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dc.citation.endPage 1411 -
dc.citation.number 7 -
dc.citation.startPage 1408 -
dc.citation.title JOULE -
dc.citation.volume 7 -
dc.contributor.author Lee, Dae-Hyung -
dc.contributor.author Gong, Minjeong -
dc.contributor.author Lee, Eunryeol -
dc.contributor.author Seo, Dong-Hwa -
dc.date.accessioned 2023-12-21T11:50:07Z -
dc.date.available 2023-12-21T11:50:07Z -
dc.date.created 2023-09-21 -
dc.date.issued 2023-07 -
dc.description.abstract Assigning oxidation states and understanding the oxygen redox mechanism is crucial for designing superior cathode materials in lithium-ion batteries. The working mechanism of stoichiometric LiNiO2 has been regarded as Ni-dominant redox with partial O contribution through covalent Ni-O bonding for several decades. However, in this issue of Joule, Morris, Grey, and co-workers reported that Ni rarely participates in the redox reaction, and oxygen primarily acts as the redox center through a combination of experimental analysis and computational prediction. Also, the highly reactive singlet O-2 formation mechanism was elucidated. This work provides an opportunity to reassess the current understanding of conventional cathode materials. -
dc.identifier.bibliographicCitation JOULE, v.7, no.7, pp.1408 - 1411 -
dc.identifier.doi 10.1016/j.joule.2023.06.023 -
dc.identifier.issn 2542-4351 -
dc.identifier.scopusid 2-s2.0-85164396040 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/65713 -
dc.identifier.wosid 001047731600001 -
dc.language 영어 -
dc.publisher CELL PRESS -
dc.title Oxygen redox in LiNiO2 cathodes -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Physical; Energy & Fuels; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Chemistry; Energy & Fuels; Materials Science -
dc.type.docType Editorial Material -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

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