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Development of P3-K0.69CrO2 as an ultra-high-performance cathode material for K-ion batteries

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dc.contributor.authorHwang, Jang-Yeon-
dc.contributor.authorKim, Jongsoon-
dc.contributor.authorYu, Tae-Yeon-
dc.contributor.authorMyung, Seung-Taek-
dc.contributor.authorSun, Yang-Kook-
dc.date.accessioned2021-07-30T05:24:33Z-
dc.date.available2021-07-30T05:24:33Z-
dc.date.created2021-05-12-
dc.date.issued2018-10-
dc.identifier.issn1754-5692-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/4670-
dc.description.abstractPotassium-ion batteries (KIBs) are emerging as a promising energy storage technology because of their low cost and high energy density. However, the large size of K+ ions hinders the reversible electrochemical potassium (de)insertion in the host structure, limiting the selection of suitable electrode materials for KIBs. Herein, we designed and exploited a new layered oxide, P3-type K0.69CrO2 (hereafter denoted as P3-K0.69CrO2), as a high-performance cathode for KIBs for the first time. The proposed P3-K0.69CrO2 cathode was successfully synthesized via an electrochemical ion-exchange route and exhibited the best cycling performance for a KIB cathode material to date. A combination of electrochemical profiles, ex situ X-ray diffraction, and first-principles calculations was used to understand the overall potassium storage mechanism of P3-K0.69CrO2. Based on a reversible phase transition, P3-K0.69CrO2 delivers a high discharge capacity of 100 mA h g−1 and exhibits extremely high cycling stability with ∼65% retention over 1000 cycles at a 1C rate. Moreover, the K-ion hopping into the P3-K0.69CrO2 structure was extremely rapid, resulting in great power capability of up to a 10C rate with a capacity retention of ∼65% (vs. the capacity at 0.1C).-
dc.language영어-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleDevelopment of P3-K0.69CrO2 as an ultra-high-performance cathode material for K-ion batteries-
dc.typeArticle-
dc.contributor.affiliatedAuthorSun, Yang-Kook-
dc.identifier.doi10.1039/c8ee01365a-
dc.identifier.scopusid2-s2.0-85053880370-
dc.identifier.wosid000448339100005-
dc.identifier.bibliographicCitationENERGY & ENVIRONMENTAL SCIENCE, v.11, no.10, pp.2821 - 2827-
dc.relation.isPartOfENERGY & ENVIRONMENTAL SCIENCE-
dc.citation.titleENERGY & ENVIRONMENTAL SCIENCE-
dc.citation.volume11-
dc.citation.number10-
dc.citation.startPage2821-
dc.citation.endPage2827-
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.journalResearchAreaEngineering-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.subject.keywordPlusLAYERED NACRO2-
dc.subject.keywordPlusSODIUM-
dc.subject.keywordPlusINTERCALATION-
dc.subject.keywordPlusLITHIUM-
dc.subject.keywordPlusANODES-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2018/EE/C8EE01365A-
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