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Tri-Metallic Catalyst for Oxygen Evolution Reaction Enables Continuous Operation of Anion Exchange Membrane Electrolyzer at 1A cm<SUP>-2</SUP> for Hundreds of Hours

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dc.contributor.authorAbdelhafiz, Ali-
dc.contributor.authorMohammed, Mona H.-
dc.contributor.authorAbed, Jehad-
dc.contributor.authorLee, Dong-Chan-
dc.contributor.authorChen, Mengjie-
dc.contributor.authorHelal, Ahmed S.-
dc.contributor.authorRen, Zhichu-
dc.contributor.authorAlamgir, Faisal-
dc.contributor.authorSargent, Edward-
dc.contributor.authorKohl, Paul A.-
dc.contributor.authorElsaidi, Sameh K.-
dc.contributor.authorLi, Ju-
dc.date.accessioned2024-04-18T06:30:31Z-
dc.date.available2024-04-18T06:30:31Z-
dc.date.issued2024-03-19-
dc.identifier.issn1614-6832-
dc.identifier.issn1614-6840-
dc.identifier.urihttps://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/33041-
dc.description.abstractAlthough numerous efforts are made to synthesize active electrocatalysts for green hydrogen production; catalyst stability, and facile synthesis to scale up the production are still challenging. Herein, the production of novel non-PGM catalysts for the oxygen reduction reaction (OER) in an alkaline aqueous medium is reported, which is based on the synthesis of a trimetallic metal-organic framework (MOF) precursors. Fine-tuning of the composition of the metal centers (Ni, Co, and Fe) shows a great effect on OER activity after the MOF undergoes dynamic chemical and structural transformations under OER conditions. In situ characterization reveals the origin of OER activity enhancement as metals&apos; oxidation state increases, inducing compressive mechanical strain on metal centers, enhancing the electronic conductivity through the formation of oxygen vacancies, and stronger metal-oxygen covalency. Catalysts are used in membrane electrode assembly (MEA) setup within an industrial full-cell anion exchange membrane electrolyzer (AEMEC), showing a stable performance for 550 h without noticeable decay at 750 and 1000 mA cm(-2) industrial level current densities.-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleTri-Metallic Catalyst for Oxygen Evolution Reaction Enables Continuous Operation of Anion Exchange Membrane Electrolyzer at 1A cm&lt;SUP&gt;-2&lt;/SUP&gt; for Hundreds of Hours-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/aenm.202303350-
dc.identifier.scopusid2-s2.0-85187937646-
dc.identifier.wosid001187210800001-
dc.identifier.bibliographicCitationADVANCED ENERGY MATERIALS, v.14, no.16-
dc.citation.titleADVANCED ENERGY MATERIALS-
dc.citation.volume14-
dc.citation.number16-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnergy &amp; Fuels-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnergy &amp; Fuels-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.subject.keywordPlusELECTROCATALYSTS-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusGRAPHENE-
dc.subject.keywordPlusSUPPORT-
dc.subject.keywordPlusOXIDES-
dc.subject.keywordPlusSTRAIN-
dc.subject.keywordAuthorelectrolyzer full cell-
dc.subject.keywordAuthorin situ characterization-
dc.subject.keywordAuthormetal-organic frameworks-
dc.subject.keywordAuthormulti-metal catalyst-
dc.subject.keywordAuthoroxygen evolution reaction-
dc.subject.keywordAuthorwater electrolysis-
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