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dc.contributor.authorShin, Woochul
dc.contributor.authorSo, Kang Pyo
dc.contributor.authorStickle, William F
dc.contributor.authorSu, Cong
dc.contributor.authorLu, Jun
dc.contributor.authorLi, Ju
dc.contributor.authorJi, Xiulei
dc.date.accessioned2021-10-27T20:05:47Z
dc.date.available2021-10-27T20:05:47Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/134615
dc.description.abstract© 2019 The Royal Society of Chemistry. Lithium metal anodes suffer from a short cycle life, and the parasitic reactions of lithium with electrolytes are widely observed. Common sense is to avoid such reactions. Herein, we head in the opposite direction by using an oxidizing co-solvent, ethyl methyl sulfone, in the electrolyte, which addresses the 'dendrite' issue entirely, resulting in a dense and macroscopically smooth surface morphology of the plated lithium. However, a dendrite-free lithium metal anode does not necessarily exhibit a high coulombic efficiency.
dc.language.isoen
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.isversionof10.1039/C9CC00046A
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.sourceRoyal Society of Chemistry (RSC)
dc.titleAn ethyl methyl sulfone co-solvent eliminates macroscopic morphological instabilities of lithium metal anode
dc.typeArticle
dc.relation.journalChemical Communications
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2020-05-05T12:33:34Z
dspace.orderedauthorsShin, W; So, KP; Stickle, WF; Su, C; Lu, J; Li, J; Ji, X
dspace.date.submission2020-05-05T12:33:37Z
mit.journal.volume55
mit.journal.issue23
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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