Chinese Journal of Catalysis ›› 2026, Vol. 87: 185-196.DOI: 10.1016/S1872-2067(26)65073-5

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The organic-inorganic S-scheme heterojunction with enhanced charge separation simultaneously catalyze the production of hydrogen and imine

Hao Wua,b, Xinyu Zenga,b, Wang Wanga,b,*(), Bei Chenga,b, Jingzhao Chenga,b, Jingsan Xuc,*(), Shaowen Caoa,b,*()   

  1. a State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, Hubei, China
    b Hubei Technology Innovation Center for Advanced Composites, Wuhan University of Technology, Wuhan 430070, Hubei, China
    c School of Chemistry and Physics, Queensland University of Technology, Brisbane QLD 4001, Australia
  • Received:2025-11-26 Accepted:2025-12-26 Online:2026-08-18 Published:2026-06-24
  • Supported by:
    Scientific Research Innovation Capability Support Project for Young Faculty(ZYGXQNJSKYCXNLZCXM-M21);National Natural Science Foundation of China(52472245);National Natural Science Foundation of China(22278324);National Natural Science Foundation of China(22578040);National Natural Science Foundation of China(22102121);Natural Science Foundation of Hubei Province(2025AFA013);Natural Science Foundation of Hubei Province(2025AFB482)

Abstract:

Photocatalytic hydrogen production coupled with value-added chemical synthesis has attracted extensive research interests as a promising route to realize efficient conversion of solar energy to chemical energy. However, the rapid charge recombination hinders the improvement of conversion efficiency. Herein, a pyrene-based conjugated polymer (PyDF)/Mn0.2Cd0.8S (MCS) organic-inorganic S-scheme heterojunction photocatalyst (PMCS) was reported. The incorporation of large delocalized π-conjugation system and formation of the S-scheme heterojunction significantly enhanced the charge separation and transfer. As a result, the optimal PMCS0.5 composite exhibited a hydrogen evolution rate of 16.3 mmol h-1 g-1 with ascorbic acid as sacrificial agent. In the coupled system for benzylamine (BA) oxidation and hydrogen production, it delivered a hydrogen evolution rate of 3.72 mmol h-1 g-1, with nearly 100% conversion of 358.8 μmol BA to N-benzylidene benzylamine (NBBA) within 4 h. To elucidate the charge transfer mechanism within the S-scheme heterojunction, density functional theory calculations, in-situ X-ray photoelectron spectroscopy, and in-situ irradiated Kelvin probe force microscopy were conducted. In addition, in-situ diffuse reflectance infrared Fourier transform spectroscopy was employed to monitor the stepwise transformation of amines to imines during the photocatalytic process. This work offers a promising approach for bifunctional photocatalyst design toward simultaneous energy conversion and green synthesis.

Key words: S-scheme heterojunction, Hydrogen evolution, Imine synthesis, Bifunctional photocatalytic system, In-situ spectroscopy