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dc.contributor.authorKo, Young-Jin-
dc.contributor.authorHan Man Ho-
dc.contributor.authorKim, Haesol-
dc.contributor.authorKim, Jun Yong-
dc.contributor.authorLee, Woong Hee-
dc.contributor.authorKim, Jaewook-
dc.contributor.authorKwak, Joon Young-
dc.contributor.authorKim, Chang-Hee-
dc.contributor.authorPark, Tae-Eon-
dc.contributor.authorYu, Seung-Ho-
dc.contributor.authorLee, Wook-Seong-
dc.contributor.authorChoi, Chang Hyuck-
dc.contributor.authorStrasser, Peter-
dc.contributor.authorOh, Hyung-Suk-
dc.date.accessioned2024-01-12T02:37:16Z-
dc.date.available2024-01-12T02:37:16Z-
dc.date.created2022-10-06-
dc.date.issued2022-09-
dc.identifier.issn2667-1107-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/76017-
dc.description.abstractNi-Fe-based materials are well known as one of the most active electrocatalysts for the oxygen evolution reaction (OER) in alkaline environments. In this study, we propose a facile and scaling up synthesis route using a surfactant for Ni-Fe 2D nanostructured electrocatalysts. Furthermore, we uncovered the hidden phase transformation mechanism of 2D Ni-Fe layered double hydroxide (LDH) electrocatalysts by combining various in situ and operando analyses. The Ni-Fe LDH underwent a chemically induced phase transformation in an alkaline environment without applied potential. The resulting phase transformation product persisted throughout the entire OER mechanism cycle, such that it played a dominant role in the process. The presence of high-valent Ni and Fe was observed on the surface; hence, the OER selectivity and catalytic turnover frequency were enhanced in the low-overpotential domain. Our study not only uncovers the fundamentals of Ni-Fe LDH but also expands the potential for practical alkaline water splitting.-
dc.languageEnglish-
dc.publisherCell Press-
dc.titleUnraveling Ni-Fe 2D nanostructure with enhanced oxygen evolution via in situ and operando spectroscopies-
dc.typeArticle-
dc.identifier.doi10.1016/j.checat.2022.07.016-
dc.description.journalClass1-
dc.identifier.bibliographicCitationChem Catalysis, v.2, no.9, pp.2312 - 2327-
dc.citation.titleChem Catalysis-
dc.citation.volume2-
dc.citation.number9-
dc.citation.startPage2312-
dc.citation.endPage2327-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.identifier.scopusid2-s2.0-85137774752-
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KIST Article > 2022
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