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dc.contributor.authorKim, Sunhyung-
dc.contributor.authorHan, Jonghee-
dc.contributor.authorKwon, Yongchai-
dc.contributor.authorLee, Kug-Seung-
dc.contributor.authorLim, Tae-Hoon-
dc.contributor.authorNam, Suk Woo-
dc.contributor.authorJang, Jong Hyun-
dc.date.accessioned2024-01-20T16:05:21Z-
dc.date.available2024-01-20T16:05:21Z-
dc.date.created2021-09-04-
dc.date.issued2011-09-30-
dc.identifier.issn0013-4686-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/129976-
dc.description.abstractUsing platinum (Pt) black and carbon-supported Pt (Pt/C) as cathode catalysts, membrane-electrode assemblies (MEAs) were fabricated with various Nafion ionomer content, and their direct formic acid fuel cell (DFAFC) performances were investigated. In MEAs incorporating Pt black catalysts, the current density at 0.6 V was highest at ionomer/catalyst volume ratio of 1.0, which was consistent with the electrochemical active area (EAS) variation measured by cyclic voltammetry. However, the current density measured at 0.3 V, the cell performance increased with Nation ionomer content, especially at low ionorner loading, indicating that proton transport rate played an important role. The variation in ionic resistance (R-ion) of cathode layers with Nation ionomer content was experimentally confirmed by using the complex capacitance analysis of impedance data implemented with nitrogen (cathodes)/hydrogen (anodes) atmosphere. For Pt/C, the layer thickness and EAS of cathode were larger than those of MEA cathode using Pt black; and the current densities at 0.6V were lower than those of Pt black, suggesting that smaller fraction of EAS was utilized. (C) 2011 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectPD CATALYST-
dc.subjectMETHANOL-
dc.subjectPERFORMANCE-
dc.subjectELECTROOXIDATION-
dc.subjectPEMFC-
dc.subjectELECTRODES-
dc.subjectBLACK-
dc.subjectDMFC-
dc.titleEffect of Nafion ionomer and catalyst in cathode layers for the direct formic acid fuel cell with complex capacitance analysis on the ionic resistance-
dc.typeArticle-
dc.identifier.doi10.1016/j.electacta.2011.02.005-
dc.description.journalClass1-
dc.identifier.bibliographicCitationELECTROCHIMICA ACTA, v.56, no.23, pp.7984 - 7990-
dc.citation.titleELECTROCHIMICA ACTA-
dc.citation.volume56-
dc.citation.number23-
dc.citation.startPage7984-
dc.citation.endPage7990-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000295437500028-
dc.identifier.scopusid2-s2.0-80052738636-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.type.docTypeArticle; Proceedings Paper-
dc.subject.keywordPlusPD CATALYST-
dc.subject.keywordPlusMETHANOL-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusELECTROOXIDATION-
dc.subject.keywordPlusPEMFC-
dc.subject.keywordPlusELECTRODES-
dc.subject.keywordPlusBLACK-
dc.subject.keywordPlusDMFC-
dc.subject.keywordAuthorDirect formic acid fuel cells-
dc.subject.keywordAuthorPlatinum catalyst-
dc.subject.keywordAuthorImpedance spectroscopy-
dc.subject.keywordAuthorComplex capacitance analysis-
dc.subject.keywordAuthorIonic resistance-
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