In situ study of CdS/WO 3 and CdS/SnO 2 heterostructures: comparison of photocatalytic activity behavior

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/WO 3 ( n ), and CdS/SnO 2 ( n ) ratios in h...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2025
Hauptverfasser: Yu, Hyejin, Hoang, Dung Thanh, Kim, Hyun Sung, Lee, Hangil
Format: Artikel
Sprache:eng
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Zusammenfassung: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/WO 3 ( n ), and CdS/SnO 2 ( n ) ratios in heterostructures ( n = WO 3 or SnO 2 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/WO 3 heterostructure system demonstrated photocatalytic properties consistent with a typical Type II mechanism. In particular, the photocatalytic properties of the CdS/WO 3 (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/SnO 2 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.
ISSN:2050-7488
2050-7496
DOI:10.1039/D4TA07048H