Preparation of PtRu/C, PtBi/C and PtRuBi/C electrocatalysts by an alcohol-reduction process for ethanol oxidation

dc.contributor.authorBRANDALISE, M.pt_BR
dc.contributor.authorTUSI, M.M.pt_BR
dc.contributor.authorLINARDI, M.pt_BR
dc.contributor.authorSPINACE, E.V.pt_BR
dc.contributor.authorOLIVEIRA NETO, A.pt_BR
dc.coverageInternacionalpt_BR
dc.creator.eventoINTERNATIONAL CONFERENCE ON NANOSTRUCTURED MATERIALS, 9thpt_BR
dc.date.accessioned2014-11-19T10:35:06Zpt_BR
dc.date.accessioned2014-11-19T14:06:12Zpt_BR
dc.date.accessioned2015-04-01T12:40:59Z
dc.date.available2014-11-19T10:35:06Zpt_BR
dc.date.available2014-11-19T14:06:12Zpt_BR
dc.date.available2015-04-01T12:40:59Z
dc.date.eventoJune 1-6, 2008pt_BR
dc.description.abstractFuel cells employing alcohols directly (direct alcohol fuel cell, DAFC) are attractive as power sources for mobile, stationary and portable applications. Compared to hydrogen-fed fuel cells, which need a reforming system or have problems of hydrogen storage, DAFCs use a liquid fuel, thus simplifying the fuel delivery system [1]. Ethanol offers an attractive alternative as the direct fuel because it is produced in large quantities from biomass and it is much less toxic than others alcohols. Due to the low electrocatalytic activity of platinum for practical DAFC applications, elements like ruthenium have been added to promote electroactivity. In this aspect it is important to study new binary and ternary electrocatalysts for ethanol oxidation [1,2]. In this work Pt/C, PtRu/C (90:10), PtRu/C (50:50), PtBi/C (90:10), PtBi/C (50:50), PtRuBi/C (80:10:10) and PtRuBi/C (50:40:10) were prepared by an alcohol-reduction process [1] with metal loading of 20 wt.% using H2PtCl6.6H2O (Aldrich), RuCl3.xH2O (Aldrich),and Bi(NO3)3.5H2O (Aldrich) as metals sources and Vulcan XC 72 as support. The electrocatalysts were characterized by EDAX, X-ray diffraction (XRD) and cyclic voltammetry (CV). The electro-oxidation of ethanol was studied in acid medium by cyclic voltammetry and chronoamperometry using thin porous coating technique. The X-ray diffractograms of Pt/C, PtRu/C, PtBi/C and PtRuBi/C electrocatalysts showed a broad peak at about 2θ = 25° that was associated with the carbon support and four diffraction peaks at about 2θ = 40°, 47°, 67° and 82° characteristic of the face centered cubic structure (fcc) structure of platinum and platinum alloys. For PtBi/C (50:50) electrocatalyst it was also observed the presence of the bismuth oxide phase (Bi2O3). The Pt:Ru, Pt:Bi and Pt:Ru:Bi atomic ratios (EDAX) of the obtained electrocalysts were similar to the nominal atomic ratios used in the preparations and the average crystallite size were in the range of 2–4 nm. The electrochemical studies showed that PtRuBi/C (80:10:10) electrocatalyst had superior performance for ethanol electro-oxidation at room temperature compared to PtRu/C and PtBi/C electrocatalys.
dc.identifier.citationBRANDALISE, M.; TUSI, M.M.; LINARDI, M.; SPINACE, E.V.; OLIVEIRA NETO, A. Preparation of PtRu/C, PtBi/C and PtRuBi/C electrocatalysts by an alcohol-reduction process for ethanol oxidation. In: INTERNATIONAL CONFERENCE ON NANOSTRUCTURED MATERIALS, 9th, June 1-6, 2008, Rio de Janeiro, RJ. <b>Abstract...</b> Disponível em: http://repositorio.ipen.br/handle/123456789/19278.
dc.identifier.orcidhttps://orcid.org/0000-0003-0105-6519
dc.identifier.orcidhttps://orcid.org/0000-0002-9287-6071
dc.identifier.orcidhttps://orcid.org/0000-0002-7011-8261
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/19278pt_BR
dc.local.eventoRio de Janeiro, RJpt_BR
dc.rightsopenAccesspt_BR
dc.subjectalcohol fuel cellspt_BR
dc.subjectplatinumpt_BR
dc.subjectrutheniumpt_BR
dc.subjectcarbonpt_BR
dc.subjectbismuthpt_BR
dc.subjectelectrocatalystspt_BR
dc.subjectreductionpt_BR
dc.subjectethanolpt_BR
dc.subjectoxidationpt_BR
dc.subjectx-ray diffractionpt_BR
dc.subjectvoltametrypt_BR
dc.titlePreparation of PtRu/C, PtBi/C and PtRuBi/C electrocatalysts by an alcohol-reduction process for ethanol oxidationpt_BR
dc.typeResumo de eventos científicospt_BR
dspace.entity.typePublication
ipen.autorMARCELO LINARDI
ipen.autorALMIR OLIVEIRA NETO
ipen.autorESTEVAM VITORIO SPINACE
ipen.autorMARCELO MARQUES TUSI
ipen.autorMICHELE BRANDALISE
ipen.codigoautor279
ipen.codigoautor3541
ipen.codigoautor555
ipen.codigoautor4024
ipen.codigoautor6918
ipen.contributor.ipenauthorMARCELO LINARDI
ipen.contributor.ipenauthorALMIR OLIVEIRA NETO
ipen.contributor.ipenauthorESTEVAM VITORIO SPINACE
ipen.contributor.ipenauthorMARCELO MARQUES TUSI
ipen.contributor.ipenauthorMICHELE BRANDALISE
ipen.date.recebimento09-03pt_BR
ipen.event.datapadronizada2008pt_BR
ipen.identifier.ipendoc13591pt_BR
ipen.notas.internasAbstractpt_BR
ipen.type.genreResumo
relation.isAuthorOfPublication274f973a-ce40-4261-a1d1-6a496557ba2b
relation.isAuthorOfPublication13be55b2-f917-45c4-bc6b-5f315bd0290f
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relation.isAuthorOfPublication.latestForDiscovery2d7c0a47-1e22-4839-8656-c47feea0ce4e
sigepi.autor.atividadeBRANDALISE, M.:6918:610:Spt_BR
sigepi.autor.atividadeTUSI, M.M.:4024:610:Npt_BR
sigepi.autor.atividadeLINARDI, M.:279:610:Npt_BR
sigepi.autor.atividadeSPINACE, E.V.:555:610:Npt_BR
sigepi.autor.atividadeOLIVEIRA NETO, A.:3541:610:Npt_BR

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