Published January 2019 | Version v1
Journal article

A facile two-step method to synthesize immobilized CdS/BiOCl film photocatalysts with enhanced photocatalytic activities

  • 1. Department of Chemistry, Jinan University, Guangzhou 510632, PR (China)
  • 2. Analytical & Testing Center, Jinan University, Guangzhou 510632, PR (China)
  • 3. Department of Ecology, Jinan University, Guangzhou 510632, PR (China)

Description

Immobilized CdS/BiOCl film photocatalysts were successfully synthesized by a facile two-step hydrothermal-hydrolysis method. The structures, morphologies, photocatalytic properties and reusabilities of the samples were studied. The photocatalytic activities of CdS/BiOCl were significantly improved compared with pure BiOCl. The photocatalytic activity of 6% CdS/BiOCl was the highest and 10 times higher than pure BiOCl, which was attributed to the enhanced visible light absorption and the higher separation of photogenerated carriers. Besides, 6% CdS/BiOCl also showed good recycling performance. A new photocatalytic mechanism, totally different from other mechanisms of BiOCl-based heterostructures, was revealed. It was part of electrons on the conducting band of CdS rather than the transferred electrons on the conducting band of BiOCl that oxidized O2 into O2, and O2 together with h+ on the valence band of CdS degraded organic pollutants. BiOCl did not generate electrons and holes, but only served as the electron transferer as electrons on the conducting band of CdS transferred to the conducting band of BiOCl, facilitating the separation of hole-electron pairs. This work provided a good reference for design and synthesis of film photocatalysts and new insights into photocatalytic mechanisms for heterostructures.

Additional details

Identifiers

DOI
10.1016/j.jallcom.2018.08.317;
PII
S0925838818332122;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
771
Journal Page Range
p. 309-316
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2018 Elsevier B.V. All rights reserved.