Issue 2, 2018

Fabrication of the ternary heterojunction Cd0.5Zn0.5S@UIO-66@g-C3N4 for enhanced visible-light photocatalytic hydrogen evolution and degradation of organic pollutants

Abstract

A novel ternary heterojunction Cd0.5Zn0.5S@UIO-66@g-C3N4 (Cd0.5Zn0.5S@UCN) has been prepared by the in situ hydrothermal and precipitation approach, which exhibits superior photocatalytic activity for H2 generation and MO degradation under visible-light irradiation. The Cd0.5Zn0.5S@UCN30 composite shows the maximum photocatalytic H2 production rate (1281.1 μmol h−1 g−1) that is about 32.9 and 2.7 times higher than UIO-66@g-C3N4 and pristine Cd0.5Zn0.5S, respectively. Besides, the Cd0.5Zn0.5S@UCN30 heterojunction indicates the superior degradation efficiency of MO (82%) in 120 min. The improved photocatalytic activity of the Cd0.5Zn0.5S@UCN heterostructure can be assigned to its large surface area, enhanced visible-light absorption ability and high-efficiency separation of photogenerated electron–hole pairs, which are proved by the results of photocurrent and EIS analyses. Moreover, the photocatalytic mechanism based on the ternary heterojunction Cd0.5Zn0.5S@UCN is discussed and the transfer and separation process of photogenerated electron–hole pairs is also proposed. This work demonstrates that a novel ternary noble-metal-free photocatalytic system could provide a scientific basis for the application in the field of energy production and pollution removal.

Graphical abstract: Fabrication of the ternary heterojunction Cd0.5Zn0.5S@UIO-66@g-C3N4 for enhanced visible-light photocatalytic hydrogen evolution and degradation of organic pollutants

Supplementary files

Article information

Article type
Research Article
Submitted
16 Oct 2017
Accepted
21 Nov 2017
First published
27 Nov 2017

Inorg. Chem. Front., 2018,5, 335-343

Fabrication of the ternary heterojunction Cd0.5Zn0.5S@UIO-66@g-C3N4 for enhanced visible-light photocatalytic hydrogen evolution and degradation of organic pollutants

Q. Liang, J. Jin, C. Liu, S. Xu, C. Yao and Z. Li, Inorg. Chem. Front., 2018, 5, 335 DOI: 10.1039/C7QI00638A

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