Acta Phys. -Chim. Sin. ›› 2025, Vol. 41 ›› Issue (11): 100142.doi: 10.1016/j.actphy.2025.100142

• ARTICLE • Previous Articles     Next Articles

Enhancing photocatalytic H2O2 production via dual optimization of charge separation and O2 adsorption in Au-decorated S-vacancy-rich CdIn2S4

Yanyan Zhao1,*(), Zhen Wu1, Yong Zhang2, Bicheng Zhu3, Jianjun Zhang3,*()   

  1. 1 College of Biology Pharmacy and Food Engineering, Shangluo University, Shangluo 726000, Shaanxi Province, China
    2 School of Advanced Materials and Green Chemical Engineering, Hubei Polytechnic University, Huangshi 435003, Hubei Province, China
    3 Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430078, Hubei Province, China
  • Received:2025-06-30 Revised:2025-07-28 Accepted:2025-07-29 Published:2025-09-29
  • Contact: Email: zhaoyanyan41@163.com (Yanyan Zhao)zhangjianjun@cug.edu.cn (Jianjun Zhang)
  • Supported by:
    National Natural Science Foundation of China(22409128); National Natural Science Foundation of China(22378103)

Abstract:

Photocatalytic oxygen reduction reaction (ORR) offers a mild and cost-effective approach for hydrogen peroxide (H2O2) production. However, its practical application is significantly hindered by rapid charge carrier recombination and insufficient O2 adsorption capacity in photocatalysts. To address these limitations, we developed a strategy involving the creation of S-vacancy-rich CdIn2S4 (Sv–CIS) to facilitate charge separation and subsequent deposition of Au nanoparticles on its surface (Au–Sv–CIS) to strengthen O2 adsorption. The results suggest that the optimized Au–Sv–CIS achieves a significantly increased H2O2 production yield of 2542 μmol·h−1·g−1 in 10%-ethanol/water solution, which is about 12.8 and 1.7 times higher than that of pure CIS and Sv–CIS. Comprehensive characterizations including photoluminescence spectra, time-resolved photoluminescence spectra, transient photocurrent response, electrochemical impedance spectra, and femtosecond transient absorption spectroscopy confirm the improved charge dynamics of Au–Sv–CIS. In addition, temperature-programmed desorption of O2 combined with density functional theory calculations conclusively demonstrates the superior O2 adsorption capacity of Au–Sv–CIS. This work provides a design strategy for efficient solar-to-chemical energy conversion through cooperative photocatalyst engineering.

Key words: S vacancy, Charge separation, O2 adsorption, CdIn2S4, Hydrogen peroxide