Abstract
OH adspecies are involved in numerous electrocatalytic reactions, such as CO, H2, methanol, and ethanol oxidation and oxygen reduction reactions, as a reaction intermediate and/or reactant. In this work, we have, for the first time, identified the OH stretching band of OH adspecies on Pt, Ru, and Pt/Ru electrodes with surface-enhanced infrared absorption spectroscopy (SEIRAS) in a flow cell through potential modulation and CO displacement. We found that while Ru had a relatively constant OH coverage at potentials between 0.1 and 0.8 V, Pt had a maximum OH coverage at 0.6 V in 0.1 M HClO4 and 0.7 V in 0.1 M KOH. CO oxidation kinetics on Ru were sluggish, although adsorbed OH appeared on Ru at very low potentials. Binary Pt/Ru electrodes promote CO oxidation through a synergistic effect in which Ru promotes OH adsorption and Pt catalyzes the reaction between the CO and OH adspecies. In addition, water coadsorbed with CO at Ru sites of Pt/Ru also plays an important role. These new spectroscopic results about OH adspecies could advance the understanding of the mechanism of fuel cell related electrocatalysis.
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