Water Oxidation and Degradation Mechanisms of BiVO₄ Photoanodes in Bicarbonate Electrolytes

The photoelectrochemical hydrogen peroxide evolution reaction (HPER) has attracted increasing attention as an environmentally friendly approach to generate a commercially and industrially valuable water oxidation product. BiVO₄ photoanodes operated in bicarbonate-containing electrolytes have been shown to offer remarkable performance characteristics for HPER, with HCO₃ ^- serving as a reaction mediator. However, the factors affecting the stability of both the semiconductor photoanode and the aqueous electrolyte remain poorly understood. Here, we investigated BiVO₄ photoanodes to quantitatively assess the roles of electrolyte composition, bias potential, and illumination on competitive reaction pathways associated with HPER, oxygen evolution reaction, and photocorrosion. Our results confirm that HCO₃ ^- serves as a highly efficient mediator, leading to rapid hole extraction and near complete suppression of interfacial recombination on BiVO₄. In addition, these favorable hole transfer kinetics significantly decrease the rate of photocorrosion, leading to dramatically enhanced stability compared to bicarbonate-free electrolytes. While the elevated pH of unbuffered bicarbonate electrolyte leads to gradual chemical attack of BiVO₄, the stability is greatly enhanced in near-neutral buffered bicarbonate electrolytes. Finally, we confirm that HCO₃ ^- is regenerated during the photoanodic reaction, though pH swings during operation in an unbuffered electrolyte can lead to electrolyte instabilities. Overall, we find that BiVO₄ photoanodes operating in buffered bicarbonate-containing solutions exhibit significantly enhanced stability and can efficiently drive water oxidation reactions, including HPER, thus providing a route to robust production of high value oxidation products.