara; Bennett, William R.

    2007-01-01

    Solvent-free, solid polymer electrolytes (SPE) have the potential to improve safety, increase design flexibility and enhance performance of rechargeable lithium batteries. Solution based electrolytes are flammable and typically incompatible with lithium metal anodes, limiting energy density. We have previously demonstrated use of polyimide rod coil block copolymers doped with lithium salts as electrolytes for lithium polymer batteries. The polyimide rod blocks provide dimensional stability while the polyethylene oxide (PEO) coil portions conduct ions. Phase separation of the rods and coils in these highly branched polymers provide channels with an order of magnitude improvement in lithium conduction over polyethylene oxide itself at room temperature. In addition, the polymers have been demonstrated in coin cells to be compatible with lithium metal. For practical use at room temperature and below, however, at least an order of magnitude improvement in ion conduction is still required. The addition of nonvolatile, room temperature ionic liquids has been shown to improve the ionic conductivity of high molecular weight PEO. Herein we describe use of these molten salts to improve ionic conductivity in the rod-coil block copolymers.

  8. Preparation of LiMn{sub 2}O{sub 4} cathode thin films for thin film lithium secondary batteries by a mist CVD process

    Energy Technology Data Exchange (ETDEWEB)

    Tadanaga, Kiyoharu, E-mail: tadanaga@chem.osakafu-u.ac.jp [Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka, 599-8531 (Japan); Yamaguchi, Akihiro; Sakuda, Atsushi; Hayashi, Akitoshi; Tatsumisago, Masahiro [Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka, 599-8531 (Japan); Duran, Alicia; Aparacio, Mario [Instituto de Cerámica y Vidrio, Consejo Superior de Investigaciones Científicas, Kelsen 5 (Campus de Cantoblanco), Madrid, 28049 (Spain)

    2014-05-01

    Highlights: • LiMn{sub 2}O{sub 4} thin films were prepared by using the mist CVD process. • An aqueous solution of lithium and manganese acetates is used for the precursor solution. • The cell with the LiMn{sub 2}O{sub 4} thin films exhibited a capacity of about 80 mAh/g. • The cell showed good cycling performance during 10 cycles. - Abstract: LiMn{sub 2}O{sub 4} cathode thin films for thin film lithium secondary batteries were prepared by using so-called the “mist CVD process”, employing an aqueous solution of lithium acetate and manganese acetate, as the source of Li and Mn, respectively. The aqueous solution of starting materials was ultrasonically atomized to form mist particles, and mists were transferred by nitrogen gas to silica glass substrate to form thin films. FE-SEM observation revealed that thin films obtained by this process were dense and smooth, and thin films with a thickness of about 750 nm were obtained. The electrochemical cell with the thin films obtained by sintering at 700 °C exhibited a capacity of about 80 mAh/g, and the cell showed good cycling performance during 10 cycles.

  9. Single-Ion Block Copoly(ionic liquid)s as Electrolytes for All-Solid State Lithium Batteries.

    Science.gov (United States)

    Porcarelli, Luca; Shaplov, Alexander S; Salsamendi, Maitane; Nair, Jijeesh R; Vygodskii, Yakov S; Mecerreyes, David; Gerbaldi, Claudio

    2016-04-27

    Polymer electrolytes have been proposed as replacement for conventional liquid electrolytes in lithium-ion batteries (LIBs) due to their intrinsic enhanced safety. Nevertheless, the power delivery of these materials is limited by the concentration gradient of the lithium salt. Single-ion conducting polyelectrolytes represent the ideal solution since their nature prevents polarization phenomena. Herein, the preparation of a new family of single-ion conducting block copolymer polyelectrolytes via reversible addition-fragmentation chain transfer polymerization technique is reported. These copolymers comprise poly(lithium 1-[3-(methacryloyloxy)propylsulfonyl]-1-(trifluoromethylsulfonyl)imide) and poly(ethylene glycol) methyl ether methacrylate blocks. The obtained polyelectrolytes show low Tg values in the range of -61 to 0.6 °C, comparatively high ionic conductivity (up to 2.3 × 10(-6) and 1.2 × 10(-5) S cm(-1) at 25 and 55 °C, respectively), wide electrochemical stability (up to 4.5 V versus Li(+)/Li), and a lithium-ion transference number close to unity (0.83). Owing to the combination of all mentioned properties, the prepared polymer materials were used as solid polyelectrolytes and as binders in the elaboration of lithium-metal battery prototypes with high charge/discharge efficiency and excellent specific capacity (up to 130 mAh g(-1)) at C/15 rate.

  10. Sn–Al core–shell nanocomposite as thin film anode for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Lin; Zhang, Kai; Tao, Zhanliang, E-mail: taozhl@nankai.edu.cn; Chen, Jun

    2015-09-25

    Highlights: • Sn (core)–Al (shell) nanocomposite thin film is prepared by magnetron sputtering method. • The effect of Al on the structure and electrochemical performance has been investigated. • Improved electrochemical performance is obtained. - Abstract: In this paper, we report on the preparation of Sn (core)–Al (shell) nanocomposite thin films by co-sputtering Sn target and Al target, and their application as anode of lithium-ion batteries. Instrumental analyses of X-ray diffraction, energy dispersive X-ray analysis, scanning electron microscopy, and transmission electron microscope have been used to characterize the structure and morphology. The results reveal that the thin film is composed of core–shell structure with Sn nanoparticle core and Al amorphous shell. Furthermore, measurements of charge–discharge, cyclic voltammetry and electrochemical impedance spectroscopy have been employed to characterize the electrochemical performance of Sn–Al film. The Sn–Al thin film with 18 wt% Al delivers high capacities of 822, 460 and 313 mA h g{sup −1} in the second 2nd, 60th and 200th cycles, respectively. Meanwhile, a discharge capacity of 420 mA h g{sup −1} is obtained at 3000 mA g{sup −1}. The excellent electrochemistry performance is owing to the core–shell structure in which Al shell can alleviate the expansion of volume of Sn particles and restrain the aggregation of Sn particles. The results indicate that Sn–Al thin film is a promising anode for lithium-ion batteries.

  11. Solution-deposited Li4Ti5O12 thin films as anode for lithium ion battery

    Institute of Scientific and Technical Information of China (English)

    WU Xian-ming; XIAO Zhuo-bing; MA Ming-you; CHEN Shang; HE Ze-qiang; LIU Jian-ben

    2006-01-01

    The technique of solution deposition was employed to prepare Li4Ti5O12 thin film using lithium acetate and TiO(C4H9)4 as starting materials. The structural and electrochemical properties of the thin films were studied by X-ray diffraction, cyclic voltammetry, galvanostatic charge-discharge experiments, and potential step technique. The results show that the thin film prepared by this method is of pure phase with a spinel framework structure. The capacity of the thin film annealed at 750 ℃ for 1 h is approximately 57 μA·h/(cm2·μm). The film possesses excellent cycling behavior with a 0.08% capacity loss per cycle after being cycled 50 times. Potential step technique shows that the average chemical diffusion coefficient of lithium ion in the thin film is approximately 4.5×10-11 cm2/s.

  12. Investigation of the susceptibility of EUROFER97 in lead-lithium to liquid metal embrittlement (LME)

    Energy Technology Data Exchange (ETDEWEB)

    Bosch, R.W. [SCK-CEN, Belgian Nuclear Research Centre, Boeretang 200, B-2400 Mol (Belgium)], E-mail: rbosch@sckcen.be; Dyck, S. van; Al Mazouzi, A. [SCK-CEN, Belgian Nuclear Research Centre, Boeretang 200, B-2400 Mol (Belgium)

    2007-10-15

    Liquid metal embrittlement (LME) is defined as the brittle fracture (loss of ductility) of usually ductile materials in the presence of a liquid metal. The sensitivity to LME is likely to increase with irradiation hardening as localised stresses can promote the aggressive action of a liquid metal. To investigate the mechanical response of irradiated materials in contact with a liquid metal, an instrumented hot cell has been developed. The testing machine installed inside allows mechanical testing of active materials in liquid lead lithium under well controlled chemistry conditions. Typical mechanical tests that can be carried out are slow strain rate tests (SSRT), constant load and rising load tests at temperatures from 150 deg. C to 500 deg. C. In this paper the first results of the SSRT tests with EUROFER97 in argon and lead-lithium at different temperatures with different strain rates will be presented. The SSRT test method has been chosen due to the accelerated nature of the test, i.e., during straining the oxide layer will be ruptured and wetting of the sample surface by the lead-lithium melt is promoted. The results collected up till now showed no sign of LME. Tests with longer pre-exposure times and tests with irradiated samples will be carried out in the next phase. A longer pre-exposure time can enhance wetting and so the susceptibility to LME. An increase of the yield stress due to irradiation can also enhance the susceptibility to LME.

  13. Lithium

    Science.gov (United States)

    Lithium is used to treat and prevent episodes of mania (frenzied, abnormally excited mood) in people with bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal ...

  14. Electrode-supported thin α-alumina separators for lithium-ion batteries

    Science.gov (United States)

    Mi, Wanliang; Sharma, Gaurav; Dong, Xueliang; Jin, Yi; Lin, Y. S.

    2016-02-01

    Lithium ion batteries with an inorganic separator offer improved safety and enhanced reliability. The free-standing inorganic separators recently studied for lithium ion batteries are brittle and expensive. To address these issues, this paper reports the synthesis of a new and stable electrode-supported separator using a low-cost ceramic powder. Thin and porous α-Al2O3 separator films of thicknesses down to 40 μm were coated on Li4Ti5O12 (LTO) electrode by blade-coating a slurry of α-Al2O3, water and a small amount of polyvinyl alcohol (PVA). The performance of the LTO/Li cells with coated α-Al2O3 separator improves with decreasing PVA content. Cells with coated α-Al2O3 separator containing 0.4wt% PVA exhibit similar discharge capacity but better rate capability than those with commercial polypropylene (PP) or thick sintered α-Al2O3 separator. The coated α-Al2O3 separator does not react with LTO even after many charge/discharge cycles. Fabrication of the electrode-supported α-Al2O3 separator is scalable and cost-effective, offering high potential for practical application in industrial lithium ion battery manufacturing.

  15. Lithium-end-capped polylactide thin films influence osteoblast progenitor cell differentiation and mineralization.

    Science.gov (United States)

    Gomillion, Cheryl T; Lakhman, Rubinder Kaur; Kasi, Rajeswari M; Weiss, R A; Kuhn, Liisa T; Goldberg, A Jon

    2015-02-01

    End-capping by covalently binding functional groups to the ends of polymer chains offers potential advantages for tissue engineering scaffolds, but the ability of such polymers to influence cell behavior has not been studied. As a demonstration, polylactide (PLA) was end-capped with lithium carboxylate ionic groups (hPLA13kLi) and evaluated. Thin films of the hPLA13kLi and PLA homopolymer were prepared with and without surface texturing. Murine osteoblast progenitor cells from collagen 1α1 transgenic reporter mice were used to assess cell attachment, proliferation, differentiation, and mineralization. Measurement of green fluorescent protein expressed by these cells and xylenol orange staining for mineral allowed quantitative analysis. The hPLA13kLi was biologically active, increasing initial cell attachment and enhancing differentiation, while reducing proliferation and strongly suppressing mineralization, relative to PLA. These effects of bound lithium ions (Li(+) ) had not been previously reported, and were generally consistent with the literature on soluble additions of lithium. The surface texturing generated here did not influence cell behavior. These results demonstrate that end-capping could be a useful approach in scaffold design, where a wide range of biologically active groups could be employed, while likely retaining the desirable characteristics associated with the unaltered homopolymer backbone. © 2014 Wiley Periodicals, Inc.

  16. Sol-gel fabrication of lithium doped zinc oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Oral, A.Y.; Bahsi, Z.B. [Dept. of Materials Science and Engineering, Gebze Inst. of Tech., Kocaeli (Turkey); Aslan, M.H.; Basaran, E. [Dept. of Physics, Gebze Inst. of Tech., Kocaeli (Turkey)

    2004-07-01

    Li doped zinc oxide thin films were deposited on glass substrates by a sol-gel technique. Acetates of zinc and lithium were used as metal sources. A homogeneous and stable solution was prepared by dissolving acetates in the solution of 2-propanol and ethanolamine. ZnO:Li thin films were obtained after preheating the spin coated films at 250 C for 1 minute after each coating. A post annealing between 450-600 C was applied after the deposition of the last layers. XRD analysis revealed ZnO with zincite structure (Card no: 36-1451) in all films. The thickness of the films was measured as 75 nm per layer. The optical band gap of the films increased as doping concentration of Li increased and decreased as the post-annealing temperature increased. (orig.)

  17. Synthesis and characterization of atomic layer deposited titanium nitride thin films on lithium titanate spinel powder as a lithium-ion battery anode

    Energy Technology Data Exchange (ETDEWEB)

    Snyder, Mark Q.; Wheeler, M. Clayton [Department of Chemical and Biological Engineering, University of Maine, 5737 Jenness Hall, Orono, ME 04469 (United States); Trebukhova, Svetlana A.; Ravdel, Boris; DiCarlo, Joseph [Yardney Technical Products/Lithion Inc., Pawcatuck, CT 06379 (United States); Tripp, Carl P. [Laboratory for Surface Science and Technology (LASST), 5708 ESRB-Barrows, Orono, ME 04469 (United States); Department of Chemistry, University of Maine, Orono, ME 04469 (United States); DeSisto, William J. [Department of Chemical and Biological Engineering, University of Maine, 5737 Jenness Hall, Orono, ME 04469 (United States); Laboratory for Surface Science and Technology (LASST), 5708 ESRB-Barrows, Orono, ME 04469 (United States)

    2007-02-25

    Lithium titanate spinel (Li{sub 4}Ti{sub 5}O{sub 12}, or LTS) is receiving consideration as a nanopowder anode material for use in lithium-ion batteries. LTS has more positive working potential than traditional graphite anodes, and it does not react with electrolyte components. However, the main drawback of LTS powder is its poor interparticle electronic conductance that reduces the high-rate ability of the electrode. To improve this we have coated the surface of the LTS powder with a titanium nitride layer by atomic layer deposition (ALD). In situ infrared spectroscopy studies were conducted to confirm the attachment of the titanium precursor. The nitrogen content of films was measured by total nitrogen content testing. Transmission electron microscopy (TEM) micrographs confirmed the formation of a thin titanium nitride film around LTS particles by ALD. Finally, lithium cells with electrodes made of original and modified LTS nanopowders were assembled and tested. (author)

  18. Liquid phase deposition of electrochromic thin films

    Energy Technology Data Exchange (ETDEWEB)

    Richardson, Thomas J.; Rubin, Michael D.

    2000-08-18

    Thin films of titanium, zirconium and nickel oxides were deposited on conductive SnO2:F glass substrates by immersion in aqueous solutions. The films are transparent, conformal, of uniform thickness and appearance, and adhere strongly to the substrates. On electrochemical cycling, TiO2, mixed TiO2-ZrO2, and NiOx films exhibited stable electrochromism with high coloration efficiencies. These nickel oxide films were particularly stable compared with films prepared by other non-vacuum techniques. The method is simple, inexpensive, energy efficient, and readily scalable to larger substrates.

  19. Mechanical properties of low activation Cr-Mn austenitic steels changes in liquid lithium

    Science.gov (United States)

    Vertkov, A. V.; Evtikhin, V. A.; Lyublinski, I. E.; Syichev, A. A.; Demina, E. V.; Prusakova, M. D.

    1993-08-01

    The mechanical properties of Fe0.06C12Cr14Mn4NiAlMo, Fe0.10C12Cr20Mn W, Fe0.25C12Cr20Mn2W, Fe0.06C17Cr19Mn3NiNbN, Fe0.0713Cr20MnN steels attacked by liquid lithium were studied. Preexposure of steels was performed in static isothermal lithium at 723 and 873 K; in the hot leg of a convection loop at 723 K, and in inert atmosphere at 723 and 873 K for 2600 h. Lithium contained up to 400 ppm nitrogen and up to 1% hydrogen. The mechanical properties were determined by tensile test in lithium and in vacuum at a strain rate of 1×10 -5-1×10 -3 s -1. It was shown that mechanical properties of tested steels after exposure in the lithium changed more than for CrNi steels. The strong embrittlement of steels containing nitrogen is associated with intergranular penetration of lithium. The character of other steels mechanical properties changes is difficult to explain and may be associated with nometallic impurities redistribution and steel phase composition changes. The main mechanical properties change took place continually for the first 1000 h at 723 K exposure. Noticeable change in the mechanical properties of the steels exposed to lithium at 873 K occuredeven until 2600 h of exposure. The effect of strength and ductility reduction through absorption did not occur.

  20. Developments of high-voltage all-solid-state thin-film lithium ion batteries

    Science.gov (United States)

    Schwenzel, J.; Thangadurai, V.; Weppner, W.

    Powders of Li 2MMn 3O 8 (M = Fe, Co) were prepared by glycine nitrate combustion from the corresponding metal nitrates. The reaction products were pressed into pellets with the addition of 20 wt.% excess LiNO 3, which were used as targets for e-beam evaporation. A high-voltage all-solid-state thin-film lithium ion battery was demonstrated by the sequential deposition of spinel structured Li 2MMn 3O 8 (M = Co, Fe) as positive electrode by e-beam evaporation, LiPON as electrolyte, and metallic Al as negative electrode by sputtering in N 2 and Ar gas mixtures with specific power and gas flow rates. A lithium ion conductivity of ∼10 -6 S cm -1 was observed for the optimized thin-film LiPON electrolyte prepared under the condition of a chamber pressure of 2.6 × 10 -2 mbar and a power of 60-100 W. The chemical diffusion coefficient (D ˜) was found to be in the range 10 -13 to 10 -12 cm 2 s -1 for any composition x of Li 2- xMMn 3O 8 (M = Fe, Co) in the range from 0.1 to 1.6 by employing the galvanostatic intermittent titration technique (GITT). AC impedance studies revealed a charge transfer resistance of 260-290 Ω, a double layer capacity of ∼45-70 μF for an electrode area of 6.7 cm 2.

  1. Solvation of lithium salts in protic ionic liquids: a molecular dynamics study.

    Science.gov (United States)

    Méndez-Morales, Trinidad; Carrete, Jesús; Cabeza, Óscar; Russina, Olga; Triolo, Alessandro; Gallego, Luis J; Varela, Luis M

    2014-01-23

    The structure of solutions of lithium nitrate in a protic ionic liquid with a common anion, ethylammonium nitrate, at room temperature is investigated by means of molecular dynamics simulations. Several structural properties, such as density, radial distribution functions, hydrogen bonds, spatial distribution functions, and coordination numbers, are analyzed in order to get a picture of the solvation of lithium cations in this hydrogen-bonded, amphiphilically nanostructured environment. The results reveal that the ionic liquid mainly retains its structure upon salt addition, the interaction between the ammonium group of the cation and the nitrate anion being only slightly perturbed by the addition of the salt. Lithium cations are solvated by embedding them in the polar nanodomains of the solution formed by the anions, where they coordinate with the latter in a solid-like fashion reminiscent of a pseudolattice structure. Furthermore, it is shown that the average coordination number of [Li](+) with the anions is 4, nitrate coordinating [Li](+) in both monodentate and bidentate ways, and that in the second coordination layer both ethylammonium cations and other lithiums are also found. Additionally, the rattling motion of lithium ions inside the cages formed by their neighboring anions, indicative of the so-called caging effect, is confirmed by the analysis of the [Li](+) velocity autocorrelation functions. The overall picture indicates that the solvation of [Li](+) cations in this amphiphilically nanostructured environment takes place by means of a sort of inhomogeneous nanostructural solvation, which we could refer to as nanostructured solvation, and which could be a universal solvation mechanism in ionic liquids.

  2. Experiments on FTU with an actively water cooled liquid lithium limiter

    Energy Technology Data Exchange (ETDEWEB)

    Mazzitelli, G., E-mail: giuseppe.mazzitelli@enea.it [Associazione EURATOM-ENEA sulla Fusione, C.R. Frascati, C.P. 65-00044 Frascati, Rome (Italy); Apicella, M.L.; Apruzzese, G.; Crescenzi, F.; Iannone, F.; Maddaluno, G. [Associazione EURATOM-ENEA sulla Fusione, C.R. Frascati, C.P. 65-00044 Frascati, Rome (Italy); Pericoli-Ridolfini, V. [Associazione EURATOM-ENEA sulla Fusione, CREATE, Università di Napoli Federico II, 80125 Napoli (Italy); Roccella, S.; Reale, M.; Viola, B. [Associazione EURATOM-ENEA sulla Fusione, C.R. Frascati, C.P. 65-00044 Frascati, Rome (Italy); Lyublinski, I.; Vertkov, A. [JSC “RED STAR”, Moscow (Russian Federation)

    2015-08-15

    In order to prevent the overheating of the liquid Li surface and the consequent Li evaporation for T > 500 °C, an advanced version of the liquid lithium limiter has been realized and installed on FTU. This new system, named Cooled Lithium Limiter (CLL), has been optimized to demonstrate the lithium limiter capability to sustain thermal loads as high as 10 MW/m{sup 2} with up to 5 s of plasma pulse duration. The CLL operates with an actively cooled system with water circulation at the temperature of about 200 °C, for heating lithium up to the melting point and for the heat removal during the plasma discharges. To characterize CLL during discharges, a fast infrared camera and the spectroscopic signals from Li and D atom emission have been used. The experiments analyzed so far and simulated by ANSYS code, point out that heat loads as high as 2 MW/m{sup 2} for 1.5 s have been withstood without problems.

  3. Retention/Diffusivity Studies in Free-Surface Flowing Liquid Lithium

    Energy Technology Data Exchange (ETDEWEB)

    R.A. Stubbers; G.H. Miley; M. Nieto; W. Olczak; D.N. Ruzic; A. Hassanein

    2004-12-14

    FLIRE was designed to measure the hydrogen and helium retention and diffusivity in a flowing stream of liquid lithium, and it has accomplished these goals. Retention coefficients for helium in the flowing liquid stream were 0.1-2% for flow speeds of 44 cm/s and implantation energies between 500 and 2000 eV. The energy dependence of retention is linear for the energy range considered, as expected, and the dependence of retention on flow velocity fits the expected square-root of flow speed dependence. Estimates of the helium diffusion coefficient in the flowing lithium stream were {approx} 4 x 10{sup -7} cm{sup 2}/s, and are independent of implantation energy. This value is much lower than expected, which could be due to several factors, such as mixing, bubble formation or surface film formation. In the case of hydrogen, long term retention and release mechanisms are of greatest importance, since this relates to tritium inventory in flowing lithium PFCs for fusion applications. The amount of hydride formation was measured for flowing lithium exposed to neutral deuterium gas. Thermal desorption spectroscopy (TDS) measurements indicate that the hydride concentration was between 0.1 and 0.2% over a wide range of pressures (6.5 x 10{sup -5} to 1 Torr). This result implies that the deuterium absorption rate is limited by the surface dissociation rate, since deuterium (hydrogen/tritium) is absorbed in its atomic form, not its molecular form.

  4. β-NMR measurements of molecular-scale lithium-ion dynamics in poly(ethylene oxide)-lithium-salt thin films

    Science.gov (United States)

    McKenzie, Iain; Cortie, David L.; Harada, Masashi; Kiefl, Robert F.; Levy, C. D. Philip; MacFarlane, W. Andrew; McFadden, Ryan M. L.; Morris, Gerald D.; Ogata, Shin-Ichi; Pearson, Matthew R.; Sugiyama, Jun

    2017-06-01

    β -detected NMR (β -NMR) has been used to study the molecular-scale dynamics of lithium ions in thin films of poly(ethylene oxide) (PEO) containing either lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) or lithium trifluoroacetate (LiTFA) salts at monomer-to-salt ratios (EO/Li) of 8.3. The results are compared with previous β -NMR measurements on pure PEO and PEO with lithium triflate (LiOTf) at the same loading [McKenzie et al., J. Am. Chem. Soc. 136, 7833 (2014)]. Activated hopping of 8Li+ was observed in all of the films above ˜250 K, with the hopping parameters strongly correlated with the ionicity of the lithium salt rather than the polymer glass transition temperature. The pre-exponential factor increases exponentially with ionicity, while the activation energy for hopping increases approximately linearly, going from 6.3 ±0.2 kJ mol-1 in PEO:LiTFA to 17.8 ±0.2 kJ mol-1 in PEO:LiTFSI. The more rapid increase in the pre-exponential factor outweighs the effect of the larger activation energy and results in 8Li+ hopping being fastest in PEO followed by PEO:LiTFSI, PEO:LiOTf, and PEO:LiTFA.

  5. Drop impact on thin liquid films using TIRM

    Science.gov (United States)

    Pack, Min; Ying Sun Team

    2015-11-01

    Drop impact on thin liquid films is relevant to a number of industrial processes such as pesticide spraying and repellent surface research such as self-cleaning applications. In this study, we systematically investigate the drop impact dynamics on thin liquid films on plain glass substrates by varying the film thickness, viscosity and impact velocity. High speed imaging is used to track the droplet morphology and trajectory over time as well as observing instability developments at high Weber number impacts. Moreover, the air layer between the drop and thin film upon drop impact is probed by total internal reflection microscopy (TIRM) where the grayscale intensity is used to measure the air layer thickness and spreading radius over time. For low We impact on thick films (We ~ 10), the effect of the air entrainment is pronounced where the adhesion of the droplet to the wall is delayed by the air depletion and liquid film drainage, whereas for high We impact (We >100) the air layer is no longer formed and instead, the drop contact with the wall is limited only to the film drainage for all film thicknesses. In addition, the maximum spreading radius of the droplet is analyzed for varying thin film thickness and viscosity.

  6. Kinetic Behavior of LiFePO4/C Thin Film Cathode Material for Lithium-Ion Batteries

    OpenAIRE

    Kucinskis, G; Bajārs, G; Kleperis, J.; Smits, J.

    2010-01-01

    LiFePO4 was prepared in a solid state synthesis with various levels of carbon content. LiFePO4/C thin films were obtained via magnetron sputtering. The surface morphology and structure was examined. Electrochemical properties of LiFePO4/C were studied, by using cyclic voltammetry, chronopotentiometry and electrochemical impedance spectroscopy. Thin films acquired show a potential use as a cathode in lithium ion batteries, displaying charge capacity up to 34 mAh g-1.

  7. Liquid Metal Walls, Lithium, And Low Recycling Boundary Conditions In Tokamaks

    Energy Technology Data Exchange (ETDEWEB)

    R. Majeski

    2010-01-15

    At present, the only solid material believed to be a viable option for plasma-facing components (PFCs) in a fusion reactor is tungsten. Operated at the lower temperatures typical of present-day fusion experiments, tungsten is known to suffer from surface degradation during long-term exposure to helium-containing plasmas, leading to reduced thermal conduction to the bulk, and enhanced erosion. Existing alloys are also quite brittle at temperatures under 700oC. However, at a sufficiently high operating temperature (700 - 1000 oC), tungsten is selfannealing and it is expected that surface damage will be reduced to the point where tungsten PFCs will have an acceptable lifetime in a reactor environment. The existence of only one potentially viable option for solid PFCs, though, constitutes one of the most significant restrictions on design space for DEMO and follow-on fusion reactors. In contrast, there are several candidates for liquid metal-based PFCs, including gallium, tin, lithium, and tin-lithium eutectics. We will discuss options for liquid metal walls in tokamaks, looking at both high and low recycling materials. We will then focus in particular on one of the candidate liquids, lithium. Lithium is known to have a high chemical affinity for hydrogen, and has been shown in test stands1 and fusion experiments2,3 to produce a low recycling surface, especially when liquid. Because it is also low-Z and is usable in a tokamak over a reasonable temperature range (200 - 400 oC), it has been now been used as a PFC in several confinement experiments (TFTR, T11- M, CDX-U, NSTX, FTU, and TJ-II), with favorable results. The consequences of substituting low recycling walls for the traditional high recycling variety on tokamak equilibria are very extensive. We will discuss some of the expected modifications, briefly reviewing experimental results, and comparing the results to expectations.

  8. Nanocrystalline NiMoO4 with an ordered mesoporous morphology as potential material for rechargeable thin film lithium batteries.

    Science.gov (United States)

    Haetge, Jan; Djerdj, Igor; Brezesinski, Torsten

    2012-07-07

    Nanocrystalline nickel molybdate (NiMoO(4)) thin film electrodes with a 3D honeycomb structure of uniform 17 nm diameter pores were successfully produced through facile polymer templating strategies. These novel sol-gel type materials exhibit enhanced lithium ion storage capabilities, and thus show promise for battery applications.

  9. Quaternary Ammonium Ionic Liquids as a Less Flammable Electrolyte for Lithium Batteries

    Institute of Scientific and Technical Information of China (English)

    H.Matsumoto; Z.B.Zhou; H.Sakaebe; K.Tatsumi

    2007-01-01

    1 Results Less-flammability is one of the most valuable properties of ionic liquids (ILs) comprised of perfluoroanions such as BF-4,TFSI-([(CF3SO2)2N]-).Recently,such a unique liquid has been expected to use as an electrolyte in order to improve thermal stability and longevity of a lithium secondary battery,which have been increasingly required for an application especially to an electric vehicle and a hybrid car.We previously reported that PI13[TFSI] (PI13: N-methyl-N-propylpiperidinium) could be used ...

  10. Transport Phenomena in Thin Rotating Liquid Films Including: Nucleate Boiling

    Science.gov (United States)

    Faghri, Amir

    2005-01-01

    In this grant, experimental, numerical and analytical studies of heat transfer in a thin liquid film flowing over a rotating disk have been conducted. Heat transfer coefficients were measured experimentally in a rotating disk heat transfer apparatus where the disk was heated from below with electrical resistance heaters. The heat transfer measurements were supplemented by experimental characterization of the liquid film thickness using a novel laser based technique. The heat transfer measurements show that the disk rotation plays an important role on enhancement of heat transfer primarily through the thinning of the liquid film. Experiments covered both momentum and rotation dominated regimes of the flow and heat transfer in this apparatus. Heat transfer measurements have been extended to include evaporation and nucleate boiling and these experiments are continuing in our laboratory. Empirical correlations have also been developed to provide useful information for design of compact high efficiency heat transfer devices. The experimental work has been supplemented by numerical and analytical analyses of the same problem. Both numerical and analytical results have been found to agree reasonably well with the experimental results on liquid film thickness and heat transfer Coefficients/Nusselt numbers. The numerical simulations include the free surface liquid film flow and heat transfer under disk rotation including the conjugate effects. The analytical analysis utilizes an integral boundary layer approach from which

  11. Electrode and solid electrolyte thin films for secondary lithium-ion batteries

    Science.gov (United States)

    Chen, C. H.; Kelder, E. M.; Schoonman, J.

    Electrostatic spray deposition (ESD) was employed to prepare thin layers of Li 1.2Mn 2O 4 (nominal composition) and BPO 4:0.035Li 2O for all-solid-state thin film lithium-ion batteries. The relationships between layer morphologies and deposition conditions such as solvent composition of the precursor solutions and substrate temperature were investigated. It was found that a low substrate temperature and/or high boiling point of the solvent may lead to a relatively dense structure. Reticular porous structures are formed, if films were deposited at 250°C and a mixture of 85 vol.% butyl carbitol and 15 vol.% ethanol was used as the solvent. The Li 1.2Mn 2O 4 layers, formed in the 250-400°C temperature range, were amorphous or micro-crystalline. After annealing beyond 600 °C, they could be crystallized into a spinel-structured material. Glassy BPO 4:0.035Li 2O layers could fill the pores of porous Li 1.2Mn 2O 4 layers to form a dense intermediate electrolyte layer. Thin-film rocking-chair batteries, Li 1.2Mn 2O 4|BPO 4:0.035Li 2O|Li 1.2Mn 2O 4|Al, were prepared and revealed an open-circuit voltage of about 1.2 V after charging.

  12. Reliability of reduced-thickness and thinly veneered lithium disilicate crowns.

    Science.gov (United States)

    Silva, N R F A; Bonfante, E A; Martins, L M; Valverde, G B; Thompson, V P; Ferencz, J L; Coelho, P G

    2012-03-01

    The present investigation hypothesized that the reliability of reduced-thickness monolithic lithium disilicate crowns is high relative to that of veneered zirconia (Y-TZP) and comparable with that of metal ceramic (MCR) systems. CAD/CAM first mandibular molar full-crown preparations were produced with uniform thicknesses of either 1.0-mm or 2.0-mm occlusal and axial reduction, then replicated in composite for standard crown dies. Monolithic 1.0-mm (MON) and 2.0-mm CAD/CAM lithium disilicate crowns, the latter with a buccal thin veneer (BTV) of 0.5 mm, were fabricated and then sliding-contact-fatigued (step-stress method) until failure or suspension (n = 18/group). Crack evolution was followed, and fractography of post mortem specimens was performed and compared with that of clinical specimens. Use level probability Weibull calculation (use load = 1,200 N) showed interval overlaps between MON and BTV. There was no significant difference between the Weibull characteristic failure loads of MON and BTV (1,535 N [90% CI 1,354-1,740] and 1,609 N [90% CI 1,512-1,712], respectively), which were significantly higher than that of Y-TZP (370 N [90% CI 322-427]) and comparable with that of MCR (1,304 N [90% CI 1,203-1,414]), validating the study hypothesis.

  13. Composite Electrolytes for Lithium Batteries: Ionic Liquids in APTES Crosslinked Polymers

    Science.gov (United States)

    Tigelaar, Dean M.; Meador, Mary Ann B.; Bennett, William R.

    2007-01-01

    Solvent free polymer electrolytes were made consisting of Li(+) and pyrrolidinium salts of trifluoromethanesulfonimide added to a series of hyperbranched poly(ethylene oxide)s (PEO). The polymers were connected by triazine linkages and crosslinked by a sol-gel process to provide mechanical strength. The connecting PEO groups were varied to help understand the effects of polymer structure on electrolyte conductivity in the presence of ionic liquids. Polymers were also made that contain poly(dimethylsiloxane) groups, which provide increased flexibility without interacting with lithium ions. When large amounts of ionic liquid are added, there is little dependence of conductivity on the polymer structure. However, when smaller amounts of ionic liquid are added, the inherent conductivity of the polymer becomes a factor. These electrolytes are more conductive than those made with high molecular weight PEO imbibed with ionic liquids at ambient temperatures, due to the amorphous nature of the polymer.

  14. The collective motion of nematodes in a thin liquid layer

    CERN Document Server

    Gart, Sean; Jung, Sunghwan

    2010-01-01

    Many organisms live in confined fluidic environments such as the thin liquid layers on the skin of host organisms or in partially- saturated soil. We investigate the collective behaviour of nematodes in a thin liquid layer, which was first observed by Gray and Lissmann, [J. Exp. Biol. 41, 135 (1964)]. We show experimentally that nematodes confined by a thin liquid film come into contact and only separate again after some intervention. We attribute this collective motion to an attractive force between them arising from the surface tension of the layer and show that for nearby nematodes this force is typically stronger than the force that may be exerted by the nematodes' muscles. We believe this to be the first demonstration of the "Cheerios effect" acting on a living organism. However, we find that being grouped together does not significantly alter the body stroke and kinematic performance of the nematode: there are no statistically significant changes of the Strouhal number and the ratio of amplitude to wave...

  15. Preparation and characterization of LiFePO4 thin films as cathode materials for lithium ion battery

    Institute of Scientific and Technical Information of China (English)

    XIAO Zhuo-bing; MA Ming-you

    2006-01-01

    LiFePO4 thin films were prepared by sol-gel technique. The phase and surface morphology were characterized by X-ray diffraction and scanning electron microscopy. The electrochemical properties of the thin films were measured by cyclic voltammetry, galvanostatic charge-discharge experiments and electrochemical impedance spectroscopy in 1 mol/L LiPF6/EC-DMC solution using lithium metal as both counter and reference electrodes. The films prepared by this method are of pure LiFePO4 phase. The capacity of the film annealed at 700 ℃ for 30 min is 145 Ma·h/g, and the capacity loss per cycle is 0.06% after being cycled 50 times. The electrochemical impedance spectroscopy shows that the diffusion rate of lithium ion in LiFePO4 thin film is 5.1×10-14cm2/s.

  16. Ferroelectric domain inversion and its stability in lithium niobate thin film on insulator with different thicknesses

    Science.gov (United States)

    Shao, Guang-hao; Bai, Yu-hang; Cui, Guo-xin; Li, Chen; Qiu, Xiang-biao; Geng, De-qiang; Wu, Di; Lu, Yan-qing

    2016-07-01

    Ferroelectric domain inversion and its effect on the stability of lithium niobate thin films on insulator (LNOI) are experimentally characterized. Two sets of specimens with different thicknesses varying from submicron to microns are selected. For micron thick samples (˜28 μm), domain structures are achieved by pulsed electric field poling with electrodes patterned via photolithography. No domain structure deterioration has been observed for a month as inspected using polarizing optical microscopy and etching. As for submicron (540 nm) films, large-area domain inversion is realized by scanning a biased conductive tip in a piezoelectric force microscope. A graphic processing method is taken to evaluate the domain retention. A domain life time of 25.0 h is obtained and possible mechanisms are discussed. Our study gives a direct reference for domain structure-related applications of LNOI, including guiding wave nonlinear frequency conversion, nonlinear wavefront tailoring, electro-optic modulation, and piezoelectric devices.

  17. Argon plasma inductively coupled plasma reactive ion etching study for smooth sidewall thin film lithium niobate waveguide application

    Science.gov (United States)

    Ulliac, G.; Calero, V.; Ndao, A.; Baida, F. I.; Bernal, M.-P.

    2016-03-01

    Lithium Niobate (LN) exhibits unique physical properties such as remarkable electro-optical coefficients and it is thus an excellent material for a wide range of fields like optic communications, lasers, nonlinear optical applications, electric field optical sensors etc. In order to further enhance the optical device performance and to be competitive with silicon photonics, sub-micrometric thickness lithium niobate films are crucial. A big step has been achieved with the development of LN thin films by using smart cut technology and wafer bonding and these films are nowadays available in the market. However, it is a challenge to obtain the requirements of the high quality thin LN film waveguide. In this letter, we show smooth ridge waveguides fabricated on 700 nm thickness thin film lithium niobate (TFLN). The fabrication has been done by developing and optimizing three steps of the technological process, the mask fabrication, the plasma etching, and a final cleaning wet etching step in order to remove the lithium niobate redeposition on the side walls. We have obtained single mode propagation with light overall losses of only 5 dB/cm.

  18. Electrochemical properties of tungsten oxysulphide thin films as positive electrodes for lithium microbatteries

    Indian Academy of Sciences (India)

    I Martin-Litas; P Vinatier; A Levasseur; J C Dupin; D Gonbeau

    2003-12-01

    Several WOS tungsten oxysulphide thin films were tested as positive electrodes for lithium microbatteries. The amorphous WO1.05S2 thin film was found very promising. A capacity decrease occurred during the first few cycles, after which the films were able to intercalate reversibly up to 1.1 lithium ion per formula unit under high regime (75 A/cm2). They were tested for 250 charge–discharge cycles, between 3.0 V and 1.2 V. X-ray photoelectron spectroscopy measurements were performed on different compounds in both intercalated (Li1WO1.05S2, Li2.7WO1.05S2 and Li3.8WO1.05S2) and partially de-intercalated (Li1WO1.05S2) states in order to understand the redox processes occurring during the first discharge–charge cycle. The analysis of both the W4 and the S2 peaks has shown that the redox processes involve not only the tungsten atoms but also sulphur atoms. At the beginning of the intercalation, W6+ was first partially reduced into W5+, and then into W4+, but the important stage was the reduction of W4+ into W0. In W0, the electron binding energy was very close to that of metallic tungsten. At the same time, S$^{2-}_2$ ions were partially reduced into S2- ions. But only the reduction process of tungsten atoms appeared to be totally reversible.

  19. Effect of zwitterion on the lithium solid electrolyte interphase in ionic liquid electrolytes

    Science.gov (United States)

    Byrne, N.; Howlett, P. C.; MacFarlane, D. R.; Smith, M. E.; Howes, A.; Hollenkamp, A. F.; Bastow, T.; Hale, P.; Forsyth, M.

    An understanding of the solid electrolyte interphase (SEI) that forms on the lithium-metal surface is essential to the further development of rechargeable lithium-metal batteries. Currently, the formation of dendrites during cycling, which can lead to catastrophic failure of the cell, has mostly halted research on these power sources. The discovery of ionic liquids as electrolytes has rekindled the possibility of safe, rechargeable, lithium-metal batteries. The current limitation of ionic liquid electrolytes, however, is that when compared with conventional non-aqueous electrolytes the device rate capability is limited. Recently, we have shown that the addition of a zwitterion such as N-methyl- N-(butyl sulfonate) pyrrolidinium resulted in enhancement of the achievable current densities by 100%. It was also found that the resistance of the SEI layer in the presence of a zwitterion is 50% lower. In this study, a detailed chemical and electrochemical analysis of the SEI that forms in both the presence and absence of a zwitterion has been conducted. Clear differences in the chemical nature and also the thickness of the SEI are observed and these may account for the enhancement of operating current densities.

  20. Optically Thin Liquid Water Clouds: Their Importance and Our Challenge

    Science.gov (United States)

    Turner, D. D.; Vogelmann, A. M.; Austin, R. T.; Barnard, J. C.; Cady-Pereira, K.; Chiu, J. C.; Clough, S. A.; Flynn, C.; Khaiyer, M. M.; Liljegren, J.; Johnson, K.; Lin, B.; Long, C.; Marshak, A.; Matrosov, S. Y.; McFarlane, S. A.; Miller, M.; Min, Q.; Minnis, P.; O'Hirok, W.; Wang, Z.; Wiscombe, W.

    2006-01-01

    Many of the clouds important to the Earth's energy balance, from the tropics to the Arctic, are optically thin and contain liquid water. Longwave and shortwave radiative fluxes are very sensitive to small perturbations of the cloud liquid water path (LWP) when the liquid water path is small (i.e., challenging to retrieve their microphysical properties accurately. We describe a retrieval algorithm intercomparison that was conducted to evaluate the issues involved. The intercomparison included eighteen different algorithms to evaluate their retrieved LWP, optical depth, and effective radii. Surprisingly, evaluation of the simplest case, a single-layer overcast cloud, revealed that huge discrepancies exist among the various techniques, even among different algorithms that are in the same general classification. This suggests that, despite considerable advances that have occurred in the field, much more work must be done, and we discuss potential avenues for future work.

  1. Thin aligned organic polymer films for liquid crystal devices

    CERN Document Server

    Foster, K E

    1997-01-01

    This project was designed to investigate the possibility of producing alignment layers for liquid crystal devices by cross-linking thin films containing anisotropic polymer bound chromophores via irradiation with polarised ultraviolet light. Photocross-linkable polymers find use in microelectronics, liquid crystal displays, printing and UV curable lacquers and inks; so there is an increasing incentive for the development of new varieties of photopolymers in general. The synthesis and characterisation of two new photopolymers that are suitable as potential alignment layers for liquid crystal devices are reported in this thesis. The first polymer contains the anthracene chromophore attached via a spacer unit to a methacrylate backbone and the second used a similarly attached aryl azide group. Copolymers of the new monomers with methyl methacrylate were investigated to establish reactivity ratios in order to understand composition drift during polymerisation.

  2. Atomistic Simulation and Electronic Structure of Lithium Doped Ionic Liquids: Structure, Transport, and Electrochemical Stability

    Science.gov (United States)

    Haskins, Justin B.; Bauschlicher, Charles W.; Lawson, John W.

    2015-01-01

    Zero-temperature density functional theory (DFT), density functional theory molecular dynamics (DFT-MD), and classical molecular dynamics using polarizable force fields (PFF-MD) are employed to evaluate the influence of Lithium ion on the structure, transport, and electrochemical stability of three potential ionic liquid electrolytes: N--methyl-N-butylpyrrolidinium bis(trifluoromethanesulfonyl)imide ([pyr14][TFSI]), N--methyl-N-propylpyrrolidinium bis(fluorosulfonyl)imide ([pyr13][FSI]), and 1-ethyl-3--methylimidazolium boron tetrafluoride ([EMIM][BF4]). We characterize the Lithium ion solvation shell through zero-temperature DFT simulations of [Li(Anion)sub n](exp n-1) -clusters, DFT-MD simulations of isolated lithium ions in small ionic liquid systems, and PFF-MD simulations with high Li-doping levels in large ionic liquid systems. At low levels of Li-salt doping, highly stable solvation shells having 2-3 anions are seen in both [pyr14][TFSI] and [pyr13][FSI], while solvation shells with 4 anions dominate in [EMIM][BF sub 4]. At higher levels of doping, we find the formation of complex Li-network structures that increase the frequency of 4 anion-coordinated solvation shells. A comparison of computational and experimental Raman spectra for a wide range of [Li(Anion) sub n](exp n -1) - clusters shows that our proposed structures are consistent with experiment. We estimate the ion diffusion coefficients and quantify both size and simulation time effects. We find estimates of lithium ion diffusion are a reasonable order of magnitude and can be corrected for simulation time effects. Simulation size, on the other hand, is also important, with diffusion coefficients from long PFF-MD simulations of small cells having 20-40% error compared to large-cell values. Finally, we compute the electrochemical window using differences in electronic energy levels of both isolated cation/anion pairs and small ionic liquid systems with Li-salt doping. The single pair and liquid

  3. Controlling domain orientation of liquid crystalline block copolymer in thin films through tuning mesogenic chemical structures

    Energy Technology Data Exchange (ETDEWEB)

    Xie, He-Lou [Institute for Molecular Engineering, The University of Chicago, Chicago Illinois 60637; Li, Xiao [Institute for Molecular Engineering, The University of Chicago, Chicago Illinois 60637; Ren, Jiaxing [Institute for Molecular Engineering, The University of Chicago, Chicago Illinois 60637; Bishop, Camille [Institute for Molecular Engineering, The University of Chicago, Chicago Illinois 60637; Arges, Christopher G. [Cain Department of Chemical Engineering, Louisiana State University, Baton Rouge Louisiana 70803 USA; Nealey, Paul F. [Institute for Molecular Engineering, The University of Chicago, Chicago Illinois 60637; Materials Science Division, Argonne National Laboratory, Argonne Illinois 60439

    2017-01-24

    Controlling the macroscopic orientation of nanoscale periodic structures of amphiphilic liquid crystalline block copolymers (LC BCPs) is important to a variety of technical applications (e.g., lithium conducting polymer electrolytes). To study LC BCP domain orientation, a series of LC BCPs containing a poly(ethylene oxide) (PEO) block as a conventional hydrophilic coil block and LC blocks containing azobenzene mesogens is designed and synthesized. LC ordering in thin films of the BCP leads to the formation of highly ordered, microphase-separated nanostructures, with hexagonally arranged PEO cylinders. Substitution on the tail of the azobenzene mesogen is shown to control the orientation of the PEO cylinders. When the substitution on the mesogenic tails is an alkyl chain, the PEO cylinders have a perpendicular orientation to the substrate surface, provided the thin film is above a critical thickness value. In contrast, when the substitution on the mesogenic tails has an ether group the PEO cylinders assemble parallel to the substrate surface regardless of the film thickness value.

  4. The effects of carbon and nitrogen on the corrosion resistance of type 316 stainless steel to liquid lithium

    Science.gov (United States)

    Barker, M. G.; Frankham, S. A.

    1982-06-01

    Type 316 stainless steel plates have been exposed at 600°C to liquid lithium containing carbon and nitrogen at various chemical activities for periods of up to 672 h. The corrosion products Li 9CrN 5 and M 23C 6 have been identified on the plate surfaces and in the grain boundaries. Scanning electron microscopy has shown preferential nickel and chromium depletion at the steel surface in lithium with high nitrogen content. The diffusion coefficient of carbon in type 316 stainless steel from a lithium source was found to be 6.5 × 10 t 1¯5 m 2/s.

  5. Soft X-ray emission spectroscopy of liquids and lithium batterymaterials

    Energy Technology Data Exchange (ETDEWEB)

    Augustsson, Andreas [Uppsala Univ. (Sweden)

    2004-01-01

    Lithium ion insertion into electrode materials is commonly used in rechargeable battery technology. The insertion implies changes in both the crystal structure and the electronic structure of the electrode material. Side-reactions may occur on the surface of the electrode which is exposed to the electrolyte and form a solid electrolyte interface (SEI). The understanding of these processes is of great importance for improving battery performance. The chemical and physical properties of water and alcohols are complicated by the presence of strong hydrogen bonding. Various experimental techniques have been used to study geometrical structures and different models have been proposed to view the details of how these liquids are geometrically organized by hydrogen bonding. However, very little is known about the electronic structure of these liquids, mainly due to the lack of suitable experimental tools. In this thesis examples of studies of lithium battery electrodes and liquid systems using soft x-ray emission spectroscopy will be presented. Monochromatized synchrotron radiation has been used to accomplish selective excitation, in terms of energy and polarization. The electronic structure of graphite electrodes has been studied, before and after lithium intercalation. Changes in the electronic structure upon lithiation due to transfer of electrons into the graphite π-bands have been observed. Transfer of electrons in to the 3d states of transition metal oxides upon lithiation have been studied, through low energy excitations as dd- and charge transfer-excitations. A SEI was detected on cycled graphite electrodes. By the use of selective excitation different carbon sites were probed in the SEI. The local electronic structure of water, methanol and mixtures of the two have been examined using a special liquid cell, to separate the liquid from the vacuum in the experimental chamber. Results from the study of liquid water showed a strong influence on the 3a1 molecular

  6. Irreversible lithium storage during lithiation of amorphous silicon thin film electrodes studied by in-situ neutron reflectometry

    Science.gov (United States)

    Jerliu, Bujar; Hüger, Erwin; Horisberger, Michael; Stahn, Jochen; Schmidt, Harald

    2017-08-01

    Amorphous silicon is a promising high-capacity anode material for application in lithium-ion batteries. However, a huge drawback of the material is that the large capacity losses taking place during cycling lead to an unstable performance. In this study we investigate the capacity losses occurring during galvanostatic lithiation of amorphous silicon thin film electrodes by in-situ neutron reflectometry experiments for the first ten cycles. As determined from the analysis of the neutron scattering length density and of the film thickness, the capacity losses are due to irreversible storage of lithium in the electrode. The amount of stored lithium increases during cycling to 20% of the maximum theoretical capacity after the 10th cycle. Possible explanations are discussed.

  7. Radiation hardness and charge collection efficiency of lithium irradiated thin silicon diodes

    CERN Document Server

    Boscardin, Maurizio; Bruzzi, Mara; Candelori, Andrea; Focardi, Ettore; Khomenkov, Volodymyr P; Piemonte, Claudio; Ronchin, S; Tosi, C; Zorzi, N

    2005-01-01

    Due to their low depletion voltage, even after high particle fluences, improved tracking precision and momentum resolution, and reduced material budget, thin substrates are one of the possible choices to provide radiation hard detectors for future high energy physics experiments. In the framework of the CERN RD50 Collaboration, we have developed PIN diode detectors on membranes obtained by locally thinning the silicon substrate by means of TMAH etching from the wafer backside. Diodes of different shapes and sizes have been fabricated on 50- mu m and 100- mu m thick membranes and tested, showing a low leakage current (of 300 nA/cm/sup 3/) and a very low depletion voltage (in the order of 1 V for the 50 mu m membrane) before irradiation. Radiation damage tests have been performed with 58 MeV lithium (Li) ions up to the fluence of 10/sup 14/ Li/cm/sup 2/ in order to determine the depletion voltage and leakage current density increase after irradiation. Charge collection efficiency tests carried out with a beta /...

  8. Production of lithium positive ions from LiF thin films on the anode in PBFA II

    Energy Technology Data Exchange (ETDEWEB)

    Green, T.A.; Stinnett, R.W.; Gerber, R.A. [and others

    1995-09-01

    The production of positive lithium ions using a lithium-fluoride-coated stainless steel anode in the particle beam fusion accelerator PBFA II is considered from both the experimental and theoretical points of view. It is concluded that the mechanism of Li{sup +} ion production is electric field desorption from the tenth-micron-scale crystallites which compose the columnar growth of the LiF thin film. The required electric field is estimated to be of the order of 5 MV/cm. An essential feature of the mechanism is that the crystallites are rendered electronically conducting through electron-hole pair generation by MeV electron bombardment of the thin film during the operation of the diode. It is proposed that the ion emission mechanism is an electronic conductivity analogue to that discovered by Rollgen for lithium halide crystallites which were rendered ionically conducting by heating to several hundred degrees Celsius. Since an electric field desorption mechanism cannot operate if a surface flashover plasma has formed and reduced the anode electric field to low values, the possibility of flashover on the lithium fluoride coated anode of the PBFA II Li{sup +} ion source is studied theoretically. It is concluded with near certainty that flashover does not occur.

  9. Reduced cost design of liquid lithium target for international fusion material irradiation facility (IFMIF)

    Energy Technology Data Exchange (ETDEWEB)

    Nakamura, Hiroo; Ida, Mizuho; Sugimoto, Masayoshi; Takeuchi, Hiroshi [Department of Fussion Engineering Research, Naka Fusion Research Establishment, Japan Atomic Energy Research Institute, Tokai, Ibaraki (Japan); Yutani, Toshiaki [Toshiba Corp., Tokyo (Japan)

    2001-01-01

    The International Fusion Materials Irradiation Facility (IFMIF) is being jointly planned to provide an accelerator-based D-Li neutron source to produce intense high energy neutrons (2 MW/m{sup 2}) up to 200 dpa and a sufficient irradiation volume (500 cm{sup 3}) for testing the candidate materials and components up to about a full lifetime of their anticipated use in ITER and DEMO. To realize such a condition, 40 MeV deuteron beam with a current of 250 mA is injected into high speed liquid lithium flow with a speed of 20 m/s. Following Conceptual Design Activity (1995-1998), a design study with focus on cost reduction without changing its original mission has been done in 1999. The following major changes to the CAD target design have been considered in the study and included in the new design: i) number of the Li target has been changed from 2 to 1, ii) spare of impurity traps of the Li loop was removed although the spare will be stored in a laboratory for quick exchange, iii) building volume was reduced via design changes in lithium loop length. This paper describes the reduced cost design of the lithium target system and recent status of Key Element Technology activities. (author)

  10. Measurements of proportional scintillation in liquid xenon using thin wires

    CERN Document Server

    Aprile, E; Goetzke, L W; Fernandez, A J Melgarejo; Messina, M; Naganoma, J; Plante, G; Rizzo, A; Shagin, P; Wall, R

    2014-01-01

    Proportional scintillation in liquid xenon has a promising application in the field of direct dark matter detection, potentially allowing for simpler, more sensitive detectors. However, knowledge of the basic properties of the phenomenon as well as guidelines for its practical use are currently limited. We report here on measurements of proportional scintillation light emitted in liquid xenon around thin wires. The maximum proportional scintillation gain of $287^{+97}_{-75}$ photons per drift electron was obtained using 10 $\\mu$m diameter gold plated tungsten wire. The thresholds for electron multiplication and proportional scintillation are measured as $725^{+48}_{-139}$ and $412^{+10}_{-133}$ kV/cm, respectively. The threshold for proportional scintillation is in good agreement with a previously published result, while the electron multiplication threshold represents a novel measurement. A complete set of parameters for the practical use of the electron multiplication and proportional scintillation processe...

  11. Laser modification and characterization of Li-Mn-O thin film cathodes for lithium-ion batteries

    Science.gov (United States)

    Pröll, J.; Kohler, R.; Adelhelm, C.; Bruns, M.; Torge, M.; Heißler, S.; Przybylski, M.; Ziebert, C.; Pfleging, W.

    2011-03-01

    The development of future battery systems is mainly focused on powerful rechargeable lithium-ion batteries. To satisfy this demand, current studies are focused on cathodes based on nano-composite materials which lead to an increase in power density of the LIB primarily due to large electrochemically active surface areas. Electrode materials made of lithium manganese oxides (Li-Mn-O) are assumed to replace commonly used cathode materials like LiCoO2 due to less toxicity and lower costs. Thin films in the Li-Mn-O system were synthesized by non-reactive r.f. magnetron sputtering of a LiMn2O4 target on silicon and stainless steel substrates. In order to enhance power density and cycle stability of the cathode material, direct laser structuring methods were investigated using a laser system operating at a wavelength of 248 nm. Therefore, high aspect ratio micro-structures were formed on the thin films. Laser annealing processes were investigated in order to achieve an appropriate crystalline phase for unstructured and structured thin films as well as for an increase in energy density and control of grain size. Laser annealing was realized via a high power diode laser system. The effects of post-thermal treatment on the thin films were studied with Raman spectroscopy, X-ray diffraction and scanning electron microscopy. The formation of electrochemically active and inactive phases was discussed. Surface chemistry was investigated via X-ray photoelectron spectroscopy. Interaction between UV-laser radiation and the thin film material was analyzed through ablation experiments. Finally, to investigate the electrochemical properties, the manufactured thin film cathodes were cycled against a lithium anode. The formation of a solid electrolyte interphase on the cathode side was discussed.

  12. Longitudinal Modes along Thin Piezoelectric Waveguides for Liquid Sensing Applications

    Directory of Open Access Journals (Sweden)

    Cinzia Caliendo

    2015-06-01

    Full Text Available The propagation of longitudinally polarized acoustic modes along thin piezoelectric plates (BN, ZnO, InN, AlN and GaN is theoretically studied, aiming at the design of high frequency electroacoustic devices suitable for work in liquid environments. The investigation of the acoustic field profile across the plate revealed the presence of longitudinally polarized Lamb modes, travelling at velocities close to that of the longitudinal bulk acoustic wave propagating in the same direction. Such waves are suitable for the implementation of high-frequency, low-loss electroacoustic devices operating in liquid environments. The time-averaged power flow density, the phase velocity and the electroacoustic coupling coefficient K2 dispersion curves were studied, for the first (S0 and four higher order (S1, S2, S3, S4 symmetrical modes for different electrical boundary conditions. Two electroacoustic coupling configurations were investigated, based on interdigitated transducers, with or without a metal floating electrode at the opposite plate surface. Enhanced performances, such as a K2 as high as 8.5% and a phase velocity as high as 16,700 m/s, were demostrated for the ZnO- and BN-based waveguides, as an example. The relative velocity changes, and the inertial and viscous sensitivities of the first symmetric and anti-symmetric mode, S0 and A0, propagating along thin plates bordered by a viscous liquid were derived using the perturbation approach. The present study highlights the feasibility of the piezoelectric waveguides to the development of high-frequency, integrated-circuits compatible electroacoustic devices suitable for working in liquid environment.

  13. MoO3 Cathodes for High-Temperature Lithium Thin-Film Cells

    Science.gov (United States)

    West, William; Whitacre, Jay

    2007-01-01

    MoO3 has shown promise as a cathode material that can extend the upper limit of operating temperature of rechargeable lithium thin-film electrochemical cells. Cells of this type are undergoing development for use as energy sources in cellular telephones, wireless medical sensors, and other, similarly sized portable electronic products. The LiCoO2 and LiMn2O4 cathodes heretofore used in these cells exhibit outstanding cycle lives (of the order of hundreds of thousands of cycles) at room temperature, but operation at higher temperatures reduces their cycle lives substantially: for example, at a temperature of 150 C, cells containing LiCoO2 cathodes lose half their capacities in 100 charge/discharge cycles. The superiority of MoO3 as a cathode material was demonstrated in experiments on lithium thin-film cells fabricated on glass slides. Each cell included a layer of Ti (for adhesion to the glass slide), a patterned layer of Pt that served as a cathode current collector, a cathode layer of MoO3, a solid electrolyte layer of Li3.3 PO3.8 N0.22 ("LiPON"), and an anode layer of Li. All the layers were deposited by magnetron sputtering except for the Li layer, which was deposited by thermal evaporation. These cells, along with similar ones containing LiCoO2 cathodes, were subjected to several tests, including measurements of specific capacity in charge/discharge cycling at a temperature of 150 C. The results of these measurements, plotted in the figure, showed that whereas specific capacity of the cells containing LiCoO2 cathodes faded to about half its initial value after only 100 cycles, the specific capacity of the cells containing the MoO3 cathodes faded only slightly during the first few hundred cycles and thereafter not only recovered to its initial value but continued to increase up to at least 5,500 cycles.

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

    Science.gov (United States)

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

    2014-09-01

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

  15. LiCoO2 and SnO2 Thin Film Electrodes for Lithium-Ion Battery Applications

    Science.gov (United States)

    Maranchi, Jeffrey P.; Hepp, Aloysius F.; Kumta, Prashant N.

    2004-01-01

    There is an increasing need for small dimension, ultra-lightweight, portable power supplies due to the miniaturization of consumer electronic devices. Rechargeable thin film lithium-ion batteries have the potential to fulfill the growing demands for micro-energy storage devices. However, rechargeable battery technology and fabrication processes have not kept paced with the advances made in device technology. Economical fabrication methods lending excellent microstructural and compositional control in the thin film battery electrodes have yet to be fully developed. In this study, spin coating has been used to demonstrate the flexibility of the approach to produce both anode (SnO2) and cathode (LiCoO2) thin films. Results on the microstructure crystal structure and electrochemical properties of the thin film electrodes are described and discussed.

  16. Characteristics of free-surface wave on high-speed liquid lithium jet for IFMIF

    Energy Technology Data Exchange (ETDEWEB)

    Kanemura, Takuji, E-mail: kanemura@stu.nucl.eng.osaka-u.ac.jp [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan); Yoshihashi-Suzuki, Sachiko [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan); Kondo, Hiroo [Japan Atomic Energy Agency, 2-4 Shirane Shirakata, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Sugiura, Hirokazu; Yamaoka, Nobuo [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan); Ida, Mizuho; Nakamura, Hiroo [Japan Atomic Energy Agency, 2-4 Shirane Shirakata, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Matsushita, Izuru [Mitsubishi Heavy Industries Mechatronics Systems, Ltd., 1-16 5-chome, Komatsu-dori, Hyogo-ku, Kobe, Hyogo 652-0865 (Japan); Muroga, Takeo [National Institute for Fusion Science, 322-6 Oroshicho, Toki, Gifu 509-5292 (Japan); Horiike, Hiroshi [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan)

    2011-10-01

    The characteristics of the surface waves on a high-speed liquid lithium wall jet were examined in a Li circulation loop at Osaka University for the International Fusion Materials Irradiation Facility (IFMIF). Surface fluctuations were measured by a contact-type liquid level sensor at 175 mm downstream from the nozzle exit, which corresponds to the deuteron beam's axis in the IFMIF, and observed with a high-speed video (HSV) camera. Both the observation and measurement results indicated that the surface fluctuations were composed of various scale turbulent fluctuations. The measurement results especially showed good agreement with the log-normal distribution which is one of the turbulent intermittency theories. The dominant wavelength was found to be shorter with increase in the flow velocity, and reached approximately 4 mm at the velocity of 15 m/s, which gave close agreement with the visually observed wavelength.

  17. Liquid-Phase Processing of Barium Titanate Thin Films

    Science.gov (United States)

    Harris, David Thomas

    Processing of thin films introduces strict limits on the thermal budget due to substrate stability and thermal expansion mismatch stresses. Barium titanate serves as a model system for the difficulty in producing high quality thin films because of sensitivity to stress, scale, and crystal quality. Thermal budget restriction leads to reduced crystal quality, density, and grain growth, depressing ferroelectric and nonlinear dielectric properties. Processing of barium titanate is typically performed at temperatures hundreds of degrees above compatibility with metalized substrates. In particular integration with silicon and other low thermal expansion substrates is desirable for reductions in costs and wider availability of technologies. In bulk metal and ceramic systems, sintering behavior has been encouraged by the addition of a liquid forming second phase, improving kinetics and promoting densification and grain growth at lower temperatures. This approach is also widespread in the multilayer ceramic capacitor industry. However only limited exploration of flux processing with refractory thin films has been performed despite offering improved dielectric properties for barium titanate films at lower temperatures. This dissertation explores physical vapor deposition of barium titanate thin films with addition of liquid forming fluxes. Flux systems studied include BaO-B2O3, Bi2O3-BaB2O 4, BaO-V2O5, CuO-BaO-B2O3, and BaO-B2O3 modified by Al, Si, V, and Li. Additions of BaO-B2O3 leads to densification and an increase in average grain size from 50 nm to over 300 nm after annealing at 900 °C. The ability to tune permittivity of the material improved from 20% to 70%. Development of high quality films enables engineering of ferroelectric phase stability using residual thermal expansion mismatch in polycrystalline films. The observed shifts to TC match thermodynamic calculations, expected strain from the thermal expansion coefficients, as well as x-ray diffract measurements

  18. Development of a high energy pulsed plasma simulator for the study of liquid lithium trenches

    Energy Technology Data Exchange (ETDEWEB)

    Jung, S., E-mail: jung73@illinois.edu [Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States); Christenson, M.; Curreli, D. [Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States); Bryniarski, C. [Department of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States); Andruczyk, D.; Ruzic, D.N. [Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States)

    2014-12-15

    Highlights: • A pulse device for a liquid lithium trench study is developed. • It consists of a coaxial plasma gun, a theta pinch, and guiding magnets. • A large energy enhancement is observed with the use of the plasma gun. • A further increase in energy and velocity is observed with the theta pinch. - Abstract: To simulate detrimental events in a tokamak and provide a test-stand for a liquid-lithium infused trench (LiMIT) device [1], a pulsed plasma source utilizing a theta pinch in conjunction with a coaxial plasma accelerator has been developed. The plasma is characterized using a triple Langmuir probe, optical methods, and a calorimeter. Clear advantages have been observed with the application of a coaxial plasma accelerator as a pre-ionization source. The experimental results of the plasma gun in conjunction with the existing theta pinch show a significant improvement from the previous energy deposition by a factor of 14 or higher, resulting in a maximum energy and heat flux of 0.065 ± 0.002 MJ/m{sup 2} and 0.43 ± 0.01 GW/m{sup 2}. A few ways to further increase the plasma heat flux for LiMIT experiments are discussed.

  19. Measurement of hydrogen solubility and desorption rate in V-4Cr-4Ti and liquid lithium-calcium alloys

    Energy Technology Data Exchange (ETDEWEB)

    Park, J.H.; Erck, R.; Park, E.T. [Argonne National Lab., IL (United States)] [and others

    1997-04-01

    Hydrogen solubility in V-4Cr-4Ti and liquid lithium-calcium was measured at a hydrogen pressure of 9.09 x 10{sup {minus}4} torr at temperatures between 250 and 700{degrees}C. Hydrogen solubility in V-4Cr-4Ti and liquid lithium decreased with temperature. The measured desorption rate of hydrogen in V-4Cr-4Ti is a thermally activated process; the activation energy is 0.067 eV. Oxygen-charged V-4Cr-4Ti specimens were also investigated to determine the effect of oxygen impurity on hydrogen solubility and desorption in the alloy. Oxygen in V-4Cr-4Ti increases hydrogen solubility and desorption kinetics. To determine the effect of a calcium oxide insulator coating on V-4Cr-4Ti, hydrogen solubility in lithium-calcium alloys that contained 0-8.0 percent calcium was also measured. The distribution ratio R of hydrogen between liquid lithium or lithium-calcium and V-4Cr-4Ti increased as temperature decreased (R {approx} 10 and 100 at 700 and 250{degrees}C, respectively). However at <267{degrees}C, solubility data could not be obtained by this method because of the slow kinetics of hydrogen permeation through the vanadium alloy.

  20. Lithium-antimony-lead liquid metal battery for grid-level energy storage

    Science.gov (United States)

    Wang, Kangli; Jiang, Kai; Chung, Brice; Ouchi, Takanari; Burke, Paul J.; Boysen, Dane A.; Bradwell, David J.; Kim, Hojong; Muecke, Ulrich; Sadoway, Donald R.

    2014-10-01

    The ability to store energy on the electric grid would greatly improve its efficiency and reliability while enabling the integration of intermittent renewable energy technologies (such as wind and solar) into baseload supply. Batteries have long been considered strong candidate solutions owing to their small spatial footprint, mechanical simplicity and flexibility in siting. However, the barrier to widespread adoption of batteries is their high cost. Here we describe a lithium-antimony-lead liquid metal battery that potentially meets the performance specifications for stationary energy storage applications. This Li||Sb-Pb battery comprises a liquid lithium negative electrode, a molten salt electrolyte, and a liquid antimony-lead alloy positive electrode, which self-segregate by density into three distinct layers owing to the immiscibility of the contiguous salt and metal phases. The all-liquid construction confers the advantages of higher current density, longer cycle life and simpler manufacturing of large-scale storage systems (because no membranes or separators are involved) relative to those of conventional batteries. At charge-discharge current densities of 275 milliamperes per square centimetre, the cells cycled at 450 degrees Celsius with 98 per cent Coulombic efficiency and 73 per cent round-trip energy efficiency. To provide evidence of their high power capability, the cells were discharged and charged at current densities as high as 1,000 milliamperes per square centimetre. Measured capacity loss after operation for 1,800 hours (more than 450 charge-discharge cycles at 100 per cent depth of discharge) projects retention of over 85 per cent of initial capacity after ten years of daily cycling. Our results demonstrate that alloying a high-melting-point, high-voltage metal (antimony) with a low-melting-point, low-cost metal (lead) advantageously decreases the operating temperature while maintaining a high cell voltage. Apart from the fact that this finding

  1. Heavy lithium-doped ZnO thin films prepared by spray pyrolysis method

    Indian Academy of Sciences (India)

    M Ardyanian; N Sedigh

    2014-10-01

    Lithium-doped ZnO thin films (ZnO : Li) were prepared by spray pyrolysis method on the glass substrates for ( = [Li]/[Zn]) value varied between 5 and 70%. Structural, electrical and optical properties of the samples were studied by X-ray diffraction (XRD), UV–Vis–NIR spectroscopy, scanning electron microscopy (SEM), Hall effect and sheet resistance measurements. XRD results show that for ≤ 50%, the structure of the films tends to be polycrystals of wurtzite structure with preferred direction along (0 0 2). The best crystalline order is found at = 20% and the crystal structure is stable until = 60%. The Hall effect results describe that Li doping leads to change in the conduction type from - to -type, again it changes to -type at = 70% and is attributed to self-compensation effect. Moreover, the carrier density was calculated in the order of 1013 cm-3. The resistivity of Li-doped films decreases until 22 cm at = 50%. Optical bandgap was reduced slightly, from 3.27 to 3.24 eV as a function of the grain size. Optical transmittance in the visible range reaches = 97%, by increasing of Li content until = 20%. Electrical and optical properties are coherent with structural results.

  2. Silicon nitride coated silicon thin film on three dimensions current collector for lithium ion battery anode

    Science.gov (United States)

    Wu, Cheng-Yu; Chang, Chun-Chi; Duh, Jenq-Gong

    2016-09-01

    Silicon nitride coated silicon (N-Si) has been synthesized by two-step DC sputtering on Cu Micro-cone arrays (CMAs) at ambient temperature. The electrochemical properties of N-Si anodes with various thickness of nitride layer are investigated. From the potential window of 1.2 V-0.05 V, high rate charge-discharge and long cycle test have been executed to investigate the electrochemical performances of various N-Si coated Si-based lithium ion batteries anode materials. Higher specific capacity can be obtained after 200 cycles. The cycling stability is enhanced via thinner nitride layer coating as silicon nitride films are converted to Li3N with covered Si thin films. These N-Si anodes can be cycled under high rates up to 10 C due to low charge transfer resistance resulted from silicon nitride films. This indicates that the combination of silicon nitride and silicon can effectively endure high current and thus enhance the cycling stability. It is expected that N-Si is a potential candidate for batteries that can work effectively under high power.

  3. Development of ruthenium dioxide electrodes for pyroelectric devices based on lithium tantalate thin films

    Energy Technology Data Exchange (ETDEWEB)

    Nougaret, Laurianne [Centre d' Electronique et de Micro-optoelectronique de Montpellier, Unite mixte de Recherche du CNRS no 5507, Universite Montpellier II, Place E. Bataillon, 34095 Montpellier cedex 05 (France)]. E-mail: laurianne.nougaret@univ-montp2.fr; Combette, Philippe [Centre d' Electronique et de Micro-optoelectronique de Montpellier, Unite mixte de Recherche du CNRS no 5507, Universite Montpellier II, Place E. Bataillon, 34095 Montpellier cedex 05 (France)]. E-mail: philippe.combette@univ-montp2.fr; Arinero, Richard [Centre d' Electronique et de Micro-optoelectronique de Montpellier, Unite mixte de Recherche du CNRS no 5507, Universite Montpellier II, Place E. Bataillon, 34095 Montpellier cedex 05 (France)]. E-mail: richard.arinero@univ-montp2.fr; Podlecki, Jean [Centre d' Electronique et de Micro-optoelectronique de Montpellier, Unite mixte de Recherche du CNRS no 5507, Universite Montpellier II, Place E. Bataillon, 34095 Montpellier cedex 05 (France)]. E-mail: jean.podlecki@univ-montp2.fr; Pascal-Delannoy, Frederique [Centre d' Electronique et de Micro-optoelectronique de Montpellier, Unite mixte de Recherche du CNRS no 5507, Universite Montpellier II, Place E. Bataillon, 34095 Montpellier cedex 05 (France)]. E-mail: Frederique.delannoy@univ-montp2.fr

    2007-02-26

    The aim of this paper is the study of ruthenium dioxide (RuO{sub 2}) films, grown on low-stress silicon nitride on silicon (SiN {sub x}/Si), in order to develop thermal micro-sensors based on pyroelectric effect. The active part of these micro-sensors is constituted by a new arrangement : lithium tantalate (LiTaO{sub 3})/RuO{sub 2}/SiN{sub x}/Si. Radio-frequency (RF) sputtering is employed to deposit RuO{sub 2} on SiN {sub x}/Si substrate. Morphology, crystallinity and resistivity of RuO{sub 2} are studied as function of growth parameters. Next, RF magnetron sputtering was used to deposit LiTaO{sub 3} on this electrode. Morphology studies, pyroelectric effect and dielectric parameters obtained, indicate that RuO{sub 2} material is a suitable candidate as back electrode for LiTaO{sub 3} thin films.

  4. Liquid lithium applications for solving challenging fusion reactor issues and NSTX-U contributions

    Energy Technology Data Exchange (ETDEWEB)

    Ono, M., E-mail: mono@pppl.gov [Princeton Plasma Physics Laboratory, PO Box 451, Princeton, NJ 08543 (United States); Jaworski, M.A.; Kaita, R. [Princeton Plasma Physics Laboratory, PO Box 451, Princeton, NJ 08543 (United States); Hirooka, Y. [National Institute for Fusion Science, 322-6 Oroshi, Toki, Gifu 509-5292 (Japan); Gray, T.K. [Oak Ridge National Laboratory, PO Box 2008, Oak Ridge, TN 37831 (United States)

    2017-04-15

    Steady-state fusion reactor operation presents major divertor technology challenges, including high divertor heat flux both steady-state and transients. In addition, there are unresolved issues of long term dust accumulation and associated tritium inventory and safety concerns (Federici et al., 2001) . It has been suggested that radiative liquid lithium divertor concepts with a modest lithium-loop could provide a possible solution for these outstanding fusion reactor technology issues, while potentially improving reactor plasma performance (Ono et al., 2013, 2014) . The application of lithium (Li) in NSTX resulted in improved H-mode confinement, H-mode power threshold reduction, and reduction in the divertor peak heat flux while maintaining essentially Li-free core plasma operation even during H-modes. These promising results in NSTX and related modeling calculations motivated the radiative liquid lithium (LL) divertor (RLLD) concept (Ono et al., 2013) and its variant, the active liquid lithium divertor concept (ARLLD) (Ono et al., 2014) , taking advantage of the enhanced non-coronal Li radiation in relatively poorly confined divertor plasmas. It was estimated that only a few moles/s of lithium injection would be needed to significantly reduce the divertor heat flux in a tokamak fusion power plant. By operating at lower temperatures ≤450 °C than the first wall ∼600–700 °C, the LL-covered divertor chamber wall surfaces can serve as an effective particle pump, as impurities generally migrate toward lower temperature LL divertor surfaces. To maintain the LL purity, a closed LL loop system with a modest circulating capacity of ∼1 l/s (l/s) is envisioned to sustain the steady-state operation of a 1 GW-electric class fusion power plant. By running the Li loop continuously, it can carry the dust particles and impurities generated in the vacuum vessel to outside where the dust/impurities are removed by relatively simple filter and cold/hot trap systems. Using a

  5. Finite Element Analysis of Silicon Thin Films on Soft Substrates as Anodes for Lithium Ion Batteries

    Science.gov (United States)

    Shaffer, Joseph

    2011-12-01

    The wide-scale use of green technologies such as electric vehicles has been slowed due to insufficient means of storing enough portable energy. Therefore it is critical that efficient storage mediums be developed in order to transform abundant renewable energy into an on-demand source of power. Lithium (Li) ion batteries are seeing a stream of improvements as they are introduced into many consumer electronics, electric vehicles and aircraft, and medical devices. Li-ion batteries are well suited for portable applications because of their high energy-to-weight ratios, high energy densities, and reasonable life cycles. Current research into Li-ion batteries is focused on enhancing its energy density, and by changing the electrode materials, greater energy capacities can be realized. Silicon (Si) is a very attractive option because it has the highest known theoretical charge capacity. Current Si anodes, however, suffer from early capacity fading caused by pulverization from the stresses induced by large volumetric changes that occur during charging and discharging. An innovative system aimed at resolving this issue is being developed. This system incorporates a thin Si film bonded to an elastomeric substrate which is intended to provide the desired stress relief. Non-linear finite element simulations have shown that a significant amount of deformation can be accommodated until a critical threshold of Li concentration is reached; beyond which buckling is induced and a wavy structure appears. When compared to a similar system using rigid substrates where no buckling occurs, the stress is reduced by an order of magnitude, significantly prolonging the life of the Si anode. Thus the stress can be released at high Li-ion diffusion induced strains by buckling the Si thin film. Several aspects of this anode system have been analyzed including studying the effects of charge rate and thin film plasticity, and the results are compared with preliminary empirical measurements to

  6. Development towards cell-to-cell monolithic integration of a thin-film solar cell and lithium-ion accumulator

    Science.gov (United States)

    Agbo, Solomon N.; Merdzhanova, Tsvetelina; Yu, Shicheng; Tempel, Hermann; Kungl, Hans; Eichel, Rüdiger-A.; Rau, Uwe; Astakhov, Oleksandr

    2016-09-01

    This work focuses on the potentials of monolithic integrated thin-film silicon solar cell and lithium ion cell in a simple cell-to-cell integration without any control electronics as a compact power solution for portable electronic devices. To demonstrate this we used triple-junction thin-film silicon solar cell connected directly to a lithium ion battery cell to charge the battery and in turn discharge the battery through the solar cell. Our results show that with appropriate voltage matching the solar cell provides efficient charging for lab-scale lithium ion storage cell. Despite the absence of any control electronics the discharge rate of the Li-ion cell through the non-illuminated solar cell can be much lower than the charging rate when the current voltage (IV) characteristics of the solar cell is matched properly to the charge-discharge characteristics of the battery. This indicates good sustainability of the ultimately simple integrated device. At the maximum power point, solar energy-to-battery charging efficiency of 8.5% which is nearly the conversion efficiency of the solar cell was obtained indicating potential for loss-free operation of the photovoltaic (PV)-battery integration. For the rest of the charging points, an average of 8.0% charging efficiency was obtained.

  7. Nanostructure of mixtures of protic ionic liquids and lithium salts: effect of alkyl chain length.

    Science.gov (United States)

    Méndez-Morales, Trinidad; Carrete, Jesús; Rodríguez, Julio R; Cabeza, Óscar; Gallego, Luis J; Russina, Olga; Varela, Luis M

    2015-02-21

    The bulk structure of mixtures of two protic ionic liquids, propylammonium nitrate and butylammonium nitrate, with a salt with a common anion, is analyzed at room temperature by means of small angle X-ray scattering and classical molecular dynamics simulations. The study of several structural properties, such as density, radial distribution functions, spatial distribution functions, hydrogen bonds, coordination numbers and velocity autocorrelation functions, demonstrates that increasing the alkyl chain length of the alkylammonium cation results in more segregated, better defined polar and apolar domains, the latter having a larger size. This increase, ascribed to the erosion of the H-bond network in the ionic liquid polar regions as salt is added, is confirmed by means of small angle X-ray scattering measurements, which show a clear linear increase of the characteristic spatial sizes of the studied protic ionic liquids with salt concentration, similar to that previously reported for ethylammonium nitrate (J. Phys. Chem. B, 2014, 118, 761-770). In addition, larger ionic liquid cations lead to a lower degree of hydrogen bonding and to more sparsely packed three-dimensional structures, which are more easily perturbed by the addition of lithium salts.

  8. Stability of thin liquid films and sessile droplets under confinement.

    Science.gov (United States)

    Dörfler, Fabian; Rauscher, Markus; Dietrich, S

    2013-07-01

    The stability of nonvolatile thin liquid films and of sessile droplets is strongly affected by finite size effects. We analyze their stability within the framework of density functional theory using the sharp kink approximation, i.e., on the basis of an effective interface Hamiltonian. We show that finite size effects suppress spinodal dewetting of films because it is driven by a long-wavelength instability. Therefore nonvolatile films are stable if the substrate area is too small. Similarly, nonvolatile droplets connected to a wetting film become unstable if the substrate area is too large. This instability of a nonvolatile sessile droplet turns out to be equivalent to the instability of a volatile drop which can attain chemical equilibrium with its vapor.

  9. Evaluation of therapeutic pulmonary surfactants by thin liquid film methods.

    Science.gov (United States)

    Todorov, Roumen; Exerowa, Dotchi; Platikanov, Dimo; Bianco, Federico; Razzetti, Roberta

    2015-08-01

    An example of the application of the Black Foam Film (BFF) Method and the Wetting Film Method, using the Microinterferomertric and the Pressure Balance Techniques, for characterization interfacial properties of the animal derived therapeutic pulmonary surfactant preparations (TSP), is presented. BFF thickness, probability of black film formation, and disjoining pressure for foam films from TSP aqueous solutions are measured as well as the wetting properties of TSP solutions on solid surfaces with different hydrophobicity have been studied. Interfacial characteristics such as minimal surfactant concentration to obtain black film (critical concentration) and concentration at which a black film is 100% obtained (threshold concentration) are determined. An evaluation of the four widely used TSP – Curosurf, Infasurf, Survanta, and Alveofact – by these methods has been carried out. Thus the methods of the thin liquid films are useful tools for studying the interfacial properties of TSP solutions, as well as for their improvement.

  10. Ionic liquid electrodeposition of strain-released Germanium nanowires as stable anodes for lithium ion batteries.

    Science.gov (United States)

    Hao, Jian; Yang, Yu; Zhao, Jiupeng; Liu, Xusong; Endres, Frank; Chi, Caixia; Wang, Binsheng; Liu, Xiaoxu; Li, Yao

    2017-06-22

    With the growing demand for portable and wearable electronic devices, it is imperative to develop high performance Li-ion batteries with long life times. Germanium-based materials have recently demonstrated excellent lithium-ion storage ability and are being considered as the most promising candidates for the anodes of lithium-ion batteries. Nevertheless, the practical implementation of Ge-based materials to Li-ion batteries is greatly hampered by the poor cycling ability that resulted from the huge volume variation during lithiation/delithiation processes. Herein, we develop a simple and efficient method for the preparation of Ge nanowires without catalyst nanoparticles and templates, using ionic liquid electrodeposition with subsequent annealing treatment. The Ge nanowire anode shows improved electrochemical performance compared with the Ge dense film anode. A capacity of ∼1200 mA h g(-1) after 200 cycles at 0.1 C is obtained, with an initial coulombic efficiency of 81.3%. In addition, the Ge nanowire anode demonstrates superior rate capability with excellent capacity retention and stability (producing highly stable discharge capacities of about 620 mA h g(-1) at 5 C). The improved electrochemical performance is the result of the enhanced electron migration and electron transport paths of the nanowires, and sufficient elasticity to buffer the volume expansion. This approach encompasses a low energy processing method where all the material is electrochemically active and binder free. The improved cycling stability and rate performance characteristics make these anodes highly attractive for the most demanding lithium-ion applications.

  11. Proteins at fluid interfaces: adsorption layers and thin liquid films.

    Science.gov (United States)

    Yampolskaya, Galina; Platikanov, Dimo

    2006-12-21

    A review in which many original published results of the authors as well as many other papers are discussed. The structure and some properties of the globular proteins are shortly presented, special accent being put on the alpha-chymotrypsin (alpha-ChT), lysozyme (LZ), human serum albumin (HSA), and bovine serum albumin (BSA) which have been used in the experiments with thin liquid films. The behaviour of protein adsorption layers (PAL) is extensively discussed. The dynamics of PAL formation, including the kinetics of adsorption as well as the time evolution of the surface tension of protein aqueous solutions, are considered. A considerable place is devoted to the surface tension and adsorption isotherms of the globular protein solutions, the simulation of PAL by interacting hard spheres, the experimental surface tension isotherms of the above mentioned proteins, and the interfacial tension isotherms for the protein aqueous solution/oil interface. The rheological properties of PAL at fluid interfaces are shortly reviewed. After a brief information about the experimental methods for investigation of protein thin liquid (foam or emulsion) films, the properties of the protein black foam films are extensively discussed: the conditions for their formation, the influence of the electrolytes and pH on the film type and stability, the thermodynamic properties of the black foam films, the contact angles film/bulk and their dynamic hysteresis. The next center of attention concerns some properties of the protein emulsion films: the conditions for formation of emulsion black films, the formation and development of a dimpling in microscopic, circular films. The protein-phospholipid mixed foam films are also briefly considered.

  12. Thinning of reverse osmosis membranes by ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Meng, Hong, E-mail: menghong@mail.buct.edu.cn; Gong, Beibei; Geng, Tao; Li, Chunxi

    2014-02-15

    In this study, ionic liquids (ILs) were used to thin out the dense layer and, in turn, tune the surface properties and separation performance of commercial aromatic polyamide reverse osmosis membranes. It was observed that the structure of the ILs and dipping time had a strong impact on the dense layer thickness and morphology. This can be understood in terms of the dissolubility and interaction force between ILs and the organic membrane surface, such as hydrogen bonding and π–π interactions. Among the ILs synthesized, 1-butyl-3-methylimidazolium chloride ([BMIM]Cl) showed the most promising thinning effects. It was observed that the thickness of the dense layer on the surface decreased from 127 to 67 nm after dipping treatment with [BMIM]Cl for 24 h. The water flux was enhanced by 20% at the expense of a slight decline of salt rejection. AFM, contact angle and zeta potential analyses suggest that the surface hydrophilicity and electronegativity increased, while the roughness decreased, which improved the anti-fouling properties.

  13. Thinning of reverse osmosis membranes by ionic liquids

    Science.gov (United States)

    Meng, Hong; Gong, Beibei; Geng, Tao; Li, Chunxi

    2014-02-01

    In this study, ionic liquids (ILs) were used to thin out the dense layer and, in turn, tune the surface properties and separation performance of commercial aromatic polyamide reverse osmosis membranes. It was observed that the structure of the ILs and dipping time had a strong impact on the dense layer thickness and morphology. This can be understood in terms of the dissolubility and interaction force between ILs and the organic membrane surface, such as hydrogen bonding and π-π interactions. Among the ILs synthesized, 1-butyl-3-methylimidazolium chloride ([BMIM]Cl) showed the most promising thinning effects. It was observed that the thickness of the dense layer on the surface decreased from 127 to 67 nm after dipping treatment with [BMIM]Cl for 24 h. The water flux was enhanced by 20% at the expense of a slight decline of salt rejection. AFM, contact angle and zeta potential analyses suggest that the surface hydrophilicity and electronegativity increased, while the roughness decreased, which improved the anti-fouling properties.

  14. Allylic ionic liquid electrolyte-assisted electrochemical surface passivation of LiCoO2 for advanced, safe lithium-ion batteries

    Science.gov (United States)

    Mun, Junyoung; Yim, Taeeun; Park, Jang Hoon; Ryu, Ji Heon; Lee, Sang Young; Kim, Young Gyu; Oh, Seung M.

    2014-01-01

    Room-temperature ionic liquid (RTIL) electrolytes have attracted much attention for use in advanced, safe lithium-ion batteries (LIB) owing to their nonvolatility, high conductivity, and great thermal stability. However, LIBs containing RTIL-electrolytes exhibit poor cyclability because electrochemical side reactions cause problematic surface failures of the cathode. Here, we demonstrate that a thin, homogeneous surface film, which is electrochemically generated on LiCoO2 from an RTIL-electrolyte containing an unsaturated substituent on the cation (1-allyl-1-methylpiperidinium bis(trifluoromethanesulfonyl)imide, AMPip-TFSI), can avert undesired side reactions. The derived surface film comprised of a high amount of organic species from the RTIL cations homogenously covered LiCoO2 with a <25 nm layer and helped suppress unfavorable thermal reactions as well as electrochemical side reactions. The superior performance of the cell containing the AMPip-TFSI electrolyte was further elucidated by surface, electrochemical, and thermal analyses. PMID:25168309

  15. Laboratory experiments of uptake and release of hydrogen isotopes in liquid lithium

    Energy Technology Data Exchange (ETDEWEB)

    Oyarzabal, E., E-mail: eider.oyarzabal@externos.ciemat.es; Martin-Rojo, A.B.; Tabarés, F.L.

    2015-08-15

    Laboratory studies of hydrogen and deuterium retention/desorption and hydride formation in liquid lithium samples exposed to those gases at 200 °C and 400 °C are reported in the present work. Two distinct absorption phases with different kinetics are observed and discussed. The calculated absorption rate constants show a preferential absorption of D{sub 2} over H{sub 2} in clean lithium and a faster absorption of H{sub 2} for predeuterated samples. First dynamic experiments on Li samples preimplanted with H{sub 2} and D{sub 2} show no evidence of isotope exchange at least up to 500 °C. TDS of Li samples exposed to H/D and of Li/LiH powder mixtures present desorption peaks at ∼500 °C, well below the observed decomposition temperature for LiH powder and no precipitated LiH is detected after the complete evaporation of Li (∼700 °C). Also, preferential release of H{sub 2} retained in the solution with respect to the formation of LiH is deduced from the desorption spectra.

  16. Safety analysis of the US dual coolant liquid lead lithium ITER test blanket module

    Science.gov (United States)

    Merrill, Brad; Reyes, Susana; Sawan, Mohamed; Wong, Clement

    2007-07-01

    The US is proposing a prototype of a dual coolant liquid lead-lithium DEMO blanket concept for testing in the International Thermonuclear Experimental Reactor (ITER) as an ITER test blanket module (TBM). Because safety considerations are an integral part of the design process to ensure that this TBM does not adversely impact the safety of ITER, a safety assessment has been conducted for this TBM and its ancillary systems as requested by the ITER project. Four events were selected by the ITER international team (IT) to address specific reactor safety concerns, such as vaccum vessel (VV) pressurization, confinement building pressure build-up, TBM decay heat removal capability, tritium and activation products release from the TBM system and hydrogen and heat production from chemical reactions. This paper summarizes the results of this safety assessment conducted with the MELCOR computer code.

  17. An aprotic lithium/polyiodide semi-liquid battery with an ionic shield

    Science.gov (United States)

    Ren, Y. X.; Liu, M.; Zhao, T. S.; Zeng, L.; Wu, M. C.

    2017-02-01

    In this paper, we report a high-energy-density lithium/polyiodide (Li/PI) semi-liquid battery with soluble polyiodide in ether-based solvents as the catholyte. The challenge of shuttle effect is addressed by adopting a hybrid membrane coated with negatively charged sulfonate-ended perfluoroalkyl polymer, which allows for inhibition of polyiodide shuttles due to the electrostatic repulsion. The assembled Li/PI battery demonstrates a superior volumetric energy density (170.5 Wh L-1), a stable cycling performance (>100 cycles, averaged decay 84%, 100 cycles at 2 C), and a high coulombic efficiency (>95%, 100 cycles at 2 C). These high performances achieved suggest that the aprotic Li/polyiodide battery with a compact architecture has the potential for various energy storage applications.

  18. Metal-organic chemical vapour deposition of lithium manganese oxide thin films via single solid source precursor

    Directory of Open Access Journals (Sweden)

    Oyedotun K.O.

    2015-12-01

    Full Text Available Lithium manganese oxide thin films were deposited on sodalime glass substrates by metal organic chemical vapour deposition (MOCVD technique. The films were prepared by pyrolysis of lithium manganese acetylacetonate precursor at a temperature of 420 °C with a flow rate of 2.5 dm3/min for two-hour deposition period. Rutherford backscattering spectroscopy (RBS, UV-Vis spectrophotometry, X-ray diffraction (XRD spectroscopy, atomic force microscopy (AFM and van der Pauw four point probe method were used for characterizations of the film samples. RBS studies of the films revealed fair thickness of 1112.311 (1015 atoms/cm2 and effective stoichiometric relationship of Li0.47Mn0.27O0.26. The films exhibited relatively high transmission (50 % T in the visible and NIR range, with the bandgap energy of 2.55 eV. Broad and diffused X-ray diffraction patterns obtained showed that the film was amorphous in nature, while microstructural studies indicated dense and uniformly distributed layer across the substrate. Resistivity value of 4.9 Ω·cm was obtained for the thin film. Compared with Mn0.2O0.8 thin film, a significant lattice absorption edge shift was observed in the Li0.47Mn0.27O0.26 film.

  19. Lithium-Ion-Conducting Electrolytes: From an Ionic Liquid to the Polymer Membrane

    Science.gov (United States)

    Fernicola, A.; Weise, F. C.; Greenbaum, S. G.; Kagimoto, J.; Scrosati, B.; Soleto, A.

    2009-01-01

    This work concerns the design, the synthesis, and the characterization of the N-butyl-N-ethylpiperidinium N,N-bis(trifluoromethane)sulfonimide (PP24TFSI) ionic liquid (IL). To impart Li-ion transport, a suitable amount of lithium N,N-bis-(trifluoromethane)sulfonimide (LiTFSI) is added to the IL. The Li–IL mixture displays ionic conductivity values on the order of 10−4 S cm−1 and an electrochemical stability window in the range of 1.8–4.5 V vs Li+/Li. The voltammetric analysis demonstrates that the cathodic decomposition gives rise to a passivating layer on the surface of the working electrode, which kinetically extends the stability of the Li/IL interface as confirmed by electrochemical impedance spectroscopy measurements. The LiTFSI–PP24TFSI mixture is incorporated in a poly(vinylidene fluoride-co-hexafluoropropylene) matrix to form various electrolyte membranes with different LiTFSI–PP24TFSI contents. The ionic conductivity of all the membranes resembles that of the LiTFSI–IL mixture, suggesting an ionic transport mechanism similar to that of the liquid component. NMR measurements demonstrate a reduction in the mobility of all ions following the addition of LiTFSI to the PP24TFSI IL and when incorporating the mixture into the membrane. Finally, an unexpected but potentially significant enhancement in Li transference number is observed in passing from the liquid to the membrane electrolyte system. PMID:20354582

  20. Lithium-sulphur battery with activated carbon cloth-sulphur cathode and ionic liquid as electrolyte

    Science.gov (United States)

    Swiderska-Mocek, Agnieszka; Rudnicka, Ewelina

    2015-01-01

    In this study a binder-free activated carbon cloth-sulphur (ACC-S) composite cathode is presented. Such a cathode was obtained using the impregnating technique of microporous activated carbon cloth with elemental melted sulphur. The surface morphology of an activated carbon cloth-sulphur electrode was studied using a scanning electron microscope (SEM), which was equipped with an EDX spectroscopy attachment. Electrochemical properties of the ACC-S composite cathode was tested in an ionic liquid electrolyte consisting of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulphonyl)imide (EtMeImNTf2) and bis(trifluoromethanesulphonyl)imide (LiNTf2). The ACC-sulphur cathode working together with lithium anode was tested with the use of cyclic voltammetry (CV), galvanostatic charge/discharge cycles and electrochemical impedance spectroscopy (EIS). The capacity and cyclic stability of the ACC-S composite cathode were much better than those for the sulphur cathode (a mixture of sulphur from graphene nanoplatelets and carbon black) tested in the same ionic liquid electrolyte. The ACC-sulphur cathode showed good cyclability and coulombic efficiency (99%) with the ionic liquid electrolyte. The reversible capacity of the ACC-S|electrolyte|Li cell was ca. 830 mAh g-1 after 50 cycles.

  1. Ultrahigh-Performance Cu2ZnSnS4 Thin Film and Its Application in Microscale Thin-Film Lithium-Ion Battery: Comparison with SnO2.

    Science.gov (United States)

    Lin, Jie; Guo, Jianlai; Liu, Chang; Guo, Hang

    2016-12-21

    To develop a high-performance anode for thin-film lithium-ion batteries (TFBs, with a total thickness on the scale of micrometers), a Cu2ZnSnS4 (CZTS) thin film is fabricated by magnetron sputtering and exhibits an ultrahigh performance of 950 mAh g(-1) even after 500 cycles, which is the highest among the reported CZTS for lithium storage so far. The characterization and electrochemical tests reveal that the thin-film structure and additional reactions both contribute to the excellent properties. Furthermore, the microscale TFBs with effective footprints of 0.52 mm(2) utilizing the CZTS thin film as anode are manufactured by microfabrication techniques, showing superior capability than the analogous TFBs with the SnO2 thin film as anode. This work demonstrates the advantages of exploiting thin-film electrodes and novel materials into micropower sources by electronic manufacture methods.

  2. Conical surface structures on model thin-film electrodes and tape-cast electrode materials for lithium-ion batteries

    Science.gov (United States)

    Kohler, R.; Proell, J.; Bruns, M.; Ulrich, S.; Seifert, H. J.; Pfleging, W.

    2013-07-01

    Three-dimensional structures in cathode materials for lithium-ion batteries were investigated in this study. For this purpose, laser structuring of lithium cobalt oxide was investigated at first for a thin-film model system and in a second step for conventional tape-cast electrode materials. The model thin-film cathodes with a thickness of 3 μm were deposited using RF magnetron sputtering on stainless steel substrates. The films were structured via excimer laser radiation with a wavelength of 248 nm. By adjusting the laser fluence, self-organized conical microstructures were formed. Using conventional electrodes, tape-cast cathodes made of LiCoO2 with a film thickness of about 80 μm on aluminum substrates were studied. It was shown that self-organizing surface structures could be formed by adjustment of the laser parameters. To investigate the formation mechanisms of the conical topography, the element composition was studied by time-of-flight secondary ion mass spectrometry and X-ray photoelectron spectroscopy. Electrochemical cycling using a lithium anode and conventional electrolyte was applied to study the influence of the laser processing procedures on cell performance. For the model electrode system, a significantly higher discharge capacity of 80 mAh/g could be obtained after 110 cycles by laser structuring compared to 8 mAh/g of the unstructured thin film. On conventional tape-cast electrodes self-organized surface structures could also increase the cycling stability resulting in an 80 % increase in capacity after 110 cycles in comparison to the unstructured electrode.

  3. Lithium-antimony-lead liquid metal battery for grid-level energy storage.

    Science.gov (United States)

    Wang, Kangli; Jiang, Kai; Chung, Brice; Ouchi, Takanari; Burke, Paul J; Boysen, Dane A; Bradwell, David J; Kim, Hojong; Muecke, Ulrich; Sadoway, Donald R

    2014-10-16

    The ability to store energy on the electric grid would greatly improve its efficiency and reliability while enabling the integration of intermittent renewable energy technologies (such as wind and solar) into baseload supply. Batteries have long been considered strong candidate solutions owing to their small spatial footprint, mechanical simplicity and flexibility in siting. However, the barrier to widespread adoption of batteries is their high cost. Here we describe a lithium-antimony-lead liquid metal battery that potentially meets the performance specifications for stationary energy storage applications. This Li||Sb-Pb battery comprises a liquid lithium negative electrode, a molten salt electrolyte, and a liquid antimony-lead alloy positive electrode, which self-segregate by density into three distinct layers owing to the immiscibility of the contiguous salt and metal phases. The all-liquid construction confers the advantages of higher current density, longer cycle life and simpler manufacturing of large-scale storage systems (because no membranes or separators are involved) relative to those of conventional batteries. At charge-discharge current densities of 275 milliamperes per square centimetre, the cells cycled at 450 degrees Celsius with 98 per cent Coulombic efficiency and 73 per cent round-trip energy efficiency. To provide evidence of their high power capability, the cells were discharged and charged at current densities as high as 1,000 milliamperes per square centimetre. Measured capacity loss after operation for 1,800 hours (more than 450 charge-discharge cycles at 100 per cent depth of discharge) projects retention of over 85 per cent of initial capacity after ten years of daily cycling. Our results demonstrate that alloying a high-melting-point, high-voltage metal (antimony) with a low-melting-point, low-cost metal (lead) advantageously decreases the operating temperature while maintaining a high cell voltage. Apart from the fact that this

  4. Effects of carbon and nitrogen on the corrosion resistance of type 316 stainless steel to liquid lithium

    Energy Technology Data Exchange (ETDEWEB)

    Barker, M.G.; Frankham, S.A. (Nottingham Univ. (UK). Dept. of Chemistry)

    1982-06-01

    Type 316 stainless steel plates have been exposed at 600/sup 0/C to liquid lithium containing carbon and nitrogen at various chemical activities for periods of up to 672 h. The corrosion products Li/sub 9/CrN/sub 5/ and M/sub 23/C/sub 6/ have been identified on the plate surfaces and in the grain boundaries. Scanning electron microscopy has shown preferential nickel and chromium depletion at the steel surface in lithium with high nitrogen content. The diffusion coefficient of carbon in type 316 stainless steel from a lithium source was found to be 6.5 x 10/sup -15/ m/sup 2//s.

  5. Effect of lithium salts addition on the ionic liquid based extraction of essential oil from Farfarae Flos.

    Science.gov (United States)

    Li, Zhen-Yu; Zhang, Sha-Sha; Jie-Xing; Qin, Xue-Mei

    2015-01-01

    In this study, an ionic liquids (ILs) based extraction approach has been successfully applied to the extraction of essential oil from Farfarae Flos, and the effect of lithium chloride was also investigated. The results indicated that the oil yields can be increased by the ILs, and the extraction time can be reduced significantly (from 4h to 2h), compared with the conventional water distillation. The addition of lithium chloride showed different effect according to the structures of ILs, and the oil yields may be related with the structure of cation, while the chemical compositions of essential oil may be related with the anion. The reduction of extraction time and remarkable higher efficiency (5.41-62.17% improved) by combination of lithium salt and proper ILs supports the suitability of the proposed approach.

  6. Thin-film encapsulation of organic electronic devices based on vacuum evaporated lithium fluoride as protective buffer layer

    Science.gov (United States)

    Peng, Yingquan; Ding, Sihan; Wen, Zhanwei; Xu, Sunan; Lv, Wenli; Xu, Ziqiang; Yang, Yuhuan; Wang, Ying; Wei, Yi; Tang, Ying

    2017-03-01

    Encapsulation is indispensable for organic thin-film electronic devices to ensure reliable operation and long-term stability. For thin-film encapsulating organic electronic devices, insulating polymers and inorganic metal oxides thin films are widely used. However, spin-coating of insulating polymers directly on organic electronic devices may destroy or introduce unwanted impurities in the underlying organic active layers. And also, sputtering of inorganic metal oxides may damage the underlying organic semiconductors. Here, we demonstrated that by utilizing vacuum evaporated lithium fluoride (LiF) as protective buffer layer, spin-coated insulating polymer polyvinyl alcohol (PVA), and sputtered inorganic material Er2O3, can be successfully applied for thin film encapsulation of copper phthalocyanine (CuPc)-based organic diodes. By encapsulating with LiF/PVA/LiF trilayer and LiF/Er2O3 bilayer films, the device lifetime improvements of 10 and 15 times can be achieved. These methods should be applicable for thin-film encapsulation of all kinds of organic electronic devices. Moisture-induced hole trapping, and Al top electrode oxidation are suggest to be the origins of current decay for the LiF/PVA/LiF trilayer and LiF/Er2O3 bilayer films encapsulated devices, respectively.

  7. Effect of shear-thinning behaviour on liquid-liquid plug flow in microchannels

    Science.gov (United States)

    Roumpea, Evangelia; Chinaud, Maxime; Weheliye, Weheliye Hashi; Angeli, Panagiota; Kahouadji, Lyes; Matar, Omar K.

    2016-11-01

    The present work investigates the dynamics of plug formation of shear-thinning solutions in a 200 μm microchannel using a two-colour micro-PIV system. Measurements, including phase-averaged velocity fields, have been conducted both at the T-junction inlet and the main channel to enhance understanding of non-Newtonian liquid-liquid flows. Two aqueous glycerol solutions containing xanthan gum are used as the non-Newtonian fluids while 5 cSt silicone oil is the Newtonian phase. The current experimental results revealed a pronounced impact of the xanthan gum (shear-thinning behaviour) on the flow pattern transition boundaries, and enhance the fluid flowrates where plug flow occurred. The addition of polymer resulted also in different hydrodynamic characteristics such as a bullet-shaped plug and an increased film thickness between the plug and the wall. In the present work, the technique allows to capture the velocity field of both phases simultaneously. Experimental results are compared with the numerical simulations provided by the code BLUE. Project funded under the UK Engineering and Physical Sciences Research Council (EPSRC) Programme Grant MEMPHIS.

  8. Evaluation of 2 1/4 Cr-1 Mo steel for liquid-lithium containment. III. Effect of velocity and lead content. Unabridged final report

    Energy Technology Data Exchange (ETDEWEB)

    Wilkinson, B.D.; Edwards, G.R.

    1981-12-01

    The intergranular penetration of specially heat treated 2-1/4 Cr-1 Mo steel by lead-lithium liquids containing 0, 17.6, and 53 w/o lead has been investigated at temperatures ranging from 300 to 600/sup 0/C and for times to 1000 hours. Limited tests using a 99.3 w/o lead-lithium liquid were also conducted.

  9. A Randomized Study of Three Interventions for Aspiration of Thin Liquids in Patients with Dementia or Parkinson's Disease

    Science.gov (United States)

    Logemann, Jeri A.; Gensler, Gary; Robbins, JoAnne; Lindblad, Anne S.; Brandt, Diane; Hind, Jacqueline A.; Kosek, Steven; Dikeman, Karen; Kazandjian, Marta; Gramigna, Gary D.; Lundy, Donna; McGarvey-Toler, Susan; Miller Gardner, Patricia J.

    2008-01-01

    Purpose: This study was designed to identify which of 3 treatments for aspiration on thin liquids--chin-down posture, nectar-thickened liquids, or honey-thickened liquids--results in the most successful immediate elimination of aspiration on thin liquids during the videofluorographic swallow study in patients with dementia and/or Parkinson's…

  10. Failure Mechanism of Fast-Charged Lithium Metal Batteries in Liquid Electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Dongping; Shao, Yuyan; Lozano, Terence J.; Bennett, Wendy D.; Graff, Gordon L.; Polzin, Bryant; Zhang, Jiguang; Engelhard, Mark H.; Saenz, Natalio T.; Henderson, Wesley A.; Bhattacharya, Priyanka; Liu, Jun; Xiao, Jie

    2015-02-01

    In recent years, lithium anode has re-attracted broad interest because of the necessity of employing lithium metal in the next-generation battery technologies such as lithium sulfur (Li-S) and lithium oxygen (Li-O2) batteries. Fast capacity degradation and safety issue associated with rechargeable lithium metal batteries have been reported, although the fundamental understanding on the failure mechanism of lithium metal at high charge rate is still under debate due to the complicated interfacial chemistry between lithium metal and electrolyte. Herein, we demonstrate that, at high current density, the quick growth of porous solid electrolyte interphase towards bulk lithium, instead of towards the separator, dramatically builds up the cell impedance that directly leads to the cell failure. Understanding the lithium metal failure mechanism is very critical to gauge the various approaches used to address the stability and safety issues associated with lithium metal anode. Otherwise, all cells will fail quickly at high rates before the observation of any positive effects that might be brought from adopting the new strategies to protect lithium.

  11. Vapor-liquid equilibria of the water + 1,3-propanediol and water + 1,3-propanediol + lithium bromide systems

    Energy Technology Data Exchange (ETDEWEB)

    Mun, S.Y.; Lee, H.

    1999-12-01

    Vapor-liquid equilibrium data of the water + 1,3-propanediol and water + 1,3-propanediol + lithium bromide systems were measured at 60, 160, 300, and 760 mmHg at temperatures ranging from 315 to 488 K. The apparatus used in this work is a modified still especially designed for the measurement of low-pressure VLE, in which both liquid and vapor are continuously recirculated. For the analysis of salt-containing solutions, a method incorporating refractometry and gravimetry was used. From the experimental measurements, the effect of lithium bromide on the VLE behavior of water + 1,3-propanediol was investigated. The experimental data of the salt-free system were successfully correlated using the Wilson, NRTL, and UNIQUAC models. In addition, the extended UNIQUAC model of Sander et al. was applied to the VLE calculation of salt-containing mixtures.

  12. Mesoporous silica/ionic liquid quasi-solid-state electrolytes and their application in lithium metal batteries

    Science.gov (United States)

    Li, Xiaowei; Zhang, Zhengxi; Yin, Kun; Yang, Li; Tachibana, Kazuhiro; Hirano, Shin-ichi

    2015-03-01

    In this work, the ordered mesoporous silica, SBA-15, is chosen as the matrix for the first time to prepare quasi-solid-state electrolytes (QSSEs) with an ionic liquid, LiTFSI salt and PVdF-HFP. The as-obtained QSSEs are evaluated by electrochemical methods. Lithium metal batteries containing these QSSEs exhibit high discharge capacity and good cycle performance at room temperature, indicating successful battery operation.

  13. CRADA Final Report: Properties of Vacuum Deposited Thin Films of Lithium Phosphorous Oxynitride (Lipon) with an Expanded Composition Range

    Energy Technology Data Exchange (ETDEWEB)

    Dudney, N.J.

    2003-12-29

    Thin films of an amorphous, solid-state, lithium electrolyte, referred to as ''Lipon'', were first synthesized and characterized at ORNL in 1991. This material is typically prepared by magnetron sputtering in a nitrogen plasma, which allows nitrogen atoms to substitute for part of the oxygen ions of Li{sub 3}PO{sub 4}. Lipon is the key component in the successful fabrication of ORNL's rechargeable thin film microbatteries. Cymbet and several other US Companies have licensed this technology for commercialization. Optimizing the properties of the Lipon material, particularly the lithium ion conductivity, is extremely important, yet only a limited range of compositions had been explored prior to this program. The goal of this CRADA was to develop new methods to prepare Lipon over an extended composition range and to determine if the film properties might be significantly improved beyond those previously reported by incorporating a larger N component into the film. Cymbet and ORNL investigated different deposition processes for the Lipon thin films. Cymbet's advanced deposition process not only achieved a higher deposition rate, but also permitted independent control the O and N flux to the surface of the growing film. ORNL experimented with several modified sputtering techniques and found that by using sectored sputter targets, composed of Li{sub 3}PO{sub 4} and Li{sub 3}N ceramic disks, thin Lipon films could be produced over an expanded composition range. The resulting Lipon films were characterized by electrical impedance, infrared spectroscopy, and several complementary analytical techniques to determine the composition. When additional N plus Li are incorporated into the Lipon film, the lithium conductivity was generally degraded. However, the addition of N accompanied by a slight loss of Li gave an increase in the conductivity. Although the improvement in the conductivity was only very modest and was a disappointing conclusion of

  14. CaO insulator coatings on a vanadium-base alloy in liquid 2 at.% calcium-lithium

    Energy Technology Data Exchange (ETDEWEB)

    Park, J.H.; Kassner, T.F. [Argonne National Laboratory, IL (United States)

    1996-10-01

    The electrical resistance of CaO coatings produced on V-4%Cr-4%Ti and V-15%Cr-5%Ti by exposure of the alloy (round bottom samples 6-in. long by 0.25-in. dia.) to liquid lithium that contained 2 at.% dissolved calcium was measured as a function of time at temperatures between 300-464{degrees}C. The solute element, calcium in liquid lithium, reacted with the alloy substrate at these temperatures for 17 h to produce a calcium coating {approx}7-8 {mu}m thick. The calcium-coated vanadium alloy was oxidized to form a CaO coating. Resistance of the coating layer on V-15Cr-5Ti, measured in-situ in liquid lithium that contained 2 at.% calcium, was 1.0 x 10{sup 10} {Omega}-cm{sup 2} at 300{degrees}C and 400 h, and 0.9 x 10{sup 10} {Omega}-cm{sup 2} at 464{degrees}C and 300 h. Thermal cycling between 300 and 464{degrees}C changed the resistance of the coating layer, which followed insulator behavior. Examination of the specimen after cooling to room temperature revealed no cracks in the CaO coating. The coatings were evaluated by optical microscopy, scanning electron microscopy (SEM), electron dispersive spectroscopy (EDS), and X-ray analysis. Adhesion between CaO and vanadium alloys was enhanced as exposure time increased.

  15. Long-scale evolution of thin liquid films

    Science.gov (United States)

    Oron, Alexander; Davis, Stephen H.; Bankoff, S. George

    1997-07-01

    Macroscopic thin liquid films are entities that are important in biophysics, physics, and engineering, as well as in natural settings. They can be composed of common liquids such as water or oil, rheologically complex materials such as polymers solutions or melts, or complex mixtures of phases or components. When the films are subjected to the action of various mechanical, thermal, or structural factors, they display interesting dynamic phenomena such as wave propagation, wave steepening, and development of chaotic responses. Such films can display rupture phenomena creating holes, spreading of fronts, and the development of fingers. In this review a unified mathematical theory is presented that takes advantage of the disparity of the length scales and is based on the asymptotic procedure of reduction of the full set of governing equations and boundary conditions to a simplified, highly nonlinear, evolution equation or to a set of equations. As a result of this long-wave theory, a mathematical system is obtained that does not have the mathematical complexity of the original free-boundary problem but does preserve many of the important features of its physics. The basics of the long-wave theory are explained. If, in addition, the Reynolds number of the flow is not too large, the analogy with Reynolds's theory of lubrication can be drawn. A general nonlinear evolution equation or equations are then derived and various particular cases are considered. Each case contains a discussion of the linear stability properties of the base-state solutions and of the nonlinear spatiotemporal evolution of the interface (and other scalar variables, such as temperature or solute concentration). The cases reducing to a single highly nonlinear evolution equation are first examined. These include: (a) films with constant interfacial shear stress and constant surface tension, (b) films with constant surface tension and gravity only, (c) films with van der Waals (long-range molecular

  16. Ionic liquid gating of ultra-thin YBa2Cu3O7-x films

    Science.gov (United States)

    Fête, A.; Rossi, L.; Augieri, A.; Senatore, C.

    2016-11-01

    In this paper, we present a detailed investigation of the self-field transport properties of an ionic liquid gated ultra-thin YBa2Cu3O7-x (YBCO) film. From the high temperature dynamic of the resistivity (>220 K), different scenarios pertaining to the interaction between the liquid and the thin film are proposed. From the low temperature evolution of Jc and Tc, a comparison between the behavior of our system and the standard properties of YBCO is drawn.

  17. Three-dimensional nanoporous Fe₂O₃/Fe₃C-graphene heterogeneous thin films for lithium-ion batteries.

    Science.gov (United States)

    Yang, Yang; Fan, Xiujun; Casillas, Gilberto; Peng, Zhiwei; Ruan, Gedeng; Wang, Gunuk; Yacaman, Miguel Jose; Tour, James M

    2014-04-22

    Three-dimensional self-organized nanoporous thin films integrated into a heterogeneous Fe2O3/Fe3C-graphene structure were fabricated using chemical vapor deposition. Few-layer graphene coated on the nanoporous thin film was used as a conductive passivation layer, and Fe3C was introduced to improve capacity retention and stability of the nanoporous layer. A possible interfacial lithium storage effect was anticipated to provide additional charge storage in the electrode. These nanoporous layers, when used as an anode in lithium-ion batteries, deliver greatly enhanced cyclability and rate capacity compared with pristine Fe2O3: a specific capacity of 356 μAh cm(-2) μm(-1) (3560 mAh cm(-3) or ∼1118 mAh g(-1)) obtained at a discharge current density of 50 μA cm(-2) (∼0.17 C) with 88% retention after 100 cycles and 165 μAh cm(-2) μm(-1) (1650 mAh cm(-3) or ∼518 mAh g(-1)) obtained at a discharge current density of 1000 μA cm(-2) (∼6.6 C) for 1000 cycles were achieved. Meanwhile an energy density of 294 μWh cm(-2) μm(-1) (2.94 Wh cm(-3) or ∼924 Wh kg(-1)) and power density of 584 μW cm(-2) μm(-1) (5.84 W cm(-3) or ∼1834 W kg(-1)) were also obtained, which may make these thin film anodes promising as a power supply for micro- or even nanosized portable electronic devices.

  18. Space-charge at the lithium-lithium chloride interface

    Science.gov (United States)

    Jamnik, J.; Gaberscek, M.; Meden, A.; Pejovnik, S.

    1991-06-01

    The electrical properties of the passive layer formed on lithium as the product of the corrosion reaction in thionyl chloride are discussed. The passive layer is regarded as a thin layer of an ionic crystal placed between two party blocking electrodes (i.e., lithium and liquid electrolyte). After a short review of thermodynamic properties of the system, a model for description of the electric properties of the static space-charge regions is presented. On this basis, a comment on and partial reinterpretation of impedance measurements of the passive layer is given. The suggested approach leads to the conclusion that the quality of Li/SOCl2 batteries decisively depends on the properties of the lithium passive layer interface. Finally, experiments to confirm the model are suggested.

  19. Limiting current density in bis(trifluoromethylsulfonyl)amide-based ionic liquid for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Park, Jun-Woo; Yoshida, Kazuki; Tachikawa, Naoki; Dokko, Kaoru; Watanabe, Masayoshi [Department of Chemistry and Biotechnology, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama 240-8501 (Japan)

    2011-02-15

    The physicochemical and electrochemical properties of the binary ionic liquid (IL), lithium bis(trifluoromethylsulfonyl)amide (LiTFSA) dissolved in N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethylsulfonyl)amide (DEMETFSA), were investigated. The ionic conductivity of the binary IL decreased with an increase in LiTFSA concentration. The self-diffusion coefficients of Li{sup +}, DEME{sup +}, and TFSA{sup -} dissolved in the IL were measured by using the pulsed-field-gradient spin-echo (PGSE) NMR method. The self-diffusion coefficient of each ionic species was also found to decrease with increasing concentration of LiTFSA. The limiting current density in the IL electrolyte was evaluated by chronoamperometry using symmetric Li vertical stroke IL vertical stroke Li cell. The results suggest that the diffusion process of Li(I) in the IL dominates the limiting current density in the cell. The highest limiting current density is achieved at a concentration of 0.64 mol dm{sup -3} of LiTFSA. (author)

  20. Ether and siloxane functionalized ionic liquids and their mixtures as electrolyte for lithium-ion batteries.

    Science.gov (United States)

    Chavan, Santosh N; Tiwari, Aarti; Nagaiah, Tharamani C; Mandal, Debaprasad

    2016-06-28

    The present study deals with an investigation of two novel imidazolium ionic liquids bearing ether-ether (1O2O2-Im-2O1) or ether-siloxane (1O2O2-Im-1SiOSi) functionalities with TFSI anion and their mixtures with propylene carbonate as electrolytes in lithium-ion batteries. The electrochemical stability and conductivity of these novel ILs were analyzed by electrochemical studies, such as cyclic voltammetry, linear sweep voltammetry and impedance measurements. The applicability of these ILs as electrolytes in Li-ion batteries was studied in the presence of a high concentration of LiTFSI (1 mol kg(-1) electrolyte) and the ether-ether IL was shown to possess a high electrochemical stability window (ESW) of 5.9 V and good conductivity of 2.2 mS cm(-1). The electrochemical stability and conductivity were further complimented by self-diffusion of different ions using pulsed gradient spin-echo (PGSE) NMR, viscosity and thermal properties like TGA and DSC analysis. More importantly, we explored the effect of temperature on the electrochemical stability and conductivity of these ILs by electrochemical impedance spectroscopy.

  1. Synthesis of Mesoporous Lithium Titanate Thin Films and Monoliths as an Anode Material for High-Rate Lithium-Ion Batteries.

    Science.gov (United States)

    Balcı, Fadime Mert; Kudu, Ömer Ulaş; Yılmaz, Eda; Dag, Ömer

    2016-12-23

    Mesoporous Li4 Ti5 O12 (LTO) thin film is an important anode material for lithium-ion batteries (LIBs). Mesoporous films could be prepared by self-assembly processes. A molten-salt-assisted self-assembly (MASA) process is used to prepare mesoporous thin films of LTOs. Clear solutions of CTAB, P123, LiNO3 , HNO3 , and Ti(OC4 H9 )4 in ethanol form gel-like meso-ordered films upon either spin or spray coating. In the assembly process, the CTAB/P123 molar ratio of 14 is required to accommodate enough salt species in the mesophase, in which the Li(I) /P123 ratio can be varied between molar ratios of 28 and 72. Calcination of the meso-ordered films produces transparent mesoporous spinel LTO films that are abbreviated as Cxx-yyy-zzz or CAxx-yyy-zzz (C=calcined, CA=calcined-annealed, xx=Li(I) /P123 molar ratio, and yyy=calcination and zzz=annealing temperatures in Celsius) herein. All samples were characterized by using XRD, TEM, N2 -sorption, and Raman techniques and it was found that, at all compositions, the LTO spinel phase formed with or without an anatase phase as an impurity. Electrochemical characterization of the films shows excellent performance at different current rates. The CA40-350-450 sample performs best among all samples tested, yielding an average discharge capacity of (176±1) mA h g(-1) at C/2 and (139±4) mA h g(-1) at 50 C and keeping 92 % of its initial discharge capacity upon 50 cycles at C/2.

  2. Electrodeposited Structurally Stable V2O5 Inverse Opal Networks as High Performance Thin Film Lithium Batteries.

    Science.gov (United States)

    Armstrong, Eileen; McNulty, David; Geaney, Hugh; O'Dwyer, Colm

    2015-12-01

    High performance thin film lithium batteries using structurally stable electrodeposited V2O5 inverse opal (IO) networks as cathodes provide high capacity and outstanding cycling capability and also were demonstrated on transparent conducting oxide current collectors. The superior electrochemical performance of the inverse opal structures was evaluated through galvanostatic and potentiodynamic cycling, and the IO thin film battery offers increased capacity retention compared to micron-scale bulk particles from improved mechanical stability and electrical contact to stainless steel or transparent conducting current collectors from bottom-up electrodeposition growth. Li(+) is inserted into planar and IO structures at different potentials, and correlated to a preferential exposure of insertion sites of the IO network to the electrolyte. Additionally, potentiodynamic testing quantified the portion of the capacity stored as surface bound capacitive charge. Raman scattering and XRD characterization showed how the IO allows swelling into the pore volume rather than away from the current collector. V2O5 IO coin cells offer high initial capacities, but capacity fading can occur with limited electrolyte. Finally, we demonstrate that a V2O5 IO thin film battery prepared on a transparent conducting current collector with excess electrolyte exhibits high capacities (∼200 mAh g(-1)) and outstanding capacity retention and rate capability.

  3. Effects of lithium doping on microstructure, electrical properties, and chemical bonds of sol-gel derived NKN thin films

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Chun-Cheng [Department of Electrical Engineering, National Cheng Kung University, Tainan 701, Taiwan (China); Department of Mathematic and Physical Sciences, R.O.C. Air Force Academy, Kaohsiung 820, Taiwan (China); Chen, Chan-Ching; Weng, Chung-Ming [Department of Electrical Engineering, National Cheng Kung University, Tainan 701, Taiwan (China); Chu, Sheng-Yuan, E-mail: chusy@mail.ncku.edu.tw [Department of Electrical Engineering, National Cheng Kung University, Tainan 701, Taiwan (China); Center for Micro/Nano Science and Technology, National Cheng Kung University, Tainan 701, Taiwan (China); Hong, Cheng-Shong [Department of Electronic Engineering, National Kaohsiung Normal University, Kaohsiung 802, Taiwan (China); Tsai, Cheng-Che [Department of Digital Game and Animation Design, Tung-Fang Design University, Kaohsiung 829, Taiwan (China)

    2015-02-28

    Highly (100/110) oriented lead-free Li{sub x}(Na{sub 0.5}K{sub 0.5}){sub 1−x}NbO{sub 3} (LNKN, x = 0, 0.02, 0.04, and 0.06) thin films are fabricated on Pt/Ti/SiO{sub 2}/Si substrates via a sol-gel processing method. The lithium (Li) dopants modify the microstructure and chemical bonds of the LNKN films, and therefore improve their electrical properties. The optimal values of the remnant polarization (P{sub r} = 14.3 μC/cm{sup 2}), piezoelectric coefficient (d{sub 33} = 48.1 pm/V), and leakage current (<10{sup −5} A/cm{sup 2}) are obtained for a lithium addition of x = 0.04 (i.e., 4 at. %). The observation results suggest that the superior electrical properties are the result of an improved crystallization, a larger grain size, and a smoother surface morphology. It is shown that the ion transport mechanism is dominated by an Ohmic behavior under low electric fields and the Poole-Frenkel emission effect under high electric fields.

  4. High-power durability of LiCoO2 thin film electrode modified with amorphous lithium tungsten oxide

    Science.gov (United States)

    Hayashi, Tetsutaro; Matsuda, Yasutaka; Kuwata, Naoaki; Kawamura, Junichi

    2017-06-01

    To investigate electrochemical performances of an amorphous lithium tungsten oxide (LWO) layer, an amorphous LWO-modified LiCoO2 (LCO) thin film electrode is fabricated by pulsed laser deposition and is exposed under a humid environment. The amorphous LWO-modified LCO exhibits high capacity retention of 80% at a rapid charge-discharge rate of 20 C. Conversely, the bare LCO exhibits capacity retention of 0% at the rates of 20 C. Electrochemical impedance spectroscopy demonstrates that the LWO-modified LCO maintains a low interfacial resistance after the cycling test compared with the bare LCO. X-ray photoemission spectroscopy (XPS), scanning transmission microscopy (STEM), and electron energy loss spectroscopy (EELS) indicate the presence of Li2CO3 on the surface of the bare LCO electrode and a thick degraded surface layer of CoO structure on the surface of LCO primary particle after electrochemical tests. XPS, STEM, and EELS indicate the presence of low amounts of Li2CO3 on the surface of the LWO-modified LCO, the LCO layer remains in a normal state, and LWO layer maintains the amorphous LWO state after the tests. Thus, the amorphous LWO protective layer contributes to suppressing the degradation of LCO and maintaining an amorphous LWO state with a lithium ion conductor, resulting in high-power durability.

  5. Comparison of lithium and the eutectic lead lithium alloy, two candidate liquid metal breeder materials for self-cooled blankets

    Energy Technology Data Exchange (ETDEWEB)

    Malang, S. [Kernforschungszentrum Karlsruhe GmbH (Germany); Mattas, R. [Argonne National Lab., IL (United States)

    1994-06-01

    Liquid metals are attractive candidates for both near-term and long-term fusion applications. The subjects of this comparison are the differences between the two candidate liquid metal breeder materials Li and LiPb for use in breeding blankets in the areas of neutronics, magnetohydrodynamics, tritium control, compatibility with structural materials, heat extraction system, safety, and required R&D program. Both candidates appear to be promising for use in self-cooled breeding blankets which have inherent simplicity with the liquid metal serving as both breeders and coolant. The remaining feasibility question for both breeder materials is the electrical insulation between liquid metal and duct walls. Different ceramic coatings are required for the two breeders, and their crucial issues, namely self-healing of insulator cracks and radiation induced electrical degradation are not yet demonstrated. Each liquid metal breeder has advantages and concerns associated with it, and further development is needed to resolve these concerns.

  6. Second-harmonic generation in periodically-poled thin film lithium niobate wafer-bonded on silicon

    Science.gov (United States)

    Rao, Ashutosh; Malinowski, Marcin; Honardoost, Amirmahdi; Talukder, Javed Rouf; Rabiei, Payam; Delfyett, Peter; Fathpour, Sasan

    2016-12-01

    Second-order optical nonlinear effects (second-harmonic and sum-frequency generation) are demonstrated in the telecommunication band by periodic poling of thin films of lithium niobate wafer-bonded on silicon substrates and rib-loaded with silicon nitride channels to attain ridge waveguide with cross-sections of ~ 2 {\\mu}m2. The compactness of the waveguides results in efficient second-order nonlinear devices. A nonlinear conversion of 8% is obtained with a pulsed input in 4 mm long waveguides. The choice of silicon substrate makes the platform potentially compatible with silicon photonics, and therefore may pave the path towards on-chip nonlinear and quantum-optic applications.

  7. Second-harmonic generation in periodically-poled thin film lithium niobate wafer-bonded on silicon

    CERN Document Server

    Rao, Ashutosh; Honardoost, Amirmahdi; Talukder, Javed Rouf; Rabiei, Rayam; Delfyett, Peter; Fathpour, Sasan

    2016-01-01

    Second-order optical nonlinear effects (second-harmonic and sum-frequency generation) are demonstrated in the telecommunication band by periodic poling of thin films of lithium niobate wafer-bonded on silicon substrates and rib-loaded with silicon nitride channels to attain ridge waveguide with cross-sections of ~ 2 {\\mu}m2. The compactness of the waveguides results in efficient second-order nonlinear devices. A nonlinear conversion of 8% is obtained with a pulsed input in 4 mm long waveguides. The choice of silicon substrate makes the platform potentially compatible with silicon photonics, and therefore may pave the path towards on-chip nonlinear and quantum-optic applications.

  8. Effects of lithium doping on microstructure, electrical properties, and chemical bonds of sol-gel derived NKN thin films

    Science.gov (United States)

    Lin, Chun-Cheng; Chen, Chan-Ching; Weng, Chung-Ming; Chu, Sheng-Yuan; Hong, Cheng-Shong; Tsai, Cheng-Che

    2015-02-01

    Highly (100/110) oriented lead-free Lix(Na0.5K0.5)1-xNbO3 (LNKN, x = 0, 0.02, 0.04, and 0.06) thin films are fabricated on Pt/Ti/SiO2/Si substrates via a sol-gel processing method. The lithium (Li) dopants modify the microstructure and chemical bonds of the LNKN films, and therefore improve their electrical properties. The optimal values of the remnant polarization (Pr = 14.3 μC/cm2), piezoelectric coefficient (d33 = 48.1 pm/V), and leakage current (Poole-Frenkel emission effect under high electric fields.

  9. Small- and Large-scale Characterization and Mixing Properties in a Thermally Driven Thin Liquid Film

    CERN Document Server

    Winkler, Michael

    2015-01-01

    Thin liquid films are nanoscopic elements of foams, emulsions and suspensions, and form a paradigm for nanochannel transport that eventually test the limits of hydrodynamic descriptions. Here we use classical dynamical systems characteristics to study the complex interplay of thermal convection, interface and gravitational forces which yields turbulent mixing and transport: Lyapunov exponents and entropies. We induce a stable two eddy convection in an extremely thin liquid film by applying a temperature gradient. Experimentally, we determine the small-scale dynamics using the motion and deformation of spots of equal size/equal color, we dubbed that technique "color imaging velocimetry". The large-scale dynamics is captured by encoding the left/right motion of the liquid directed to the left or right of the separatrix between the two rolls. This way, we characterize chaos of course mixing in this peculiar fluid geometry of a thin, free-standing liquid film.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-05-13

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

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

    Science.gov (United States)

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

    2014-05-13

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

  12. Liquid phase epitaxial growth of heterostructured hierarchical MOF thin films

    KAUST Repository

    Chernikova, Valeriya

    2017-05-10

    Precise control of epitaxial growth of MOF-on-MOF thin films, for ordered hierarchical tbo-type structures is demonstrated. The heterostructured MOF thin film was fabricated by successful sequential deposition of layers from two different MOFs. The 2-periodic layers, edge-transitive 4,4-square lattices regarded as supermolecular building layers, were commendably cross-linked using a combination of inorganic/organic and organic pillars.

  13. Numerical Simulation of Vapor Bubble Growth and Heat Transfer in a Thin Liquid Film

    Institute of Scientific and Technical Information of China (English)

    TAO Yu-Jia; HUAI Xiu-Lan; LI Zhi-Gang

    2009-01-01

    A mathematical model is developed to investigate the dynamics of vapor bubble growth in a thin liquid film,movement of the interface between two fluids and the surface heat transfer characteristics. The model takes into account the effects of phase change between the vapor and liquid, gravity, surface tension and viscosity. The details of the multiphase flow and heat transfer are discussed for two cases: (1) when a water micro-droplet impacts a thin liquid fihn with a vapor bubble growing and (2) when the vapor bubble grows and merges with the vapor layer above the liquid film without the droplet impacting. The development trend of the interface between the vapor and liquid is coincident qualitatively with the available literature, mostly at the first stage. We also provide an important method to better understand the mechanism of nucleate spray cooling.

  14. Development and implementation of flowing liquid lithium limiter control system for EAST

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, XiaoLin [Institute of Plasma Physics, Chinese Academy of Sciences, Hefei 230031 (China); University of Science and Technology of China, Hefei 230031 (China); Chen, Yue [Institute of Plasma Physics, Chinese Academy of Sciences, Hefei 230031 (China); Hu, JianSheng, E-mail: hujs@ipp.ac.cn [Institute of Plasma Physics, Chinese Academy of Sciences, Hefei 230031 (China); Li, JianGang; Zuo, GuiZhong; Ren, Jun; Zhou, Yue; Li, ChangZheng; Sun, Zheng; Xu, Wei; Meng, XianCai; Huang, Ming; Zheng, XingWei; Yao, Xingjia [Institute of Plasma Physics, Chinese Academy of Sciences, Hefei 230031 (China)

    2016-11-15

    Highlights: • Development of a FLiLi remote control system for EAST. • Intelligent instruments are used to realize FLiLi remote control. • Good operating results of the control system were obtained in the EAST campaign. - Abstract: A control system of a flowing liquid lithium (FLiLi) limiter for the Experimental Advanced Superconducting Tokamak (EAST) was developed and implemented. The control system is not only able to control the direct current (DC) electromagnetic pump and heating power but can also set scanning parameters, receive the shot number, acquire the temperature, etc. The system consists of multifunctional LAN eXtensions for Instrumentation (LXI) instrument, temperature-acquisition module, programmable DC power supply, and programmable logic controller (PLC). The multi-range DC power supply is programmed to meet the operational requirements of the DC electromagnetic pump. The LXI instrument and temperature-acquisition module are used to obtain temperature data. The PLC is adopted to control the temperature of the FLiLi limiter. A safety interlock and protection function was developed for the FLiLi limiter control system. The software was designed by using LabVIEW to achieve data interaction between multiple protocols. The FLiLi limiter control system can acquire experimental data at a speed of 100 S/s and store it for later analysis. The control system was successfully applied to a FLiLi limiter to study the interaction between plasma and a fixed wall in the EAST campaign. This paper presents the framework, the implementation details, and results of the control system.

  15. Analysis of SEI formed with cyano-containing imidazolium-based ionic liquid electrolyte in lithium secondary batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Liwei; Yamaki, Jun-ichi [Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-Koen, Kasuga, Fukuoka 816-8580 (Japan); Egashira, Minato [Department of Applied Chemistry and Chemical Engineering, Faculty of Engineering, Yamaguchi University, 2-16-1, Yamaguchi 755-8611 (Japan)

    2007-12-06

    Two kinds of cyano-containing imidazolium-based ionic liquid, 1-cyanopropyl-3-methylimidazolium-bis(trifluoromethanesulfonyl)imide (CpMI-TFSI) and 1-cyanomethyl-3-methylimidazolium-bis(trifluoromethanesulfonyl)imide (CmMI-TFSI), each of which contained 20 wt% dissolved LiTFSI, were used as electrolytes for lithium secondary batteries. Compared with 1-ethyl-3-methylimidazolium-bis(trifluoromethane-sulfonyl)imide (EMI-TFSI) electrolyte, a reversible lithium deposition/dissolution on a stainless-steel working electrode was observed during CV measurements in these cyano-containing electrolytes, which indicated that a passivation layer (solid electrolyte interphase, SEI) was formed during potential scanning. The morphology of the working electrode with each electrolyte system was studied by SEM. Different dentrite forms were found on the electrodes with each electrolyte. The SEI that formed in CpMI-TFSI electrolyte showed the best passivating effect, while the deposited film formed in EMI-TFSI electrolyte showed no passivating effect. The chemical characteristics of the deposited films on the working electrodes were compared by XPS measurements. A component with a cyano group was found in SEIs in CpMI-TFSI and CmMI-TFSI electrolytes. The introduction of a cyano functional group suppressed the decomposition of electrolyte and improved the cathodic stability of the imidazolium-based ionic liquid. The reduction reaction route of imidazolium-based ionic liquid was considered to be different depending on whether or not the molecular structure contained a cyano functional group. (author)

  16. Lithium secondary batteries using an asymmetric sulfonium-based room temperature ionic liquid as a potential electrolyte

    Institute of Scientific and Technical Information of China (English)

    LUO ShiChun; ZHANG ZhengXi; YANG Li

    2008-01-01

    A new asymmetric sulfonium-based ionic liquid, 1-butyldimethylsulfonium bis(trifluoromethylsulfonyl) imide (S114TFSI), was developed as electrolyte material for lithium secondary battery. Its cathodic po-tential was a little more positive against the Li/Li+, so vinylene carbonate (VC) was added into the LiTFSI/S114TFSI ionic liquid electrolyte to ensure the formation of a solid electrolyte interface (SEI), which effectively prevented the decomposition of the electrolyte. The properties of the Li/LiMn2O4 cell containing S114TFSI-based electrolyte were studied and the cycle performances were compared to Electrochemical impedance spectroscopy (EIS) and X-ray diffraction (XRD) were conducted to analyze the mechanisms affecting the cell performances at different temperatures. The lithium secondary bat-tery system, using the above ionic liquid electrolyte material, shows good cycle performances and good safety at room temperature, and is worthwhile to further investigate so as to find out the potential application.

  17. Liquid-phase plasma synthesis of silicon quantum dots embedded in carbon matrix for lithium battery anodes

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Ying [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou (China); College of Chemistry and Chemical Engineering, Bohai University, Jinzhou 121000 (China); Yu, Hang; Li, Haitao; Ming, Hai; Pan, Keming; Huang, Hui [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou (China); Liu, Yang, E-mail: yangl@suda.edu.cn [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou (China); Kang, Zhenhui, E-mail: zhkang@suda.edu.cn [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou (China)

    2013-10-15

    Graphical abstract: - Highlights: • Silicon quantum dots embedded in carbon matrix (SiQDs/C) were fabricated. • SiQDs/C exhibits excellent battery performance as anode materials with high specific capacity. • The good performance was attributed to the marriage of small sized SiQDs and carbon. - Abstract: Silicon quantum dots embedded in carbon matrix (SiQDs/C) nanocomposites were prepared by a novel liquid-phase plasma assisted synthetic process. The SiQDs/C nanocomposites were demonstrated to show high specific capacity, good cycling life and high coulmbic efficiency as anode materials for lithium-ion battery.

  18. Self-assembled ordered structures in thin films of HAT5 discotic liquid crystal

    Directory of Open Access Journals (Sweden)

    Piero Morales

    2010-05-01

    Full Text Available Thin films of the discotic liquid crystal hexapentyloxytriphenylene (HAT5, prepared from solution via casting or spin-coating, were investigated by atomic force microscopy and polarizing optical microscopy, revealing large-scale ordered structures substantially different from those typically observed in standard samples of the same material. Thin and very long fibrils of planar-aligned liquid crystal were found, possibly formed as a result of an intermediate lyotropic nematic state arising during the solvent evaporation process. Moreover, in sufficiently thin films the crystallization seems to be suppressed, extending the uniform order of the liquid crystal phase down to room temperature. This should be compared to the bulk situation, where the same material crystallizes into a polymorphic structure at 68 °C.

  19. A Long-Life Lithium Ion Battery with Enhanced Electrode/Electrolyte Interface by Using an Ionic Liquid Solution.

    Science.gov (United States)

    Elia, Giuseppe Antonio; Ulissi, Ulderico; Mueller, Franziska; Reiter, Jakub; Tsiouvaras, Nikolaos; Sun, Yang-Kook; Scrosati, Bruno; Passerini, Stefano; Hassoun, Jusef

    2016-05-10

    In this paper, we report an advanced long-life lithium ion battery, employing a Pyr14 TFSI-LiTFSI non-flammable ionic liquid (IL) electrolyte, a nanostructured tin carbon (Sn-C) nanocomposite anode, and a layered LiNi1/3 Co1/3 Mn1/3 O2 (NMC) cathode. The IL-based electrolyte is characterized in terms of conductivity and viscosity at various temperatures, revealing a Vogel-Tammann-Fulcher (VTF) trend. Lithium half-cells employing the Sn-C anode and NMC cathode in the Pyr14 TFSI-LiTFSI electrolyte are investigated by galvanostatic cycling at various temperatures, demonstrating the full compatibility of the electrolyte with the selected electrode materials. The NMC and Sn-C electrodes are combined into a cathode-limited full cell, which is subjected to prolonged cycling at 40 °C, revealing a very stable capacity of about 140 mAh g(-1) and retention above 99 % over 400 cycles. The electrode/electrolyte interface is further characterized through a combination of electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) investigations upon cell cycling. The remarkable performances reported here definitively indicate that IL-based lithium ion cells are suitable batteries for application in electric vehicles.

  20. Visualization of Thin Liquid Crystal Bubbles in Microgravity

    Science.gov (United States)

    Park, C. S.; Clark, N. A.; Maclennan, J. E.; Glaser, M. A.; Tin, P.; Stannarius, R.; Hall, N.; Storck, J.; Sheehan, C.

    2015-01-01

    The Observation and Analysis of Smectic Islands in Space (OASIS) experiment exploits the unique characteristics of freely suspended liquid crystals in a microgravity environment to advance the understanding of fluid state physics.

  1. COMPENSATION EFFECT OF POLYIMIDE THIN FILMS ON NORMALLY WHITE TWISTED NEMATIC LIQUID CRYSTAL DISPLAYS

    Institute of Scientific and Technical Information of China (English)

    LI Baozhong; HE Tianbai; DING Mengxian

    1997-01-01

    The disadvantages of Normally White Twisted Nematic Liquid Crystal Display (NW-TN-LCD) were discussed. The reason that the negative birefringent polyimide thin films were used to compensate NW-TN-LCD to decrease off-axis leakage, improve contrast ratios and enlarge viewing angles' was explained in this paper. A certain polyimide thin film was taken as an example to show compensation effect on NW-TN-LCD.

  2. Influence of Polar Organic Solvents in an Ionic Liquid Containing Lithium Bis(fluorosulfonyl)amide: Effect on the Cation-Anion Interaction, Lithium Ion Battery Performance, and Solid Electrolyte Interphase.

    Science.gov (United States)

    Lahiri, Abhishek; Li, Guozhu; Olschewski, Mark; Endres, Frank

    2016-12-14

    Ionic liquid-organic solvent mixtures have recently been investigated as potential battery electrolytes. However, contradictory results with these mixtures have been shown for battery performance. In this manuscript, we studied the influence of the addition of polar organic solvents into the ionic liquid electrolyte 1 M lithium bis(fluorosulfonyl)amide (LiFSI)-1-butyl-1-methylpyrrolidinium bis(fluorosulfonyl)amide ([Py1,4]FSI) and tested it for lithium ion battery applications. From infrared and Raman spectroscopy, clear changes in the lithium solvation and cation-anion interactions in the ionic liquid were observed on addition of organic solvents. From the lithiation/delithiation studies on electrodeposited Ge, the storage capacity for the ionic liquid-highly polar organic solvent (acetonitrile) mixture was found to be the highest at low C-rates (0.425 C) compared to using an ionic liquid alone and ionic liquid-less polar solvent (dimethyl carbonate) mixtures. Furthermore, XPS and AFM were used to evaluate the solid electrolyte interphase (SEI) and to correlate its stability with Li storage capacity.

  3. Improved liquid-solid-gas interface deposition of nanoparticle thin films

    Institute of Scientific and Technical Information of China (English)

    Diao Jia-Jie; Chen Guang-De; Qiu Fu-Sheng; Yan Guo-Jun

    2004-01-01

    A liquid-solid-gas interface deposition method to prepare nanoparticle thin films is presented in this paper. The nanoparticles in the part of suspension located close to the solid-liquid-gas interface grow on the substrate under the influence of interface force when the partially immersed substrate moves relatively to the suspension. By using statistical theory of the Brownian motion, growth equations for mono-component and multi-component nanoparticle thin films are obtained and some parameters for deposition process are discussed.

  4. Rupture of thin liquid films induced by impinging air-jets.

    Science.gov (United States)

    Berendsen, Christian W J; Zeegers, Jos C H; Kruis, Geerit C F L; Riepen, Michel; Darhuber, Anton A

    2012-07-01

    Thin liquid films on partially wetting substrates are subjected to laminar axisymmetric air-jets impinging at normal incidence. We measured the time at which film rupture occurs and dewetting commences as a function of diameter and Reynolds number of the air-jet. We developed numerical models for the air flow as well as the height evolution of the thin liquid film. The experimental results were compared with numerical simulations based on the lubrication approximation and a phenomenological expression for the disjoining pressure. We achieved quantitative agreement for the rupture times. We found that the film thickness profiles were highly sensitive to the presence of minute quantities of surface-active contaminants.

  5. Synthesis and ionic liquid gating of hexagonal WO{sub 3} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Phillip M., E-mail: philwu@stanford.edu, E-mail: beasley@stanford.edu; Munakata, Ko; Hammond, R. H.; Geballe, T. H.; Beasley, M. R., E-mail: philwu@stanford.edu, E-mail: beasley@stanford.edu [Department of Applied Physics, Stanford University, Stanford, California 94305, USA and Geballe Laboratory for Advanced Materials, Stanford University, Stanford, California 94305 (United States); Ishii, Satoshi; Tanabe, Kenji; Tokiwa, Kazuyasu [Department of Applied Electronics, Tokyo University of Science, Katsushika-ku, Tokyo 125-8585 (Japan)

    2015-01-26

    Via thin film deposition techniques, the meta-stable in bulk crystal hexagonal phase of tungsten oxide (hex-WO{sub 3}) is stabilized as a thin film. The hex-WO{sub 3} structure is potentially promising for numerous applications and is related to the structure for superconducting compounds found in WO{sub 3}. Utilizing ionic liquid gating, carriers were electrostatically induced in the films and an insulator-to-metal transition is observed. These results show that ionic liquid gating is a viable technique to alter the electrical transport properties of WO{sub 3}.

  6. The Spite Lithium Plateau Ultra-Thin but Post-Primordial

    CERN Document Server

    Ryan, S G; Beers, T C; Ryan, Sean G.; Norris, John E.; Beers, Timothy C.

    1999-01-01

    We have studied 23 very metal-poor field turnoff stars, specifically chosen to enable a precise measurement of the dispersion in the lithium abundance of the Spite Li plateau. We concentrated on stars having a narrow range of effective temperature and very low metallicities ([Fe/H] < -2.5) to reduce the effects of systematic errors, and have made particular efforts to minimize random errors in equivalent width and effective temperature. A typical formal error for our abundances is 0.033 dex (1-sigma), which represents a factor of two improvement on most previous studies. Our observed spread about the Li Spite plateau is a mere 0.031 dex (1-sigma), hence we conclude the intrinsic spread is effectively zero at the very metal-poor halo turnoff. We recover a robust dependence of lithium abundance with metallicity, dA(Li)/d[Fe/H] = 0.118 +/- 0.023 dex per dex. Previous claims for a lack of dependence of A(Li) on [Fe/H] are shown to have arisen from the use of noisier estimates of effective temperatures and meta...

  7. Determination of ginsenoside compound K in human plasma by liquid chromatography–tandem mass spectrometry of lithium adducts

    Science.gov (United States)

    Chen, Yunhui; Lu, Youming; Yang, Yong; Chen, Xiaoyan; Zhu, Liang; Zhong, Dafang

    2015-01-01

    Ginsenoside compound K (GCK), the main metabolite of protopanaxadiol constituents of Panax ginseng, easily produces alkali metal adduct ions during mass spectrometry particularly with lithium. Accordingly, we have developed a rapid and sensitive liquid chromatography–tandem mass spectrometric method for analysis of GCK in human plasma based on formation of a lithium adduct. The analyte and paclitaxel (internal standard) were extracted from 50 µL human plasma using methyl tert-butyl ether. Chromatographic separation was performed on a Phenomenex Gemini C18 column (50 mm×2.0 mm; 5 μm) using stepwise gradient elution with acetonitrile–water and 0.2 mmol/L lithium carbonate at a flow rate of 0.5 mL/min. Detection was performed in the positive ion mode using multiple reaction monitoring of the transitions at m/z 629→449 for the GCK-lithium adduct and m/z 860→292 for the adduct of paclitaxel. The assay was linear in the concentration range 1.00–1000 ng/mL (r2>0.9988) with intra- and inter-day precision of ±8.4% and accuracy in the range of −4.8% to 6.5%. Recovery, stability and matrix effects were all satisfactory. The method was successfully applied to a pharmacokinetic study involving administration of a single GCK 50 mg tablet to healthy Chinese volunteers. PMID:26579476

  8. Electrolyte properties of 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids for lithium secondary batteries

    Energy Technology Data Exchange (ETDEWEB)

    Seki, Shiro; Kobayashi, Takeshi; Serizawa, Nobuyuki; Kobayashi, Yo; Takei, Katsuhito; Miyashiro, Hajime [Materials Science Research Laboratory, Central Research Institute of Electric Power Industry (CRIEPI), 2-11-1, Iwado-kita, Komae, Tokyo 201-8511 (Japan); Hayamizu, Kikuko; Tsuzuki, Seiji [National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Center 5, Tsukuba, Ibaraki 305-8565 (Japan); Mitsugi, Takushi; Umebayashi, Yasuhiro [Department of Chemistry, Faculty of Science, Kyushu University, Hakozaki, Higashi-ku, Fukuoka 812-8581 (Japan); Watanabe, Masayoshi [Department of Chemistry and Biotechnology, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, Kanagawa (Japan)

    2010-09-15

    The physicochemical and electrochemical properties of three 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids with various alkyl chain lengths were investigated. The temperature dependences of density, viscosity, and ionic conductivity were obtained by precise measurements. Electrolyte properties of these room-temperature ionic liquids were also examined from the viewpoint of their uses in lithium secondary batteries ([LiCoO{sub 2} positive electrode vertical stroke electrolyte vertical stroke lithium metal negative electrode]). It was found that the alkyl chain length affects the charge-discharge performances of cells. (author)

  9. Bendable and thin sulfide solid electrolyte film: a new electrolyte opportunity for free-standing and stackable high-energy all-solid-state lithium-ion batteries.

    Science.gov (United States)

    Nam, Young Jin; Cho, Sung-Ju; Oh, Dae Yang; Lim, Jun-Muk; Kim, Sung Youb; Song, Jun Ho; Lee, Young-Gi; Lee, Sang-Young; Jung, Yoon Seok

    2015-05-13

    Bulk-type all-solid-state lithium batteries (ASLBs) are considered a promising candidate to outperform the conventional lithium-ion batteries. Unfortunately, the current technology level of ASLBs is in a stage of infancy in terms of cell-based (not electrode-material-based) energy densities and scalable fabrication. Here, we report on the first ever bendable and thin sulfide solid electrolyte films reinforced with a mechanically compliant poly(paraphenylene terephthalamide) nonwoven (NW) scaffold, which enables the fabrication of free-standing and stackable ASLBs with high energy density and high rate capabilities. The ASLB, using a thin (∼70 μm) NW-reinforced SE film, exhibits a 3-fold increase of the cell-energy-density compared to that of a conventional cell without the NW scaffold.

  10. Solid-state lithium battery

    Science.gov (United States)

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

    2014-11-04

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

  11. A Thin Liquid Film and Its Effects in an Atomic Force Microscopy Measurement

    Institute of Scientific and Technical Information of China (English)

    LIN Jing; ZHENG Zhi-Jun; YU Ji-Lin; BAI Yi-Long

    2009-01-01

    Recently,it has been observed that a liquid film spreading on a sample surface will significantly distort atomic force microscopy (AFM) measurements.In order to elaborate on the effect,we establish an equation governing the deformation of liquid film under its interaction with the AFM tip and substrate.A key issue is the critical liquid bump height yoc,at which the liquid film jumps to contact the AFM tip.It is found that there are three distinct regimes in the variation of yoc with film thickness H,depending on Hamaker constants of tip,sample and liquid.Noticeably,there is a characteristic thickness H* physically defining what a thin fihn is;namely,once the film thickness H is the same order as H*,the effect of film thickness should be taken into account.The value of H* is dependent on Hamaker constants and liquid surface tension as well as tip radius.

  12. Homo-junction ferroelectric field-effect-transistor memory device using solution-processed lithium-doped zinc oxide thin films

    KAUST Repository

    Nayak, Pradipta K.

    2012-06-22

    High performance homo-junction field-effect transistor memory devices were prepared using solution processed transparent lithium-doped zinc oxide thin films for both the ferroelectric and semiconducting active layers. A highest field-effect mobility of 8.7 cm2/Vs was obtained along with an Ion/Ioff ratio of 106. The ferroelectric thin filmtransistors showed a low sub-threshold swing value of 0.19 V/dec and a significantly reduced device operating voltage (±4 V) compared to the reported hetero-junction ferroelectrictransistors, which is very promising for low-power non-volatile memory applications.

  13. Synthesis and Compatibility of Ionic Liquid Containing Rod-Coil Polyimide Gel Electrolytes with Lithium Metal Electrodes

    Science.gov (United States)

    Tigelaar, Dean M.; Palker, Allyson E.; Meador, Mary Ann B.; Bennett, William R.

    2008-01-01

    A highly cross-linked polyimide-polyethylene oxide copolymer has been synthesized that is capable of holding large volumes of liquid component, simultaneously maintaining good dimensional stability. An amine end capped oligomer was made that was imidized in solution, followed by reaction with a triisocyanate in the presence of desired additives at ambient temperature. Polymer films are able to hold over 4 times their weight in room temperature ionic liquid RTIL or carbonate solvent. Electrolytes were studied that contained varying amounts of RTIL, lithium trifluoromethanesulfonimide LiTFSi, and alumina nanoparticles. Electrochemical stability of these electrolytes with lithium metal electrodes was studied by galvanic cycling and impedance spectroscopy. Improved cycling stability and decreased interfacial resistance were observed when increasing amounts of RTIL and LiTFSi were added. The addition of small amounts of alumina further decreased interfacial resistance by nearly an order of magnitude. During the course of the study, cycling stability increased from less than 3 to greater than 1000 h at 60 C and 0.25 mA/cm2 current density.

  14. Synthesis and Compatibility of Ionic Liquid Containing Rod-Coil Polyimide Gel Electrolytes with Lithium Metal Electrodes

    Science.gov (United States)

    Tigelaar, Dean M.; Palker, Allyson E.; Meador, Mary Ann B.; Bennett, William R.

    2008-01-01

    A highly cross-linked polyimide-polyethylene oxide copolymer has been synthesized that is capable of holding large volumes of liquid component, simultaneously maintaining good dimensional stability. An amine end capped oligomer was made that was imidized in solution, followed by reaction with a triisocyanate in the presence of desired additives at ambient temperature. Polymer films are able to hold over 4 times their weight in room temperature ionic liquid RTIL or carbonate solvent. Electrolytes were studied that contained varying amounts of RTIL, lithium trifluoromethanesulfonimide LiTFSi, and alumina nanoparticles. Electrochemical stability of these electrolytes with lithium metal electrodes was studied by galvanic cycling and impedance spectroscopy. Improved cycling stability and decreased interfacial resistance were observed when increasing amounts of RTIL and LiTFSi were added. The addition of small amounts of alumina further decreased interfacial resistance by nearly an order of magnitude. During the course of the study, cycling stability increased from less than 3 to greater than 1000 h at 60 C and 0.25 mA/cm2 current density.

  15. Enhanced energy capacity of lithium-oxygen batteries with ionic liquid electrolytes by addition of ammonium ions

    Science.gov (United States)

    Matsuda, Shoichi; Uosaki, Kohei; Nakanishi, Shuji

    2017-07-01

    Lithium-oxygen (Li-O2) batteries with ionic liquid-based electrolytes have attracted much attention because of their superior battery performance and high safety. However, the practical energy capacities achieved to date are markedly lower than those of Li-ion batteries. A dominant factor that limits the energy capacities of Li-O2 batteries is the insulating characteristics and insolubility of lithium peroxide (Li2O2), which gradually accumulates on the positive electrode as a discharge product. Herein, we report that ammonium ions function as a promoter for the solution-route formation of Li2O2, which results in a significant improvement of the energy capacity of Li-O2 cells. Scanning electron microscopy analyses revealed that the structure of Li2O2 changed from spherical particles to toroidal particles with an increase in the ammonium ions concentration. Ionic additives that have been reported to function as promoters the solution-route formation of Li2O2 in ether-based electrolyte systems do not exhibit a promoting effect in ionic liquid-based electrolytes.

  16. Structural, morphological, optical and electrical properties of spray deposited lithium doped CdO thin films

    Energy Technology Data Exchange (ETDEWEB)

    Velusamy, P.; Babu, R. Ramesh, E-mail: rampap2k@yahoo.co.in [Crystal Growth and Thin Films Laboratory, Department of Physics, Bharathidasan University, Tiruchirappalli-620 024, Tamil Nadu (India); Ramamurthi, K. [Crystal Growth and Thin Films Laboratory, Department of Physics and Nanotechnology, Faculty of Engineering and Technology, SRM University, Kattankulathur – 603 203, Tamil Nadu (India)

    2016-05-23

    In the present work, CdO and Li doped CdO thin films were deposited on microscopic glass substrates at 300°C by a spray pyrolysis experimental setup. The deposited CdO and Li doped CdO thin films were subjected to XRD, SEM, UV-VIS spectroscopy and Hall measurement analyses. XRD studies revealed the polycrystalline nature of the deposited films and confirmed that the deposited CdO and Li doped CdO thin films belong to cubic crystal system. The Scanning electron microscopy analysis revealed the information on shape of CdO and Li doped CdO films. Electrical study reveals the n-type semiconducting nature of CdO and the optical band gap is varied between 2.38 and 2.44 eV, depending on the Li doping concentrations.

  17. Structural, morphological, optical and electrical properties of spray deposited lithium doped CdO thin films

    Science.gov (United States)

    Velusamy, P.; Babu, R. Ramesh; Ramamurthi, K.

    2016-05-01

    In the present work, CdO and Li doped CdO thin films were deposited on microscopic glass substrates at 300˚C by a spray pyrolysis experimental setup. The deposited CdO and Li doped CdO thin films were subjected to XRD, SEM, UV-VIS spectroscopy and Hall measurement analyses. XRD studies revealed the polycrystalline nature of the deposited films and confirmed that the deposited CdO and Li doped CdO thin films belong to cubic crystal system. The Scanning electron microscopy analysis revealed the information on shape of CdO and Li doped CdO films. Electrical study reveals the n-type semiconducting nature of CdO and the optical band gap is varied between 2.38 and 2.44 eV, depending on the Li doping concentrations.

  18. Low-temperature anodic bonding using thin films of lithium-niobate-phosphate glass

    Science.gov (United States)

    Woetzel, S.; Kessler, E.; Diegel, M.; Schultze, V.; Meyer, H.-G.

    2014-09-01

    This paper reports on the investigation of a low-temperature anodic bonding process with layers of a lithium-niobate-phosphate glass on chip level. The glass layers are deposited by means of rf sputtering. The applied glass is characterised by its high ion conductivity, enabling anodic bonding at room temperature. Results of the optimisation process concerning the intrinsic stress of the glass layers and the thermal exposure of the substrates through the deposition process are presented. The stoichiometry of the glass layers is verified through Rutherford backscattering spectroscopy (RBS). The bonding strength is measured by tensile tests. Microfabricated atomic vapour cells are used for hermeticity tests of the bonding by absorption measurements of the caesium D1 line.

  19. Failure Mechanism for Fast-Charged Lithium Metal Batteries with Liquid Electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Lv, DP; Shao, YY; Lozano, T; Bennett, WD; Graff, GL; Polzin, B; Zhang, JG; Engelhard, MH; Saenz, NT; Henderson, WA; Bhattacharya, P; Liu, J; Xiao, J

    2014-09-11

    In recent years, the Li metal anode has regained a position of paramount research interest because of the necessity for employing Li metal in next-generation battery technologies such as Li-S and Li-O-2. Severely limiting this utilization, however, are the rapid capacity degradation and safety issues associated with rechargeable Li metal anodes. A fundamental understanding of the failure mechanism of Li metal at high charge rates has remained elusive due to the complicated interfacial chemistry that occurs between Li metal and liquid electrolytes. Here, it is demonstrated that at high current density the quick formation of a highly resistive solid electrolyte interphase (SEI) entangled with Li metal, which grows towards the bulk Li, dramatically increases up the cell impedance and this is the actual origin of the onset of cell degradation and failure. This is instead of dendritic or mossy Li growing outwards from the metal surface towards/through the separator and/or the consumption of the Li and electrolyte through side reactions. Interphase, in this context, refers to a substantive layer rather than a thin interfacial layer. Discerning the mechanisms and consequences for this interphase formation is crucial for resolving the stability and safety issues associated with Li metal anodes.

  20. Microscopic thin film optical anisotropy imaging at the solid-liquid interface

    Science.gov (United States)

    Miranda, Adelaide; De Beule, Pieter A. A.

    2016-04-01

    Optical anisotropy of thin films has been widely investigated through ellipsometry, whereby typically an optical signal is averaged over a ˜1 cm2 elliptical area that extends with increasing angle-of-incidence (AOI). Here, we report on spectroscopic imaging ellipsometry at the solid-liquid interface applied to a supported lipid bilayer (SLB). We detail how a differential spectrally resolved ellipsometry measurement, between samples with and without optically anisotropic thin film on an absorbing substrate, can be applied to recover in and out of plane refractive indices of the thin film with known film thickness, hence determining the thin film optical anisotropy. We also present how optimal wavelength and AOI settings can be determined ensuring low parameter cross correlation between the refractive indices to be determined from a differential measurement in Δ ellipsometry angle. Furthermore, we detail a Monte Carlo type analysis that allows one to determine the minimal required optical ellipsometry resolution to recover a given thin film anisotropy. We conclude by presenting a new setup for a spectroscopic imaging ellipsometry based on fiber supercontinuum laser technology, multi-wavelength diode system, and an improved liquid cell design, delivering a 5 ×-10 × ellipsometric noise reduction over state-of-the-art. We attribute this improvement to increased ellipsometer illumination power and a reduced light path in liquid through the use of a water dipping objective.

  1. High contrast switching of transmission due to electrohydrodynamic effect in stacked thin systems of liquid crystals.

    Science.gov (United States)

    Serak, Svetlana V; Hrozhyk, Uladzimir; Hwang, Jeoungyeon; Tabiryan, Nelson V; Steeves, Diane; Kimball, Brian R

    2016-10-20

    We study the opportunity of using electrohydrodynamic instabilities in a nematic liquid crystal mixture with negative dielectric anisotropy for controlling laser beams. Switching between naturally transparent and diffuse light scattering states is achieved by application of low frequency, low amplitude voltages. The specifics of diffuse light scattering state depending on the orientation and thickness of the liquid crystal layer are revealed. The switching occurs on a milliseconds time scale. Combination of thin, flexible liquid crystal cells allows polarization independent, high contrast, fast switching in a broad band of visible wavelengths.

  2. Preliminary assessment of interactions between the FMIT deuteron beam and liquid-lithium target

    Energy Technology Data Exchange (ETDEWEB)

    Hassberger, J A

    1983-03-01

    Scoping calculations were performed to assess the limit of response of the FMIT lithium target to the deuteron-beam interactions. Results indicate that most response modes have acceptably minor impacts on the lithium-target behavior. Individual modes of response were studied separately to assess sensitivity of the target to various phenomena and to identify those needing detailed evaluation. A few responses are of sufficient magnitude to warrant further investigation. Potential for several different responses combining additively is identified as the major area requiring further consideration.

  3. Preconcentration in gas or liquid phases using adsorbent thin films

    Directory of Open Access Journals (Sweden)

    Antonio Pereira Nascimento Filho

    2006-03-01

    Full Text Available The possibility of preconcentration on microchannels for organic compounds in gas or liquid phases was evaluated. Microstructures with different geometries were mechanically machined using poly(methyl methacrylate - PMMA as substrates and some cavities were covered with cellulose. The surfaces of the microchannels were modified by plasma deposition of hydrophilic or hydrophobic films using 2-propanol and hexamethyldisilazane (HMDS, respectively. Double layers of HMDS + 2-propanol were also used. Adsorption characterization was made by Quartz Crystal Measurements (QCM technique using reactants in a large polarity range that showed the adsorption ability of the structures depends more on the films used than on the capillary phenomena. Cellulose modified by double layer film showed a high retention capacity for all gaseous compounds tested. However, structures without plasma deposition showed low retention capacity. Microchannels modified with double layers or 2-propanol plasma films showed higher retention than non-modified ones on gas or liquid phase.

  4. Enhanced drainage and thinning of liquid films between bubbles and solids that support surface waves

    Science.gov (United States)

    Horesh, Amihai; Morozov, Matvey; Manor, Ofer

    2017-05-01

    We study the thinning and drainage of the intermediate liquid film between a bubble and a solid surface at close proximity in the presence of a surface acoustic wave (SAW) in the solid. Specifically, we employ the diffraction of light to observe a long air bubble confined in a solid rectangular channel filled with silicone oil. This setup, constituting a two-dimensional physical model of thin film drainage, allows us to analyze the influence of a SAW on the rate of thinning of the micron-thick liquid film separating the bubble and the solid substrate. The viscous penetration of the SAW into the liquid imposes a convective drift of mass, redistributing the fluid in the film against capillary resistance and producing a net drift of liquid out of the film. The rate of drainage of liquid from the film increases by one to several orders of magnitude in comparison to the rate of drainage due to the Laplace pressure of the bubble alone. The experimental findings agree well with a newly developed theory describing the SAW-enhanced drainage as a competition between the capillary flow and SAW-induced streaming.

  5. Lithium ion diffusion measurements in high quality LiCoO{sub 2} thin film battery cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Bahn, C.S.; McGraw, J.M.; Perkins, J.D.; Parilla, P.A.; Ginley, D.S.

    2000-07-01

    Highly crystalline, textured thin films of LiCo{sub x}Al{sub 1{minus}x}O{sub 2} (x = 0, 0.5) have been grown by pulsed laser deposition. Films of both stoichiometries were dense and uniaxially textured with Li, Co (or Co,Al) layers parallel to the substrate. It was found that crystal quality depended strongly on oxygen partial pressure, substrate temperature, and substrate material. The deposition of LiCo{sub 0.5}Al{sub 0.5}O{sub 2} is also highly dependent upon laser fluence, requiring at least 12.8 J/cm{sup 2} for high quality films. Chemical diffusion measurements were performed over a wide range of lithium contents using the potentiostatic intermittent titration technique. Maximum and minimum effective {tilde D} for LiCoO{sub 2} were 4.0 x 10{sup {minus}11} and 1.2 x 10{sup {minus}12}/s, respectively, and for LiCo{sub 0.5}Al{sub 0.5}O{sub 2}, 2.2 x 10{sup {minus}12} and 8.0 x 10{sup {minus}17} cm{sup 2}/s, respectively.

  6. Study of the corrosion behaviors of 304 austenite stainless steel specimens exposed to static liquid lithium at 600 K

    Science.gov (United States)

    Meng, Xiancai; Zuo, Guizhong; Ren, Jun; Xu, Wei; Sun, Zhen; Huang, Ming; Hu, Wangyu; Hu, Jiansheng; Deng, Huiqiu

    2016-11-01

    Investigation of corrosion behavior of stainless steel served as one kind of structure materials exposed to liquid lithium (Li) is one of the keys to apply liquid Li as potential plasma facing materials (PFM) or blanket coolant in the fusion device. Corrosion experiments of 304 austenite stainless steel (304 SS) were carried out in static liquid Li at 600 K and up to1584 h at high vacuum with pressure less than 4 × 10-4 Pa. After exposure to liquid Li, it was found that the weight of 304 SS slightly decreased with weight loss rate of 5.7 × 10-4 g/m2/h and surface hardness increased by about 50 HV. Lots of spinel-like grains and holes were observed on the surface of specimens measured by SEM. By further EDS, XRD and metallographic analyzing, it was confirmed that the main compositions of spinel-like grains were M23C6 carbides, and 304 SS produced a non-uniform corrosion behavior by preferential grain boundary attack, possibly due to the easy formation of M23C6 carbides and/or formation of Li compound at grain boundaries.

  7. Water-free titania-bronze thin films with superfast lithium-ion transport.

    Science.gov (United States)

    Zhang, Kui; Katz, Michael B; Li, Baihai; Kim, Sung Joo; Du, Xianfeng; Hao, Xiaoguang; Jokisaari, Jacob R; Zhang, Shuyi; Graham, George W; Van der Ven, Anton; Bartlett, Bart M; Pan, Xiaoqing

    2014-11-19

    Using pulsed laser deposition, TiO2 (-) B and its recently discovered variant Ca:TiO2 (-) B (CaTi5O11) are synthesized as highly crystalline thin films for the first time by a completely water-free process. Significant enhancement in the Li-ion battery performance is achieved by manipulating the crystal orientation of the films, used as anodes, with a demonstration of extraordinary structural stability under extreme conditions.

  8. Effect of ion structure on conductivity in lithium-doped ionic liquid electrolytes: A molecular dynamics study

    Science.gov (United States)

    Liu, Hongjun; Maginn, Edward

    2013-09-01

    Molecular dynamics simulations were performed to examine the role cation and anion structure have on the performance of ionic liquid (IL) electrolytes for lithium conduction over the temperature range of 320-450 K. Two model ionic liquids were studied: 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide ([bmim][Tf2N]) and 1-butyl-4-methylpyridinium pyrrolide ([bmpyr][pyl]) doped with Li[Tf2N] and Li[pyl], respectively. The results have demonstrated that the Li+ doped IL containing the planar [bmpyr] cation paired with the planar [pyl] anion significantly outperformed the [bmim][Tf2N] IL. The different coordination of Li+ with the [Tf2N]- or [pyl]- anions produces a remarkable change in IL structure with a concomitant effect on the transport of all ions. For the doped [bmim][Tf2N], each Li+ is coordinated by four oxygen atoms from [Tf2N]- anions. Formation of a rigid structure between Li+ and [Tf2N]- induces a decrease in the mobility of all ions. In contrast, for the doped [bmpyr][pyl], each Li+ is coordinated by two nitrogen atoms from [pyl]- anions. The original alternating structure cation|anion|cation in the neat [bmpyr][pyl] is replaced by another alternating structure cation|anion|Li+|anion|cation in the doped [bmpyr][pyl]. Increases of Li+ mole fraction in doped [bmpyr][pyl] affects the dynamics to a much lesser extent compared with [bmim][Tf2N] and leads to reduced diffusivities of cations and anions, but little change in the dynamics of Li+. More importantly, the calculations predict that the Li+ ion conductivity of doped [bmpyr][pyl] is comparable to that observed in organic liquid electrolytes and is about an order of magnitude higher than that of doped [bmim][Tf2N]. Such Li+ conductivity improvement suggests that this and related ILs may be promising candidates for use as electrolytes in lithium ion batteries and capacitors.

  9. NMR Studies on Diffusion and Molecular Motions of Imidazolium Ionic Liquids doped by Lithium Salts Related to Ionic Conductivity and Computational Interaction Energy

    Institute of Scientific and Technical Information of China (English)

    Kikuko; Hayamizua; Seiji; Tsuzuki; Shiro; Seki

    2007-01-01

    1 Results Room-temperature Ionic liquids (RTILs) are special class of compounds, where a combination of cations and anions produces neutral, stable and viscous liquids with high ionic conductivity. Widely spread applications are proposed to use conductors, electrolytes, clean solvents and others. Especially, RTILs are expected to be safe electrolytes in the ion-lithium batteries. In this study, NMR methods are used to clarify the basic properties of the individual movements of the anions and cations of ...

  10. Sulfonic Acid- and Lithium Sulfonate-Grafted Poly(Vinylidene Fluoride) Electrospun Mats As Ionic Liquid Host for Electrochromic Device and Lithium-Ion Battery.

    Science.gov (United States)

    Zhou, Rui; Liu, Wanshuang; Leong, Yew Wei; Xu, Jianwei; Lu, Xuehong

    2015-08-05

    Electrospun polymer nanofibrous mats loaded with ionic liquids (ILs) are promising nonvolatile electrolytes with high ionic conductivity. The large cations of ILs are, however, difficult to diffuse into solid electrodes, making them unappealing for application in some electrochemical devices. To address this issue, a new strategy is used to introduce proton conduction into an IL-based electrolyte. Poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) copolymer is functionalized with sulfonic acid through covalent attachment of taurine. The sulfonic acid-grafted P(VDF-HFP) electrospun mats consist of interconnected nanofibers, leading to remarkable improvement in dimensional stability of the mats. IL-based polymer electrolytes are prepared by immersing the modified mats in 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM(+)BF4(-)). It is found that the SO3(-) groups can have Lewis acid-base interactions with the cations (BMIM(+)) of IL to promote the dissociation of ILs, and provide additional proton conduction, resulting in significantly improved ionic conductivity. Using this novel electrolyte, polyaniline-based electrochromic devices show higher transmittance contrast and faster switching behavior. Furthermore, the sulfonic acid-grafted P(VDF-HFP) electrospun mats can also be lithiated, giving additional lithium ion conduction for the IL-based electrolyte, with which Li/LiCoO2 batteries display enhanced C-rate performance.

  11. Low Temperature Coating of Anatase Thin Films on Silica Glass Fibers by Liquid Phase Deposition

    Institute of Scientific and Technical Information of China (English)

    LI Shun; LIU Jiachen; FENG Tiecheng

    2007-01-01

    Uniform crystalline TiO2 thin films were coated on silica glass fibers by liquid phase deposition from aqueous solution of ammonium hexafluorotitanate at low temperature. TiO2 thin films and nanopowders were prepared by adding H3BO3 into (NH4)2TiF6 solution supersaturated with anatase nano-crystalline TiO2 at 40 ℃. The effects of the deposition conditions on the surface morphology, section morphology, thickness of the deposited TiO2 thin films were investigated. The results indicate that the growth rate and particle size of the thin films were controlled by both the deposition conditions and the amount of anatase nano-crystalline TiO2.

  12. Atomic layer deposited tungsten nitride thin films as a new lithium-ion battery anode.

    Science.gov (United States)

    Nandi, Dip K; Sen, Uttam K; Sinha, Soumyadeep; Dhara, Arpan; Mitra, Sagar; Sarkar, Shaibal K

    2015-07-14

    This article demonstrates the atomic layer deposition (ALD) of tungsten nitride using tungsten hexacarbonyl [W(CO)6] and ammonia [NH3] and its use as a lithium-ion battery anode. In situ quartz crystal microbalance (QCM), ellipsometry and X-ray reflectivity (XRR) measurements are carried out to confirm the self-limiting behaviour of the deposition. A saturated growth rate of ca. 0.35 Å per ALD cycle is found within a narrow temperature window of 180-195 °C. In situ Fourier transform infrared (FTIR) vibrational spectroscopy is used to determine the reaction pathways of the surface bound species after each ALD half cycle. The elemental presence and chemical composition is determined by XPS. The as-deposited material is found to be amorphous and crystallized to h-W2N upon annealing at an elevated temperature under an ammonia atmosphere. The as-deposited materials are found to be n-type, conducting with an average carrier concentration of ca. 10(20) at room temperature. Electrochemical studies of the as-deposited films open up the possibility of this material to be used as an anode material in Li-ion batteries. The incorporation of MWCNTs as a scaffold layer further enhances the electrochemical storage capacity of the ALD grown tungsten nitride (WNx). Ex situ XRD analysis confirms the conversion based reaction mechanism of the as-grown material with Li under operation.

  13. Asymptotic heat transfer model in thin liquid films

    CERN Document Server

    Chhay, Marx; Gisclon, Marguerite; Ruyer-Quil, Christian

    2015-01-01

    In this article, we present a modelling of heat transfer occuring through a liquid film flowing down a vertical wall. This model is formally derived thanks to asymptotic developpment, by considering the physical ratio of typical length scales of the study. A new Nusselt thermal solution is proposed, taking into account the hydrodynamic free surface variations and the contributions of the higher order terms in the asymptotic model are numerically pointed out. The comparisons are provided against the resolution of the full Fourier equations in a steady state frame.

  14. Discerning the Impact of a Lithium Salt Additive in Thin-Film Light-Emitting Electrochemical Cells with Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Bastatas, Lyndon D; Lin, Kuo-Yao; Moore, Matthew D; Suhr, Kristin J; Bowler, Melanie H; Shen, Yulong; Holliday, Bradley J; Slinker, Jason D

    2016-09-20

    Light-emitting electrochemical cells (LEECs) from small molecules, such as iridium complexes, have great potential as low-cost emissive devices. In these devices, ions rearrange during operation to facilitate carrier injection, bringing about efficient operation from simple, single-layer devices. Prior work has shown that the luminance, efficiency, and responsiveness of iridium LEECs is greatly enhanced by the inclusion of small fractions of lithium salts, but much remains to be understood about the origin of this enhancement. Recent work with planar devices demonstrates that lithium additives in iridium LEECs enhance double-layer formation. However, the quantitative influence of lithium salts on the underlying physics of conventional thin-film, sandwich structure LEECs, which beneficially operate at low voltages and generate higher luminance, has yet to be clarified. Here, we use electrochemical impedance spectroscopy to discern the impact of the lithium salt concentration on double-layer formation within the device and draw correlations with performance metrics, such as current, luminance, and external quantum efficiency.

  15. Pulsed laser deposited Cr{sub 2}O{sub 3} nanostructured thin film on graphene as anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Khamlich, S., E-mail: skhamlich@gmail.com [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa); Nuru, Z.Y. [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa); Bello, A.; Fabiane, M.; Dangbegnon, J.K.; Manyala, N. [Department of Physics, SARChI Chair in Carbon Technology and Materials, Institute of Applied Materials, University of Pretoria, Pretoria (South Africa); Maaza, M. [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa)

    2015-07-15

    Graphical abstract: A different approach for the fabrication of an anode material system that comprises pulsed laser-deposited (PLD) Cr{sub 2}O{sub 3} grown on few layer graphene (FLG) by chemical vapor deposition (CVD) was used. The electrochemical performance of Cr{sub 2}O{sub 3} nanostructured thin film was improved by FLG, which make it a promising candidate for future lithium-ion batteries application. - Highlights: • Pulsed laser deposition technique was used to deposit Cr{sub 2}O{sub 3} on few-layer graphene (FLG). • FLG improved the electrochemical performance of Cr{sub 2}O{sub 3} nanostructured thin film. • Good stable cycle of Cr{sub 2}O{sub 3}/FLG/Ni electrode make it one of the promise anode materials for future lithium-ion batteries. - Abstract: Pulsed laser deposition technique was used to deposit Cr{sub 2}O{sub 3} nanostructured thin film on a chemical vapor deposited few-layer graphene (FLG) on nickel (Ni) substrate for application as anode material for lithium-ion batteries. The experimental results show that graphene can effectively enhance the electrochemical property of Cr{sub 2}O{sub 3}. For Cr{sub 2}O{sub 3} thin film deposited on Ni (Cr{sub 2}O{sub 3}/Ni), a discharge capacity of 747.8 mA h g{sup −1} can be delivered during the first lithiation process. After growing Cr{sub 2}O{sub 3} thin film on FLG/Ni, the initial discharge capacity of Cr{sub 2}O{sub 3}/FLG/Ni was improved to 1234.5 mA h g{sup −1}. The reversible lithium storage capacity of the as-grown material is 692.2 mA h g{sup −1} after 100 cycles, which is much higher than that of Cr{sub 2}O{sub 3}/Ni (111.3 mA h g{sup −1}). This study reveals the differences between the two material systems and emphasizes the role of the graphene layers in improving the electrochemical stability of the Cr{sub 2}O{sub 3} nanostructured thin film.

  16. Gravitational instability of thin gas layer between two thick liquid layers

    Science.gov (United States)

    Pimenova, A. V.; Goldobin, D. S.

    2016-12-01

    We consider the problem of gravitational instability (Rayleigh-Taylor instability) of a horizontal thin gas layer between two liquid half-spaces (or thick layers), where the light liquid overlies the heavy one. This study is motivated by the phenomenon of boiling at the surface of direct contact between two immiscible liquids, where the rate of the "break-away" of the vapor layer growing at the contact interface due to development of the Rayleigh-Taylor instability on the upper liquid-gas interface is of interest. The problem is solved analytically under the assumptions of inviscid liquids and viscous weightless vapor. These assumptions correspond well to the processes in real systems, e.g., they are relevant for the case of interfacial boiling in the system water- n-heptane. In order to verify the results, the limiting cases of infinitely thin and infinitely thick gas layers were considered, for which the results can be obviously deduced from the classical problem of the Rayleigh-Taylor instability. These limiting cases are completely identical to the well-studied cases of gravity waves at the liquidliquid and liquid-gas interfaces. When the horizontal extent of the system is long enough, the wavenumber of perturbations is not limited from below, and the system is always unstable. The wavelength of the most dangerous perturbations and the rate of their exponential growth are derived as a function of the layer thickness. The dependence of the exponential growth rate on the gas layer thickness is cubic.

  17. The design status of the liquid lithium target facility of IFMIF at the end of the engineering design activities

    Energy Technology Data Exchange (ETDEWEB)

    Nitti, F.S., E-mail: francesco.nitti@enea.it [IFMIF/EVEDA Project Team, Rokkasho Japan (Japan); Ibarra, A. [CIEMAT, Madrid (Spain); Ida, M. [IHI Corporation, Tokyo (Japan); Favuzza, P. [ENEA Research Center Firenze (Italy); Furukawa, T. [JAEA Research Center, Tokai-mura, Ibaraki (Japan); Groeschel, F. [KIT Research Center, Karlsruhe (Germany); Heidinger, R. [F4E Research Center, Garching (Germany); Kanemura, T. [JAEA Research Center, Tokai-mura, Ibaraki (Japan); Knaster, J. [IFMIF/EVEDA Project Team, Rokkasho Japan (Japan); Kondo, H. [JAEA Research Center, Tokai-mura, Ibaraki (Japan); Micchiche, G. [ENEA Research Center, Brasimone (Italy); Sugimoto, M. [JAEA Research Center, Rokkasho Japan (Japan); Wakai, E. [JAEA Research Center, Tokai-mura, Ibaraki (Japan)

    2015-11-15

    Highlights: • Results of validation and design activity for the Li loop facility of IFMIF. • Demonstration of Li target stability, with surface disturbance <1 mm. • Demonstration of start-up and shut down procedures of Li loop. • Complete design of the heat removal system and C and O purification system. • Conceptual design of N and H isotopes purification systems. - Abstract: The International Fusion Material Irradiation Facility (IFMIF) is an experimental facility conceived for qualifying and characterizing structural materials for nuclear fusion applications. The Engineering Validation and Engineering Design Activity (EVEDA) is a fundamental step towards the final design. It presented two mandates: the Engineering Validation Activities (EVA), still on-going, and the Engineering Design Activities (EDA) accomplished on schedule in June 2013. Five main facilities are identified in IFMIF, among which the Lithium Target Facility constituted a technological challenge overcome thanks to the success of the main validation challenges impacting the design. The design of the liquid Lithium Target Facility at the end of the EDA phase is here detailed.

  18. Novel choline-based ionic liquids as safe electrolytes for high-voltage lithium-ion batteries

    Science.gov (United States)

    Yong, Tianqiao; Zhang, Lingzhi; Wang, Jinglun; Mai, Yongjin; Yan, Xiaodan; Zhao, Xinyue

    2016-10-01

    Three choline-based ionic liquids functionalized with trimethylsilyl, allyl, and cynoethyl groups are synthesized in an inexpensive route as safe electrolytes for high-voltage lithium-ion batteries. The thermal stabilities, viscosities, conductivities, and electrochemical windows of these ILs are reported. Hybrid electrolytes were formulated by doping with 0.6 M LiPF6/0.4 M lithium oxalydifluoroborate (LiODFB) as salts and dimethyl carbonate (DMC) as co-solvent. By using 0.6 M LiPF6/0.4 M LiODFB trimethylsilylated choline-based IL (SN1IL-TFSI)/DMC as electrolyte, LiCoO2/graphite full cell showed excellent cycling performance with a capacity of 152 mAh g-1 and 99% capacity retention over 90 cycles at a cut-off voltage of 4.4 V. The propagation rate of SN1IL-TFSI)/DMC electrolyte is only one quarter of the commercial electrolyte (1 M LiPF6 EC/DEC/DMC, v/v/v = 1/1/1), suggesting a better safety feature.

  19. Optimized Setup for 2D Convection Experiments in Thin Liquid Films

    CERN Document Server

    Winkler, Michael

    2015-01-01

    We present a novel experimental setup to investigate two-dimensional thermal convection in a freestanding thin liquid film. We develop a setup for the reproducible generation of freestanding thin liquid films. Such films can be produced in a controlled way on the scale of 5 to 1000 nanometers. Our primary goal is to investigate the statistics of reversals in Rayleigh-B\\'enard convection with varying aspect ratio; here numerical works are quite expensive and 3D experiments prohibitively complicated and costly. However, as well questions regarding the physics of liquid films under controlled conditions can be investigated, like surface forces, or stability under varying thermodynamical parameters. The thin liquid film has a well-defined and -chosen chemistry in order to fit our particular requirements, it has a thickness to area ratio of approximately 10^8 and is supported by a frame which is adjustable in height and width to vary the aspect ratio from 0.16 to 10. The top and bottom frame elements can be set to...

  20. A liquid-like model for the morphology evolution of ion bombarded thin films

    Energy Technology Data Exchange (ETDEWEB)

    Repetto, L., E-mail: luca.repetto@unige.it [Department of Physics and Nanomed Labs, Università di Genova, Via Dodecaneso 33, 16146 Genova (Italy); Lo Savio, R. [Department of Physics and Nanomed Labs, Università di Genova, Via Dodecaneso 33, 16146 Genova (Italy); Šetina Batič, B. [Inštitut Za Kovinske Materiale in Tehnologije, Lepi pot 11, 1000 Ljubljana (Slovenia); Firpo, G.; Angeli, E.; Valbusa, U. [Department of Physics and Nanomed Labs, Università di Genova, Via Dodecaneso 33, 16146 Genova (Italy)

    2015-07-01

    Thin solid films exposed to ion irradiation exhibit a peculiar evolution that can differ substantially from what is observed for bulk samples. The phenomenology of the patterns that self-organize on the substrate is very rich, with morphologies that display several degrees of order upon the modification of initial film characteristics and irradiation parameters. This richness paves the way for the fabrication of novel functional surfaces, but it is also an indication of the complexity of the underlying driving mechanisms. A remarkable simplification for the comprehension of these phenomena can come from the noteworthy similarity of the obtained patterns with those showing up when liquids dewet from their substrates. Here, we analyze the possibility to apply a liquid-like model to explain the morphology evolution of ion bombarded thin films for the whole phenomenology showing up in experiments. In establishing this connection between liquids and ion bombarded thin films, we propose to use also for liquids the insight gained for our system with recent experiments that stress the importance of the substrate topography for the selection of the dewetting mechanism. If confirmed, this result would lead to a reconsideration of the importance of capillary waves in spinodal dewetting, and will help to understand the low reproducibility of the related experimental results.

  1. Rupture mechanism of liquid crystal thin films realized by large-scale molecular simulations

    Science.gov (United States)

    Nguyen, Trung Dac; Carrillo, Jan-Michael Y.; Matheson, Michael A.; Brown, W. Michael

    2014-02-01

    The ability of liquid crystal (LC) molecules to respond to changes in their environment makes them an interesting candidate for thin film applications, particularly in bio-sensing, bio-mimicking devices, and optics. Yet the understanding of the (in)stability of this family of thin films has been limited by the inherent challenges encountered by experiment and continuum models. Using unprecedented large-scale molecular dynamics (MD) simulations, we address the rupture origin of LC thin films wetting a solid substrate at length scales similar to those in experiment. Our simulations show the key signatures of spinodal instability in isotropic and nematic films on top of thermal nucleation, and importantly, for the first time, evidence of a common rupture mechanism independent of initial thickness and LC orientational ordering. We further demonstrate that the primary driving force for rupture is closely related to the tendency of the LC mesogens to recover their local environment in the bulk state. Our study not only provides new insights into the rupture mechanism of liquid crystal films, but also sets the stage for future investigations of thin film systems using peta-scale molecular dynamics simulations.The ability of liquid crystal (LC) molecules to respond to changes in their environment makes them an interesting candidate for thin film applications, particularly in bio-sensing, bio-mimicking devices, and optics. Yet the understanding of the (in)stability of this family of thin films has been limited by the inherent challenges encountered by experiment and continuum models. Using unprecedented large-scale molecular dynamics (MD) simulations, we address the rupture origin of LC thin films wetting a solid substrate at length scales similar to those in experiment. Our simulations show the key signatures of spinodal instability in isotropic and nematic films on top of thermal nucleation, and importantly, for the first time, evidence of a common rupture mechanism

  2. Electrochemical performance and kinetic behavior of lithium ion in Li{sub 4}Ti{sub 5}O{sub 12} thin film electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Jianqiu, E-mail: jqdeng2003@163.com [School of Material Science and Engineering, Guilin University of Electronic Technology, Guilin 541004 (China); Lu, Zhouguang; Chung, C.Y. [Department of Physics and Materials Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong SAR (China); Han, Xiaodong [Institute of Microstructure and Property of Advanced Materials, Beijing University of Technology, Beijing 100022 (China); Wang, Zhongmin; Zhou, Huaiying [School of Material Science and Engineering, Guilin University of Electronic Technology, Guilin 541004 (China)

    2014-09-30

    Highlights: • Li{sub 4}Ti{sub 5}O{sub 12} thin film electrodes show favorable specific capacities and cycle performance. • The chemical diffusion coefficients are in a range of 10{sup −15} to 10{sup −12} cm{sup 2} s{sup −1}. • The dependence of R{sub ct} on cell voltage is explained by two-phase transition. - Abstract: Li{sub 4}Ti{sub 5}O{sub 12} thin film electrodes are successfully deposited on Pt/Ti/SiO{sub 2}/Si substrates by pulsed laser deposition (PLD) technique. The microstructure and morphology of Li{sub 4}Ti{sub 5}O{sub 12} thin films are characterized by XRD and ESEM. The electrochemical properties of Li{sub 4}Ti{sub 5}O{sub 12} thin film electrodes are evaluated by galvanostatic cycling test. The kinetic behavior of lithium ions in Li{sub 4}Ti{sub 5}O{sub 12} thin film electrodes is also conducted using cyclic voltammetry (CV), galvanostatic intermittent titration technique (GITT), and electrochemical impedance spectroscopy (EIS). Li{sub 4}Ti{sub 5}O{sub 12} thin film electrodes show favorable specific capacities and cycle performance. The chemical diffusion coefficients are found to be in a range of 10{sup −15} to 10{sup −12} cm{sup 2} s{sup −1} determined by GITT method. The kinetic parameters obtained from impedance spectra as a function of the cell voltage are investigated in details. The decrease of the charge-transfer resistance (R{sub ct}) can be explained by the two-phase transition during lithium insertion into Li{sub 4}Ti{sub 5}O{sub 12}.

  3. High power accelerator-based boron neutron capture with a liquid lithium target and new applications to treatment of infectious diseases

    Energy Technology Data Exchange (ETDEWEB)

    Halfon, S. [Soreq NRC, Yavne 81800 (Israel); Racah Institute of Physics, Hebrew University, Jerusalem 91904 (Israel)], E-mail: halfon@phys.huji.ac.il; Paul, M. [Racah Institute of Physics, Hebrew University, Jerusalem 91904 (Israel); Steinberg, D. [Biofilm Laboratory, Institute of Dental Sciences, Faculty of Dentistry, Hebrew University-Hadassah (Israel); Nagler, A.; Arenshtam, A.; Kijel, D. [Soreq NRC, Yavne 81800 (Israel); Polacheck, I. [Clinical Microbiology and Infectious Diseases, Hadassah-Hebrew University Medical Center (Israel); Srebnik, M. [Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Hebrew University, Jerusalem 91120 (Israel)

    2009-07-15

    A new conceptual design for an accelerator-based boron neutron capture therapy (ABNCT) facility based on the high-current low-energy proton beam driven by the linear accelerator at SARAF (Soreq Applied Research Accelerator Facility) incident on a windowless forced-flow liquid-lithium target, is described. The liquid-lithium target, currently in construction at Soreq NRC, will produce a neutron field suitable for the BNCT treatment of deep-seated tumor tissues, through the reaction {sup 7}Li(p,n){sup 7}Be. The liquid-lithium target is designed to overcome the major problem of solid lithium targets, namely to sustain and dissipate the power deposited by the high-intensity proton beam. Together with diseases conventionally targeted by BNCT, we propose to study the application of our setup to a novel approach in treatment of diseases associated with bacterial infections and biofilms, e.g. inflammations on implants and prosthetic devices, cystic fibrosis, infectious kidney stones. Feasibility experiments evaluating the boron neutron capture effectiveness on bacteria annihilation are taking place at the Soreq nuclear reactor.

  4. High power accelerator-based boron neutron capture with a liquid lithium target and new applications to treatment of infectious diseases.

    Science.gov (United States)

    Halfon, S; Paul, M; Steinberg, D; Nagler, A; Arenshtam, A; Kijel, D; Polacheck, I; Srebnik, M

    2009-07-01

    A new conceptual design for an accelerator-based boron neutron capture therapy (ABNCT) facility based on the high-current low-energy proton beam driven by the linear accelerator at SARAF (Soreq Applied Research Accelerator Facility) incident on a windowless forced-flow liquid-lithium target, is described. The liquid-lithium target, currently in construction at Soreq NRC, will produce a neutron field suitable for the BNCT treatment of deep-seated tumor tissues, through the reaction (7)Li(p,n)(7)Be. The liquid-lithium target is designed to overcome the major problem of solid lithium targets, namely to sustain and dissipate the power deposited by the high-intensity proton beam. Together with diseases conventionally targeted by BNCT, we propose to study the application of our setup to a novel approach in treatment of diseases associated with bacterial infections and biofilms, e.g. inflammations on implants and prosthetic devices, cystic fibrosis, infectious kidney stones. Feasibility experiments evaluating the boron neutron capture effectiveness on bacteria annihilation are taking place at the Soreq nuclear reactor.

  5. Nano-Sponge Ionic Liquid-Polymer Composite Electrolytes for Solid-State Lithium Power Sources

    Science.gov (United States)

    2010-01-01

    Journal of Power Sources 195 (2010) 867–871 Contents lists available at ScienceDirect Journal of Power Sources journa l homepage: www.e lsev ier .com...locate / jpowsour Short communication Nano-sponge ionic liquid–polymer composite electrolytes for solid-state lithium power sources Kang-Shyang...As storage becomesmore important in alternative technologies, these systems are evolving the need for safe, compact, rechargeable power sources continues

  6. Lithium outdiffusion in LiTi2O4 thin films grown by pulsed laser deposition

    Science.gov (United States)

    Mesoraca, S.; Kleibeuker, J. E.; Prasad, B.; MacManus-Driscoll, J. L.; Blamire, M. G.

    2016-11-01

    We report surface chemical cation composition analysis of high quality superconducting LiTi2O4 thin films, grown epitaxially on MgAl2O4 (111) substrates by pulsed laser deposition. The superconducting transition temperature of the films was 13.8 K. Surface chemical composition is crucial for the formation of a good metal/insulator interface for integrating LiTi2O4 into full-oxide spin-filtering devices in order to minimize the formation of structural defects and increase the spin polarisation efficiency. In consideration of this, we report a detailed angle resolved x-ray photoelectron spectroscopy analysis. Results show Li segregation at the surface of LiTi2O4 films. We attribute this process due to outdiffusion of Li toward the outermost LiTi2O4 layers.

  7. Comparison of liquid-liquid extraction-thin layer chromatography with solid-phase extraction-high-performance thin layer chromatography in detection of urinary morphine.

    Science.gov (United States)

    Ahadi, Ali; Partoazar, Alireza; Abedi-Khorasgani, Mohammad-Hassan; Shetab-Boushehri, Seyed Vahid

    2011-09-01

    Liquid-liquid extraction-thin layer chromatography (LLE-TLC) has been a common and routine combined method for detection of drugs in biological materials. Solid-phase extraction (SPE) is gradually replacing the traditional LLE method. High performance thin layer chromatography (HPTLC) has several advantages over TLC. The present work studied the higher efficiency of a new SPE-HPTLC method over that of a routine LLE-TLC method, in extraction and detection of urinary morphine. Fifty-eight urine samples, primarily identified as morphine-positive samples by a strip test, were re-screened by LLE-TLC and SPE-HPTLC. The results of LLE-TLC and SPE-HPTLC were then compared with each other. The results showed that the SPE-HPTLC detected 74% of total samples as morphine-positive samples whereas the LLE-TLC detected 48% of the same samples. We further discussed the effect of codeine abuse on TLC analysis of urinary morphine. Regarding the importance of morphine detection in urine, the present combined SPE-HPTLC method is suggested as a replacement method for detection of urinary morphine by many reference laboratories.

  8. Preparation and Characterization of Silver Liquid Thin Films for Magnetic Fluid Deformable Mirror

    Directory of Open Access Journals (Sweden)

    Lianchao Zhang

    2015-01-01

    Full Text Available Silver liquid thin film, formed by silver nanoparticles stacking and spreading on the surface of the liquid, is one of the important parts of magnetic fluid deformable mirror. First, silver nanoparticles were prepared by liquid phase chemical reduction method using sodium citrate as reducing agent and stabilizer and silver nitrate as precursor. Characterization of silver nanoparticles was studied using X-ray diffractometer, UV-vis spectrophotometer, and transmission electron microscope (TEM. The results showed that silver nanoparticles are spherical and have a good monodispersity. Additionally, the effect of the reaction conditions on the particle size of silver is obvious. And then silver liquid thin films were prepared by oil-water two-phase interface technology using as-synthesized silver nanoparticles. Properties of the film were investigated using different technology. The results showed that the film has good reflectivity and the particle size has a great influence on the reflectivity of the films. SEM photos showed that the liquid film is composed of multilayer silver nanoparticles. In addition, stability of the film was studied. The results showed that after being stored for 8 days under natural conditions, the gloss and reflectivity of the film start to decrease.

  9. Surface patterns of laterally extended thin liquid films in three dimensions.

    Science.gov (United States)

    Bestehorn, M; Neuffer, K

    2001-07-23

    We examine the fully nonlinear behavior of a thin liquid film in three spatial dimension for a large lateral extension. A partial differential equation is used for the spatiotemporal evolution of the height of the film. To take intermolecular forces in the liquid into account, we concentrate on a recently formulated model of Pismen and Pomeau, who derived an expression for the disjoining pressure only from the wetting properties of the fluid. Finally, the motion of a falling film on an inclined plane is studied within this model.

  10. Nanoscale investigations on interchain organization in thin films of polymer-liquid crystal blend

    Science.gov (United States)

    Villeneuve-Faure, C.; Le Borgne, D.; Ventalon, V.; Seguy, I.; Moineau-Chane Ching, K. I.; Bedel-Pereira, E.

    2017-07-01

    Optimized nanomorphology in organic thin active layers is crucial for good performance in organic solar cells. However, the relation between morphology and electronic properties at nanoscale remains not completely understood. Here, we study the effect of film thickness and temperature annealing on the ordering of poly(3-hexylthiophene) chains when the polymer is blended with a columnar liquid crystalline molecule. Electronic absorption, atomic force microscopy measurements, and Raman spectroscopy show that morphology and chain ordering of the blend depend on the film thickness. We highlight the benefit of using a liquid crystal in organic blends, opening the way to use simple processing methods for the fabrication of organic electronic devices.

  11. Rare earth-doped alumina thin films deposited by liquid source CVD processes

    Energy Technology Data Exchange (ETDEWEB)

    Deschanvres, J.L.; Meffre, W.; Joubert, J.C.; Senateur, J.P. [Ecole Nat. Superieure de Phys. de Grenoble, St. Martin d`Heres (France). Lab. des Materiaux et du Genie Phys.; Robaut, F. [Consortium des Moyens Technologiques Communs, Institut National Polytechnique de Grenoble, BP 75, 38402 St Martin d`Heres (France); Broquin, J.E.; Rimet, R. [Laboratoire d`Electromagnetisme, Microondes et Optoelectronique, CNRS-Ecole Nationale Superieure d`Electronique et Radioelectricite de Grenoble, BP 257, 38016 Grenoble, Cedex (France)

    1998-07-24

    Two types of liquid-source CVD processes are proposed for the growth of rare earth-doped alumina thin films suitable as amplifying media for integrated optic applications. Amorphous, transparent, pure and erbium- or neodymium-doped alumina films were deposited between 573 and 833 K by atmospheric pressure aerosol CVD. The rare earth doping concentration increases by decreasing the deposition temperature. The refractive index of the alumina films increases as a function of the deposition temperature from 1.53 at 573 K to 1.61 at 813 K. Neodymium-doped films were also obtained at low pressure by liquid source injection CVD. (orig.) 7 refs.

  12. Anchoring Strength of Thin Aligned-Polymer Films Formed by Liquid Crystalline Monomer

    Science.gov (United States)

    Murashige, Takeshi; Fujikake, Hideo; Ikehata, Seiichiro; Sato, Fumio

    2003-04-01

    We have evaluated the polar anchoring strength of a thin molecule-aligned polymer film formed by a liquid crystalline monomer. The polymer film was obtained by photopolymerization of the monomer oriented by a rubbed polyimide alignment layer in a chamber filled with N2 gas. We fabricated a nematic liquid crystal cell using the thin aligned-polymer films as alignment layers, and then evaluated the anchoring strength of the polymer by measuring the optical retardation curve of the cell driven by voltages. The experimental result showed that the anchoring strength was one order of magnitude lower than that of a conventional rubbed polyimide alignment layer, and decreased with increasing the cure temperature of the monomer film.

  13. Marangoni effects on a thin liquid film coating a sphere with axial or radial thermal gradients

    Science.gov (United States)

    Kang, Di; Nadim, Ali; Chugunova, Marina

    2016-11-01

    We study the time evolution of a thin liquid film coating the outer surface of a sphere in the presence of gravity, surface tension and thermal gradients. We derive the fourth-order nonlinear partial differential equation that models the thin film dynamics, including Marangoni terms arising from the dependence of surface tension on temperature. We consider two different heating regimes with axial or radial thermal gradients. We analyze the stability of a uniform coating under small perturbations and carry out numerical simulations in COMSOL for a range of parameter values. In the case of an axial temperature gradient, we find steady states with either uniform film thickness, or with drops forming at the top or bottom of the sphere, depending on the total volume of liquid in the film, dictating whether gravity or Marangoni effects dominate. In the case of a radial temperature gradient, a stability analysis reveals the most unstable non-axisymmetric modes on an initially uniform coating film.

  14. Capillary-driven, spatially-directed liquid transport on and through thin porous substrates

    Science.gov (United States)

    Chatterjee, Souvick; Sinha Mahapatra, Pallab; Ibrahim, Ali; Ganguly, Ranjan; Megaridis, Constantine; Yu, Lisha; Dodge, Richard

    2016-11-01

    Thin porous substrates exhibit good wicking properties for liquid distribution. The low cost of such common substrates often makes them useful for point of care biomedical diagnostics. Isotropic and anisotropic liquid transport through porous media has been studied extensively in literature. Moreover, previous research has demonstrated spatially-directed liquid transport on textured surfaces featuring surface-tension confined track. Combining both these features, here we demonstrate and analyze capillary-driven, directional liquid transport both on the surface of, and through, a wettability-patterned, horizontal porous substrate. The vertical (through) penetration is governed by Darcy's law. The horizontal (on surface) transport is driven by the Laplace pressure gradient caused by the geometry of the meniscus on the wettability-confined track. The transport rate on the substrate is found to far exceed the liquid permeation rate through it. Consequently, the penetration resistance can be estimated using a quasi-static approach. Using a semi-analytical model, we analyze the effect of the liquid curvature on the penetration rate of a sessile drop placed on the substrate. The model accounts for the back pressure caused by the liquid on the opposing side. The transport model is validated against the experiments, and the geometry, wettability and substrate porosity parameters causing fastest transport are identified.

  15. Phase equilibria in stratified thin liquid films stabilized by colloidal particles

    OpenAIRE

    Blawzdziewicz, J.; Wajnryb, E.

    2005-01-01

    Phase equilibria between regions of different thickness in thin liquid films stabilized by colloidal particles are investigated using a quasi-two-dimensional thermodynamic formalism. Appropriate equilibrium conditions for the film tension, normal pressure, and chemical potential of the particles in the film are formulated, and it is shown that the relaxation of these parameters occurs consecutively on three distinct time scales. Film stratification is described quantitatively for a hard-spher...

  16. Effect of nanostructures and electrostatic interactions on disjoining pressure of ultra-thin liquid film

    Science.gov (United States)

    Hu, Han; Weinberger, Christopher; Sun, Ying

    2014-11-01

    Disjoining pressure, the excess pressure that stems from the long-range intermolecular interactions, plays a key role in the stability of thin films in applications such as lubrication, wetting, boiling, condensation and evaporation. In recent years, nanostructures have been introduced as a means to control the stability of thin films. However, the classic theory of disjoining pressure assumes atomically smooth surface and neglects the electrostatic interactions. In the present study, the effect of nanostructures and electrostatic interactions on disjoining pressure is examined with combined modeling and molecular dynamics simulations. A model of meniscus shape and disjoining pressure for a thin liquid film on a nanostructured surface is derived based on minimization of system free energy and Derjaguin approximation. The scaled healing length ξ / D (D the nanostructure depth) is used to characterize the competition between the liquid surface tension and solid-liquid intermolecular forces. The result shows disjoining pressure increases with D. The model prediction agrees well with molecular dynamics simulations for a water-gold system. The electrostatic interactions enhance the disjoining pressure effect but the strength of the electrostatic interactions becomes weaker as the aspect ratio of the nanostructures increases.

  17. Self-assembled thin film of imidazolium ionic liquid on a silicon surface: Low friction and remarkable wear-resistivity

    Energy Technology Data Exchange (ETDEWEB)

    Gusain, Rashi [CSIR-Indian Institute of Petroleum, Mohkampur, Dehardun 248005 (India); Academy of Scientific and Innovative Research, New Delhi 110025 (India); Kokufu, Sho [Department of Materials Science and Engineering, Kyoto University, Kyoto 606-8501 (Japan); Bakshi, Paramjeet S. [CSIR-Indian Institute of Petroleum, Mohkampur, Dehardun 248005 (India); Utsunomiya, Toru; Ichii, Takashi; Sugimura, Hiroyuki [Department of Materials Science and Engineering, Kyoto University, Kyoto 606-8501 (Japan); Khatri, Om P., E-mail: opkhatri@iip.res.in [CSIR-Indian Institute of Petroleum, Mohkampur, Dehardun 248005 (India); Academy of Scientific and Innovative Research, New Delhi 110025 (India)

    2016-02-28

    Graphical abstract: - Highlights: • Ionic liquid thin film is deposited on a silicon surface via covalent interaction. • Chemical and morphological features of ionic liquid thin film are probed by XPS and AFM. • Ionic liquid thin film exhibited low and steady friction along with remarkable wear-resistivity. - Abstract: Imidazolium-hexafluorophosphate (ImPF{sub 6}) ionic liquid thin film is prepared on a silicon surface using 3-chloropropyltrimethoxysilane as a bifunctional chemical linker. XPS result revealed the covalent grafting of ImPF{sub 6} thin film on a silicon surface. The atomic force microscopic images demonstrated that the ImPF{sub 6} thin film is composed of nanoscopic pads/clusters with height of 3–7 nm. Microtribological properties in terms of coefficient of friction and wear-resistivity are probed at the mean Hertzian contact pressure of 0.35–0.6 GPa under the rotational sliding contact. The ImPF{sub 6} thin film exhibited low and steady coefficient of friction (μ = 0.11) along with remarkable wear-resistivity to protect the underlying silicon substrate. The low shear strength of ImPF{sub 6} thin film, the covalent interaction between ImPF{sub 6} ionic liquid thin film and underlying silicon substrate, and its regular grafting collectively reduced the friction and improved the anti-wear property. The covalently grafted ionic liquid thin film further shows immense potential to expand the durability and lifetime of M/NEMS based devices with significant reduction of the friction.

  18. Liquid-Phase Deposition of CIS Thin Layers: Final Report, February 2003--July 2005

    Energy Technology Data Exchange (ETDEWEB)

    Ernst, F.; Pirouz, P.

    2006-02-01

    The goal of this project was to fabricate single-phase CIS (a-Cu-In-Se, stoichiometric composition: CuInSe2) thin films for photovoltaic applications from a liquid phase - a Cu-In-Se melt of appropriate composition. This approach of liquid-phase deposition (LPD) is based on the new phase diagram we have established for Cu-In-Se, the first complete equilibrium phase diagram of this system. The liquidus projection exhibits four composition fields in which the primary solid phase, i.e., the first solid material that forms on cooling down from an entirely liquid state, is a-CuInSe2. Remarkably, none of the four composition fields is anywhere near the stoichiometric composition (CuInSe2) of a-CuInSe2. The results demonstrate that the proposed technique is indeed capable of producing films with a particularly large grain size and a correspondingly low density of grain boundaries. To obtain films sufficiently thin for solar cell applications and with a sufficiently smooth surface, it is advantageous to employ a sliding boat mechanism. Future work on liquid-phase deposition of CIS should focus on the interaction between the melt and the substrate surface, the resulting CIS interfaces, the surface morphology of the LPD-grown films, and, of course, the electronic properties of the material.

  19. Stabilization of thin liquid films by repulsive van der waals force

    KAUST Repository

    Li, Erqiang

    2014-05-13

    Using high-speed video recording of bubble rise experiments, we study the stability of thin liquid films trapped between a rising bubble and a surfactant-free liquid-liquid meniscus interface. Using different combinations of nonpolar oils and water that are all immiscible, we investigate the extent to which film stability can be predicted by attractive and repulsive van der Waals (vdW) interactions that are indicated by the relative magnitude of the refractive indices of the liquid combinations, for example, water (refractive index, n = 1.33), perfluorohexane (n = 1.23), and tetradecane (n = 1.43). We show that, when the film-forming phase was oil (perfluorohexane or tetradecane), the stability of the film could always be predicted from the sign of the vdW interaction, with a repulsive vdW force resulting in a stable film and an attractive vdW force resulting in film rupture. However, if aqueous electrolyte is the film-forming bulk phase between the rising air bubble and the upper oil phase, the film always ruptured, even when a repulsive vdW interaction was predicted. We interpret these results as supporting the hypothesis that a short-ranged hydrophobic attraction determines the stability of the thin water film formed between an air phase and a nonpolar oil phase. © 2014 American Chemical Society.

  20. Stabilization of thin liquid films by repulsive van der Waals force.

    Science.gov (United States)

    Li, Er Qiang; Vakarelski, Ivan U; Chan, Derek Y C; Thoroddsen, Sigurdur T

    2014-05-13

    Using high-speed video recording of bubble rise experiments, we study the stability of thin liquid films trapped between a rising bubble and a surfactant-free liquid-liquid meniscus interface. Using different combinations of nonpolar oils and water that are all immiscible, we investigate the extent to which film stability can be predicted by attractive and repulsive van der Waals (vdW) interactions that are indicated by the relative magnitude of the refractive indices of the liquid combinations, for example, water (refractive index, n = 1.33), perfluorohexane (n = 1.23), and tetradecane (n = 1.43). We show that, when the film-forming phase was oil (perfluorohexane or tetradecane), the stability of the film could always be predicted from the sign of the vdW interaction, with a repulsive vdW force resulting in a stable film and an attractive vdW force resulting in film rupture. However, if aqueous electrolyte is the film-forming bulk phase between the rising air bubble and the upper oil phase, the film always ruptured, even when a repulsive vdW interaction was predicted. We interpret these results as supporting the hypothesis that a short-ranged hydrophobic attraction determines the stability of the thin water film formed between an air phase and a nonpolar oil phase.

  1. Liquid oxygen LOX compatibility evaluations of aluminum lithium (Al-Li) alloys: Investigation of the Alcoa 2090 and MMC weldalite 049 alloys

    Science.gov (United States)

    Diwan, Ravinder M.

    1989-01-01

    The behavior of liquid oxygen (LOX) compatibility of aluminum lithium (Al-Li) alloys is investigated. Alloy systems of Alcoa 2090, vintages 1 to 3, and of Martin Marietta Corporation (MMC) Weldalite 049 were evaluated for their behavior related to the LOX compatibility employing liquid oxygen impact test conditions under ambient pressures and up to 1000 psi. The developments of these aluminum lithium alloys are of critical and significant interest because of their lower densities and higher specific strengths and improved mechanical properties at cryogenic temperatures. Of the different LOX impact tests carried out at the Marshall Space Flight Center (MSFC), it is seen that in certain test conditions at higher pressures, not all Al-Li alloys are LOX compatible. In case of any reactivity, it appears that lithium makes the material more sensitive at grain boundaries due to microstructural inhomogeneities and associated precipitate free zones (PFZ). The objectives were to identify and rationalize the microstructural mechanisms that could be relaxed to LOX compatibility behavior of the alloy system in consideration. The LOX compatibility behavior of Al-Li 2090 and Weldalite 049 is analyzed in detail using microstructural characterization techniques with light optical metallography, scanning electron microscopy (SEM), electron microprobe analysis, and surface studies using secondary ion mass spectrometry (SIMS), electron spectroscopy in chemical analysis (ESCA) and Auger electron spectroscopy (AES). Differences in the behavior of these aluminum lithium alloys are assessed and related to their chemistry, heat treatment conditions, and microstructural effects.

  2. Large deformation of liquid capsules enclosed by thin shells immersed in the fluid

    Science.gov (United States)

    Le, Duc-Vinh; Tan, Zhijun

    2010-06-01

    The deformation of a liquid capsule enclosed by a thin shell in a simple shear flow is studied numerically using an implicit immersed boundary method. We present a thin-shell model for computing the forces acting on the shell middle surface during the deformation within the framework of the Kirchhoff-Love theory of thin shells. This thin-shell model takes full account of finite-deformation kinematics which allows thickness stretching as well as large deflections and bending strains. For hyperelastic materials, the plane-stress assumption is used to compute the hydrostatic pressure and the incompressibility condition yields the thickness strain component and the corresponding change in the thickness. The stresses developing over the cross-section of the shell are integrated over the thickness to yield the stress and moment resultants which are then used to compute the forces acting on the shell middle surface. The immersed boundary method is employed for calculating the hydrodynamics and fluid-structure interaction effects. The location of the thin shell is updated implicitly using the Newton-Krylov method. The present numerical technique has been validated by several examples including an inflation of a spherical shell and deformations of spherical and oblate spheroidal capsules in the shear flow.

  3. Droplet impact on a thin liquid film: anatomy of the splash

    CERN Document Server

    Josserand, Christophe; Zaleski, Stéphane

    2015-01-01

    We investigate the dynamics of drop impact on a thin liquid film at short times in order to identify the mechanisms of splashing formation. Using numerical simulations and scaling analysis, we show that the splashing formation depends both on the inertial dynamics of the liquid and the cushioning of the gas. Two asymptotic regimes are identified, characterized by a new dimensionless number $J$: when the gas cushioning is weak, the jet is formed after a sequence of bubbles are entrapped and the jet speed is mostly selected by the Reynolds number of the impact. On the other hand, when the air cushioning is important, the lubrication of the gas beneath the drop and the liquid film controls the dynamics, leading to a single bubble entrapment and a weaker jet velocity.

  4. Droplet impact on a thin liquid film: anatomy of the splash

    Science.gov (United States)

    Josserand, Christophe; Ray, Pascal; Zaleski, Stéphane

    2016-09-01

    We investigate the dynamics of drop impact on a thin liquid film at short times in order to identify the mechanisms of splashing formation. Using numerical simulations and scaling analysis, we show that the splashing formation depends both on the inertial dynamics of the liquid and the cushioning of the gas. Two asymptotic regimes are identified, characterized by a new dimensionless number $J$: when the gas cushioning is weak, the jet is formed after a sequence of bubbles are entrapped and the jet speed is mostly selected by the Reynolds number of the impact. On the other hand, when the air cushioning is important, the lubrication of the gas beneath the drop and the liquid film controls the dynamics, leading to a single bubble entrapment and a weaker jet velocity.

  5. Hard X-ray photoelectron spectroscopy of Li{sub x}Ni{sub 1−x}O epitaxial thin films with a high lithium content

    Energy Technology Data Exchange (ETDEWEB)

    Kumara, L. S. R., E-mail: KUMARA.Rosantha@nims.go.jp; Yang, Anli [Synchrotron X-ray Station at SPring-8, National Institute for Materials Science (NIMS), 1-1-1 Kouto, Sayo, Hyogo 679-5148 (Japan); Sakata, Osami, E-mail: SAKATA.Osami@nims.go.jp [Synchrotron X-ray Station at SPring-8, National Institute for Materials Science (NIMS), 1-1-1 Kouto, Sayo, Hyogo 679-5148 (Japan); Synchrotron X-ray Group, Quantum Beam Unit, NIMS, 1-1-1 Kouto, Sayo, Hyogo 679-5148 (Japan); Department of Innovative and Engineered Materials, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259-J3-16, Nagatsuta, Midori, Yokohama 226-8502 (Japan); Yamauchi, Ryosuke; Matsuda, Akifumi; Yoshimoto, Mamoru [Department of Innovative and Engineered Materials, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259-J3-16, Nagatsuta, Midori, Yokohama 226-8502 (Japan); Taguchi, Munetaka [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), Ikoma, Nara 630-0192 (Japan)

    2014-07-28

    The core-level and valence-band electronic structures of Li{sub x}Ni{sub 1−x}O epitaxial thin films with x = 0, 0.27, and 0.48 were studied by hard X-ray photoelectron spectroscopy. A double peak structure, consisting of a main peak and a shoulder peak, and a satellite structure were observed in the Ni 2p{sub 3/2} core-level spectra. The intensity ratio of the shoulder to main peak in this double peak structure increased with increasing lithium content in Li{sub x}Ni{sub 1−x}O. This lithium doping dependence of the Ni 2p{sub 3/2} core-level spectra was investigated using an extended cluster model, which included the Zhang–Rice (ZR) doublet bound states arising from a competition between O 2p – Ni 3d hybridization and the Ni on-site Coulomb interaction. The results indicated that the change in the intensity ratio in the main peak is because of a reduction in the ZR doublet bound states from lithium substitutions. This strongly suggests that holes compensating Li doping in Li{sub x}Ni{sub 1−x}O are of primarily ZR character.

  6. The liquid phase epitaxy method for the construction of oriented ZIF-8 thin films with controlled growth on functionalized surfaces

    KAUST Repository

    Shekhah, Osama

    2013-01-01

    Highly-oriented ZIF-8 thin films with controllable thickness were grown on an -OH-functionalized Au substrate using the liquid phase epitaxy method at room temperature, as evidenced by SEM and PXRD. The adsorption-desorption properties of the resulting ZIF-8 thin film were investigated for various VOCs using the QCM technique. © The Royal Society of Chemistry 2013.

  7. Electrochemical characterisation of a lithium-ion battery electrolyte based on mixtures of carbonates with a ferrocene-functionalised imidazolium electroactive ionic liquid.

    Science.gov (United States)

    Forgie, John C; El Khakani, Soumia; MacNeil, Dean D; Rochefort, Dominic

    2013-05-28

    Electrolytic solutions of lithium-ion batteries can be modified with additives to improve their stability and safety. Electroactive molecules can be used as such additives to act as an electron (redox) shuttle between the two electrodes to prevent overcharging. The electroactive ionic liquid, 1-ferrocenylmethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide (TFSI), was synthesised and its electrochemical properties were investigated when diluted with ethylene carbonate-diethyl carbonate solvent at various concentrations. Cyclic voltammetry data were gathered to determine the redox potential, diffusion coefficient and heterogeneous rate constants of the electroactive imidazolium TFSI ionic liquid in the carbonate solution. The properties of this molecule as an additive in lithium battery electrolytes were studied in standard coin cells with a metallic Li anode and a Li4Ti5O12 cathode.

  8. Structures and Electronic Properties of Lithium Chelate-Based Ionic Liquids.

    Science.gov (United States)

    Si, Dawei; Chen, Kexian; Yao, Jia; Li, Haoran

    2016-04-28

    The conformations, electronic properties, and interaction energies of four chelate-based ionic liquids [Li(EA)][Tf2N], [Li(HDA)][Tf2N], [Li(DEA)][Tf2N], and [Li(DOBA)][Tf2N] have been theoretically explored. The reliability of the located conformers has been confirmed via the comparison between the simulated and experimental infrared spectra. Our results show that the N-Li and O-Li coordinate bonds in cation are elongated as the numbers of coordinate heteroatoms of alkanolamine ligands to Li(+) increased. Also the binding energies between Li(+) and ligands are increased and the interaction energies between cations and Tf2N anion are decreased. The cation-anion interaction energies follow the order of [Li(DOBA)][Tf2N] ionic liquids. Interestingly, the strongest stabilization orbital interactions in these ionic liquids and their cations revealed by the natural bond orbital analysis lie in the interaction between the lone pair (LP) of the coordinate heteroatoms in ligands or anion as donors and the vacant valence shell nonbonding orbital (LP*) of Li(+) as acceptors, which are very different from that of conventional ionic liquids. Moreover, the charges transferred from cations to anion are quite similar, and the charge of Li(+) is proposed for possibly predicting the order of the interaction energies of ionic liquids in series. The present study allows for the deeper understanding the differences between chelate-based ionic liquids and conventional ionic liquids.

  9. Atomistic molecular point of view for liquid lead and lithium in Nuclear Fusion technology

    Energy Technology Data Exchange (ETDEWEB)

    Fraile, A. [Instituto de Fusión Nuclear, ETSI Industriales, Universidad Politécnica de Madrid, José Gutierrez Abascal, 2, 28006 Madrid (Spain); Cuesta-López, S., E-mail: scuesta@ubu.es [Universidad de Burgos, Parque Científico I-D-I, Plaza Misael Bañuelos s/n, 09001 Burgos (Spain); Iglesias, R. [Universidad de Oviedo, Departamento de Física, Calvo Sotelo s/n, 33007 Oviedo (Spain); Caro, A. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Perlado, J.M. [Instituto de Fusión Nuclear, ETSI Industriales, Universidad Politécnica de Madrid, José Gutierrez Abascal, 2, 28006 Madrid (Spain)

    2013-09-15

    Understanding the behavior and properties of liquid metals is a crucial milestone in different current Nuclear Technology developments. Extracting both structural and dynamical properties of liquid metals via Molecular Dynamics simulations, represents a strong pillar for multiscale modeling efforts aiming to understand the suitability of these compounds. Here we present first results on the validation of two semi-empirical potentials for Li and Pb in liquid phase. Our results establish a solid base as a previous, but crucial step, to implement a LiPb cross potential. Structural and thermodynamical analyses confirm that the analyzed potentials for Li and Pb are sufficiently accurate to simulate both elements in the liquid phase, and in conditions of interest for Nuclear Technology.

  10. Demonstration of a high-intensity neutron source based on a liquid-lithium target for Accelerator based Boron Neutron Capture Therapy.

    Science.gov (United States)

    Halfon, S; Arenshtam, A; Kijel, D; Paul, M; Weissman, L; Berkovits, D; Eliyahu, I; Feinberg, G; Kreisel, A; Mardor, I; Shimel, G; Shor, A; Silverman, I; Tessler, M

    2015-12-01

    A free surface liquid-lithium jet target is operating routinely at Soreq Applied Research Accelerator Facility (SARAF), bombarded with a ~1.91 MeV, ~1.2 mA continuous-wave narrow proton beam. The experiments demonstrate the liquid lithium target (LiLiT) capability to constitute an intense source of epithermal neutrons, for Accelerator based Boron Neutron Capture Therapy (BNCT). The target dissipates extremely high ion beam power densities (>3 kW/cm(2), >0.5 MW/cm(3)) for long periods of time, while maintaining stable conditions and localized residual activity. LiLiT generates ~3×10(10) n/s, which is more than one order of magnitude larger than conventional (7)Li(p,n)-based near threshold neutron sources. A shield and moderator assembly for BNCT, with LiLiT irradiated with protons at 1.91 MeV, was designed based on Monte Carlo (MCNP) simulations of BNCT-doses produced in a phantom. According to these simulations it was found that a ~15 mA near threshold proton current will apply the therapeutic doses in ~1h treatment duration. According to our present results, such high current beams can be dissipated in a liquid-lithium target, hence the target design is readily applicable for accelerator-based BNCT.

  11. Experiments on Heat Transfer in a Thin Liquid Film Flowing Over a Rotating Disk

    Science.gov (United States)

    Sankaran, Subramanian (Technical Monitor); Ozar, B.; Cetegen, B. M.; Faghri, A.

    2004-01-01

    An experimental study of heat transfer into a thin liquid film on a rotating heated disk is described. Deionized water was introduced at the center of a heated. horizontal disk with a constant film thickness and uniform radial velocity. Radial distribution of the disk surface temperatures was measured using a thermocouple/slip ring arrangement. Experiments were performed for a range of liquid flow rates between 3.01pm and 15.01pm. The angular speed of the disk was varied from 0 rpm to 500 rpm. The local heat transfer coefficient was determined based on the heat flux supplied to the disk and the temperature difference between the measured disk surface temperature and the liquid entrance temperature onto the disk. The local heat transfer coefficient was seen to increase with increasing flow rate as well as increasing angular velocity of the disk. Effect of rotation on heat transfer was largest for the lower liquid flow rates with the effect gradually decreasing with increasing liquid flow rates. Semi-empirical correlations are presented in this study for the local and average Nusselt numbers.

  12. Thin-film lithium-ion battery derived from Li1.3Al0.3Ti1.7(PO4)3 sintered pellet

    Institute of Scientific and Technical Information of China (English)

    XIAO Zhuo-bing; MA Ming-you; WU Xian-ming; HE Ze-qiang; CHEN Shang

    2006-01-01

    Thin-film lithium-ion battery of LiMn2O4/Li1.3Al0.3Ti1.7(PO4)3/LiMn2O4 was fabricated using Li1.3Al0.3Ti1.7(PO4)3 sintered pellet as both substrate and electrolyte. Li1.3Al0.3Ti1.7(PO4)3 sintered pellet was prepared by sol-gel technique, and the thin-film battery was heat-treated by rapid thermal annealing. Phase identification, morphology and electrochemical properties of the components and thin-film battery were investigated by X-ray diffractometry, scanning electron microscopy, electrochemical impedance spectroscopy and galvanostatic charge-discharge experiments. The results show that Li1.3Al0.3Ti1.7(PO4)3 possesses a electrochemical window of 2.4 V and an ionic conductivity of 1.2×10-4 S/cm. With Li1.3Al0.3Ti1.7(PO4)3 sintered pellet as both substrate and solid electrolyte, the fabricated thin-film battery with an open circuit voltage of 1.2V can be easily cycled.

  13. Nanocrystalline SnO2:F Thin Films for Liquid Petroleum Gas Sensors

    OpenAIRE

    Sutichai Chaisitsak

    2011-01-01

    This paper reports the improvement in the sensing performance of nanocrystalline SnO2-based liquid petroleum gas (LPG) sensors by doping with fluorine (F). Un-doped and F-doped tin oxide films were prepared on glass substrates by the dip-coating technique using a layer-by-layer deposition cycle (alternating between dip-coating a thin layer followed by a drying in air after each new layer). The results showed that this technique is superior to the conventional technique for both improving the ...

  14. Nanocrystal Diffusion in a Liquid Thin Film Observed by in situ Transmission Electron Microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Haimei; Claridge, Shelley A.; Minor, Andrew M.; Alivisatos, A. Paul; Dahmen, Ulrich

    2009-04-17

    We have directly observed motion of inorganic nanoparticles during fluid evaporation using a Transmission Electron Microscope. Tracking real-time diffusion of both spherical (5-15 nm) and rod-shaped (5x10 nm) gold nanocrystals in a thin-film of water-15percentglycerol reveals complex movements, such as rolling motions coupled to large-step movements and macroscopic violations of the Stokes-Einstein relation for diffusion. As drying patches form during the final stages of evaporation, particle motion is dominated by the nearby retracting liquid front.

  15. Tribological Behavior of Si3N4/Ti3SiC2 Contacts Lubricated by Lithium-Based Ionic Liquids

    Directory of Open Access Journals (Sweden)

    Haizhong Wang

    2014-01-01

    Full Text Available The tribological performance of Si3N4 ball sliding against Ti3SiC2 disc lubricated by lithium-based ionic liquids (ILs was investigated using an Optimol SRV-IV oscillating reciprocating friction and wear tester at room temperature (RT and elevated temperature (100°C. Glycerol and the conventional imidazolium-based IL 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonylimide (L-F106 were used as references under the same experimental conditions. The results show that the lithium-based ILs had higher thermal stabilities than glycerol and lower costs associated with IL preparation than L-F106. The tribotest results show that the lithium-based ILs were effective in reducing the friction and wear of Si3N4/Ti3SiC2 contacts. [Li(urea]TFSI even produced better tribological properties than glycerol and L-F106 both at RT and 100°C. The SEM/EDS and XPS results reveal that the excellent tribological endurance of Si3N4/Ti3SiC2 contacts lubricated by lithium-based ILs was mainly attributed to the formation of surface protective films composed of various tribochemical products.

  16. Nanocharacterization and nanofabrication of a Nafion thin film in liquids by atomic force microscopy.

    Science.gov (United States)

    Umemura, Kazuo; Wang, Tong; Hara, Masahiko; Kuroda, Reiko; Uchida, On; Nagai, Masayuki

    2006-03-28

    We demonstrated the nanocharacterization and nanofabrication of a Nafion thin film using atomic force microscopy (AFM). AFM images showed that the Nafion molecules form nanoclusters in water, in 5% methanol, and in acetic acid. Young's modulus E of a Nafion film was estimated by sequential force curve measurements in water and in 5% methanol on one sample surface. Ewater/E5% methanol was 1.75 +/- 0.40, so the film was much softer in 5% methanol than in water. Even when solvent was replaced from 5% methanol to water, Young's modulus was not recovered soon. We showed the first example of the mechanical properties of a Nafion film on the nanoscale. Furthermore, we succeeded in fabricating 3D nanostructures on a Nafion surface by AFM nanolithography in liquids. Our results showed the new potential of the AFM nanolithography of a polymer film by softening the molecules in liquids.

  17. The requirements for processing tritium recovered from liquid lithium blankets: The blanket interface

    Energy Technology Data Exchange (ETDEWEB)

    Clemmer, R.G.; Finn, P.A.; Greenwood, L.R.; Grimm, T.L.; Sze, D.K.; Bartlit, J.R.; Anderson, J.L.; Yoshida, H.; Naruse

    1988-03-01

    We have initiated a study to define a blanket processing mockup for Tritium Systems Test Assembly. Initial evaluation of the requirements of the blanket processing system have been started. The first step of the work is to define the condition of the gaseous tritium stream from the blanket tritium recovery system. This report summarizes this part of the work for one particular blanket concept, i.e., a self-cooled lithium blanket. The total gas throughput, the hydrogen to tritium ratio, the corrosive chemicals, and the radionuclides are defined. The key discoveries are: the throughput of the blanket gas stream (including the helium carrier gas) is about two orders of magnitude higher than the plasma exhaust stream;the protium to tritium ratio is about 1, the deuterium to tritium ratio is about 0.003;the corrosion chemicals are dominated by halides;the radionuclides are dominated by C-14, P-32, and S-35;their is high level of nitrogen contamination in the blanket stream. 77 refs., 6 figs., 13 tabs.

  18. Temperature dependence of the liquid eutectic lead-lithium alloy density

    Institute of Scientific and Technical Information of China (English)

    Alchagirov; Boris; B.; Mozgovoi; Alexandr; G.; Taova; Tamara; M.

    2005-01-01

    Lead-lithium alloys are of great interest for practice as the advanced materials to be used in new technique, nuclear energetics, and so forth. Terefore, study on the physico-chemical properties of the latter is of major significance. An analysis of the available literature shows that there are a few works, devoted to study of Pb-Li alloys densities. However, temperature dependence of the density ρ(T), and its temperature coefficientK=dρ/dT for eutectic alloy were obtained by either extrapolation of the density data up to the eutectic alloy's composition, or calculation method. There is a certain discrepancy amounting to as high as 4%, while the allowable error in the density measurements is less than 0.5%. The discrepancy between the results for the temperature coefficients of density amounts to 80%.In this work we present the experimental data on the temperature dependence of Ph0.83 Li0.17 eutectic alloy's density in the temperature range 520K to 643 K. The alloys were prepared using Pb and Li with 99. 999% and 99.8% contents of the basic elements, respectively. We use the improved device, which permits to get the results with error less than 0. 15%. The results of 115 measurements of density in 520K to 643K temperature range were processed by the least-square method. Density polytherm of Pb0.83 Li0. 17 eutectic alloy is described by linear equation ρ(T) =9507.89-0. 79813(T-508) , kg/m3 ,where T is the absolute temperature by K. Mearsurement error was 0. 12% at 95% reliability.Discrepancy in the temperature coefficient data was 1.08%.Thus, the temperature dependence of the Pb-Li eutectic alloy density was studied by the precise two-capillary method. The obtained results may be recommended as the most reliable reference data.

  19. Fabrication and lithium intercalation properties of epitaxial Li{sub 2}RuO{sub 3} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Zheng Yueming [Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502 (Japan); School of Electronic and Information Engineering, Xi' an Jiaotong University, Xi' an 710049 (China); Taminato, Sou; Suzuki, Kota [Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502 (Japan); Hirayama, Masaaki, E-mail: hirayama@echem.titech.ac.jp [Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502 (Japan); Kanno, Ryoji [Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502 (Japan)

    2012-05-31

    Lithium intercalation in a lithium excess layered material Li{sub 2}RuO{sub 3} was investigated using two-dimensional model electrodes with a restricted reaction plane of (002). Li{sub 2}RuO{sub 3} films were synthesized on Al{sub 2}O{sub 3}(0001) substrate by a pulsed laser deposition, and X-ray diffraction measurements confirmed epitaxial growth of Li{sub 2}RuO{sub 3}(002). Electrochemical characterization using cyclic voltammetry and charge/discharge measurements indicated electrochemical reactions with a discharge capacity of 200 mAh g{sup -1} for the film deposited at 400 Degree-Sign C followed by post-annealing at 550 Degree-Sign C. The electrochemical activity on the (002) plane indicated three-dimensional lithium diffusion in the two-dimensional layered rocksalt structure through the lithium sites in the transition metal layer. - Highlights: Black-Right-Pointing-Pointer Epitaxial Li{sub 2}RuO{sub 3} (002) films were successfully synthesized on Al{sub 2}O{sub 3} (0001). Black-Right-Pointing-Pointer Li{sub 2}RuO{sub 3} (002) films exhibited a discharge capacity of 200 mAh g{sup -1}. Black-Right-Pointing-Pointer 3-dimensional Li diffusion was confirmed in the 2-dimensional layered structure. Black-Right-Pointing-Pointer Mechanistic studies using epitaxial films clarify the intercalation mechanism.

  20. Thin liquid films with time-dependent chemical reactions sheared by an ambient gas flow

    Science.gov (United States)

    Bender, Achim; Stephan, Peter; Gambaryan-Roisman, Tatiana

    2017-08-01

    Chemical reactions in thin liquid films are found in many industrial applications, e.g., in combustion chambers of internal combustion engines where a fuel film can develop on pistons or cylinder walls. The reactions within the film and the turbulent outer gas flow influence film stability and lead to film breakup, which in turn can lead to deposit formation. In this work we examine the evolution and stability of a thin liquid film in the presence of a first-order chemical reaction and under the influence of a turbulent gas flow. Long-wave theory with a double perturbation analysis is used to reduce the complexity of the problem and obtain an evolution equation for the film thickness. The chemical reaction is assumed to be slow compared to film evolution and the amount of reactant in the film is limited, which means that the reaction rate decreases with time as the reactant is consumed. A linear stability analysis is performed to identify the influence of reaction parameters, material properties, and environmental conditions on the film stability limits. Results indicate that exothermic reactions have a stabilizing effect whereas endothermic reactions destabilize the film and can lead to rupture. It is shown that an initially unstable film can become stable with time as the reaction rate decreases. The shearing of the film by the external gas flow leads to the appearance of traveling waves. The shear stress magnitude has a nonmonotonic influence on film stability.

  1. Liquid film condensation along a vertical surface in a thin porous medium with large anisotropic permeability.

    Science.gov (United States)

    Sanya, Arthur S O; Akowanou, Christian; Sanya, Emile A; Degan, Gerard

    2014-01-01

    The problems of steady film condensation on a vertical surface embedded in a thin porous medium with anisotropic permeability filled with pure saturated vapour are studied analytically by using the Brinkman-Darcy flow model. The principal axes of anisotropic permeability are oriented in a direction that non-coincident with the gravity force. On the basis of the flow permeability tensor due to the anisotropic properties and the Brinkman-Darcy flow model adopted by considering negligible macroscopic and microscopic inertial terms, boundary-layer approximations in the porous liquid film momentum equation is solved analytically. Scale analysis is applied to predict the order-of-magnitudes involved in the boundary layer regime. The first novel contribution in the mathematics consists in the use of the anisotropic permeability tensor inside the expression of the mathematical formulation of the film condensation problem along a vertical surface embedded in a porous medium. The present analytical study reveals that the anisotropic permeability properties have a strong influence on the liquid film thickness, condensate mass flow rate and surface heat transfer rate. The comparison between thin and thick porous media is also presented.

  2. A simple method of measuring profiles of thin liquid films for microfluidics experiments by means of interference reflection microscopy

    CERN Document Server

    Berejnov, V

    2010-01-01

    A simple method was developed to observe the interference patterns of the light reflected by the interfaces of thin liquid films. Employing a fluorescent microscope with epi-illumination, we collected the 2D patterns of interference fringes containing information of the liquid film topography at microscale. To demonstrate the utility of the proposed visualization method we developed a framework for reconstructing the profiles of liquid films by analysing the reflected interferograms numerically. Both the visualization and reconstruction methods should be useful for variety of microfluidic applications involving the flows with droplets and bubbles in which the knowledge of the topography of the interfacial liquid film is critical.

  3. Synthesis and Properties of Tin Sulfide Thin Films from Nanocolloids Prepared by Pulsed Laser Ablation in Liquid.

    Science.gov (United States)

    Johny, Jacob; Sepulveda-Guzman, Selene; Krishnan, Bindu; Avellaneda, David A; Aguilar Martinez, Josue A; Shaji, Sadasivan

    2016-12-15

    Tin sulfide (SnS) nanoparticles were synthesized by pulsed laser ablation in liquid (PLAL) technique using an Nd:YAG laser operated at 532 nm. SnS thin films were deposited by spraying the colloidal suspension onto the heated substrates. The influence of different liquid media (dimethyl formamide and isopropyl alcohol) on the thin film properties were studied. Morphology, crystalline structure, and chemical composition of the nanoparticles were identified using transmission electron microscopy with energy dispersive X-ray analysis. The crystalline structure of the thin films was analyzed by using grazing incidence X-ray diffraction, and the chemical states by X-ray photoelectron spectroscopy. Scanning electron microscopy was employed for the morphological analysis of the thin films. Annealing the films at 380 °C improved the crystallinity of the films exhibiting a layered morphology, which may be useful in optoelectronic and sensing applications. Cyclic voltammetry studies showed that the films have good electrochemical properties.

  4. Investigation of Symphytum cordatum alkaloids by liquid-liquid partitioning, thin-layer chromatography and liquid chromatography-ion-trap mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Mroczek, Tomasz [Department of Pharmacognosy with Medicinal Plants Laboratory, Medical University, 1 Chodzki St., 20-093 Lublin (Poland)]. E-mail: tmroczek@pharmacognosy.org; Ndjoko-Ioset, Karine [Laboratoire de Pharmacognosie et Phytochimie, Ecole de Pharmacie Geneve-Lausanne, Universite de Geneve, Quai Ernest-Ansermet 30, CH-1211 Geneva 4 (Switzerland); Glowniak, Kazimierz [Department of Pharmacognosy with Medicinal Plants Laboratory, Medical University, 1 Chodzki St., 20-093 Lublin (Poland); Mietkiewicz-Capala, Agnieszka [Department of Pharmacognosy with Medicinal Plants Laboratory, Medical University, 1 Chodzki St., 20-093 Lublin (Poland); Hostettmann, Kurt [Laboratoire de Pharmacognosie et Phytochimie, Ecole de Pharmacie Geneve-Lausanne, Universite de Geneve, Quai Ernest-Ansermet 30, CH-1211 Geneva 4 (Switzerland)

    2006-05-04

    From the alkalised crude extract of Symphytum cordatum (L.) W.K. roots, pyrrolizidine alkaloids (PAs) were extracted as free tertiary bases and polar N-oxides in a merely one-step liquid-liquid partitioning (LLP) in separation funnel and subsequently pre-fractionated by preparative multiple-development (MD) thin-layer chromatography (TLC) on silica gel plates. In this way three alkaloid fractions of different polarities and retention on silica gel plates were obtained as: the most polar N-oxides of the highest retention, the tertiary bases of medium retention, and diesterified N-oxides of the lowest retention. The former fraction was reduced into free bases by sodium hydrosulfite and purified by LLP on Extrelut-NT3 cartridge. It was further analysed together with the two other fractions by high-performance liquid chromatography (HPLC)-ion-trap mass spectrometry with atmospheric pressure chemical ionization (APCI) interface on XTerra C{sub 18} column using a gradient elution. Based on MS {sup n} spectra, 18 various alkaloids have been tentatively determined for the first time in this plant as the following types of structure: echimidine-N-oxide (three diasteroisomers), 7-sarracinyl-9-viridiflorylretronecine (two diasteroisomers), echimidine (two diasteroisomers), lycopsamine (two diasteroisomers), dihydroechinatine-N-oxide, dihydroheliospathuline-N-oxide, lycopsamine-N-oxide (three diasteroisomers), 7-acetyllycopsamine-N-oxide, symphytine-N-oxide (two diasteroisomers) and 2'',3''-epoxyechiumine-N-oxide.

  5. A graphene-oxide-based thin coating on the separator: an efficient barrier towards high-stable lithium-sulfur batteries

    Science.gov (United States)

    Zhang, Yunbo; Miao, Lixiao; Ning, Jing; Xiao, Zhichang; Hao, Long; Wang, Bin; Zhi, Linjie

    2015-06-01

    The electrochemical performance of lithium-sulfur (Li-S) batteries can be significantly improved by simply coating a thin barrier layer on the separator. The spray-coating of a mixture of graphene oxides (GO) and oxidized carbon nanotubes (o-CNT) can achieve a barrier coating of only 0.3 mg cm-2, which is much less than conventional interlayers and has no negative impact on the energy density but significantly enhances the electrochemical performances of the whole battery device. Due to the binding forces induced by functional groups on GO and the interconnected nanoscale channels provided by o-CNT, the thus fabricated Li-S batteries show dramatically improved specific discharge capacities of up to 750 mAh g-1 at 1 C even after 100 cycles, more than twice those of batteries without barrier coatings.

  6. Evaporation characteristics of thin film liquid argon in nano-scale confinement: A molecular dynamics study

    Science.gov (United States)

    Hasan, Mohammad Nasim; Shavik, Sheikh Mohammad; Rabbi, Kazi Fazle; Haque, Mominul

    2016-07-01

    Molecular dynamics simulation has been carried out to explore the evaporation characteristics of thin liquid argon film in nano-scale confinement. The present study has been conducted to realize the nano-scale physics of simultaneous evaporation and condensation inside a confined space for a three phase system with particular emphasis on the effect of surface wetting conditions. The simulation domain consisted of two parallel platinum plates; one at the top and another at the bottom. The fluid comprised of liquid argon film at the bottom plate and vapor argon in between liquid argon and upper plate of the domain. Considering hydrophilic and hydrophobic nature of top and bottom surfaces, two different cases have been investigated: (i) Case A: Both top and bottom surfaces are hydrophilic, (ii) Case B: both top and bottom surfaces are hydrophobic. For all cases, equilibrium molecular dynamics (EMD) was performed to reach equilibrium state at 90 K. Then the lower wall was set to four different temperatures such as 110 K, 120 K, 130 K and 140 K to perform non-equilibrium molecular dynamics (NEMD). The variation of temperature and density as well as the variation of system pressure with respect to time were closely monitored for each case. The heat fluxes normal to top and bottom walls were estimated and discussed to illuminate the effectiveness of heat transfer in both hydrophilic and hydrophobic confinement at various boundary temperatures of the bottom plate.

  7. On the breakup of a thin liquid film subject to interfacial shear

    Science.gov (United States)

    Saber, Hamed H.; El-Genk, Mohamed S.

    2004-02-01

    The breakup of a thin non-evaporating liquid film that is either flowing down or climbing on a vertical or inclined surface and subject to cocurrent or countercurrent interfacial shear (or gas flow) is investigated analytically. Analytical expressions for the dimensionless liquid film thickness, Delta_{scriptsizemin}, and wetting rate, Gamma_{scriptsizemin}, at breakup are derived based on the minimization of the total energy of a stable rivulet, formed following the film breakup. For a downflowing liquid film, increasing the cocurrent interfacial shear (or gas velocity) or decreasing the equilibrium contact angle, theta_{o}, decreases both Delta_{scriptsizemin} and Gamma _{scriptsizemin}, below their values with zero interfacial shear. Conversely, increasing the countercurrent interfacial shear or theta_{o}, increases both Delta_{scriptsizemin} and Gamma_{scriptsizemin}, above their values with zero interfacial shear. The predictions of Delta _{scriptsizemin} and Gamma _{scriptsizemin} for a climbing water film on a vertical surface are in good agreement with reported experimental data for a wide range of cocurrent gas velocities.

  8. Lithium generated by cosmic rays: an estimator of the time that Mars had a thicker atmosphere and liquid water

    CERN Document Server

    Durand-Manterola, Hector Javier

    2012-01-01

    Lithium is overabundant in cosmic rays because protons impact on carbon and oxygen nuclei and fission them. Among the products of this fission is lithium. Given this preference for carbon and oxygen atoms, in this work I propose that in an atmosphere of almost pure CO2, such as Mars and Venus atmospheres, lithium nuclei are produced by interaction with cosmic rays. I calculated the production rate of lithium and came to the conclusion that, for pressures of two bars or greater, are produced between 21 and 81 lithium nuclei for each primary cosmic rays proton. For lower pressures, the production is less and almost nil with the current pressure of Mars or Earth (pressure of CO2). Assuming a rate of cosmic ray arrival at Mars equal to that of Earth, and a pressure greater than two bars throughout the history of Mars, the amount of lithium that would occur would be between 162 and 642 million metric tons (in the Earth lithium estimated reserves are 30 million metric tons). These values are an upper limit; the act...

  9. Vertical phase separation and liquid-liquid dewetting of thin PS/PCL blend films during spin coating.

    Science.gov (United States)

    Ma, Meng; He, Zhoukun; Yang, Jinghui; Wang, Qi; Chen, Feng; Wang, Ke; Zhang, Qin; Deng, Hua; Fu, Qiang

    2011-02-01

    Thin films of an amorphous polymer, polystyrene (PS), and a crystalline polymer, poly(ε-caprolactone) (PCL), blend were prepared by spin coating a toluene solution. Surface chemical compositions of the blend films were measured by X-ray photoelectron spectroscopy (XPS), and the surface and interface topographical changes were followed by atomic force microscopy (AFM). By changing the PS concentration and keeping the PCL concentration of the solution at 1 wt %, a great variety of morphologies were constructed. The results show that the morphology of the blend films can be divided into three regions with increasing PS concentration. In region I, PS island domains are embedded in PCL crystals when the PS concentration is lower than 0.3 wt % and the size of the PS island increases with increasing PS concentration. In region II, holes with different sizes surrounded by a low rim are obtained when the concentration of PS is between 0.35 and 0.5 wt %. After selectively washing the PS domains, we studied the interface morphology of PS/PCL and found that the upper PS-rich layer extended into the bottom PCL layer, forming a trench surrounding the holes. In region III, an enriched two-layer structure with the PS-rich layer on top of the blend films and the PCL-rich crystal layer underneath is obtained when the concentration of PS is higher than 0.5 wt %. Last, the formation mechanism of the different surface and interface morphologies is further discussed in terms of the vertical phase separation to a layered structure, followed by liquid-liquid dewetting and crystallization processes during spin coating.

  10. Optimization of Pore Structure of Cathodic Carbon Supports for Solvate Ionic Liquid Electrolytes Based Lithium-Sulfur Batteries.

    Science.gov (United States)

    Zhang, Shiguo; Ikoma, Ai; Li, Zhe; Ueno, Kazuhide; Ma, Xiaofeng; Dokko, Kaoru; Watanabe, Masayoshi

    2016-10-04

    Lithium-sulfur (Li-S) batteries are a promising energy-storage technology owing to their high theoretical capacity and energy density. However, their practical application remains a challenge because of the serve shuttle effect caused by the dissolution of polysulfides in common organic electrolytes. Polysulfide-insoluble electrolytes, such as solvate ionic liquids (ILs), have recently emerged as alternative candidates and shown great potential in suppressing the shuttle effect and improving the cycle stability of Li-S batteries. Redox electrochemical reactions in polysulfide-insoluble electrolytes occur via a solid-state process at the interphase between the electrolyte and the composite cathode; therefore, creating an appropriate interface between sulfur and a carbon support is of great importance. Nevertheless, the porous carbon supports established for conventional organic electrolytes may not be suitable for polysulfide-insoluble electrolytes. In this work, we investigated the effect of the porous structure of carbon materials on the Li-S battery performance in polysulfide-insoluble electrolytes using solvate ILs as a model electrolyte. We determined that the pore volume (rather than the surface area) exerts a major influence on the discharge capacity of S composite cathodes. In particular, inverse opal carbons with three-dimensionally ordered interconnected macropores and a large pore volume deliver the highest discharge capacity. The battery performance in both polysulfide-soluble electrolytes and solvate ILs was used to study the effect of electrolytes. We propose a plausible mechanism to explain the different porous structure requirements in polysulfide-soluble and polysulfide-insoluble electrolytes.

  11. Crosslinked polymer gel electrolytes based on polyethylene glycol methacrylate and ionic liquid for lithium battery applications

    Energy Technology Data Exchange (ETDEWEB)

    Liao, Chen [ORNL; Sun, Xiao-Guang [ORNL; Dai, Sheng [ORNL

    2013-01-01

    Gel polymer electrolytes were synthesized by copolymerization polyethylene glycol methyl ether methacrylate with polyethylene glycol dimethacrylate in the presence of a room temperature ionic liquid, methylpropylpyrrolidinium bis(trifluoromethanesulfonyl)imide (MPPY TFSI). The physical properties of gel polymer electrolytes were characterized by thermal analysis, impedance spectroscopy, and electrochemical tests. The ionic conductivities of the gel polymer electrolytes increased linearly with the amount of MPPY TFSI and were mainly attributed to the increased ion mobility as evidenced by the decreased glass transition temperatures. Li||LiFePO4 cells were assembled using the gel polymer electrolytes containing 80 wt% MPPY TFSI via an in situ polymerization method. A reversible cell capacity of 90 mAh g 1 was maintained under the current density of C/10 at room temperature, which was increased to 130 mAh g 1 by using a thinner membrane and cycling at 50 C.

  12. Mixtures of room temperature ionic liquid/ethanol solutions as electrolytic media for cerium oxide thin layer electrodeposition

    Energy Technology Data Exchange (ETDEWEB)

    Lair, V., E-mail: virginie-lair@chimie-paristech.f [Laboratoire d' Electrochimie, Chimie des Interfaces et Modelisation pour l' Energie, LECIME, CNRS UMR 7575-Chimie Paristech (ENSCP)-Paris, 11, rue Pierre et Marie Curie, 75231 Paris Cedex 05 (France); Sirieix-Plenet, J.; Gaillon, L.; Rizzi, C. [UPMC University Paris 06, UMR 7195, Laboratoire de Physicochimie des Electrolytes, Colloides et Sciences Analytiques (PECSA), F-75005 Paris (France); CNRS, UMR 7195, PECSA, F-75005 Paris (France); ESPCI, UMR 7195, PECSA, F-75005 Paris (France); Ringuede, A. [Laboratoire d' Electrochimie, Chimie des Interfaces et Modelisation pour l' Energie, LECIME, CNRS UMR 7575-Chimie Paristech (ENSCP)-Paris, 11, rue Pierre et Marie Curie, 75231 Paris Cedex 05 (France)

    2010-12-30

    A cerium oxide thin layer was electrodeposited onto stainless steel, using mixed room temperature ionic liquid (the 1-methyl-3-butylimidazolium bis(trifluoromethyl sulfonyl)imide)/ethanol solutions, as electrolytic medium. The hydrophobic ionic liquid content is one of the main parameters in the morphology control influencing the ceria growth rate and crystallinity. Micro-nano structural properties and electrical behaviour are presented, using XRD, SEM/EDS and impedance spectroscopy, as a function of electrodeposition conditions.

  13. Aerosol indirect effects on the nighttime Arctic Ocean surface from thin, predominantly liquid clouds

    Science.gov (United States)

    Zamora, Lauren M.; Kahn, Ralph A.; Eckhardt, Sabine; McComiskey, Allison; Sawamura, Patricia; Moore, Richard; Stohl, Andreas

    2017-06-01

    Aerosol indirect effects have potentially large impacts on the Arctic Ocean surface energy budget, but model estimates of regional-scale aerosol indirect effects are highly uncertain and poorly validated by observations. Here we demonstrate a new way to quantitatively estimate aerosol indirect effects on a regional scale from remote sensing observations. In this study, we focus on nighttime, optically thin, predominantly liquid clouds. The method is based on differences in cloud physical and microphysical characteristics in carefully selected clean, average, and aerosol-impacted conditions. The cloud subset of focus covers just ˜ 5 % of cloudy Arctic Ocean regions, warming the Arctic Ocean surface by ˜ 1-1.4 W m-2 regionally during polar night. However, within this cloud subset, aerosol and cloud conditions can be determined with high confidence using CALIPSO and CloudSat data and model output. This cloud subset is generally susceptible to aerosols, with a polar nighttime estimated maximum regionally integrated indirect cooling effect of ˜ -0.11 W m-2 at the Arctic sea ice surface (˜ 8 % of the clean background cloud effect), excluding cloud fraction changes. Aerosol presence is related to reduced precipitation, cloud thickness, and radar reflectivity, and in some cases, an increased likelihood of cloud presence in the liquid phase. These observations are inconsistent with a glaciation indirect effect and are consistent with either a deactivation effect or less-efficient secondary ice formation related to smaller liquid cloud droplets. However, this cloud subset shows large differences in surface and meteorological forcing in shallow and higher-altitude clouds and between sea ice and open-ocean regions. For example, optically thin, predominantly liquid clouds are much more likely to overlay another cloud over the open ocean, which may reduce aerosol indirect effects on the surface. Also, shallow clouds over open ocean do not appear to respond to aerosols as

  14. Aerosol indirect effects on the nighttime Arctic Ocean surface from thin, predominantly liquid clouds

    Directory of Open Access Journals (Sweden)

    L. M. Zamora

    2017-06-01

    Full Text Available Aerosol indirect effects have potentially large impacts on the Arctic Ocean surface energy budget, but model estimates of regional-scale aerosol indirect effects are highly uncertain and poorly validated by observations. Here we demonstrate a new way to quantitatively estimate aerosol indirect effects on a regional scale from remote sensing observations. In this study, we focus on nighttime, optically thin, predominantly liquid clouds. The method is based on differences in cloud physical and microphysical characteristics in carefully selected clean, average, and aerosol-impacted conditions. The cloud subset of focus covers just ∼ 5 % of cloudy Arctic Ocean regions, warming the Arctic Ocean surface by ∼ 1–1.4 W m−2 regionally during polar night. However, within this cloud subset, aerosol and cloud conditions can be determined with high confidence using CALIPSO and CloudSat data and model output. This cloud subset is generally susceptible to aerosols, with a polar nighttime estimated maximum regionally integrated indirect cooling effect of ∼ −0.11 W m−2 at the Arctic sea ice surface (∼ 8 % of the clean background cloud effect, excluding cloud fraction changes. Aerosol presence is related to reduced precipitation, cloud thickness, and radar reflectivity, and in some cases, an increased likelihood of cloud presence in the liquid phase. These observations are inconsistent with a glaciation indirect effect and are consistent with either a deactivation effect or less-efficient secondary ice formation related to smaller liquid cloud droplets. However, this cloud subset shows large differences in surface and meteorological forcing in shallow and higher-altitude clouds and between sea ice and open-ocean regions. For example, optically thin, predominantly liquid clouds are much more likely to overlay another cloud over the open ocean, which may reduce aerosol indirect effects on the surface. Also, shallow clouds over

  15. The flow of a thin liquid film on a stationary and rotating disk. II - Theoretical prediction

    Science.gov (United States)

    Rahman, M. M.; Faghri, A.; Hankey, W. L.

    1990-01-01

    The existing theoretical models are improved and a systematic procedure to compute the free surface flow of a thin liquid film is suggested. The solutions for axisymmetric radial flow on a stationary horizontal disk and for the disk rotating around its axis are presented. The theoretical predictions are compared with the experimental data presented in Part I of this report. The analysis shows results for both supercritical and subcritical flows and the flow structure in the vicinity of a hydraulic jump which isolates these two flow types. The detailed flow structure in a hydraulic jump was computed and shown to contain regions of separation including a 'surface roller'. The effects of surface tension are found to be important near the outer edge of the disk where the fluid experiences a free fall. At other locations, the surface tension is negligible. For a rotating disk, the frictional resistance in the angular direction is found to be as important as that in the radial direction.

  16. Liquid- and Gas-Phase Diffusion of Ferrocene in Thin Films of Metal-Organic Frameworks

    Directory of Open Access Journals (Sweden)

    Wencai Zhou

    2015-06-01

    Full Text Available The mass transfer of the guest molecules in nanoporous host materials, in particular in metal-organic frameworks (MOFs, is among the crucial features of their applications. By using thin surface-mounted MOF films in combination with a quartz crystal microbalance (QCM, the diffusion of ferrocene vapor and of ethanolic and hexanic ferrocene solution in HKUST-1 was investigated. For the first time, liquid- and gas-phase diffusion in MOFs was compared directly in the identical sample. The diffusion coefficients are in the same order of magnitude (~10−16 m2·s−1, whereas the diffusion coefficient of ferrocene in the empty framework is roughly 3-times smaller than in the MOF which is filled with ethanol or n-hexane.

  17. Liquid- and Gas-Phase Diffusion of Ferrocene in Thin Films of Metal-Organic Frameworks

    Science.gov (United States)

    Zhou, Wencai; Wöll, Christof; Heinke, Lars

    2015-01-01

    The mass transfer of the guest molecules in nanoporous host materials, in particular in metal-organic frameworks (MOFs), is among the crucial features of their applications. By using thin surface-mounted MOF films in combination with a quartz crystal microbalance (QCM), the diffusion of ferrocene vapor and of ethanolic and hexanic ferrocene solution in HKUST-1 was investigated. For the first time, liquid- and gas-phase diffusion in MOFs was compared directly in the identical sample. The diffusion coefficients are in the same order of magnitude (~10−16 m2·s−1), whereas the diffusion coefficient of ferrocene in the empty framework is roughly 3-times smaller than in the MOF which is filled with ethanol or n-hexane.

  18. Liquid Density Sensing Using Resonant Flexural Plate Wave Device with Sol-Gel PZT Thin Films

    CERN Document Server

    Yu, Jyh-Cheng

    2008-01-01

    This paper presents the design, fabrication and preliminary experimental results of a flexure plate wave (FPW) resonator using sol-gel derived lead zirconate titanates (PZT) thin films. The resonator adopts a two-port structure with reflecting grates on the composite membrane of PZT and SiNx. The design of the reflecting grate is derived from a SAW resonator model using COM theory to produce a sharp resonant peak. The comparison between the mass and the viscosity effects from the theoretical expression illustrates the applications and the constraints of the proposed device in liquid sensing. Multiple coatings of sol-gel derived PZT films are adopted because of the cost advantage and the high electromechanical coupling effect over other piezoelectric films. The fabrication issues of the proposed material structure are addressed. Theoretical estimations of the mass and the viscosity effects are compared with the experimental results. The resonant frequency has a good linear correlation with the density of low v...

  19. Dopamine/TiO{sub 2} hybrid thin films prepared by the liquid phase deposition method

    Energy Technology Data Exchange (ETDEWEB)

    Gutierrez-Tauste, David [Departament de Quimica, Universitat Autonoma de Barcelona, Campus UAB, Edifici Cn, 08290 Cerdanyola del Valles, Barcelona (Spain)], E-mail: davidg@qf.uab.es; Domenech, Xavier [Departament de Quimica, Universitat Autonoma de Barcelona, Campus UAB, Edifici Cn, 08290 Cerdanyola del Valles, Barcelona (Spain); Domingo, Concepcion [Instituto de Ciencia de Materiales (CSIC), Campus UAB, 08290 Cerdanyola del Valles, Barcelona (Spain); Ayllon, Jose A. [Departament de Quimica, Universitat Autonoma de Barcelona, Campus UAB, Edifici Cn, 08290 Cerdanyola del Valles, Barcelona (Spain)

    2008-04-30

    Liquid phase deposition method is applied to one-step production of a hybrid material composed by dopamine(DA) and TiO{sub 2} anatase. An optimized amount of the enediol derivative is added to a fluoride titania precursor aqueous solution in order to entrap this modifier within the growing TiO{sub 2}, yielding a DA/TiO{sub 2} nanocomposite material. Uniform, well-adhered and brown-colored thin films are deposited on indium tin oxide covered glass substrate. The DA/TiO{sub 2} hybrid material has been characterized by infrared spectroscopy, electronic microscopy, X-ray diffraction and UV-vis spectroscopy. The formation of the hybrid material seems to be reasonably explained by linkage of different TiO{sub 2} nanocrystallites taking advantage of both enediol and amine groups of DA.

  20. The effect of surfaces on molecular ordering in thin liquid-crystal systems

    Science.gov (United States)

    Śliwa, I.; JeŻewski, W.; Zakharov, A. V.

    2016-08-01

    A theoretical method for analyzing the interplay between pair long-range intermolecular forces and nonlocal, relatively short-range, surface interactions in liquid crystals, confined between plates of thin planar cells, is developed. It is shown that this method, as involving the concept of local orientational and translational order parameters, enables detailed investigations of the emergence of smectic A, nematic, and isotopic phases, as well as yields an insight into phase transitions between them, in cases of systems strongly affected by surfaces. The evidence of various surface effects, including the coexistence of different phases and the inward propagation of surface melting under the increase of temperature, is also given. The underlying numerical procedure, based on the algorithm of self-consistent calculations of local order parameters, is found to be very effective, allowing one to consider model systems of rather large thicknesses, corresponding to thicknesses of real sample cells.

  1. A Liquid Inorganic Electrolyte Showing an Unusually High Lithium Ion Transference Number: A Concentrated Solution of LiAlCl4 in Sulfur Dioxide

    Directory of Open Access Journals (Sweden)

    Martin Winter

    2013-08-01

    Full Text Available We report on studies of an inorganic electrolyte: LiAlCl4 in liquid sulfur dioxide. Concentrated solutions show a very high conductivity when compared with typical electrolytes for lithium ion batteries that are based on organic solvents. Our investigations include conductivity measurements and measurements of transference numbers via nuclear magnetic resonance (NMR and by a classical direct method, Hittorf’s method. For the use of Hittorf’s method, it is necessary to measure the concentration of the electrolyte in a selected cell compartment before and after electrochemical polarization very precisely. This task was finally performed by potentiometric titration after hydrolysis of the salt. The Haven ratio was determined to estimate the association behavior of this very concentrated electrolyte solution. The measured unusually high transference number of the lithium cation of the studied most concentrated solution, a molten solvate LiAlCl4 × 1.6SO2, makes this electrolyte a promising alternative for lithium ion cells with high power ability.

  2. Liquid-lithium nitrate: candidate fusion reactor coolant or chemical curiosity

    Energy Technology Data Exchange (ETDEWEB)

    Adamson, M.G.

    1986-01-01

    On the basis of the recent Blanket Comparison and Selection Study, 700 K was selected as the threshold for useful high-temperature operation of a liquid nitrate coolant and 800 K was assumed as a realistic upper operating limit. Both standard Second Law equilibrium calculations and computerized Gibbs energy minimization methods were used to determine equilibrium compositions of multiphase, multicomponent salt systems at specified temperatures under certain condensed were performed on the LiNO/sub 3/-LiNO/sub 2/, NaNO/sub 3/- NaNO/sub 2/, and KNO/sub 3/-KNO/sub 2/ systems, and then predicted decomposition pressures were compared for equivalent degrees of decomposition at temperatures ranging from 600 to 900K. Two approaches were taken in calculating decomposition pressures over MNO/sub 3/-MNO/sub 2/ systems: (a) allowing the formation of molecular N/sub 2/ as a gaseous reaction product and (b) not allowing its formation. In calculations of MNO/sub 2/-M/sub 2/O-MOH-H/sub 2/O equilibria, which were used to evaluate the reversibility of tritium dissolution and release, the activity of hydroxide reaction product was determined as a function of water activity at two representative temperatures. Preliminary results and conclusions are summarized.

  3. Electric batteries. Lithium batteries; Piles electrique. Piles au lithium

    Energy Technology Data Exchange (ETDEWEB)

    Sarrazin, Ch. [Delegation Generale pour l' Armement, DGA/DRET, 75 - Paris (France)

    2002-05-01

    Lithium has the most negative potential and the highest mass capacity of all solid anode materials. It is the metal that allows to reach the highest mass energies in batteries when associated to a high potential cathode. The search for high performance cathodes has led to many different types of lithium batteries (transition metal oxides or sulfides, halogenides, oxi-halogenides, carbon, organic compounds etc..). These batteries can have a solid cathode (Li/CuO, Li/MnO{sub 2}, Li/CF{sub x}, etc..), or a liquid cathode (Li/SOCl{sub 2}, Li/SO{sub 2}, etc..) and in some cases they can have also a solid electrolyte, but not all types of lithium battery led to important industrial fabrication. The increasing use of lithium batteries is linked with the development of portable equipments for which, the compactness of the energy source is a key point. This article examines only the lithium batteries that have been the object of a significant industrial fabrication: lithium-sulfur dioxide, lithium-thionyl chloride, lithium-manganese dioxide, lithium-copper oxide, lithium-carbon fluoride, lithium-iron disulfide, other types of lithium batteries. (J.S.)

  4. Experiments on the Flow of a Thin Liquid Film Over a Horizontal Stationary and Rotating Disk Surface

    Science.gov (United States)

    Ozar, B.; Cetegen, B. M.; Faghri, A.

    2003-01-01

    Experiments on characterization of thin liquid films flowing over stationary and rotating disk surfaces are described. The thin liquid film was created by introducing deionized water from a flow collar at the center of an aluminum disk with a known initial film thickness and uniform radial velocity. Radial film thickness distribution was measured using a non-intrusive laser light interface reflection technique that enabled the measurement of the instantaneous film thickness over a finite segment of the disk. Experiments were performed for a range of flow rates between 3.01pm and 15.01pm, corresponding to Reynolds numbers based on the liquid inlet gap height and velocity between 238 and 1,188. The angular speed of the disk was varied from 0 rpm to 300 rpm. When the disk was stationary, a circular hydraulic jump was present in the liquid film. The liquid-film thickness in the subcritical region (down-stream of the hydraulic jump) was an order of magnitude greater than that in the supercritical region (upstream of the hydraulic jump) which was of the order of 0.3 mm. As the Reynolds number increased, the hydraulic jump migrated toward the edge of the disk. In the case of rotation, the liquid-film thickness exhibited a maximum on the disk surface. The liquid-film inertia and friction influenced the inner region where the film thickness progressively increased. The outer region where the film thickness decreased was primarily affected by the centrifugal forces. A flow visualization study of the thin film was also performed to determine the characteristics of the waves on the free surface. At high rotational speeds, spiral waves were observed on the liquid film. It was also determined that the angle of the waves which form on the liquid surface was a function of the ratio of local radial to tangential velocity.

  5. Experimental analysis and flow visualization of a thin liquid film on a stationary and rotating disk

    Science.gov (United States)

    Thomas, S.; Faghri, A.; Hankey, W.

    1991-01-01

    The mean thickness of a thin liquid film of deionized water with a free surface on a stationary and rotating horizontal disk has been measured with a nonobtrusive capacitance technique. The measurements were taken when the rotational speed ranged from 0-300 rpm and the flow rate varied from 7.0-15.0 lpm. A flow visualization study of the thin film was also performed to determine the characteristics of the waves on the free surface. When the disk was stationary, a circular hydraulic jump was present on the disk. Upstream from the jump, the film thickness was determined by the inertial and frictional forces on the fluid, and the radial spreading of the film. The surface tension at the edge of the disk affected the film thickness downstream from the jump. For the rotating disk, the film thickness was dependent upon the inertial and frictional forces near the center of the disk and the centrifugal forces near the edge of the disk.

  6. Increased Hierarchical Wrinklons on Stiff Metal Thin Film on a Liquid Meniscus.

    Science.gov (United States)

    Deng, Shikai; Berry, Vikas

    2016-09-21

    Wrinklons-the hierarchical merging of wrinkles-are observed on several surfaces including thin films, curtains, graphene sheets, and skin. Wrinklons are a consequence of the interplay between bending, stretching, and gravitational energies and generally exhibit 1 to 2 hierarchical transitions (λn+1 = 2λn). Here we show that parallel and self-similar wrinklons on ultrathin cobalt/chromium film atop a contracting silicone oil meniscus can produce up to 5 hierarchical wrinklon transitions near the fluid-solid boundary. Further, these wrinklons do not follow the standard von-Kármán wrinklon scaling near the edge, attributed to the added surface energy (L/λ ∝ (A/t)(0.31)). A model developed via scale analysis shows (a) the relationship between wavelength and length of the wrinkles and (b) a linear relation between the amplitude and the length of wrinkles at all observed hierarchic levels (L ∝ A), fitted well with previous literature results. This work provides a mechanism for thin-film metal wrinkling on liquids and shows that surface stretching effects can allow increased hierarchical levels in wrinklons.

  7. GeO2 Thin Film Deposition on Graphene Oxide by the Hydrogen Peroxide Route: Evaluation for Lithium-Ion Battery Anode.

    Science.gov (United States)

    Medvedev, Alexander G; Mikhaylov, Alexey A; Grishanov, Dmitry A; Yu, Denis Y W; Gun, Jenny; Sladkevich, Sergey; Lev, Ovadia; Prikhodchenko, Petr V

    2017-03-15

    A peroxogermanate thin film was deposited in high yield at room temperature on graphene oxide (GO) from peroxogermanate sols. The deposition of the peroxo-precursor onto GO and the transformations to amorphous GeO2, crystalline tetragonal GeO2, and then to cubic elemental germanium were followed by electron microscopy, XRD, and XPS. All of these transformations are influenced by the GO support. The initial deposition is explained in view of the sol composition and the presence of GO, and the different thermal transformations are explained by reactions with the graphene support acting as a reducing agent. As a test case, the evaluation of the different materials as lithium ion battery anodes was carried out revealing that the best performance is obtained by amorphous germanium oxide@GO with >1000 mAh g(-1) at 250 mA g(-1) (between 0 and 2.5 V vs Li/Li(+) cathode), despite the fact that the material contained only 51 wt % germanium. This is the first demonstration of the peroxide route to produce peroxogermanate thin films and thereby supported germanium and germanium oxide coatings. The advantages of the process over alternative methodologies are discussed.

  8. A very light and thin liquid hydrogen/deuterium heat pipe target for COSY experiments

    Science.gov (United States)

    Abdel-Bary, M.; Abdel-Samad, S.; Kilian, K.

    2005-07-01

    A liquid hydrogen/deuterium heat pipe (HP) target is used at the COSY external experiments TOF, GEM and MOMO. The target liquid is produced at a cooled condenser and guided through a central tube assisted by gravitation into the target cell. An aluminum condenser is used instead of copper, which requires less material, improves conductivities and provides shorter cooling down time. Residual condenser temperature fluctuations in the order of ≈0.4 K are reduced by using thermal resistances between the cooling machine and the condenser of the heat pipe combined with a controlled heating power. A new design with only a 7-mm-diameter HP has been developed. The diameter of the condenser part remains at 16 mm to provide enough condensation area. The small amount of material ensures short cooling down times. A cold gas deuterium HP target has been designed and developed which allows protons with energy ⩽1 MeV to be measured. A 7-mm-diameter HP is used to fill a cooling jacket around the D 2 gas cell with LH 2. The D 2 gas is stabilized at 200 mbar to allow for thin windows. Its density is increased by factor 15 compared to room temperature.

  9. Numerical study of heat and mass transfer during evaporation of a thin liquid film

    Directory of Open Access Journals (Sweden)

    Oubella M’hand

    2015-01-01

    Full Text Available A numerical study of mixed convection heat and mass transfer with film evaporation in a vertical channel is developed. The emphasis is focused on the effects of vaporization of three different liquid films having widely different properties, along the isothermal and wetted walls on the heat and mass transfer rates in the channel. The induced laminar downward flow is a mixture of blowing dry air and vapour of water, methanol or acetone, assumed as ideal gases. A two-dimensional steady state and elliptical flow model, connected with variable thermo-physical properties, is used and the phase change problem is based on thin liquid film assumptions. The governing equations of the model are solved by a finite volume method and the velocity-pressure fields are linked by SIMPLE algorithm. The numerical results, including the velocity, temperature and concentration profiles, as well as axial variations of Nusselt numbers, Sherwood number and dimensionless film evaporation rate are presented for two values of inlet temperature and Reynolds number. It was found that lower the inlet temperature and Re, the higher the induced flows cooling with respect of most volatile film. The better mass transfer rates related with film evaporation are found for a system with low mass diffusion coefficient.

  10. High resolution imaging of 2D distribution of lithium in thin samples measured with multipixel detectors in sandwich geometry

    Science.gov (United States)

    Tomandl, I.; Vacík, J.; Mora Sierra, Y.; Granja, C.; Kraus, V.

    2017-02-01

    A method that enables visualization of lateral distribution of Li in thin films is described. The method is based on the simultaneous detection of the reaction products of the 6Li(n,α)t nuclear reaction with thermal neutrons measured with two multipixel detectors in a sandwich geometry with a sample. Here, the principle and basic methodological parameters of the method, including tests with thin polymers with known Li microstructure, are discussed.

  11. Tuning the Band Gap of Cu₂ZnSn(S,Se)₄ Thin Films via Lithium Alloying.

    Science.gov (United States)

    Yang, Yanchun; Kang, Xiaojiao; Huang, Lijian; Pan, Daocheng

    2016-03-02

    Alkali metal doping plays a crucial role in fabricating high-performance Cu(In,Ga)(S,Se)2 and Cu2ZnSn(S,Se)4 (CZTSSe) thin film solar cells. In this study, we report the first experimental observation and characterizations of the alloyed Li(x)Cu(2-x)ZnSn(S,Se)4 thin films. It is found that Cu(+) ions in Cu2ZnSn(S,Se)4 thin films can be substituted with Li(+) ions, forming homogeneous Li(x)Cu(2-x)ZnSn(S,Se)4 (0 ≤ x ≤ 0.29) alloyed thin films. Consequently, the band gap, conduction band minimum, and valence band maximum of Li(x)Cu(2-x)ZnSn(S,Se)4 thin films are profoundly affected by Li/Cu ratios. The band alignment at the Li(x)Cu(2-x)ZnSn(S,Se)4/CdS interface can be tuned by changing the Li/Cu ratio. We found that the photovoltaic parameters of the Li(x)Cu(2-x)ZnSn(S,Se)4 solar cell devices are strongly influenced by the Li/Cu ratios. Besides, the lattice constant, carrier concentration, and crystal growth of Li(x)Cu(2-x)ZnSn(S,Se)4 thin films were studied in detail.

  12. Growth of LiMn{sub 2}O{sub 4} thin films by pulsed-laser deposition and their electrochemical properties in lithium microbatteries

    Energy Technology Data Exchange (ETDEWEB)

    Julien, C. [Univ. Pierre et Marie Curie, Paris (France). LMDH; Haro-Poniatowski, E. [Laboratorio de Optica Cuantica, Universidad Autonoma Metropolitana Iztapalapa, Apdo. Postal 55-534, Mexico (Mexico); Camacho-Lopez, M.A. [LMDH, UMR 7603, Universite Pierre et Marie Curie, 4 place Jussieu, 75252, Paris (France); Escobar-Alarcon, L. [Departamento de Fisica, Instituto Nacional de Investigaciones Nucleares, Apdo. Postal 18-1027, Mexico (Mexico); Jimenez-Jarquin, J. [Laboratorio de Optica Cuantica, Universidad Autonoma Metropolitana Iztapalapa, Apdo. Postal 55-534, Mexico (Mexico)

    2000-03-01

    Films of LiMn{sub 2}O{sub 4} were grown by pulsed-laser deposition (PLD) onto silicon wafers using sintered targets which consisted in the mixture of LiMn{sub 2}O{sub 4} and Li{sub 2}O powders. The film formation has been studied as a function of the preparation conditions, i.e. composition of the target, substrate temperature, and oxygen partial pressure in the deposition chamber. Composition, morphology and structural properties of PLD films have been investigated using Rutherford backscattering spectroscopy, scanning electron microscopy, X-ray diffraction and Raman scattering spectroscopy. The films deposited from target LiMn{sub 2}O{sub 4}+15% Li{sub 2}O have an excellent crystallinity when deposited onto silicon substrate maintained at 300 C in an oxygen partial pressure of 100 mTorr. It is found that such a film crystallizes in the spinel structure (Fd3m symmetry) as evidenced by X-ray diffraction. Well-textured polycrystalline films exhibit crystallite size of 300 nm. Pulsed-laser deposited LiMn{sub 2}O{sub 4} thin films obtained with a polycrystalline morphology were successfully used as cathode materials in lithium microbatteries. The Li//LiMn{sub 2}O{sub 4} thin film cells have been tested by cyclic voltammetry and galvanostatic charge-discharge techniques in the potential range 3.0-4.2 V. Specific capacity as high as 120 mC/cm{sup 2} {mu}m was measured on polycrystalline films. The chemical diffusion coefficients for the Li{sub x}Mn{sub 2}O{sub 4} thin films appear to be in the range of 10{sup -11}-10{sup -12} cm{sup 2}/s. Electrochemical measurements show a good cycleability of PLD films when cells are charged-discharged at current densities of 5-25 {mu}A/cm{sup 2}. (orig.)

  13. Interfacial characteristics of a PEGylated imidazolium bistriflamide ionic liquid electrolyte at a lithium ion battery cathode of LiMn2O4.

    Science.gov (United States)

    Rock, Simon E; Wu, Lin; Crain, Daniel J; Krishnan, Sitaraman; Roy, Dipankar

    2013-03-01

    Nonvolatile and nonflammable ionic liquids (ILs) have distinct thermal advantages over the traditional organic solvent electrolytes of lithium ion batteries. However, this beneficial feature of ILs is often counterbalanced by their high viscosity (a limiting factor for ionic conductivity) and, sometimes, by their unsuitable electrochemistry for generating protective layers on electrode surfaces. In an effort to alleviate these limiting aspects of ILs, we have synthesized a PEGylated imidazolium bis(trifluoromethylsulfonyl)amide (bistriflamide) IL that exhibited better thermal and electrochemical stability than a conventional electrolyte based on a blend of ethylene carbonate and diethyl carbonate. The electrochemical performance of this IL has been demonstrated using a cathode consisting of ball-milled LiMn2O4 particles. A direct comparison of the ionic liquid electrolyte with the nonionic low-viscosity conventional solvent blend is presented.

  14. A long life 4 V class lithium-ion polymer battery with liquid-free polymer electrolyte

    Science.gov (United States)

    Kobayashi, Yo; Shono, Kumi; Kobayashi, Takeshi; Ohno, Yasutaka; Tabuchi, Masato; Oka, Yoshihiro; Nakamura, Tatsuya; Miyashiro, Hajime

    2017-02-01

    Ether-based solid polymer electrolyte (SPE) is one of the most well-known lithium ion conductors. Unlike the other inorganic electrolytes, SPE exhibits advantages of flexibility and large-area production, enabling low cost production of large size batteries. However, because the ether group is oxidized at 4 V versus Li/Li+ cathode, and due to its high irreversibility with the carbon anode, ether-based SPE was believed to be inapplicable to 4 V class lithium-ion batteries with carbon anode. Here we report a remarkably stable SPE in combination with a 4 V class cathode and carbon anode achieved by the proper design at the interface. The introduced boron-based lithium salt prohibits further oxidation of SPE at the cathode interface. The surface modification of graphite by the annealing of polyvinyl chloride mostly prohibits the continuous consumption of lithium at the graphite anode. Using above interface design, we achieved 60% capacity retention after 5400 cycles. The proposed battery provides a possible approach for realizing flammable electrolyte-free lithium-ion batteries, which achieve innovative safety improvements of large format battery systems for stationary use.

  15. Growth and decomposition of Lithium and Lithium hydride on Nickel

    DEFF Research Database (Denmark)

    Engbæk, Jakob; Nielsen, Gunver; Nielsen, Jane Hvolbæk

    2006-01-01

    In this paper we have investigated the deposition, structure and decomposition of lithium and lithium-hydride films on a nickel substrate. Using surface sensitive techniques it was possible to quantify the deposited Li amount, and to optimize the deposition procedure for synthesizing lithium......-hydride films. By only making thin films of LiH it is possible to study the stability of these hydride layers and compare it directly with the stability of pure Li without having any transport phenomena or adsorbed oxygen to obscure the results. The desorption of metallic lithium takes place at a lower...... temperature than the decomposition of the lithium-hydride, confirming the high stability and sintering problems of lithium-hydride making the storage potential a challenge. (c) 2006 Elsevier B.V. All rights reserved....

  16. Nanocrystalline SnO2:F thin films for liquid petroleum gas sensors.

    Science.gov (United States)

    Chaisitsak, Sutichai

    2011-01-01

    This paper reports the improvement in the sensing performance of nanocrystalline SnO(2)-based liquid petroleum gas (LPG) sensors by doping with fluorine (F). Un-doped and F-doped tin oxide films were prepared on glass substrates by the dip-coating technique using a layer-by-layer deposition cycle (alternating between dip-coating a thin layer followed by a drying in air after each new layer). The results showed that this technique is superior to the conventional technique for both improving the film thickness uniformity and film transparency. The effect of F concentration on the structural, surface morphological and LPG sensing properties of the SnO(2) films was investigated. Atomic Force Microscopy (AFM) and X-ray diffraction pattern measurements showed that the obtained thin films are nanocrystalline SnO(2) with nanoscale-textured surfaces. Gas sensing characteristics (sensor response and response/recovery time) of the SnO(2):F sensors based on a planar interdigital structure were investigated at different operating temperatures and at different LPG concentrations. The addition of fluorine to SnO(2) was found to be advantageous for efficient detection of LPG gases, e.g., F-doped sensors are more stable at a low operating temperature (300 °C) with higher sensor response and faster response/recovery time, compared to un-doped sensor materials. The sensors based on SnO(2):F films could detect LPG even at a low level of 25% LEL, showing the possibility of using this transparent material for LPG leak detection.

  17. Nanocrystalline SnO2:F Thin Films for Liquid Petroleum Gas Sensors

    Directory of Open Access Journals (Sweden)

    Sutichai Chaisitsak

    2011-07-01

    Full Text Available This paper reports the improvement in the sensing performance of nanocrystalline SnO2-based liquid petroleum gas (LPG sensors by doping with fluorine (F. Un-doped and F-doped tin oxide films were prepared on glass substrates by the dip-coating technique using a layer-by-layer deposition cycle (alternating between dip-coating a thin layer followed by a drying in air after each new layer. The results showed that this technique is superior to the conventional technique for both improving the film thickness uniformity and film transparency. The effect of F concentration on the structural, surface morphological and LPG sensing properties of the SnO2 films was investigated. Atomic Force Microscopy (AFM and X-ray diffraction pattern measurements showed that the obtained thin films are nanocrystalline SnO2 with nanoscale-textured surfaces. Gas sensing characteristics (sensor response and response/recovery time of the SnO2:F sensors based on a planar interdigital structure were investigated at different operating temperatures and at different LPG concentrations. The addition of fluorine to SnO2 was found to be advantageous for efficient detection of LPG gases, e.g., F-doped sensors are more stable at a low operating temperature (300 °C with higher sensor response and faster response/recovery time, compared to un-doped sensor materials. The sensors based on SnO2:F films could detect LPG even at a low level of 25% LEL, showing the possibility of using this transparent material for LPG leak detection.

  18. Sandwiched Thin-Film Anode of Chemically Bonded Black Phosphorus/Graphene Hybrid for Lithium-Ion Battery.

    Science.gov (United States)

    Liu, Hanwen; Zou, Yuqin; Tao, Li; Ma, Zhaoling; Liu, Dongdong; Zhou, Peng; Liu, Hongbo; Wang, Shuangyin

    2017-09-01

    A facile vacuum filtration method is applied for the first time to construct sandwich-structure anode. Two layers of graphene stacks sandwich a composite of black phosphorus (BP), which not only protect BP from quickly degenerating but also serve as current collector instead of copper foil. The BP composite, reduced graphene oxide coated on BP via chemical bonding, is simply synthesized by solvothermal reaction at 140 °C. The sandwiched film anode used for lithium-ion battery exhibits reversible capacities of 1401 mAh g(-1) during the 200th cycle at current density of 100 mA g(-1) indicating superior cycle performance. Besides, this facile vacuum filtration method may also be available for other anode material with well dispersion in N-methyl pyrrolidone (NMP). © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Three-dimensional architecture of lithium-anodes made from graphite fibers coated with thin-films of silicon oxycarbide: Design, performance and manufacturability

    Science.gov (United States)

    Saleh, Ibrahim; Raj, Rishi

    2016-04-01

    Silicon oxycarbide (SiCO) is an amorphous molecular network of Sisbnd Csbnd O tetrahedra anchored to graphene-like carbon. The graphene forms a three dimensional cellular network with a domain size of ∼5 nm. Therefore nanometer thick films of SiCO grown on graphite may be expected to have unusual behavior. We grow these films on a bed of commercially available graphite fibers that serve the dual function of a current collector. The electrochemical behavior of the composite is measured as a function of the thickness of the SiCO films. Thick films approach the typical behavior of bulk SiCO (which has three times the capacity of graphite, but suffers from poor first cycle efficiency). However, films, approximately 100 nm thick, show high first cycle efficiency as well as high capacity. The composite performs better than the prediction from the rule-of-mixtures, which further substantiates the unusual behavior of the thin-film architecture. The Raman spectra of these thin films also differ from bulk SiCO. The development of thin graphite fibers, with a high surface to volume ratio that have the same capacity as the current graphite-powder technology, coupled with manufacturing of these thin-films by a liquid-polymer precursor based process, can propel these results toward commercialization.

  20. Organic solar cells based on liquid crystalline and polycrystalline thin films

    Science.gov (United States)

    Yoo, Seunghyup

    This dissertation describes the study of organic thin-film solar cells in pursuit of affordable, renewable, and environmentally-friendly energy sources. Particular emphasis is given to the molecular ordering found in liquid crystalline or polycrystalline films as a way to leverage the efficiencies of these types of cells. Maximum efficiencies estimated based on excitonic character of organic solar cells show power conversion efficiencies larger than 10% are possible in principle. However, their performance is often limited due to small exciton diffusion lengths and poor transport properties which may be attributed to the amorphous nature of most organic semiconductors. Discotic liquid crystal (DLC) copper phthalocyanine was investigated as an easily processible building block for solar cells in which ordered molecular arrangements are enabled by a self-organization in its mesophases. An increase in photocurrent and a reduction in series resistance have been observed in a cell which underwent an annealing process. X-ray diffraction (XRD) and atomic force microscopy (AFM) measurements suggest that structural and morphological changes induced after the annealing process are related to these improvements. In an alternative approach, p-type pentacene thin films prepared by physical vapor deposition were incorporated into heterojunction solar cells with C60 as n-type layers. Power conversion efficiencies of 2.7% under broadband illumination (350--900 nm) with a peak external quantum efficiency of 58% have been achieved with the broad spectral coverage across the visible spectrum. Analysis using an exciton diffusion model shows this efficient carrier generation is mainly due to the large exciton diffusion length of pentacene films. Joint XRD and AFM studies reveal that the highly crystalline nature of pentacene films can account for the observed large exciton diffusion length. In addition, the electrical characteristics are studied as a function of light intensity using

  1. High-power electron beam tests of a liquid-lithium target and characterization study of (7)Li(p,n) near-threshold neutrons for accelerator-based boron neutron capture therapy.

    Science.gov (United States)

    Halfon, S; Paul, M; Arenshtam, A; Berkovits, D; Cohen, D; Eliyahu, I; Kijel, D; Mardor, I; Silverman, I

    2014-06-01

    A compact Liquid-Lithium Target (LiLiT) was built and tested with a high-power electron gun at Soreq Nuclear Research Center (SNRC). The target is intended to demonstrate liquid-lithium target capabilities to constitute an accelerator-based intense neutron source for Boron Neutron Capture Therapy (BNCT) in hospitals. The lithium target will produce neutrons through the (7)Li(p,n)(7)Be reaction and it will overcome the major problem of removing the thermal power >5kW generated by high-intensity proton beams, necessary for sufficient therapeutic neutron flux. In preliminary experiments liquid lithium was flown through the target loop and generated a stable jet on the concave supporting wall. Electron beam irradiation demonstrated that the liquid-lithium target can dissipate electron power densities of more than 4kW/cm(2) and volumetric power density around 2MW/cm(3) at a lithium flow of ~4m/s, while maintaining stable temperature and vacuum conditions. These power densities correspond to a narrow (σ=~2mm) 1.91MeV, 3mA proton beam. A high-intensity proton beam irradiation (1.91-2.5MeV, 2mA) is being commissioned at the SARAF (Soreq Applied Research Accelerator Facility) superconducting linear accelerator. In order to determine the conditions of LiLiT proton irradiation for BNCT and to tailor the neutron energy spectrum, a characterization of near threshold (~1.91MeV) (7)Li(p,n) neutrons is in progress based on Monte-Carlo (MCNP and Geant4) simulation and on low-intensity experiments with solid LiF targets. In-phantom dosimetry measurements are performed using special designed dosimeters based on CR-39 track detectors.

  2. Numerical Modeling of Thermocapillary Deformation and Film Breakdown in a Locally Heated Thin Horizontal Volatile Liquid Layer

    Directory of Open Access Journals (Sweden)

    Barakhovskaya Ella

    2016-01-01

    Full Text Available The problem of thermocapillary deformation and film breakdown in a thin horizontal layer of viscous incompressible liquid with a free surface is considered. The deformable liquid layer is locally heated. The problem of thermocapillary deformation of the locally heated horizontal liquid layer has been solved numerically for two-dimensional unsteady case. The lubrication approximation theory is used. Capillary pressure, viscosity and gravity are taken into account. Evaporating rate is supposed to be proportional to the temperature difference between the liquid and ambient. Heat transfer in the substrate is also simulated. The numerical algorithm for the joint solution of the energy equation and the evolution equation for the thickness of liquid layer has been developed. The model predicts the thermocapillary deformation of the liquid surface and the formation of dry spots. The dynamics of liquid surface, the dry spots formation and the velocity of the contact line have been calculated. The deformation of the free surface has been calculated for different values of the heating power and thickness of the liquid layer. The effect of surface tension coefficient and wetting contact angle on the velocity of the contact line motion has been analyzed. It has been obtained that the velocity of the contact line increases with the increase of the wetting contact angle value and of the surface tension coefficient.

  3. Preparation of Nano-Particles (Pb,La)TiO3 Thin Films by Liquid Source Misted Chemical Deposition

    Institute of Scientific and Technical Information of China (English)

    张之圣; 曾建平; 李小图

    2004-01-01

    Nano-particles lanthanum-modified lead titanate (PLT) thin films are grown on Pt/Ti/SiO2/Si substrate by liquid source misted chemical deposition (LSMCD). PLT films are deposited for 4-8 times, and then annealed at various temperature. XRD and SEM show that the prepared films have good crystallization behavior and perovskite structure. The crystallite is about 60 nm. The deposition speed is 3 nm/min. This deposition method can exactly control stoichiometry ratios, doping concentration ratio and thickness of PLT thin films. The best annealing process is to bake at 300 ℃ for 10 min and anneal at 600 ℃ for 1 h.

  4. Towards Li(Ni0.33Mn0.33Co0.33)O2/graphite batteries with ionic liquid-based electrolytes. I. Electrodes' behavior in lithium half-cells

    Science.gov (United States)

    Simonetti, E.; Maresca, G.; Appetecchi, G. B.; Kim, G.-T.; Loeffler, N.; Passerini, S.

    2016-11-01

    Lithium cells based on NMC cathodes or graphite anodes and ionic liquid-based electrolyte mixtures are investigated. The electrode tapes, using water-soluble natural binders, as well as the ionic liquid materials, are prepared through eco-friendly routes involving H2O as the only processing solvent. The Li/NMC and Li/graphite half-cells are studied by cyclic voltammetry, impedance spectroscopy and galvanostatic cycling tests at different temperatures. The results herein reported, demonstrate the performance improvement in terms of cycling behavior and ageing resistance, granted by the ionic liquid mixtures with respect to the electrolytes reported in literature based on a single ionic liquid.

  5. Long Term Effects of Multiple DBD Pulses on Thin Liquid Layers Over Tissue: Reactive Fluences and Electric Fields

    Science.gov (United States)

    Tian, Wei; Kushner, Mark J.

    2014-10-01

    Atmospheric dielectric barrier discharges (DBDs) are used in treatment of tissue, often covered by thin liquid layers. The reactivity reaching the tissue depends on the plasma dose, composition and acidification of the liquid, and the cumulative delivery of electric fields through the liquid. In this paper, we report on a computational investigation of the interaction of DBDs with a thin liquid layer covering tissue over many minutes. We used nonPDPSIM, a 2-d model in which Poisson's equation, the electron temperature equation, transport equations for charged and neutral species and radiation transport are solved in both the gas and liquid. The liquid layer, 100's μm thick, is water with dissolved gases [O2aq (aq is aqueous), CO2aq], metal ions (Feaq2+ , Feaq3+) , and organics (RHaq) . Hundreds of pulses at 100 Hz are computed, followed by minutes of afterglow. In the liquid, transient radicals (OHaq, Haq) are produced during the discharge pulse and are consumed during the interpulse period. Terminal species (H2O2aq, O3aq) accumulate and diffuse to the tissue. Ions are dominated by NO3-aq, O2-aq and H3Oaq+.Production of HNO3aq and HOONOaq is assisted by O2aq for the first pulses and then O3aq. Accumulating nitric acid lowers the pH. RHaq consumes most reactive oxygen species in the early plasma treatment leaving Raq. With longer exposure, RHaq can be consumed, enabling more ROS to reach the tissue. The cumulative exposure of electric fields to the tissue depends on the increasing conductivity of the liquid. Work supported by DOE Office of Fusion Energy Science and NSF.

  6. Near-Field Birefringence Response of Liquid Crystal Molecules in Thickness Direction of Liquid Crystal Thin Film Orientated by Shear Force

    Institute of Scientific and Technical Information of China (English)

    Jing QIN; Norihiro UMEDA

    2007-01-01

    Information of molecular orientation in nematic liquid crystal (LC) is attractive and important for applications in the field of display devices. We demonstrate a novel method using a birefringence scanning near-field optical microscope (Bi-SNOM) with a probe which is inserted into the LC thin film to detect the molecular orientation from its birefringence responses in the thickness direction of the LC thin film. The probe is laterally vibrated when going forward into the LC thin film, and the retardation and azimuth angle are recorded as the probe going down. Firstly, the thickness of the LC thin film is measured by the shear force detection. Since the shear force acts as a stimulation to reorientate the LC molecules above the substrate surface, we can detect the molecular orientation caused by a polyimide alignment substrate and the effect to molecular orientation caused by vibration of fibre probe. As a result, the orientation profiling of the LC film in depth direction is obtained in both the cases that the direction of probe vibrating is vertical/parallel to the rubbing direction of the alignment film.Furthermore, the thickness of completely orientated layers just above the substrate surface can also be obtained by either vibrating probe or no-vibrating probe. Ultimately, the LC thin film can be modelled in thickness direction from all the results using this method.

  7. Thin-film Nanofibrous Composite Membranes Containing Cellulose or Chitin Barrier Layers Fabricated by Ionic Liquids

    Energy Technology Data Exchange (ETDEWEB)

    H Ma; B Hsiao; B Chu

    2011-12-31

    The barrier layer of high-flux ultrafiltration (UF) thin-film nanofibrous composite (TFNC) membranes for purification of wastewater (e.g., bilge water) have been prepared by using cellulose, chitin, and a cellulose-chitin blend, regenerated from an ionic liquid. The structures and properties of regenerated cellulose, chitin, and a cellulose-chitin blend were analyzed with thermogravimetric analysis (TGA) and wide-angle X-ray diffraction (WAXD). The surface morphology, pore size and pore size distribution of TFNC membranes were determined by SEM images and molecular weight cut-off (MWCO) methods. An oil/water emulsion, a model of bilge water, was used as the feed solution, and the permeation flux and rejection ratio of the membranes were investigated. TFNC membranes based on the cellulose-chitin blend exhibited 10 times higher permeation flux when compared with a commercial UF membrane (PAN10, Sepro) with a similar rejection ratio after filtration over a time period of up to 100 h, implying the practical feasibility of such membranes for UF applications.

  8. Wrinkling of a thin film on a nematic liquid-crystal elastomer

    Science.gov (United States)

    Soni, Harsh; Pelcovits, Robert A.; Powers, Thomas R.

    2016-07-01

    Wrinkles commonly develop in a thin film deposited on a soft elastomer substrate when the film is subject to compression. Motivated by recent experiments [Agrawal et al., Soft Matter 8, 7138 (2012)], 10.1039/c2sm25734c that show how wrinkle morphology can be controlled by using a nematic elastomer substrate, we develop the theory of small-amplitude wrinkles of an isotropic film atop a nematic elastomer. The directors of the nematic elastomer are initially uniform. For uniaxial compression of the film along the direction perpendicular to the elastomer directors, the system behaves as a compressed film on an isotropic substrate. When the uniaxial compression is along the direction of nematic order, we find that the soft elasticity characteristic of liquid-crystal elastomers leads to a critical stress for wrinkling which is very small compared to the case of an isotropic substrate. We also determine the wavelength of the wrinkles at the critical stress and show how the critical stress and wavelength depend on substrate depth and the anisotropy of the polymer chains in the nematic elastomer.

  9. Wrinkling of a thin film on a nematic liquid-crystal elastomer.

    Science.gov (United States)

    Soni, Harsh; Pelcovits, Robert A; Powers, Thomas R

    2016-07-01

    Wrinkles commonly develop in a thin film deposited on a soft elastomer substrate when the film is subject to compression. Motivated by recent experiments [Agrawal et al., Soft Matter 8, 7138 (2012)]1744-683X10.1039/c2sm25734c that show how wrinkle morphology can be controlled by using a nematic elastomer substrate, we develop the theory of small-amplitude wrinkles of an isotropic film atop a nematic elastomer. The directors of the nematic elastomer are initially uniform. For uniaxial compression of the film along the direction perpendicular to the elastomer directors, the system behaves as a compressed film on an isotropic substrate. When the uniaxial compression is along the direction of nematic order, we find that the soft elasticity characteristic of liquid-crystal elastomers leads to a critical stress for wrinkling which is very small compared to the case of an isotropic substrate. We also determine the wavelength of the wrinkles at the critical stress and show how the critical stress and wavelength depend on substrate depth and the anisotropy of the polymer chains in the nematic elastomer.

  10. Advanced fabrication method for the preparation of MOF thin films: Liquid-phase epitaxy approach meets spin coating method.

    KAUST Repository

    Chernikova, Valeriya

    2016-07-14

    Here we report a new and advanced method for the fabrication of highly oriented/polycrystalline metal-organic framework (MOF) thin films. Building on the attractive features of the liquid-phase epitaxy (LPE) approach, a facile spin coating method was implemented to generate MOF thin films in a high-throughput fashion. Advantageously, this approach offers a great prospective to cost-effectively construct thin-films with a significantly shortened preparation time and a lessened chemicals and solvents consumption, as compared to the conventional LPE-process. Certainly, this new spin-coating approach has been implemented successfully to construct various MOF thin films, ranging in thickness from a few micrometers down to the nanometer scale, spanning 2-D and 3-D benchmark MOF materials including Cu2(bdc)2•xH2O, Zn2(bdc)2•xH2O, HKUST-1 and ZIF-8. This method was appraised and proved effective on a variety of substrates comprising functionalized gold, silicon, glass, porous stainless steel and aluminum oxide. The facile, high-throughput and cost-effective nature of this approach, coupled with the successful thin film growth and substrate versatility, represents the next generation of methods for MOF thin film fabrication. Thereby paving the way for these unique MOF materials to address a wide range of challenges in the areas of sensing devices and membrane technology.

  11. Advanced Fabrication Method for the Preparation of MOF Thin Films: Liquid-Phase Epitaxy Approach Meets Spin Coating Method.

    Science.gov (United States)

    Chernikova, Valeriya; Shekhah, Osama; Eddaoudi, Mohamed

    2016-08-10

    Here, we report a new and advanced method for the fabrication of highly oriented/polycrystalline metal-organic framework (MOF) thin films. Building on the attractive features of the liquid-phase epitaxy (LPE) approach, a facile spin coating method was implemented to generate MOF thin films in a high-throughput fashion. Advantageously, this approach offers a great prospective to cost-effectively construct thin-films with a significantly shortened preparation time and a lessened chemicals and solvents consumption, as compared to the conventional LPE-process. Certainly, this new spin-coating approach has been implemented successfully to construct various MOF thin films, ranging in thickness from a few micrometers down to the nanometer scale, spanning 2-D and 3-D benchmark MOF materials including Cu2(bdc)2·xH2O, Zn2(bdc)2·xH2O, HKUST-1, and ZIF-8. This method was appraised and proved effective on a variety of substrates comprising functionalized gold, silicon, glass, porous stainless steel, and aluminum oxide. The facile, high-throughput and cost-effective nature of this approach, coupled with the successful thin film growth and substrate versatility, represents the next generation of methods for MOF thin film fabrication. Therefore, paving the way for these unique MOF materials to address a wide range of challenges in the areas of sensing devices and membrane technology.

  12. Dynamic response of a thin sessile drop of conductive liquid to an abruptly applied or removed electric field

    Science.gov (United States)

    Corson, L. T.; Mottram, N. J.; Duffy, B. R.; Wilson, S. K.; Tsakonas, C.; Brown, C. V.

    2016-10-01

    We consider, both theoretically and experimentally, a thin sessile drop of conductive liquid that rests on the lower plate of a parallel-plate capacitor. We derive analytical expressions for both the initial deformation and the relaxation dynamics of the drop as the electric field is either abruptly applied or abruptly removed, as functions of the geometrical, electrical, and material parameters, and investigate the ranges of validity of these expressions by comparison with full numerical simulations. These expressions provide a reasonable description of the experimentally measured dynamic response of a drop of conductive ionic liquid 1-butyl-3-methyl imidazolium tetrafluoroborate.

  13. Solution-processed lithium-doped zinc oxide thin-film transistors at low temperatures between 100 and 300 °C

    Science.gov (United States)

    Liu, Fangmei; Qian, Chuan; Sun, Jia; Liu, Peng; Huang, Yulan; Gao, Yongli; Yang, Junliang

    2016-04-01

    Lithium-doped zinc oxide (Li-ZnO) thin-film transistors (TFTs) were fabricated by solution process at the low temperatures ranged from 100 to 300 °C. Li-ZnO TFTs fabricated at 300 °C under nitrogen condition showed a mobility of 1.2 cm2/Vs. Most importantly, the mobility of Li-ZnO TFT devices fabricated at 100 °C could be increased significantly from 0.08 to 0.4 cm2/Vs by using double spin-coated and UV irradiation-treated Li-ZnO film, and the on-/off-current ratio is in the order of 106. Notably, the XPS analyses proved that the performance improvement was originated from the chemical composition or stoichiometry evolution, in which the hydroxide was converted into metal oxide and accelerated the formation of the oxygen vacancies. Furthermore, low-voltage operating Li-ZnO TFTs were demonstrated by using a high-capacitance ion gel gate dielectrics. The Li-ZnO TFTs with an operating voltage as low as 2 V exhibited the carrier mobilities of 2.1 and 0.65 cm2/Vs for the devices treated at 300 and 100 °C, respectively. The low-temperature, solution-processed Li-ZnO TFTs showed greatly potential applications in flexible displays, smart label, and sensors.

  14. Super-aligned carbon nanotube films with a thin metal coating as highly conductive and ultralight current collectors for lithium-ion batteries

    Science.gov (United States)

    Wang, Ke; Wu, Yang; Wu, Hengcai; Luo, Yufeng; Wang, Datao; Jiang, Kaili; Li, Qunqing; Li, Yadong; Fan, Shoushan; Wang, Jiaping

    2017-05-01

    Cross-stacked super-aligned carbon nanotube (SACNT) films are promising for use as current collectors in lithium-ion batteries because of their outstanding capability to decrease the weight and thickness of inactive material and strong adhesion to the electrodes. However, the relatively poor conductivity of SACNT films may limit their application to large-size electrodes or at high current rate. Herein, a facile approach is proposed to improve the conductivity of SACNT films by electron-beam deposition of a thin metal film on their surface. Such modification lowers the sheet resistance by three orders of magnitude while keeping the extremely small fraction of SACNT current collectors. The metal-coated SACNT films strongly inhibit polarization during the electrochemical reaction, resulting in improved cell performance compared with that of metal and uncoated CNT current collectors. The improvement in conductivity and cell performance achieved by this approach is so large that the effect of the increase of inactive material is overwhelmed, leading to increased gravimetric energy density.

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

    Science.gov (United States)

    Chu, Hsun-Chen; Tuan, Hsing-Yu

    2017-04-01

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

  16. 3D strain engineered self-rolled thin-film architecture for high-energy density lithium-ion batteries

    Science.gov (United States)

    Godbey, Griffin; Gong, Chen; Yu, Cynthia; Blythe, Clayton; Leite, Marina

    Recently, multiple 3D geometries have been implemented into energy storage devices (e . g . nanowire anodes and arrays of interdigitated rods) in order to better accommodate the large volume expansion experienced by the anode during lithiation and to increase the structure energy density. However, most approached structures are difficult to scale up. Here we show how self-rolled thin-films can maintain a high energy density and can potentially accommodate the volume expansion suffered by the anode. The self-rolled tubes are fabricated by physical deposition of the active layers, creating a stress gradient between thin-film stack due to differences in coefficient of thermal expansion. Upon a sacrificial layer removal, the thin-film rolls to relieve this built-in stress. We predict the final dimension of self-rolled battery tubes using known elastic properties of materials commonly used as the active layers of the device. We will discuss an appropriate figure-of-merit that defines how the winding process can ultimately affect the volumetric capacity of 3D self-rolled batteries.

  17. The flow of a thin liquid film on a stationary and rotating disk. I - Experimental analysis and flow visualization

    Science.gov (United States)

    Thomas, S.; Faghri, A.; Hankey, W.

    1990-01-01

    The mean thickness of a thin liquid film of deionized water with a free surface on a stationary and rotating horizontal disk has been measured with a nonobtrusive capacitance technique. The measurements were taken when the rotational speed was 0-300 RPM and the flow rate was 7.0-15.0 LPM. A flow visualization study of the thin film was also performed to determine the characteristics of the waves on the free surface. When the disk was stationary, a circular hydraulic jump was present on the disk. Surface waves were found in the supercritical and subcritical regions at all flow rates studied. When the rotational speed of the disk is low, a standing wave at the edge of the disk was present. As the rotational speed increased, the surface waves changed from the wavy-laminar region to a region in which the waves ran nearly radially across the disk on top of a thin substrate of fluid.

  18. Atomistic modelling of evaporation and explosive boiling of thin film liquid argon over internally recessed nanostructured surface

    Science.gov (United States)

    Hasan, Mohammad Nasim; Shavik, Sheikh Mohammad; Rabbi, Kazi Fazle; Haque, Mominul

    2016-07-01

    Molecular dynamics (MD) simulations have been carried out to investigate evaporation and explosive boiling phenomena of thin film liquid argon on nanostructured solid surface with emphasis on the effect of solid-liquid interfacial wettability. The nanostructured surface considered herein consists of trapezoidal internal recesses of the solid platinum wall. The wetting conditions of the solid surface were assumed such that it covers both the hydrophilic and hydrophobic conditions and hence effect of interfacial wettability on resulting evaporation and boiling phenomena was the main focus of this study. The initial configuration of the simulation domain comprised of a three phase system (solid platinum, liquid argon and vapor argon) on which equilibrium molecular dynamics (EMD) was performed to reach equilibrium state at 90 K. After equilibrium of the three-phase system was established, the wall was set to different temperatures (130 K and 250 K for the case of evaporation and explosive boiling respectively) to perform non-equilibrium molecular dynamics (NEMD). The variation of temperature and density as well as the variation of system pressure with respect to time were closely monitored for each case. The heat flux normal to the solid surface was also calculated to illustrate the effectiveness of heat transfer for hydrophilic and hydrophobic surfaces in cases of both nanostructured surface and flat surface. The results obtained show that both the wetting condition of the surface and the presence of internal recesses have significant effect on normal evaporation and explosive boiling of the thin liquid film. The heat transfer from solid to liquid in cases of surface with recesses are higher compared to flat surface without recesses. Also the surface with higher wettability (hydrophilic) provides more favorable conditions for boiling than the low-wetting surface (hydrophobic) and therefore, liquid argon responds quickly and shifts from liquid to vapor phase faster in

  19. Magnetic Propulsion of Intense Lithium Streams in a Tokamak Magnetic Field

    Energy Technology Data Exchange (ETDEWEB)

    Leonid E. Zakharov

    2002-03-13

    The paper gives the theory of magnetic propulsion of liquid lithium streams and their stability in tokamaks. In the approximation of a thin flowing layer the MHD equations are reduced to one integro-differential equation which takes into account the propulsion effect, viscosity and the drag force due to magnetic pumping and other interactions with the magnetic field. A criterion is obtained for the stabilization of the ''sausage'' instability of the streams by centrifugal force.

  20. Imidazolium ionic liquid induced one-step synthesis of -Fe2O3 nanorods and nanorod assemblies for lithium-ion battery

    Directory of Open Access Journals (Sweden)

    Shuting Xie

    2016-12-01

    Full Text Available α-Fe2O3 nanorods and nanorod assemblies are prepared via a facile one-step method with the assistance of imidazolium-based ionic liquid. The aspect ratio of synthesized nanorods is determined by the alkyl chain length of [Cnmim]+. The inter-molecular π−π interaction and intra-molecular dipole-dipole interaction among imidazole rings of [C4mim]+[PhCOO]− play critical roles in both nucleation and assembly processes of α-Fe2O3 nanorods. The α-Fe2O3 nanorod assemblies show an excellent performance in lithium-ion batteries with a reversible capacity of 1007.3 mA h g−1 at the rate of 500 mA g−1 after 150 cycles.

  1. Lithium ion conducting PVdF-HFP composite gel electrolytes based on N-methoxyethyl- N-methylpyrrolidinium bis(trifluoromethanesulfonyl)-imide ionic liquid

    Science.gov (United States)

    Ferrari, S.; Quartarone, E.; Mustarelli, P.; Magistris, A.; Fagnoni, M.; Protti, S.; Gerbaldi, C.; Spinella, A.

    Blends of PVdF-HFP and ionic liquids (ILs) are interesting for application as electrolytes in plastic Li batteries. They combine the advantages of the gel polymer electrolytes (GPEs) swollen by conventional organic liquid electrolytes with the nonflammability, and high thermal and electrochemical stability of ILs. In this work we prepared and characterized PVdF-HFP composite membranes swollen with a solution of LiTFSI in ether-functionalized pyrrolidinium-imide ionic liquid (PYRA 12O1TFSI). The membranes were filled in with two different types of silica: (i) mesoporous SiO 2 (SBA-15) and (ii) a commercial nano-size one (HiSil™ T700). The ionic conductivity and the electrochemical properties of the gel electrolytes were studied in terms of the nature of the filler. The thermal and the transport properties of the composite membranes are similar. In particular, room temperature ionic conductivities higher than 0.25 mS cm -1 are easily obtained at defined filler contents. However, the mesoporous filler guarantees higher lithium transference numbers, a more stable electrochemical interface and better cycling performances. Contrary to the HiSil™-based membrane, the Li/LiFePO 4 cells with PVdF-HFP/PYRA 12O1TFSI-LiTFSI films containing 10 wt% of SBA-15 show good charge/discharge capacity, columbic efficiency close to unity, and low capacity losses at medium C-rates during 180 cycles.

  2. Research of cathode material LiCoO2 micro thin films lithium-ion batteries%微型薄膜锂离子电池正极材料LiCoO2薄膜研究

    Institute of Scientific and Technical Information of China (English)

    刘琦; 刘畅; 吴长青; 郭航

    2016-01-01

    As positive electrode material,LiCoO2 thin films used for all-solid-state thin film lithium ion microbattery are studied. The phase of LiCoO2 thin films are amorphous,it is fabricated by magnetron sputtering in low gas pressure and it changes to crystalline and array closely after annealed at 400 ℃ . The electrochemical properties of LiCoO2 thin-films are then investigated. The cyclic voltammetry and constant current charge-discharge tests indicate that the LiCoO2 thin films without annealed have no oxidation/ reduction peaks,which indicates that they do not have lithium-ion insertion/ extrusion of reversibility,while the LiCoO2 thin films after annealed have a good reversibility from the second lap. The prepared LiCoO2 thin films closely adhere to the substrate with good crystalline state,close texture and good cycling performance,can be used for all-solid-states thin film lithium-ion microbatteries.%研究了应用于微型全固态薄膜锂离子电池的正极材料钴酸锂 LiCoO2薄膜材料,采用磁控溅射法来制备,对其进行400℃退火处理后,进行 XRD 分析和 SEM 分析,表明在低气压条件下制备的薄膜呈非晶态,经过退火后,形成了排列致密的晶体结构,薄膜沿(003)晶面平行于基底择优生长;循环伏安测试和恒电流充放电测试表明,未经过退火处理的 LiCoO2薄膜不具有锂离子嵌入/脱出的可逆性,而经过退火处理的 LiCoO2薄膜从第二圈开始具有较好的可逆性。制备的 LiCoO2薄膜结晶状态优良、质地紧密、与衬底薄膜紧密接触、循环性能和循环充放电性能良好,可以用于微型全固态薄膜锂离子电池。

  3. Rechargeable lithium batteries based on Li{sub 1+x}V{sub 3}O{sub 8} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Bonino, F. [Dept. of Chemistry, Rome Univ. `La Sapienza` (Italy); Panero, S. [Dept. ICMMPM, Rome Univ. `La Sapienza` (Italy); Pasquali, M. [Dept. ICMMPM, Rome Univ. `La Sapienza` (Italy); Pistoia, G. [Centro di Studio per l`Elettrochimica e la Chimica Fisica delle Interfasi, CNR, Rome (Italy)

    1995-08-01

    Low-temperature thin films of Li{sub 1+x}V{sub 3}O{sub 8} have been fabricated and tested in LiClO{sub 4}/propylene carbonate-1,2-dimethoxyethane/Li cells. These cells show very good intercalation kinetics, and at 0.4 C discharge rate produce a specific energy of {approx}110 Wh/kg. The films could be used in microbatteries for electronic devices, and applications requiring more power could also be envisaged. (orig.)

  4. Numerical experiments on evaporation and explosive boiling of ultra-thin liquid argon film on aluminum nanostructure substrate

    Science.gov (United States)

    Wang, Weidong; Zhang, Haiyan; Tian, Conghui; Meng, Xiaojie

    2015-04-01

    Evaporation and explosive boiling of ultra-thin liquid film are of great significant fundamental importance for both science and engineering applications. The evaporation and explosive boiling of ultra-thin liquid film absorbed on an aluminum nanostructure solid wall are investigated by means of molecular dynamics simulations. The simulated system consists of three regions: liquid argon, vapor argon, and an aluminum substrate decorated with nanostructures of different heights. Those simulations begin with an initial configuration for the complex liquid-vapor-solid system, followed by an equilibrating system at 90 K, and conclude with two different jump temperatures, including 150 and 310 K which are far beyond the critical temperature. The space and time dependences of temperature, pressure, density number, and net evaporation rate are monitored to investigate the phase transition process on a flat surface with and without nanostructures. The simulation results reveal that the nanostructures are of great help to raise the heat transfer efficiency and that evaporation rate increases with the nanostructures' height in a certain range.

  5. Numerical experiments on evaporation and explosive boiling of ultra-thin liquid argon film on aluminum nanostructure substrate.

    Science.gov (United States)

    Wang, Weidong; Zhang, Haiyan; Tian, Conghui; Meng, Xiaojie

    2015-01-01

    Evaporation and explosive boiling of ultra-thin liquid film are of great significant fundamental importance for both science and engineering applications. The evaporation and explosive boiling of ultra-thin liquid film absorbed on an aluminum nanostructure solid wall are investigated by means of molecular dynamics simulations. The simulated system consists of three regions: liquid argon, vapor argon, and an aluminum substrate decorated with nanostructures of different heights. Those simulations begin with an initial configuration for the complex liquid-vapor-solid system, followed by an equilibrating system at 90 K, and conclude with two different jump temperatures, including 150 and 310 K which are far beyond the critical temperature. The space and time dependences of temperature, pressure, density number, and net evaporation rate are monitored to investigate the phase transition process on a flat surface with and without nanostructures. The simulation results reveal that the nanostructures are of great help to raise the heat transfer efficiency and that evaporation rate increases with the nanostructures' height in a certain range.

  6. Simultaneous determination of cyclodol and diprazin by thin layer chromatography and high performance liquid chromatography.

    Science.gov (United States)

    Makharadze, R; Adeishvili, L; Chelidze, T; Imnadze, N; Nizharadze, N

    2009-11-01

    Ciklodol (trihexyphenidil)--the central and peripheral m-cholinoblocker is currently used with other antipsychotic drugs such as phenotiazines and tricycle antidepressants. For the purpose of simultaneous determination of ciklodol and diprazine, were selected two methods of analysis: Thin Layer Chromatography (TLC) and High Performance Liquid Chromatography (HPLC). During development of TLC method was studied the 10 visualizing system and 24 mobile systems. For individual or simultaneous determination of ciklodol and diprazine were recommended the following solvents' systems: 1. Toluene-acetone-ethanole-25%NH(4)OH (45:45: 7.5:2.5), 2. Hexane-ethyl acetate (15:5), 3. Chloroform-heptene-25%NH(4)OH (16:3:3), 4. Ethylacetate-hexane (10:10), 5. Acetonitrile-metanol (10:10) and 6.Heptene-chloroform-ethanol-25% NH(4)OH (5:10:3:1). As visualizing systems were chosen: Iodine vapors, blacklight (UV254) and reagent of FNP. Reagent of FNP gives colored spot just with diprazine and it is also could be used for separation of both objects in simultaneous analysis. Developed HPLC method of simultaneous determination of ciklodol and diprazine: like mobile phase is recommended: Acetonitril- 0.05M KH(2)PO4 (55:45) (v/v) +H(3)PO(4) (pH3.5), column EC250 x 4.6mm, with solid phase Nucleosil, flow rate 1ml/min, sample volume 40 microl. In given conditions, the retention time of ciklodol is 6.005min and diprazine 7.227min. Developed method of simultaneous determination and separation of ciklodol and diprazine in respective mixtures could be successfully applied as in the pharmaceutical, as well in the chemical-toxicological laboratories.

  7. Effects of Surface Roughness of Capillary Wall on the Profile of Thin Liquid Film and Evaporation Heat Transfer

    Institute of Scientific and Technical Information of China (English)

    Qu Wei; Ma Tongze

    2001-01-01

    The surface of capillary wall can be treated to have a periodic microrelief mathematically. The roughness is micro enough compared with the thickness of the liquid film. So, the surface roughness only exerts influence on the adsorptive potential. Macroscopically, the flow field of the liquid film can be considered as that when the rough surface has an equivalent smooth surface, whose position is at the crests of the microrelief. The mechanism of heat transfer is in connection with two resistances: the thermal resistance of the liquid film conduction and the thermal resistance of the interfacial evaporation. The capillary pressure between the two sides of the vapor-liquid interface due to the interfacial curvature and the disjoining pressure owing to the thin liquid film are considered simultaneously. Several micro tubes with different micro rough surfaces are studied. The length of the evaporating interfacial region decreases with the increase of roughness angle and/or the increase of the roughness height. The heat transfer coefficient and the temperature of the vapor-liquid interface will change to fit the constant mass flow rate.

  8. Blacking of nano-CdS thin film from gas/liquid interface for enhanced photoelectrochemical performances

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Xiaoqing; Yin, Xiangle; Pu, Fang; Xia, Yue, E-mail: xiayue_chem@126.com; Huang, Wei; Li, Zelin, E-mail: lizelin@hunnu.edu.cn

    2014-09-15

    Graphical abstract: Thin films of CdS nanoparticles prepared rapidly at gas/liquid interface became black under visible light irradiation and exhibited enhanced photoelectrochemical performance in splitting water for hydrogen production in alkaline solution of methanol. - Highlights: • Thin films of CdS nanoparticles were facilely obtained at gas/liquid interface. • It involved reaction between CdCl{sub 2} and Na{sub 2}S and assembly of CdS nanoparticles. • The film became black under visible light irradiation in methanol alkaline solution. • The phase composition of the black film was characterized by HRTEM and XRD. • The black film exhibited enhanced PEC performance for H{sub 2}-production from water. - Abstract: Thin films of CdS nanoparticles were prepared rapidly at gas/liquid interface by dropping Na{sub 2}S ethanol solution onto CdCl{sub 2} solution surface with the help of a surfactant (dodecyl sulfate). The photoelectrochemical cell that comprised of the prepared thin film photoanode of CdS nanoparticles and a Pt cathode generated a photocurrent density as high as 2.8 mA cm{sup −2} at a bias voltage of 0.6 V under visible light illumination of 100 mW cm{sup −2} in an alkaline solution of methanol, which was larger than that in other solutions under investigation. It can be ascribed to methanol-assisted transformation of CdS nanoparticles into black Cd/Cd(OH){sub 2}/CdS nanocomposites. At 2.8 mA, the decrease of bias voltage reached 2.49 V for hydrogen production with a solar-to-electricity efficiency of 4.65%.

  9. Deposition and characterization of thin films of materials with application in cathodes for lithium rechargeable micro batteries; Deposito y caracterizacion de peliculas delgadas de materiales con aplicacion en catodos para microbaterias recargables de litio

    Energy Technology Data Exchange (ETDEWEB)

    Lopez I, J. [UAEM, Facultad de Quimica, 50000 Toluca, Estado de Mexico (Mexico)

    2007-07-01

    In this thesis work is reported the deposition and characterization of thin films of materials of the type LiMO{sub 2}, with M=Co and Ni, which have application in cathodes for micro-batteries of lithium ions. In the last years some investigators have reported that the electrochemical operation of the lithium ions batteries it can improve recovering the cathode, in bundle form, with some metal oxides as the Al{sub 2}O{sub 3}; for that the study of the formation of thin films in bilayer form LiMO{sub 2}/AI{sub 2}O{sub 3} is of interest in the development of lithium ions micro batteries. The thin films were deposited using the laser ablation technique studying the effect of some deposit parameters in the properties of the one formed material, as: laser fluence, substrate temperature and working atmosphere, with the purpose of optimizing it. In the case of the LiCoO{sub 2} it was found that to use an inert atmosphere of argon allows to obtain the material with the correct composition. Additionally, with the use of a temperature in the substrate of 150 C is possible to obtain to the material with certain crystallinity grade that to the subjected being to a post-deposit thermal treatment at 300 C for three hours, it gives as result a totally crystalline material. In the case of the thin films of LiNiO{sub 2}, it was necessary to synthesize the oxide starting from a reaction of solid state among nickel oxide (NiO) and lithium oxide (Li{sub 2}O) obtaining stoichiometric LiNiO{sub 2}. For the formation of the thin films of LiNiO{sub 2} it was used an argon atmosphere and the laser fluence was varied, the deposits were carried out to two different substrates temperatures, atmosphere and 160 C. In both cases the material it was recovered with an alumina layer, found that this layer didn't modify the structural properties of the base oxide (LiCoO{sub 2} and LiNiO{sub 2}). (Author)

  10. Atomic thin titania nanosheet-coupled reduced graphene oxide 2D heterostructures for enhanced photocatalytic activity and fast lithium storage

    Science.gov (United States)

    Li, Dong Jun; Huang, Zhegang; Hwang, Tae Hoon; Narayan, Rekha; Choi, Jang Wook; Kim, Sang Ouk

    2016-03-01

    Realizing practical high performance materials and devices using the properties of 2D materials is of key research interest in the materials science field. In particular, building well-defined heterostructures using more than two different 2D components in a rational way is highly desirable. In this paper, a 2D heterostructure consisting of atomic thin titania nanosheets densely grown on reduced graphene oxide surface is successfully prepared through incorporating polymer functionalized graphene oxide into the novel TiO2 nanosheets synthesis scheme. As a result of the synergistic combination of a highly accessible surface area and abundant interface, which can modulate the physicochemical properties, the resultant heterostructure can be used in high efficiency visible light photocatalysis as well as fast energy storage with a long lifecycle. [Figure not available: see fulltext.

  11. Electrolytic Manganese Dioxide Coatings on High Aspect Ratio Micro-Pillar Arrays for 3D Thin Film Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Yafa Zargouni

    2017-05-01

    Full Text Available In this work, we present the electrochemical deposition of manganese dioxide (MnO2 thin films on carbon-coated TiN/Si micro-pillars. The carbon buffer layer, grown by plasma enhanced chemical vapor deposition (PECVD, is used as a protective coating for the underlying TiN current collector from oxidation, during the film deposition, while improving the electrical conductivity of the stack. A conformal electrolytic MnO2 (EMD coating is successfully achieved on high aspect ratio C/TiN/Si pillar arrays by tailoring the deposition process. Lithiation/Delithiation cycling tests have been performed. Reversible insertion and extraction of Li+ through EMD structure are observed. The fabricated stack is thus considered as a good candidate not only for 3D micorbatteries but also for other energy storage applications.

  12. Nanostructured CuO thin film electrodes prepared by spray pyrolysis: a simple method for enhancing the electrochemical performance of CuO in lithium cells

    Energy Technology Data Exchange (ETDEWEB)

    Morales, J.; Sanchez, L. [Cordoba Univ. (Spain). Departamento de Qumica Inorganica e Ingenieria Quimica; Martin, F.; Ramos-Barrado, J.R.; Sanchez, M. [Malaga Univ. (Spain). Lab. de Materiales y Superficie

    2004-10-15

    Nanostructured CuO thin films were prepared by using a spray pyrolysis method, copper acetate as precursor and stainless steel as substrate. The textural and structural properties of the films were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The SEM images revealed thorough coating of the substrate and thickness of 450-1250 nm; the average particle size as determined from the AFM images ranged from 30 to 160 nm. The XRD patterns revealed the formation of CuO alone and the XPS spectra confirmed the presence of Cu{sup 2+} as the main oxidation state on the surface. The films were tested as electrodes in lithium cells and their electrochemical properties evaluated from galvanostatic and step potential electrochemical spectroscopy (SPES) measurements. The discharge STEP curves exhibited various peaks consistent with the processes CuO {r_reversible} Cu{sub 2}O {r_reversible}Cu and with decomposition of the electrolyte, a reversible process in the light of the AFM images. The best electrode exhibited capacity values of 625 Ah kg{sup -1} over more than 100 cycles. This value, which involves a CuO {r_reversible} Cu reversible global reaction, is Ca. 50% higher than that reported for bulk CuO. The nanosize of the particles and the good adherence of the active material to the substrate are thought to be the key factors accounting for the enhanced electrochemical activity found. (author)

  13. A Lithium Ion Highway by Surface Coordination Polymerization: In Situ Growth of Metal-Organic Framework Thin Layers on Metal Oxides for Exceptional Rate and Cycling Performance.

    Science.gov (United States)

    Han, Yuzhen; Yu, Danni; Zhou, Junwen; Xu, Peiyu; Qi, Pengfei; Wang, Qianyou; Li, Siwu; Fu, Xiaotao; Gao, Xing; Jiang, Chenghao; Feng, Xiao; Wang, Bo

    2017-08-25

    A thin layer of a highly porous metal-organic framework material, ZIF-8, is fabricated uniformly on the surface of nanostructured transition metal oxides (ZnO nanoflakes and MnO2 nanorods) to boost the transfer of lithium ions. The novel design and uniform microstructure of the MOF-coated TMOs (ZIF-8@TMOs) exhibit dramatically enhanced rate and cycling performance comparing to their pristine counterparts. The capacities of ZIF-8@ZnO (nanoflakes) and ZIF-8@MnO2 (nanorods) are 28 % and 31 % higher that of the pristine ones at the same current density. The nanorods of ZIF-8@MnO2 show a capacity of 1067 mAh g(-1) after 500 cycles at 1 Ag(-1) and without any fading. To further improve the conductivity and capacity, the ZIF-8-coated materials are pyrolyzed at 700 °C in an N2 atmosphere (ZIF-8@TMO-700 N). After pyrolysis, a much higher capacity improvement is achieved: ZIF-8@ZnO-700 N and ZIF-8@MnO2 -700 N have 54 % and 69 % capacity increases compared with the pristine TMOs, and at 1 Ag(-1) , the capacity of ZIF-8@MnO2 -700 N is 1060 mAh g(-1) after cycling for 300 cycles. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Structural evolution of bias sputtered LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} thin film cathodes for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Su, Shih-Hsuan, E-mail: minimono42@gmail.com [Department of Materials Science and Engineering, Feng Chia University, 100 Wenhwa Rd., Taichung 40724, Taiwan (China); Chiu, Kuo-Feng [Department of Materials Science and Engineering, Feng Chia University, 100 Wenhwa Rd., Taichung 40724, Taiwan (China); Leu, Hoang-Jyh [Department of Fiber and Composite Materials, Feng Chia University, 100 Wenhwa Rd., Taichung 40724, Taiwan (China)

    2014-12-01

    LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} (LNMO) thin films have been deposited on stainless steel substrates using radio frequency (f = 13.56 MHz) magnetron sputtering, followed by thermal annealing in ambient atmosphere. Various negative biases were applied on the substrates during deposition. The structural evolution of LNMO thin films under different negative biases has been investigated and characterized by X-ray diffraction. All of the deposited films exhibit a crystalline spinel structure with a space group of Fd-3m, which is a so-called disordered phase. The results also indicate that particle size decreases with increasing negative bias. The electrochemical properties of the LNMO thin films as cathode materials for lithium ion batteries were investigated. Two distinctive voltage plateaus at ∼ 4.7 V and at ∼ 4.0 V (vs. Li{sup +}/Li) can be observed in the discharge curves, corresponding to the reactions of the disordered phase. The capacity of LNMO thin film electrodes under suitable negative bias can be optimized. - Highlights: • LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} thin films have been deposited on stainless steel substrates. • Various negative biases were applied on the substrates during deposition. • The particle sizes of LNMO thin films decrease with increasing negative bias.

  15. Irreversible change of electric conduction in ionic-liquid-gated (La,Sr)MnO3 thin films

    Science.gov (United States)

    Lee, Tae Kwon; Jung, Jong Hoon

    2016-10-01

    We have investigated the ionic-liquid-gating effect on electric conduction in (La0.8Sr0.2)MnO3(LSMO) thin films. The gating effect is significant for the LSMO thin films grown at low oxygen partial pressures. We observed that the channel resistance of LSMO was altered only for a positive gating voltage, not for a negative one, mainly through the changes of mobility rather than the carrier density. The increased sheet resistance at positive voltage does not return to the original value even after the removal of gating voltage as well as the application of a negative voltage. Through the Mn 2 p X-ray absorption, the increased resistance of LSMO after a positive voltage is found to be associated with the increase of the Mn3+ ions over Mn4+ ones. We proposed that oxygen vacancy and electrochemical reactions should play a role for the irreversible electric conduction in ionic-liquid-gated (La,Sr)MnO3 thin films.

  16. Fabrication of composite thin films with microstructures of honeycomb, foam, and nanosphere arrays through adsorption and self-assembly of block copolymers at the liquid/liquid interface.

    Science.gov (United States)

    Liu, Yanan; Chen, Lifang; Geng, Yuanyuan; Lee, Yong-Ill; Li, Ying; Hao, Jingcheng; Liu, Hong-Guo

    2013-10-01

    The adsorption and self-organization behaviors of two kinds of block copolymers, polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) and poly(4-vinylpyridine)-block-polystyrene-block-poly(4-vinylpyridine) (P4VP-b-PS-b-P4VP), at planar liquid/liquid interfaces were investigated. A gel film decorating with honeycomb-like microstructures forms at the liquid/liquid interface between PS-b-P4VP chloroform solution and chloroauric acid aqueous solution. However, foam films were developed when the chloroauric acid aqueous solution was replaced by a chloroplatinic acid solution or a silver nitrate solution. Furthermore, a free-standing film containing the ordered arrays of nanospheres appeared at the liquid/liquid interface between P4VP-b-PS-b-P4VP chloroform solution and chloroauric acid aqueous solution. The formation of these microstructures was attributed to the adsorption of polymer molecules, combining with inorganic ions and the self-assembly of the composite species at the interface. The doped metal ions and complex ions were transformed to metal nanoparticles after further treatment. This is a facile and convenient method to prepare polymer/inorganic nanoparticle composites. These results also indicate the great influences of the polymer structures and the inorganic species in the aqueous phases on the self-assembly behaviors of the polymers at the interfaces, the final morphology, and structure of the composites. In addition, the formed thin composite films doped with well-dispersed, homogeneous small noble metal nanoparticles exhibit great and durable catalytic activities for the reduction of 4-nitrophenol (4-NP) by potassium borohydride.

  17. Effects of Ni doping on photocatalytic activity of TiO2 thin films prepared by liquid phase deposition technique

    Indian Academy of Sciences (India)

    Noor Shahina Begum; H M Farveez Ahmed; K R Gunashekar

    2008-10-01

    The TiO2 thin films doped by Ni uniformly and non-uniformly were prepared on glass substrate from an aqueous solution of ammonium hexa-fluoro titanate and NiF2 by liquid phase deposition technique. The addition of boric acid as an – scavenger will shift the equilibrium to one side and thereby deposition of the film is progressed. The rate of the reaction and the nature of deposition depend on growing time and temperature. The resultant films were characterized by XRD, EDAX, UV and SEM. The result shows that the deposited films have amorphous background, which becomes crystalline at 500°C. The EDAX data confirms the existence of Ni atoms in TiO2 matrix. XRD analysis reveals the peaks corresponding to Ni but no peak of crystalline NiO was found. The transmittance spectra of Ni uniformly and non-uniformly doped TiO2 thin films show `blue shift and red shift’, respectively. Ni-doped TiO2 thin films can be used as photocatalyst for the photodegradation of methyl orange dye. It was found that, organic dye undergoes degradation efficiently in presence of non-uniformly Ni-doped TiO2 thin films when compared to uniformly doped films and pure TiO2 films under visible light. The photocatalytic activity increases with increase in the concentration of Ni in case of nonuniformly doped thin films but decreases with the concentration when uniformly doped thin films were used.

  18. Evidence of extended solidlike layering in [Bmim][NTf2] ionic liquid thin films at room-temperature.

    Science.gov (United States)

    Bovio, Simone; Podestà, Alessandro; Lenardi, Cristina; Milani, Paolo

    2009-05-14

    We report the direct observation of solidlike ordering at room temperature of thin films of [Bmim][NTf2] ionic liquid on mica, amorphous silica, and oxidized Si(110). A statistical quantitative analysis of atomic force microscopy topographies shows that on these surfaces [Bmim][NTf2] forms layered structures, characterized by a perpendicular structural periodicity of approximately 0.6 nm. Remarkably, even the highest structures, up to 50 nm high, behave solidlike against the AFM probe. Conversely, on highly oriented pyrolitic graphite the ionic liquid forms nanometer-sized, liquidlike domains. The results of this study are directly relevant for those applications where ILs are employed in form of thin films supported on solid surfaces, such as in microelectromechanical or microelectronic devices. More generally, they suggest that at the liquid/solid interface the structural properties of ILs can be far more complex than those depicted so far, and prompt new fundamental investigations of the forces that drive supported ILs through a liquidlike-to-solidlike transition.

  19. Influence of the structure of the anion in an ionic liquid electrolyte on the electrochemical performance of a silicon negative electrode for a lithium-ion battery

    Science.gov (United States)

    Yamaguchi, Kazuki; Domi, Yasuhiro; Usui, Hiroyuki; Shimizu, Masahiro; Matsumoto, Kuninobu; Nokami, Toshiki; Itoh, Toshiyuki; Sakaguchi, Hiroki

    2017-01-01

    We investigated the influence of the anions in ionic liquid electrolytes on the electrochemical performance of a silicon (Si) negative electrode for a lithium-ion battery. While the electrode exhibited poor cycle stability in tetrafluoroborate-based and propylene carbonate-based electrolytes, better cycle performance was achieved in bis(fluorosulfonyl)amide (FSA-)- and bis(trifluoromethanesulfonyl)amide (TFSA-)-based electrolytes, in which the discharge capacity of a Si electrode was more than 1000 mA h g-1 at the 100th cycle. It is considered that a surface film derived from FSA-- and TFSA--based electrolytes effectively suppressed continuous decomposition of the electrolyte. In a capacity limitation test, a discharge capacity of 1000 mA h g-1 was maintained even after about the 1600th cycle in the FSA--based electrolyte, which corresponds to a cycle life almost twice as long as that in TFSA--based electrolyte. This result should be explained by the high structural stability of FSA--derived surface film. In addition, better rate capability with a discharge capacity of 700 mA h g-1 was obtained at a high current rate of 6 C (21 A g-1) in FSA--based electrolyte, which was 7-fold higher than that in TFSA--based electrolyte. These results clarified that FSA--based ionic liquid electrolyte is the most promising candidate for Si-based negative electrodes.

  20. Ionic Liquid-Organic Carbonate Electrolyte Blends To Stabilize Silicon Electrodes for Extending Lithium Ion Battery Operability to 100 °C.

    Science.gov (United States)

    Ababtain, Khalid; Babu, Ganguli; Lin, Xinrong; Rodrigues, Marco-Tulio F; Gullapalli, Hemtej; Ajayan, Pulickel M; Grinstaff, Mark W; Arava, Leela Mohana Reddy

    2016-06-22

    Fabrication of lithium-ion batteries that operate from room temperature to elevated temperatures entails development and subsequent identification of electrolytes and electrodes. Room temperature ionic liquids (RTILs) can address the thermal stability issues, but their poor ionic conductivity at room temperature and compatibility with traditional graphite anodes limit their practical application. To address these challenges, we evaluated novel high energy density three-dimensional nano-silicon electrodes paired with 1-methyl-1-propylpiperidinium bis(trifluoromethanesulfonyl)imide (Pip) ionic liquid/propylene carbonate (PC)/LiTFSI electrolytes. We observed that addition of PC had no detrimental effects on the thermal stability and flammability of the reported electrolytes, while largely improving the transport properties at lower temperatures. Detailed investigation of the electrochemical properties of silicon half-cells as a function of PC content, temperature, and current rates reveal that capacity increases with PC content and temperature and decreases with increased current rates. For example, addition of 20% PC led to a drastic improvement in capacity as observed for the Si electrodes at 25 °C, with stability over 100 charge/discharge cycles. At 100 °C, the capacity further increases by 3-4 times to 0.52 mA h cm(-2) (2230 mA h g(-1)) with minimal loss during cycling.

  1. Biological treatment of thin-film transistor liquid crystal display (TFT-LCD) wastewater.

    Science.gov (United States)

    Lei, C N; Whang, L M; Lin, H L

    2008-01-01

    The amount of pollutants produced during manufacturing processes of TFT-LCD (thin-film transistor liquid crystal display) substantially increases due to an increasing production of the opto-electronic industry in Taiwan. The total amount of wastewater from TFT-LCD manufacturing plants is expected to exceed 200,000 CMD in the near future. Typically, organic solvents used in TFT-LCD manufacturing processes account for more than 33% of the total TFT-LCD wastewater. The main components of these organic solvents are composed of the stripper (dimethyl sulphoxide (DMSO) and monoethanolamine (MEA)), developer (tetra-methyl ammonium hydroxide (TMAH)) and chelating agents. These compounds are recognized as non-or slow-biodegradable organic compounds and little information is available regarding their biological treatability. In this study, the performance of an A/O SBR (anoxic/oxic sequencing batch reactor) treating synthetic TFT-LCD wastewater was evaluated. The long-term experimental results indicated that the A/O SBR was able to achieve stable and satisfactory removal performance for DMSO, MEA and TMAH at influent concentrations of 430, 800, and 190 mg/L, respectively. The removal efficiencies for all three compounds examined were more than 99%. In addition, batch tests were conducted to study the degradation kinetics of DMSO, MEA, and TMAH under aerobic, anoxic, and anaerobic conditions, respectively. The organic substrate of batch tests conducted included 400 mg/L of DMSO, 250 mg/L of MEA, and 120 mg/L of TMAH. For DMSO, specific DMSO degradation rates under aerobic and anoxic conditions were both lower than 4 mg DMSO/g VSS-hr. Under anaerobic conditions, the specific DMSO degradation rate was estimated to be 14 mg DMSO/g VSS-hr, which was much higher than those obtained under aerobic and anoxic conditions. The optimum specific MEA and TMAH degradation rates were obtained under aerobic conditions with values of 26.5 mg MEA/g VSS-hr and 17.3 mg TMAH/g VSS

  2. III-Vs at Scale: A PV Manufacturing Cost Analysis of the Thin Film Vapor-Liquid-Solid Growth Mode

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Maxwell; Horowitz, Kelsey; Woodhouse, Michael; Battaglia, Corsin; Kapadia, Rehan; Javey, Ali

    2016-06-01

    The authors present a manufacturing cost analysis for producing thin-film indium phosphide modules by combining a novel thin-film vapor-liquid-solid (TF-VLS) growth process with a standard monolithic module platform. The example cell structure is ITO/n-TiO2/p-InP/Mo. For a benchmark scenario of 12% efficient modules, the module cost is estimated to be $0.66/W(DC) and the module cost is calculated to be around $0.36/W(DC) at a long-term potential efficiency of 24%. The manufacturing cost for the TF-VLS growth portion is estimated to be ~$23/m2, a significant reduction compared with traditional metalorganic chemical vapor deposition. The analysis here suggests the TF-VLS growth mode could enable lower-cost, high-efficiency III-V photovoltaics compared with manufacturing methods used today and open up possibilities for other optoelectronic applications as well.

  3. Low power optical limiting studies on nanocrystalline benzimidazole thin films prepared by modified liquid phase growth technique

    Indian Academy of Sciences (India)

    P A Praveen; S P Prabhakaran; R Ramesh Babu; K Sethuraman; K Ramamurthi

    2015-06-01

    In the present work, benzimidazole (BMZ), a well known nonlinear optical material, thin films were deposited using the modified liquid phase growth technique at different solution temperatures. The prepared samples were subjected to spectral, structural and surface analyses. Linear optical properties and third-order optical nonlinearity of the deposited BMZ thin films were analysed using UV–visible–NIR spectrum and -scan technique, respectively. The experimental results show that the BMZ films exhibit reverse saturable absorption and positive nonlinearity at 650 nm CW laser of power 5 mW. The measured third-order nonlinear susceptibility of the films is about 10−10 esu. Optical limiting studies were performed using the same laser source and the potentiality of the BMZ films is reported.

  4. Superacid-Based Lithium Salts For Polymer Electrolytes

    Science.gov (United States)

    Nagasubramanian, Ganesan; Prakash, Surya; Shen, David H.; Surampudi, Subbarao; Olah, George

    1995-01-01

    Solid polymer electrolytes exhibiting high lithium-ion conductivities made by incorporating salts of superacids into thin films of polyethylene oxide (PEO). These and other solid-polymer electrolytes candidates for use in rechargeable lithium-based electrochemical cells. Increases in room-temperature lithium-ion conductivities of solid electrolytes desirable because they increase achievable power and energy densities.

  5. Theoretical analysis based on fundamental functions of thin plate and experimental measurement for vibration characteristics of a plate coupled with liquid

    Science.gov (United States)

    Liao, Chan-Yi; Wu, Yi-Chuang; Chang, Ching-Yuan; Ma, Chien-Ching

    2017-04-01

    This study combined theoretical, experimental, and numerical analysis to investigate the vibration characteristics of a thin rectangular plate positioned horizontally at the bottom of a rectangular container filled with liquid. Flow field pressure was derived using an equation governing the behavior of incompressible fluids. Analytic solutions to vibrations in a thin plate in air served as the fundamental function of the thin plate coupled with liquid. We then used liquid pressure, and the out-of-plane deflection of the thin plate for the construction of frequency response functions for the analysis of vibration characteristics in the liquid-plate coupling system. Two experimental methods were employed to measure the vibration characteristics of the thin plate immersed in water. The first involved using sensors of polyvinylidene difluoride (PVDF) to measure transient signals of fluid-plate system subjected an impact at the thin plate. These were then converted to the frequency domain in order to obtain the resonant frequencies of the fluid-plate coupling system. The second method was amplitude-fluctuation electronic speckle pattern interferometry (AF-ESPI), which was used to measure the dynamic characteristics of the thin plate in the flow field. This method was paired with the image processing techniques, temporal speckle pattern interferometry (TSPI) and temporal standard deviation (TSTD), to obtain clear mode shapes of the thin plate and resonant frequencies. Comparison of the results from theoretical analysis, finite element method, and experimental measurements confirmed the accuracy of our theoretical analysis, which was superior to the conventional approach based on beam mode shape functions. The experimental methods proposed in this study can be used to measure the resonant frequencies of underwater thin plates, and clear mode shapes can be obtained using AF-ESPI. Our results indicate that the resonant frequencies of thin plates underwater are lower than

  6. Lithium Intoxication

    Directory of Open Access Journals (Sweden)

    Sermin Kesebir

    2011-09-01

    Full Text Available Lithium has been commonly used for the treatment of several mood disorders particularly bipolar disorder in the last 60 years. Increased intake and decreased excretion of lithium are the main causes for the development of lithium intoxication. The influence of lithium intoxication on body is evaluated as two different groups; reversible or irreversible. Irreversible damage is usually related with the length of time passed as intoxicated. Acute lithium intoxication could occur when an overdose of lithium is received mistakenly or for the purpose of suicide. Patients may sometimes take an overdose of lithium for self-medication resulting in acute intoxication during chronic, while others could develop chronic lithium intoxication during a steady dose treatment due to a problem in excretion of drug. In such situations, it is crucial to be aware of risk factors, to recognize early clinical symptoms and to conduct a proper medical monitoring. In order to justify or exclude the diagnosis, quantitative evaluation of lithium in blood and toxicologic screening is necessary. Following the monitoring schedules strictly and urgent intervention in case of intoxication would definitely reduce mortality and sequela related with lithium intoxication. In this article, the etiology, frequency, definition, clinical features and treatment approaches to the lithium intoxication have been briefly reviewed.

  7. A low-power all-optical bistable device based on a liquid crystal layer embedded in thin gold films

    Science.gov (United States)

    Takase, Yuki; Tien Thanh, Pham; Fujimura, Ryushi; Kajikawa, Kotaro

    2014-04-01

    An all-optical bistable (AOB) resonator device composed of a 430-nm-thick liquid crystal (LC) layer embedded in two thin gold films (MLM) is reported in this paper. This device allows the use of the incident illumination at normal incidence, whereas the previous AOB devices based on twisted nematic (TN)-LC function only for illumination at oblique incidence. The fastest switching time was measured to be 1.8 ms, which is significantly faster than that of TN-LC. Because the MLM device operates free from electronic circuits, it is promising for two-dimensional optical data processing, random access optical memories, and spatial light modulators.

  8. Separation of Berberine Hydrochloride and Tetrahydropalmatine and Their Quantitative Analysis with Thin Layer Chromatography Involved with Ionic Liquids

    Directory of Open Access Journals (Sweden)

    Jing Lu

    2015-01-01

    Full Text Available [BMIM]OH was used in mobile and stationary phase of thin layer chromatography (TLC to analyze berberine hydrochloride and tetrahydropalmatine for the first time. Supported imidazole ionic liquid with hydroxide ion on silica gel (SiO2·Im+·OH− was synthesized through simple procedure and characterized by Fourier transform infrared spectroscopy (FT-IR, elemental analysis, and scanning electron microscope (SEM. Moreover, on the plates prepared by SiO2·Im+·OH−, the contents of the above alkaloids in the Chinese patent medicine (CPM of “Stomacheasy” capsule were successfully determined by TLC scanner. The key conditions and chromatographic behaviors were also investigated in detail. According to similar ways, ionic liquids (ILs also can be used in other planar chromatographies in two modes. This study is expected to be helpful in expanding the application of IL and its bonded silica gel in TLC separation field.

  9. Lithium ion conducting PVdF-HFP composite gel electrolytes based on N-methoxyethyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)-imide ionic liquid

    Energy Technology Data Exchange (ETDEWEB)

    Ferrari, S.; Quartarone, E.; Mustarelli, P.; Magistris, A. [Dept. of Physical Chemistry, University of Pavia, Via Taramelli 16, 27100 Pavia (Italy); Fagnoni, M.; Protti, S. [Dept. of Organic Chemistry, University of Pavia, Via Taramelli 12, 27100 Pavia (Italy); Gerbaldi, C. [Dept. of Material Science and Chemical Engineering, Politecnico di Torino, C.so Duca degli Abruzzi, 24, 10129 Torino (Italy); Spinella, A. [Centro Grandi Apparecchiature - UniNetLab, University of Palermo, Via F. Marini 14, 90128 Palermo (Italy)

    2010-01-15

    Blends of PVdF-HFP and ionic liquids (ILs) are interesting for application as electrolytes in plastic Li batteries. They combine the advantages of the gel polymer electrolytes (GPEs) swollen by conventional organic liquid electrolytes with the nonflammability, and high thermal and electrochemical stability of ILs. In this work we prepared and characterized PVdF-HFP composite membranes swollen with a solution of LiTFSI in ether-functionalized pyrrolidinium-imide ionic liquid (PYRA{sub 12O1}TFSI). The membranes were filled in with two different types of silica: (i) mesoporous SiO{sub 2} (SBA-15) and (ii) a commercial nano-size one (HiSil trademark T700). The ionic conductivity and the electrochemical properties of the gel electrolytes were studied in terms of the nature of the filler. The thermal and the transport properties of the composite membranes are similar. In particular, room temperature ionic conductivities higher than 0.25 mS cm{sup -1} are easily obtained at defined filler contents. However, the mesoporous filler guarantees higher lithium transference numbers, a more stable electrochemical interface and better cycling performances. Contrary to the HiSil trademark -based membrane, the Li/LiFePO{sub 4} cells with PVdF-HFP/PYRA{sub 12O1}TFSI-LiTFSI films containing 10 wt% of SBA-15 show good charge/discharge capacity, columbic efficiency close to unity, and low capacity losses at medium C-rates during 180 cycles. (author)

  10. Molecular dynamics analysis of the effect of electronic polarization on the structure and single-particle dynamics of mixtures of ionic liquids and lithium salts.

    Science.gov (United States)

    Lesch, Volker; Montes-Campos, Hadrián; Méndez-Morales, Trinidad; Gallego, Luis Javier; Heuer, Andreas; Schröder, Christian; Varela, Luis M

    2016-11-28

    We report a molecular dynamics study on the effect of electronic polarization on the structure and single-particle dynamics of mixtures of the aprotic ionic liquid 1-ethyl-3-methylimidazolium bis-(trifluoromethylsulfonyl)-imide ([EMIM][TFSI]) doped with a lithium salt with the same anion at 298 K and 1 bar. In particular, we analyze the effect of electron density fluctuations on radial distribution functions, velocity autocorrelation functions, cage correlation functions, mean-squared displacements, and vibrational densities of states, comparing the predictions of the quantum-chemistry-based Atomistic Polarizable Potential for Liquids, Electrolytes, & Polymers (APPLE&P) with those of its nonpolarizable version and those of the standard non-polarizable Optimized Potentials for Liquid Simulations-All Atom (OPLS-AA). We found that the structure of the mixture is scarcely modified by the fluctuations in electron charge of their constituents, but their transport properties are indeed quite drastically changed, with larger mobilities being predicted for the different species in the bulk mixtures with the polarizable force field. Specifically, the mean-squared displacements are larger for the polarizable potentials at identical time intervals and the intermediate subdiffusive plateaus are greatly reduced, so the transition to the diffusive regime takes place much earlier than in the non-polarizable media. Moreover, the correlations of the added cations inside their cages are weakened out earlier and their vibrational densities of states are slightly red-shifted, reflecting the weakening effect of the electronic polarization on the Coulomb coupling in these dense ionic media. The comparison of OPLS-AA with non-polarizable APPLE&P indicates that adding polarization to OPLS-AA is not sufficient to achieve results close to experiments.

  11. Molecular dynamics analysis of the effect of electronic polarization on the structure and single-particle dynamics of mixtures of ionic liquids and lithium salts

    Science.gov (United States)

    Lesch, Volker; Montes-Campos, Hadrián; Méndez-Morales, Trinidad; Gallego, Luis Javier; Heuer, Andreas; Schröder, Christian; Varela, Luis M.

    2016-11-01

    We report a molecular dynamics study on the effect of electronic polarization on the structure and single-particle dynamics of mixtures of the aprotic ionic liquid 1-ethyl-3-methylimidazolium bis-(trifluoromethylsulfonyl)-imide ([EMIM][TFSI]) doped with a lithium salt with the same anion at 298 K and 1 bar. In particular, we analyze the effect of electron density fluctuations on radial distribution functions, velocity autocorrelation functions, cage correlation functions, mean-squared displacements, and vibrational densities of states, comparing the predictions of the quantum-chemistry-based Atomistic Polarizable Potential for Liquids, Electrolytes, & Polymers (APPLE&P) with those of its nonpolarizable version and those of the standard non-polarizable Optimized Potentials for Liquid Simulations-All Atom (OPLS-AA). We found that the structure of the mixture is scarcely modified by the fluctuations in electron charge of their constituents, but their transport properties are indeed quite drastically changed, with larger mobilities being predicted for the different species in the bulk mixtures with the polarizable force field. Specifically, the mean-squared displacements are larger for the polarizable potentials at identical time intervals and the intermediate subdiffusive plateaus are greatly reduced, so the transition to the diffusive regime takes place much earlier than in the non-polarizable media. Moreover, the correlations of the added cations inside their cages are weakened out earlier and their vibrational densities of states are slightly red-shifted, reflecting the weakening effect of the electronic polarization on the Coulomb coupling in these dense ionic media. The comparison of OPLS-AA with non-polarizable APPLE&P indicates that adding polarization to OPLS-AA is not sufficient to achieve results close to experiments.

  12. Ultrafast and scalable laser liquid synthesis of tin oxide nanotubes and its application in lithium ion batteries.

    Science.gov (United States)

    Liu, Zhikun; Cao, Zeyuan; Deng, Biwei; Wang, Yuefeng; Shao, Jiayi; Kumar, Prashant; Liu, C Richard; Wei, Bingqing; Cheng, Gary J

    2014-06-07

    Laser-induced photo-chemical synthesis of SnO2 nanotubes has been demonstrated by employing a nanoporous polycarbonate membrane as a template. The SnO2 nanotube diameter can be controlled by the nanoporous template while the nanotube length can be tuned by laser parameters and reaction duration. The microstructure characterization of the nanotubes indicates that they consist of mesoporous structures with sub 5 nm size nanocrystals connected by the twinning structure. The application of SnO2 nanotubes as an anode material in lithium ion batteries has also been explored, and they exhibited high capacity and excellent cyclic stability. The laser based emerging technique for scalable production of crystalline metal oxide nanotubes in a matter of seconds is remarkable. The compliance of the laser based technique with the existing technologies would lead to mass production of novel nanomaterials that would be suitable for several emerging applications.

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

    Energy Technology Data Exchange (ETDEWEB)

    Park, J.H.; Dragel, G. [Argonne National Lab., Chicago, IL (United States)

    1995-04-01

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

  14. New lithium gas sorbent

    Energy Technology Data Exchange (ETDEWEB)

    Chuntonov, K. [Nanoshell Materials R and D GmbH, Primoschgasse 3, 9020 Klagenfurt (Austria)], E-mail: konstantin@chuntonov.com; Setina, J. [Institute of Metals and Technology, 1000 Ljubljana (Slovenia); Ivanov, A.; Permikin, D. [Ural State University, Lenin Avenue 51, 620083 Ekaterinburg (Russian Federation)

    2008-07-28

    The kinetics of lithium evaporation from Ag-Li wire has been studied experimentally in the temperature interval 520-630 deg. C. The initial stage of the process takes place in the kinetic regime and finishes with the formation of a thin layer of silver on the surface of the alloy. Then the process moves to the diffusion region where the evaporation flow and the mass of the deposited film can be described quantitatively with the help of simple analytical expressions.

  15. Tunable terahertz fishnet metamaterials based on thin nematic liquid crystal layers for fast switching.

    Science.gov (United States)

    Zografopoulos, Dimitrios C; Beccherelli, Romeo

    2015-08-14

    The electrically tunable properties of liquid-crystal fishnet metamaterials are theoretically investigated in the terahertz spectrum. A nematic liquid crystal layer is introduced between two fishnet metallic structures, forming a voltage-controlled metamaterial cavity. Tuning of the nematic molecular orientation is shown to shift the magnetic resonance frequency of the metamaterial and its overall electromagnetic response. A shift higher than 150 GHz is predicted for common dielectric and liquid crystalline materials used in terahertz technology and for low applied voltage values. Owing to the few micron-thick liquid crystal cell, the response speed of the tunable metamaterial is calculated as orders of magnitude faster than in demonstrated liquid-crystal based non-resonant terahertz components. Such tunable metamaterial elements are proposed for the advanced control of electromagnetic wave propagation in terahertz applications.

  16. Accelerating rate calorimetry studies of the reactions between ionic liquids and charged lithium ion battery electrode materials

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yadong; Dahn, J.R. [Department of Physics and Atmospheric Science, Dalhousie University, Halifax, NS (Canada); Zaghib, K.; Guerfi, A. [Institut de Recherche d' Hydro-Quebec, 1800 Lionel-Boulet, Varennes, Que. (Canada); Bazito, Fernanda F.C.; Torresi, Roberto M. [Instituto de Quimica Universidade de Sao Paulo, CP 26077, 05513-970 Sao Paulo (Brazil)

    2007-06-30

    Using accelerating rate calorimetry (ARC), the reactivity between six ionic liquids (with and without added LiPF{sub 6}) and charged electrode materials is compared to the reactivity of standard carbonate-based solvents and electrolytes with the same electrode materials. The charged electrode materials used were Li{sub 1}Si, Li{sub 7}Ti{sub 4}O{sub 12} and Li{sub 0.45}CoO{sub 2}. The experiments showed that not all ionic liquids are safer than conventional electrolytes/solvents. Of the six ionic liquids tested, 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide (EMI-FSI) shows the worst safety properties, and is much worse than conventional electrolyte. 1-Ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) and 1-propyl-1-methylpyrrolidinium bis(fluorosulfonyl)imide (Py13-FSI) show similar reactivity to carbonate-based electrolyte. The three ionic liquids 1-butyl-2,3-dimethylimidazolium bis(trifluoromethanesulfonyl)imide (BMMI-TFSI), 1-butyl-1-methylpiperidinium bis(trifluoromethanesulfonyl)imide (Pp14-TFSI) and N-trimethyl-N-butylammonium bis(trifluoromethanesulfonyl)imide (TMBA-TFSI) show similar reactivity and are much safer than the conventional carbonate-based electrolyte. A comparison of the reactivity of ionic liquids with common anions and cations shows that ionic liquids with TFSI{sup -} are safer than those with FSI{sup -}, and liquids with EMI{sup +} are worse than those with BMMI{sup +}, Py13{sup +}, Pp14{sup +} and TMBA{sup +}. (author)

  17. Surface-induced solid-liquid phase transitions in ultra-thin water films at T > 0 ^oC

    Science.gov (United States)

    Chakraborty, Animesh; Gellman, Andrew; Baker, Layton; Broitman, Estebahn

    2008-03-01

    We report here the measurements of both the adsorption isotherms and the dissipation in ultra-thin films of water adsorbed on the surfaces of SiO2 . The measurements were made in a small high vacuum chamber in which we have mounted a QCM. The chamber was evacuated to ˜10-8 Torr and then filled with water vapor at pressures ranging from 10-3 -- 40 Torr (the vapor pressure of water at room temperature is ˜22 Torr). In addition the temperature of the apparatus can be varied in the range 10 -- 60^oC. This is sufficient to measure the adsorption isotherm and to probe the phase of adsorbed water films over the range of conditions. Recently published work studying the adsorption of water on the SiO2 layer formed on Si single crystals has suggested that the phase of the water at temperatures well above 0^oC is actually that of a solid, ice-like structure rather than liquid water [1]. That work is based on the comparison of the vibrational spectrum of thin water films with those of liquid water and ice. In our study we are using the QCM to investigate the possibility of formation of Ice-like structures on SiO2. [1] Asay, D. B. and Kim, S.H., Evolution of the Adsorbed Water Layer Structure on Silicon Oxide at Room Temperature. J. Phys. Chem. B. 2005, 109, 16760-16763

  18. Hydrogen, lithium, and lithium hydride production

    Science.gov (United States)

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

    2014-03-25

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

  19. CaO insulator and Be intermetallic coatings on V-base alloys for liquid-lithium fusion blanket applications

    Energy Technology Data Exchange (ETDEWEB)

    Park, J.H.; Kassner, T.F. [Argonne National Laboratory, Chicago, IL (United States)

    1996-04-01

    The objective of this study is to develop (a) stable CaO insulator coatings at the Liquid-Li/structural-material interface, with emphasis on electrically insulating coating that prevent adverse MHD-generated currents from passing through the V-alloy wall, and (b) stable Be-V intermetallic coating for first-wall components that face the plasma. Electrically insulating and corrosion-resistant coatings are required at the liquid-Li/structural interface in fusion first-wall/blanket application. The electrical resistance of CaO coatings produced on oxygen-enriched surface layers of V-5%Cr-5%Ti by exposing the alloy to liquid Li that contained 0.5-85 wt% dissolved Ca was measured as a function of time at temperatures between 250 and 600{degrees}C. Crack-free Be{sub 2}V intermetallic coatings were also produced by exposing V-alloys to liquid Li that contained Be as a solute. These techniques can be applied to various shapes (e.g., inside/outside of tubes, complex geometrical shapes) because the coatings are formed by liquid-phase reactions.

  20. Characterization and photocatalytic activity of boron-doped TiO2 thin films prepared by liquid phase deposition technique

    Indian Academy of Sciences (India)

    Noor Shahina Begum; H M Farveez Ahmed; O M Hussain

    2008-10-01

    Boron doped TiO2 thin films have been successfully deposited on glass substrate and silicon wafer at 30°C from an aqueous solution of ammonium hexa-fluoro titanate and boron trifluoride by liquid phase deposition technique. The boric acid was used as an – scavenger. The resultant films were characterized by XRD, EDAX, UV and microstructures by SEM. The result shows the deposited film to be amorphous which becomes crystalline between 400 and 500°C. The EDAX and XRD data confirm the existence of boron atom in TiO2 matrix and a small peak corresponding to rutile phase was also found. Boron doped TiO2 thin films can be used as photocatalyst for the photodegradation of chlorobenzene which is a great environmental hazard. It was found that chlorobenzene undergoes degradation efficiently in presence of boron doped TiO2 thin films by exposing its aqueous solution to visible light. The photocatalytic activity increases with increase in the concentration of boron.

  1. Lithium Poisoning

    DEFF Research Database (Denmark)

    Baird-Gunning, Jonathan; Lea-Henry, Tom; Hoegberg, Lotte C G

    2017-01-01

    is required. The cause of lithium poisoning influences treatment and 3 patterns are described: acute, acute-on-chronic, and chronic. Chronic poisoning is the most common etiology, is usually unintentional, and results from lithium intake exceeding elimination. This is most commonly due to impaired kidney...... function caused by volume depletion from lithium-induced nephrogenic diabetes insipidus or intercurrent illnesses and is also drug-induced. Lithium poisoning can affect multiple organs; however, the primary site of toxicity is the central nervous system and clinical manifestations vary from asymptomatic...... supratherapeutic drug concentrations to clinical toxicity such as confusion, ataxia, or seizures. Lithium poisoning has a low mortality rate; however, chronic lithium poisoning can require a prolonged hospital length of stay from impaired mobility and cognition and associated nosocomial complications. Persistent...

  2. Detection of chemical substances in water using an oxide nanowire transistor covered with a hydrophobic nanoparticle thin film as a liquid-vapour separation filter

    Science.gov (United States)

    Lim, Taekyung; Lee, Jonghun; Ju, Sanghyun

    2016-08-01

    We have developed a method to detect the presence of small amounts of chemical substances in water, using a Al2O3 nanoparticle thin film covered with phosphonic acid (HDF-PA) self-assembled monolayer. The HDF-PA self-assembled Al2O3 nanoparticle thin film acts as a liquid-vapour separation filter, allowing the passage of chemical vapour while blocking liquids. Prevention of the liquid from contacting the SnO2 nanowire and source-drain electrodes is required in order to avoid abnormal operation. Using this characteristic, the concentration of chemical substances in water could be evaluated by measuring the current changes in the SnO2 nanowire transistor covered with the HDF-PA self-assembled Al2O3 nanoparticle thin film.

  3. Detection of chemical substances in water using an oxide nanowire transistor covered with a hydrophobic nanoparticle thin film as a liquid-vapour separation filter

    Directory of Open Access Journals (Sweden)

    Taekyung Lim

    2016-08-01

    Full Text Available We have developed a method to detect the presence of small amounts of chemical substances in water, using a Al2O3 nanoparticle thin film covered with phosphonic acid (HDF-PA self-assembled monolayer. The HDF-PA self-assembled Al2O3 nanoparticle thin film acts as a liquid-vapour separation filter, allowing the passage of chemical vapour while blocking liquids. Prevention of the liquid from contacting the SnO2 nanowire and source-drain electrodes is required in order to avoid abnormal operation. Using this characteristic, the concentration of chemical substances in water could be evaluated by measuring the current changes in the SnO2 nanowire transistor covered with the HDF-PA self-assembled Al2O3 nanoparticle thin film.

  4. Analysis of gas absorption to a thin liquid film in the presence of a zero-order chemical reaction

    Science.gov (United States)

    Rajagopalan, S.; Rahman, M. M.

    1995-01-01

    The paper presents a detailed theoretical analysis of the process of gas absorption to a thin liquid film adjacent to a horizontal rotating disk. The film is formed by the impingement of a controlled liquid jet at the center of the disk and subsequent radial spreading of liquid along the disk. The chemical reaction between the gas and the liquid film can be expressed as a zero-order homogeneous reaction. The process was modeled by establishing equations for the conservation of mass, momentum, and species concentration and solving them analytically. A scaling analysis was used to determine dominant transport processes. Appropriate boundary conditions were used to solve these equations to develop expressions for the local concentration of gas across the thickness of the film and distributions of film height, bulk concentration, and Sherwood number along the radius of the disk. The partial differential equation for species concentration was solved using the separation of variables technique along with the Duhamel's theorem and the final analytical solution was expressed using confluent hypergeometric functions. Tables for eigenvalues and eigenfunctions are presented for a number of reaction rate constants. A parametric study was performed using Reynolds number, Ekman number, and dimensionless reaction rate as parameters. At all radial locations, Sherwood number increased with Reynolds number (flow rate) as well as Ekman number (rate of rotation). The enhancement of mass transfer due to chemical reaction was found to be small when compared to the case of no reaction (pure absorption), but the enhancement factor was very significant when compared to pure absorption in a stagnant liquid film. The zero-order reaction processes considered in the present investigation included the absorption of oxygen in aqueous alkaline solutions of sodiumdithionite and rhodium complex catalyzed carbonylation of methanol. Present analytical results were compared to previous theoretical

  5. Control of structure and growth of polymorphic crystalline thin films of amphiphilic molecules on liquid surfaces

    DEFF Research Database (Denmark)

    Weinbach, S.P.; Kjær, K.; Bouwman, W.G.;

    1994-01-01

    The spontaneous formation and coexistence of crystalline polymorphic trilayer domains in amphiphilic films at air-liquid interfaces is demonstrated by grazing incidence synchrotron x-ray diffraction. These polymorphic crystallites may serve as models for the early stages of crystal nucleation...... and growth, helping to elucidate the manner in which additives influence the progress of crystal nucleation, growth, and polymorphism and suggesting ways of selectively generating and controlling multilayers on liquid surfaces. Auxiliary molecules have been designed to selectively inhibit development...

  6. Quaternary ammonium room-temperature ionic liquid including an oxygen atom in side chain/lithium salt binary electrolytes: ab initio molecular orbital calculations of interactions between ions.

    Science.gov (United States)

    Tsuzuki, Seiji; Hayamizu, Kikuko; Seki, Shiro; Ohno, Yasutaka; Kobayashi, Yo; Miyashiro, Hajime

    2008-08-14

    Interactions of the lithium bis(trifluoromethylsulfonyl)amide (LiTFSA) complex with N, N-diethyl-N-methyl-N-(2-methoxyethyl) ammonium (DEME), 1-ethyl-3-methylimidazolium (EMIM) cations, neutral diethylether (DEE), and the DEMETFSA complex were studied by ab initio molecular orbital calculations. An interaction energy potential calculated for the DEME cation with the LiTFSA complex has a minimum when the Li atom has contact with the oxygen atom of DEME cation, while potentials for the EMIM cation with the LiTFSA complex are always repulsive. The MP2/6-311G**//HF/6-311G** level interaction energy calculated for the DEME cation with the LiTFSA complex was -18.4 kcal/mol. The interaction energy for the neutral DEE with the LiTFSA complex was larger (-21.1 kcal/mol). The interaction energy for the DEMETFSA complex with LiTFSA complex is greater (-23.2 kcal/mol). The electrostatic and induction interactions are the major source of the attraction in the two systems. The substantial attraction between the DEME cation and the LiTFSA complex suggests that the interaction between the Li cation and the oxygen atom of DEME cation plays important roles in determining the mobility of the Li cation in DEME-based room temperature ionic liquids.

  7. In situ SEM observation of the Si negative electrode reaction in an ionic-liquid-based lithium-ion secondary battery.

    Science.gov (United States)

    Tsuda, Tetsuya; Kanetsuku, Tsukasa; Sano, Teruki; Oshima, Yoshifumi; Ui, Koichi; Yamagata, Masaki; Ishikawa, Masashi; Kuwabata, Susumu

    2015-06-01

    By exploiting characteristics such as negligible vapour pressure and ion-conductive nature of an ionic liquid (IL), we established an in situ scanning electron microscope (SEM) method to observe the electrode reaction in the IL-based Li-ion secondary battery (LIB). When 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)amide ([C2mim][FSA]) with lithium bis(trifluoromethanesulfonyl)amide (Li[TFSA]) was used as the electrolyte, the Si negative electrode exhibited a clear morphology change during the charge process, without any solid electrolyte interphase (SEI) layer formation, while in the discharge process, the appearance was slightly changed, suggesting that a morphology change is irreversible in the charge-discharge process. On the other hand, the use of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ([C2mim][TFSA]) with Li[TFSA] did not induce a change in the Si negative electrode. It is interesting to note this distinct contrast, which could be attributed to SEI layer formation from the electrochemical breakdown of [C2mim](+) at the Si negative electrode|separator interface in the [C2mim][TFSA]-based LIB. This in situ SEM observation technique could reveal the effect of the IL species electron-microscopically on the Si negative electrode reaction.

  8. Effects of compatibility of polymer binders with solvate ionic liquid electrolytes on discharge and charge reactions of lithium-sulfur batteries

    Science.gov (United States)

    Nakazawa, Toshitada; Ikoma, Ai; Kido, Ryosuke; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi

    2016-03-01

    Electrochemical reactions in Li-S cells with a solvate ionic liquid (SIL) electrolyte composed of tetraglyme (G4) and Li[TFSA] (TFSA: bis(trifluoromethanesulfonyl)amide) are studied. The sulfur cathode (S cathode) comprises sulfur, carbon powder, and a polymer binder. Poly(ethylene oxide) (PEO) and poly(vinyl alcohol) (PVA-x) with different degrees of saponification (x%) are used as binders to prepare the composite cathodes. For the Li-S cell containing PEO binder, lithium polysulfides (Li2Sm, 2 ≤ m ≤ 8), reaction intermediates of the S cathode, dissolve into the electrolyte, and Li2Sm acts as a redox shuttle in the Li-S cell. In contrast, in the Li-S cell with PVA-x binder, the dissolution of Li2Sm is suppressed, leading to high columbic efficiencies during charge-discharge cycles. The compatibility of the PVA-x binder with the SIL electrolyte changes depending on the degree of saponification. Decreasing the degree of saponification leads to increased electrolyte uptake by the PVA-x binder, increasing the charge and discharge capacities of Li-S cell. The rate capability of Li-S cell is also enhanced by the partial swelling of the PVA-x binder. The enhanced performance of Li-S cell containing PVA-x is attributed to the lowering of resistance of Li+ ion transport in the composite cathode.

  9. One-pot synthesis of SnO{sub 2}/reduced graphene oxide nanocomposite in ionic liquid-based solution and its application for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Gu, Changdong, E-mail: cdgu@zju.edu.cn; Zhang, Heng; Wang, Xiuli; Tu, Jiangping

    2013-10-15

    Graphical abstract: - Highlights: • A facile and low-temperature method is developed for SnO{sub 2}/graphene composite. • Synthesis performed in a choline chloride-based ionic liquid. • The composite shows an enhanced cycling stability as anode for Li-ion batteries. • 4 nm SnO{sub 2} nanoparticles mono-dispersed on the surface of reduced graphene oxide. - Abstract: A facile and low-temperature method is developed for SnO{sub 2}/graphene composite which involves an ultrasonic-assistant oxidation–reduction reaction between Sn{sup 2+} and graphene oxide in a choline chloride–ethylene glycol based ionic liquid under ambient conditions. The reaction solution is non-corrosive and environmental-friendly. Moreover, the proposed technique does not require complicated infrastructures and heat treatment. The SnO{sub 2}/graphene composite consists of about 4 nm sized SnO{sub 2} nanoparticles with cassiterite structure mono-dispersed on the surface of reduced graphene oxide. As anode for lithium-ion batteries, the SnO{sub 2}/graphene composite shows a satisfying cycling stability (535 mAh g{sup −1} after 50 cycles @100 mA g{sup −1}), which is significantly prior to the bare 4 nm sized SnO{sub 2} nanocrsytals. The graphene sheets in the hybrid nanostructure could provide a segmentation effect to alleviate the volume expansion of the SnO{sub 2} and restrain the small and active Sn-based particles aggregating into larger and inactive clusters during cycling.

  10. Study of LiNiVO{sub 4} thin films used as anodes in lithium micro-batteries; Etude de couches minces de type LiNiVO{sub 4} utilisables en tant qu'electrode negative dans des microbatteries au lithium

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, V.

    2003-03-01

    Since fifteen years, considerable effort has been invested in developing thin film solid state micro-batteries as possible integrated components in microelectronics. The recent technological improvement concerning miniaturized systems opens a large field of applications for the future use of micro-batteries. LiNiVO{sub 4} thin films are promising materials as anodes for lithium micro-batteries. All the thin films have been prepared by radio-frequency magnetron sputtering using a LiNiVO{sub 4} target. The discharge gas was either pure argon or a mixture of argon and oxygen. We have studied the influence of some experimental parameters such as the oxygen partial pressure, the sputtering power, the target-substrate distance, the total pressure and the substrate temperature on the composition, the microstructure and the electrochemical properties. The chemical composition of the thin films has been determined by Rutherford backscattering spectroscopy combined with nuclear reaction analysis. Among all experimental parameters investigated, only the partial pressure of oxygen has a considerable influence on the thin film composition. Auger spectroscopy has revealed a good homogeneity of the thin films. X-ray diffraction shows that the as-deposited thin films are amorphous. The near-stoichiometric composition Li{sub 1.12}NiV{sub 1.02}O{sub 4}.11 has highlighted good electrochemical properties in the potential range [3 V - 0.02 V]. This particular composition displays a high capacity of 1000 mAh/g which is enhanced when the film is annealed at 300 degrees C. (author)

  11. Liquid phase epitaxy and optical investigation of KYb(WO4)2 thin layers

    NARCIS (Netherlands)

    Romanyuk, Y.E.; Ehrentraut, D.; Aznar, A.; Sole, R.; Aguilo, M.; Gerner, P.; Güdel, H.U.; Pollnau, M.

    2003-01-01

    In recent years, Yb3+ has attracted much attention as an activating ion because of its small quantum defect for laser emission from 2F5/2 to 2F7/2 at ~1.03 µm [1], which provides high efficiency and reduced heat generation. Of high practical interest is the thin-disk laser concept [2], which possess

  12. Testing automated liquid-based cytology samples with a manual liquid-based cytology method using residual cell suspensions from 500 ThinPrep cases.

    Science.gov (United States)

    Maksem, John A; Dhanwada, Vijaya; Trueblood, Joy E; Weidmann, James; Kane, Bruce; Bolick, David R; Bedrossian, Carlos W M; Kurtycz, Daniel F I; Stewart, Jim

    2006-06-01

    We report a technical improvement upon a previously disclosed manual liquid-based cytology (MLBC) method; and, we use the improved method to prepare slides from residual ThinPrep specimens in order to see how often ThinPrep diagnoses correspond to diagnoses derived from exhaustive examination of their parent sample suspensions. Residual cell suspensions from 500 ThinPrep cases comprising (1) 20 low-grade squamous intraepithelial lesions (LSILs); (2) 200 high risk (HR) negatives and 20 ASC-US; and (3) 260 screening cytology specimens were studied. Institutional review committee guidelines allowed us to know diagnoses by groups of specimens, but did not allow us to know individual patient diagnoses, so we could not perform case-by-case matched outcome-comparisons. Cells were concentrated by conventional centrifugation and sedimented into a polymer gel that was then vortex-mixed and converted into a viscous cell-rich suspension. The cell suspension was smeared between two clean glass slides, which were air-dried and stained with the Papanicolaou stain. Two study-sets were created, comprising one slide from each case. Each of the two study sets was examined by two cytopathologists, and discordant diagnoses were adjudicated. Because of the ambiguity involved in the "atypical" (ASC-US, ASC-H, AGC) diagnosis categories, only outcomes at the level of LSIL or greater were recorded. All MLBC SILs were digitally imaged and abnormal slides plus digital images were sent to the laboratory that provided the residual automated liquid-based cytology (ALBC) suspensions. The final diagnoses were confirmed by the laboratory that provided the residual ALBC specimens. MLBC slides of the 20 LSIL cases afforded 2 high-grade squamous intraepithelial lesions (HSILs) and 18 LSILs. Those of the 200 HR-Negatives showed 3 HSILs and 30 LSILs; and those of the 20 HR-ASC-US showed 3 HSILs and 9 LSILs. MLBC slides of the 260 screening cytology specimens showed 1 Carcinoma, 3 HSILs and 20 LSILs

  13. Studying the Dynamics of Breakdown of Thin Horizontal Liquid Layers with Local Heating

    Directory of Open Access Journals (Sweden)

    Spesivtsev Serafim

    2016-01-01

    Full Text Available Experimental study of liquid layers breakdown when heated locally from the substrate side was made. Water and ethanol were used as working liquids with a layer thickness of 300 μm. Basic steps of the breakdown process were found and mean velocities of the dry spot formation were determined; the values are 0.06 mm/sec for ethanol and 5.15 mm/sec for water. The formation of residual layer over the hot-spot before the breakdown has been found for both liquids. The creation of a droplet cluster near the heating region is observed when using water as a working fluid. It was shown that evaporation is one of the general factors influencing the process of layer breakdown and dry spot formation as well as thermocapillary effect.

  14. Janus Solid-Liquid Interface Enabling Ultrahigh Charging and Discharging Rate for Advanced Lithium-Ion Batteries.

    Science.gov (United States)

    Zheng, Jiaxin; Hou, Yuyang; Duan, Yandong; Song, Xiaohe; Wei, Yi; Liu, Tongchao; Hu, Jiangtao; Guo, Hua; Zhuo, Zengqing; Liu, Lili; Chang, Zheng; Wang, Xiaowei; Zherebetskyy, Danylo; Fang, Yanyan; Lin, Yuan; Xu, Kang; Wang, Lin-Wang; Wu, Yuping; Pan, Feng

    2015-09-09

    LiFePO4 has long been held as one of the most promising battery cathode for its high energy storage capacity. Meanwhile, although extensive studies have been conducted on the interfacial chemistries in Li-ion batteries,1-3 little is known on the atomic level about the solid-liquid interface of LiFePO4/electrolyte. Here, we report battery cathode consisted with nanosized LiFePO4 particles in aqueous electrolyte with an high charging and discharging rate of 600 C (3600/600 = 6 s charge time, 1 C = 170 mAh g(-1)) reaching 72 mAh g(-1) energy storage (42% of the theoretical capacity). By contrast, the accessible capacity sharply decreases to 20 mAh g(-1) at 200 C in organic electrolyte. After a comprehensive electrochemistry tests and ab initio calculations of the LiFePO4-H2O and LiFePO4-EC (ethylene carbonate) systems, we identified the transient formation of a Janus hydrated interface in the LiFePO4-H2O system, where the truncated symmetry of solid LiFePO4 surface is compensated by the chemisorbed H2O molecules, forming a half-solid (LiFePO4) and half-liquid (H2O) amphiphilic coordination environment that eases the Li desolvation process near the surface, which makes a fast Li-ion transport across the solid/liquid interfaces possible.

  15. The bridge between thin layer chromatography-mass spectrometry and high-performance liquid chromatography-mass spectrometry: The realization of liquid thin layer chromatography-mass spectrometry (LTLC-MS).

    Science.gov (United States)

    Li, Yafeng; Wang, Jianing; Zhan, Lingpeng; Wleklinski, Michael; Wang, Jiyun; Xiong, Caiqiao; Liu, Huihui; Zhou, Yueming; Nie, Zongxiu

    2016-08-19

    The combination of thin layer chromatography (TLC) and mass spectrometry (MS) has been studied for decades, but for most cases MS detection is done after TLC separation is finished. Here, an online simultaneous TLC-MS analysis system, liquid thin layer chromatography-mass spectrometry (LTLC-MS), is developed which successfully synchronize TLC separation process and MS detection process like GC-MS and HPLC-MS do. And there's no need to use specially designed TLC, just regular TLC plates are enough. LTLC-MS method is composed of a newly developed ambient ionization method, glow discharge-matrix assisted infrared desorption ionization (GD-MAIRDI), and forced-flow TLC (FFTLC) technique, which guarantees the MS detection process does not disturb the TLC separation process throughout the whole analysis. The whole LTLC-MS analysis only need two steps and less than 15min. Mixtures as well as the two main components of a pain relief pills have been successfully analyzed by LTLC-MS. This proof of concept study opens up new possibilities of combining TLC with MS, and will further broaden the application abilities of TLC.

  16. A thin film degradation study of a fluorinated polyether liquid lubricant using an HPLC method

    Science.gov (United States)

    Morales, W.

    1986-01-01

    A High Pressure Liquid Chromatography (HPLC) separation method was developed to study and analyze a fluorinated polyether fluid which is promising liquid lubricant for future applications. This HPLC separation method was used in a preliminary study investigating the catalytic effect of various metal, metal alloy, and ceramic engineering materials on the degradation of this fluid in a dry air atmosphere at 345 C. Using a 440 C stainless steel as a reference catalytic material it was found that a titanium alloy and a chromium plated material degraded the fluorinated polyether fluid substantially more than the reference material.

  17. Qualitative Behaviour of Solutions in Two Models of Thin Liquid Films

    Directory of Open Access Journals (Sweden)

    Matthew Michal

    2016-01-01

    Full Text Available For the thin-film model of a viscous flow which originates from lubrication approximation and has a full nonlinear curvature term, we prove existence of nonnegative weak solutions. Depending on initial data, we show algebraic or exponential dissipation of an energy functional which implies dissipation of the solution arc length that is a well known property for a Hele-Shaw flow. For the classical thin-film model with linearized curvature term, under some restrictions on parameter and gradient values, we also prove analytically the arc length dissipation property for positive solutions. We compare the numerical solutions for both models, with nonlinear and with linearized curvature terms. In regimes when solutions develop finite time singularities, we explain the difference in qualitative behaviour of solutions.

  18. Liquid film condensation along a vertical surface in a thin porous medium with large anisotropic permeability

    OpenAIRE

    Sanya, Arthur S O; Akowanou, Christian; Sanya, Emile A; Degan, Gerard

    2014-01-01

    The problems of steady film condensation on a vertical surface embedded in a thin porous medium with anisotropic permeability filled with pure saturated vapour are studied analytically by using the Brinkman-Darcy flow model. The principal axes of anisotropic permeability are oriented in a direction that non-coincident with the gravity force. On the basis of the flow permeability tensor due to the anisotropic properties and the Brinkman-Darcy flow model adopted by considering negligible macros...

  19. Lithium nephrotoxicity.

    Science.gov (United States)

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

    2010-01-01

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

  20. Gelled Electrolytes For Lithium Batteries

    Science.gov (United States)

    Nagasubramanian, Ganesan; Attia, Alan; Halpert, Gerald

    1993-01-01

    Gelled polymer electrolyte consists of polyacrylonitrile (PAN), LiBF4, and propylene carbonate (PC). Thin films of electrolyte found to exhibit stable bulk conductivities of order of 10 to the negative 3rd power S/cm at room temperature. Used in thinfilm rechargeable lithium batteries having energy densities near 150 W h/kg.

  1. Numerical simulation of fluid flow and heat transfer in a thin liquid film over a rotating disk

    Science.gov (United States)

    Rahman, M. M.; Faghri, A.

    1992-01-01

    The results of a numerical simulation of the flow field and associated heat transfer coefficient are presented for the free surface flow of a thin liquid film adjacent to a horizontal rotating disk. The computation has been performed for different flow rates and rotational velocities using a three-dimensional boundary-fitted coordinate system. Since the geometry of the free surface is unknown and dependent on flow rate, rate of rotation, and other parameters, an interative procedure had to be used to ascertain its location. The computed film height agreed well with existing experimental measurements. The flow was dominated by inertia near the entrance and close to the free surface, and dominated by centrifugal force at larger radii and adjacent to the disk. The rotation enhanced the heat transfer coefficient by a significant amount.

  2. Hairy foam : thin layers of carbon nanofibers as catalyst support for liquid phase reactions

    NARCIS (Netherlands)

    Chinthaginjala, Jitendra Kumar

    2010-01-01

    Catalytic multiphase reactors are at the heart of many chemical industries. They allow efficient contact between gas and/or liquid reactant phases with solid catalysts increasing reaction rates. In practice, the higher reaction rates can be taken advantage of only under the condition that the transf

  3. Hairy foam : thin layers of carbon nanofibers as catalyst support for liquid phase reactions

    NARCIS (Netherlands)

    Chinthaginjala, J.K.

    2010-01-01

    Catalytic multiphase reactors are at the heart of many chemical industries. They allow efficient contact between gas and/or liquid reactant phases with solid catalysts increasing reaction rates. In practice, the higher reaction rates can be taken advantage of only under the condition that the

  4. Accuracy of reading liquid based cytology slides using the ThinPrep Imager compared with conventional cytology: prospective study

    Science.gov (United States)

    d'Assuncao, Jefferson; Irwig, Les; Macaskill, Petra; Chan, Siew F; Richards, Adele; Farnsworth, Annabelle

    2007-01-01

    Objective To compare the accuracy of liquid based cytology using the computerised ThinPrep Imager with that of manually read conventional cytology. Design Prospective study. Setting Pathology laboratory in Sydney, Australia. Participants 55 164 split sample pairs (liquid based sample collected after conventional sample from one collection) from consecutive samples of women choosing both types of cytology and whose specimens were examined between August 2004 and June 2005. Main outcome measures Primary outcome was accuracy of slides for detecting squamous lesions. Secondary outcomes were rate of unsatisfactory slides, distribution of squamous cytological classifications, and accuracy of detecting glandular lesions. Results Fewer unsatisfactory slides were found for imager read cytology than for conventional cytology (1.8% v 3.1%; Pcytology (7.4% v 6.0% overall and 2.8% v 2.2% for cervical intraepithelial neoplasia of grade 1 or higher). Among 550 patients in whom imager read cytology was cervical intraepithelial neoplasia grade 1 or higher and conventional cytology was less severe than grade 1, 133 of 380 biopsy samples taken were high grade histology. Among 294 patients in whom imager read cytology was less severe than cervical intraepithelial neoplasia grade 1 and conventional cytology was grade 1 or higher, 62 of 210 biopsy samples taken were high grade histology. Imager read cytology therefore detected 71 more cases of high grade histology than did conventional cytology, resulting from 170 more biopsies. Similar results were found when one pathologist reread the slides, masked to cytology results. Conclusion The ThinPrep Imager detects 1.29 more cases of histological high grade squamous disease per 1000 women screened than conventional cytology, with cervical intraepithelial neoplasia grade 1 as the threshold for referral to colposcopy. More imager read slides than conventional slides were satisfactory for examination and more contained low grade cytological

  5. Indium oxide thin film prepared by low temperature atomic layer deposition using liquid precursors and ozone oxidant

    Energy Technology Data Exchange (ETDEWEB)

    Maeng, W.J. [Department of Materials Science and Engineering, University of Wisconsin Madison, Madison, WI 53706 (United States); Choi, Dong-Won [Division of Materials Science and Engineering, 222 Wangsimni-ro, Seongdong-gu, Hanyang University, Seoul, 133-719 (Korea, Republic of); Park, Jozeph, E-mail: jozeph.park@gmail.com [Department of Materials Science and Engineering, KAIST, Daejeon 305-701 (Korea, Republic of); Park, Jin-Seong, E-mail: jsparklime@hanyang.ac.kr [Division of Materials Science and Engineering, 222 Wangsimni-ro, Seongdong-gu, Hanyang University, Seoul, 133-719 (Korea, Republic of)

    2015-11-15

    Transparent conducting Indium oxide (InO{sub x}) thin films were deposited by atomic layer deposition at low deposition temperatures below 100 °C. For the comparative study with liquid precursors in low temperature thermal ALD, diethyl[1,1,1-trimethyl-N-(trimethylsilyl)silanaminato]-Indium, [3-(dimethylamino-kN)propyl-kC]dimethyl-Indium, and triethyl indium (TEIn) were used as the In precursors. Ozone was used as the oxidant for all precursors. InO{sub x} films grown using the three precursors all exhibit relatively low electrical resistivity below 10{sup −3} Ω cm at temperatures above 150 °C. Below 100 °C, the lowest resistivity (2 × 10{sup −3} Ω cm) was observed in the films grown with TEIn. The electrical, structural and optical properties were systematically investigated as functions of the deposition temperature and precursors. - Highlights: • InO{sub x} thin films were deposited by ALD at extremely low deposition temperatures below 100 °C. • InO{sub x} films exhibit relatively low electrical resistivity below 10{sup −3} Ω cm at temperatures above 150 °C. • Ozone stimulate the chemical reactions to yield dense indium oxide films at low temperatures.

  6. Numerical and experimental analysis of a thin liquid film on a rotating disk related to development of a spacecraft absorption cooling system

    Science.gov (United States)

    Faghri, Amir; Swanson, Theodore D.

    1989-01-01

    The numerical and experimental analysis of a thin liquid film on a rotating and a stationary disk related to the development of an absorber unit for a high capacity spacecraft absorption cooling system, is described. The creation of artificial gravity by the use of a centrifugal field was focused upon in this report. Areas covered include: (1) One-dimensional computation of thin liquid film flows; (2) Experimental measurement of film height and visualization of flow; (3) Two-dimensional computation of the free surface flow of a thin liquid film using a pressure optimization method; (4) Computation of heat transfer in two-dimensional thin film flow; (5) Development of a new computational methodology for the free surface flows using a permeable wall; (6) Analysis of fluid flow and heat transfer in a thin film in the presence and absence of gravity; and (7) Comparison of theoretical prediction and experimental data. The basic phenomena related to fluid flow and heat transfer on rotating systems reported here can also be applied to other areas of space systems.

  7. Research on Y-Ba-Cu-O superconducting thin films at liquid nitrogen temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Li Yuan; Yang Senzu; Ji Zhengming; Sun Zhijian; Jing Dong; Wu Peiheng; Zhang Shiyan; Wang Hao; Zhou Ningsheng; Fan Depei; and others

    1988-12-01

    The Y-Ba-Cu-O superconducting thin films on several kinds of substrates of single crystal ZrO/sub 2/, YSZ and polycrystalline SrTiO/sub 3/ have been successfully prepared by mean of /ital rf/ reactive magnetron sputtering. The zero resistance temperature obtained is 81 K. The thickness of the films is about 1--2 ..mu..m. In this paper the composition of the films, the substrates, /ital R/-/ital T/ curves, X-ray diffraction patterns and the heat treatment process of the films are described.

  8. Thermocapillarity driven Instabilities in thin liquid layers subject to long-wave analysis

    Science.gov (United States)

    Narendranath, Aneet; Hermanson, James; Struthers, Allan; Kolkka, Robert; Allen, Jeffrey

    2012-11-01

    An evolution equation describing the dynamics of an evaporating liquid film has previously been developed from the governing equations of fluid dynamics after the application of the lubrication approximation and the choice of a viscous time scale. The authors have solved the evaporating liquid film evolution equation with a validated numeric program. The role of domain size and thermocapillarity on the formation of secondary finger like structures is studied. The effect that gravity has on the formation of these finger patterns is evaluated. It is observed that the formation of secondary structures is strongly tied to a balance between destabilizing thermocapillarity and stabilizing surface tension. The secondary structures are amplified in a zero gravity environment.

  9. Dynamics of thin liquid films on a porous substrate in zero gravity

    CERN Document Server

    Narendranath, Aneet Dharmavaram

    2016-01-01

    The long-wave dynamics of liquid films on isothermal substrates show a dynamic competition between various physical mechanisms. If the destabilizing effect of thermocapillarity overcomes the stabilizing effect of surface tension and gravity, the liquid film ruptures in finite time, through the formation of primary and secondary thermocapillary finger structures. The long-wave evolution dynamics are compared for two different substrate types: isothermal non-porous and isothermal porous for small Biot number in a zero gravity environment. The multi-time-scale dynamics is revealed through time scales obtained from a method of similarity solutions. It is observed that with an isothermal porous substrate, in zero gravity, secondary thermocapillary structures are damped through imbibition and that primary thermocapillary structures persist for long times without rupture.

  10. Theory for particle settling and shear-induced migration in thin-film liquid flow.

    Science.gov (United States)

    Cook, Benjamin P

    2008-10-01

    Particles suspended in a film flow can either settle out of the flow, remain well mixed, or even advance faster than the fluid, accumulating at the moving contact line. Recent experiments by Zhou et al. [Phys. Rev. Lett. 94, 117803 (2005)] have demonstrated that these three settling behaviors can be achieved by control of the average particle concentration phi and inclination angle theta . This work presents a theory for determining the settling behavior in the Stokes regime by calculating the depth profile of phi and the depth-averaged velocities of the liquid and particle phases. It is found that shear-induced particle fluxes can lead to an inversely stratified flow, in which the particles move on average faster than the liquid. The theory is directly compared to Zhou et al.'s experimental data, and the implications of stratification for lubrication-type models are also discussed.

  11. Molecular dynamics study on the effect of boundary heating rate on the phase change characteristics of thin film liquid

    Science.gov (United States)

    Hasan, Mohammad Nasim; Morshed, A. K. M. Monjur; Rabbi, Kazi Fazle; Haque, Mominul

    2016-07-01

    In this study, theoretical investigation of thin film liquid phase change phenomena under different boundary heating rates has been conducted with the help of molecular dynamics simulation. To do this, the case of argon boiling over a platinum surface has been considered. The study has been conducted to get a better understanding of the nano-scale physics of evaporation/boiling for a three phase system with particular emphasis on the effect of boundary heating rate. The simulation domain consisted of liquid and vapor argon atoms placed over a platinum wall. Initially the whole system was brought to an equilibrium state at 90K with the help of equilibrium molecular dynamics and then the temperature of the bottom wall was increased to a higher temperature (250K/130K) over a finite heating period. Depending on the heating period, the boundary heating rate has been varied in the range of 1600×109 K/s to 8×109 K/s. The variations of argon region temperature, pressure, net evaporation number with respect to time under different boundary heating rates have been determined and discussed. The heat fluxes normal to platinum wall for different cases were also calculated and compared with theoretical upper limit of maximum possible heat transfer to elucidate the effect of boundary heating rate.

  12. Liquid Microjunction Surface Sampling Probe Electrospray Mass Spectrometry for Detection of Drugs and Metabolites in Thin Tissue Sections

    Energy Technology Data Exchange (ETDEWEB)

    Van Berkel, Gary J [ORNL; Kertesz, Vilmos [ORNL; Koeplinger, Kenneth A. [Merck Research Laboratories; Vavek, Marissa [Merck Research Laboratories; Kong, Ah-Ng Tony [Rutgers University

    2008-01-01

    A self-aspirating, liquid micro-junction surface sampling probe/electrospray emitter mass spectrometry system was demonstrated for use in the direct analysis of spotted and dosed drugs and their metabolites in thin tissue sections. Proof-of-principle sampling and analysis directly from tissue without the need for sample preparation was demonstrated first by raster scanning a region on a section of rat liver onto which reserpine was spotted. The mass spectral signal from selected reaction monitoring was used to develop a chemical image of the spotted drug on the tissue. The probe was also used to selectively spot sample areas of sagittal whole mouse body tissue sections that had been dosed orally (90 mg/kg) with R,S-sulforaphane 3 hrs prior to sacrifice. Sulforaphane and its glutathione and N-acetyl cysteine conjugates were monitored with selected reaction monitoring and detected in the stomach and various other tissues from the dosed mouse. No signal for these species was observed in the tissue from a control mouse. The same dosed tissue section was used to illustrate the possibility of obtaining a line scan across the whole body section. In total these results illustrate the potential for rapid screening of the distribution of drugs and metabolites in tissue sections with the micro-liquid junction surface sampling probe/electrospray mass spectrometry approach.

  13. FULL SCALE TESTING TECHNOLOGY MATURATION OF A THIN FILM EVAPORATOR FOR HIGH-LEVEL LIQUID WASTE MANAGEMENT AT HANFORD - 12125

    Energy Technology Data Exchange (ETDEWEB)

    TEDESCHI AR; CORBETT JE; WILSON RA; LARKIN J

    2012-01-26

    Simulant testing of a full-scale thin-film evaporator system was conducted in 2011 for technology development at the Hanford tank farms. Test results met objectives of water removal rate, effluent quality, and operational evaluation. Dilute tank waste simulant, representing a typical double-shell tank supernatant liquid layer, was concentrated from a 1.1 specific gravity to approximately 1.5 using a 4.6 m{sup 2} (50 ft{sup 2}) heated transfer area Rototherm{reg_sign} evaporator from Artisan Industries. The condensed evaporator vapor stream was collected and sampled validating efficient separation of the water. An overall decontamination factor of 1.2E+06 was achieved demonstrating excellent retention of key radioactive species within the concentrated liquid stream. The evaporator system was supported by a modular steam supply, chiller, and control computer systems which would be typically implemented at the tank farms. Operation of these support systems demonstrated successful integration while identifying areas for efficiency improvement. Overall testing effort increased the maturation of this technology to support final deployment design and continued project implementation.

  14. Numerical and experimental modeling of liquid metal thin film flows in a quasi-coplanar magentic field

    Energy Technology Data Exchange (ETDEWEB)

    Morley, Neil B. [Univ. of California, Los Angeles, CA (United States)

    1994-01-01

    Liquid metal film protection of plasma-facing surfaces in fusion reactors is proposed in an effort to counter the adverse effects of high heat and particle fluxes from the burning plasma. Concerns still exist about establishing the required flow in presence of strong magnetic fields and plasma momentum flux typical of a reactor environment. In this work, the flow behavior of the film is examined under such conditions. Analysis of MHD equations as they apply to liquid metal flows with a free surface in the fully-developed limit was undertaken. Solution yields data for velocity profiles and uniform film heights vs key design parameters (channel size, magnetic field magnitude/orientation, channel slope, wall conductivity). These results are compared to previous models to determine accuracy of simplifying assumptions, in particular Hartmann averaging of films along {rvec B}. Effect of a plasma momentum flux on the thin films is also analyzed. The plasma momentum is strong enough in the cases examined to seriously upset the film, especially for lighter elements like Li. Ga performed much better and its possible use is bolstered by calculations. In an experiment in the MeGA-loop MHD facility, coplanar, wide film flow was found to be little affected by the magnetic field due to the elongated nature of the film. Both MHD drag and partial laminarization are observed, supporting the fully- developed film model predictions of the onset of MHD drag and duct flow estimations for flow laminarization.

  15. Influence of evaporation on a thin binary liquid film flowing down a heated inclined plate

    Science.gov (United States)

    Kamrak, Juthamas; Scheid, Benoit; Colinet, Pierre

    2012-11-01

    We investigate the evolution of a two-component liquid film (here consisting of glycerine in water) falling down a heated plate, while water evaporates (glycerine is assumed to be non-volatile). The liquid phase is separated from pure water vapour by a deformable interface. We study the influence of both heat and mass transfer on the evolution of the liquid film. The temperature and concentration variations due to the evaporation of the solvent induce thermal and solutal Marangoni stresses on the free surface, thus affecting the evolution of the film. The mathematical model is developed by combining the lubrication theory with a weighted residuals approach. We obtain a set of coupled equations for the evolution of the film thickness, the velocity, the temperature and the concentration fields, at first-order. Stationary solutions are then calculated for different control parameters and show an intricate dependence of the different variables in the transition region where the evaporation flux reaches its maximum. Supported by FRIA, by the Marie Curie MULTIFLOW Network, and by FRS-FNRS.

  16. Ionic Liquid Hybrid Electrolytes for Lithium-Ion Batteries: A Key Role of the Separator-Electrolyte Interface in Battery Electrochemistry.

    Science.gov (United States)

    Huie, Matthew M; DiLeo, Roberta A; Marschilok, Amy C; Takeuchi, Kenneth J; Takeuchi, Esther S

    2015-06-10

    Batteries are multicomponent systems where the theoretical voltage and stoichiometric electron transfer are defined by the electrochemically active anode and cathode materials. While the electrolyte may not be considered in stoichiometric electron-transfer calculations, it can be a critical factor determining the deliverable energy content of a battery, depending also on the use conditions. The development of ionic liquid (IL)-based electrolytes has been a research area of recent reports by other researchers, due, in part, to opportunities for an expanded high-voltage operating window and improved safety through the reduction of flammable solvent content. The study reported here encompasses a systematic investigation of the physical properties of IL-based hybrid electrolytes including quantitative characterization of the electrolyte-separator interface via contact-angle measurements. An inverse trend in the conductivity and wetting properties was observed for a series of IL-based electrolyte candidates. Test-cell measurements were undertaken to evaluate the electrolyte performance in the presence of functioning anode and cathode materials, where several promising IL-based hybrid electrolytes with performance comparable to that of conventional carbonate electrolytes were identified. The study revealed that the contact angle influenced the performance more significantly than the conductivity because the cells containing IL-tetrafluoroborate-based electrolytes with higher conductivity but poorer wetting showed significantly decreased performance relative to the cells containing IL-bis(trifluoromethanesulfonyl)imide electrolytes with lower conductivity but improved wetting properties. This work contributes to the development of new IL battery-based electrolyte systems with the potential to improve the deliverable energy content as well as safety of lithium-ion battery systems.

  17. A Lithium/Polysulfide Battery with Dual-Working Mode Enabled by Liquid Fuel and Acrylate-Based Gel Polymer Electrolyte.

    Science.gov (United States)

    Liu, Ming; Ren, Yuxun; Zhou, Dong; Jiang, Haoran; Kang, Feiyu; Zhao, Tianshou

    2017-01-25

    The low density associated with low sulfur areal loading in the solid-state sulfur cathode of current Li-S batteries is an issue hindering the development of this type of battery. Polysulfide catholyte as a recyclable liquid fuel was proven to enhance both the energy density and power density of the battery. However, a critical barrier with this lithium (Li)/polysulfide battery is that the shuttle effect, which is the crossover of polysulfides and side deposition on the Li anode, becomes much more severe than that in conventional Li-S batteries with a solid-state sulfur cathode. In this work, we successfully applied an acrylate-based gel polymer electrolyte (GPE) to the Li/polysulfide system. The GPE layer can effectively block the detrimental diffusion of polysulfides and protect the Li metal from the side passivation reaction. Cathode-static batteries utilizing 2 M catholyte (areal sulfur loading of 6.4 mg cm(-2)) present superior cycling stability (727.4 mAh g(-1) after 500 cycles at 0.2 C) and high rate capability (814 mAh g(-1) at 2 C) and power density (∼10 mW cm(-2)), which also possess replaceable and encapsulated merits for mobile devices. In the cathode-flow mode, the Li/polysulfide system with catholyte supplied from an external tank demonstrates further improved power density (∼69 mW cm(-2)) and stable cycling performance. This novel and simple Li/polysulfide system represents a significant advancement of high energy density sulfur-based batteries for future power sources.

  18. Electrochemical performance of Si@TiN composite anode synthesized in a liquid ammonia for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Tu, Jiguo; Wang, Wei [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Jiao, Shuqiang, E-mail: sjiao@ustb.edu.cn [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Hou, Jungang; Huang, Kai [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Zhu, Hongmin, E-mail: hzhu@metall.ustb.edu.cn [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China)

    2012-10-15

    High-efficiency Si@TiN composite anode was synthesized by a homogeneous reduction reaction in the liquid ammonia, then calcinated at 950 Degree-Sign C for 2 h in vacuum. The crystal structure and morphology of the obtained in-situ coated composites were characterized by XRD, FESEM. The results showed that the micron-sized Si particles were almost coated by the TiN nanoparticles with the average size of 50 nm, while the morphology of Si@TiN composite was almost unchanged over 50 discharge-charge cycles. The electrochemical performances of Si@TiN composite anode were studied by galvanostatic discharge-charge tests, cyclic voltammetry (CV) and electrochemical impedance spectrum (EIS). The CV curves showed that the two redox peaks remained stable and were attributed to the alloying/dealloying process of Li with active Si particles. It could be seen from the EIS curves that the charge transfer resistance (R{sub ct}) for fresh was larger than that for the 50th cycle, which was mainly because the electrons and Li ions conducted on the electrode surface more difficultly for fresh. The cycle stability of the as-prepared Si@TiN composite anode was investigated, with the result showing that the cycling performance was stable and optimal at a rate of 0.2 C. The initial charge capacity was as high as 3226.99 mAh g{sup -1}, which was kept as 467.02 mAh g{sup -1} over 50 cycles. -- Highlights: Black-Right-Pointing-Pointer Si@TiN composite anode was synthesized in-situ in a liquid ammonia. Black-Right-Pointing-Pointer The size of TiN nanoparticles was about 50 nm. Black-Right-Pointing-Pointer The initial charge capacity was as high as 3226.99 mAh g{sup -1}.

  19. Anchoring and electro-optical dynamics of thin liquid crystalline films in a polyimide cell: Experiment and theory

    Science.gov (United States)

    Lee, Lay Min; Kwon, Hye J.; Kang, Joo H.; Nuzzo, Ralph G.; Schweizer, Kenneth S.

    2006-07-01

    The surface-dependent anchoring and electro-optical (EO) dynamics of thin liquid crystalline films have been examined using Fourier transform infrared spectroscopy. A simple nematic liquid crystal, 4-n-pentyl-4'-cyanobiphenyl (5CB), is confined as 40, 50, and 390nm thick films in nanocavities defined by gold interdigitated electrode arrays (IDEAs) patterned on polyimide-coated zinc selenide (ZnSe) substrates [Noble et al., J. Am. Chem. Soc. 124, 15020 (2002)]. New strategies for controlling the anchoring interactions and EO dynamics are explored based on coating a ZnSe surface with an organic polyimide layer in order to both planarize the substrate and induce a planar alignment of the liquid crystalline film. The polyimide layer can be further treated so as to induce a strong alignment of the nematic director along a direction parallel to the electrode digits of the IDEA. Step-scan time-resolved spectroscopy measurements were made to determine the rate constants for the electric-field-induced orientation and thermal relaxation of the 5CB films. In an alternate set of experiments, uncoated ZnSe substrates were polished unidirectionally to produce a grooved surface presenting nanometer-scale corrugations. The dynamical rate constants measured for several nanoscale film thicknesses and equilibrium organizations of the director in these planar alignments show marked sensitivities. The orientation rates are found to vary strongly with both the magnitude of the applied potential and the initial anisotropy of the alignment of the director within the IDEA. The relaxation rates do not vary in this same way. The marked variations seen in EO dynamics can be accounted for by a simple coarse-grained dynamical model.

  20. Bifurcation in a thin liquid film flowing over a locally heated surface

    CERN Document Server

    Katkar, Harshwardhan H

    2014-01-01

    We investigate the non-linear dynamics of a two-dimensional film flowing down a finite heater, for a non-volatile and a volatile liquid. An oscillatory instability is predicted beyond a critical value of Marangoni number using linear stability theory. Continuation along the Marangoni number using non-linear evolution equation is used to trace bifurcation diagram associated with the oscillatory instability. Hysteresis, a characteristic attribute of a sub-critical Hopf bifurcation, is observed in a critical parametric region. The bifurcation is universally observed for both, a non-volatile film and a volatile film.

  1. Nematic ordering of SWNT in meso-structured thin liquid films of polystyrenesulfonate.

    Science.gov (United States)

    Itzhak-Cohen, Racheli; Nativ-Roth, Einat; Levi-Kalisman, Yael; Josef, Elinor; Szleifer, Igal; Yerushalmi-Rozen, Rachel

    2014-12-16

    The formation of nematic-like islands of single-walled carbon nanotubes (SWNT) in polystyrenesulfonate (PSS) dispersions confined into nanometrically thin films is reported. The SWNT are observed to assemble into orientationally ordered phases, where the intertube distance, as measured via transmission electron microscopy at cryogenic temperatures, matches the polyelectrolyte's bulk correlation length deduced from X-ray scattering. The micrometers-long islands of orientationally ordered carbon nanotubes are observed in both SWNT and double-walled carbon nanotubes (DWNT) but not in specimens prepared from similar dispersions of multiwalled carbon nanotubes (MWNT). These observations, together with relaxation and rheological experiments, suggest that the orientational ordering may result from coupling between confinement of the polymer-wrapped SWNT and DWNT and the microstructure of the solvated polyelectrolyte.

  2. [Lithium nephropathy].

    Science.gov (United States)

    Kaczmarczyk, Ireneusz; Sułowicz, Władysław

    2013-01-01

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

  3. Liquid metal actuators: correctable mounting and assembly of thin-shell x-ray telescope mirrors

    Science.gov (United States)

    Bruccoleri, Alexander R.; Klingensmith, Martin; Chalifoux, Brandon; Heilmann, Ralf K.; Schattenburg, Mark L.

    2015-09-01

    An ideal bonding agent for thin-shell x-ray mirrors could be quickly applied to joints and set with deterministic and stable properties. Unfortunately, mirror assembly methods have typically utilized various epoxy formulations which are messy, slow to apply and cure, and far from deterministic or stable. Problems include shrinkage, creep and high thermal and humidity sensitivity. Once the bond is set errors are frozen in and cannot be corrected. We are developing a new method for bonding thin-foil mirrors that has the potential to solve these problems. Our process to bond mirrors to housing reference points is achieved via small beads of a low-melting-point bonding agent (such as solder or thermoset). The mirror is bonded to small contact surface points under real-time metrology. If the position of the mirror needs to be adjusted after bonding, a small force is applied normal or parallel to the contact surface and a pulsed fiber laser is used to melt an ultrathin layer of the solder for a very short time. The joint is then compressed, stretched or sheared while molten before refreezing in a new position, enabling repeatable and stable mirror position adjustments along the direction of the force in nm-level steps with minimal heat input. We present results from our prototype apparatus demonstrating proof of principle. The initial experiment includes developing a technique to bond D263 glass to Kovar, designing and building a one-dimensional stage to precisely apply force, and using an infrared laser pulse to heat the joint while measuring position and force.

  4. Non-volatile polymer electrolyte based on poly(propylene carbonate), ionic liquid, and lithium perchlorate for electrochromic devices.

    Science.gov (United States)

    Zhou, Dan; Zhou, Rui; Chen, Chuanxiang; Yee, Wu-Aik; Kong, Junhua; Ding, Guoqiang; Lu, Xuehong

    2013-06-27

    A series of solvent-free ionic liquid (IL)-based polymer electrolytes composed of amorphous and biodegradable poly(propylene carbonate) (PPC) host, LiClO4, and 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM(+)BF4(-)) were prepared and characterized for the first time. FTIR studies reveal that the interaction between PPC chains and imidazolium cations weakens the complexation between PPC chains and Li(+) ions. Thermal analysis (DSC and TGA) results show that the incorporation of BMIM(+)BF4(-) into PPC/LiClO4 remarkably decreases the glass transition temperature and improves the thermal stability of the electrolytes. AC impedance results show that the ionic conductivities of the electrolytes are significantly increased with the increase of BMIM(+)BF4(-) amount, the ambient ionic conductivity of the electrolyte at a PPC/LiClO4/BMIM(+)BF4(-) weight ratio of 1/0.2/3 is 1.5 mS/cm, and the ionic transport behavior follows the Arrhenius equation. Both PPC/LiClO4/BMIM(+)BF4(-) and PPC/BMIM(+)BF4(-) electrolytes were applied in electrochromic devices with polyaniline as the electrochromic layer. The PPC/LiClO4/BMIM(+)BF4(-)-based device exhibits much better electrochromic performance in terms of optical contrast and switching time due to the presence of much smaller cations.

  5. Toward uniform and ultrathin carbon layer coating on lithium iron phosphate using liquid carbon dioxide for enhanced electrochemical performance

    Science.gov (United States)

    Hong, Seung-Ah; Kim, Dong Hyun; Chung, Kyung Yoon; Chang, Wonyoung; Yoo, Jibeom; Kim, Jaehoon

    2014-09-01

    In this communication, uniform and ultrathin carbon coating on LiFePO4 (LFP) particles are performed using liquid carbon dioxide (l-CO2)-based free-meniscus coating. The uniform and conformal coverage of the carbon layer on LFP with a thickness of 3.3 nm, and a uniform distribution of carbon on the entire surface of the LFP particle are confirmed. The carbon-coated LFP (C-LFP) with a carbon content of 1.9 wt.% obtained using l-CO2-based coating exhibits a discharge capacity of 169 mAh g-1 at 0.1 C and 71 mAh g-1 at 30 C, while much lower discharge capacity of 146 mAh g-1 at 0.1 C and 17 mAh g-1 at 30 C is observed when C-LFP with an optimized carbon content of 6.0 wt.% is prepared using conventional aqueous-based coating.

  6. Coarsening Dynamics and Marangoni Effects in Thin Liquid Crystal Bubbles in Microgravity

    Science.gov (United States)

    Clark, Noel; Glaser, Matthew; Maclennan, Joseph; Park, Cheol; Tin, Padetha; Hall, Nancy R.; Sheehan, Christopher; Storck, Jennifer

    2015-01-01

    The Observation and Analysis of Smectic Islands in Space (OASIS) flight hardware was successfully launched on SpaceX-6 on April 15, 2015 and was operated in the Microgravity Science Glovebox (MSG) on board the International Space Station (ISS). The OASIS project comprises a series of experiments that probe the interfacial and hydrodynamic behavior of spherical-bubble freely suspended liquid crystal (FSLC) membranes in space. These are the thinnest known stable condensed phase structures, making them ideal for studies of two-dimensional (2D) coarsening dynamics and thermocapillary phenomena in microgravity. The OASIS experimental investigation was carried out using four different smectic A and C liquid crystal materials in four separate sample chambers housed inside the MSG. In this report, we present the behavior of collective dynamics on 2D bubble surface, including the equilibrium spatial organization and interaction of islands in electric fields and temperature gradients, and the diffusion and coalescence-driven coarsening dynamics of island emulsions in microgravity. We have observed spontaneous bubble thickening behavior caused by gradients between the bubble-blowing needle and ambient air temperatures. A uniform, thicker band forms during coarsening as a result of non-uniform heating by the LED illumination panels. These are proposed to be a result of Marangoni convection on the bubble surface.

  7. Chinese Tritium Technology of the Liquid Lithium-lead Alloy Experimental Loop for ITER%ITER中国液态锂铅实验回路中的氚技术

    Institute of Scientific and Technical Information of China (English)

    谢波; 吴宜灿; 翁葵平; 杨通在; 刘云怒; 宋勇; FDS团队

    2011-01-01

    The multinational cooperation in the International Thermonuclear Experimental Reactor (ITER) plan aims to show that fusion reactors are a new and viable way to address global energy concerns.The Chinese Dual Function Lithium Lead Testing Blanket Module (DFLL-TBM) is one of the major research programs and uses liquid lithium-lead as both breeder and cooler, and a helium-hydrogen gas bubbling method is used to extract tritium.So, tritium technology is a key issue in the liquid metal blanket.Based on the development strategy for Chinese liquid lithium-lead experimental blanket technology, development of Chinese tritium technology for liquid lithiumlead loops between 2004 and 2010 was elaberated in three fields, namely, theoretical analysis and calculation, experimental research, and engineering design.Some important information were introduced, such as the simulation-design-develop of liquid lithium-lead bubbler,tritium analysis and permeation barriers in the loops, tritium release from lithium-lead after irradiation, design of tritium extraction system for the blanket, etc.These works indicate that it is possible to completely overcome the difficulties involving very small solubility of tritium in the lithium-lead, accumulation of Magneto-Hydro-Dynamics (MHD) after a long period of continuous operation, materials corrosion together with the pressure drop caused by wall stress, and many technical problems, such as tritium retention, penetration,recovery and environment pollution, can be thoroughly solved.%多方合作的国际热核实验堆(ITER)计划是全球能源问题关注的一个重要进展标志,中国参与提出的双功能液态锂铅包层模块(DFLL-TBM)是一重要组成部分,采用液态锂铅合金作为氚增殖剂和冷却剂,氢-氦混合气鼓泡方式提取氚.因此,氚技术成为关系液态金属包层成败的关键问题之一.结合中国液态锂铅实验包层技术的发展战略,从理论分析与计算

  8. Study on property-gradient polymer electrolyte for rechargeable lithium batteries; Lithium niji denchi no tame no keisha tokusei kobunshi denkaishitsu no sosei ni kansuru kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    Kokumi, Z.; Kanemura, S.; Inaba, M.; Takehara, Z.; Yao, K.; Uchimoto, Y. [Kyoto University, Kyoto (Japan)

    1997-02-01

    This paper describes the fundamental experiments for creating property-gradient polymer electrolyte for rechargeable lithium batteries. The rechargeable lithium battery is composed of an anodic composite agent section with high ion conductivity, a separator equivalent section with high mechanical strength (high bridging degree), and a section surpressing the precipitation of metal lithium by contacting with it. The continuous property-gradient polymer electrolyte was tried to be synthesized by means of the plasma polymerization method. As a result, plasma polymerization electrolyte with high ion conductivity could be prepared from the liquid phase by using a monomer with low vapor pressure. Porous material simulating the anodic composite agent was impregnated by the monomer, which was plasma-polymerized. As a result, it was found that the bridging degree decreased from the surface towards the inside of the plasma-polymerized porous material. In addition, polymer was prepared using fluorine-base monomer. Thus, LiF thin film could be prepared through the reaction between the polymer and metal lithium. 3 figs.

  9. Flow of a thin liquid film coating a horizontal stationary cylinder.

    Science.gov (United States)

    Cachile, M; Aguirre, M A; Lenschen, M; Calvo, A

    2013-12-01

    An experimental and theoretical study of the flow of liquid films around a stationary horizontal cylinder is reported. The film presents two different behaviors: The flow is stable in the upper zone (up to ∼150° with the vertical) and Rayleigh-Taylor-like instabilities appear in the lower zone. For the stable region, film thickness evolution could be described by numerically integrating an evolution equation obtained using a lubrication approximation. For the unstable region, a linear stability analysis allows us to determine the maximum growth wavelength for the Rayleigh-Taylor instability. Approximate analytical solutions were obtained for generatrices at an angle with the vertical θ=0 (stable region) and θ=π (where the instability appears).

  10. Elastic anisotropy effects on the electrical responses of a thin sample of nematic liquid crystal

    Science.gov (United States)

    Gomes, O. A.; Yednak, C. A. R.; Ribeiro de Almeida, R. R.; Teixeira-Souza, R. T.; Evangelista, L. R.

    2017-03-01

    The electrical responses of a nematic liquid crystal cell are investigated by means of the elastic continuum theory. The nematic medium is considered as a parallel circuit of a resistance and a capacitance and the electric current profile across the sample is determined as a function of the elastic constants. In the reorientation process of the nematic director, the resistance and capacitance of the sample are determined by taking into account the elastic anisotropy. A nonmonotonic profile for the current is observed in which a minimum value of the current may be used to estimate the elastic constants values. This scenario suggests a theoretical method to determine the values of the bulk elastic constants in a single planar aligned cell just by changing the direction of applied electrical field and measuring the resulting electrical current.

  11. Lithium and magnesium separation from salt lake brine by ionic liquids containing tributyl phosphate%离子液体-磷酸三丁酯体系分离盐湖卤水镁锂

    Institute of Scientific and Technical Information of China (English)

    石成龙; 贾永忠; 景燕

    2015-01-01

    In the present work, a typical room temperature ionic liquids (RTILs), 1-octyl-3-methyl-imidazolium hexafluorophosphate ([C8mim][PF6]), was used as an alternative solvent to study liquid/liquid extraction of lithium from salt lake brine. In this system, the ionic liquids and tributyl phosphate (TBP) were used as extraction medium and extractant respectively. The effects of solution pH value, phase ratio and other factors on lithium extraction efficiency had been investigated. The preliminary experimental results had demonstrated that, compared with using conventional extraction system, the extraction efficiency had been increased greatly in this ionic liquid system. Optimal extraction conditions of this system include the ratio of TBP/ILs at 9/1(vol), O/A at 2:1 and unadjusted pH. Under the optimal conditions, the single extraction efficiency of lithium ion and magnesium ion were 80.64% and 5.30%, respectively. And total extraction efficiency of 99.42% was obtained by triple-stage countercurrent extraction. The single stripping rate of lithium ion and magnesium ion were 98.78% and 99.15%, respectively, at 80℃ when the A/O phase ratio was 2. The Mg/Li ratio was 3.03 in the aqueous phase after stripping, which have dropped 93.41% when compared with the initial value.To evaluate the potential use of RTILs to replace traditional volatile organic compounds (VOCs) in liquid/liquid extraction of lithium, the extractions of lithium ion with VOCs and ionic liquid were compared. Compared with using conventional extraction system, the extraction efficiency had been increased greatly in this ionic liquid system. In addition, the equipment corrosion and the environmental pollution had been avoided in this new extraction system. The extraction mechanism was deduced based on the ultraviolet-visible(UV) absorption. Cation exchange was proposed to be the mechanism of extraction followed in ionic liquid. So the ionic liquid was not only regarded as the solvent but also the co

  12. Investigation of the shear thinning behavior of epoxy resins for utilization in vibration assisted liquid composite molding processes

    Science.gov (United States)

    Meier, R.; Kirdar, C.; Rudolph, N.; Zaremba, S.; Drechsler, K.

    2014-05-01

    Efficient production and consumption of energy are of greatest importance for contemporary industries and their products. This has led to an increasing application of lightweight materials in general and of Carbon Fiber Reinforced Plastics (CFRP) in particular. However, broader application of CFRP is often limited by high costs and manual labor production processes. These constraints are addressed by Liquid Composite Molding (LCM) processes. In LCM a dry fibrous preform is placed into a cavity and infiltrated mostly by thermoset resins; epoxy resins are wide spread in CFRP applications. One crucial parameter for a fast mold filling is the viscosity of the resin, which is affected by the applied shear rates as well as temperature and curing time. The work presented focuses on the characterization of the shear thinning behavior of epoxy resins. Furthermore, the correlation with the conditions in vibration assisted LCM processes, where additional shear rates are created during manufacture, is discussed. Higher shear rates result from high frequencies and/or high amplitudes of the vibration motions which are created by a vibration engine mounted on the mold. In rheological investigations the shear thinning behavior of a representative epoxy resin is studied by means of rotational and oscillatory experiments. Moreover, possible effects of shear rates on the chemical curing reaction are studied. Here, the time for gelation is measured for different levels of shear rates in a pre-shearing phase. Based on the rheological studies, the beneficial effect of vibration assistance in LCM processes with respect to mold filling can further be predicted and utilized.

  13. Shape optimization of a sheet swimming over a thin liquid layer

    Energy Technology Data Exchange (ETDEWEB)

    Wilkening, J.; Hosoi, A.E.

    2008-12-10

    Motivated by the propulsion mechanisms adopted by gastropods, annelids and other invertebrates, we consider shape optimization of a flexible sheet that moves by propagating deformation waves along its body. The self-propelled sheet is separated from a rigid substrate by a thin layer of viscous Newtonian fluid. We use a lubrication approximation to model the dynamics and derive the relevant Euler-Lagrange equations to simultaneously optimize swimming speed, efficiency and fluid loss. We find that as the parameters controlling these quantities approach critical values, the optimal solutions become singular in a self-similar fashion and sometimes leave the realm of validity of the lubrication model. We explore these singular limits by computing higher order corrections to the zeroth order theory and find that wave profiles that develop cusp-like singularities are appropriately penalized, yielding non-singular optimal solutions. These corrections are themselves validated by comparison with finite element solutions of the full Stokes equations, and, to the extent possible, using recent rigorous a-priori error bounds.

  14. Three-dimensional modelling of thin liquid films over spinning disks

    Science.gov (United States)

    Zhao, Kun; Wray, Alex; Yang, Junfeng; Matar, Omar

    2016-11-01

    In this research the dynamics of a thin film flowing over a rapidly spinning, horizontal disk is considered. A set of non-axisymmetric evolution equations for the film thickness, radial and azimuthal flow rates are derived using a boundary-layer approximation in conjunction with the Karman-Polhausen approximation for the velocity distribution in the film. These highly nonlinear partial differential equations are then solved numerically in order to reveal the formation of two and three-dimensional large-amplitude waves that travel from the disk inlet to its periphery. The spatio-temporal profile of film thickness provides us with visualization of flow structures over the entire disk and by varying system parameters(volumetric flow rate of fluid and rotational speed of disk) different wave patterns can be observed, including spiral, concentric, smooth waves and wave break-up in exceptional conditions. Similar types of waves can be found by experimentalists in literature and CFD simulation and our results show good agreement with both experimental and CFD results. Furthermore, the semi-parabolic velocity profile assumed in our model under the waves is directly compared with CFD data in various flow regimes in order to validate our model. EPSRC UK Programme Grant EP/K003976/1.

  15. Frictional Response of Molecularly Thin Liquid Polymer Films Subject to Constant Shear Stress

    Science.gov (United States)

    Tschirhart, Charles; Troian, Sandra

    2014-03-01

    Measurements of the frictional response of nanoscale viscous films are typically obtained using the surface force apparatus in which a fluid layer is confined between smooth solid substrates approaching at constant speed or force. The squeezing pressure causes lateral flow from which the shear viscosity can be deduced. Under these conditions however, molecularly thin films tend to solidify wholly or partially and estimates of the shear viscosity can exceed those in macroscale films by many orders of magnitude. This problem can be avoided altogether by examining the response of an initially flat, supported, free surface film subject to comparable values of surface shear stress by application of an external inert gas stream. This method was first conceived by Derjaguin in 1944; more recent studies by Mate et al. at IBM Almaden on complex polymeric systems have uncovered fluid layering and other interesting behaviors. The only drawback is that this alternative technique requires an accurate model for interface distortion. We report on ellipsometric measurements of ultrathin polymeric films in efforts to determine whether the usual interface equations for free surface films based purely on continuum models can be properly extended to nanoscale films. Supported by a Fred and Jean Felberg Fellowship and G. W. Housner Student Discovery Fund.

  16. Module of lithium divertor for KTM tokamak

    Energy Technology Data Exchange (ETDEWEB)

    Lyublinski, I., E-mail: yublinski@yandex.ru [FSUE ' Red Star' , Moscow (Russian Federation); Vertkov, A.; Evtikhin, V.; Balakirev, V.; Ionov, D.; Zharkov, M. [FSUE ' Red Star' , Moscow (Russian Federation); Tazhibayeva, I. [IAE NNC RK, Kurchatov (Kazakhstan); Mirnov, S. [TRINITI, Troitsk, Moscow Region (Russian Federation); Khomiakov, S.; Mitin, D. [OJSC Dollezhal Institute, Moscow (Russian Federation); Mazzitelli, G. [ENEA RC Frascati (Italy); Agostini, P. [ENEA RC Brasimone (Italy)

    2012-10-15

    Highlights: Black-Right-Pointing-Pointer Problems of PFE degradation, tritium accumulation and plasma pollution can be overcome by the use of liquid lithium-metal with low Z. Black-Right-Pointing-Pointer Capillary-porous system (CPS) - new material in which liquid lithium fill a solid matrix from porous material. Black-Right-Pointing-Pointer Lithium divertor module for KTM tokamak is under development. Black-Right-Pointing-Pointer Lithium filled tungsten felt is offered as the base plasma facing material of divertor. Black-Right-Pointing-Pointer Results of this project addresses to the progress in the field of fusion neutrons source and fusion energy source creation. - Abstract: Activity on projects of ITER and DEMO reactors has shown that solution of problems of divertor target plates and other plasma facing elements (PFEs) based on the solid plasma facing materials cause serious difficulties. Problems of PFE degradation, tritium accumulation and plasma pollution can be overcome by the use of liquid lithium-metal with low Z. Application of lithium will allow to create a self-renewal and MHD stable liquid metal surface of the in-vessel devices possessing practically unlimited service life; to reduce power flux due to intensive re-irradiation on lithium atoms in plasma periphery that will essentially facilitate a problem of heat removal from PFE; to reduce Z{sub eff} of plasma to minimally possible level close to 1; to exclude tritium accumulation, that is provided with absence of dust products and an opportunity of the active control of the tritium contents in liquid lithium. Realization of these advantages is based on use of so-called lithium capillary-porous system (CPS) - new material in which liquid lithium fill a solid matrix from porous material. The progress in development of lithium technology and also activity in lithium experiments in the tokamaks TFTR, T-11M, T-10, FTU, NSTX, HT-7 and stellarator TJ II permits of solving the problems in development of

  17. Navy Lithium Battery Safety

    Science.gov (United States)

    2010-07-14

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

  18. Laser-adjusted three-dimensional Li-Mn-O cathode architectures for secondary lithium-ion cells

    Science.gov (United States)

    Pröll, J.; Kohler, R.; Torge, M.; Bruns, M.; Przybylski, M.; Ulrich, S.; Seifert, H. J.; Pfleging, W.

    2012-03-01

    Three-dimensional cathode architectures for rechargeable lithium-ion cells can provide better Li-ion diffusion due to larger electrochemical active surface area and therefore, may stabilize the cycling behaviour of an electrochemical cell. This features show great importance when aiming for long-life batteries, e.g. in stationary or portable power devices. In this study, lithium manganese oxide thin films were used as cathode material with the goal to stabilize their cycling behavior and to counter degradation effects which come up within the lithium manganese oxide system. Firstly, appropriate laser ablation parameters were selected in order to achieve defined three-dimensional structures with features sizes down to micro- and sub-micrometer scale by using mask imaging technique. Laser annealing was also applied onto the laser structured material in a second step in order to form an electrochemically active phase. Process development led to a laser annealing strategy for a flexible adjustment of crystallinity and grain size. Laser annealing was realized using a high power diode laser system operating at a wavelength of 940 nm. Information on the surface composition, chemistry and topography as well as studies on the crystalline phase of the material were obtained by using Raman spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy and X-ray diffraction analysis. The electrochemical activity of the laser modified lithium manganese oxide cathodes was explored by cyclic voltammetry measurements and galvanostatic testing by using a lithium anode and standard liquid electrolyte.

  19. Differentiation of coloured inks of inkjet printer cartridges by thin layer chromatography and high performance liquid chromatography.

    Science.gov (United States)

    Poon, N L; Ho, S S H; Li, C K

    2005-01-01

    Document examiners are frequently asked to determine whether or not a colour printout has originated from a particular inkjet printer. The printer can rarely be identified unless some unique defects or irregularities of the printer are present on the printout. However, it is possible to decipher the make and/or model of the printer by comparing the ink-profile of the questioned printout with that of a seized inkjet printer cartridge or from one in a database. This paper presents an overview of a systematic approach to characterising and discriminating the inks of different inkjet printer cartridges using thin layer chromatography (TLC) and high pressure liquid chromatography (HPLC) with multi-wavelength ultra-violet/visible (UV/Vis) detection. Ink samples from 23 different inkjet printer cartridges (including originals and substitutes) of different brands and colour printouts, printed by known printers were examined with newly developed chromatographic methods. Subsequently, a database of the ink-profiles was generated. The methods provide a useful tool for discriminating coloured inks in inkjet printer cartridges of different brands.

  20. Exposure to volatile organic compounds and kidney dysfunction in thin film transistor liquid crystal display (TFT-LCD) workers.

    Science.gov (United States)

    Chang, Ta-Yuan; Huang, Kuei-Hung; Liu, Chiu-Shong; Shie, Ruei-Hao; Chao, Keh-Ping; Hsu, Wen-Hsin; Bao, Bo-Ying

    2010-06-15

    Many volatile organic compounds (VOCs) are emitted during the manufacturing of thin film transistor liquid crystal displays (TFT-LCDs), exposure to some of which has been reported to be associated with kidney dysfunction, but whether such an effect exists in TFT-LCD industry workers is unknown. This cross-sectional study aimed to investigate the association between exposure to VOCs and kidney dysfunction among TFT-LCD workers. The results showed that ethanol (1811.0+/-1740.4 ppb), acetone (669.0+/-561.0 ppb), isopropyl alcohol (187.0+/-205.3 ppb) and propylene glycol monomethyl ether acetate (PGMEA) (102.9+/-102.0 ppb) were the four dominant VOCs present in the workplace. The 63 array workers studied had a risk of kidney dysfunction 3.21-fold and 3.84-fold that of 61 cell workers and 18 module workers, respectively. Workers cumulatively exposed to a total level of isopropyl alcohol, PGMEA and propylene glycol monomethyl ether> or =324 ppb-year had a significantly higher risk of kidney dysfunction (adjusted OR=3.41, 95% CI=1.14-10.17) compared with those exposed to LCD industry, and cumulative exposure to specific VOCs might be associated with kidney dysfunction.

  1. Use of thin film transistor liquid crystal display (TFT-LCD) waste glass in the production of ceramic tiles.

    Science.gov (United States)

    Lin, Kae-Long

    2007-09-05

    In this study, we employ the following operating conditions: varied pressure (25 kgf/cm(2)), sintering temperature (900-1200 degrees C), sintering time (6h), percentage of thin film transistor liquid crystal display (TFT-LCD) waste glass by weight (0-50%) and temperature rising at a rate of 5 degrees C/min, to fabricate clay tiles. The sintering characteristics of the clay blended with TFT-LCD waste glass tiles are examined to evaluate the feasibility of the reuse of TFT-LCD waste glass. TFT-LCD waste glass contains large amounts of glass. The TCLP leaching concentrations all met the ROC EPAs current regulatory thresholds. The addition of TFT-LCD waste glass to the mixture, increased the apparent weight loss. The incorporation of 50% TFT-LCD waste glass resulted in a significant increase in the porosity ratio of the specimens compared to the porosity ratio of the ceramic tile containing TFT-LCD waste glass. The main constituent in both the clay tile and the clay with TFT-LCD waste glass samples is quartz. Increasing the temperature resulted in an increase in the flexural strength and resistance to abrasion in the tiles. The porosity ratio decreases as shrinkage increases. The relation between the porosity ratio and the hardness of the tiles used in the study is also shown.

  2. Novel polymer electrolyte from poly(carbonate-ether) and lithium tetrafluoroborate for lithium-oxygen battery

    Science.gov (United States)

    Lu, Qi; Gao, Yonggang; Zhao, Qiang; Li, Ji; Wang, Xianhong; Wang, Fosong

    2013-11-01

    Novel polymer electrolyte based on low-molecular weight poly(carbonate-ether) and lithium tetrafluoroborate has been prepared and used in lithium-oxygen battery for the first time, the electrolyte with approximate 17% of LiBF4 showed ionic conductivity of 1.57 mS cm-1. Infrared spectra analysis indicates that obvious interaction between the lithium ions and partial oxygen atoms in the host polymer exists, and the lithium salt and the host polymer have good miscibility. The lithium-oxygen battery from this polymer electrolyte shows similar cyclic stability to traditional liquid electrolyte observed by FT-IR, AFM and electrochemical measurements, which may provide a new choice for fabrication of all-solid-state high-capacity rechargeable lithium-oxygen battery with better safety.

  3. Vacuum distillation refining of crude lithium (Ⅰ)——Thermodynamics on separating impurities from lithium

    Institute of Scientific and Technical Information of China (English)

    陈为亮; 杨斌; 柴立元; 闵小波; 戴永年; 于霞; 张传福

    2001-01-01

    Thermodynamics on vacuum refining process of the crude lithium has been studied by using separation coefficients of impurities in the crude lithium and vapor-liquid equilibrium composition diagrams of Li-i binary alloy (i stands for an impurity) at different temperatures. Behaviors of impurities in the vacuum distillation process have been examined.The results show that fractional vacuum distillation should be taken to obtain metal lithium with high purity more than 99.99 % Li, in which metal K, Na and partial Mg are volatilized at lower temperature of 673~873 K. Lithium is distilled from the residual liquid containing other impurities, such as Ca, Mg, Al, Si, Fe and Ni at higher temperature of 873~1 073 K and the chamber pressure is less than the critical pressure of lithium.

  4. New method of solving the optimized paired-phonon analysis equations and stability of thin films of liquid 4He at T=0 K

    Science.gov (United States)

    Szybisz, L.; Ristig, M. L.

    1989-09-01

    We propose a novel numerical method to solve the two-body Euler-Lagrange equation derived by Krotscheck, Qian, and Kohn in the paired-phonon analysis for an inhomogeneous Bose liquid at zero temperature. The new algorithm is applied to thin films of liquid 4He supported by an external potential. Numerical results are reported for density profiles, chemical potentials, binding energies, and corrective Jastrow correlation factors as a function of the particle number of the film and the strength of the external potential. The stability of this kind of film is discussed in detail. Some evidence for a long-wavelength instability of free thin films is provided. In addition, in order to unify results obtained from different derivations, it is proved that the expression for the Hartree potential reported by Krotscheck et al. is equal, within the framework of the hypernetted-chain theory, to a previously published one by Saarela, Pietiläinen, and Kallio.

  5. A lithium superionic conductor.

    Science.gov (United States)

    Kamaya, Noriaki; Homma, Kenji; Yamakawa, Yuichiro; Hirayama, Masaaki; Kanno, Ryoji; Yonemura, Masao; Kamiyama, Takashi; Kato, Yuki; Hama, Shigenori; Kawamoto, Koji; Mitsui, Akio

    2011-07-31

    Batteries are a key technology in modern society. They are used to power electric and hybrid electric vehicles and to store wind and solar energy in smart grids. Electrochemical devices with high energy and power densities can currently be powered only by batteries with organic liquid electrolytes. However, such batteries require relatively stringent safety precautions, making large-scale systems very complicated and expensive. The application of solid electrolytes is currently limited because they attain practically useful conductivities (10(-2) S cm(-1)) only at 50-80 °C, which is one order of magnitude lower than those of organic liquid electrolytes. Here, we report a lithium superionic conductor, Li(10)GeP(2)S(12) that has a new three-dimensional framework structure. It exhibits an extremely high lithium ionic conductivity of 12 mS cm(-1) at room temperature. This represents the highest conductivity achieved in a solid electrolyte, exceeding even those of liquid organic electrolytes. This new solid-state battery electrolyte has many advantages in terms of device fabrication (facile shaping, patterning and integration), stability (non-volatile), safety (non-explosive) and excellent electrochemical properties (high conductivity and wide potential window).

  6. Mitigation of plasma–material interactions via passive Li efflux from the surface of a flowing liquid lithium limiter in EAST

    Science.gov (United States)

    Zuo, G. Z.; Hu, J. S.; Maingi, R.; Ren, J.; Sun, Z.; Yang, Q. X.; Chen, Z. X.; Xu, H.; Tritz, K.; Zakharov, L. E.; Gentile, C.; Meng, X. C.; Huang, M.; Xu, W.; Chen, Y.; Wang, L.; Yan, N.; Mao, S. T.; Yang, Z. D.; Li, J. G.; EAST Team

    2017-04-01

    A new flowing liquid Li limiter (FLiLi) based on the concept of a thin flowing film has been successfully designed and tested in the EAST device in 2014. A bright Li radiative mantle at the plasma edge was observed during discharges using FLiLi, resulting from passive Li injection and transport in the scrape-off layer (SOL) plasma. Li particle efflux from the FLiLi surface into the plasma was estimated at  >5  ×  1020 atom s‑1, due to surface evaporation and sputtering, and accompanied with a few small Li droplets ~1 mm diameter that were ejected from FLiLi. The Li efflux from FLiLi was ionized by the SOL plasma and formed a Li radiation band that originated from the FLiLi surface, and then spread toroidally by SOL plasma flow. The Li radiative mantle appeared to partly isolate the plasma from the wall, reducing impurity release from the wall materials, and possibly leading to a modest improvement in confinement. In addition, strong Li radiation reduced the particle and heat fluxes impacting onto the divertor plate, with certain similarities to heat flux reduction and detachment onset via low-Z impurity injection.

  7. Stable Lithium Deposition Generated from Ceramic-Cross-Linked Gel Polymer Electrolytes for Lithium Anode.

    Science.gov (United States)

    Tsao, Chih-Hao; Hsiao, Yang-Hung; Hsu, Chun-Han; Kuo, Ping-Lin

    2016-06-22

    In this work, a composite gel electrolyte comprising ceramic cross-linker and poly(ethylene oxide) (PEO) matrix is shown to have superior resistance to lithium dendrite growth and be applicable to gel polymer lithium batteries. In contrast to pristine gel electrolyte, these nanocomposite gel electrolytes show good compatibility with liquid electrolytes, wider electrochemical window, and a superior rate and cycling performance. These silica cross-linkers allow the PEO to form the lithium ion pathway and reduce anion mobility. Therefore, the gel not only features lower polarization and interfacial resistance, but also suppresses electrolyte decomposition and lithium corrosion. Further, these nanocomposite gel electrolytes increase the lithium transference number to 0.5, and exhibit superior electrochemical stability up to 5.0 V. Moreover, the lithium cells feature long-term stability and a Coulombic efficiency that can reach 97% after 100 cycles. The SEM image of the lithium metal surface after the cycling test shows that the composite gel electrolyte with 20% silica cross-linker forms a uniform passivation layer on the lithium surface. Accordingly, these features allow this gel polymer electrolyte with ceramic cross-linker to function as a high-performance lithium-ionic conductor and reliable separator for lithium metal batteries.

  8. Lithium ion sources

    Science.gov (United States)

    Roy, Prabir K.; Greenway, Wayne G.; Grote, Dave P.; Kwan, Joe W.; Lidia, Steven M.; Seidl, Peter A.; Waldron, William L.

    2014-01-01

    A 10.9 cm diameter lithium alumino-silicate ion source has been chosen as a source of ˜100mA lithium ion current for the Neutralized Drift Compression Experiment (NDCX-II) at LBNL. Research and development was carried out on lithium alumino-silicate ion sources prior to NDCX-II source fabrication. Space-charge-limited emission with the current density exceeding 1 mA/cm2 was measured with 0.64 cm diameter lithium alumino-silicate ion sources at 1275 °C. The beam current density is less for the first 10.9 cm diameter NDCX-II source, and it may be due to an issue of surface coverage. The lifetime of a thin coated (on a tungsten substrate) source is varied, roughly 40-50 h, when pulsed at 0.05 Hz and with pulse length of 6μs each, i.e., a duty factor of 3×10-7, at an operating temperature of 1250-1275 °C. The 10.9 cm diameter source lifetime is likely the same as of a 0.64 cm source, but the lifetime of a source with a 2 mm diameter (without a tungsten substrate) is 10-15 h with a duty factor of 1 (DC extraction). The lifetime variation is dependent on the amount of deposition of β-eucryptite mass, and the surface temperature. The amount of mass deposition does not significantly alter the current density. More ion source work is needed to improve the large source performance.

  9. Lithium ion sources

    Energy Technology Data Exchange (ETDEWEB)

    Roy, Prabir K., E-mail: pkroy@lbl.gov [Lawrence Berkeley National Laboratory (LBNL), One Cyclotron Road, Berkeley, California CA-94720 (United States); Greenway, Wayne G. [Lawrence Berkeley National Laboratory (LBNL), One Cyclotron Road, Berkeley, California CA-94720 (United States); Grote, Dave P. [Lawrence Livermore National Laboratory LLC, CA-94550 (United States); Kwan, Joe W.; Lidia, Steven M.; Seidl, Peter A.; Waldron, William L. [Lawrence Berkeley National Laboratory (LBNL), One Cyclotron Road, Berkeley, California CA-94720 (United States)

    2014-01-01

    A 10.9 cm diameter lithium alumino-silicate ion source has been chosen as a source of ∼100mA lithium ion current for the Neutralized Drift Compression Experiment (NDCX-II) at LBNL. Research and development was carried out on lithium alumino-silicate ion sources prior to NDCX-II source fabrication. Space-charge-limited emission with the current density exceeding 1 mA/cm{sup 2} was measured with 0.64 cm diameter lithium alumino-silicate ion sources at 1275 °C. The beam current density is less for the first 10.9 cm diameter NDCX-II source, and it may be due to an issue of surface coverage. The lifetime of a thin coated (on a tungsten substrate) source is varied, roughly 40–50 h, when pulsed at 0.05 Hz and with pulse length of 6μs each, i.e., a duty factor of 3×10{sup −7}, at an operating temperature of 1250–1275 °C. The 10.9 cm diameter source lifetime is likely the same as of a 0.64 cm source, but the lifetime of a source with a 2 mm diameter (without a tungsten substrate) is 10–15 h with a duty factor of 1 (DC extraction). The lifetime variation is dependent on the amount of deposition of β-eucryptite mass, and the surface temperature. The amount of mass deposition does not significantly alter the current density. More ion source work is needed to improve the large source performance.

  10. Low-temperature liquid-phase epitaxy and optical waveguiding of rare-earth-ion-doped KY(WO4)2 thin layers

    NARCIS (Netherlands)

    Romanyuk, Y.E.; Utke, I.; Ehrentraut, D.; Apostolopoulos, V.; Pollnau, Markus; Garcia-Revilla, S.; Valiente, B.

    2004-01-01

    Crystalline $KY(WO_{4})_{2}$ thin layers doped with different rare-earth ions were grown on b-oriented, undoped $KY(WO_{4})_{2}$ substrates by liquid-phase epitaxy employing a low-temperature flux. The ternary chloride mixture of NaCl, KCl, and CsCl with a melting point of 480°C was used as a solven

  11. Evaporation temperature-tuned physical vapor deposition growth engineering of one-dimensional non-Fermi liquid tetrathiofulvalene tetracyanoquinodimethane thin films

    DEFF Research Database (Denmark)

    Sarkar, I.; Laux, M.; Demokritova, J.

    2010-01-01

    We describe the growth of high quality tetrathiofulvalene tetracyanoquinodimethane (TTF-TCNQ) organic charge-transfer thin films which show a clear non-Fermi liquid behavior. Temperature dependent angle resolved photoemission spectroscopy and electronic structure calculations show that the growth...... of TTF-TCNQ films is accompanied by the unfavorable presence of neutral TTF and TCNQ molecules. The quality of the films can be controlled by tuning the evaporation temperature of the precursor in physical vapor deposition method....

  12. Low-temperature liquid-phase epitaxy and optical waveguiding of rare-earth-ion-doped $KY(WO_{4})_{2}$ thin layers

    NARCIS (Netherlands)

    Romanyuk, Y.E.; Utke, I.; Ehrentraut, D.; Apostolopoulos, V.; Pollnau, M.; Garcia-Revilla, S.; Valiente, B.

    2004-01-01

    Crystalline $KY(WO_{4})_{2}$ thin layers doped with different rare-earth ions were grown on b-oriented, undoped $KY(WO_{4})_{2}$ substrates by liquid-phase epitaxy employing a low-temperature flux. The ternary chloride mixture of NaCl, KCl, and CsCl with a melting point of 480°C was used as a solven

  13. Development of technology for fabrication of lithium CPS on basis of CNT-reinforced carboxylic fabric

    Energy Technology Data Exchange (ETDEWEB)

    Tazhibayeva, Irina, E-mail: tazhibayeva@ntsc.kz [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Baklanov, Viktor; Ponkratov, Yuriy [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Abdullin, Khabibulla [Institute of Experimental and Theoretical Physics of Kazakh National University, Almaty (Kazakhstan); Kulsartov, Timur; Gordienko, Yuriy; Zaurbekova, Zhanna [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan); Lyublinski, Igor [JSC «Red Star», Moscow (Russian Federation); NRNU «MEPhI», Moscow (Russian Federation); Vertkov, Alexey [JSC «Red Star», Moscow (Russian Federation); Skakov, Mazhyn [Institute of Atomic Energy, National Nuclear Center of RK, Kurchatov (Kazakhstan)

    2017-04-15

    Highlights: • Preliminary study of carboxylic fabric wettability with liquid lithium is presented. • Preliminary studies of carboxylic fabric wettability with liquid lithium consist in carrying out of experiments at temperatures 673,773 and 873 К in vacuum during long time. • A scheme of experimental device for manufacturing of lithium CPS and matrix filling procedure with liquid lithium are presented. • The concept of lithium limiter with CPS on basis of CNT-reinforced carboxylic fabric is proposed. - Abstract: The paper describes the analysis of liquid lithium interaction with materials based on carbon, the manufacture technology of capillary-porous system (CPS) matrix on basis of CNT-reinforced carboxylic fabric. Preliminary study of carboxylic fabric wettability with liquid lithium is presented. The development of technology includes: microstructural studies of carboxylic fabric before its CNT-reinforcing; validation of CNT-reinforcing technology; mode validation of CVD-method for CNT synthesize; study of synthesized carbon structures. Preliminary studies of carboxylic fabric wettability with liquid lithium consist in carrying out of experiments at temperatures 673, 773 and 873 К in vacuum during long time. The scheme of experimental device for manufacturing of lithium CPS and matrix filling procedure with liquid lithium are presented. The concept of lithium limiter with CPS on basis of CNT-reinforced carboxylic fabric is proposed.

  14. Results of R and D for lithium/vanadium breeding blanket design

    Energy Technology Data Exchange (ETDEWEB)

    Mattas, R.F.; Smith, D.L.; Reed, C.B.; Park, J.H. [Argonne National Lab., IL (United States); Kirillov, I.R. [D.V. Efremov Scientific Research Inst. of Electrophysical Apparatus, St. Petersburg (Russian Federation); Strebkov, Yu.S. [Research and Development Inst. of Power Engineering, Moscow (Russian Federation); Rusanov, A.E. [Inst. of Physics and Power Engineering, Obninsk (Russian Federation); Votinov, S.N. [A.A. Bochvar Inst. of Non-Organic Materials, Moscow (Russian Federation)

    1997-04-01

    The self-cooled lithium/vanadium blanket concept has several attractive features for fusion power systems, including reduced activation, resistance to radiation damage, accommodation of high heat loads and operating to temperatures of 650--700 C. The primary issue associated with the lithium/vanadium concept is the potentially high MHD pressure drop experienced by the lithium as it flows through the high magnetic field of the tokamak. The solution to this issue is to apply a thin insulating coating to the inside of the vanadium alloy to prevent the generation of eddy currents within the structure that are responsible for the high MHD forces and pressure drop. This paper presents progress in the development of an insulator coating that is capable of operating in the severe fusion environment, progress in the fabrication development of vanadium alloys, and a summary of MHD testing. A large number of small scale tests of vanadium alloy specimens coated with CaO and AlN have been conducted in liquid lithium to determine the resistivity and stability of the coating. In-situ measurements in lithium have determined that CaO coatings, {approximately} 5 {micro}m thick, have resistivity times thickness values exceeding 10{sup 6} {Omega}-cm{sup 2}. These results have been used to identify fabrication procedures for coating a large vanadium alloy (V-4Cr-4Ti) test section that was tested in the ALEX (Argonne Liquid metal Experiment) facility. Similar test sections have been produced in both Russia and the US.

  15. A method to form semiconductor quantum dot (QD) thin films by igniting a flame at air-liquid interface: CdS and WO3.

    Science.gov (United States)

    Jadhav, Aarti H; Patil, Sagar H; Sathaye, Shivaram D; Patil, Kashinath R

    2015-02-01

    We reveal an easy, inexpensive, efficient one stepflame synthesis of semiconductor/metal oxide thin films at air-liquid interface, subsequently, transferred on suitable substrate. The method has been illustrated by the formation of CdS and WO3 QDs thin films. The features of the present method are (1) Growth of thin films consisting of0.5-2.0nm sized Quantum Dots (QDs)/(ultra-small nanoparticles) in a short time, at the air-liquid interface which can be suitably transferred by a well-known Blodgett technique to an appropriate substrate, (2) The method is suitable to apply layer by layer (LbL) technique to increase the film thickness as well as forming various compositions as revealed by AFM measurements. The films are characterized for their structure (SAED), morphology (TEM), optical properties (UV-Vis.) and photoluminescence (PL). Possible mechanism of formation of QDs thin film and effect of capping in case of CdS QDs is discussed. Copyright © 2014 Elsevier Inc. All rights reserved.

  16. Fabrication of ionic liquid electrodeposited Cu--Sn--Zn--S--Se thin films and method of making

    Science.gov (United States)

    Bhattacharya, Raghu Nath

    2016-01-12

    A semiconductor thin-film and method for producing a semiconductor thin-films comprising a metallic salt, an ionic compound in a non-aqueous solution mixed with a solvent and processing the stacked layer in chalcogen that results in a CZTS/CZTSS thin films that may be deposited on a substrate is disclosed.

  17. Physical chemistry studies of ionic conduction gel electrolytes for lithium batteries; Etudes physico-chimiques d'electrolytes gelifies a conduction ionique pour batteries au lithium

    Energy Technology Data Exchange (ETDEWEB)

    Caillon-Caravanier, M.

    2002-12-01

    With the development of new electronic technologies, the research on gel electrolytes basic properties has been widely increased. The use of these materials, produced under thin plastic films, improves the stored energy - battery volume ratio. The ionic gel conductivity, liquid-type, is ensured by the ion migration in the liquid electrolyte incorporated to the polymer network. Thus a preliminary study of liquid phases to be incorporated has been done before the gel investigation. In order to optimize the conductive properties of liquid electrolytes, a simplified model of ionic conductivity has been established. It is based on the ion pair dissociation equilibrium. The ionic mobility is supposed to be inversely proportional to the macroscopic medium viscosity. The liquid electrolytes are then incorporated in the polymer network, based on di-acrylate monomers (DAC) or fluorinated copolymer (PVdF-HFP/SiO{sub 2}). The conductivity loss of the liquid encapsulated phases, more pronounced in the DAC case, is attributed to ion-polymer network interactions, which lead to a decrease of both the concentration and the mobility of free ions in the system. In the case of gel electrolytes DAC based, these interactions are quantified from an ionic transport model, which relies on the hypothesis of a 3D quasi-cubic reticulation. This hypothesis also allows anticipating the network maximal ability to contain the liquid phase. For gel electrolytes PVdF-HFP/SiO{sub 2} based, the kinetic study of the liquid phase absorption has allowed us to optimize the elaboration conditions. The ion-ion, ion-solvent and ion-polymer interactions have. been qualitatively and quantitatively studied by the mean of Raman spectroscopy. The performance of elaborated gel electrolytes is also estimated in cyclability terms towards commercial electrodes for lithium batteries. So the gel behavior has been studied with half-batteries associating a metal lithium electrode to a carbon anode or a lithiated cobalt

  18. [Liquid-based cervical cytology ThinPrep screening in Hungary].

    Science.gov (United States)

    Bak, Mihály; Séberné Éll, Mária; Bóka, Melinda; Veleczki, Zsuzsanna; Nyári, Tibor; Pete, Imre; Szentirmay, Zoltán

    2014-05-04

    Bevezetés: A hagyományos Papanicolaou-cervixkenetet világszerte az úgynevezett folyadékalapú (liquid-based) citológia váltotta fel. Egyértelműen bizonyított, hogy a folyadékalapú citológia alternatív módszer. Célkitűzés: A dolgozat célja a folyadékalapú méhnyakrákszűrés magyarországi eredményeinek, diagnózisainak követése, citohisztológiai összehasonlítása, illetve minőségbiztosítása volt. Módszer: 4573 folyadékalapú citológiai cervixkenetet a Bethesda (2001) beosztás szerint klasszifikálták. A humán papillomavírus tipizálását valós idejű polimeráz láncreakció módszerével határozták meg. Eredmények: A diagnózisok megoszlása: negatív 2323 (50,8%), egyéb, nem neoplasticus 2017 (44,1%) és kóros, neoplasticus 233 (5,1%). A nem értékelhető kenetek száma 43 (0,9%) volt, mérsékelt fokú intraepithelialis laesiót 87 esetben (1,9%), kifejezett fokú intraepithelialis laesiót 24 esetben (0,5%), carcinomát 23 esetben (0,5%) észleltek. A citológiai és hisztológiai leletek közötti korreláció alapján a módszer szenzitivitása 93,2%, specificitása 100%, pozitív prediktív értéke 100%-nak bizonyult. A folyadékalapú citológiai módszerrel a mérsékelt és kifejezett fokú intraepithelialis laesiót mutató kenetek aránya az előző évek azonos időtartamához viszonyítva 0,82%-ról 2,51%-ra emelkedett. Humán papillomavírus-DNS-meghatározást 81 esetben végeztek (pozitív prediktív érték 99%). Az 51 kóros hámelváltozás kapcsán 50 (98%) esetben igazolódott humán papillomavírus-fertőzés, ezek közül 20 (24,7%) alacsony, 46 (56,8%) pedig magas kockázatú volt. Következtetések: A szerzők megállapították, hogy tanulmányukban a folyadékalapú cervixcitológiai vizsgálat minőségbiztosítási eredményei megfelelnek a nemzetközileg elvártaknak. A folyadékalapú vizsgálat alternatív cervixcitológiai módszer, és hatékonysága, valamennyi paramétert tekintve

  19. Lithium Circuit Test Section Design and Fabrication

    Science.gov (United States)

    Godfroy, Thomas; Garber, Anne; Martin, James

    2006-01-01

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

  20. Hydrogen-bonding-mediated synthesis of atomically thin TiO2 films with exposed (001) facets and applications in fast lithium insertion/extraction.

    Science.gov (United States)

    Zhang, Hongye; Yang, Zhenzhen; Gan, Wei; Zhao, Yanfei; Yu, Bo; Xu, Huanjun; Ma, Zhishuang; Hao, Leiduan; Chen, Dechao; Miao, Shiding; Liu, Zhimin

    2015-10-05

    Ultrathin two-dimensional (2D) crystalline materials show high specific surface area (SA) of high energy (HE) facets, imparting a significant improvement in their performances. Herein we report a novel route to synthesize TiO2 nanofilms (NFs) with atomic thickness (TiO2 NFs have nearly 100 % exposed (001) facets and give an extremely high SA up to 487 m(2)  g(-1) . The synergistic effect of HQ and choline chloride plays a vital role in the formation of TiO2 NFs and in the exposure of HE (001) facets. Because of its ultrathin feature and exposed (001) facet, the N2 -annealled TiO2 NFs showed fast kinetics of lithium insertion/extraction, demonstrating foreseeable applications in the energy storage. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Arabidopsis thaliana Polar Glycerolipid Profiling by Thin Layer Chromatography (TLC) Coupled with Gas-Liquid Chromatography (GLC)

    Science.gov (United States)

    Wang, Zhen; Benning, Christoph

    2011-01-01

    Biological membranes separate cells from the environment. From a single cell to multicellular plants and animals, glycerolipids, such as phosphatidylcholine or phosphatidylethanolamine, form bilayer membranes which act as both boundaries and interfaces for chemical exchange between cells and their surroundings. Unlike animals, plant cells have a special organelle for photosynthesis, the chloroplast. The intricate membrane system of the chloroplast contains unique glycerolipids, namely glycolipids lacking phosphorus: monogalactosyldiacylglycerol (MGDG), digalactosyldiacylglycerol (DGDG), sulfoquinovosyldiacylglycerol (SQDG)4. The roles of these lipids are beyond simply structural. These glycolipids and other glycerolipids were found in the crystal structures of photosystem I and II indicating the involvement of glycerolipids in photosynthesis8,11. During phosphate starvation, DGDG is transferred to extraplastidic membranes to compensate the loss of phospholipids9,12. Much of our knowledge of the biosynthesis and function of these lipids has been derived from a combination of genetic and biochemical studies with Arabidopsis thaliana14. During these studies, a simple procedure for the analysis of polar lipids has been essential for the screening and analysis of lipid mutants and will be outlined in detail. A leaf lipid extract is first separated by thin layer chromatography (TLC) and glycerolipids are stained reversibly with iodine vapor. The individual lipids are scraped from the TLC plate and converted to fatty acyl methylesters (FAMEs), which are analyzed by gas-liquid chromatography coupled with flame ionization detection (FID-GLC) (Figure 1). This method has been proven to be a reliable tool for mutant screening. For example, the tgd1,2,3,4 endoplasmic reticulum-to-plastid lipid trafficking mutants were discovered based on the accumulation of an abnormal galactoglycerolipid: trigalactosyldiacylglycerol (TGDG) and a decrease in the relative amount of 18:3 (carbons

  2. Thin film detection of High Energy Materials: Optical Pumping Approach

    CERN Document Server

    Barthwal, Sachin

    2014-01-01

    We present our work on High Energy Material detection based on thin film of Lithium using the phenomenon of Optical Pumping. The Li atoms present in the thin film are optically pumped to one of the ground hyperfine energy levels so that they can no more absorb light from the resonant light source. Now in presence of a RF signal, which quantifies the ambient magnetic field, this polarized atomic system is again randomized thus making it reabsorb the resonant light. This gives a quantified measurement of the magnetic field surrounding the thin film detector. This is then mapped to the presence of magnetic HEM and hence the HEM are detected. Our approach in this regard starts with verifying the stability of Lithium atoms in various solvents so as to get a suitable liquid medium to form a thin film. In this regard, various UV-visible characterization spectra are presented to finally approach a stable system for the detection. We have worked on around 10 polar and non- polar solvents to see the stability criteria....

  3. Lithium as a blanket coolant

    Energy Technology Data Exchange (ETDEWEB)

    Wells, W.M.

    1977-01-01

    Recent re-assessment of tokamak reactors which move towards smaller size and lower required field strength (higher beta)/sup 2/ change the picture as regards the magnitude of MHD effects on flow resistance for lithium coolant. Perhaps the most important consequence of this as regards use of this coolant is that of clear acceptability of such effects when the flow is predominantly transverse to the magnetic field. This permits defining a blanket that consists entirely of round tubes containing the circulated lithium with voids between the tubes. Required thermal-hydraulic calculations are then on bases which are well established, especially in view of recent results dealing with perturbations of ducts and magnetic fields. Mitigation of MHD effects is feasible through tapering of tube wall thickness or use of insulated layers, but their use was not mandatory for the assumed conditions. Blanket configurations utilizing flowing lithium in round tubes immersed in static lithium may be suitable, but calculational methods do not now exist for this situation. Use of boiling potassium or cesium appears to be prohibitive in terms of vapor flow area when temperature levels are consistent with stainless steel. Liquid sodium, in addition to not being a breeding material, requires higher velocity than lithium for the same heat removal.

  4. RECOVERY OF LITHIUM FROM WASTE MATERIALS

    Directory of Open Access Journals (Sweden)

    JITKA JANDOVÁ

    2012-03-01

    Full Text Available In this study, processes based on roasting-leaching-crystallization steps and condensation-precipitation steps for Li2CO3 separation from spent Li/MnO2 batteries and lithium-containing wastewaters were developed and verified on a laboratory scale. Spent Li/MnO2 batteries were roasted under reduced pressure at 650°C, which split the castings and deactivated the batteries by reduction of LiMnO2 and MnO2 with residual lithium metal and graphite to form MnO and Li2CO3. The resultant lithium carbonate was selectively solubilised in water with manganese remaining in the leach residue. Li2CO3 of 99.5 % purity was obtained after evaporation of 95 % water. Processing of lithium-containing alkaline wastewaters from the production of liquid rubber comprises condensation up to lithium concentration of 12-13 g/l Li and a two-step precipitation of lithium carbonate using CO2 as a precipitation agent. Sparingly soluble Li2CO3 was produced in the second step at 95°C, whilst most impurities remain in the solution. Obtained lithium carbonate products contained on average more than 99.5 % Li2CO3. The lithium precipitation efficiency was about 90 %.

  5. 层层自组装技术在薄膜锂电池上的应用研究进展%Thin Film Lithium-Ion Battery Assembly via Layer-by-Layer Technique

    Institute of Scientific and Technical Information of China (English)

    王国建; 顾贤科

    2011-01-01

    Thin film lithium battery is a very important micro energy device, which has showed tremendous potential application. In order to further improve the performance of the thin film battery, it requires better assembling method. Layer-by-layer (LbL) technique provides a simple, safe and affordable route in assembling thin film electrolytes and electrodes. The technique is very important to construct nanoscale thin film which has showed unique property compared with bulk film. Here, we review the design of LbL films for electrolytes and electrodes and recent progress. Furthermore, material choice is significant to affect the properties of LBL battery. Hence, we review the recent progress of LBL film battery incorporating carbon nanotubes(CNT) due to its excellent electronic property.%薄膜锂电池作为一种重要的微型能源形式已经显示出巨大的应用前景,为了进一步提高薄膜锂电池的性能,要求有更好的技术对这种薄膜锂电池进行组装。层层自组装(Layer-by-Layer self-assembly,LBL)技术正是一种非常安全、经济、简便的薄膜组装方式,这对于组装薄膜电解质和薄膜电极是一个非常好的选择。更重要的是,由于纳米尺寸已经在电化学领域显示出优异的特性,因此LBL技术组装纳米结构的薄膜锂电池具有非常重要的意义。本文综述了使用LBL技术组装固体薄膜电解质和电极的进展和成就。同时,由于纳米材料选

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-01-01

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

  7. Lithium in 2012

    Science.gov (United States)

    Jaskula, B.W.

    2013-01-01

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

  8. Capillary Electrophoresis as Analysis Technique for Battery Electrolytes: (i Monitoring Stability of Anions in Ionic Liquids and (ii Determination of Organophosphate-Based Decomposition Products in LiPF6-Based Lithium Ion Battery Electrolytes

    Directory of Open Access Journals (Sweden)

    Marcelina Pyschik

    2017-09-01

    Full Text Available In this work, a method for capillary electrophoresis (CE hyphenated to a high-resolution mass spectrometer was presented for monitoring the stability of anions in ionic liquids (ILs and in commonly used lithium ion battery (LIB electrolytes. The investigated ILs were 1-methyl-1-propylpyrrolidinium bis(trifluoromethanesulfonylimide (PYR13TFSI and 1-methyl-1-propylpyrrolidinium bis(fluorosulfonylimide (PYR13FSI. The method development was conducted by adjusting the following parameters: buffer compositions, buffer concentrations, and the pH value. Also the temperature and the voltage applied on the capillary were optimized. The ILs were aged at room temperature and at 60 °C for 16 months each. At both temperatures, no anionic decomposition products of the FSI− and TFSI− anions were detected. Accordingly, the FSI− and TFSI− anions were thermally stable at these conditions. This method was also applied for the investigation of LIB electrolyte samples, which were aged at 60 °C for one month. The LP30 (50/50 wt. % dimethyl carbonate/ethylene carbonate and 1 M lithium hexafluorophosphate electrolyte was mixed with the additive 1,3-propane sultone (PS and with one of the following organophosphates (OP: dimethyl phosphate (DMP, diethyl phosphate (DEP, and triethyl phosphate (TEP, to investigate the influence of these compounds on the formation of OPs.

  9. Controllability study on the preparation of pure phase BiFeO{sub 3} thin films by liquid phase self-assembled method

    Energy Technology Data Exchange (ETDEWEB)

    Ren Xuanru, E-mail: renxuanru1986@163.com [C/C Composites Research Center, State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, Xi' an, Shaanxi 710072 (China); Tan Guoqiang; Miao Hongyan; Li Ziyu [College of Material Science and Engineering, Shaanxi University of Science and Technology, Xi' an, Shaanxi 710021 (China)

    2012-08-01

    Pure phase BiFeO{sub 3} (BFO) thin films were prepared on the ITO/glass substrates covered with functionalized OTS self-assembled monolayers (SAMs) by controllable liquid phase self-assembled method. The hydrophobic surface of OTS-SAMs was changed into hydrophilic surface after UV irradiation, which is helpful to make BFO precursor solutions fully wet the substrate surface. A dense film was formed only on the hydrophilic silnaol group regions, which shows the selectively deposition of BFO precursors. Changing the pH value of BFO precursor solutions will affect the phase purity. The pure phase BFO thin films can be obtained under various pH values, which indicates that the liquid phase self-assembled method is controllable. All pure phase BFO films are dense, smooth, well-grown polycrystalline films, but the size of grains increased gradually along with the increase of pH values. The micropattern of BiFeO{sub 3} film has clear edges. The possible growth mechanism of BFO thin films was discussed.

  10. Ionic-Liquid-Tethered Nanoparticles: Hybrid Electrolytes

    KAUST Repository

    Moganty, Surya S.

    2010-10-22

    A new class of solventless electrolytes was created by tethering ionic liquids to hard inorganic ZrO2 nanostructures (see picture; NIM=nanoscale ionic material). These hybrid fluids exhibit exceptional redox stability windows, excellent thermal stability, good lithium transference numbers, long-term interfacial stability in the presence of a lithium anode and, when doped with lithium salt, reasonable ionic conductivities.

  11. Liquid cathode primary batteries

    Science.gov (United States)

    Schlaikjer, Carl R.

    1985-03-01

    Lithium/liquid cathode/carbon primary batteries offer from 3 to 6 times the volumetric energy density of zinc/alkaline manganese cells, improved stability during elevated temperature storage, satisfactory operation at temperatures from -40 to +150 °C, and efficient discharge at moderate rates. he lithium/sulfur dioxide cell is the most efficient system at temperatures below 0 °C. Although chemical reactions leading to electrolyte degradation and lithium corrosion are known, the rates of these reactions are slow. While the normal temperature cell reaction produces lithium dithionite, discharge at 60 °C leads to a reduction in capacity due to side reactions involving sulfur dioxide and discharge intermediates. Lithium/thionyl chloride and lithium/sulfuryl chloride cells have the highest practical gravimetric and volumetric energy densities when compared with aqueous and most other nonaqueous systems. For thionyl chloride, discharge proceeds through a series of intermediates to sulfur, sulfur dioxide and lithium chloride. Catalysis, leading to improved rate capability and capacity, has been achieved. The causes of rapid reactions leading to thermal runaway are thought to be chemical in nature. Lithium/sulfuryl chloride cells, which produce sulfur dioxide and lithium chloride on discharge, experience more extensive anode corrosion. An inorganic cosolvent and suitable salt are capable of alleviating this corrosion. Calcium/oxyhalide cells have been studied because of their promise of increased safety without substantial sacrifice of energy density relative to lithium cells. Anode corrosion, particularly during discharge, has delayed practical development.

  12. Liquid cathode primary batteries

    Energy Technology Data Exchange (ETDEWEB)

    Schlaikjer, C.R.

    1985-01-15

    Lithium/liquid cathode/carbon primary batteries offer from 3 to 6 times the volumetric energy density of zinc/alkaline manganese cells, improved stability during elevated temperature storage, satisfactory operation at temperatures from -40 to +150/sup 0/C, and efficient discharge at moderate rates. The lithium/sulfur dioxide cell is the most efficient system at temperatures below 0/sup 0/C. Although chemical reactions leading to electrolyte degradation and lithium corrosion are known, the rates of these reactions are slow. While the normal temperature cell reaction produces lithium dithionite, discharge at 60/sup 0/C leads to a reduction in capacity due to side reactions involving sulfur dioxide and discharge intermediates. Lithium/thionyl chloride and lithium/sulfuryl chloride cells have the highest practical gravimetric and volumetric energy densities when compared with aqueous and most other nonaqueous systems. For thionyl chloride, discharge proceeds through a series of intermediates to sulfur, sulfur dioxide and lithium chloride. Catalysis, leading to improved rate capability and capacity, has been achieved. The causes of rapid reactions leading to thermal runaway are thought to be chemical in nature. Lithium/sulfuryl chloride cells, which produce sulfur dioxide and lithium chloride on discharge, experience more extensive anode corrosion. An inorganic cosolvent and suitable salt are capable of alleviating this corrosion. Calcium/oxyhalide cells have been studied because of their promise of increased safety without substantial sacrifice of energy density relative to lithium cells. Anode corrosion, particularly during discharge, has delayed practical development.

  13. Decoupling of dynamic processes in surfactant-based liquid mixtures: the case of lithium-containing bis(2-ethylhexyl)phosphoric acid/bis(2-ethylhexyl)amine systems.

    Science.gov (United States)

    Nicotera, Isabella; Oliviero Rossi, Cesare; Turco Liveri, Vincenzo; Calandra, Pietro

    2014-07-22

    Pure surfactant liquids and their binary mixtures, because of the amphiphilic nature of the molecules involved, can exhibit nanosegregation and peculiar transport properties. The idea that inspired this work is that the possibility of including in such media salts currently used for technological applications should lead to a synergy between the properties of the salt and those of the medium. Therefore, the dynamic features of bis(2-ethylhexyl)amine (BEEA) and bis(2-ethylhexyl)phosphoric acid (HDEHP) liquid mixtures were investigated as a function of composition and temperature by (1)H nuclear magnetic resonance (NMR) spectroscopy and rheometry. Inclusion of litium trifluoromethanesulfonate (LiT) has been investigated by infrared spectroscopy, pulsed field gradient NMR, and conductimetry methods to highlight the solubilizing and confining properties of these mixtures as well as the lithium conductivity. It was found that BEEA/HDEHP binary liquid mixtures show zero-threshold percolating self-assembly with a maximum in viscosity and a minimum in molecular diffusion at a 1:1 composition. Dissolution of LiT in such system can occur via confinement in the locally self-assembled polar domains. Despite this confinement, Li(+) conduction is scarcely dependent on the medium composition because of the possibility of a field-induced hopping decoupled by the structural and dynamical features of the medium.

  14. Thin film rechargeable electrodes based on conductive blends of nanostructured olivine LiFePO4 and sucrose derived nanocarbons for lithium ion batteries.

    Science.gov (United States)

    Praveen, P; Jyothsna, U; Nair, Priya; Ravi, Soumya; Balakrishnan, A; Subramanian, K R V; Nair, A Sreekumaran; Nair, V Shantikumar; Sivakumar, N

    2013-08-01

    The present study provides the first reports of a novel approach of electrophoretic co-deposition technique by which titanium foils are coated with LiFePO4-carbon nanocomposites synthesized by sol gel route and processed into high-surface area cathodes for lithium ion batteries. The study elucidates how sucrose additions as carbon source can affect the surface morphology and the redox reaction behaviors underlying these cathodes and thereby enhance the battery performance. The phase and morphological analysis were done using XRD and XPS where the LiFePO4 formed was confirmed to be a high purity orthorhombic system. From the analysis of the relevant electrochemical parameters using cyclic voltammetry and electrochemical impedance spectroscopy, a 20% increment and 90% decrement in capacity and impedance values were observed respectively. The composite electrodes also exhibited a specific capacity of 130 mA h/g. It has been shown that cathodes based on such composite systems can allow significant room for improvement in the cycling performance at the electrode/electrolyte interface.

  15. Influence of reactive oxygen ambience on the structural, morphological and optical properties of pulsed laser ablated potassium lithium niobate thin films

    Energy Technology Data Exchange (ETDEWEB)

    Jayasree, V. [Department of Optoelectronics, University of Kerala, Kariavattom, Thiruvananthapuram 695 581, Kerala (India); Ratheesh, R. [Centre for Materials for Electronics Technology, Athani P. O, Thrissur, Kerala (India); Ganesan, V.; Reddy, V.R. [UGC-DAE Consortium for Scientific Research, Indore Centre, Madhya Pradesh (India); Sudarsanakumar, C. [School of Pure and Applied Physics, Mahatma Gandhi University, Kottayam, Kerala (India); Pillai, V.P. Mahadevan [Department of Optoelectronics, University of Kerala, Kariavattom, Thiruvananthapuram 695 581, Kerala (India)], E-mail: vpmpillai9@rediffmail.com; Nayar, V.U. [Department of Optoelectronics, University of Kerala, Kariavattom, Thiruvananthapuram 695 581, Kerala (India)

    2008-11-28

    The effect of oxygen ambience on the structure and properties of potassium lithium niobate (K{sub 3}Li{sub 2}Nb{sub 5}O{sub 15}: KLN) films prepared on glass substrates by pulsed laser ablation technique (PLD) are studied. The influence of annealing on the properties of vacuum deposited films is also investigated. The Gracing Incidence X-ray Diffraction (GIXRD) data suggests the tetragonal structure for the KLN film whose grain sizes increase on thermal annealing. The Atomic Force Microscopic (AFM) analysis reveals the four-fold symmetric nature of the grains in the films. Self assembly of grains in the form of rings and rods are observed in AFM images of the films deposited in an oxygen ambience of 2 Pa. The films deposited at higher oxygen ambience show a blue shift in optical band gap. The direct current (DC) resistance measurement on the films deposited at non-reactive ambience reveals resistivity in the range of k{omega} m.

  16. Protection of lithium metal surfaces using chlorosilanes.

    Science.gov (United States)

    Marchioni, Filippo; Star, Kurt; Menke, Erik; Buffeteau, Thierry; Servant, Laurent; Dunn, Bruce; Wudl, Fred

    2007-11-01

    In this paper, we present a new approach for protecting metallic lithium surfaces based on a reaction between the thin native layer of lithium hydroxide present on the surface and various chlorosilane derivatives. The chemical composition of the resulting layer and the chemistry involved in layer formation were analyzed by polarization modulated infrared reflection absorption spectroscopy (PM-IRRAS), X-ray photoelectron spectroscopy (XPS), and energy dispersive X-ray analysis (EDX). Spectroscopy shows the disappearance of surface hydroxide groups and the appearance of silicon and chloride on the lithium surface. Differential scanning calorimetry (DSC) and electrochemical impedance spectroscopy (EIS) show that this surface treatment protects the lithium from certain gas-phase reactions and is ionically conductive.

  17. Cervical histology after routine ThinPrep or SurePath liquid-based cytology and computer-assisted reading in Denmark

    Science.gov (United States)