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Carbon-supported TiO2-Au hybrids as catalysts for the electrogeneration of hydrogen peroxide: Investigating the effect of TiO2 shape

dc.contributor.authorReis, Flavia V. E. dos
dc.contributor.authorAntonin, Vanessa S.
dc.contributor.authorHammer, Peter [UNESP]
dc.contributor.authorSantos, Mauro C.
dc.contributor.authorCamargo, Pedro H. C.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal do ABC (UFABC)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-10-22T06:17:08Z
dc.date.available2015-10-22T06:17:08Z
dc.date.issued2015-06-01
dc.description.abstractTiO2-Au hybrid materials are promising as electrocatalysts for the in situ production of H2O2 via the oxygen reduction reaction (ORR). However, the synthesis of uniform and well-controlled TiO2-Au materials, which is crucial to establish morphology-performance relationships, remains challenging. We describe herein the synthesis of hybrid materials composed of TiO2 colloidal spheres and wires decorated with Au nanoparticles. We employed TiO2 colloidal spheres and wires as physical templates for Au deposition, which enabled the uniform deposition of Au NPs with monodisperse sizes over the TiO2 surface. Then, the electrocatalytic activities toward the electrogeneration of H2O2 by the ORR were investigated as a function of the TiO2 shape and TiO2-Au loading on Vulcan XC-72R carbon. We found that the electrocatalytic activities were strongly dependent on the TiO2 shape and TiO2-Au loading in the catalysts. The utilization of TiO2 colloidal spheres led to higher activities relative to pure carbon and commercial Pt/C, and the optimal TiO2-Au loading corresponded to 3%. Conversely, the TiO2 wires led to detrimental effects over the catalytic performances for all hybrid materials. These results could be explained based on the morphological and conductivity differences among TiO2-Au/C electrode materials. We believe the results described herein can have important implication for the design of TiO2-based hybrid nanostructures for the electrogeneration of H2O2 by the ORR. (C) 2015 Elsevier Inc. All rights reserved.en
dc.description.affiliationUniv Sao Paulo, Inst Quim, Dept Quim Fundamental, BR-05508000 Sao Paulo, SP, Brazil
dc.description.affiliationUniv Fed Abc, CCNH, LEMN, BR-09210170 Santo Andre, SP, Brazil
dc.description.affiliationUNESP, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 2013/19861-6
dc.description.sponsorshipIdFAPESP: 2011/21656-6
dc.description.sponsorshipIdCNPq: 471245/2012-7
dc.description.sponsorshipIdCNPq: 474913/2012-0
dc.description.sponsorshipIdCNPq: 406612/2013-7
dc.format.extent100-106
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0021951715000937
dc.identifier.citationJournal Of Catalysis. San Diego: Academic Press Inc Elsevier Science, v. 326, p. 100-106, 2015.
dc.identifier.doi10.1016/j.jcat.2015.04.007
dc.identifier.issn0021-9517
dc.identifier.lattes6466841023506131
dc.identifier.orcid0000-0002-3823-0050
dc.identifier.urihttp://hdl.handle.net/11449/129618
dc.identifier.wosWOS:000355356900011
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal Of Catalysis
dc.relation.ispartofjcr6.759
dc.relation.ispartofsjr2,397
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectElectrocatalysisen
dc.subjectOxygen reduction reactionen
dc.subjectHydrogen peroxideen
dc.subjectTitanium dioxideen
dc.subjectGold nanoparticlesen
dc.titleCarbon-supported TiO2-Au hybrids as catalysts for the electrogeneration of hydrogen peroxide: Investigating the effect of TiO2 shapeen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes6466841023506131[3]
unesp.author.orcid0000-0002-3823-0050[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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