Thematische Bibliographien / Diffusion du lithium

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Auswahl der wissenschaftlichen Literatur zum Thema „Diffusion du lithium“

Autor: Grafiati

Veröffentlicht am 29. März 2025

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Zeitschriftenartikel zum Thema "Diffusion du lithium"

Jun, KyuJung, und Gerbrand Ceder. „(Battery Division Student Research Award Sponsored by Mercedes-Benz Research & Development) Rationalizing Fast Lithium-ion Diffusion in Inorganic Lithium Superionic Conductors“. ECS Meeting Abstracts MA2023-02, Nr. 7 (22.12.2023): 985. http://dx.doi.org/10.1149/ma2023-027985mtgabs.

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All-solid-state batteries are gaining attention due to the potential advantage that solid electrolytes provide in terms of safety and energy density. Understanding the mechanism of fast lithium-ion diffusion in inorganic materials has become one of the key challenges in materials science. Among various factors that affect lithium mobility, the topology of the crystal structure strongly dictates which materials can accommodate fast lithium-ion motion. Despite this, the intrinsic mechanism that connects the lithium-ion diffusion to the structural feature of the crystal structure and motion of the non-diffusing framework remains unclear, hindering the rational design of novel fast-conducting solid electrolytes. This talk focuses on the fundamental understanding of the structure-property relationship of lithium-ionic conductivities. We first discuss the structural factors governing fast lithium-ion diffusion in oxide materials. We find that both the topology of the lithium-ion diffusion network as well as the connectivity of the non-diffusing framework strongly affect lithium-ions diffusion in oxide materials. Structural features that allow lithium superionic conductivity in oxide materials are identified, which led to the discovery of 16 novel fast lithium-ion conducting frameworks. In the second part of the talk, we present our statistical framework for understanding the correlation between anion-group rotational motion and lithium-ion translational motion. Using event-detection algorithms on long ab-initio molecular dynamics trajectories, we detect and differentiate various types of rotational motion of anion groups. This allows us to obtain a statistically rigorous understanding of how each type of anion group rotational motion affects lithium-ion diffusion events. These fundamental understandings provide design guidelines towards the development of fast-diffusing inorganic materials optimal for all-solid-state batteries.

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Ociepa, Jozef. „The Search for the Materials That Are Attractive to "Natural" Li Diffusion“. ECS Meeting Abstracts MA2022-02, Nr. 3 (09.10.2022): 296. http://dx.doi.org/10.1149/ma2022-023296mtgabs.

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"Natural" Li diffusion is defined as the process of Li atom/ions migration under a concentration gradient and activated by thermal energy from atomic vibrations of the host structure at room temperature. This process of passive Li diffusion is important for a better understanding of the active diffusion processes that are happening in lithium-ion batteries (LIBs), where external energy component such as electrical potential is applied. It is expected that materials that exhibit good “natural” Li diffusion properties will perform much better under the external electrical potential. This approach offers a unique opportunity to observe the free movement of lithium atoms/ions into the solid structure and simplify the understanding of diffusion processes especially if single-crystal structures are used. The single-crystal structures are free from grain boundaries and the lithium diffusion process is limited to lattice diffusions such as interstitial, vacancies, and dislocations. This approach allows for categorizing materials that are attractive to lithium diffusion based on the pure lattice component. The characterizing techniques are Auger electron spectroscopy (AES) for tracing Lithium concentration on the surface (Li-KVV peak at 52 eV) and Low Energy Electron Diffraction (LEED) for surface crystallography changes. The lithium concentration gradient is created on the surface of the host material by the evaporation of ultra-thin film of lithium with an effective thickness of 10 Angstrom under ultra-high vacuum conditions. The data obtained from these experiments are showing different lithium diffusion behavior on the selected materials and there is an indication of three categories of the studied materials. 1-Rapid lattice diffusion of Li into HOPG and no change in the surface crystalline structure. 2-Moderate lattice diffusion of Li into CVD Diamond, SiC-6H, LiNbO3, and TiO2 and some change in the surface crystalline structure. 3-No lattice diffusion of Li into Si single crystals, Ga2O3 and SrTiO3, and no long-range order in the surface crystalline structure. Most likely rapid diffusion occurs only in graphite but there are several materials with moderate diffusion properties, and these are potential for novel LIBs electrodes or chemically stable interfaces with enhanced performance. The materials with passive no-diffusion properties present challenges in application to LIBs as there is a special need to create active diffusion paths because there is no lattice diffusion contribution. In addition, this method of tracing lithium passive diffusion using AES is suitable for comparing fabricated polycrystalline LIBs electrodes as a metrology tool for quality control.

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Xu, Gao, Feng Hao, Mouyi Weng, Jiawang Hong, Feng Pan und Daining Fang. „Strong influence of strain gradient on lithium diffusion: flexo-diffusion effect“. Nanoscale 12, Nr. 28 (2020): 15175–84. http://dx.doi.org/10.1039/d0nr03746j.

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Loburets, A. T., N. B. Senenko, M. A. Mukhtarov, Yu S. Vedula und A. G. Naumovets. „Surface Diffusion in Coadsorbed Layers with Different Mobilities of Adsorbates: (Li +Dy) on Mo(112) and (Li+Sr) on W(112)“. Defect and Diffusion Forum 277 (April 2008): 201–6. http://dx.doi.org/10.4028/www.scientific.net/ddf.277.201.

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With the aim to study the regularities of surface diffusion in coadsorbed layers, we investigated diffusion of lithium on the (112) surfaces of Mo and W precovered with submonolayers of dysprosium and strontium, which have substantially lower mobilities than lithium. Experiments were carried out using scanning contact-potential microscopy, and Li diffusion parameters were extracted from diffusional evolution of coverage profiles. Dy and Sr preadsorbed in amounts of ∼10–1 of a monolayer were found to reduce the diffusion rate of Li by orders of magnitude. The strong impact of coadsorbates with low mobility on Li diffusion can be caused by important role of collective mechanisms in surface diffusion, which entails pronounced pinning effects, as well as by the possibility of formation of surface alloys and surface vitrification.

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Roselieb, Knut, Marc Chaussidon, Denis Mangin und Albert Jambon. „Lithium diffusion in vitreous jadeite (NaAlSi206): An ion microprobe investigation“. Neues Jahrbuch für Mineralogie - Abhandlungen 172, Nr. 2-3 (01.05.1998): 245–57. http://dx.doi.org/10.1127/njma/172/1998/245.

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Rupp, Rico, Bart Caerts, André Vantomme, Jan Fransaer und Alexandru Vlad. „Lithium Diffusion in Copper“. Journal of Physical Chemistry Letters 10, Nr. 17 (22.08.2019): 5206–10. http://dx.doi.org/10.1021/acs.jpclett.9b02014.

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Park, Jong Hyun, Hana Yoon, Younghyun Cho und Chung-Yul Yoo. „Investigation of Lithium Ion Diffusion of Graphite Anode by the Galvanostatic Intermittent Titration Technique“. Materials 14, Nr. 16 (19.08.2021): 4683. http://dx.doi.org/10.3390/ma14164683.

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Graphite is used as a state-of-the-art anode in commercial lithium-ion batteries (LIBs) due to its highly reversible lithium-ion storage capability and low electrode potential. However, graphite anodes exhibit sluggish diffusion kinetics for lithium-ion intercalation/deintercalation, thus limiting the rate capability of commercial LIBs. In order to determine the lithium-ion diffusion coefficient of commercial graphite anodes, we employed a galvanostatic intermittent titration technique (GITT) to quantify the quasi-equilibrium open circuit potential and diffusion coefficient as a function of lithium-ion concentration and potential for a commercial graphite electrode. Three plateaus are observed in the quasi-equilibrium open circuit potential curves, which are indicative of a mixed phase upon lithium-ion intercalation/deintercalation. The obtained diffusion coefficients tend to increase with increasing lithium concentration and exhibit an insignificant difference between charge and discharge conditions. This study reveals that the diffusion coefficient of graphite obtained with the GITT (1 × 10−11 cm2/s to 4 × 10−10 cm2/s) is in reasonable agreement with literature values obtained from electrochemical impedance spectroscopy. The GITT is comparatively simple and direct and therefore enables systematic measurements of ion intercalation/deintercalation diffusion coefficients for secondary ion battery materials.

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Dörrer, Lars, Philipp Tuchel, Daniel Uxa und Harald Schmidt. „Lithium tracer diffusion in proton-exchanged lithium niobate“. Solid State Ionics 365 (Juli 2021): 115657. http://dx.doi.org/10.1016/j.ssi.2021.115657.

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Zuo, Peng, und Ya-Pu Zhao. „A phase field model coupling lithium diffusion and stress evolution with crack propagation and application in lithium ion batteries“. Physical Chemistry Chemical Physics 17, Nr. 1 (2015): 287–97. http://dx.doi.org/10.1039/c4cp00563e.

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Lee, Danwon, Chihyun Nam, Juwon Kim, Bonho Koo, Hyejeong Hyun, Jinkyu Chung, Sungjae Seo et al. „(Battery Student Slam 8 Award Winner) Multi-Clustered Lithium Diffusion in Single-Crystalline NMC Battery Particles“. ECS Meeting Abstracts MA2024-01, Nr. 5 (09.08.2024): 704. http://dx.doi.org/10.1149/ma2024-015704mtgabs.

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Understanding the diffusion dynamics of lithium within solid-state electrodes is pivotal for developing high-performance batteries. In this context, layered oxides were utilized as a promising cathode material due to their high energy density and fast intraparticle lithium diffusivity. Despite advancements in material composition, coating, and doping, the understanding of intraparticle lithium diffusion has long been described by Fick's law. Conventionally, lithium diffusion is assumed to generate a monotonic lithium concentration gradient within solid-solution single-crystalline battery materials during cycling. This raises fundamental questions about diffusion in layered oxides; (1) Can the diffusion of Li in solids be interpreted as Fickian diffusion, similar to diffusion in gases or liquids, even though it involves structural and phase evolution throughout the battery cycle? and, (2) Does the fast diffusivity (10-11-10-9 cm2/s) support the homogenization of Li? In this study, we address these questions surrounding lithium diffusion in layered oxide by utilizing operando scanning transmission X-ray microscopy. We revealed the formation of mobile Li-dense/-dilute nano-domains within individual single-crystalline LiNi1/3Mn1/3Co1/3O2 (scNMC) during battery cycles. We term this phenomenon ‘multi-clustered lithium diffusion’, distinguishing our findings from the conventionally suggested Fickian diffusion model in solid-solution materials. These domains persist for at least 4 hours during relaxation, accompanied by locally residing strained domains, as confirmed by Bragg coherent diffraction imaging (BCDI), within a single particle. We believe these domains arise due to the compensation of localized chemical potential gradients that are generated by the sustained presence of strain within the battery particles during cycling. While maintaining integrity of Li-dense/-dilute domain at various C-rates, STXM result further show that Li-dilute domains maintain during the discharging. Given the lower concentration of Li at insertion boundaries, which could lower the surface charge transfer impedance of the system, Li-dilute domains facilitate lithium transport by functioning as low-resistance pathways. Through a comprehensive analysis of electrical impedance spectroscopy (EIS), STXM imaging and finite element analysis (FEA), we showed that controlling the local domain fraction is crucial for controlling the overpotential during subsequent charging. Our study introduces new insights into nanoscale solid-state diffusion, thereby enabling the fabrication of high-performance batteries. Figure 1

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Dissertationen zum Thema "Diffusion du lithium"

Senyshyn, A., M. Monchak, O. Dolotko und H. Ehrenberg. „Lithium Diffusion and Diffraction“. Diffusion fundamentals 21 (2014) 4, S.1, 2014. https://ul.qucosa.de/id/qucosa%3A32392.

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In the current contribution the application of bond valence method for the prediction (and diffraction-based techniques for the evalution) of ion diffusion pathways in different materials for electrochemical energy conversion and storage will be presented and discussed.

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Li, Juchuan. „UNDERSTANDING DEGRADATION AND LITHIUM DIFFUSION IN LITHIUM ION BATTERY ELECTRODES“. UKnowledge, 2012. http://uknowledge.uky.edu/cme_etds/12.

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Lithium-ion batteries with higher capacity and longer cycle life than that available today are required as secondary energy sources for a wide range of emerging applications. In particular, the cycling performance of several candidate materials for lithium-ion battery electrodes is insufficient because of the fast capacity fading and short cycle life, which is mainly a result of mechanical degradation. This dissertation mainly focuses on the issue of mechanical degradation in advanced lithium-ion battery electrodes. Thin films of tin electrodes were studied where we observed whisker growth as a result of electrochemical cycling. These whiskers bring safety concerns because they may penetrate through the separator, and cause short-circuit of the electrochemical cells. Cracking patterns generated in amorphous silicon thin film electrodes because of electrochemical cycling were observed and analyzed. A two-dimensional spring-block model was proposed to successfully simulate the observed cracking patterns. With semi-quantitative study of the cracking pattern features, two strategies to void cracking in thin-film electrodes were proposed, namely reducing the film thickness and patterning the thin-film electrodes. We also investigated electrodes consisting of low melting point elements and showed that cracks can be self-healed by the solid-to-liquid phase transformation upon cycling. Using gallium as an example, mechanical degradation as a failure mechanism for lithium-ion battery electrodes can be eliminated. In order to quantitatively understand the effect of surface modification on electrodes, we analyzed diffusion equations with boundary conditions of finite interfacial reactions, and proposed a modified potentialstatic intermittent titration technique (PITT) as an electro-analytical technique to study diffusion and interfacial kinetics. The modified PITT has been extended to thin-film geometry and spherical geometry, and thus can be used to study thin-film and composite electrodes consisting of particles as active materials.

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Heitjans, Paul. „Diffusion in lithium ion conductors – from fundamentals to applications“. Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-181798.

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Swanson, Claudia H., Michael Schulz, Holger Fritze, Jianmin Shi, Klaus-Dieter Becker, Peter Fielitz und Günter Borchardt. „Examinations of high-temperature properties of stoichiometric lithium niobate“. Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-186802.

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Epp, Viktor, Christian Brünig, Martin Wilkening, Michael Binnewies und Paul Heitjans. „Lithium diffusion studies of gas-phase synthesized amorphous oxides“. Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-188235.

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Heitjans, Paul. „Diffusion in lithium ion conductors – from fundamentals to applications“. Diffusion fundamentals 20 (2013) 19, S. 1-2, 2013. https://ul.qucosa.de/id/qucosa%3A13583.

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Rahn, J., E. Hüger, E. Witt, P. Heitjans und H. Schmidt. „Lithium Self-Diffusion in Single Crystalline and Amorphous LiAlO2“. Diffusion fundamentals 21 (2014) 16, S.1, 2014. https://ul.qucosa.de/id/qucosa%3A32425.

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Berggren, Elin. „Diffusion of Lithium in Boron-doped Diamond Thin Films“. Thesis, Uppsala universitet, Molekyl- och kondenserade materiens fysik, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413090.

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In this thesis, the diffusion of lithium was studied on boron-doped diamond (BDD) as a potential anode material in lithium ion batteries (LIB). The initial interaction between deposited lithium and BDD thin films was studied using X-ray Photoelectron Spectroscopy (XPS). Diffusion is directly linked to reactions between lithium and carbon atoms in the BDD-lithium interface. By measuring binding energies of core-electrons of carbon and lithium before and after deposition, these reactions can be analyzed. Scanning Electron Microscopy (SEM) was used to study the BDD surface and the behaviour of deposited lithium. Experiments show that a chemical interaction occurs between lithium and carbon atoms in the surfacelayers of the BDD. The diffusion of lithium is discussed from spectroscopic data and suggests that surface diffusion is occurring and no proof of bulk diffusion was found. The results do not exclude bulk diffusion in later states but it was not found in the initial interaction at the interface after depositing lithium. SEM images show that lithium clusters in the nanometer range are formed on the BDD surface. The results of this study give insights in the initial diffusion behaviour of lithium at the BDD interface and possible following events are discussed.

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Ohlendorf, Gerd, Denny Richter, Jan Sauerwald und Holger Fritze. „High-temperature electrical conductivity and electromechanical properties of stoichiometric lithium niobate“. Universitätsbibliothek Leipzig, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-192902.

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High temperature properties such as electrical conductivity (σ) and resonance behaviour of stoichiometric lithium niobate (LiNbO3) are determined in the temperature range from 20 to 950 °C. The activation energy of the conductivity is found to be 0.9 and 1.7 eV in the temperature range from 500 to 750 °C and from 800 to 950 °C, respectively. During thermal treatments in ambient air up to 950 °C and back, the conductivity remains unchanged at a given temperature, i.e., the crystal is stable under these conditions. The oxygen partial pressure (pO2) dependence of the conductivity shows two distinct ranges. At 750 °C, the property remains unchanged down to 10−15 bar. Below 10−15 bar, the conductivity increases according to σ ~ (pO2)−1/5. Z-cut LiNbO3 plates can be excited to thickness mode vibrations up to at least 900 °C. At this temperature, the quality factor Q is found to be between 30 and 100. As for changes of the conductivity, a decrease of the resonance frequency is observed below 10−15 bar indicating a correlation of both properties. In order to evaluate the lithium evaporation, the crystals are tempered at 900 °C in ambient air for 24 h. A depth profile of the constituents does not indicate lithium loss within the accuracy of the secondary ion mass spectroscopy. The preliminary results underline the potential of stoichiometric LiNbO3 for high-temperature applications and justify its closer investigation.

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Moore, Charles J. (Charles Jacob). „Ab initio screening of lithium diffusion rates in transition metal oxide cathodes for lithium ion batteries“. Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/79562.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2012.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 57-62).
A screening metric for diffusion limitations in lithium ion battery cathodes is derived using transition state theory and common materials properties. The metric relies on net activation barrier for lithium diffusion. Several cathode materials are screened using this approach: [beta]'-LiFePO4, hexagonal LiMnBO3, monoclinic LiMnBO3, Li 3Mn(CO3)(PO4), and Li9V3 (P2O7)3(PO4) 2. The activation barriers for the materials are determined using a combined approach. First, an empirical potential model is used to identify the lithium diffusion topology. Second, density functional theory is used to determine migration barriers. The accuracy of the empirical potential diffusion topologies, the density functional theory migration barriers, and the overall screening metric are compared against experimental evidence to validate the methodology. The accuracy of the empirical potential model is also evaluated against the density functional theory migration barriers.
by Charles J. Moore.
S.M.

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Bücher zum Thema "Diffusion du lithium"

Attiah, Abdul-Redha Dinar. Diffusion of tritium in neutron irradiated lithium fluoride and lithium carbonate. Salford: University of Salford, 1992.

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Lucuta, P. G. Diffusion of tritium in lithium-based fusion blanket ceramics: A review. Chalk River, Ont: Fuel Materials Branch Chalk River Laboratories, 1991.

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V, George Mathews Pharr. Diffusion, Deformation, and Damage in Lithium-Ion Batteries and Microelectronics. 2014.

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L'industrie lithique des populations blicquiennes: Organisation des productions et réseaux de diffusion. British Archaeological Reports Oxford Ltd, 2017.

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Buchteile zum Thema "Diffusion du lithium"

Julien, Christian, und Alain Mauger. „Diffusion“. In Rechargeable Lithium Metal Batteries, 1–24. Cham: Springer Nature Switzerland, 2024. https://doi.org/10.1007/978-3-031-67470-9_1.

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Winkelmann, Jochen. „Diffusion coefficient of lithium(6) in lithium“. In Diffusion in Gases, Liquids and Electrolytes, 1328. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1104.

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Winkelmann, Jochen. „Diffusion coefficient of lithium(7) in lithium“. In Diffusion in Gases, Liquids and Electrolytes, 1879. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1307.

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Winkelmann, Jochen. „Diffusion coefficient of lithium(6) in lithium“. In Diffusion in Gases, Liquids and Electrolytes, 1880. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1308.

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Michaud, G., und G. Beaudet. „Lithium Abundance, Diffusion and Turbulence“. In Highlights of Astronomy, 459–60. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-010-9374-3_78.

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Winkelmann, Jochen. „Self-diffusion coefficient of lithium“. In Diffusion in Gases, Liquids and Electrolytes, 534–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_320.

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Luong, Huu Duc, Thien Lan Tran und Van An Dinh. „Small Polaron–Li-Ion Complex Diffusion in the Cathodes of Rechargeable Li-Ion Batteries“. In Lithium-Related Batteries, 29–39. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003263807-2.

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Skullerud, H. R., T. Eide und Thorarinn Stefansson. „Transverse Diffusion of Lithium Ions in Helium“. In Swarm Studies and Inelastic Electron-Molecule Collisions, 81. New York, NY: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4612-4662-6_9.

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Shokuhfar, Ali, Arash Rezaei, S. M. M. Hadavi, Shahram Ahmadi und H. Azimi. „Effect of Homogenization Process on Hot Rolling of Aluminum-Lithium Alloys“. In Defect and Diffusion Forum, 20–25. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/3-908451-36-1.20.

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Winkelmann, Jochen. „Diffusion coefficient of lithium dodecyl sulfate in water“. In Diffusion in Gases, Liquids and Electrolytes, 1476. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_996.

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Konferenzberichte zum Thema "Diffusion du lithium"

Di Fonso, Roberta, Francesco Simonetti, Remus Teodorescu und Pallavi Bharadwaj. „A Fast Technique for Lithium-Ion Diffusion Coefficient Determination in Batteries“. In 2024 International Symposium on Power Electronics, Electrical Drives, Automation and Motion (SPEEDAM), 656–60. IEEE, 2024. http://dx.doi.org/10.1109/speedam61530.2024.10609072.

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Rocca, Dario, Matthias Loipersberger, Jérôme F. Gonthier, Robert M. Parrish, Jisook Hong, Byeol Kang, Chanshin Park und Hong Woo Lee. „Towards Quantum Simulations of Lithium Diffusion in Solid State Electrolytes for Battery Applications“. In 2024 IEEE International Conference on Quantum Computing and Engineering (QCE), 655–61. IEEE, 2024. https://doi.org/10.1109/qce60285.2024.00082.

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Suntsov, Sergiy, Sarah Kretschmann, Kore Hasse und Detlef Kip. „Diffusion-Doped Lithium Tantalate Waveguides for Watt-level Nonlinear Frequency Conversion in the Near UV“. In CLEO: Science and Innovations, SM4N.2. Washington, D.C.: Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_si.2024.sm4n.2.

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Highly photorefractive optical damage resistant ridge waveguides for near UV and short-wavelength visible ranges have been fabricated using high-temperature diffusion doping with different metal ions and vapor transport equilibration method of commercially available congruently melting LiTaO3 crystals.

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Sivan, V., L. Bui, D. Venkatachalam, S. Bhargava, T. Priest, A. Holland und A. Mitchell. „Etching lithium niobate during Ti diffusion process“. In Microelectronics, MEMS, and Nanotechnology, herausgegeben von Hark Hoe Tan, Jung-Chih Chiao, Lorenzo Faraone, Chennupati Jagadish, Jim Williams und Alan R. Wilson. SPIE, 2007. http://dx.doi.org/10.1117/12.759612.

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Hoff, Christiana, Sarah Penniston-Dorland, Philip Piccoli, Danny Stockli und Lisa Stockli. „Lithium diffusion in pyrope-almandine rich garnets“. In Goldschmidt2022. France: European Association of Geochemistry, 2022. http://dx.doi.org/10.46427/gold2022.12298.

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Garvey, Brendan, Megan Holycross und Gabe Larouche. „Multi-pathway diffusion of lithium in feldspar“. In Goldschmidt 2024. United States of America: Geochemical Society, 2024. https://doi.org/10.46427/gold2024.22282.

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RUZIN, ARIE, NIKOLAI ABROSIMOV und PIOTR LITOVCHENKO. „STUDY OF LITHIUM DIFFUSION INTO SILICON-GERMANIUM CRYSTALS“. In Proceedings of the 10th Conference. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812819093_0102.

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Wang, Airong, Guangming Wu, Hui-yu Yang, Ming-xia Zhang, Xingmei Fang, Xiao-yun Yang, Bin Zhou und 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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Yost, Cheyenne R., Emily Cahoon, Adam Kent, Scott Toney und Kyle Nunely. „COPPER AND LITHIUM DIFFUSION IN EASTER OREGON SUNSTONES“. In Cordilleran Section - 119th Annual Meeting - 2023. Geological Society of America, 2023. http://dx.doi.org/10.1130/abs/2023cd-387527.

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Gan, X. F., F. Zhang, X. Y. He, Y. Z. Cao, J. Z. Yang und X. D. Huang. „Sio2by chemical vapor deposition as lithium diffusion barrier layer for integrated lithium-ion battery“. In 2017 International Conference on Electron Devices and Solid-State Circuits (EDSSC). IEEE, 2017. http://dx.doi.org/10.1109/edssc.2017.8333232.

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Berichte der Organisationen zum Thema "Diffusion du lithium"

Bhatia, Harsh, Attila Gyulassy, Mitchell Ong, Vincenzo Lordi, Erik Draeger, John Pask, Valerio Pascucci und Peer Timo Bremer. Understanding Lithium Solvation and Diffusion through Topological Analysis of First-Principles Molecular Dynamics. Office of Scientific and Technical Information (OSTI), September 2016. http://dx.doi.org/10.2172/1331475.

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Balapanov, M. Kh, K. A. Kuterbekov, M. M. Kubenova, R. Kh Ishembetov, B. M. Akhmetgaliev und R. A. Yakshibaev. Effect of lithium doping on electrophysical and diffusion proper-ties of nonstoichiometric superionic copper selenide Cu1.75Se. Phycal-Technical Society of Kazakhstan, Dezember 2017. http://dx.doi.org/10.29317/ejpfm.2017010203.

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Friend, James, An Huang, Ping Liu und Haodong Liu. Final project report for: Rapid charging made practical in graphite-based lithium batteries: surface-acoustic wave turbulent electrolyte mixing to overcome diffusion limited charging rates. Office of Scientific and Technical Information (OSTI), April 2021. http://dx.doi.org/10.2172/1778016.

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Stotler, D. P., C. H. Skinner, W. R. Blanchard, P. S. Krstic, H. W. Kugel, H. Schneider und L. E. Zakharov. Simulation of Diffusive Lithium Evaporation Onto the NSTX Vessel Walls. Office of Scientific and Technical Information (OSTI), Dezember 2010. http://dx.doi.org/10.2172/1001673.

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Environmental Assessment for the sale of excess lithium hydroxide stored at the Oak Ridge K-25 Site and the Portsmouth Gaseous Diffusion Plant. Office of Scientific and Technical Information (OSTI), April 1993. http://dx.doi.org/10.2172/10173192.

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