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

被引:0
|
作者
Yu, Hyejin [1 ]
Hoang, Dung Thanh [2 ]
Kim, Hyun Sung [1 ]
Lee, Hangil [2 ]
机构
[1] Pukyong Natl Univ, Dept Chem, BB21 Plus Program, Busan 48513, South Korea
[2] Sookmyung Womens Univ, Dept Chem, Seoul 04310, South Korea
基金
新加坡国家研究基金会;
关键词
CDS; REDUCTION; PERFORMANCE; NANOSHEETS; MECHANISM; NANORODS;
D O I
10.1039/d4ta07048h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:6049 / 6058
页数:10
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