Insights into the mechanism of the enhanced visible-light photocatalytic activity of black phosphorus/BiVO4 heterostructure: a first-principles study. Issue 39 (28th September 2018)

• Record Type: Journal Article
• Authors: Chen, Yuxuan; Shi, Tingting; Liu, Pengyi; Ma, Xinguo; Shui, Lingling; Shang, Chaoqun; Chen, Zhihong; Wang, Xin; Kempa, Krzysztof; Zhou, Guofu
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 39(2018)
• Page Start: 19167
• Page End: 19175
• Publication Date: 2018-09-28
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8ta07321j
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Photocatalytic water splitting was observed on black phosphorus/BiVO4 heterostructure under visible light irradiation. Abstract : Bismuth vanadate (BiVO4 )-based photocatalysts as a typical solar-water-splitting material have attracted much interest due to their moderate band gap, fine hole conductivity and good stability. In this work, we perform a comprehensive first-principles study of the structural, electronic and optical properties of a black phosphorus BP/BiVO4 heterostructure, which was realized with remarkable performance in pure water splitting in a very recent experiment. Firstly, the optoelectronic properties and charge transport between BP and BiVO4 are systematically elucidated. We find that the positions of the valence/conduction band edge of BP and BiVO4 change with the Fermi level and form a type-II heterostructure with a high optical absorption coefficient. Furthermore, the charge density difference and Bader charge analysis indicated that the internal electric field will facilitate the separation of e − /h + pairs at the BP/BiVO4 interface and restrain the carrier recombination. Therefore, the present work provides insightful understanding of the physical mechanism and superior photocatalytic performance of this new synthesized system and offers instructions for fabricating superior BiVO4 -based heterostructure photocatalysts.