Acta Phys. -Chim. Sin. ›› 2025, Vol. 41 ›› Issue (11): 100136.doi: 10.1016/j.actphy.2025.100136

• ARTICLE • Previous Articles     Next Articles

Ultrafast electron transfer at the ZIS1−x/UCN S-scheme interface enables efficient H2O2 photosynthesis coupled with tetracycline degradation

Shumin Zhang1, Yaqi Wang1, Zelin Wang1, Libo Wang2, Changsheng An1,*(), Difa Xu*,1()   

  1. 1 Hunan Key Laboratory of Applied Environmental Photocatalysis, Changsha University, Changsha 410022, Hunan Province, China
    2 Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430078, Hubei Province, China
  • Received:2025-06-24 Revised:2025-07-20 Accepted:2025-07-23 Published:2025-09-29
  • Contact: Email: z20190628@ccsu.edu.cn. Tel: +86-18932463886 (Changsheng An)xudifa@sina.com. +86-13687382717 (Difa Xu)
  • Supported by:
    the Research Foundation Bureau of Hunan Province(24B0787); the National Natural Science Foundation of China(52204307); the National Natural Science Foundation of China(52202376)

Abstract:

Coupling H2O2 production with organic pollutant degradation can effectively overcome the sluggish kinetics of water oxidation while concurrently addressing environmental pollution challenges. In this work, an S-defect-rich ZnIn2S4/g-C3N4 (ZIS1−x/UCN) S-scheme heterojunction photocatalyst was constructed by in situ growing ZIS1−x nanosheets on porous ultrathin UCN. The designed ZIS1−x/UCN photocatalyst demonstrates enhanced visible light absorption, abundant active sites, and intimate interfacial contact. The optimized ZIS1−x/UCN-1.0 photocatalyst exhibits outstanding dual functionality, simultaneously achieving an H2O2 production rate of 2902.2 µmol·g−1·h−1 and 91.3% tetracycline (50 mg·L−1) degradation efficiency. This H2O2 performance represents a 1.63-fold enhancement compared to its activity in pure water (1777.0 µmol·g−1·h−1). Through comprehensive characterization including femtosecond transient absorption spectroscopy (fs-TAS), in situ irradiation X-ray photoelectron spectroscopy (ISI-XPS), and in situ X-ray absorption fine structure spectroscopy (XAFS), we unequivocally confirm the S-scheme charge transfer mechanism. This S-scheme induced unique electronic structure not only fosters ultrafast electron transfer at the interface (3.54 ps) but also significantly enhances the redox capacity of photogenerated carriers. Collectively, this work opens new avenues for the dual application of photocatalytic technology in both energy production and environmental remediation.

Key words: S-scheme heterojunction, H2O2 photosynthesis, Tetracycline degradation, fs-TA spectroscopy