Low-Bias Solar Water Oxidation on Photoanodes Composed of Oxygen-Vacancy-Rich BiVO4 Nanopyramid Arrays Coated with Nanoscale Co–Fe-Layered Double Hydroxide Films

Despite the great potential of bismuth vanadate (BiVO4) photoanode in photoelectrochemical (PEC) water splitting applications, the pressing bottleneck of its sluggish surface reaction kinetics and significant charge losses remains to be resolved. Further optimizing the intrinsic charge transport for the enhancement of the solar-to-hydrogen conversion has emerged as a critical priority. Herein, a nanoscale cobalt–iron layered double hydroxide (CoFe-LDH) film was conformally encapsulated on oxygen-vacancy-rich BiVO4 (OV-BiVO4) nanopyramid arrays, forming a distinctive highly ordered OV-BiVO4/CoFe-LDH core–shell photoanode. Experimental and computational studies revealed that the successful introduction of oxygen vacancies on the BiVO4 lattice, via the electrochemical reduction process, remarkably increases the overall carrier density, electrical conductivity, and built-in photovoltage, devoted to the promotion of both bulk and surface charge separation. The synergistically integrated CoFe-LDH nanofilm as the cocatalyst and protective layer further strengthens interfacial hole extraction and surface wettability, thereby enhancing water oxidation kinetics and charge injection efficiency. As a result, the nanostructured OV-BiVO4/CoFe-LDH photoanode achieved a considerably improved photocurrent density of 2.33 mA/cm2 at 1.23 VRHE, the relatively lower onset potential of 0.21 VRHE, a higher photon-to-electron conversion efficiency of 53.7%, and better photocorrosion resistance. This work offers valuable insights into the impact of defect engineering on the PEC behavior and also demonstrates a feasible nanoscale collaborative strategy to optimize photoanodes, enabling efficient solar water oxidation.