Construction of ZnIn2S4/CdS/PdS S-Scheme Heterostructure for Efficient Photocatalytic H2 Production

被引:59
|
作者
Sun, Guotai [1 ]
Tai, Zige [1 ]
Li, Fan [1 ]
Ye, Qian [1 ]
Wang, Ting [1 ]
Fang, Zhiyu [1 ]
Jia, Lichao [2 ]
Liu, Wei [3 ]
Wang, Hongqiang [1 ]
机构
[1] Northwestern Polytech Univ, Ctr Nano Energy Mat, Sch Mat Sci & Engn, State Key Lab Solidificat Proc, Xian 710072, Peoples R China
[2] Shaanxi Normal Univ, Sch Mat Sci & Engn, Xian 710119, Peoples R China
[3] Nanjing Univ Sci & Technol, Nano & Heterogeneous Mat Ctr, Sch Mat Sci & Engn, Nanjing 210094, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
co-catalysts; hydrogen generation; photocatalysis; S-scheme mechanisms; water splitting; HYDROGEN-PRODUCTION; CHARGE SEPARATION; CDS NANOWIRES; ZNIN2S4; FABRICATION; HETEROJUNCTION; SEMICONDUCTOR; PERFORMANCE; EVOLUTION; MOS2;
D O I
10.1002/smll.202207758
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is facing a tremendous challenge to develop the desirable hybrids for photocatalytic H-2 generation by integrating the advantages of a single semiconductor. Herein, an all-sulfide ZnIn2S4/CdS/PdS heterojunction is constructed for the first time, where CdS and PdS nanoparticles anchor in the spaces of ZnIn2S4 micro-flowers due to the confinement effects. The morphology engineering can guarantee rapid charge transfer owing to the short carrier migration distances and the luxuriant reactive sites provided by ZnIn2S4. The S-scheme mechanism between ZnIn2S4 and CdS assisted by PdS cocatalyst is testified by in situ irradiated X-ray photoelectron spectroscopy and electron paramagnetic resonance (EPR), where the electrons and holes move in reverse driven by work function difference and built-in electric field at the interfaces. The optimal ZnIn2S4/CdS/PdS performs a glaring photocatalytic activity of 191.9 mu mol h(-1) (10 mg of catalyst), and the largest AQE (apparent quantum efficiency) can reach a high value of 26.26%. This work may afford progressive tactics to design multifunctional photocatalysts.
引用
收藏
页数:10
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