Synergistic Effect of BiVO4/P-g-C3N4 Heterojunction with Enhanced Optoelectronic Properties on Synthetic Colorants under Visible Light

Author:

Chowdhury Anuradha1,Balu Sridharan12ORCID,Lan Kuo-Wei1ORCID,Wei-Chih Lee Louis3,Yang Thomas C.-K.12ORCID

Affiliation:

1. Department of Chemical Engineering and Biotechnology, National Taipei University of Technology, No. 1, Sec. 3, Zhongxiao East Road, Taipei 10608, Taiwan

2. Precision Analysis and Materials Research Center, National Taipei University of Technology, No. 1, Sec. 3, Zhongxiao East Road, Taipei 10608, Taiwan

3. Asia Electronic Material Co., Ltd., Taihe Village, Zhubei City, Hsinchu 30267, Taiwan

Abstract

Environmental remediation in the presence of robust semiconductor photocatalysts by utilizing renewable energy sources is of keen interest among researchers. In this study, we synthesize a BiVO4/P-g-C3N4 semiconductor heterojunction photocatalytic system through a hydrothermal route followed by utilizing a total-solvent evaporation method. The optical and electronic properties of the as-prepared heterojunction are characterized via various spectroscopic techniques. Rhodamine B (RhB) and Congo Red (CR) are used as synthetic colorants to evaluate the photocatalytic performances of BiVO4/P-g-C3N4. In addition, the chemical environment of the photocatalyst and its mechanistic pathways are confirmed through X-ray photoelectron spectroscopy and electrochemical Mott–Schottky analysis. The BiVO4/P-g-C3N4 photocatalyst shows higher photodegradation (96.94%) of the mixed synthetic dyes under simulated solar-light irradiation. The as-synthesized BiVO4/P-g-C3N4 heterojunction significantly promotes the quick separation of photoexcited carriers due to the excellent synergetic properties, the extended light absorption, and the photoelectrochemical response. Furthermore, a possible type-II charge transfer mechanism is adopted for the BiVO4/P-g-C3N4 system after investigating the band potentials, active species, and charge carrier migration over the heterojunction interface.

Funder

National Science and Technology Council, Taiwan

Asia Electronic Material Co., Ltd.

Publisher

MDPI AG

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