Efficient photoelectrocatalytic performances using a WO3/BiVO4 heterojunction photoanode: applied bias-promoted photoinduced charge transfer and separation

Abstract

Combining tungsten trioxide (WO3) with bismuth vanadate (BiVO4) to form a heterojunction photoanode offers a promising solution to achieving highly efficient photoelectrocatalytic (PEC) performances. In this work, we successfully fabricated the WO3/BiVO4 heterojunction on tungsten (W) foil via a hydrothermal route, followed by a successive ionic layer adsorption and reaction (SILAR) process. The PEC performances for synergetic H2 evolution and organic pollutant degradation were significantly enhanced after the BiVO4 nanoparticles were loaded on the WO3 photoanode. The PEC performance with the WO3/BiVO4 heterojunction as the photoanode was demonstrated to be much more dependent on the applied bias potential (Vab) than that with pristine WO3 as the photoanode. Based on the various photoelectrochemical features and fundamental theory of semiconductor heterojunctions, it was well elucidated that, under the applied bias potential, the gradual diminishment and eventual reversal of the energy band bending at the heterojunction interface could achieve the efficient transfer and separation of more photogenerated charges, thereby enhancing overall PEC performances. This work highlights the roles of the evolution of the band bending in the WO3/BiVO4 heterojunction interface by applied bias in promoting the efficient transfer and separation of photogenerated charges.

Graphical abstract: Efficient photoelectrocatalytic performances using a WO3/BiVO4 heterojunction photoanode: applied bias-promoted photoinduced charge transfer and separation

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Article information

Article type
Paper
Submitted
15 May 2025
Accepted
02 Jul 2025
First published
03 Jul 2025

Phys. Chem. Chem. Phys., 2025, Advance Article

Efficient photoelectrocatalytic performances using a WO3/BiVO4 heterojunction photoanode: applied bias-promoted photoinduced charge transfer and separation

Y. Liu, Y. Kang, Z. Zhang and J. Lin, Phys. Chem. Chem. Phys., 2025, Advance Article , DOI: 10.1039/D5CP01826A

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