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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/76545
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dc.contributor.authorGeraldes, Adriana Napoleão-
dc.contributor.authorDa Silva, Dionisio Furtunato-
dc.contributor.authorPino, Eddy Segura-
dc.contributor.authorDa Silva, Júlio César Martins-
dc.contributor.authorDe Souza, Rodrigo Fernando Brambilla-
dc.contributor.authorHammer, Peter-
dc.contributor.authorSpinacé, Estevam Vitório-
dc.contributor.authorNeto, Almir Oliveira-
dc.contributor.authorLinardi, Marcelo-
dc.contributor.authorDos Santos, Mauro Coelho-
dc.date.accessioned2014-05-27T11:30:41Z-
dc.date.accessioned2016-10-25T18:54:06Z-
dc.date.available2014-05-27T11:30:41Z-
dc.date.available2016-10-25T18:54:06Z-
dc.date.issued2013-09-11-
dc.identifierhttp://dx.doi.org/10.1016/j.electacta.2013.08.021-
dc.identifier.citationElectrochimica Acta, v. 111, p. 455-465.-
dc.identifier.issn0013-4686-
dc.identifier.urihttp://hdl.handle.net/11449/76545-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/76545-
dc.description.abstractCarbon-supported Pd, Au and bimetallic PdAu (Pd:Au 90:10, 50:50 and 30:70 atomic ratios) electrocatalysts were prepared using electron beam irradiation. The obtained materials were characterized by energy dispersive X-ray analysis (EDX), X-ray diffraction (XRD) and transmission electron microscopy (TEM), and their catalytic activities toward ethanol electro-oxidation were evaluated in an alkaline medium using electrochemical techniques, in situ attenuated total reflectance Fourier transformed infrared spectroscopy (ATR-FTIR) analysis and a single alkaline direct ethanol fuel cell (ADEFC). EDX analyses showed that the actual Pd: Au atomic ratios were very similar to the nominal ones. X-ray diffractograms of PdAu/C electrocatalysts evidenced the presence of Pd-rich (fcc) and Au-rich (fcc) phases. TEM analysis showed a homogeneous dispersion of nanoparticles on the carbon support, with an average size in the range of 3-5 nm and broad size distributions. Cyclic voltammetry (CV) and chronoamperometry (CA) experiments revealed the superior ambient activity toward ethanol electro-oxidation of PdAu/C electrocatalysts with Pd: Au ratios of 90:10 and 50:50. In situ ATR-FTIR spectroscopy measurements have shown that the mechanism for ethanol electro-oxidation is dependent on catalyst composition, leading to different reaction products, such as acetaldehyde and acetate, depending on the number of electrons transferred. Experiments on a single ADEFC were conducted between 50 and 900 C, and the best performance of 44 mW cm-2 in 2.0molL-1 ethanol was obtained at 850C for the Pd:Au 90:10 catalysts. This superior performance is most likely associated with enhancement of ethanol adsorption on Pd, oxidation of the intermediates, the presence of gold oxide-hydroxyl species, low mean particle diameters and better distribution of particles on the support. © 2013 Elsevier Ltd. All rights reserved.en
dc.format.extent455-465-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAlkaline direct ethanol fuel cell-
dc.subjectDAAFC-
dc.subjectElectron beam irradiation-
dc.subjectEthanol electro-oxidation-
dc.subjectFuel cell-
dc.subjectPdAu/C-
dc.subjectAttenuated total reflectance-
dc.subjectElectrochemical techniques-
dc.subjectEnergy dispersive x-ray analysis (EDX)-
dc.subjectFourier transformed infrared spectroscopy-
dc.subjectCarbon-
dc.subjectCatalyst activity-
dc.subjectChronoamperometry-
dc.subjectCyclic voltammetry-
dc.subjectDirect ethanol fuel cells (DEFC)-
dc.subjectElectrocatalysts-
dc.subjectElectrolysis-
dc.subjectElectron beams-
dc.subjectElectrooxidation-
dc.subjectEthanol-
dc.subjectExperiments-
dc.subjectFourier transform infrared spectroscopy-
dc.subjectFuel cells-
dc.subjectIrradiation-
dc.subjectReaction intermediates-
dc.subjectTransmission electron microscopy-
dc.subjectX ray diffraction-
dc.subjectPalladium-
dc.titleEthanol electro-oxidation in an alkaline medium using Pd/C, Au/C and PdAu/C electrocatalysts prepared by electron beam irradiationen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal do ABC (UFABC)-
dc.contributor.institutionInstituto de Pesquisas Energéticas e Nucleares (IPEN)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationLaboratorio de Eletroquímica e Materials Nanoestruturados Centro de Ciencias Naturais e Humanas Uníversídade Federal Do ABC, Rua Santa Adélia, 166, 09210-170 Santo-André, SP-
dc.description.affiliationInstituto de Pesquisas Energéticas e Nucleares-Comissao Nacional de Energia Nuclear, Av. Prof. Lineu Prestes, 2242, 05508-900 Sao Paulo, SP-
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho Instituto de Química de Araraquara, Rua Prof. Francisco Degni, 55 Quitandinha, 14800-060 Araraquara, SP-
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho Instituto de Química de Araraquara, Rua Prof. Francisco Degni, 55 Quitandinha, 14800-060 Araraquara, SP-
dc.identifier.doi10.1016/j.electacta.2013.08.021-
dc.identifier.wosWOS:000329531100061-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofElectrochimica Acta-
dc.identifier.scopus2-s2.0-84883524606-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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