Photocatalytic ethane conversion on rutile TiO2(110): identifying the role of the ethyl radical

被引:6
作者
Li, Fangliang [1 ,2 ]
Lai, Yuemiao [1 ,2 ]
Zeng, Yi [1 ,2 ]
Chen, Xiao [1 ,2 ]
Wang, Tao [1 ,2 ]
Yang, Xueming [1 ,2 ,3 ,4 ]
Guo, Qing [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Shenzhen Key Lab Energy Chem, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Guangdong, Peoples R China
[3] Chinese Acad Sci, State Key Lab Mol React Dynam, Dalian Inst Chem Phys, Dalian 116023, Liaoning, Peoples R China
[4] Hefei Natl Lab, Hefei 230088, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
FINAL-STATE DISTRIBUTIONS; H BOND ACTIVATION; OXIDATIVE DEHYDROGENATION; SULFATED ZIRCONIA; REDOX CATALYSTS; OXIDE CATALYSTS; SURFACE; PHOTOOXIDATION; METHANE; METAL;
D O I
10.1039/d3sc05623f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxidative dehydrogenation of ethane (C2H6, ODHE) is a promising approach to producing ethene (C2H4) in the chemical industry. However, the ODHE needs to be operated at a high temperature, and realizing the ODHE under mild conditions is still a big challenge. Herein, using photocatalytic ODHE to obtain C2H4 has been achieved successfully on a model rutile(R)-TiO2(110) surface with high selectivity. Initially, the C2H6 reacts with hole trapped O-Ti(-) centers to produce ethyl radicals , which can be precisely detected by a sensitive TOF method, and then the majority of the radicals spontaneously dehydrogenate into C2H4 without another photo-generated hole. In addition, parts of the radicals rebound with diversified surface sites to produce C-2 products via migration along the surface. The mechanistic model built in this work not only advances our knowledge of the C-H bond activation and low temperature C2H6 conversion, but also provides new opportunities for realizing the ODHE with high C2H4 efficiency under mild conditions.
引用
收藏
页码:307 / 316
页数:10
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