Evaluation of polycrystalline platinum and rhodium surfaces for the electro-oxidation of aqueous sulfur dioxide

Abstract

Polycrystalline Rh and Pt were studied to ascertain their electrocatalytic activity for the electro-oxidation of SO2, an important reaction in sulfur dioxide depolarized electrolyzers used to produce hydrogen. Cyclic voltammetry and linear polarization methods were employed to evaluate the catalytic activity of these surfaces. Rh exhibited 25-fold lower catalytic activity than Pt and was more susceptible to poisoning by adsorbed intermediate sulfur species. Koutecky-Levich analysis indicated a two-electron transfer reaction on the Pt surface, which corresponded to the most commonly accepted SO2 electro-oxidation reaction mechanism. The Tafel slopes in the low potential region (near the onset potential), in conjunction with an analysis of well-known reaction mechanisms, suggested that the step leading to the oxidation of water to form adsorbed hydroxyl species was the rate-determining step (RDS). This mechanistic model predicts a decrease in Tafel slope with increasing coverage of catalyst active surface sites by adsorbed sulfur species. For Pt, we estimate a surface sulfur coverage of 4 % based on the experimentally measured Tafel slope. In the case of Rh, the sulfur coverage was calculated to be approximately 1 %. The Tafel slopes obtained changed from 106 mV decade−1 for Rh and 80 mV decade−1 for Pt at potentials below 0.7 V vs. standard hydrogen electrode (SHE) to 210 mV decade−1 for Rh and 162 mV decade−1 for Pt at potentials above 0.7 V vs. SHE, suggesting a change in the reaction mechanism corresponding to a change in the surface of the electrocatalyst