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dc.contributor.authorYasuda, Koujien
dc.contributor.authorShimao, Takeyukien
dc.contributor.authorHagiwara, Rikaen
dc.contributor.authorHomma, Takayukien
dc.contributor.authorNohira, Toshiyukien
dc.contributor.alternative安田, 幸司ja
dc.contributor.alternative萩原, 理加ja
dc.contributor.alternative野平, 俊之ja
dc.date.accessioned2017-05-24T02:18:17Z-
dc.date.available2017-05-24T02:18:17Z-
dc.date.issued2017-05-04-
dc.identifier.issn0013-4651-
dc.identifier.urihttp://hdl.handle.net/2433/224952-
dc.description.abstractA new electrolytic production process for solar-grade Si has been proposed utilizing liquid Si–Zn alloy cathode in molten CaCl2. To establish this process, the behavior of liquid Zn metal in molten CaCl2 at 1123 K was investigated. Evaporation of Zn metal was largely suppressed by immersion in the molten salt, which enabled the use of a Zn electrode despite its high vapor pressure. Cyclic voltammetry results suggested that the reduction of SiO2 on a Zn cathode proceeded at a more negative than 1.45 V vs. Ca2+/Ca. After potentiostatic electrolysis at 0.9 V, Si particles with sizes of 2–30 μm were precipitated in the solidified Zn matrix by a slow cooling process. The rate-determining step for electrochemical reduction of SiO2 on the Zn cathode was discussed on the basis of a measurement of the alloying rate between solid Si and liquid Zn.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElectrochemical Societyen
dc.rights© The Author(s) 2017. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited.en
dc.subjectElectrolysisen
dc.subjectMolten Salten
dc.subjectSilicaen
dc.subjectSolar-grade Siliconen
dc.subjectZincen
dc.titleElectrolytic Production of Silicon Using Liquid Zinc Alloy in Molten CaCl2en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleJournal of The Electrochemical Societyen
dc.identifier.volume164-
dc.identifier.issue8-
dc.identifier.spageH5049-
dc.identifier.epageH5056-
dc.relation.doi10.1149/2.0121708jes-
dc.textversionpublisher-
dcterms.accessRightsopen access-
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