Enhanced photocatalytic hydrogen evolution of CdS@CuS core-shell nanorods under visible light

被引:9
|
作者
Liang, Hui [1 ,2 ]
Mei, Junwei [1 ]
Sun, Han [2 ]
Cao, Lixin [1 ]
机构
[1] Ocean Univ China, Sch Mat Sci & Engn, 238 Songling Rd, Qingdao 266100, Shandong, Peoples R China
[2] Yancheng Inst Technol, Sch Chem & Chem Engn, 1,Middle Hope Ave, Yancheng City, Jiangsu Provinc, Peoples R China
基金
中国国家自然科学基金;
关键词
CdS@CuS Core-shell; Nanorods; Hydrogen evolution; REDUCED GRAPHENE OXIDE; NASCENT FORMED OXYGEN; STABLE PHOTOCATALYST; ELECTRON MEDIATOR; WATER; EFFICIENT; SYSTEM; METAL; H-2; SEMICONDUCTORS;
D O I
10.1016/j.mssp.2022.107105
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Desigin of earth-abundant highly efficient photocatalysts with unique nanostrcuture has become of great importance for solar energy conversion. Herein, novel CdS@CuS core-shell nanorods with ultrathin CuS shell and intimately contacted interfaces via cation exchange method were constructed for efficient hydrogen evolution under visible light. CdS@CuS core-shell nanorods could establish the Z-Scheme which promote the efficiency of charge separation. Moreover, the intimately contacted interfaces between the CdS core and CuS shell boost photocatalytic hydrogen evolution reaction more efficiently. In consequence, the obtained CdS@CuS core-shell photocatalysts exhibited remarkable photocatalytic activity (13.45 mmol/g/h), which was 8.3 times higher than that of pristine CdS. This work not only demonstrates the synthesis of a novel core-shell structured photocatalyst with high hydrogen evolution rate, but also provides a modal system for further improvement in photocatalyst design for hydrogen production.
引用
收藏
页数:7
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