Auswahl der wissenschaftlichen Literatur zum Thema „Spectroscopie du lithium“
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Zeitschriftenartikel zum Thema "Spectroscopie du lithium"
Hanquet, B., B. Tabyaoui, J. C. Caille, M. Farnier und R. Guilard. „Synthèse stéréosélective de (±) boschnialactone, (±) 7-épiteucriumlactone et (±) 7-épiisoiridomyrmécine. Étude de la stéréochimie par spectroscopie de résonance magnétique nucléaire“. Canadian Journal of Chemistry 68, Nr. 4 (01.04.1990): 620–27. http://dx.doi.org/10.1139/v90-095.
Der volle Inhalt der QuelleSeo, Ambrose, Andrew Meyer, Sujan Shrestha, Ming Wang, Xingcheng Xiao und Yang-Tse Cheng. „Observation of the surface layer of lithium metal using in situ spectroscopy“. Applied Physics Letters 120, Nr. 21 (23.05.2022): 211602. http://dx.doi.org/10.1063/5.0096546.
Der volle Inhalt der QuelleZhang, Li, Tao Qian, Xingyu Zhu, Zhongli Hu, Mengfan Wang, Liya Zhang, Tao Jiang, Jing-Hua Tian und Chenglin Yan. „In situ optical spectroscopy characterization for optimal design of lithium–sulfur batteries“. Chemical Society Reviews 48, Nr. 22 (2019): 5432–53. http://dx.doi.org/10.1039/c9cs00381a.
Der volle Inhalt der QuelleMeyer, Lydia, Collin Kinder und Jason Morgan Porter. „Chemometric and Machine Learning Analysis of Lithium Concentration and Solvation Behavior in Li-Ion Battery Electrolytes“. ECS Meeting Abstracts MA2022-02, Nr. 6 (09.10.2022): 618. http://dx.doi.org/10.1149/ma2022-026618mtgabs.
Der volle Inhalt der QuelleCai Jiahua, 才家华, 张保龙 Zhang Baolong, 耿春艳 Geng Chunyan, 郝思博 Hao Sibo, 陈赛 Chen Sai und 吴晓君 Wu Xiaojun. „铌酸锂强场太赫兹非线性时域光谱系统“. Chinese Journal of Lasers 50, Nr. 17 (2023): 1714012. http://dx.doi.org/10.3788/cjl230435.
Der volle Inhalt der QuelleMuhammad, F. H., A. F. M. Fadzil und Tan Winie. „FTIR and Electrical Studies of Hexanoyl Chitosan-Based Nanocomposite Polymer Electrolytes“. Advanced Materials Research 1043 (Oktober 2014): 36–39. http://dx.doi.org/10.4028/www.scientific.net/amr.1043.36.
Der volle Inhalt der QuelleKatime-Santrich, Orlando J., Bruno V. Castilho, Carlos A. O. Torres und Germano R. Quast. „Photometric and spectroscopic analysis of the stellar association AB Doradus“. Proceedings of the International Astronomical Union 5, S265 (August 2009): 370–71. http://dx.doi.org/10.1017/s1743921310000979.
Der volle Inhalt der QuelleFritzke, Jana Beatrice, Sunita Dey, Christopher A. O'Keefe und Clare P. Grey. „NMR Spectroscopic Investigations of the Performance Limiting Mechanisms of Lithium-Sulfur Batteries“. ECS Meeting Abstracts MA2023-02, Nr. 55 (22.12.2023): 2692. http://dx.doi.org/10.1149/ma2023-02552692mtgabs.
Der volle Inhalt der QuelleBezdomnikov, Alexey A., Liudmila I. Demina, Lyudmila G. Kuz’mina, Galina V. Kostikova, Valeriy I. Zhilov und Aslan Yu Tsivadze. „Study of Lithium-Extraction Systems Based on Benzo-15-Crown-5 Ether and Alkylimidazolium-Based Ionic Liquid“. Molecules 28, Nr. 3 (17.01.2023): 935. http://dx.doi.org/10.3390/molecules28030935.
Der volle Inhalt der QuelleJin, Yan, Lin Zhou, Jianyu Yu, Jie Liang, Wenshan Cai, Huigang Zhang, Shining Zhu und Jia Zhu. „In operando plasmonic monitoring of electrochemical evolution of lithium metal“. Proceedings of the National Academy of Sciences 115, Nr. 44 (15.10.2018): 11168–73. http://dx.doi.org/10.1073/pnas.1808600115.
Der volle Inhalt der QuelleDissertationen zum Thema "Spectroscopie du lithium"
Iezzi, Gianluca. „Cristallochimie des amphiboles à lithium“. Orléans, 2001. http://www.theses.fr/2001ORLE2035.
Der volle Inhalt der QuelleSafrany, Renard Marianne. „Propriétés électrochimiques et réponse structurale du polymorphe gamma'-V2O5 vis-à-vis de l'insertion du lithium et du sodium“. Thesis, Paris Est, 2017. http://www.theses.fr/2017PESC1185/document.
Der volle Inhalt der QuelleThe question of energy storage is currently at the heart of many international issues. The development of storage systems such as lithium ion (LIB) and sodium ion (SIB) batteries is therefore today the subject of many researches.In this context, layered materials having an interlayer space allowing insertion of cationic species seem ideal in the context of use as a positive electrode material for these LIB and SIB systems. Among these structures, vanadium pentoxide, in its alpha form, is a model compound with many advantages as an attractive cathode material for lithium batteries. This material also has numerous stable polymorphs allowing a wide field of study of this compound.In this thesis we were interested in the gamma'-V2O5 polymorph, which exhibits a layered structure with very large interlayer space allowing an easier insertion. Therefore, increased electrochemical performances are expected for this compound. The aim of this thesis was to study the electrochemical properties and the structural response of this compound toward the insertion of lithium and sodium ions.The first part of this thesis proposes a review of the current literature studies devoted to lithium-ion and sodium batteries.In a second part, a thorough study of the electrochemical lithium and sodium insertion in the alpha-V2O5 phase are depicted. The electrochemical and structural properties of alpha-V2O5 will make it possible to highlight the advantage of using the polymorph gamma'-V2O5 as a positive electrode material for LIB and SIB.The third part of this thesis presents the synthesis and characterization of the gamma'-V2O5 polymorph. The complete study of this system is presented in the case of the insertion of lithium with a study of electrochemical performances, a kinetic study of the insertion reaction carried out by complex impedance spectroscopy and a description of the structural changes studied by X-ray diffraction and by Raman spectroscopy.In the fourth chapter, the insertion of sodium into the polymorph gamma'-V2O5 is studied, using the same approach than that adopted in the case of lithium. The structural mechanism involved during the electrochemical process is solved. The formation of a new sodium vanadium bronze, gamma-Na0.97V2O5 , is revealed and its structural determination is carried out. Due to its remarkable electrochemical characteristics, especially its high voltage of 3,3V and excellent cycling stability, the gamma'-V2O5 oxide ranks among the most performant cathode materials for sodium batteries
Dridi, Zrelli Yosra. „Électrochimie et spectroscopie Raman de matériaux d’électrode positive pour batteries Li-ion“. Thesis, Paris Est, 2012. http://www.theses.fr/2012PEST1126/document.
Der volle Inhalt der QuelleIn this work, we show the relevance of Raman spectroscopy as a useful technique to investigate the local changes induced by the electrochemical reaction of intercalation/deintercalation of lithium in positive electrode materials for rechargeable lithium ion batteries.Raman investigations concern three types of high voltage cathode materials (4-5Volts) which are layered LiCoO2 and cubic LiMn2O4 and LiNi0.4Mn1.6O4.During electrochemical deintercalation of LiCoO2, we show the existence of a two phase region where the initial hexagonal phase coexist with a second hexagonal phase with a 3% expansion of the lattice parameter indicating a weakening of the Co-O bond in the Li1-xCoO2 material.On the other hand, a new assignment of LiMn2O4 Raman spectrum was proposed. During the charge in the 4V region, a three region phase (initial LiMn2O4 phase, intermediary phase and poor lithium phase) was described using Raman spectroscopy. RX measurements can not detect this intermediary phase. Lithiated phase Raman signature shows a specific local order: Fd3m for extreme phases and F43m for partially lithiated phase. A rich Raman band spectrum is attributed to this later phase in coherence with literature calculations. Structural changes reversibility is demonstrated. Identification of this intermediary phase as a major component of a cycled electrode, underline the incomplete reduction and explain the important loss of capacity observed during cycling. Raman study of LiMn2O4 electrochemical insertion in the 3V region, has demonstrated for the first time a progressive formation of tetragonal Li2Mn2O4 phase, which is in coexistence with initial cubic phase and is pure at the end of discharge. Structural transition reversibility was also demonstrated.In the case of LiNi0.4Mn1.6O4, the assignment of the Raman spectrum of LiNi0.4Mn1.6O4 is provided for the first time. DRX study in function of the state of charge and discharge, exhibit cubic structure conservation with moderate lattice parameters variations. The Raman spectrum of the spinel oxide exhibits drastic spectral changes during Li extraction. These changes have been directly related to the Mn and Ni oxidation states in the cathode material under operation. It comes out that electrochemical reactions of LiNi0.4Mn1.6O4 are reversible and based on three redox couples of Mn3+/Mn4+, Ni2+/Ni3+, and Ni3+/Ni4+. An original and concrete Raman spectroscopy application is the study of self discharge mechanism of completely charged LiNi0.4Mn1.6O4. Raman spectra evolution exhibits a quantitative Ni4+ reduction during the first hours, and then a slower Ni3+ reduction process. Finally, LiNi0.4Mn1.6O4 lithium insertion has been explored for the first time using Raman spectroscopy, and a tetragonal Li2Ni0.4Mn1.6O4 phase has been identified.The originality of this work is the important number of experimental Raman data of 4V electrode materials. New assignment of initial compound has been proposed and original vibrationnal data of compound during charge/discharge has been presented. These Raman data has permitted to propose a quantitative explanation which must be completed with ab initio calculations to simulate vibrationnal modes frequencies/ intensities
Morales, Ugarte Jorge Eduardo. „Etude Operando des accumulateurs au lithium par couplage spectroscopie à photoémission des rayons X et spectroscopie d’impédance“. Thesis, Université Grenoble Alpes (ComUE), 2019. http://www.theses.fr/2019GREAI082.
Der volle Inhalt der QuelleFaced with the major industrial challenges in the field of electrochemical energy storage, a fundamental research effort on the materials involved and their interfaces is nowadays essential for a gain in performance, durability and safety.In this context, it is essential to understand the interfacial processes involved that induce the degradation of the lithium metal-electrolyte interface and lead to a decrease in Coulombic efficiency and promote dendritic growth.In this thesis, we propose a study coupling electrochemical techniques such as impedance spectroscopy with surface analysis techniques such as X-ray photo-emission spectroscopy to study the chemical and electrochemical reactivity between electrolytes and a lithium metal electrode.To this end, special attention has been paid to the ionic liquids based electrolytes, which have been proposed as solvents for lithium salts, particularly for their low saturation vapor pressure, which considerably increases the safety of the batteries thus designed.Finally, this work was devoted in particular to the development of operando XPS assemblies and measurements in order to follow the chemical evolution of the interfaces inside a battery in real time
Mignoni, Sabrina. „Investigation par spectroscopie Raman des propriétés photoréfractives et microstructurales de LiNbO3 dopé“. Thesis, Metz, 2010. http://www.theses.fr/2010METZ017S/document.
Der volle Inhalt der QuelleLithium niobate LiNbO3 (LN) is an excellent material for various applications in particular thanks to its photorefractive (PR) properties. One of the research goals for this material consists in performing efficient PR optical waveguides for integrated optics.The objective of the thesis is to determine the optimum performing conditions for the iron (Fe) diffusion in LN, by controling its microstructure and estimating its PR properties with only one technique, Raman spectroscopy.Several LN:Fe samples have been studied within this work. The aim is, among others, to control the iron diffusion profile, and to estimate the influence of the oxidizing or reducing treatment on the different crystals.Indeed I was able to show that the microstructure has been affected not only by the introduction of a dopant as Fe, but also by the various treatments. I showed for the first time the mecanism of Fe ions incorporation in LN structures obtained by diffusion.Otherwise, I proposed a new approach of the Raman activity rules, in the way they can take into account optical nonlinearities of the second order, which is generally neglected in litterature. Thus I have established the Raman configurations where, or the intensities of the lines are enhanced, or new lines are activated by a nonlinear process. These predictions have been confirmed by experimental results obtained on many samples. At last, I was able to propose a new method for the estimation of the PR efficiency, allowing to compare usefully several samples according to their doping or treatments
Guichard, Jordan. „Etude de l'hydrolyse de l'hydrure de lithium“. Thesis, Dijon, 2015. http://www.theses.fr/2015DIJOS050/document.
Der volle Inhalt der QuelleThe hydrolysis of LiH at room temperature and under low water vapor pressure (PH2O < 10 hPa) is investigated by thermogravimetry and FTIR spectroscopy with low sample mass. Then, to be closer to industrial conditions, hydrolysis of LiH is studied by manometry either in closed (adjustable PH2O) or open (constant PH2O) system using larger amounts of sample and heavy water. Products of the reaction are characterized by X-ray diffraction and FTIR spectroscopy. The first set of experiments show that the mechanism of hydrolysis starts with the formation of lithium oxide Li2O. Then, when the oxide layer is sufficiently thick, the hydrolysis reaction is followed by the formation of lithium hydroxide LiOH and afterwards with the formation of lithium hydroxide monohydrate LiOH, H2O. Besides, the Li2O/LiOH outer layer forms a protective barrier on the surface of LiH. The second set of experiments clearly highlights for the first time that the hydrolysis reaction occurs in two steps: first water is adsorbed on the LiH surface and then the hydrolysis reaction starts. The reaction rate is however extremely low and only a very small fraction of LiH is hydrolysed. The kinetic can be well predicted by the shrinking-core model limited by the diffusion through the external ash layer (Li2O and/or LiOH). For practical application, it is concluded that if the LiH powder is stored for several years under a controlled atmosphere or in a sealed container where the vapor water pressure is less than 0.04 hPa, there is no major risk of LiOH formation
Seung, Do-Young. „Approche structurale et étude de la conduction ionique de verres à base de thioarsenite de lithium et de verres à formateur mixte, thioborate et thioarsenite de lithium“. Bordeaux 1, 1995. http://www.theses.fr/1995BOR10544.
Der volle Inhalt der QuelleFleutot, Benoit. „Amélioration des performances des microbatteries au lithium : corrélation entre la structure locale et la conductivité ionique d’électrolytes solides amorphes“. Thesis, Bordeaux 1, 2010. http://www.theses.fr/2010BOR14162/document.
Der volle Inhalt der QuelleMicrobatteries are energy sources well-adapted to power microsystems such as the real time clock of mobile phones, smart tags RFID. To be considered as a microelectronic component, the microbattery must be compatible with the solder-reflow process which reaches a temperature of 260 °C during few seconds. During this Ph-D, various thin films of LiPON (lithium phosphate oxynitride) used as amorphous solid electrolyte have been prepared by sputtering. As this material presents limited performances for an application of the microbattery at low temperature, we have investigated the influence of its composition and local structure on its electrical performances. In addition, a decrease of its performances has been noticed after solder-reflow. In this work, we have proposed a new material, much more thermally stable. Finally, we have studied the compatibility of other active layers as well as the all-solid-state microbattery towards the solder-reflow
Dollé, Mickael. „Etude par spectroscopie d'impédance électrochimique, couplée à la microscopie électronique, d'interfaces de batteries au lithium et à ions lithium“. Amiens, 2002. http://www.theses.fr/2002AMIE0207.
Der volle Inhalt der QuelleZhang, Wanjie. „Etude des interfaces de batteries lithium-ion : application aux anodes de conversion“. Thesis, Pau, 2014. http://www.theses.fr/2014PAUU3024/document.
Der volle Inhalt der QuelleIn the past decades, the need for portable power has accelerated due to the miniaturization of electronic appliances. It continues to drive research and development of advanced energy systems, especially for lithium ion battery systems. As a consequence, conversion materials for lithium-ion batteries, including Sb and Sn-based compounds, have attracted much intense attention for their high storage capacities. Among conversion materials, TiSnSb has been recently developed as a negative electrode for lithium-ion batteries. This material is able to reversibly take up 6.5 Li per formula unit which corresponds to a specific capacity of 580 mAh/g. In the field of lithium-ion battery research, the solid electrolyte interphase (SEI) as a protective passivation film formed at electrode surface owing to the reduction of the electrolyte components, has been considered as a determinant factor on the performances of lithium-ion battery. Thus it has been a focused topic of many researches. However, little information can be found about the formation and composition of the SEI layer formed on TiSnSb conversion electrode at this time. With the aim to investigate the influences of the SEI layer on the performances of composite TiSnSb electrode, we first studied the electrochemical properties of the electrode from various aspects, including the effects of cycling rates, electrolyte additives, as well as room temperature ionic liquids (RTILs). Especially, a RTILs-based electrolyte system was developed and optimized by evaluating its physicochemical properties to be able to further improve the performances of TiSnSb electrode. In order to characterize the SEI layer formed at electrode surface, we performed X-ray photoelectron spectroscopy (XPS) and electrochemical impedance spectroscopy (EIS). This study allowed to target some essential parameters concerning electrochemical performances linked with the nature of the solid electrolyte interphase.*
Bücher zum Thema "Spectroscopie du lithium"
Fergani, Hadi. Determination of lithium in geological samples by using atomic absorption spectroscopy. Sudbury, Ont: Laurentian University, 1991.
Den vollen Inhalt der Quelle findenBullen, Peter Stanley. Domain Broadening in Periodic Poling of Thinned Lithium Niobate and Spectroscopic Methods for Whole Blood Analysis. [New York, N.Y.?]: [publisher not identified], 2019.
Den vollen Inhalt der Quelle findenGarbarino, John R. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory: Determination of dissolved arsenic, boron, lithium, selenium, strontium, thallium, and vanadium using inductively coupled plasma-mass spectrometry. Denver, Colo: U.S. Geological Survey, 1999.
Den vollen Inhalt der Quelle findenLithium, magnesium, calcium, strontium, and barium in waters and sewage effluents by atomic absorption spectrophotometry, 1987. London: H.M.S.O., 1987.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Spectroscopie du lithium"
Sebban, Muriel, Laure Guilhaudis und Hassan Oulyadi. „Spectroscopic Advances in Structural Lithium Chemistry: Diffusion-Ordered Spectroscopy and Solid-State NMR“. In Lithium Compounds in Organic Synthesis, 85–122. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch4.
Der volle Inhalt der QuelleZhang, Jianbo, Shangshang Wang und Kei Ono. „Electrochemical Impedance Spectroscopy“. In Microscopy and Microanalysis for Lithium-Ion Batteries, 301–50. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003299295-11.
Der volle Inhalt der QuelleJones, Amanda C. „Spectroscopic Advances in Organolithium Reactivity: The Contribution of Rapid-Injection NMR (RINMR)“. In Lithium Compounds in Organic Synthesis, 53–84. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch3.
Der volle Inhalt der QuelleAlcántara, Ricardo, Pedro Lavela, Carlos Pqérez Vicente und José L. Tirado. „Applications of Mössbauer Spectroscopy in The Study of Lithium Battery Materials“. In Mössbauer Spectroscopy, 552–63. Hoboken, New Jersey: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118714614.ch28.
Der volle Inhalt der QuelleZuerch, Michael. „Ultrafast Second-Harmonic XUV Spectroscopy: A Novel Probe for Symmetry“. In Springer Proceedings in Physics, 169–76. Cham: Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-47938-0_16.
Der volle Inhalt der QuelleDedryvere, R., S. Denis, J. Olivier-Fourcade und J. C. Jumas. „Lithium Insertion Mechanism in Copper Indium Tin Sulfospinels Studied by 119Sn Mössbauer Spectroscopy and Rietveld Analysis“. In Materials for Lithium-Ion Batteries, 577–80. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4333-2_43.
Der volle Inhalt der QuelleHandke, Miroslaw, und Marek Nocuń. „Vibrational Spectroscopy of Lithium Silicates and Aluminosilicates in Crystalline Form“. In Progress in Fourier Transform Spectroscopy, 507–10. Vienna: Springer Vienna, 1997. http://dx.doi.org/10.1007/978-3-7091-6840-0_124.
Der volle Inhalt der Quellevan Wijngaarden, W. A., und G. A. Noble. „Precision Laser Spectroscopy of Li+ and Neutral Lithium“. In Precision Physics of Simple Atoms and Molecules, 111–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75479-4_7.
Der volle Inhalt der QuellePruneri, V., S. D. Butterworth, J. Webjörn, P. St J. Russell und D. C. Hanna. „Green-Light Generation from Picosecond Pulses Via First-Order Quasi-Phase-Matched Lithium Niobate“. In Ultrafast Processes in Spectroscopy, 365–67. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4615-5897-2_82.
Der volle Inhalt der QuelleDeliyannis, C. P., J. R. King und A. M. Boesgaard. „Lithium in the Old Open Cluster M 67: Constraints for the Cause of the Boesgaard Li Gap“. In Wide-Field Spectroscopy, 201–4. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5722-3_33.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Spectroscopie du lithium"
Mashburn, Carter, Kristina Chang, Tsung-Han Wu, Luis Ledezma, Ryoto Sekine, Alireza Marandi und Scott A. Diddams. „Towards UV-Visible Dual-Comb Spectroscopy with Lithium Niobate Nanophotonic Waveguides“. In CLEO: Science and Innovations, SW4F.3. Washington, D.C.: Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_si.2024.sw4f.3.
Der volle Inhalt der QuelleKishkin, Krasimir, Dimitar Arnaudov, Kaspars Kroics und Vladimir Dimitrov. „Comparison of the Characretistics of a Lithium Ion and a Lithium Titanate Oxide Battery by Impedance Spectroscopy“. In 2024 23rd International Symposium on Electrical Apparatus and Technologies (SIELA), 1–5. IEEE, 2024. http://dx.doi.org/10.1109/siela61056.2024.10637828.
Der volle Inhalt der QuelleEngleman, R., L. J. Radziemski und J. W. Brault. „Reanalysis of 6Li I and 7Li I transitions using hollow cathode Fourier transform spectra“. In Fourier Transform Spectroscopy. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/fts.1995.ffd3.
Der volle Inhalt der Quellede Almeida, Jose M. M. M., Antonio M. P. P. Leite und Jaymin Amin. „Spectroscopy of doped lithium niobate“. In Symposium on Integrated Optoelectronics, herausgegeben von Shibin Jiang. SPIE, 2000. http://dx.doi.org/10.1117/12.382863.
Der volle Inhalt der QuelleBaxter, G. W., Y. He und B. J. Orr. „A pulsed, injection-seeded optical parametric oscillator system based on periodically poled lithium niobate for high-resolution spectroscopy“. In The European Conference on Lasers and Electro-Optics. Washington, D.C.: Optica Publishing Group, 1998. http://dx.doi.org/10.1364/cleo_europe.1998.cfh3.
Der volle Inhalt der QuelleIsler, R. C. „Spectroscopic techniques for studying magnetic fusion plasmas“. In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1989. http://dx.doi.org/10.1364/oam.1989.wy3.
Der volle Inhalt der QuelleSarkas, H. W., S. T. Arnold, Jackie Hendricks, V. L. Slager und Kit Bowen. „Photoelectron spectroscopy of lithium dimer anion“. In OE/LASE'93: Optics, Electro-Optics, & Laser Applications in Science& Engineering, herausgegeben von Cheuk Yiu Ng. SPIE, 1993. http://dx.doi.org/10.1117/12.143090.
Der volle Inhalt der QuelleChiuHuang, Cheng-Kai, Chuanzhen Zhou und Hsiao-Ying Shadow Huang. „Exploring Lithium-Ion Intensity and Distribution via a Time-of-Flight Secondary Ion Mass Spectroscopy“. In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-63013.
Der volle Inhalt der QuelleDonnelly, T. D., T. E. Glover, E. A. Lipman, M. Hofer, R. W. Falcone, L. Da Silva, S. Morwka und D. C. Eder. „Experiments with Short-Wavelength Lasers Driven by Ultra-Short Pulse, High-Intensity Lasers“. In High Resolution Fourier Transform Spectroscopy. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/hrfts.1994.wb2.
Der volle Inhalt der QuelleQi, Zhi-mei, Lichao Zhang und Ning Xue. „Design of a High-resolution Static Fourier Transform Spectrometer on Thin-film Lithium Niobate Substrate“. In Fourier Transform Spectroscopy. Washington, D.C.: OSA, 2021. http://dx.doi.org/10.1364/fts.2021.fw3d.3.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Spectroscopie du lithium"
Benn, D., R. Linnen und T. Martins. Evaluating white mica as an indicator mineral for lithium bearing pegmatites, Wekusko Lake pegmatite field, Manitoba, Canada. Natural Resources Canada/CMSS/Information Management, 2021. http://dx.doi.org/10.4095/328982.
Der volle Inhalt der QuelleTachikawa, Hiroyasu. In situ Raman spectroscopy of lithium electrode surface in ambient temperature lithium secondary battery. Final report. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/10160397.
Der volle Inhalt der QuelleAugustsson, Andreas. Soft X-ray emission spectroscopy of liquids and lithium batterymaterials. Office of Scientific and Technical Information (OSTI), Oktober 2004. http://dx.doi.org/10.2172/878312.
Der volle Inhalt der QuelleBarbour, R., Sunghyun Kim, D. Tryk und D. A. Scherson. In situ spectroscopic applications to the study of rechargeable lithium batteries. Final report. Office of Scientific and Technical Information (OSTI), August 1993. http://dx.doi.org/10.2172/10105605.
Der volle Inhalt der QuelleGofer, Y., R. Barbour, Yuyan Luo, In Tae Bae, Lin-Feng Li und D. A. Scherson. In situ spectroscopic applications to the study of rechargeable lithium batteries. Final report. Office of Scientific and Technical Information (OSTI), Juli 1996. http://dx.doi.org/10.2172/409896.
Der volle Inhalt der QuelleKilroy, W. P., S. A. Chmielewski und D. W. Bennett. Investigation of Li/SO2 Cell Hazards. 3. Raman Spectroscopy of Lithium Dithionite. Fort Belvoir, VA: Defense Technical Information Center, September 1988. http://dx.doi.org/10.21236/ada205756.
Der volle Inhalt der QuelleScherson, D., und G. Chottiner. Ex-situ and in-situ spectroscopic studies of the passive film on lithium in non-aqueous solvents. Office of Scientific and Technical Information (OSTI), Oktober 1990. http://dx.doi.org/10.2172/6009064.
Der volle Inhalt der QuelleKopasz, J. P., C. E. Johnson und J. Ortiz-Villafuerte. An investigation of the desorption of hydrogen from lithium oxide using temperature programmed desorption and diffuse reflectance infrared spectroscopy. Office of Scientific and Technical Information (OSTI), April 1995. http://dx.doi.org/10.2172/114938.
Der volle Inhalt der QuelleKopasz, J. P., C. E. Johnson und J. Ortiz-Villafuerte. An investigation of the desorption of hydrogen from lithium oxide using temperature programmed desorption and diffuse reflectance infrared spectroscopy. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/10181972.
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