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dc.contributor.authorKim, Sechul-
dc.contributor.authorJung, Changhoon-
dc.contributor.authorKim, Jandee-
dc.contributor.authorRhee, Choong Kyun-
dc.contributor.authorChoi, Sung-Min-
dc.contributor.authorLim, Tae-Hoon-
dc.date.accessioned2024-01-20T19:33:57Z-
dc.date.available2024-01-20T19:33:57Z-
dc.date.created2021-09-02-
dc.date.issued2010-03-16-
dc.identifier.issn0743-7463-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/131629-
dc.description.abstractThis work presents formic acid oxidation on Pt deposits on Au nanoparticles dispersed oil Vulcan XC-72R. The Pt deposits were produced using spontaneous deposition method contacting the Au nanoparticles with solutions containing Pt complex ions in various concentrations. The Pt deposits were characterized using CO stripping coulometry, X-ray photoelectron spectroscopy, and inductively coupled plasma atomic emission spectroscopy. When the Pt concentration is 10(-5)-10(-4) M, the Pt deposits are nanoislands of monatomic height. In the concentration range of 10(-4)-10(-3) M, the Pt deposits are most likely two-layer-thick nanofeatures. As Pt concentration increases further, the deposits become wider and thicker. Voltammetric behavior of Pt deposits reveals that on Pt deposits, dehydrogenation path is activated at the expense of poison-fori-ning dehydration path. Furthermore, chronoamperometric measurement of the catalytic activity of Pt deposits supports that the two-layer-thick Pt deposits are most efficient in formic acid oxidation among the studied Pt deposits on Au nanoparticles. The enhancement factor of the particular Pt deposits is 2 in terms of turnover frequency, compared with a commercial Pt catalyst. Details are discussed in conjunction with Pt deposits on Au(111).-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectIRREVERSIBLY ADSORBED ADATOMS-
dc.subjectCO MONOLAYER OXIDATION-
dc.subjectPT-RU ALLOY-
dc.subjectMETHANOL OXIDATION-
dc.subjectPARTICLE-SIZE-
dc.subjectELECTROCATALYTIC OXIDATION-
dc.subjectSINGLE-CRYSTAL-
dc.subjectHETEROGENEOUS ELECTROCATALYSIS-
dc.subjectPLATINUM NANOPARTICLES-
dc.subjectCATALYTIC-ACTIVITY-
dc.titleModification of Au Nanoparticles Dispersed on Carbon Support Using Spontaneous Deposition of Pt toward Formic Acid Oxidation-
dc.typeArticle-
dc.identifier.doi10.1021/la903357c-
dc.description.journalClass1-
dc.identifier.bibliographicCitationLANGMUIR, v.26, no.6, pp.4497 - 4505-
dc.citation.titleLANGMUIR-
dc.citation.volume26-
dc.citation.number6-
dc.citation.startPage4497-
dc.citation.endPage4505-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000275226700105-
dc.identifier.scopusid2-s2.0-77957952196-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusIRREVERSIBLY ADSORBED ADATOMS-
dc.subject.keywordPlusCO MONOLAYER OXIDATION-
dc.subject.keywordPlusPT-RU ALLOY-
dc.subject.keywordPlusMETHANOL OXIDATION-
dc.subject.keywordPlusPARTICLE-SIZE-
dc.subject.keywordPlusELECTROCATALYTIC OXIDATION-
dc.subject.keywordPlusSINGLE-CRYSTAL-
dc.subject.keywordPlusHETEROGENEOUS ELECTROCATALYSIS-
dc.subject.keywordPlusPLATINUM NANOPARTICLES-
dc.subject.keywordPlusCATALYTIC-ACTIVITY-
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