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A high-capacity Li[Ni0.8Co0.06Mn0.14]O-2 positive electrode with a dual concentration gradient for next-generation lithium-ion batteries

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dc.contributor.authorPark, Kang-Joon-
dc.contributor.authorLim, Byung-Beom-
dc.contributor.authorChoi, Moon-Ho-
dc.contributor.authorJung, Hun-Gi-
dc.contributor.authorSun, Yang Kook-
dc.contributor.authorHaro, Marta-
dc.contributor.authorVicente, Nuria-
dc.contributor.authorBisquert, Juan-
dc.contributor.authorGarcia-Belmonte, Germa-
dc.date.accessioned2021-08-02T17:54:14Z-
dc.date.available2021-08-02T17:54:14Z-
dc.date.created2021-05-12-
dc.date.issued2015-09-
dc.identifier.issn2050-7488-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/24866-
dc.description.abstractTo increase the reversible capacity of layered lithium nickel-cobalt-manganese oxide, a Li [Ni0.8Co0.06Mn0.14]O-2 positive electrode with a two-sloped full concentration gradient (TSFCG) was successfully synthesized via co-precipitation. The TSFCG maximizes the Ni concentration in the particle core and the Mn concentration on the particle surface. The TSFCG Li[Ni0.8Co0.06Mn0.14]O-2 positive electrode showed improved overall electrochemical properties (i.e., reversible capacity, cycle life, and rate capability) and thermal stability compared to a conventional positive electrode (CC) Li [Ni0.8Co0.06Mn0.14]O-2 without a concentration gradient. Electrochemical impedance spectroscopy showed that the high stability of the outer surface composition of Li[Ni0.64Co0.06Mn0.30]O-2 is responsible for reduction in surface resistance and charge transfer resistance by decreasing the parasitic reaction with the electrolyte. These reduced resistances explain the superior rate capability of TSFCG positive electrodes.-
dc.language영어-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleA high-capacity Li[Ni0.8Co0.06Mn0.14]O-2 positive electrode with a dual concentration gradient for next-generation lithium-ion batteries-
dc.typeArticle-
dc.contributor.affiliatedAuthorSun, Yang Kook-
dc.identifier.doi10.1039/c5ta05657h-
dc.identifier.scopusid2-s2.0-84946550135-
dc.identifier.wosid000364080400029-
dc.identifier.bibliographicCitationJOURNAL OF MATERIALS CHEMISTRY A, v.3, no.44, pp.22183 - 22190-
dc.relation.isPartOfJOURNAL OF MATERIALS CHEMISTRY A-
dc.citation.titleJOURNAL OF MATERIALS CHEMISTRY A-
dc.citation.volume3-
dc.citation.number44-
dc.citation.startPage22183-
dc.citation.endPage22190-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusCATHODE MATERIAL-
dc.subject.keywordPlusELECTROCHEMICAL PROPERTIES-
dc.subject.keywordPlusHIGH-ENERGY-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusKINETICS-
dc.subject.keywordPlusSURFACE-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2015/TA/C5TA05657H-
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