Chemical reduction-induced surface oxygen vacancies of BiVO4 photoanodes with enhanced photoelectrochemical performance. Issue 8 (31st March 2021)

• Record Type: Journal Article
• Authors: Peng, Yong; Wu, Hao; Yuan, Mingjian; Li, Fang-Fang; Zou, Xingli; Ng, Yun Hau; Hsu, Hsien-Yi
• Is Part Of: Sustainable energy & fuels. Volume 5:Issue 8(2021)
• Page Start: 2284
• Page End: 2293
• Publication Date: 2021-03-31
• Subjects: Renewable energy sources -- Periodicals; Fuel cells -- Periodicals; Electric batteries -- Periodicals; Electrochemistry -- Periodicals; 660.297
• DOI: 10.1039/d0se01901a
• Languages: English
• ISSNs: 2398-4902

Abstract

Abstract : A facile chemical treatment employing a reducing agent sodium sulfite with a mild reduction activity is used to alter the surface states of BiVO4 photoanodes. The sulfite-treated BiVO4 (S-BiVO4 ) exhibits an enhanced photoelectrochemical performance. Abstract : Bismuth vanadate (BiVO4 ) is one of the highly promising photoanodes for photoelectrochemical (PEC) water splitting but suffers from severe carrier recombination and undesirable charge transfer at the semiconductor–electrolyte interface. Herein, we employ an effective surface-engineered sulfite treatment to improve the PEC performance of BiVO4 without illumination. This post-synthetic treatment on BiVO4 photoanodes can substantially enhance the interfacial charge transfer efficiency because of decreased charge carrier recombination arising from both surface oxygen vacancies (Ovac ) and surface disordered layers. The as-prepared BiVO4 exhibits a photocurrent density of 2.2 mA cm −2 at 1.23 V vs. the reversible hydrogen electrode (RHE) under 1-sun illumination, which is 1.7-times higher than that of pristine BiVO4 . By coating the amorphous FeOOH cocatalyst, the photocurrent density can be further improved to 2.8 mA cm −2 . We demonstrate that the chemical reaction employing a reducing agent with a mild reduction activity can controllably alter the surface states of BiVO4 photoanodes, providing a facile, efficient, and low-cost strategy to achieve high-performance photoelectrodes.