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Updated: Jun 5, 2026

Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition
Published on: May 2, 2014
In Situ Generated Ti3+ over Ag/TiO2 Enables Highly Efficient Photocatalytic Oxidative Coupling of Methane in Flow
Shihua Zhu1, Yachao Wang1, Mengya Yang1
1Anhui Basic Discipline Research Center for Clean Energy and Catalysis, Key Laboratory of Functional Molecular Solids Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, P. R. China.
Abstract:
Photocatalytic oxidative coupling of methane (OCM) is a promising sustainable technology for chemical and fuel synthesis, but current photocatalysts suffer from limited activity and selectivity. Here, we report a highly active Ag/TiO2 catalyst for OCM in a flow reactor, achieving a C2 hydrocarbon production rate of 1.9 mmol g-1 h-1 and selectivity of up to 92% with enhanced stability exceeding 150 h. This performance surpasses that of most reported semiconductor-based photocatalysts. The enhanced performance is attributed to a synergistic effect between in situ photogenerated Ti3+ and Ag on TiO2, where Ti3+ acts as a hole trap promoting hole transfer and C-H activation, and Ag serves as an electron acceptor and catalytic center to accelerate electron transfer and C-C coupling. These findings not only provide valuable mechanistic insights into photocatalytic OCM but also demonstrate the utility of in situ/operando techniques for establishing the structure-activity relation of catalysts "at work".
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