A BiVO4Photoanode with a VOxLayer Bearing Oxygen Vacancies Offers Improved Charge Transfer and Oxygen Evolution Kinetics in Photoelectrochemical Water Splitting

Author:

Liu Boyan1,Wang Xin1,Zhang Yingjuan1,Xu Liangcheng1,Wang Tingsheng1,Xiao Xiong1,Wang Songcan1,Wang Lianzhou2ORCID,Huang Wei1

Affiliation:

1. Frontiers Science Center for Flexible Electronics Xi'an Institute of Flexible Electronics (IFE) Xi'an Institute of Biomedical Materials & Engineering Northwestern Polytechnical University 127 West Youyi Road Xi'an 710072 China

2. Nanomaterials Centre School of Chemical Engineering and Australian Institute for Bioengineering and Nanotechnology The University of Queensland Brisbane QLD 4072 Australia

Abstract

AbstractSluggish oxygen evolution kinetics are one of the key limitations of bismuth vanadate (BiVO4) photoanodes for efficient photoelectrochemical (PEC) water splitting. To address this issue, we report a vanadium oxide (VOx) with enriched oxygen vacancies conformally grown on BiVO4photoanodes by a simple photo‐assisted electrodeposition process. The optimized BiVO4/VOxphotoanode exhibits a photocurrent density of 6.29 mA cm−2at 1.23 V versus the reversible hydrogen electrode under AM 1.5 G illumination, which is ca. 385 % as high as that of its pristine counterpart. A high charge‐transfer efficiency of 96 % is achieved and stable PEC water splitting is realized, with a photocurrent retention rate of 88.3 % upon 40 h of testing. The excellent PEC performance is attributed to the presence of oxygen vacancies in VOxthat forms undercoordinated sites, which strengthen the adsorption of water molecules onto the active sites and promote charge transfer during the oxygen evolution reaction. This work demonstrates the potential of vanadium‐based catalysts for PEC water oxidation.

Funder

National Natural Science Foundation of China

Australian Research Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

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