Construction of Cu7.2S4/g-C3N4 photocatalyst for efficient NIR photocatalysis of H2 production

被引:21
|
作者
Yu, Rui [1 ]
Luo, Bifu [3 ]
Chen, Min [1 ]
Xu, Dongbo [1 ]
Wu, Xiaojie [1 ]
Li, Di [2 ]
Huang, Yuanyong [1 ]
Xie, Zhongkai [1 ]
Shen, Nanjun [1 ]
Meng, Suci [1 ]
Shi, Weidong [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Inst Energy Res, Zhenjiang 212013, Peoples R China
[3] Guizhou Normal Univ, Sch Chem & Mat Sci, Key Lab Funct Mat Chem Guizhou Prov, Guiyang 550001, Peoples R China
基金
中国国家自然科学基金;
关键词
Near-infrared light responsive; Cu7; Hydrogen production; HYDROGEN-PRODUCTION; G-C3N4; WATER; NANOSHEETS; CO2; NANOPARTICLES; EVOLUTION;
D O I
10.1016/j.ijhydene.2023.03.167
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
Graphite-like carbon nitride (g-C3N4) has been regarded as a promising photocatalyst for solar-to-chemical conversion. Nevertheless, the narrow absorption of light extremely limited its photocatalytic performance under near-infrared (NIR) irradiation. Herein, the Cu7.2S4 with outstanding NIR absorption was successfully introduced to g-C3N4 nanosheets through a simple in-situ growth procedure. As expected, the constructed Cu7.2S4/g-C3N4 (CSCN) photocatalysts exhibit superior H2 production activity of 82 mmol g-1 h-1 under NIR light irradiation (l > 800 nm), which outperforms currently reported g-C3N4-based NIR-driven H2 production systems. Especially, the optimal sample CSCN-5 displays a robust activity of 66 mmol g-1 h-1 at l = 850 nm monochromatic light irradiation. The excellent photocatalytic performance is linked to the extended optical absorption as well as the efficient separation efficiency of photoinduced carriers, which are evidenced by the UV -visible absorption spectroscopy and photoelectrochemical test. This work provides an effective approach for constructing a Cu7.2S4/g-C3N4 photocatalytic system for the trans-formation of NIR solar energy into hydrogen.& COPY; 2023 Published by Elsevier Ltd on behalf of Hydrogen Energy Publications LLC.
引用
收藏
页码:24285 / 24294
页数:10
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