Relevant bibliographies by topics / Lithium film

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Lithium film'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Lithium film"

1

Zhang, Ji-Guang, Edwin C. Tracy, David K. Benson, and Satyen K. Deb. "The influence of microstructure on the electrochromic properties of LixWO3 thin films: Part I. Ion diffusion and electrochromic properties." Journal of Materials Research 8, no. 10 (October 1993): 2649–56. http://dx.doi.org/10.1557/jmr.1993.2649.

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The chemical diffusion coefficients of lithium ions in LixWO3 films were investigated as a function of lithium concentration and film porosity. Thin films were deposited with different porosities by thermal evaporation of WO3 powder in various partial water pressures. Our results indicate that diffusion coefficients increase with film porosity and decrease with increasing lithium concentration. Large diffusion coefficients that were found for small lithium concentrations appear to be due to the contribution of protons generated from ion exchange reactions between lithium and water incorporated in the film. Simultaneous electrical and in situ optical measurements were carried out to study the effect of porosity on the electrochromic properties of LixWO3. The coloring efficiency of porous WO3 films increases by approximately 70% when deposited in partial water pressure of 10−4 Torr, but decreases with further increments in water pressure.
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Xu, Mengyue, Mingbo He, Yuntao Zhu, Lin Liu, Lifeng Chen, Siyuan Yu, and Xinlun Cai. "Integrated thin film lithium niobate Fabry–Perot modulator [Invited]." Chinese Optics Letters 19, no. 6 (2021): 060003. http://dx.doi.org/10.3788/col202119.060003.

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Wu, Xu Yong, De Yin Zhang, and Kun Li. "Preparation and Characterization of Novel Lithium Tantalate Target." Applied Mechanics and Materials 117-119 (October 2011): 840–44. http://dx.doi.org/10.4028/www.scientific.net/amm.117-119.840.

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The novel lithium enriched lithium tantalate (LiTaO3) targets were papered by employing the sol-gel process and the high temperature sintered process. The sol of LiTaO3 was firstly prepared through reacting lithium ethoxide with tantalum ethoxide. The LiTaO3 powder was fabricated by presintered LiTaO3 dry gel 4 hour, at 800°C. The 11cm13cm1cm lithium enriched LiTaO3 target samples were prepared by sintered the pressed LiTaO3 powder billet 4 hour in the 850°C muffle furnace. The density of the 5% overdose lithium enriched LiTaO3 target is measured 5.96g/cm3. The XRD measured results show that the ion beam enhanced deposited (IBED) thin film samples using the prepared 5% overdose lithium enriched LiTaO3 target have the polycrystal structure of LiTaO3, but there has remanent Ta2O5 existed in the IBED thin film samples. The main reason for the remanent Ta2O5 growth was due to the stoichiometric proportion mismatch between Li and Ta in the IBED thin film samples during the high temperature annealed process, which caused the lithium oxide evaporation loss from the IBED thin film samples and made the proportion of Ta2O5 increase. After multipule repeated target prepared experiments, the 8.76% overdose lithium enriched LiTaO3 target is suitable for fabricating the 550°C annealed IBED LiTaO3 thin film. After the repeated process experiments, the suitable deposited process parameters of the IBED-C600M instrument for the 8.76% overdose lithium enriched LiTaO3 target were obtained. The SEM micrographs of the 550°C annealed IBED LiTaO3 thin films prepared by the 8.76% overdose lithium enriched LiTaO3 target reveal the prepared thin films are uniform, smooth and crack-free on the surface, and the perfect adhesion between the thin film and the substrate. The successfully fabricated LiTaO3 thin film samples verify the prepared processes of novel LiTaO3 sputtering target are effective.
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Liang, Hai Xia, Run Xia Jiang, Liang Xiao, and Han Xing Liu. "Structure and Electrochemical Properties of Li1-XNi0.5Mn0.5O2 Thin Film Using Different Raw Material by Sol-Gel Method." Applied Mechanics and Materials 44-47 (December 2010): 2259–63. http://dx.doi.org/10.4028/www.scientific.net/amm.44-47.2259.

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Lithium-deficient thin films Li1-xNi0.5Mn0.5O2 were synthesized by sol-gel method using metal lithium, manganese and nickel acetate salts and acetylacetonate salts as started materials, respectively. The microstructures and electrochemical performance of Li1-xNi0.5Mn0.5O2 thin films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and galvanostatic charge–discharge measurements. Lithium-deficient was due to the formation of spinel LiNi0.5Mn1.5O4 impurities. The lithium-deficient was more seriously for SB film due to contain crystal water in the acetate salts. The raw material had great influence on the morphology of the films. The SA film had better electrochemical properties than that of SB film. The first discharge capacity was about 51 μAh/cm2-μm. After 40 cycles, 76% of its discharge capacity can be retained. The metal acetylacetonate salts without crystal water are more suitable for the preparation of LiNi0.5Mn0.5O2 film by sol-gel method.
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Perrotta, A. J., S. Y. Tzeng, W. D. Imbrogno, R. Rolles, and M. S. Weather. "Hydrotalcite formation on aluminum sheet and powder." Journal of Materials Research 7, no. 12 (December 1992): 3306–13. http://dx.doi.org/10.1557/jmr.1992.3306.

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We have observed the formation of the hydrotalcite-like phase of lithium dialuminate, LiAl2(OH)6OH · 2H2O, and also the carbonate analog, by the oxidation of aluminum sheet and also aluminum powder in aqueous lithium hydroxide or lithium carbonate solutions. A secondary phase, bayerite, was also observed following the oxidation process, except when the aluminum was treated with lithium oxalate solutions where it is the principal phase. Results have been obtained for the time required to form a passivating film to hydrogen formation as a function of temperature and oxidizing solution. Grazing incidence x-ray diffraction of aluminum sheet samples, combined with polycrystalline x-ray diffraction on similarly treated aluminum powder, were used to evaluate the formation of the films. Both transmission and reflectance infrared absorption spectra on powder and sheet samples were used to support the x-ray observations. Scanning and transmission electron microscopies show morphological differences between preparations, film thicknesses of 10–20 μm, and also film defects. Additional SIMS analysis determined the relative lithium and aluminum concentrations in the films, suggesting that a higher concentration of lithium occurs when lithium carbonate is present in the reacting solutions.
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Xu, Fan, Nancy J. Dudney, Gabriel M. Veith, Yoongu Kim, Can Erdonmez, Wei Lai, and Yet-Ming Chiang. "Properties of lithium phosphorus oxynitride (Lipon) for 3D solid-state lithium batteries." Journal of Materials Research 25, no. 8 (August 2010): 1507–15. http://dx.doi.org/10.1557/jmr.2010.0193.

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The thin film electrolyte known as Lipon (lithium phosphorous oxynitride) has proven successful for planar thin film battery applications. Here, the sputter deposition of the amorphous LiPON electrolyte onto more complex 3D structures is examined. The 3D structures include off-axis alignment of planar substrates and also 10–100 μm arrays of pores, columns, and grooves. For magnetron sputtering in N2 gas at 2.6 Pa, the Lipon film deposition is not restricted to be line-of-sight to the target, but forms conformal and dense films over the 3D and off-axis substrates. The deposition rate decreases for areas and grooves that are less accessible by the sputtered flux. The composition varies, but remains within the range that gives sufficient Li+ ionic conductivity, 2 ± 1 μS/cm.
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Utamarat, Nisida, Lek Sikong, and Kanadit Chetpattananondh. "Electrochromic Properties of Lithium Vanadate Doped Tungsten Trioxide Film." Applied Mechanics and Materials 873 (November 2017): 9–13. http://dx.doi.org/10.4028/www.scientific.net/amm.873.9.

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Lithium vanadate doped tungsten trioxide films were coated on conducting fluorine doped tin oxide substrate by the sol-gel and dip coating methods using lithium vanadate and peroxotungstic acid sol. The concentration of lithium vanadatewas varied and the effects of lithium vanadate on morphology, microstructure and electrochromic properties of WO3 film were investigated. The synthesized tungsten trioxide with 10 wt.% lithium vanadate can be identified as amorphous structure. It observed that the crystallinity of the films are increase and more smooth when Li concentration increased and exhibits excellent properties in electrochromic performance in terms of diffusion coefficient is about as 2.6×10-9 cm2s-1 with the potential scan from -1.0 to +1.0 V as a scan rate of 100 mVs-1 in 0.5 M H2SO4 solution.
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Badilescu, Simona, Khalid Boufker, P. V. Ashrit, Fernand E. Girouard, and Vo-Van Truong. "FT-IR/ATR Study of Lithium Intercalation into Molybdenum Oxide Thin Film." Applied Spectroscopy 47, no. 6 (June 1993): 749–52. http://dx.doi.org/10.1366/0003702934066866.

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Molybdenum oxide thin films are deposited by thermal evaporation and sputtering, and lithium is inserted by a dry lithiation method. The FT-IR/ATR technique is used to study the formation and evolution of lithium bronze and lithium molybdate species. The mechanism of lithium intercalation is found to be dependent on the method of film preparation. The involvement of water molecules in the kinetics of lithiation is stressed.
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Wu, Jiaxiong, Wei Cai, and Guangyi Shang. "Electrochemical Behavior of LiFePO4 Thin Film Prepared by RF Magnetron Sputtering in Li2SO4 Aqueous Electrolyte." International Journal of Nanoscience 14, no. 01n02 (February 2015): 1460027. http://dx.doi.org/10.1142/s0219581x14600278.

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LiFePO 4 films were deposited on Au / Si substrate by radio-frequency magnetron sputtering. The effect of annealing on the crystallization and morphology of LiFePO 4 thin film has been investigated. X-ray diffraction revealed that the films through annealing were well crystallized compared with as-deposited films. The surface morphology of the thin film was also observed by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Electrochemical tests in 1M Li 2 SO 4 showed that the annealed thin film in 500°C exhibits larger Li -ion diffusion coefficient (3.46 × 10-7 cm2s-1) than as-deposited film and powder. Furthermore, cyclic voltammetry demonstrate a well-defined lithium intercalation/deintercalation reaction at around 0.45 V versus SCE (i.e., 3.6 V versus Li +/ Li ), suggesting that the annealed LiFePO 4 thin film is a promising candidate cathode film for lithium microbatteries.
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Bates, J. "Thin-film lithium and lithium-ion batteries." Solid State Ionics 135, no. 1-4 (November 1, 2000): 33–45. http://dx.doi.org/10.1016/s0167-2738(00)00327-1.

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Dissertations / Theses on the topic "Lithium film"

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Slaven, Simon. "Thin film carbon for lithium ion batteries /." Thesis, Connect to Dissertations & Theses @ Tufts University, 1996.

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Thesis (Ph.D.)--Tufts University, 1996.
Adviser: Ronald B. Goldner. Submitted to the Dept. of Electrical Engineering. Includes bibliographical references. Access restricted to members of the Tufts University community. Also available via the World Wide Web;
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Gavanier, Beatrice. "Stability of thin film insertion electrodes." Thesis, University of Southampton, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324003.

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Li, Chiung-Nan. "Microstructural stability of nanocrystalline LiCoO₂ cathode in lithium thin-film batteries." Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1580828921&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Mui, Simon C. 1976. "Electrochemical kinetics of thin film vanadium pentoxide cathodes for lithium batteries." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/33607.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2005.
Includes bibliographical references (p. 147-154).
Electrochemical experiments were performed to investigate the processing-property-performance relations of thin film vanadium pentoxide cathodes used in lithium batteries. Variations in microstructures were achieved via sputtering and anneal treatments, resulting in films with different morphologies, grain size distributions, and orientations. Key findings included (1) grain size distributions largely did not affect the current rate performance of the cathodes. Rather, the film orientation and the ability to undergo rapid phase transformation were more vital to improving performance; (2) interfacial resistance and ohmic polarization were also dominant at the high current rates used (> 600 [mu]A/cm²) in addition to solid diffusion; and (3) optimization of thin film batteries requires that film thickness be < 500 nm to avoid diminishing returns in power and energy densities. Kinetic parameters including the transfer coefficient ([alpha] = 0.90± 0.05) and standard rate constant (k⁰ [approx.] 2 x 10⁻⁶ cm/s) for vanadium pentoxide films were quantified using slow scan DC cyclic voltammetry and AC cyclic voltammetry. The reaction rate was found to be potentially limiting at moderate to high current rates (> 200 [mu]A/cm²).
(cont.) An analysis of the wide variation in current-rate performance for different V₂0₅ architectures (including composite, nanofiber, and thin film) shows a convergence in results when the area of active material has been factored into the metric. This convergence suggests that either the reaction rate or interfacial resistance is limiting in V₂0₅ as opposed to diffusion.
by Simon C. Mui.
Ph.D.
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Bieber, Christalee. "Self-assembly of conformal polymer electrolyte film for lithium ion microbatteries." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/40910.

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Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Physics, 2007.
Includes bibliographical references (leaves 37-39).
I apply the theory of polar and apolar intermolecular interactions to predict the behavior of combinations of common battery materials, specifically the cathode substrate lithium cobalt oxide (LCO) and the polymer separator poly(ethylene oxide). These predictions were first tested qualitatively using hexane and PTFE, which have well-established surface energies, and then by measuring the contact angles of PEO on LCO in hexane and hexadecane, chosen for their immiscibility in PEO. For better comparison, these experiments were repeated using water instead of PEO, for a total of four systems tested. This data allowed an estimate for the experimental surface energy components of LCO to be derived, resulting in 18.3 ± 1 mJ/m2 for [gamma]LW, 0.22 ± 0.02 mJ/m2 for [gamma]+, and 5.8 ± 1.6 mJ/m2 for [gamma]-, compared to the previously reported values of 40.8 mJ/m2 for [gamma]LW, 0.0008 mJ/m2 for [gamma]+, and 0.21 mJ/m2 for [gamma]-. This variation is probably due to a variety of factors, including instrumental uncertainty in the contact angle measurement, a difference in contact angle measurement procedure, and inevitable contamination by water and other materials. Using this new data, self-assembling electrolyte-cathode systems are predicted, like LCO-polyacrylonitrile-chloroform.
by Christalee Bieber.
S.B.
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Gil, Rashapal Ram. "Aluminium and its alloy as substrates for the lithium rechargeable electrode." Thesis, University of Newcastle Upon Tyne, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363538.

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Lin, Qian. "A Plastic-Based Thick-Film Li-Ion Microbattery for Autonomous Microsensors." Diss., CLICK HERE for online access, 2006. http://contentdm.lib.byu.edu/ETD/image/etd1175.pdf.

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Jeong, Soon-ki. "Studies on Surface Film Formation on Graphite Negative Electrodes in Lithium-Ion Batteries." 京都大学 (Kyoto University), 2002. http://hdl.handle.net/2433/149782.

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Hlongwa, Ntuthuko Wonderboy. "Nanoparticles-infused lithium manganese phosphate coated with magnesium-gold composite thin film - a possible novel material for lithium ion battery olivine cathode." University of the Western Cape, 2014. http://hdl.handle.net/11394/4467.

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>Magister Scientiae - MSc
Architecturally enhanced electrode materials for lithium ion batteries (LIB) with permeable morphologies have received broad research interests over the past years for their promising properties. However, literature based on modified porous nanoparticles of lithium manganese phosphate (LiMnPO₄) is meagre. The goal of this project is to explore lithium manganese phosphate (LiMnPO₄) nanoparticles and enhance its energy and power density through surface treatment with transition metal nanoparticles. Nanostructured materials offer advantages of a large surface to volume ratio, efficient electron conducting pathways and facile strain relaxation. The material can store lithium ions but have large structure change and volume expansion during charge/discharge processes, which can cause mechanical failure. LiMnPO₄ is a promising, low cost and high energy density (700 Wh/kg) cathode material with high theoretical capacity and high operating voltage of 4.1 V vs. Ag/AgCl which falls within the electrochemical stability window of conventional electrolyte solutions. LiMnPO₄ has safety features due to the presence of a strong P–O covalent bond. The LiMnPO₄ nanoparticles were synthesized via a sol-gel method followed by coating with gold nanoparticles to enhance conductivity. A magnesium oxide (MgO) nanowire was then coated onto the LiMnPO₄/Au, in order to form a support for gold nanoparticles which will then form a thin film on top of LiMnPO₄ nanoparticles crystals. The formed products will be LiMnPO₄/Mg-Au composite. MgO has good electrical and thermal conductivity with improved corrosion resistance. Thus the electronic and optical properties of MgO nanowires were sufficient for the increase in the lithium ion diffusion. The pristine LiMnPO₄ and LiMnPO₄/Mg-Au composite were examined using a combination of spectroscopic and microscopic techniques along with cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Microscopic results revealed that the LiMnPO₄/Mg-Au composite contains well crystallized particles and regular morphological structures with narrow size distributions. The composite cathode exhibits better reversibility and kinetics than the pristine LiMnPO₄ due to the presence of the conductive additives in the LiMnPO₄/Mg-Au composite. This is demonstrated in the values of the diffusion coefficient (D) and the values of charge and discharge capacities determined through cyclic voltammetry. For the composite cathode, D= 2.0 x 10⁻⁹ cm²/s while for pristine LiMnPO₄ D = 4.81 x 10⁻¹⁰ cm2/s. The charge capacity and the discharge capacity for LiMnPO₄/Mg-Au composite were 259.9 mAh/g and 157.6 mAh/g, respectively, at 10 mV/s. The corresponding values for pristine LiMnPO₄ were 115 mAh/g and 44.75 mAh/g, respectively. A similar trend was observed in the results obtained from EIS measurements. These results indicate that LiMnPO₄/Mg-Au composite has better conductivity and will facilitate faster electron transfer and therefore better electrochemical performance than pristine LiMnPO₄. The composite cathode material (LiMnPO₄/Mg-Au) with improved electronic conductivity holds great promise for enhancing electrochemical performances, discharge capacity, cycle performance and the suppression of the reductive decomposition of the electrolyte solution on the LiMnPO₄ surface. This study proposes an easy to scale-up and cost-effective technique for producing novel high-performance nanostructured LiMnPO₄ nanopowder cathode material.
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Prakash, Shruti. "The development and fabrication of miniaturized direct methanol fuel cells and thin-film lithium ion battery hybrid system for portable applications." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/28279.

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Thesis (M. S.)--Chemical Engineering, Georgia Institute of Technology, 2009.
Committee Chair: Kohl, Paul; Committee Member: Fuller, Tom; Committee Member: Gray, Gary; Committee Member: Liu, Meilin; Committee Member: Meredith, Carson; Committee Member: Rincon-Mora, Gabriel.
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Books on the topic "Lithium film"

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Foong, T. M. Film growth on aluminium-lithium alloys. Manchester: UMIST, 1991.

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Symposium on Thin Film Solid Ionic Devices and Materials (1995 Chicago, Ill.). Proceedings of the Symposium on Thin Film Solid Ionic Devices and Materials. Pennington, NJ: Electrochemical Society, 1996.

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Dutt, A. B. A pictorial atlas of Gondwana lithic fill in Indian Peninsula. Calcutta: Geological Survey of India, 1993.

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Sato, Mitsunobu, Li Lu, and Hiroki Nagai, eds. Lithium-ion Batteries - Thin Film for Energy Materials and Devices. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.73346.

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Kim, Won-Seok. Enhanced electrochemical characteristics of lithium manganese oxide thin film cathodes for li-ion rechargeable microbatteries. 2004.

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Book chapters on the topic "Lithium film"

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Kulova, Tatiana, Alexander Mironenko, Alexander Rudy, and Alexander Skundin. "Modern Lithium and Lithium-Ion Rechargeable Batteries." In All Solid State Thin-Film Lithium-Ion Batteries, 1–28. First edition. | Boca Raton : CRC Press, 2021.: CRC Press, 2021. http://dx.doi.org/10.1201/9780429023736-1.

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Kulova, Tatiana, Alexander Mironenko, Alexander Rudy, and Alexander Skundin. "Materials for All-Solid-State Thin-Film Batteries." In All Solid State Thin-Film Lithium-Ion Batteries, 29–73. First edition. | Boca Raton : CRC Press, 2021.: CRC Press, 2021. http://dx.doi.org/10.1201/9780429023736-2.

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Shim, Heung Taek, Joong Kee Lee, and Byung Won Cho. "DLC Film Coating on a Lithium Metal as an Anode of Lithium Secondary Batteries." In Solid State Phenomena, 919–22. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-31-0.919.

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Nilsen, Ola, Knut B. Gandrud, Ruud Amund, and Fjellvåg Helmer. "Atomic Layer Deposition for Thin-Film Lithium-Ion Batteries." In Atomic Layer Deposition in Energy Conversion Applications, 183–207. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527694822.ch6.

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Maranchi, J. P., P. N. Kumta, and A. F. Hepp. "Amorphous Silicon Thin Film Anodes for Lithium-Ion Batteries." In Ceramic Transactions Series, 121–29. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118407189.ch13.

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Patil, Vaishali, Arun Patil, Ji-Won Choi, and Seok-Jin Yoon. "Chemically Deposited Sb2Se3 Anode for Thin Film Lithium Batteries." In Communications in Computer and Information Science, 221–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-35248-5_31.

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Kulova, Tatiana, Alexander Mironenko, Alexander Rudy, and Alexander Skundin. "Diagnostics of Functional Layers of All-Solid-State Thin-Film Lithium-Ion Batteries." In All Solid State Thin-Film Lithium-Ion Batteries, 89–192. First edition. | Boca Raton : CRC Press, 2021.: CRC Press, 2021. http://dx.doi.org/10.1201/9780429023736-4.

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Kulova, Tatiana, Alexander Mironenko, Alexander Rudy, and Alexander Skundin. "Conclusion." In All Solid State Thin-Film Lithium-Ion Batteries, 193–96. First edition. | Boca Raton : CRC Press, 2021.: CRC Press, 2021. http://dx.doi.org/10.1201/9780429023736-5.

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Kulova, Tatiana, Alexander Mironenko, Alexander Rudy, and Alexander Skundin. "PVD Methods for Manufacturing All-Solid-State Thin-Film Lithium-Ion Batteries." In All Solid State Thin-Film Lithium-Ion Batteries, 74–88. First edition. | Boca Raton : CRC Press, 2021.: CRC Press, 2021. http://dx.doi.org/10.1201/9780429023736-3.

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Ribeiro, J. F., M. F. Silva, J. P. Carmo, L. M. Gonçalves, M. M. Silva, and J. H. Correia. "Solid-State Thin-Film Lithium Batteries for Integration in Microsystems." In Scanning Probe Microscopy in Nanoscience and Nanotechnology 3, 575–619. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-25414-7_20.

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Conference papers on the topic "Lithium film"

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Owen, J. R. "Prospects for thin film lithium batteries." In IEE Colloquium on Compact Power Sources. IEE, 1996. http://dx.doi.org/10.1049/ic:19960677.

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Ribeiro, J. F., R. Sousa, J. A. Sousa, L. M. Goncalves, M. M. Silva, L. Dupont, and J. H. Correia. "Flexible thin-film rechargeable lithium battery." In 2013 Transducers & Eurosensors XXVII: The 17th International Conference on Solid-State Sensors, Actuators and Microsystems (TRANSDUCERS & EUROSENSORS XXVII). IEEE, 2013. http://dx.doi.org/10.1109/transducers.2013.6627248.

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Rao, Ashutosh, Sasan Fathpour, and Kartik Srinivasan. "Integrated Thin-Film Lithium Niobate Photonics." In Integrated Photonics Research, Silicon and Nanophotonics. Washington, D.C.: OSA, 2020. http://dx.doi.org/10.1364/iprsn.2020.itu1a.2.

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Itabashi, Haruka, Naoaki Kuwata, Daichi Fujimoto, Yasutaka Matsuda, and Junichi Kawamura. "Characterization of Lithium Borate and Lithium Silicate Thin-Films as Solid Electrolyte for Thin-Film Battery." In 14th Asian Conference on Solid State Ionics (ACSSI 2014). Singapore: Research Publishing Services, 2014. http://dx.doi.org/10.3850/978-981-09-1137-9_166.

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Wang, Airong, Guangming Wu, Hui-yu Yang, Ming-xia Zhang, Xingmei Fang, Xiao-yun Yang, Bin Zhou, and Jun Shen. "Study of lithium diffusion through vanadium pentoxide aerogel." In Sixth International Conference on Thin Film Physics and Applications. SPIE, 2008. http://dx.doi.org/10.1117/12.792630.

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Wu, Guangming, Yonggang Wu, Xingyuan Ni, Zhen Zhou, Huiqin Zhang, Zhemin Jin, and Xiang Wu. "Infrared properties of lithium-intercalated vanadium pentoxide films." In Third International Conference on Thin Film Physics and Applications, edited by Shixun Zhou, Yongling Wang, Yi-Xin Chen, and Shuzheng Mao. SPIE, 1998. http://dx.doi.org/10.1117/12.300708.

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Kutbee, Arwa T., Mohamed T. Ghoneim, and Muhammad M. Hussain. "Flexible lithium-ion planer thin-film battery." In 2015 IEEE 15th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2015. http://dx.doi.org/10.1109/nano.2015.7388906.

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8

Renyuan Wang, Sunil A. Bhave, and Kushal Bhattacharjee. "Thin-film Lithium Niobate contour-mode resonators." In 2012 IEEE International Ultrasonics Symposium. IEEE, 2012. http://dx.doi.org/10.1109/ultsym.2012.0074.

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Bhave, Sunil A. "Multi-frequency lithium niobate thin-film resonators." In 2014 72nd Annual Device Research Conference (DRC). IEEE, 2014. http://dx.doi.org/10.1109/drc.2014.6872277.

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Stenger, Vincent, Michael Shnider, Sri Sriram, Donald Dooley, and Mark Stout. "Thin Film Lithium Tantalate (TFLT) Pyroelectric Detectors." In SPIE OPTO, edited by Laurence P. Sadwick and Créidhe M. O'Sullivan. SPIE, 2012. http://dx.doi.org/10.1117/12.908523.

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Reports on the topic "Lithium film"

1

Dudney, N. J., J. B. Bates, and D. Lubben. Thin-film rechargeable lithium batteries. Office of Scientific and Technical Information (OSTI), June 1995. http://dx.doi.org/10.2172/102151.

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2

Momozaki, Y. Research proposal for development of an electron stripper using a thin liquid lithium film for rare isotope accelerator. Office of Scientific and Technical Information (OSTI), March 2006. http://dx.doi.org/10.2172/917981.

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3

Reddy, Arava L., Anchal Srivastava, Sanketh R. Gowda, Hemtej Gullapalli, Madan Dubey, and Pulickel M. Ajayan. Synthesis of Nitrogen-Doped Graphene Films for Lithium Battery Application. Fort Belvoir, VA: Defense Technical Information Center, January 2010. http://dx.doi.org/10.21236/ada552925.

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4

Green, T. A., R. W. Stinnett, and R. A. Gerber. Production of lithium positive ions from LiF thin films on the anode in PBFA II. Office of Scientific and Technical Information (OSTI), September 1995. http://dx.doi.org/10.2172/116623.

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5

Fujita, M., H. Tanaka, H. Muramatsu, H. Asoh, and S. Ono. Corrosion Resistance Improvement Technology of Anodic Oxide Films on Aluminum Alloy that uses a Lithium Hydroxide Solution. Warrendale, PA: SAE International, October 2013. http://dx.doi.org/10.4271/2013-32-9049.

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6

Dudney, N. J. CRADA Final Report: Properties of Vacuum Deposited Thin Films of Lithium Phosphorous Oxynitride (Lipon) with an Expanded Composition Range. Office of Scientific and Technical Information (OSTI), December 2003. http://dx.doi.org/10.2172/885850.

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