Synergic Effects of Surface Chemistry and Applied Potentials on the Kinetics of the Electrocatalytic Oxygen Evolution Reaction in IrO2

Improving the efficacy of the oxygen evolution reaction (OER) through water oxidation is critical for advancing photoelectrochemical water splitting. Among the catalysts, IrO2 exhibits a high OER catalytic activity and stability under acidic conditions. The OER mechanism in this system has been a topic of intense research; however, many mechanistic understandings are lacking. In this work, we carried out first-principles calculations with an implicit solvation model at a constant potential to study the OER behavior on the IrO2(110) surface. We find that the surface hydrogen coverage has a significant effect on OER kinetics and transition states. We then develop a microkinetics model that accounts for the continuous evolution of both OER activation energy and hydrogen coverage as a function of an applied potential. We show that this inclusion leads to significant improvement in the simulated Tafel plot compared to available experiments. Our results point to a complex interplay between surface chemistry and the applied potential on OER kinetics.

Automated summary

This study investigates the OER behavior and mechanism on the IrO2(110) surface using first-principles calculations and a microkinetics model. The research finds that the surface hydrogen coverage has a significant effect on OER kinetics and transition states. A continuous evolution model related to the applied potential is developed, leading to significant improvement in the simulated Tafel plot compared to available experiments.