Photocatalytic Oxidative Coupling of Methane over Au1Ag Single‐Atom Alloy Modified ZnO with Oxygen and Water Vapor: Synergy of Gold and Silver

Author:

Wang Yuxiong1,Hong Guang2,Zhang Yaoyu1,Liu Yue13ORCID,Cen Wanglai2,Wang Lianzhou4,Wu Zhongbiao13

Affiliation:

1. Key Laboratory of Environment Remediation and Ecological Health Ministry of Education College of Environmental and Resource Sciences Zhejiang University Hangzhou 310058 China

2. Institute of New Energy and Low-Carbon Technology National Engineering Research Center for Flue Gas Desulfurization Sichuan University Chengdu 610207 China

3. Zhejiang Provincial Engineering Research Center of Industrial Boiler & Furnace Flue Gas Pollution Control Hangzhou 310058 China

4. Nanomaterials Centre School of Chemical Engineering and Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia QLD, 4072 Australia

Abstract

AbstractC−H dissociation and C−C coupling are two key steps in converting CH4 into multi‐carbon compounds. Here we report a synergy of Au and Ag to greatly promote C2H6 formation over Au1Ag single‐atom alloy nanoparticles (Au1Ag NPs)‐modified ZnO catalyst via photocatalytic oxidative coupling of methane (POCM) with O2 and H2O. Atomically dispersed Au in Au1Ag NPs effectively promotes the dissociation of O2 and H2O into *OOH, promoting C−H activation of CH4 on the photogenerated O to form *CH3. Electron‐deficient Au single atoms, as hopping ladders, also facilitate the migration of electron donor *CH3 from ZnO to Au1Ag NPs. Finally, *CH3 coupling can readily occur on Ag atoms of Au1Ag NPs. An excellent C2H6 yield of 14.0 mmol g−1 h−1 with a selectivity of 79 % and an apparent quantum yield of 14.6 % at 350 nm is obtained via POCM with O2 and H2O, which is at least two times that of the photocatalytic system. The bimetallic synergistic strategy offers guidance for future catalyst design for POCM with O2 and H2O.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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