First-principles study of crystalline CoWO4 as oxygen evolution reaction catalyst

Abstract

Cobalt tungstate (CoWO₄) was recently reported as a catalyst that drives the oxygen evolution reaction. Interestingly, the catalytic activity of crystalline CoWO₄ is orders of magnitude lower than its amorphous counterpart. In order to better understand the mechanical origin of these observations, herein we study the oxygen evolution on the crystalline CoWO₄ surface using first-principles calculations. By comparing the calculated data with experimental measurements, we demonstrate that GGA + U calculations with U = 4.5 effectively predict the structural and electronic properties of crystalline CoWO₄. With this U value the overpotential for oxygen evolution on the crystalline CoWO₄ surface is 0.97 V. This prediction agrees fairly well with experimental estimation, and is consistent with the low catalytic activity of crystalline CoWO₄. By a comprehensive analysis of the reaction process, such high overpotential is attributed to the instability of oxygen radicals formed during the oxygen evolution. Our results highlight the importance to stabilize oxygen radicals during oxygen evolution reaction. It also paves the road for future optimization of CoWO₄ as oxygen evolution catalyst.