Borate and iron hydroxide co-modified BiVO4 photoanodes for high-performance photoelectrochemical water oxidation

BiVO4 has attracted tremendous attention as a promising photoanode material for photoelectrochemical (PEC) water oxidation, but the serious surface charge recombination and the slow water oxidation kinetics restrict its progress. To settle this problem, a two-step simple solution impregnation method is developed for fabricating a high-performance photoanode by anchoring an ultrathin beta-FeOOH nanolayer with enriched active sites on borate-post-treated nanoporous BiVO4 (B-BiVO4). The resultant beta-FeOOH-B-BiVO4 photoanode shows an extremely high photocurrent density of 4.96 mA cm(-2) at 1.23 V vs. RHE (1 sun illumination), over 3-fold larger than that of pure BiVO4 (1.45 mA cm(-2)) and also superior to that of B-BiVO4 (3.80 mA cm(-2)). The half-cell solarto-hydrogen conversion efficiency and the surface charge transfer efficiency of beta-FeOOH-B-BiVO4 photoanode are determined as 1.94% (ca. 0.62 V vs. RHE) and 90.2% (1.23 V vs. RHE), respectively. These PEC property enhancement is systematially confirmed to be ascribed to restrain surface charge recombination of BiVO4, accelerated hole transfer from B-BiVO4 to the catalytic sites of beta-FeOOH, and abundant oxygen vacancies from ultrathin p-FeOOH nanolayers. Further, a sustainable photostability is gained for the beta-FeOOH-B-BiVO4 photoanode only by tuning electrolyte composition. This study offers a viable route to fabricate low-cost and highperformance catalysts for solar water splitting.

Automated summary

By anchoring an ultrathin β-FeOOH nanolayer on borate-post-treated nanoporous BiVO4, a high-performance photoanode was fabricated, showing significantly improved photocurrent density, solar-to-hydrogen conversion efficiency, and surface charge transfer efficiency.