Published May 2021 | Version v1
Journal article

Facile construction of novel Co3O4/Bi12O17Cl2 heterojunction composites with enhanced photocatalytic performance

  • 1. School of Petrochemical Engineering, Liaoning Shihua University, Fushun, 113001 (China)

Description

Highlights: • Co3O4/Bi12O17Cl2 photocatalyst have been prepared for the first time. • The improved photocatalytic performance was gained over Co3O4/Bi12O17Cl2 photocatalyst. • Co3O4/Bi12O17Cl2 photocatalyst might keep excellent sustained degraded ability. • A reasonable photocatalytic mechanism over Co3O4/Bi12O17Cl2 catalyst was revealed. A novel Co3O4/Bi12O17Cl2 heterojunction catalyst has been constructed for the first time via a sample hydrothermal course. The chemical, optical and physical properties of as-constructed materials were examined by XRD, XPS, TEM, and DRS methods. These results demonstrated that Co3O4 nanoparticles evenly dispersed on Bi12O17Cl2 flakes, forming heterojunction nanostructure. When Co3O4/Bi12O17Cl2 photocatalyst was used for degrading rhodamine b (RhB), the best Co3O4/Bi12O17Cl2 sample (0.122 min−1) exhibited 2.5 folds higher rate constant than bare Bi12O17Cl2 (0.048 min−1), which owed to the collaborative interactions of heterojunction between Co3O4 and Bi12O17Cl2, accelerating validly the separation of photo-generated carriers, boosting visible light absorbance. Simultaneously, various radical scavenger tests indicated that ·O2 and h+ were prime parts for heightening activity. Eventually, depending on the above experimental conclusions, a photocatalytic mechanism was presented for the Co3O4/Bi12O17Cl2 heterojunction.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2021.122066

Additional details

Identifiers

DOI
10.1016/j.jssc.2021.122066;
PII
S0022459621001110;

Publishing Information

Journal Title
Journal of Solid State Chemistry (Print)
Journal Volume
297
Journal Page Range
vp.
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2021 Elsevier Inc. All rights reserved.