dc.contributorUniversidade Federal do ABC (UFABC)
dc.contributorInstituto de Pesquisas Energéticas e Nucleares (IPEN)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:30:41Z
dc.date.accessioned2022-10-05T18:59:17Z
dc.date.available2014-05-27T11:30:41Z
dc.date.available2022-10-05T18:59:17Z
dc.date.created2014-05-27T11:30:41Z
dc.date.issued2013-09-11
dc.identifierElectrochimica Acta, v. 111, p. 455-465.
dc.identifier0013-4686
dc.identifierhttp://hdl.handle.net/11449/76545
dc.identifier10.1016/j.electacta.2013.08.021
dc.identifierWOS:000329531100061
dc.identifier2-s2.0-84883524606
dc.identifier6466841023506131
dc.identifier0000-0002-3823-0050
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3925428
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.
dc.languageeng
dc.relationElectrochimica Acta
dc.relation5.116
dc.relation1,439
dc.rightsAcesso restrito
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 irradiation
dc.typeArtigo


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