Abstract
Platinum is the most investigated catalyst for the electrochemical oxidation of small organic molecules. This metal presents high overpotentials for the oxidation of organic compounds and the poisoning of active sites by strongly adsorbed intermediates, mainly CO, which decrease the efficiency of a direct alcohol fuel cell (DAFC). Ethanol is an ideal fuel for these DAFC systems due to its high energy density, but one of the problems with the electro-oxidation of this fuel is the low yield for the total oxidation to CO 2. The purpose of the work reported here was to study the influence of the composition of Pt-Rh/C catalysts on the CO 2 yields. In addition, using the differential electrochemical mass spectrometry (DEMS) technique, it is shown that Pt-Rh/C catalysts enhance the total ethanol oxidation with respect to pure Pt/C by driving the reaction via the CO 2 route. The faradaic current efficiency for the oxidation of ethanol to CO 2 increased from 0.08 on pure Pt/C to 0.5 on the Pt 47Rh 53/C catalyst at 0.7 V vs. RHE. It was concluded that electronic effects play a key role in the mechanism of ethanol oxidation on Pt-Rh/C electrodes.
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