异质结
非阻塞I/O
光催化
材料科学
光致发光
紫外线
光化学
光电子学
化学工程
化学
催化作用
生物化学
工程类
作者
Wentao Xiang,Zhenzhen Yu,Rui Gao,Zhengyi Yi,Kun Gong,Kang‐Qiang Lu,Weiya Huang,Changlin Yu,Zeshu Zhang,Man Zhou,Kai Yang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2025-04-17
卷期号:30 (8): 1804-1804
被引量:1
标识
DOI:10.3390/molecules30081804
摘要
Rapid charge separation and transfer is the key scientific problem in photocatalysis. The construction of S-scheme heterojunction is one of the effective strategies to promote charge separation and maintain the strong redox properties. Herein, the NiO, K0.2WO3, and NiWO4 ternary double S-scheme K0.2WO3/NiO/NiWO4 heterojunction (W/NiO) was created by a one-step molten salt method. Ultraviolet-visible (UV-Vis) diffuse reflectance spectra, photoluminescence (PL) spectra, photoelectrochemistry tests, and other analyses revealed that the double S-scheme heterostructure broadened the spectral response range of NiO and promoted its separation of photocarriers. Compared with pristine NiO, the modified double S-scheme heterojunction enhanced the surface adsorption of water molecules and the accumulation of intermediate product of HCOO−, and optimized the CO2 reduction system, realizing the improved CO yield of 373 μmol·g−1·h−1 in Ru(byp)32+/ethanolamine of CO2 reduction system. This study indicates that double S-scheme heterojunction could facilitate efficient photogenerated charge transfer and separation, thereby achieving high activity and selectivity for CO2 photoreduction. Our work provides a reference for the one-step construction of double S-scheme heterojunction.
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