Issue 8, 2025

In situ study of CdS/WO3 and CdS/SnO2 heterostructures: comparison of photocatalytic activity behavior

Abstract

Despite extensive research on photocatalysts, there remains a significant gap in understanding the comparative photocatalytic behaviors of CdS-based heterostructures under visible light irradiation. This study presents the synthesis of CdS with varying CdS/WO3(n), and CdS/SnO2(n) ratios in heterostructures (n = WO3 or SnO2 wt%). The photocatalytic conversion efficiency of a biomass molecule under visible light and the production efficiency of the desired target products were evaluated using these heterostructures under optimized conditions. In addition, an in-depth study of photocatalytic activity in the visible-light region was conducted using in situ X-ray photoelectron spectroscopy. The CdS/WO3 heterostructure system demonstrated photocatalytic properties consistent with a typical Type II mechanism. In particular, the photocatalytic properties of the CdS/WO3(50) heterostructure system exhibited 31% increase in efficiency at the interface, compared to conventional CdS, when evaluating the 2,5-hydroxymethylfurfural oxidation reaction. However, the photocatalytic properties of the CdS/SnO2 heterostructures displayed a gradually decreasing trend with increasing relative amount of CdS, resulting in a clear difference between the two systems. These results indicate that the identification of the optimized conditions for CdS-based heterostructures contributes to the advancement of photocatalytic science and opens new avenues for the development of efficient and sustainable technologies for chemical synthesis and environmental remediation.

Graphical abstract: In situ study of CdS/WO3 and CdS/SnO2 heterostructures: comparison of photocatalytic activity behavior

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Article information

Article type
Paper
Submitted
02 Oct 2024
Accepted
21 Jan 2025
First published
22 Jan 2025

J. Mater. Chem. A, 2025,13, 6049-6058

In situ study of CdS/WO3 and CdS/SnO2 heterostructures: comparison of photocatalytic activity behavior

H. Yu, D. T. Hoang, H. S. Kim and H. Lee, J. Mater. Chem. A, 2025, 13, 6049 DOI: 10.1039/D4TA07048H

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