催化作用
选择性
化学
光化学
二氧化钛
甲醇
纳米团簇
激进的
甲烷厌氧氧化
氧化还原
无机化学
氧气
甲烷
材料科学
有机化学
冶金
作者
Hui Song,Xianguang Meng,Shengyao Wang,Wei Zhou,Shuang Song,Tetsuya Kako,Jinhua Ye
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-11-23
卷期号:10 (23): 14318-14326
被引量:172
标识
DOI:10.1021/acscatal.0c04329
摘要
Direct and selective oxidation of CH4 with dioxygen to methanol is a "dream reaction" in modern catalysis yet remains a great challenge. Here, we report that TiO2 loaded with dual cocatalysts, that is, nanometals and cobalt oxide (CoOx) nanoclusters, is capable of selectively catalyzing CH4 to CH3OH at room temperature under photoexcitation using abundant and inexpensive O2 as an oxidant. The best activity for the formation of the primary products, CH3OOH and CH3OH, is up to 50.8 μmol for 2 h with 95% selectivity. Mechanistic studies elucidate that the superior activity and selectivity result from the synergistic effect of nanometals and CoOx. Nanometals enhance CH4 conversion by promoting the separation of the photoexcited electron and the reduction of O2. The CoOx mediates a mild CH4 oxidation process by suppressing the formation of highly oxidative •OH radicals that can further oxidize CH3OH to HCHO and CO2, thereby preserving a high selectivity toward oxygenated products. This work provides a prototype in designing efficient photocatalysts for selective oxidation of CH4 to CH3OH with O2 under mild conditions.
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