Metal-organic framework-derived ZnxCd1-xS/ZnxCd1-x-MOF heterostructures promoting charge separation for photocatalytic hydrogen evolution

被引:2
|
作者
Ma, Siqing [1 ]
Wang, Xin [1 ]
Wan, Kang [1 ]
Liu, Boyan [1 ]
Yang, Yilong [1 ,2 ,3 ]
Wang, Songcan [1 ]
机构
[1] Northwestern Polytech Univ, Xian Inst Flexible Elect IFE, Frontiers Sci Ctr Flexible Elect, 127 West Youyi Rd, Xian 710072, Peoples R China
[2] Henan Univ Urban Construct, Sch Mat & Chem Engn, Pingdingshan 467000, Peoples R China
[3] Henan Yicheng New Energy Co Ltd, Zhengzhou 450018, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalytic hydrogen evolution; Heterojunctions; Charge separation; Metal-organic frameworks; CADMIUM-SULFIDE; CARBON NITRIDE; HETEROJUNCTION;
D O I
10.1016/j.seppur.2024.129089
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Severe charge recombination is a bottleneck for efficient photocatalytic hydrogen production. Herein, ZnxCd1-xS/ZnxCd1-x-MOF heterostructures with enhanced photocatalytic hydrogen evolution activity are synthesized by a two-step solvothermal process based on a metalorganic framework (MOF) template method. By carefully tuning the composition and the reaction temperatures, the obtained Zn0.2Cd0.8S/Zn0.2Cd0.8-MOF heterojunction can continuously generate hydrogen for 25 h, with an optimized hydrogen production rate of 13.3 mmol g-1h-1. An impressive apparent quantum yield of 24.1 % at 420 nm monochromatic light is achieved. Zn0.2Cd0.8S nanoparticles are embedded in the Zn0.2Cd0.8-MOF skeleton during the solvothermal process, resulting in excellent distribution and interfacial contact in the obtained heterojunction. Such a heterostructure not only promotes charge separation, but also alleviates photocorrosion. The proof-of-concept demonstrated in this work provides an alternative way for the design of high-performance metal sulfide-based photocatalysts for efficient solar hydrogen production.
引用
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页数:10
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