Vertical-crystalline Fe-doped beta-Ni oxyhydroxides for highly active and stable evolution reaction

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dc.contributor.authorKim, Byeongyoonko
dc.contributor.authorKabiraz, Mrinal Kantiko
dc.contributor.authorLee, Jaewanko
dc.contributor.authorChoi, Changhyeokko
dc.contributor.authorBaik, Hionsuckko
dc.contributor.authorJung, Yousungko
dc.contributor.authorOh, Hyung-Sukko
dc.contributor.authorChoi, Sang-Ilko
dc.contributor.authorLee, Kwangyeolko
dc.date.accessioned2021-11-30T06:41:34Z-
dc.date.available2021-11-30T06:41:34Z-
dc.date.created2021-11-29-
dc.date.created2021-11-29-
dc.date.created2021-11-29-
dc.date.created2021-11-29-
dc.date.created2021-11-29-
dc.date.issued2021-11-
dc.identifier.citationMATTER, v.4, no.11, pp.3585 - 3604-
dc.identifier.issn2590-2393-
dc.identifier.urihttp://hdl.handle.net/10203/289666-
dc.description.abstractThe layered transition metal oxyhydroxides have received increasing interest owing to the efficient energy conversion performance and material stability during the oxygen evolution reaction (OER). In particular, Fe-doped NiOOH has shown record-high OER performance in alkaline media among various catalysts. Theoretically, undercoordinated facets including Ni4+, exposed at the edges of NiOOH, were predicted to perform highly active OER. Therefore, here we suggest a rational catalyst design, a vertical-crystalline beta-Fe/NiOOH layer built on faceted Fe/Ni nanocrystals, which exposes Ni4+ sites and could improve the OER performance dramatically. Electrochemical OER tests recorded the overpotential of 210 mV at a current density of 10 mA cm(-2) GEO and stable operation for 5 days. In situ/operando and density functional theory studies revealed that the Ni valence cycle between +2 and +4 assisted by Fe dopant is the key engine that greatly accelerates OER kinetics and that the vertical-crystalline beta-Fe/NiOOH layers on Ni octahedra are stable under harsh OER conditions.-
dc.languageEnglish-
dc.publisherELSEVIER-
dc.titleVertical-crystalline Fe-doped beta-Ni oxyhydroxides for highly active and stable evolution reaction-
dc.typeArticle-
dc.identifier.wosid000717520800003-
dc.identifier.scopusid2-s2.0-85123000978-
dc.type.rimsART-
dc.citation.volume4-
dc.citation.issue11-
dc.citation.beginningpage3585-
dc.citation.endingpage3604-
dc.citation.publicationnameMATTER-
dc.identifier.doi10.1016/j.matt.2021.09.003-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorJung, Yousung-
dc.contributor.nonIdAuthorKim, Byeongyoon-
dc.contributor.nonIdAuthorKabiraz, Mrinal Kanti-
dc.contributor.nonIdAuthorLee, Jaewan-
dc.contributor.nonIdAuthorBaik, Hionsuck-
dc.contributor.nonIdAuthorOh, Hyung-Suk-
dc.contributor.nonIdAuthorChoi, Sang-Il-
dc.contributor.nonIdAuthorLee, Kwangyeol-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusMEMBRANE WATER ELECTROLYSIS-
dc.subject.keywordPlusOXYGEN-EVOLUTION-
dc.subject.keywordPlusELECTRONIC-STRUCTURE-
dc.subject.keywordPlusREACTION DYNAMICS-
dc.subject.keywordPlusREDOX STATES-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusELECTROCATALYSTS-
dc.subject.keywordPlusOXIDE-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusXANES-
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