چکیده
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In this study, the electrocatalytic activity of the Co@Pt core-shell nanoparticles
toward the ethanol oxidation reaction has been investigated in detail by cyclic
voltammetry and chronoamperometry in an acidic and alkaline media. The
physicochemical data obtained in an alkaline solution were compared to those in an acidic solution. The obtained results demonstrate that while Co@Pt core-shell
nanoparticles exhibit a good electrocatalytic performance for ethanol oxidation
reaction in both media; the Co@Pt core-shell catalyst presents more catalytic activity (1.4 times), exchanges current densities (about 8 times), and high electrochemical active surface area (1.2 times) and stability (about 2 times) in the alkaline medium. The effect of some experimental factors such as electrolytes (H2SO4 and NaOH) and ethanol concentrations was studied and optimum conditions were suggested. From these points, we concluded that the ethanol oxidation reaction can be improved with an alkaline electrolyte and the oxidation reaction is highly dependent on the pH of the electrolyte. These results indicate that the system studied in the present work; Co@Pt core-shell nanoparticles on a carbon-ceramic electrode, is the most promising system for use in alkaline fuel cells.
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