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Off-stoichiometry induced few-nanometer surface layer for high-performance layered cathode in nonaqueous and aqueous electrolytes

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dc.contributor.authorLee, Hyeon Jeong-
dc.contributor.authorLee, Ji Hoon-
dc.contributor.authorSon, In Hyuk-
dc.contributor.authorHan, Sangil-
dc.contributor.authorByeon, Pilgyu-
dc.contributor.authorPark, Min-Sik-
dc.contributor.authorChung, Sung-Yoon-
dc.contributor.authorChoi, Jang Wook-
dc.date.accessioned2020-03-16T11:08:12Z-
dc.date.available2020-03-16T11:08:12Z-
dc.date.created2019-05-30-
dc.date.issued2018-10-
dc.identifier.citationACS Applied Energy Materials, Vol.1 No.10, pp.5726-5734-
dc.identifier.issn2574-0962-
dc.identifier.other74515-
dc.identifier.urihttps://hdl.handle.net/10371/164636-
dc.description.abstractDespite the long history in commercial lithium-ion batteries, layered lithium cobalt oxide (LiCoO2) suffers from structural degradations that shorten the cycle life when operating at high voltages (i.e., 4.5 V vs Li/Li+) in nonaqueous electrolytes or even at moderate voltages in aqueous electrolytes. This limited performance originates from the O3-to-O1 phase transition involving cobalt dissolution or the leaching of Li2O. Here, we report a one-pot synthesis that yields LiCoO2 bearing a spinel-Co3O4 surface structure with a thickness of 2 nm via lithium-deficient stoichiometry (Li:Co = 0.98:1). The lithium-deficiency induces the spinel structure, a thermodynamically preferred phase at the given stoichiometry, by temperature-specific phase separation. The spinel surface layer mitigates cobalt dissolution and oxygen gas evolution or avoids direct contact with the electrolyte causing the leaching of Li2O, improving the cyclability in nonaqueous and aqueous electrolytes by 35% and 20% after 100 cycles compared to that of LiCoO2 when the upper cutoff voltages were imposed at 4.5 V (vs Li/Li+) and 0.8 V (vs Ag/AgCl), respectively.-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleOff-stoichiometry induced few-nanometer surface layer for high-performance layered cathode in nonaqueous and aqueous electrolytes-
dc.typeArticle-
dc.contributor.AlternativeAuthor최장욱-
dc.identifier.doi10.1021/acsaem.8b01317-
dc.citation.journaltitleACS Applied Energy Materials-
dc.identifier.wosid000458706600068-
dc.identifier.scopusid2-s2.0-85061879902-
dc.citation.endpage5734-
dc.citation.number10-
dc.citation.startpage5726-
dc.citation.volume1-
dc.identifier.sci000458706600068-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorChoi, Jang Wook-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusLITHIUM-ION BATTERIES-
dc.subject.keywordPlusLICOO2 CATHODE-
dc.subject.keywordPlusCAPACITY RETENTION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusINTERCALATION-
dc.subject.keywordPlusEVOLUTION-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusLIXCOO2-
dc.subject.keywordPlusOXYGEN-
dc.subject.keywordPlus1ST-PRINCIPLES-
dc.subject.keywordAuthoraqueous rechargeable battery-
dc.subject.keywordAuthorhigh operating voltage-
dc.subject.keywordAuthorlithium cobalt oxide-
dc.subject.keywordAuthoroff-stoichiometry-
dc.subject.keywordAuthorsurface modification-
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area Physics, Materials Science

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