Chinese Journal of Catalysis ›› 2026, Vol. 80: 189-199.DOI: 10.1016/S1872-2067(25)64854-6

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Tuning radical generation rate for efficient CH4 photooxidation to CH3OH over AgPd alloy and Co3O4 cascade active sites

Shuqi Lianga,1, Zhen Xiaoa,1, Jinni Shena, Wenxin Daia,b, Zizhong Zhanga,*()   

  1. aState Key Laboratory of Chemistry for NBC Hazards Protection, Fuzhou University, Fuzhou 350116, Fujian, China
    bQingyuan Innovation Laboratory, Quanzhou 362801, Fujian, China
  • Received:2025-07-12 Accepted:2025-09-05 Online:2026-01-18 Published:2026-01-05
  • Contact: Zizhong Zhang
  • About author:First author contact:1These authors contributed equally.

Abstract:

The direct conversion of methane into methanol under mild conditions represents a highly appealing pathway. Regulating the generation of hydroxyl radicals (•OH) is a representative method, but excessive release of •OH will inevitably lead to the over-oxidation of CH3OH. Here, we design AgPd alloy and Co3O4 cascade active sites on the TiO2 surface (AgPd-Co/TiO2) to control the release rate of •OH to improve the selectivity of CH3OH. By incorporating Co3O4 as a hole buffer and storage center, the kinetics of •OH generation at the TiO2 interface can be effectively modulated. This confines the spatial distribution of •OH to the active sites of the AgPd alloy, thus facilitating the directional combination of •CH3 and •OH. The optimal AgPd-Co/TiO2 photocatalyst demonstrates outstanding catalytic performance with the selectivity of CH3OH reaching up to 93% in the liquid phase. AgPd-Co/TiO2 exhibited significantly enhanced selectivity relative to reported TiO2-based photocatalytic systems, while simultaneously achieving comparable methanol yields. This research offers valuable insights for the precise design of composite photocatalysts to achieve highly selective methane oxidation.

Key words: Methane conversion, AgPd alloy, Co3O4, TiO2, Photocatalysis