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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
来源:
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.
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页数:10
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