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Cited 60 time in webofscience Cited 61 time in scopus
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dc.contributor.authorLee, Jooyoung-
dc.contributor.authorJUNG, HYEONJUNG-
dc.contributor.authorPark, Yoo Sei-
dc.contributor.authorWoo, Seongwon-
dc.contributor.authorYang, Juchan-
dc.contributor.authorJang, Myeong Je-
dc.contributor.authorJeong, Jaehoon-
dc.contributor.authorKwon, Nayoung-
dc.contributor.authorLim, Byungkwon-
dc.contributor.authorHan, Jeong Woo-
dc.contributor.authorChoi, Sung Mook-
dc.date.accessioned2021-11-20T13:50:03Z-
dc.date.available2021-11-20T13:50:03Z-
dc.date.created2021-11-19-
dc.date.issued2021-07-
dc.identifier.issn1613-6810-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/107547-
dc.description.abstractDeveloping high-efficiency and low-cost oxygen-evolving electrodes in anion exchange membrane (AEM) water electrolysis technology is one of the major challenges. Herein, it is demonstrated that the surface corrosion of a conventional Ni foam electrode in the presence of Fe3+ and V3+ cations can transform it into an electrode with a high catalytic performance for oxygen evolution reaction (OER). The corroded electrode consists of a ternary NiFeV layered double hydroxide (LDH) nanosheet array supported on the Ni foam surface. This NiFeV LDH electrode achieves an OER current density of 100 mA cm(-2) at an overpotential of 272 mV in 1 m KOH, outperforming the IrO2 catalyst by 180 mV. Density functional theory calculations reveal that the unique structure and the presence of vanadium in NiFeV LDH play a key role in achieving improved OER activity. When coupled with a commercial Pt/C cathode catalyst, the resulting AEM water electrolyzer achieves a cell current density as high as 2.1 A cm(-2) at a voltage of only 1.8 V-cell in 1 m KOH, which is similar to the performance of the proton exchange membrane water electrolyzer obtained from the IrO2 and Pt/C catalysts pair.-
dc.languageEnglish-
dc.publisherWiley - V C H Verlag GmbbH & Co.-
dc.relation.isPartOfSmall-
dc.titleHigh‐Efficiency Anion‐Exchange Membrane Water Electrolyzer Enabled by Ternary Layered Double Hydroxide Anode-
dc.typeArticle-
dc.identifier.doi10.1002/smll.202100639-
dc.type.rimsART-
dc.identifier.bibliographicCitationSmall, v.17, no.28, pp.2100639-
dc.identifier.wosid000657391500001-
dc.citation.number28-
dc.citation.startPage2100639-
dc.citation.titleSmall-
dc.citation.volume17-
dc.contributor.affiliatedAuthorJUNG, HYEONJUNG-
dc.contributor.affiliatedAuthorHan, Jeong Woo-
dc.identifier.scopusid2-s2.0-85107046750-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.type.docTypeArticle-
dc.subject.keywordPlusOXYGEN EVOLUTION-
dc.subject.keywordPlusHYDROGEN EVOLUTION-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusNICKEL-
dc.subject.keywordPlusELECTROCATALYSTS-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusCATALYST-
dc.subject.keywordPlusIRON-
dc.subject.keywordPlusELECTRODES-
dc.subject.keywordPlusPARAMETERS-
dc.subject.keywordAuthoranion exchange membrane water electrolyzers-
dc.subject.keywordAuthorelectrocatalysts-
dc.subject.keywordAuthoroxygen evolution reaction-
dc.subject.keywordAuthortransition metals-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-

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한정우HAN, JEONG WOO
Dept. of Chemical Enginrg
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