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Статті в журналах з теми "Glassy Electrolytes"

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Morales, Daniel J., and Steven Greenbaum. "NMR Investigations of Crystalline and Glassy Solid Electrolytes for Lithium Batteries: A Brief Review." International Journal of Molecular Sciences 21, no. 9 (May 11, 2020): 3402. http://dx.doi.org/10.3390/ijms21093402.

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The widespread use of energy storage for commercial products and services have led to great advancements in the field of lithium-based battery research. In particular, solid state lithium batteries show great promise for future commercial use, as solid electrolytes safely allow for the use of lithium-metal anodes, which can significantly increase the total energy density. Of the solid electrolytes, inorganic glass-ceramics and Li-based garnet electrolytes have received much attention in the past few years due to the high ionic conductivity achieved compared to polymer-based electrolytes. This review covers recent work on novel glassy and crystalline electrolyte materials, with a particular focus on the use of solid-state nuclear magnetic resonance spectroscopy for structural characterization and transport measurements.
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Wheaton, Jacob, and Steve Martin. "Electrochemical Characterization of a Drawn Thin-Film Mixed Oxy-Sulfide Glassy Electrolyte Material for Solid-State Battery Applications." ECS Meeting Abstracts MA2022-02, no. 4 (October 9, 2022): 489. http://dx.doi.org/10.1149/ma2022-024489mtgabs.

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Solid-state batteries are a promising avenue for next-generation lithium-ion batteries due to their enabling of the lithium metal anode, while simultaneously removing the flammable organic electrolyte. Glassy materials are particularly interesting as solid-state electrolytes due to their intrinsic lack of grain boundaries, their low temperature forming capabilities, and their highly tunable chemistries. Much work has been done to study the electrochemical properties of glasses in the Li2S – SiS2 – LixMOy phase space, and several compositions have shown high ionic conductivities (~ 10-3 S/cm), large electrochemical stability windows (0-5 V vs. Li/Li+), and good glass forming ability. These glasses, however, have not been well studied at thicknesses that are viable for commercialization of solid electrolytes (< 100 μm). Utilizing a glass working method known as the redraw process, a rectangular preform of glass can be reheated and drawn from ~ 5 mm in thickness to thin films of less than 100 μm. The electrochemical behavior of thin-film glasses in the Li2S – SiS2 – LiPO3 phase space created through the glass redraw process are studied utilizing electrochemical impedance spectroscopy, cyclic voltammetry, and galvanostatic symmetric cell cycling. These results show that thin-film glassy solid electrolytes made through the glass redraw method are a viable new research direction for generation of highly conducting thin-film solid-state electrolytes.
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TSIULYANU, D., I. STRATAN, and M. CIOBANU. "INFLUENCE OF GLASSY BACKBONE ON THE PHOTOFORMATION AND PROPERTIES OF SOLID ELECTROLYTES Ag : As-S-Ge." Chalcogenide Letters 17, no. 1 (January 2020): 9–14. http://dx.doi.org/10.15251/cl.2020.171.9.

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The effect of the glassy backbone on the process of fabrication and some properties of solid electrolytes obtained via photodissolution (PD) of Ag into chalcogenide glasses (ChG) of the system As-S-Ge have been studied with respect to XRD and far IR spectroscopy analyses. The compositional tie – line (GeS4)x (AsS3)1-x has been chosen to realize the monotonic transition of the structural units of glassy backbone from trigonal to tetragonal configuration. It is shown that the process of solid electrolyte formation occurs in three steps, but the last two steps, as well as the electrical properties of the finally fabricated electrolyte, are strongly influenced by chemical composition and microstructure of the used ChG backbone. The rate of solid electrolyte formation exhibit a maximum around of glassy backbone composition (GeS4)0.33(AsS3)0.67 but the electrical resistivity of fabricated solid electrolytes reaches a minimum at this composition. Based on IR transmission spectra analyses, it is assumed that these peculiarities are due to glass homogenization, which results from building in this alloyed composition of an amalgamation of tetrahedral and trigonal structural units connected in a random network, without clustering. Such homogenization promotes the transport of both electrons and ions involved in photoreaction because of lack of phase boundaries and additional defects.
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Okkema, Mary, Madison Martin, and Steve Martin. "Electrochemical Characterization of a Drawn Thin-Film Glassy Mixed Oxy-Sulfide-Nitride Phosphate Electrolyte Material for Applications in Solid-State Batteries." ECS Meeting Abstracts MA2022-02, no. 4 (October 9, 2022): 414. http://dx.doi.org/10.1149/ma2022-024414mtgabs.

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Thin-film glassy solid-state electrolytes are often considered for applications in energy storage devices; fully-dense thin-film glassy electrolyte materials are able to minimize power loss while suppressing dendrite growth. The glass with the composition Na4P2S5.8O0.92N0.18 (NaPSON) was chosen because it balances the high conductivity of a sulfide chemistry with the high processability and electrochemical stability of an oxy-nitride chemistry. NaPSON thin-film glassy solid-state electrolyte ribbons with thicknesses that range from 75 to 600 μm were drawn using a process of softening and drawing of a cast and annealed preform. Raman spectroscopy was run on the thin-film samples to ensure the material was structurally similar after processing across different thicknesses and remelts. Electrochemical impedance spectroscopy (EIS) was used on varying thicknesses of thin-film to investigate and compare the ionic conductivity of Na+ in the thin film compared to the bulk sample. Area specific resistance models as a function of time were created to compare the trend of bulk and interfacial resistances of different thicknesses. Thin-film samples were made into symmetric cells and cycled. The cycling of the symmetric cells gave insight into the behavior and durability of the electrolyte under applied voltage and sustained current. These results show that drawn thin-film electrolytes are a solid research direction.
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Martin, Madison, Mary Okkema, and Steve Martin. "Electrochemical Characterization of a Drawn Thin-Film Glassy Mixed Oxy-Sulfide-Nitride Phosphate Electrolyte for Applications in Solid-State Batteries." ECS Meeting Abstracts MA2022-02, no. 4 (October 9, 2022): 530. http://dx.doi.org/10.1149/ma2022-024530mtgabs.

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Thin-film glassy solid-state electrolytes (GSEs) are being considered for applications in energy storage devices; fully-dense thin-film glassy electrolyte materials are able to minimize power loss while suppressing dendrite growth. The glass with the composition Na4P2S5.8O0.92N0.18 (NaPSON) was chosen because it balances the high conductivity of a sulfide chemistry with the high processability and electrochemical stability of an oxy-nitride chemistry. NaPSON thin-film GSE ribbons with thicknesses that range from 50 to 150 μm were drawn using a process of softening and drawing of a cast and annealed preform. Electrochemical impedance spectroscopy (EIS) was used on varying thicknesses of thin-film to investigate and compare the ionic conductivity of Na+ in the thin film compared to the bulk sample. Area specific resistance models as a function of time were created to compare the trend of bulk and interfacial resistances of different thicknesses. Thin-film samples were made into symmetric cells and cycled. The cycling of the symmetric cells gave insight into the behavior and durability of the electrolyte under applied voltage and sustained current. These results show that drawn thin-film electrolytes are a viable research direction for all solid-state batteries.
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Bin, Wu, and Fan Chun. "Summary of Lithium-Ion Battery Polymer Electrolytes." Advanced Materials Research 535-537 (June 2012): 2092–99. http://dx.doi.org/10.4028/www.scientific.net/amr.535-537.2092.

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Polymer electrolyte is a good ion conductor in lithium-ion battery with an excellent performance in conductivity, ion mobility and ion transport number. Some researches show strengthening mechanisms of polymer electrolyte membranes correlated with macromolecules group weight of PEGDME such as concentration of compounded Li+ salt. Ion transport in glassy polymer electrolytes including polymer backbones with same mesogenic chains can affect amorphous structure and relaxation at ambient temperature. In addition, singe crystal structure polymer electrolytes have various internal microstructures and external properties such as conductivity and charge or discharge stability in electrochemical that correlating with layers of ion diffusion and forming.
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Ingram, M. "Ion transport in glassy electrolytes." Solid State Ionics 94, no. 1-4 (February 1, 1997): 49–54. http://dx.doi.org/10.1016/s0167-2738(96)00610-8.

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Choi, H., H. K. Kim, Y. W. Koo, K. H. Nam, S. M. Koo, W. J. Cho, and H. B. Chung. "Investigation of Electrical Properties in Chalcogenide Thin Film According to Wave Length." Advanced Materials Research 31 (November 2007): 135–37. http://dx.doi.org/10.4028/www.scientific.net/amr.31.135.

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Programmable metallization cell (PMC) memory is based on the electrochemical control of nanoscale quantities of metal in thin films of solid electrolyte. We investigate the nature of thin films formed by the photo-dissolution of Ag into Ge-Se-Te glasses for use in programmable metallization cell devices. Glassy alloys of a-Ge25Se75-xTex(x = 0, 25) are prepared by well known melt-quenching technique. Thin films of a-Ge25Se75-xTex(x = 0, 25) glassy alloys are evaporated by vacuum evaporation technique at ~10-6 torr on glass substrate at room temperature. Optical properties in this study concerns photo-diffusion of Ag on Ag-doped Ge-Se-Te electrolytes. With these promising properties, the composition a-Ge25Se75-xTex(x = 0, 25) is recommended as a potential candidate for PMC-RAM.
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Vukicevic, Natasa, Vesna Cvetkovic, Nebojsa Nikolic, Goran Brankovic, Tanja Barudzija, and Jovan Jovicevic. "Formation of the honeycomb-like MgO/Mg(OH)2 structures with controlled shape and size of holes by molten salt electrolysis." Journal of the Serbian Chemical Society 83, no. 12 (2018): 1351–62. http://dx.doi.org/10.2298/jsc180913084v.

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Анотація:
Synthesis of the honeycomb-like MgO/Mg(OH)2 structures, with controlled shape and size of holes, by the electrolysis from magnesium nitrate hexahydrate melt onto glassy carbon is presented. The honeycomb-like structures were made up of holes, formed from detached hydrogen bubbles, surrounded by walls, built up of thin intertwined needles. For the first time, it was shown that the honeycomb-like structures can be obtained by molten salt electrolysis and not exclusively by electrolysis from aqueous electrolytes. Analogies with the processes of the honeycomb-like metal structures formation from aqueous electrolytes are presented and discussed. Rules established for the formation of these structures from aqueous electrolytes, such as the increase of number of holes, the decrease of holes size and coalescence of neighbouring hydrogen bubbles observed with increasing cathodic potential, appeared to be valid for the electrolysis of the molten salt used.
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Fettkether, Will, Steve Martin, and Jacob Wheaton. "Development and Optimization of Composite Cathode Materials for Use with Thin-Film Glassy Solid Electrolytes in Solid-State Batteries." ECS Meeting Abstracts MA2022-02, no. 4 (October 9, 2022): 515. http://dx.doi.org/10.1149/ma2022-024515mtgabs.

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The electrochemical properties and thermal behavior of thin-film glassy solid electrolytes (GSE) in the [Li2S - SiS2 - LiPO3] system make them viable candidates for inclusion in solid-state batteries. To properly assess these electrolytes in the full-cell format, compatible composite cathode materials must be developed. These materials must be electronically and ionically conductive, and form a stable interface in contact with the GSE. A composite blend of redox-active lithium iron phosphate (LiFePO4), a mixed-oxy-sulfide glassy electrolyte, carbon nanotubes, a lithium solvate ionic liquid (SIL), and styrene butadiene rubber binder (SBR) was utilized to create the cathode material. Mixing time and order of component mixing were controlled in order to optimize for ionic and electronic conductivities within the bulk composite powder. With the addition of the SIL and SBR, a composite cathode blend capable of stably cycling in contact with the GSE was created.
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Дисертації з теми "Glassy Electrolytes"

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Reuter, Daniel [Verfasser], and Alois [Akademischer Betreuer] Loidl. "Ionic and Dipolar Dynamics in Glassy Electrolytes / Daniel Reuter ; Betreuer: Alois Loidl." Augsburg : Universität Augsburg, 2020. http://d-nb.info/1222437201/34.

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Karlsson, Christian. "Ionic conduction in glasses and nanocomposite polymer electrolytes /." Göteborg : Chalmers university of technology, 2003. http://catalogue.bnf.fr/ark:/12148/cb392991306.

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Salami, Taiye James. "Novel Conductive Glass-Perovskites as Solid Electrolytes in Lithium – ion Batteries." University of Toledo / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1533220964477566.

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Novita, Deassy I. "Evidence for Intermediate Phase in Solid Electrolyte Glasses." University of Cincinnati / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1234751813.

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Mahapatra, Manoj Kumar. "Study of Seal Glass for Solid Oxide Fuel/Electrolyzer Cells." Diss., Virginia Tech, 2009. http://hdl.handle.net/10919/77281.

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Seal glass is essential and plays a crucial role in solid oxide fuel/electrolyzer cell performance and durability. A seal glass should have a combination of thermal, chemical, mechanical, and electrical properties in order to seal different cell components and stacks and prevent gas leakage. All the desired properties can simultaneously be obtained in a seal glass by suitable compositional design. In this dissertation, SrO-La₂O₃-A₂O₃-B₂O₃3-SiO₂ based seal glasses have been developed and composition-structure-property relationships have been investigated. B₂O₃ free SrO-La₂O₃-Al₂O₃-SiO₂ based seal glass is the most suitable and its compatibility with the metallic interconnects and sealing performances have been evaluated. A seal glass should be stable for 5,000-40,000 hrs in the oxidizing and reducing atmospheres at 600-900°C but both the thermal and chemical stability is a persistent problem. The effect of Al₂O₃ on a SrO-La₂O₃-Al₂O₃-B₂O₃-SiO₂ based seal glass has been studied to improve the thermal properties, such as glass transition temperature, softening temperature and thermal expansion coefficient, and the thermal stability. Al₂O₃ improves the thermal stability but does not significantly affect the thermal properties of the seal glass. Comprehensive understanding of composition-structure-property relationships is needed to design a suitable seal glass. The thermal properties and stability of a borosilicate seal glass depend on the B2O3:SiO2 ratio in the composition. The role of B₂O₃:SiO₂ ratio on the glass network structure of the SrO-La₂O₃-Al₂O₃-B₂O₃-SiO₂ based seal glasses has been studied using Raman spectroscopy and nuclear magneto resonance spectroscopy. The thermal properties and thermal stability were correlated with the glass network structure and the calculated network connectivity. This study shows that the thermal properties degrade with increasing B₂O₃:SiO₂ ratio due to increase in the non-bridging oxygen and decrease in the network connectivity. High B₂O₃:SiO₂ ratio induces BO4 and SiO4 structural unit ordering, increases micro-heterogeneity, and subsequently degrades thermal stability. B₂O₃ free SrO-La₂O₃-Al₂O₃-SiO₂ seal glass shows the best combination of the thermal properties and thermal stability among the studied glasses. Nickel or nickel oxide is added into a seal glass to modify the thermal properties depending on the specific composition. The role of nickel as a network former or modifier and its effect on the thermal properties and thermal stability of the SrO-La₂O₃-Al₂O₃-SiO₂ based seal glasses have been investigated. Nickel is a modifier in this glass system and does not improve the thermal properties but degrades thermal stability by decreasing network connectivity and inducing micro-heterogeneity. The interconnect-seal glass interface stability is the most crucial for solid oxide fuel/electrolyzer cell. Crofer 22 APU and AISI 441 alloys are the preferred interconnects. The interfacial stability of the SrO-La₂O₃-Al₂O₃-SiO₂ based seal glass with these alloys have been studied as a function of time (0-1000 hrs), temperature (700-850°C), atmospheres (air, argon, and H₂O/H₂) using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray diffraction analysis (XRD). Complementary analytical techniques such as wave length dispersive spectroscopy (WDS) and SEM of thin samples were also carried out for selected samples. This study shows good interfacial stability of the SrO-La₂O₃-Al₂O₃-SiO₂ based seal glass with these alloys for the studied conditions. A suitable seal glass should be hermetic and withstand 100-1000 thermal cycles for practical application. Sealing performances of the SrO-La2O3-Al2O3-SiO2 based seal glass have been evaluated by pressure-leakage method. The seal glass is hermetic for at least 2000 hrs and withstands 100 thermal cycles. Overall, present work shows that the SrO-La₂O₃-Al₂O₃-SiO₂ based glass has all the desired properties and suitable for solid oxide fuel/electrolyzer cell seal.
Ph. D.
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Cohen, Sally Elizabeth. "Synthesis and characterisation of glass electrolytes for sensing bismuth and antimony in non ferrous metals." Thesis, University of Leeds, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275676.

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Wachtman, Jacob L. "Molecular structure of (AsSe)₁₋x̳ (Ag₂Se)x̳ solid electrolyte glasses." Cincinnati, Ohio : University of Cincinnati, 2009. http://rave.ohiolink.edu/etdc/view.cgi?acc_num=ucin1250625212.

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Thesis (M.S.)--University of Cincinnati, 2009.
On t.p. "x̳" is subscript. Advisor: P. Boolchand. Title from electronic thesis title page (viewed Jan. 14, 2010). Includes abstract. Keywords: AsSe; Ag2Se; AgAsSe; solid electrolyte glass; raman. Includes bibliographical references.
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Pablo, Fleurdelis, of Western Sydney Nepean University, and Faculty of Science and Technology. "Adsorptive stripping voltammetry of trace elements on a glassy carbon mercury film electrode." THESIS_FST_XXX_Pablo_F.xml, 1994. http://handle.uws.edu.au:8081/1959.7/207.

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This thesis describes the development of new adsorptive cathodic stripping voltammetric methods for reliable determination of some trace metals in biological and environmental materials on a glassy carbon mercury film electrode. In particular, the development of these methods involved selection of a suitable complexing agent for the respective metal ion studied, characterization of the electrode processes, investigation of factors affecting the voltammetric response such as concentration and pH of supporting electrolyte, concentration of complexing agent, accumulation potential, accumulation time and electrode rotation rate. Also, organic and inorganic interferences, linear concentration range, and detection limits were carefully considered. Furthermore, the analytical application of the method was demonstrated for each metal in biological and/or environmental materials, after optimization of the sample decomposition procedure. Some conclusions : the results obtained by the AdCSV method for the determination of tin in juices agreed reasonably with those obtained by atomic absorption method; the use of the adsorptive voltammetric technique after dry-ashing and UV treatment of the samples was successfully demonstrated for the determination of vanadium in standard reference materials such as urban particulate matter, peach leaves, apple leaves and bovine liver; and, the use of the adsorptive stripping voltammetric technique, after decomposition of samples by dry-ashing and UV treatment, was successfully demonstrated for the determination of molybdenum in peach leaves, apple leaves and bovine liver samples.
Doctor of Philosophy (PhD)
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Jui, Sumit Kumar Narendrakumar. "Study of Micro-Electrochemical Discharge Machining (ECDM) Using Low Electrolyte Concentration." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1384870046.

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Castro, Alexandre. "Développement de batteries tout solide sodium ion à base d’électrolyte en verre de chalcogénures." Thesis, Rennes 1, 2018. http://www.theses.fr/2018REN1S126/document.

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L'évolution des consommations énergétiques au cours des dernières décennies entraîne des modifications majeures dans la conception des systèmes électriques autonomes à fournir, que ce soit pour des applications électriques ou électroniques. La nécessité présente de réaliser des générateurs capables de délivrer l'énergie suffisante, avec une garantie de sûreté maximale, impose à la recherche l'exploration de nouvelles voies de stockage. Les voies actuelles par accumulateurs au lithium tendent à montrer leurs limites, tant stratégiques qu'environnementales. Dans ce cadre, la construction de nouveaux systèmes électrochimiques mettant en œuvre le sodium ouvre une possibilité de réalisation d'accumulateurs sans lithium. Le besoin de batteries toujours plus performantes oblige à des conceptions innovantes, abandonnant la voie liquide au profit de systèmes tout solide plus sécuritaires. De plus, la miniaturisation de l'électronique conduit à revoir le dimensionnement des batteries, vers des batteries de type micro, pour lesquelles l'intérêt d'un empilement tout solide n'est plus à démontrer. Aujourd'hui, des verres de chalcogénures au soufre permettent l'accès à des conductivités ioniques qui laissent entrevoir la possibilité d'une réalisation de batteries tout solide, à la fois sous forme de micro batteries ou de batteries massives. Un effort de recherche a été porté à la formulation de ces verres de chalcogénures afin d'obtenir des conductivités ioniques maximales et des propriétés autorisant leur utilisation comme électrolyte. La modification de ces verres met alors en lumière l'intérêt des différents éléments les composant. L'étude de la mise en forme de l'électrolyte par dépôts de type couches minces (obtenues par Radio Fréquence Magnétron Sputering, RFMS) prouve la faisabilité de ces micro batteries tout solide au sodium. Par la suite, la réalisation de batteries massives tout solide a demandé la synthèse de deux matériaux de cathode (NaCrO2 et Na[Ni0,25Fe0,5Mn0,25]O2) et de deux matériaux d'anode (Na15Sn4 et Na) permettant ainsi la mise en œuvre de quatre empilements électrochimiques, tous caractérisés comme accumulateurs. Enfin, l'amélioration des interfaces grâce à un gel-polymère a permis de perfectionner les propriétés des assemblages avec notamment une augmentation des vitesses de charge/décharge et une mobilisation accrue des matériaux actifs de cathode
The evolution of energy consumption in recent decades has led to major changes in the design of autonomous electrical systems dedicated to either electrical or electronic applications. The present demand to build generators capable of delivering sufficient energy, with a guarantee of maximum safety, requires to explore new storage routes. The current lithium battery routes tend to show their limits, both strategic and environmental. In this context, the construction of new electrochemical systems implementing sodium opens the way of the lithium-free accumulators production. The need for ever more efficient batteries requires innovative designs, giving up the liquid path in favor of stronger solid systems. In addition, the miniaturization of electronics leads to a review of the size of the batteries, to micro-type batteries, for which the interest of a solid stack is no longer to demonstrate. Today, sulfur chalcogenide glasses allow access to ionic conductivities that suggest the possibility of a realization of all solid batteries, both in the form of micro batteries or massive batteries. A research effort has been made to formulate these chalcogenide glasses in order to obtain a maximum of ionic conductivity and properties allowing their use as electrolytes. The composition of these glasses highlights the interest of the different elements for such properties. The study of the electrolyte shaping by thin-film deposition (obtained by Radio Frequency Magnetron Sputering, RFMS) proves the feasibility of these all-solid sodium micro-batteries. Subsequently, the realization of massive all solid batteries required the synthesis of two cathode materials (NaCrO2 and Na [Ni0.25Fe0.5Mn0.25]O2) and two anode materials (Na15Sn4 and Na) thus allowing the implementation of four electrochemical stacks, all characterized as accumulators. Finally, the improvement of the interfaces thanks to a gel-polymer made it possible to improve the properties of the assemblies with notably an increase of the speeds of charge / discharge and an enhanced mobilization of the cathode active materials
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Книги з теми "Glassy Electrolytes"

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Bhattacharya, Sanjib, and Koyel Bhattacharya, eds. Lithium Ion Glassy Electrolytes. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4.

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Bhattacharya, Koyel, and Sanjib Bhattacharya. Lithium Ion Glassy Electrolytes: Properties, Fundamentals, and Applications. Springer, 2022.

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Частини книг з теми "Glassy Electrolytes"

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Poddar, Asmita, Madhab Roy, and Sanjib Bhattacharya. "Electrodes." In Lithium Ion Glassy Electrolytes, 137–46. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_13.

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Bhattacharya, Koyel, and Sanjib Bhattacharya. "Methods of Preparation of Lithium Ion-Doped Glassy Systems." In Lithium Ion Glassy Electrolytes, 21–29. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_3.

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Acharya, Amartya, Koyel Bhattacharya, Chandan Kr Ghosh, and Sanjib Bhattacharya. "Electrochemical Applications." In Lithium Ion Glassy Electrolytes, 175–81. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_16.

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Bhattacharya, Sanjib. "Experimental Tools for Characterizations of Lithium-Ion Doped Glassy Systems." In Lithium Ion Glassy Electrolytes, 41–52. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_5.

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Bhattacharya, Sanjib. "Features of Lithium-Ion Doped Glassy Systems." In Lithium Ion Glassy Electrolytes, 31–40. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_4.

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Mondal, Ajit, Debasish Roy, Arun Kumar Bar, and Sanjib Bhattacharya. "Mechanical Properties of Some Li-Doped Glassy Systems." In Lithium Ion Glassy Electrolytes, 103–18. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_10.

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Acharya, Amartya, Chandan Kr Ghosh, and Sanjib Bhattacharya. "Fundamentals of Lithium-Ion Containing Glassy Systems." In Lithium Ion Glassy Electrolytes, 3–12. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_1.

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Halder, Prolay, and Sanjib Bhattacharya. "Battery Applications." In Lithium Ion Glassy Electrolytes, 159–73. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_15.

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Acharya, Amartya, Koyel Bhattacharya, Chandan Kr Ghosh, and Sanjib Bhattacharya. "Dielectric Properties and Analysis of Some Li-Doped Glassy Systems." In Lithium Ion Glassy Electrolytes, 75–86. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_8.

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Ojha, Swarupa, Madhab Roy, and Sanjib Bhattacharya. "Photonic Glass Ceramics." In Lithium Ion Glassy Electrolytes, 147–57. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3269-4_14.

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Тези доповідей конференцій з теми "Glassy Electrolytes"

1

Souquet, Jean Louis. "Crystalline, Glassy and Polymeric Electrolytes: Similarities and Differences in Ionic Transport Mechanisms." In Proceedings of the 10th Asian Conference. WORLD SCIENTIFIC, 2006. http://dx.doi.org/10.1142/9789812773104_0003.

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Paul, Lijo, and Arun B. Kumar. "Improvement in Micro Feature Generation in ECDM Process With Powder Mixed Electrolyte." In ASME 2018 13th International Manufacturing Science and Engineering Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/msec2018-6348.

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Анотація:
Electrochemical discharge machining (ECDM), also known as spark assisted chemical engraving (SACE), is an effective micro-machining process for machining of electrically nonconducting materials. It involves melting and etching process under the high electrical discharge on the electrode tip during electrolysis that enables the ECDM process to machine very hard and non-conducting materials such as borosilicate glass, quartz, ceramics etc. efficiently and economically. In the current study micro holes are machined on borosilicate glass with an electrolyte mixed with graphite powder. The conductive graphite powder in electrolyte has shown improvement in machining with more quantity of spark during machining. The main parameters taken in the study are voltage, tool rotation and duty factor along with concentration of powder in electrolyte. The main output responses taken in the study are Material Removal Rate (MRR) and lower Radial Overcut (ROC) along the machined holes. A multi-objective optimization is carried out for higher MRR and lower ROC with Grey Relation Analysis (GRA) in order to obtain the best parameters combination. From the experimental study the optimum values of parameters for MRR and ROC are found to be, voltage of 40 V, Graphite powder concentration 1.25% by weight, duty factor 70% and tool rotation of 500 rpm. From the microscopic images of the machined surface, presence graphite powder in electrolyte has improved the machined features due to its conductive nature.
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Ziki, Jana Abou, Nand Kishor M. Dhawale, and Rolf Wu¨thrich. "Modeling the Forces Exerted on the Tool-Electrode During Spark Assisted Chemical Engraving Constant Velocity Feed-Drilling." In ASME 2010 8th International Conference on Nanochannels, Microchannels, and Minichannels collocated with 3rd Joint US-European Fluids Engineering Summer Meeting. ASMEDC, 2010. http://dx.doi.org/10.1115/fedsm-icnmm2010-31047.

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Spark Assisted Chemical Engraving (SACE) is an interesting technology for micro-machining several types of non-conductive materials like glass, quartz, polymers and some ceramics. The process takes place in an electrochemical cell with two electrodes immersed in an electrolyte. The electrolytic solution is typically sodium hydroxide (30%wt NaOH) or potassium hydroxide (KOH). The cathode is used as tool and the anode as counter-electrode. When the applied voltage is higher than a critical value (typically around 30V, depending on the electrolyte and tool-electrode geometry) bubbles grow so dense on the electrode surface that they coalesce into a gas film. Electrical discharges occur between the electrode and the electrolyte. Machining begins consequently if the electrode is placed close enough to the surface to be machined (typically 25μm for glass). In the present paper, the forces exerted on the tool-electrode during constant velocity feed drilling is investigated experimentally and a model is proposed. The setup is composed of a machine head mounted on XYZ precision linear stage holding the tool-electrode. The machining head further incorporates a force sensor which is able to monitor, during drilling operation, the force exerted on the tool-electrode based on the zero displacement measurement principle.
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4

Munoz, Francisco, and Peter Hockicko. "Electrical and acoustic properties of solid-state glass electrolytes." In 2018 ELEKTRO. IEEE, 2018. http://dx.doi.org/10.1109/elektro.2018.8398240.

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Pokhmurskii, V., G. Nykyforchyn, M. Student, M. Klapkiv, G. V. Karpenko, H. Pokhmurska, B. Wielage, T. Grund, and A. Wank. "Plasma Electrolytic Oxidation of Arc Sprayed Aluminium Coatings." In ITSC2007, edited by B. R. Marple, M. M. Hyland, Y. C. Lau, C. J. Li, R. S. Lima, and G. Montavon. ASM International, 2007. http://dx.doi.org/10.31399/asm.cp.itsc2007p1029.

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Abstract Different post treatment methods such as heat treatment, mechanical processing, sealing, etc. are known to be capable to improve microstructure and exploitation properties of thermal spray coatings. In this work a plasma electrolytic oxidation of aluminium coatings obtained by arc spraying on aluminium and carbon steel substrates is carried out. Microstructure and properties of oxidised layers formed on sprayed coating as well as on bulk material are investigated. Oxidation is performed in electrolyte containing KOH and liquid glass under different process parameters. It is shown that thick uniform oxidised layers can be formed on arc sprayed aluminium coatings as well as on solid material. Distribution of alloying elements and phase composition of obtained layers are investigated. A significant improvement of wear resistance of treated layers in two types of abrasive wear conditions is observed.
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Amamoto, Ippei, Naoki Mitamura, Tatsuya Tsuzuki, Yasushi Takasaki, Atsushi Shibayama, Tetsuji Yano, Masami Nakada, and Yoshihiro Okamoto. "Removal of Fission Products in the Spent Electrolyte Using Iron Phosphate Glass as a Sorbent." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40272.

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This study is carried out to make the pyroprocessing hold a competitive advantage from the viewpoint of environmental load reduction and economical improvement. As one of the measures to reduce the volume of the high-level radioactive waste (HLW), the phosphate conversion method is applied for removal of fission products (FP) from the melt, referring to the spent electrolyte in this paper. Among the removing target chlorides in the spent electrolyte i.e., alkali metals, alkaline earth metals and rare earth elements, only the rare earth elements and lithium form the precipitates as insoluble phosphates by reaction with Li3PO4. The sand filtration method was applied to separate FP precipitates from the spent electrolyte. The iron phosphate glass (IPG) powder, which is a compatible material for the immobilization of FP, was used as a filter medium. After filtration experiment, it was proven that insoluble FP could almost be completely removed from the spent electrolyte. Subsequently, we attempted to separate the dissolved FP from the spent electrolyte. The IPG was being used once again but this time as a sorbent instead. This is possible because the IPG has some unique characteristics, e.g., changing the valence of iron, which is one of its network modifiers due to its manufacturing temperature. Therefore, it would be likely to sorb some FP when the chemical condition of IPG is unstable. We produced three kinds of IPG under different manufacturing temperature and confirmed that those glasses could sorb FP as anticipated. According to the experimental result, its sorption efficiency of metal cations was attained at around 20–40%.
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Sadineni, S. B., R. Hurt, C. K. Halford, and R. F. Boehm. "Reclaiming Electrolysis Reject Water With a Solar Still." In ASME 2007 Energy Sustainability Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/es2007-36001.

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Electrolysis is one sustainable pathway to hydrogen production. During this process, however, it is common to reject a large portion of the water during the pretreatment process to carry away impurities. We have been examining water-conserving approaches to this problem with low energy devices. One such approach is to couple the water purification step with a solar still, thus allowing some of the wastewater to be recycled and utilized in the hydrogen production. This paper reports on a study of a weir type solar still. A weir type solar still is an inclined solar still with the absorber plate formed to make weirs, as well as a top basin and a bottom basin. Raw water flows from the top basin through the weirs and to the bottom basin that is circulated back to the top basin by a small pump. Purified water is collected from condensate on the glass cover. The weir type solar still with 0.61 m width and 1.82 m length (net aperture area 0.97 m2) was constructed and tested for the Las Vegas weather conditions. A data acquisition system with temperature and flow rate sensors was also installed to record the transient variation of temperature and flow rate. The distillate productivity of the still with double-pane and single-pane glass covers is compared. The average distillate productivities for double-pane and single-pane glass covers were approximately 1.9 l/m2/day and 5.5 l/m2/day in the months of August and September in Las Vegas respectively. A double-pane glass reduced the productivity of a solar still significantly due to the reduced temperature difference between the raw water and the glass inner surface. The productivity of the weir type still is also compared with the basin type still tested at the same location side by side and is found that the weir type still productivity was approximately 20% higher. The quality of distillate from the still was also analyzed to verify the product will meet the purity required by electrolyzers.
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Kofuji, Hirohide, Tetsuji Yano, Munetaka Myochin, Kanae Matsuyama, Takeshi Okita, and Shinya Miyamoto. "Optimization of Chemical Composition in the Iron Phosphate Glass as the Matrix of High Level Waste Generated From Pyroprocessing." In 2014 22nd International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/icone22-30688.

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As part of ongoing research and development of nuclear waste disposal techniques suitable for the pyrochemical processing system [1], iron-phosphate glass was examined as an alternative waste form for high level waste generated from the electro-refining process [2]. To enhance the waste element content in the glass matrix and improve the durability of the waste form, optimization experiments of the glass composition were performed, and the effects of other additional transition metal oxides were determined. From the surface analysis of iron phosphate glass, a leaching mechanism was assumed for various elements contained in the glass matrix. We have selected suitable a glass composition for the treatment of radioactive waste generated from the spent electrolytes of pyrochemical processing.
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Liu, Zhijian, Jiaming Gao, Tianze Wu, Sen Wu, Zixiao Fan, Ziyi Yuan, Yongxin Song, and Xinxiang Pan. "Probing zeta potential of glass in electrolyte solutions by colloidal probe technique." In 2021 IEEE 16th International Conference on Nano/Micro Engineered and Molecular Systems (NEMS). IEEE, 2021. http://dx.doi.org/10.1109/nems51815.2021.9451307.

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Razfar, Mohammad Reza, Jun Ni, Ali Behroozfar, and Shuhuai Lan. "An Investigation on Electrochemical Discharge Micro-Drilling of Glass." In ASME 2013 International Manufacturing Science and Engineering Conference collocated with the 41st North American Manufacturing Research Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/msec2013-1135.

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Анотація:
Electrochemical Discharge Machining (ECDM) as an innovative spark-based micromachining method has been successfully applied for fabricating micro-holes in non-conductive brittle materials such as glass. However, the effects of influencing parameters for attaining accurate structures and dimensions remain to be explored. This paper attempts to analyze the effects of process parameters including applied voltage, tool immersion depth and electrolyte concentration on process outputs such as radial overcut (ROC), material removal rate (MRR), heat affected zone (HAZ) thickness and roundness error (RE) of the holes. In this regard, a set of experiments based on response surface experiment design method were conducted on soda lime glass. The relevant experimental data were used to establish mathematical models for process outputs using the response surface methodology (RSM). The obtained results show that applied voltage significantly increases the ROC, MRR, HAZ and RE. Also, electrolyte concentration has the same effects on mentioned outputs except the ROC. In addition, greater tool immersion depth decreases the MRR and HAZ thickness. The adequacy of the developed mathematical models was also evaluated by an analysis of variance (ANOVA) test. The relevant results show the capability of the proposed approach to investigate the ECDM process of glass.
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Звіти організацій з теми "Glassy Electrolytes"

1

Martin, Steve W. Development of New Fast Proton Conducting Chalcogenide Glassy Electrolytes. Fort Belvoir, VA: Defense Technical Information Center, March 2005. http://dx.doi.org/10.21236/ada430645.

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