A CO2-philic ferrocene-based porous organic polymer for solar-driven CO2 conversion from flue gas

被引:12
作者
Fang, Zhou [1 ,2 ]
Wang, Yuqi [1 ,2 ]
Hu, Yue [1 ,2 ]
Yao, Bing [1 ,2 ]
Ye, Zhizhen [1 ,2 ]
Peng, Xinsheng [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat & Adv Semicond Mat, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ, Inst Wenzhou, Wenzhou Key Lab Novel Optoelect & Nanomat, Wenzhou 325006, Peoples R China
基金
中国国家自然科学基金;
关键词
CARBON-DIOXIDE; EFFICIENT CYCLOADDITION; CHEMICAL FIXATION; FRAMEWORK; CATALYST; EPOXIDES; MILD; SEPARATION; NANOSHEETS; AMMONIUM;
D O I
10.1039/d3ta03622g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Conversion of CO2 to high value chemicals from diluted CO2 flue gas is challenging but attractive in reducing CO2 emission. Herein, CO2-philic ferrocene-based porous organic polymers (Fc-POPs) are designed and demonstrate outstanding catalytic activity and recyclability for CO2 cycloaddition under solar irradiation. The yield of cyclic carbonate reaches 94.7% in pure CO2 (0.3 W cm(-2)), while the productivity is around 93% in diluted CO2 (15 vol%, 0.4 W cm(-2)). Notably, the functional groups enable Fc-POPs to possess high-efficiency photothermal adsorption and outstanding affinity for CO2 at low pressure (0.15 bar, 5.38 wt%) at room temperature. Density functional theory calculations indicate that the Lewis acid-base synergistic effect and intramolecular interaction reduce the energy barrier, synergistically promoting catalytic activities. In terms of the excellent catalytic performance, Fc-POPs are regarded as promising candidates for efficient fixation and conversion of flue gas.
引用
收藏
页码:18272 / 18279
页数:8
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