Aerobic Oxidative Carboxylation of Styrene Over Cobalt Catalysts: Integrated CO2 Capture and Conversion

被引:0
|
作者
Chen, Junjun [1 ,2 ]
Liu, Xiaofang [1 ]
Zhang, Peipei [3 ]
Zhang, Shunan [4 ]
Zhou, Haozhi [4 ]
Li, Lin [1 ,2 ]
Luo, Hu [1 ]
Wang, Hui [1 ,4 ]
Sun, Yuhan [1 ,4 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Low Carbon Convers Sci & Engn, Shanghai Adv Res Inst, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] CNOOC Inst Chem & Adv Mat Beijing Co Ltd, Beijing 102209, Peoples R China
[4] Shanghai Tech Univ, Inst Carbon Neutral, Shanghai 201203, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
single-atom catalyst; cobalt catalyst; carbon dioxide utilization; oxidative carboxylation; flue gas; N-C CATALYST; TOTAL-ENERGY CALCULATIONS; ONE-POT SYNTHESIS; CYCLIC CARBONATES; PROPYLENE EPOXIDATION; ORGANIC CARBONATES; MOLECULAR-OXYGEN; OLEFINS; DIOXIDE; REDUCTION;
D O I
10.1002/cssc.202301567
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The direct synthesis of cyclic carbonates through oxidative carboxylation of alkenes using CO2 and O-2 offers a sustainable and carbon-neutral method for CO(2)utilization, which is, however, still a largely unexplored field. Here we develop a single-atom catalyst (SAC) Co-N/O-C as the earth-abundant metal catalyst for the oxidative carboxylation of styrene with CO2 and O-2. Remarkably, even using the flue gas as an impureCO(2) and O2 source, desired cyclic carbonate could be obtained with moderate productivity, which shows the potential for integrated CO2 capture and conversion, leveraging the high CO2 adsorption capacity of Co-N/O-C. In addition, the catalyst can be reused five times without an obvious decline in activity. Detailed characterizations and theoretical calculations elucidate the crucial role of single Co atoms in activating O-2 and CO2, as well as controlling selectivity.
引用
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页数:9
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