Hollow Nanobox-Shaped Cu2-xS@ZnxCd1-xS Heterojunction by Light Multireflection with Z-Scheme Mechanism for Enhanced Photocatalytic Hydrogen Production

被引:0
|
作者
Wang, Lihui [1 ]
Xiao, Han [1 ]
Yang, Lei [1 ]
Li, Jiaxing [1 ]
Zi, Jiangzhi [1 ]
Lian, Zichao [1 ]
机构
[1] School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai,200093, China
基金
中国国家自然科学基金;
关键词
Cadmium alloys - Electron resonance - Negative ions - Paramagnetic resonance - Photocatalytic activity - Positive ions - Redox reactions - Zinc alloys;
D O I
10.1002/adfm.202416358
中图分类号
学科分类号
摘要
Achieving efficient spatial photoinduced charge separation and light utilization for improving the high photocatalytic activity is still a major obstacle. Here, a Cu2-xS@ZnxCd1-xS (Cu2-xS@ZnCdS) heterojunction is reported featuring a distinctive core–shell hollow nanobox structure. The Cu2-xS@ZnxCd1-xS exhibits high photocatalytic activity in hydrogen evolution reaction (HER) at the rate of 8175 µmol∙g−1∙h−1 under visible light irradiation, outperforming pristine ZnCdS nanoparticles and Cu2-xS hollow nanoboxes. The remarkable activity and outstanding stability of Cu2-x@ZnCdS are attributed to the development of robust interfacial electric fields, and improved light multireflection absorption efficiency as well as the Z-scheme mechanism. The electron paramagnetic resonance (EPR) and in situ X-ray photoelectron spectroscopy (XPS) measurements gave the direct evidence of the formation of the Z-scheme, which maintained the high redox potentials of each ZnCdS and Cu2-xS. This study gives the guideline for the design of heterojunction with the Z-scheme mechanism, leading to the high photocatalytic performance and remarkable stability. © 2024 Wiley-VCH GmbH.
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