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dc.contributor.authorLee, Woong Hee-
dc.contributor.authorHan, Man Ho-
dc.contributor.authorKo, Young-Jin-
dc.contributor.authorMin, Byoung Koun-
dc.contributor.authorChae, Keun Hwa-
dc.contributor.authorOh, Hyung-Suk-
dc.date.accessioned2024-01-19T12:33:36Z-
dc.date.available2024-01-19T12:33:36Z-
dc.date.created2022-04-05-
dc.date.issued2022-02-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/115650-
dc.description.abstractThe phase and spin state affect catalytic activity of Co-based catalysts for oxygen evolution reaction. Herein, the authors demonstrate a simple reconstruction strategy to fabricate electrodes maintaining a Fe-CoOOH phase and an intermediate-spin state during catalysis. Computational calculations and experimental studies reveal that the CoOOH phase and the intermediate-spin (IS) state are the key factors for realizing efficient Co-based electrocatalysts for the oxygen evolution reaction (OER). However, according to thermodynamics, general cobalt oxide converts to the CoO2 phase under OER condition, retarding the OER kinetics. Herein, we demonstrate a simple and scalable strategy to fabricate electrodes with maintaining Fe-CoOOH phase and an IS state under the OER. The changes of phase and spin states were uncovered by combining in-situ/operando X-ray based absorption spectroscopy and Raman spectroscopy. Electrochemical reconstruction of chalcogenide treated Co foam affords a highly enlarged active surface that conferred excellent catalytic activity and stability in a large-scale water electrolyzer. Our findings are meaningful in that the calculated results were experimentally verified through the operando analyses. It also proposes a new strategy for electrode fabrication and confirms the importance of real active phases and spin states under a particular reaction condition.-
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.titleElectrode reconstruction strategy for oxygen evolution reaction: maintaining Fe-CoOOH phase with intermediate-spin state during electrolysis-
dc.typeArticle-
dc.identifier.doi10.1038/s41467-022-28260-5-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNature Communications, v.13-
dc.citation.titleNature Communications-
dc.citation.volume13-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000749535300014-
dc.identifier.scopusid2-s2.0-85123974390-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.type.docTypeArticle-
dc.subject.keywordPlusWATER ELECTROLYSIS-
dc.subject.keywordPlusCOBALT OXIDE-
dc.subject.keywordPlusELECTROCATALYSTS-
dc.subject.keywordPlusCO3O4-
dc.subject.keywordPlusCO-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusSUBSTITUTION-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusCONVERSION-
dc.subject.keywordPlusREDUCTION-
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