Ternary Pt45Ru45M10/C (M=Mn, Mo and W) catalysts for methanol and ethanol electro-oxidation

Cited 14 time in webofscience Cited 0 time in scopus
  • Hit : 555
  • Download : 7
DC FieldValueLanguage
dc.contributor.authorJeon, Min-Kuko
dc.contributor.authorLee, Ki-Rakko
dc.contributor.authorWoo, Seong-Ihlko
dc.date.accessioned2013-03-11T16:25:10Z-
dc.date.available2013-03-11T16:25:10Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-07-
dc.identifier.citationKOREAN JOURNAL OF CHEMICAL ENGINEERING, v.26, no.4, pp.1028 - 1033-
dc.identifier.issn0256-1115-
dc.identifier.urihttp://hdl.handle.net/10203/99594-
dc.description.abstractTernary Pt45Ru45Mn10/C, Pt45Ru45Mo10/C and Pt45Ru45W10/C catalysts were synthesized and physical and electrochemical properties were characterized. Particle sizes of the catalysts were determined by X-ray diffraction to be 3.9, 4.8 and 4.6 nm for the Mn, Mo and W incorporated catalysts, respectively. Electrochemically active surface areas were calculated from CO stripping results, which were 17.7, 17.2 and 15.7 m(2)/g (catal) for the Pt45Ru45Mn10/C, Pt45Ru45Mo10/C and Pt45Ru45W10/C catalysts, respectively. In methanol electro-oxidation, the Pt45Ru45W10/C catalyst showed highest mass and specific activities of 2.78 A/g (cat.) and 177 mA/m(2), respectively, which were 22 and 100% higher than those of commercial PtRu/C. In the case of ethanol electro-oxidation, the Pt45Ru45Mo10/C catalyst exhibited highest mass and specific activities of 4.8 A/g (catal) and 280 mA/m(2), respectively. Specific activity of the Pt45Ru45Mo10/C catalyst was 56% higher than that of the commercial PtRu/C.-
dc.languageEnglish-
dc.publisherKOREAN INST CHEM ENGINEERS-
dc.subjectMEMBRANE FUEL-CELLS-
dc.subjectANODE ELECTROCATALYSTS-
dc.subjectELECTRONIC-STRUCTURE-
dc.subjectCO-TOLERANCE-
dc.subjectACID-MEDIUM-
dc.subjectOXIDATION-
dc.subjectPERFORMANCE-
dc.subjectNI-
dc.subjectTRANSITION-
dc.subjectRUTHENIUM-
dc.titleTernary Pt45Ru45M10/C (M=Mn, Mo and W) catalysts for methanol and ethanol electro-oxidation-
dc.typeArticle-
dc.identifier.wosid000267670500018-
dc.identifier.scopusid2-s2.0-67651193770-
dc.type.rimsART-
dc.citation.volume26-
dc.citation.issue4-
dc.citation.beginningpage1028-
dc.citation.endingpage1033-
dc.citation.publicationnameKOREAN JOURNAL OF CHEMICAL ENGINEERING-
dc.identifier.doi10.2478/s11814-009-0171-1-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorWoo, Seong-Ihl-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorElectrocatalyst-
dc.subject.keywordAuthorDirect Alcohol Fuel Cell-
dc.subject.keywordAuthorMethanol Electro-oxidation-
dc.subject.keywordAuthorEthanol Electro-oxidation-
dc.subject.keywordAuthorCO Stripping-
dc.subject.keywordPlusMEMBRANE FUEL-CELLS-
dc.subject.keywordPlusANODE ELECTROCATALYSTS-
dc.subject.keywordPlusELECTRONIC-STRUCTURE-
dc.subject.keywordPlusCO-TOLERANCE-
dc.subject.keywordPlusACID-MEDIUM-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusNI-
dc.subject.keywordPlusTRANSITION-
dc.subject.keywordPlusRUTHENIUM-
Appears in Collection
CBE-Journal Papers(저널논문)
Files in This Item
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 14 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0