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Bimetallic core-shell Ag@Pt nanoparticle-decorated MWNT electrodes for amperometric H-2 sensors and direct methanol fuel cells

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dc.contributor.authorRashid, Muhammad-
dc.contributor.authorJun, Tae-Sun-
dc.contributor.authorJung, Yongju-
dc.contributor.authorKim, Yong Shin-
dc.date.accessioned2021-06-22T20:23:07Z-
dc.date.available2021-06-22T20:23:07Z-
dc.date.created2021-01-21-
dc.date.issued2015-03-
dc.identifier.issn0925-4005-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/18799-
dc.description.abstractBimetallic core-shell Ag@Pt nanoparticles (NPs) attached on multiwall carbon nanotube (Ag@Pt-MWNT) were synthesized via the formation of Ag NPs on a MWNT surface through chemical reduction and subsequent galvanic replacement of Ag with PtCl62-. The successful synthesis of Ag@Pt-MWNT was confirmed by probing chemical compositions, absorption, and microstructures using various material analysis methods (UV-vis, SEM, EDS, and TEM). The bimetallic particles were found to have a core-shell structure in the TEM image: an Ag core with an average size of approximately 7 nm was enclosed by a shell composedof small Pt NPs. The electrochemical surface area of the Ag@Pt-MWNT-modified glassy carbon electrode was 896 cm(2)/mg, which was 1.5 times higher than that of commercial 20 wt% Pt-C (E-Tek). The Ag@Pt-MWNTs electrode also exhibited a higher peak current for methanol oxidation than those of comparable Pt-MWNT and Pt-C under the same amount of Pt loading, thus providing evidence for its higher electro-catalytic activity and CO tolerance. Furthermore, an amperometric gas-sensing electrode was fabricated by filtering an Ag@Pt-MWNT solution on a porous PTFE sheet. The as-fabricated electrode displayed a high sensitivity of 1.1 mu A/ppm in H-2 detection and an excellent linear response over the wide concentration range of 5-1000 ppm, together with fairly good detection times and long-term stability. This enhanced performance was correlated and discussed to be a result of the unique nanostructural features of the Ag@Pt core-shell structure with a porous Pt layer and the strong anchoring of the bimetallic NPs on the activated MWNT surface, which provides a highly active surface area and effective interactions between Ag and Pt. (C) 2014 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherElsevier BV-
dc.titleBimetallic core-shell Ag@Pt nanoparticle-decorated MWNT electrodes for amperometric H-2 sensors and direct methanol fuel cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Yong Shin-
dc.identifier.doi10.1016/j.snb.2014.11.005-
dc.identifier.scopusid2-s2.0-84911452221-
dc.identifier.wosid000346000500002-
dc.identifier.bibliographicCitationSensors and Actuators, B: Chemical, v.208, pp.7 - 13-
dc.relation.isPartOfSensors and Actuators, B: Chemical-
dc.citation.titleSensors and Actuators, B: Chemical-
dc.citation.volume208-
dc.citation.startPage7-
dc.citation.endPage13-
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.journalResearchAreaInstruments & Instrumentation-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryInstruments & Instrumentation-
dc.subject.keywordPlusMULTIWALLED CARBON NANOTUBES-
dc.subject.keywordPlusGALVANIC REPLACEMENT-
dc.subject.keywordPlusCATALYTIC-ACTIVITY-
dc.subject.keywordPlusHOLLOW-
dc.subject.keywordPlusGRAPHENE-
dc.subject.keywordPlusNANOSTRUCTURES-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordAuthorAg@Pt-MWNT electrode-
dc.subject.keywordAuthorGalvanic replacement reaction-
dc.subject.keywordAuthorAmperometric H-2 sensor-
dc.subject.keywordAuthorDirect methanol fuel cell-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0925400514013598?via%3Dihub-
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