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Insights into the ethanol electro-oxidation reaction mechanism on palladium in alkaline media are presented combining polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) and density functional theory (DFT) calculations. The synergy between PM-IRRAS and DFT calculations helps to explain why the C–C bond is not broken during ethanol electro-oxidation, and the reaction stops at acetate. Coupling chronoamperometry (CA) with in situ PM-IRRAS enables us to simultaneously identify ethanol electro-oxidation products on the catalyst surface and in the bulk solution. We show that, at lower potential, it is possible to break the C–C bond on Pd/C in alkaline media to form CO₂. However, the selectivity is poor, because of competition with the formation of acetate and other side products, which gets worse at higher potentials. DFT computations complete the picture using the computational …