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Optimization of active sites by sulfurization of the core–shell ZIF 67@ZIF 8 for rapid oxygen reduction kinetics in acidic media

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dc.contributor.authorLee, Jung Su-
dc.contributor.authorRajan, Hashikaa-
dc.contributor.authorChristy, Maria-
dc.contributor.authorYi, Sung Chul-
dc.date.accessioned2021-07-30T04:48:13Z-
dc.date.available2021-07-30T04:48:13Z-
dc.date.created2021-05-13-
dc.date.issued2021-03-
dc.identifier.issn0360-3199-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/1368-
dc.description.abstractAchieving a highly active cathode surface with extremely efficient electrocatalysts for oxygen reduction kinetics is a fundamental necessity for durable fuel cells. Developing such active materials into desirable nanostructures is crucial in the pursuit of electrocatalysis. A facile preparation of cobalt decorated nitrogen and sulfur co-doped carbon nanostructures (Co-NSC) with the added advantage of Zeolitic imidazolate frameworks (ZIF), ZIF 67@ZIF 8 is reported here. The as-prepared Co, N, S, co-doped carbon (Co-NSC) electrocatalyst comes under platinum group metal-free (PGM-free) catalysts which intends to replace the scarce and highly expensive commercial Pt catalysts. Facile preparation of the Co-NSC catalyst that is scalable, low cost and highly ORR active makes the material advantageous. Co-doping sulfur has dramatically enhanced the intrinsic catalytic activity of the catalyst, and the degree of variation in sulfurization greatly influences the overall catalytic property. Co-NSC 200 with high sulfur doping exhibit a positively shifted onset potential of 0.81 V, and a high yielding current density of 5.5 mA cm(-2) at 20 mV s(-1).-
dc.language영어-
dc.language.isoen-
dc.publisherElsevier Ltd-
dc.titleOptimization of active sites by sulfurization of the core–shell ZIF 67@ZIF 8 for rapid oxygen reduction kinetics in acidic media-
dc.typeArticle-
dc.contributor.affiliatedAuthorYi, Sung Chul-
dc.identifier.doi10.1016/j.ijhydene.2020.12.159-
dc.identifier.scopusid2-s2.0-85099314826-
dc.identifier.wosid000623642900012-
dc.identifier.bibliographicCitationInternational Journal of Hydrogen Energy, v.46, no.18, pp.10739 - 10748-
dc.relation.isPartOfInternational Journal of Hydrogen Energy-
dc.citation.titleInternational Journal of Hydrogen Energy-
dc.citation.volume46-
dc.citation.number18-
dc.citation.startPage10739-
dc.citation.endPage10748-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.subject.keywordPlusCarbon-
dc.subject.keywordPlusElectrocatalysis-
dc.subject.keywordPlusElectrocatalysts-
dc.subject.keywordPlusElectrolytic reduction-
dc.subject.keywordPlusFuel cells-
dc.subject.keywordPlusNanostructures-
dc.subject.keywordPlusOxygen-
dc.subject.keywordPlusPlatinum metals-
dc.subject.keywordPlusSulfur-
dc.subject.keywordPlusActive material-
dc.subject.keywordPlusCatalytic properties-
dc.subject.keywordPlusCathode surface-
dc.subject.keywordPlusFacile preparation-
dc.subject.keywordPlusOnset potential-
dc.subject.keywordPlusOxygen reduction kinetics-
dc.subject.keywordPlusPlatinum group metals-
dc.subject.keywordPlusZeolitic imidazolate frameworks-
dc.subject.keywordPlusCatalyst activity-
dc.subject.keywordAuthorMetal organic frameworks-
dc.subject.keywordAuthorZeolitic imidazolate frameworks-
dc.subject.keywordAuthorOxygen reduction reaction-
dc.subject.keywordAuthorSulfurization-
dc.subject.keywordAuthorReaction kinetics-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0360319920347911?via%3Dihub-
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