Cobalt Imidazolate Metal-Organic Frameworks Photosplit CO2 under Mild Reaction Conditions

被引:524
|
作者
Wang, Sibo [1 ,2 ]
Yao, Wangshu [1 ,2 ]
Lin, Jinliang [1 ,2 ]
Ding, Zhengxin [1 ,2 ]
Wang, Xinchen [1 ,2 ]
机构
[1] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
[2] Fuzhou Univ, Coll Chem & Chem Engn, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon dioxide; cobalt; metal-organic frameworks; photochemistry; zeolites; CARBON-DIOXIDE; PHOTOCHEMICAL REDUCTION; THERMAL-STABILITY; ROOM-TEMPERATURE; PROPYLENE-OXIDE; IONIC LIQUIDS; HYDROGEN; EFFICIENT; SEPARATION; CATALYSIS;
D O I
10.1002/anie.201309426
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-organic frameworks (MOFs) have shown great promise for CO2 capture and storage. However, the operation of chemical redox functions of framework substances and organic CO2-trapping entities which are spatially linked together to catalyze CO2 conversion has had much less attention. Reported herein is a cobalt-containing zeolitic imidazolate framework (Co-ZIF-9) which serves as a robust MOF cocatalyst to reduce CO2 by cooperating with a ruthenium-based photosensitizer. The catalytic turnover number of Co-ZIF-9 was about 450 within 2.5hours under mild reaction conditions, while still keeping its original reactivity during prolonged operation.
引用
收藏
页码:1034 / 1038
页数:5
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