Citation: Zheng Liu, Yuqing Bian, Graham Dawson, Jiawei Zhu, Kai Dai. Rational constructing of Zn0.5Cd0.5S-diethylenetriamine/g-C3N4 S-scheme heterojunction with enhanced photocatalytic H2O2 production[J]. Chinese Chemical Letters, ;2025, 36(9): 111272. doi: 10.1016/j.cclet.2025.111272 shu

Rational constructing of Zn0.5Cd0.5S-diethylenetriamine/g-C3N4 S-scheme heterojunction with enhanced photocatalytic H2O2 production

    * Corresponding authors.
    E-mail addresses: zjw1584038799@mail.ustc.edu.cn (J. Zhu), daikai940@chnu.edu.cn (K. Dai).
    1 These authors contributed equally to this work.
  • Received Date: 27 January 2025
    Revised Date: 25 April 2025
    Accepted Date: 27 April 2025
    Available Online: 28 April 2025

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  • Photocatalytic hydrogen peroxide (H2O2) production (PHP) offers significant advantages to traditional production methods, including solar energy utilization, mild reaction conditions, environmental friendliness, pollution-free processes, sustainability, and high selectivity. However, despite its potential as a green and sustainable technology, photocatalytic H2O2 production (PHP) is constrained by limited visible light absorption by photocatalysts and the rapid recombination of photogenerated charge carriers, which reduce yield and efficiency. In this study, we synthesized an organic amine constrained Zn0.5Cd0.5S-DETA/g-C3N4 (ZCS-D/CN) S-scheme heterojunction via a hydrothermal method to enhance PHP. Anchoring ZCS-D on the surface of CN and forming an S-scheme heterojunction effectively prevented ZCS-D agglomeration, modulated the band structure of CN, and enhanced the migration and redox capabilities of photogenerated charge carriers. The optimized heterojunction (ZCS-D/CN) achieved a H2O2 yield of 5124 µmol g-1 h-1 in pure H2O, significantly outperforming pure CN (24 µmol g-1 h-1) and ZCS-D (4012 µmol g-1 h-1). These results demonstrate that ZCS-D/CN S-scheme heterojunction holds substantial potential for photocatalytic applications, particularly in the efficient production of H2O2.
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