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Thermally reduced rGO-wrapped CoP/Co2P hybrid microflower as an electrocatalyst for hydrogen evolution reaction

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dc.contributor.authorKim, Taek-Seung-
dc.contributor.authorSong, Hee Jo-
dc.contributor.authorDar, Mushtaq Ahmad-
dc.contributor.authorShim, Hyun-Woo-
dc.contributor.authorKim, Dong-Wan-
dc.date.accessioned2021-09-02T06:47:04Z-
dc.date.available2021-09-02T06:47:04Z-
dc.date.created2021-06-16-
dc.date.issued2018-09-
dc.identifier.issn0002-7820-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/73258-
dc.description.abstractCobalt phosphides (CoPx) are potential candidates for use as high-efficiency hydrogen evolution reaction electrocatalysts that can replace noble metals, such as Pt. Typically, CoPx can be synthesized by phosphidation with Co-based precursors such as oxides or hydroxides. In this study, we propose a new strategy for synthesizing CoPx through the thermal reduction in cobalt phosphate (Co-3(PO4)(2)). A reduced graphene oxide-wrapped CoP/Co2P hybrid microflower was successfully synthesized by a facile coprecipitation method in a Co-3(PO4)(2) matrix, followed by a thermal reduction process. Co-3(PO4)(2) can be transformed to CoP/Co2P by treatment at 700 degrees C for 1hour, maintaining the original particle morphology with the assistance of reduced graphene oxide (rGO). In a 0.5mol/L H2SO4 solution, the rGO-CoP/Co2P microflower catalyzes the hydrogen evolution reaction with an overpotential of 156 mV at a current density of 10mA cm(-2), a Tafel slope of 53.8mV dec(-1), and good stability as observed through long-term CV and chronoamperometry tests.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectMOLYBDENUM-
dc.subjectOXIDATION-
dc.subjectCATALYSTS-
dc.subjectPHOSPHIDE-
dc.subjectCOAL-
dc.titleThermally reduced rGO-wrapped CoP/Co2P hybrid microflower as an electrocatalyst for hydrogen evolution reaction-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.identifier.doi10.1111/jace.15581-
dc.identifier.scopusid2-s2.0-85045770242-
dc.identifier.wosid000436943300002-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CERAMIC SOCIETY, v.101, no.9, pp.3749 - 3754-
dc.relation.isPartOfJOURNAL OF THE AMERICAN CERAMIC SOCIETY-
dc.citation.titleJOURNAL OF THE AMERICAN CERAMIC SOCIETY-
dc.citation.volume101-
dc.citation.number9-
dc.citation.startPage3749-
dc.citation.endPage3754-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Ceramics-
dc.subject.keywordPlusMOLYBDENUM-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusPHOSPHIDE-
dc.subject.keywordPlusCOAL-
dc.subject.keywordAuthorcatalysts-
dc.subject.keywordAuthorcatalysis-
dc.subject.keywordAuthorcobalt-
dc.subject.keywordAuthorcobalt compounds-
dc.subject.keywordAuthorgraphene oxide-
dc.subject.keywordAuthorhydrogen evolution reaction-
dc.subject.keywordAuthorphosphates-
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