Mitigating Redox Mediator-Induced Surface Recombination for Efficient Photoelectrocatalytic Benzyl Alcohol Oxidation on Mo-Doped Bismuth Vanadate

Abstract

Synthetic photoelectrochemistry offers a sustainable route for selective organic transformations under visible light, yet carrier recombination losses at the electrode-electrolyte interfaces remain a critical bottleneck. Although redox mediators are often employed to improve selectivity and circumvent kinetic barriers, their interactions with the photoelectrodes are not well understood. Here we show that N-hydroxysuccinimide (NHS), a widely used hydrogen atom transfer (HAT) mediator, dynamically adsorbs onto oxygen vacancies on BiVO₄ photoanodes, forming extrinsic interfacial states that trap photogenerated holes. Time-resolved photoelectrochemical and voltametric analyses reveal a direct correlation between this interfacial recombination pathway, photocurrent declines, and diminished reaction yields. Incorporating Mo dopant in BiVO₄ increases the oxygen-vacancy formation energy, while electrolyte cation tuning modulates the electrochemical double-layer structure, jointly suppressing NHS chemisorption and mitigating surface recombination. During selective PEC oxidation of benzyl alcohol to benzaldehyde, optimized Mo-doped BiVO₄ photoanodes achieve a conversion rate of 19.1 ± 1.4 μmol cm^-2 h^-1 with >92% Faradaic efficiency, representing the highest performance reported for BiVO₄-based benzylic alcohol oxidation. These findings identify interfacial mediator adsorption as a previously overlooked recombination channel and establish rational interfacial design as a powerful strategy for broadly tunable, high-efficiency light-driven organic synthesis.