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dc.contributor.authorFukunaga, Ryo
dc.contributor.authorAllanore, Antoine
dc.contributor.authorYagi, Shunsuke
dc.date.accessioned2022-05-11T15:40:39Z
dc.date.available2022-05-11T15:40:39Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/142473
dc.description.abstractThe redox behavior of Cu2S in a Li2S-dissolving aprotic electrolyte was investigated to examine the practical viability of rechargeable batteries using sulfide ions as carrier ions. We established aprotic electrolytes, dimethyl sulfoxide and dimethylformamide containing S2- at over 0.10 M concentration by adding NH4NO3 to increase the solubility of Li2S, which is hardly soluble in almost all aprotic solvents. Two redox reactions of Cu2S, Cu/Cu2S and Cu2S/CuS, were observed at -0.25 V and 0.60 V vs Mo, respectively. In addition, it was found that elemental S is electrodeposited/stripped at approximately 0.1 V vs Mo on graphite but not on platinum.en_US
dc.language.isoen
dc.publisherThe Electrochemical Societyen_US
dc.relation.isversionof10.1149/1945-7111/ABADBDen_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.sourceIOP Publishingen_US
dc.titleCommunication—Redox Behavior of Cu 2 S in Li 2 S-Dissolving Aprotic Electrolyte for Sulfide-Ion Batteriesen_US
dc.typeArticleen_US
dc.identifier.citationFukunaga, Ryo, Allanore, Antoine and Yagi, Shunsuke. 2020. "Communication—Redox Behavior of Cu 2 S in Li 2 S-Dissolving Aprotic Electrolyte for Sulfide-Ion Batteries." Journal of the Electrochemical Society, 167 (12).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.relation.journalJournal of the Electrochemical Societyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-05-11T15:33:18Z
dspace.orderedauthorsFukunaga, R; Allanore, A; Yagi, Sen_US
dspace.date.submission2022-05-11T15:33:19Z
mit.journal.volume167en_US
mit.journal.issue12en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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