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3D/3D C-MoO2/Cd0.9Zn0.1S composite with an S-scheme electron transfer pathway enables highly efficient photocatalytic hydrogen evolution
a
School of Mechanical Engineering and Transportation, Changzhou Vocational
Institute of Industry Technology, Changzhou, 213164, P. R China
b
School of Materials Engineering, Jiangsu University of Technology, Changzhou,
213001, P. R China
c
School of Physics and Electronic Engineering, Jiangsu University, Zhenjiang,
212013, P. R. China
* Corresponding Author:
Chalcogenide Letters 2025, 22(8), 665-677. https://doi.org/10.15251/CL.2025.228.665
Received 18 April 2025; Accepted 01 August 2025;
Abstract
Constructing heterojunctions represents a crucial strategy for enhancing semiconductor photocatalysts. In this study, the C-MoO2/Cd0.9Zn0.1S S-scheme heterojunction composite was successfully fabricated through a self-assembly approach. XPS analysis confirmed the spontaneous transfer of intrinsic electrons from Cd0.9Zn0.1S to C-MoO2 in the dark, establishing an internal electric field at the C-MoO2/Cd0.9Zn0.1S interface. Under visible light irradiation, the C-MoO2/Cd0.9Zn0.1S composite exhibited significantly enhanced hydrogen evolution activity, achieving a 6.3-fold improvement compared to pristine Cd0.9Zn0.1S. PL, TRPL, and electrochemical measurements collectively demonstrated that the incorporation of C-MoO2 effectively suppressed the recombination of photogenerated electrons in Cd0.9Zn0.1S. The outstanding photocatalytic performance and improved charge carrier separation efficiency can be attributed to the S-scheme heterojunction configuration, which facilitates efficient electron transfer from Cd0.9Zn0.1S to C-MoO2. This work provides valuable experimental guidance for designing and constructing S-scheme heterojunction photocatalytic systems for solar hydrogen production.Keywords
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Copyright © 2025 The Author(s). Published by Tech Science Press.This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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