A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes

Abstract

The hydrogen oxidation reaction (hor) was studied on a polycrystalline ruthenium electrode in H2SO4 solution at different rotation rates (ω). The experimental polarization curves recorded on steady state show the existence of a maximum current with a non-linear dependence of the current density on ω1/2. On the basis of the Tafel-Heyrovsky-Volmer kinetic mechanism, coupled with a process of inhibition of active sites by the reversible electroadsorption of hydroxyl species, it was possible to appropriately describe the origin of the maximum current. The corresponding set of kinetic parameters was also calculated from the correlation of the experimental results with the proposed kinetic model.