甲烷氧化偶联
光催化
甲烷
选择性
催化作用
三元运算
产量(工程)
化学
材料科学
合理设计
光化学
化学工程
纳米技术
有机化学
计算机科学
工程类
冶金
程序设计语言
作者
Chao Wang,Xiyi Li,Yifei Ren,Haimiao Jiao,Feng Ryan Wang,Junwang Tang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2023-03-02
卷期号:13 (6): 3768-3774
被引量:29
标识
DOI:10.1021/acscatal.2c06093
摘要
Oxidation of methane into valuable chemicals, such as C2+ molecules, has been long sought after but the dilemma between high yield and high selectivity of desired products remains. Herein, methane is upgraded through the photocatalytic oxidative coupling of methane (OCM) over a ternary Ag–AgBr/TiO2 catalyst in a pressurized flow reactor. The ethane yield of 35.4 μmol/h with a high C2+ selectivity of 79% has been obtained under 6 bar pressure. These are much better than most of the previous benchmark performance in photocatalytic OCM processes. These results are attributed to the synergy between Ag and AgBr, where Ag serves as an electron acceptor and promotes the charge transfer and AgBr forms a heterostructure with TiO2 not only to facilitate charge separation but also to avoid the overoxidation process. This work thus demonstrates an efficient strategy for photocatalytic methane conversion by both the rational design of the catalyst for the high selectivity and reactor engineering for the high conversion.
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