dc.contributor | Universidade Federal do ABC (UFABC) | |
dc.contributor | Instituto de Pesquisas Energéticas e Nucleares (IPEN) | |
dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-27T11:30:41Z | |
dc.date.available | 2014-05-27T11:30:41Z | |
dc.date.created | 2014-05-27T11:30:41Z | |
dc.date.issued | 2013-09-11 | |
dc.identifier | Electrochimica Acta, v. 111, p. 455-465. | |
dc.identifier | 0013-4686 | |
dc.identifier | http://hdl.handle.net/11449/76545 | |
dc.identifier | 10.1016/j.electacta.2013.08.021 | |
dc.identifier | WOS:000329531100061 | |
dc.identifier | 2-s2.0-84883524606 | |
dc.identifier | 6466841023506131 | |
dc.identifier | 0000-0002-3823-0050 | |
dc.description.abstract | Carbon-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.language | eng | |
dc.relation | Electrochimica Acta | |
dc.relation | 5.116 | |
dc.relation | 1,439 | |
dc.rights | Acesso restrito | |
dc.source | Scopus | |
dc.subject | Alkaline direct ethanol fuel cell | |
dc.subject | DAAFC | |
dc.subject | Electron beam irradiation | |
dc.subject | Ethanol electro-oxidation | |
dc.subject | Fuel cell | |
dc.subject | PdAu/C | |
dc.subject | Attenuated total reflectance | |
dc.subject | Electrochemical techniques | |
dc.subject | Energy dispersive x-ray analysis (EDX) | |
dc.subject | Fourier transformed infrared spectroscopy | |
dc.subject | Carbon | |
dc.subject | Catalyst activity | |
dc.subject | Chronoamperometry | |
dc.subject | Cyclic voltammetry | |
dc.subject | Direct ethanol fuel cells (DEFC) | |
dc.subject | Electrocatalysts | |
dc.subject | Electrolysis | |
dc.subject | Electron beams | |
dc.subject | Electrooxidation | |
dc.subject | Ethanol | |
dc.subject | Experiments | |
dc.subject | Fourier transform infrared spectroscopy | |
dc.subject | Fuel cells | |
dc.subject | Irradiation | |
dc.subject | Reaction intermediates | |
dc.subject | Transmission electron microscopy | |
dc.subject | X ray diffraction | |
dc.subject | Palladium | |
dc.title | Ethanol electro-oxidation in an alkaline medium using Pd/C, Au/C and PdAu/C electrocatalysts prepared by electron beam irradiation | |
dc.type | Artículos de revistas | |