选择性
光催化
甲烷
甲烷氧化偶联
催化作用
光化学
激进的
化学
异质结
甲烷厌氧氧化
纳米颗粒
化学工程
材料科学
纳米技术
有机化学
工程类
光电子学
作者
Shuang Song,Hui Song,Luming Li,Shengyao Wang,Wei Chu,Kang Peng,Xianguang Meng,Qi Wang,Bowen Deng,Qianxia Liu,Zhuan Wang,Yuxiang Weng,Huilin Hu,Huiwen Lin,Tetsuya Kako,Jinhua Ye
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2021-11-29
卷期号:4 (12): 1032-1042
被引量:213
标识
DOI:10.1038/s41929-021-00708-9
摘要
Direct oxidation of methane to valuable chemicals is a great challenge as catalysts with both high activity and selectivity for the activation of inert C–H bonds are required. Here, we report the highly efficient and selective photo-oxidation of methane to ethane with dioxygen in a flow reactor using a Au nanoparticle (NP) loaded ZnO/TiO2 hybrid. An ethane production rate of over 5,000 μmol g−1 h−1 with 90% selectivity is achieved, which is more than one order of magnitude higher than the state-of-the-art photocatalytic systems. Detailed characterizations and theoretical studies show that the formation of heterojunctions between ZnO and TiO2 leads to enhanced photocatalytic activity, while maintaining high selectivity owing to the weak overoxidation ability of the main component ZnO. Moreover, the Au cocatalyst enables the facile desorption of methyl (CH3) species as •CH3 radicals in the gas phase, thereby facilitating C2H6 formation and inhibiting overoxidation of CH4 to CO2.
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