Effects of thermal activation on the oxidation pathways of methanol at bulk Pt-Ru alloy electrodes

The competition between pathways that lead to adsorbed CO and CO, during th e electrochemical oxidation of 1.0 M methanol in 0.1 M HClO4 on two bulk Pt -Ru alloys (10 at.% Ru (X-Ru approximate to 0.1) and 90 at.% Ru (X-Ru appro ximate to 0.9)) was investigated for temperatures in the range of 25-80 deg reesC. On the high Ru content alloy studied (X-Ru approximate to 0.9), the dissociative chemisorption of methanol was inhibited below 70 degreesC; the faradaic current for methanol oxidation was low, and only small quantities of adsorbed CO and CO, were detected with infrared spectroscopy between 0. 2-0.8 V (vs. RHE). At 80 degreesC, strong infrared bands from CO2 and adsor bed, atop coordinated CO were observed over the potential ranges of 0.4-0.8 V and 0.2-0.8 V, respectively. The infrared measurements are consistent wi th the observation that bulk, high Ru content alloy electrodes appear passi vated toward methanol oxidation below 70 degreesC. On the low Ru content ah oy studied (X-Ru approximate to 0.1), the methanol surface chemistry was si milar to that of pure, polycrystalline Pt, but the electrode was more poiso n resistant than Pt. For both alloys, the persistence of strong adsorbed CO bands and rapid CO2 production between 0.4-0.8 V suggests CO functions as a reactive species with high steady-state coverages at these potentials. (C ) 2001 Elsevier Science B.V. All rights reserved.