Determination of the Gibbs excess of H and OH adsorbed at a Pt(1 1 1) electrode surface using a thermodynamic method

Abstract

The thermodynamics of the so-called perfectly polarized electrode were employed to analyze the total charge densities for a Pt(1 1 1) electrode in a series of solutions (0.1− x) M HClO 4+ x M KClO 4 with a constant ionic strength and a variable hydronium ion concentration. The total charge densities were calculated by integration of cyclic voltammetry curves. A complete thermodynamic analysis using charge and potential as independent variables has been performed. The Gibbs excesses of adsorbed hydrogen and OH were determined without the need to introduce an arbitrary correction for the so-called charging of the double layer and further assumptions about the charge number per adsorbed species. We found that the maximum surface concentration of H amounts to ∼11×10 14 ions cm −2 or to a coverage 0.73 monolayer (ML) in good agreement with previous estimates. The maximum surface coverage of OH is equal to ∼8×10 14 ions cm −2 or to a coverage ∼0.53 ML. Using the thermodynamic method, the charge numbers at a constant potential (electrosorption valency) and at a constant chemical potential (reciprocal of the Esin–Markov coefficient) for adsorbed H and OH were calculated using the Gibbs excess data. The charge numbers are equal to ∼1 for H and to ∼−1 for OH. These values suggest that the adsorbed species is hydrogen atom and discharged OH species.