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Cobalt encapsulated in the nitrogen and sulfur co-doped carbon nanotube supported platinum for the oxygen reduction reaction catalyst

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dc.contributor.authorKim, Tae-Hyun-
dc.contributor.authorJung, Chi-Young-
dc.contributor.authorBose, Ranjith-
dc.contributor.authorYi, Sung-Chul-
dc.date.accessioned2022-07-10T23:01:24Z-
dc.date.available2022-07-10T23:01:24Z-
dc.date.created2021-05-12-
dc.date.issued2018-11-
dc.identifier.issn0008-6223-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/149051-
dc.description.abstractIn this paper, cobalt encapsulated in nitrogen and sulfur co-doped carbon nanotube (Co-NST) was synthesized through a simple pyrolysis method to impregnate platinum (Pt) nanoparticles. The Co-NST presented a bamboo-like morphology with the high degree of graphitization. Owing to the dual heteroatoms co-doped in the carbon matrix, the Pt supported on the Co-NST (Pt/Co-NST) showed the well-dispersed morphology of the Pt nanoparticles. In addition, the synergistic effect between the Co-NST support and the Pt nanoparticle was observed from the physicochemical characterizations. As a result, the Pt/Co-NST presented improved oxygen reduction reaction (ORR) activity and stability compared to the commercial Pt/C. The mass activity and specific activity of the Pt/Co-NST presented 508.48 mA mg(pt)(-1) and 723.93 mu A cm(pt)(-2), respectively, which exhibited more than 3 times higher compared to those of the commercial Pt/C. After repeating 5000 potential cycles, the Pt/Co-NST showed improved stability with 29 mV loss in half-wave potential, while the half-wave potential of the commercial Pt/C was severely decreased by 118 mV.-
dc.language영어-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleCobalt encapsulated in the nitrogen and sulfur co-doped carbon nanotube supported platinum for the oxygen reduction reaction catalyst-
dc.typeArticle-
dc.contributor.affiliatedAuthorYi, Sung-Chul-
dc.identifier.doi10.1016/j.carbon.2018.07.031-
dc.identifier.scopusid2-s2.0-85053106412-
dc.identifier.wosid000446063100075-
dc.identifier.bibliographicCitationCARBON, v.139, pp.656 - 665-
dc.relation.isPartOfCARBON-
dc.citation.titleCARBON-
dc.citation.volume139-
dc.citation.startPage656-
dc.citation.endPage665-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusMEMBRANE FUEL-CELLS-
dc.subject.keywordPlusCATHODE CATALYST-
dc.subject.keywordPlusHIGHLY EFFICIENT-
dc.subject.keywordPlusELECTROCATALYTIC ACTIVITY-
dc.subject.keywordPlusCOMPOSITE CATALYST-
dc.subject.keywordPlusGRAPHENE-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusDURABILITY-
dc.subject.keywordPlusROUTE-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0008622318306730?via%3Dihub-
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