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Article Abstract

Excessive hole-accumulation-induced photocorrosion is considered a key factor that limits the activity of the photoelectrochemical water splitting reaction. In this study, a heterogeneous catalyst was prepared by a simple impregnation method, i.e., modification of different ratios of heterometallic oxyhydroxides (FeCoOOH) on in situ photoreduction-treated BiVO (Bi-BVO). This work demonstrates for the first time that adjusting the FeCo ratio can greatly enhance the separation, transport, and directional control of electron-hole pairs, thus inhibiting photocorrosion. The Bi-BVO/FeCoOOH composite exhibited a photocurrent density of 0.243 mA cm at 1.23 V (4.5 times that of pure BiVO under 1.5 G AM illumination) in a sacrificial agent-free NaSO electrolyte. After 20 h of continuous illumination, the photocurrent density of the optimized samples showed negligible attenuation (7.2%). The strong stability under light conditions can be attributed to Fe and Co acting as hole shuttling mediators, which efficiently match the hole generation rate of Bi-BVO and enhance hole transport to the surface active sites. Furthermore, formation of Co-O-V bonds and passivation of surface states, which immobilize V in the lattice, further inhibit photocorrosion. This bimetallic oxyhydroxide modification strategy provides valuable insights into mitigating photocorrosion and offers an optimization approach for photoelectrochemical water splitting.

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http://dx.doi.org/10.1021/acsami.5c05130DOI Listing

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