脱氢
丙烯
丙烷
光催化
选择性
键裂
光化学
放热反应
化学
金红石
催化作用
材料科学
有机化学
作者
Fangliang Li,Binli Wang,Xiao Chen,Yuemiao Lai,Tao Wang,Hongjun Fan,Xueming Yang,Qing Guo
出处
期刊:JACS Au
[American Chemical Society]
日期:2022-10-27
卷期号:2 (11): 2607-2616
被引量:25
标识
DOI:10.1021/jacsau.2c00512
摘要
High Resolution Image Download MS PowerPoint Slide Oxidative dehydrogenation of propane (ODHP) as an exothermic process is a promising method to produce propene (C 3 H 6 ) with lower energy consumption in chemical industry. However, the selectivity of the C 3 H 6 product is always poor because of overoxidation. Herein, the ODHP reaction into C 3 H 6 on a model rutile(R)-TiO 2 (110) surface at low temperature via photocatalysis has been realized successfully. The results illustrate that photocatalytic oxidative dehydrogenation of propane (C 3 H 8 ) into C 3 H 6 can occur efficiently on R-TiO 2 (110) at 90 K via a stepwise manner, in which the initial C–H cleavage occurs via the hole coupled C–H bond cleavage pathway followed by a radical mediated C–H cleavage to the C 3 H 6 product. An exceptional selectivity of ∼90% for C 3 H 6 production is achieved at about 13% propane conversion. The mechanistic model constructed in this study not only advances our understanding of C–H bond activation but also provides a new pathway for highly selective ODHP into C 3 H 6 under mild conditions.
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