Item

Abstract

In this work, we employ electronic structure methods to investigate the structure and reactivity of IrO_x nanoparticle models as catalysts for the oxygen evolution reaction (OER). Based on the explicit inclusion of the potential and pH in a constant potential framework, a computational approach is applied to investigate the thermodynamics of the proton and electron transfer process of IrO_x cluster models. We address structural changes of the clusters under electrochemical conditions by constructing potential–pH diagrams from our computational results. Comparison of two IrO_x cluster structures suggests that the charge transport to the clusters strongly depends on the pH. As a result, structures with a maximum number of on-top hydroxyl (OH_μ1) species are stable at low potentials and deprotonation becomes favorable with increasing potential. An assessment of the Ir oxidation states in our models shows that mixed oxidation states, i.e., Ir^IV and Ir^V, occur around the OER onset potential and increase to higher oxidation states (Ir^VI) in the high potential regime. Furthermore, an investigation of the water adsorption mechanism is carried out at different potentials.The results suggest that the potential controls the energetics of intermediates as well as transition states during the OER.