CO2 photoreduction with high selectivity of C2H4 production on conjugated microporous polymer with Cu single atoms

被引:2
|
作者
Li, Jing [1 ]
Chan, Tingshan [3 ]
Jing, Chuanyong [1 ,2 ]
Wang, Jin [1 ,4 ,5 ]
机构
[1] Beijing Jiaotong Univ, Sch Environm, Beijing Key Lab Aqueous Typ Pollutants Control & W, Beijing 100044, Peoples R China
[2] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
[3] Natl Synchrotron Radiat Res Ctr, 101 Hsin-Ann Rd,Hsinchu Sci Pk, Hsinchu 30076, Taiwan
[4] Beijing Jiaotong Univ, Tangshan Res Inst, Tangshan 063000, Peoples R China
[5] 3 Shangyuancun, Beijing 100044, Peoples R China
关键词
Conjugated microporous polymer; Cu single atoms; Synergistic effect; CO2; photoreduction; Highly selective ethylene production; CARBON-DIOXIDE REDUCTION; NITROGEN;
D O I
10.1016/j.fuel.2023.130020
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Selective conversion of CO2 to fuels and chemicals has been considered one of the key challenges in the photocatalytic CO2 reduction reaction. The multi-electron reduction reaction requires the design of photocatalysts that can adsorb CO2 and transfer electrons. Herein, Cu single atoms are confined in a conjugated microporous polymer (CMP) to construct Cun@CMP photocatalyst for CO2 reduction to produce C2H4 and CH4. By adjusting Cu loading, Cu-0.012@CMP exhibited a high performance with production yields of 236.81 mu mol center dot g(-1)center dot h(-1) for C2H4, and 78.2 % selectivity for C2H4 formation. DFT calculations displayed the band structure and confirmed Cu-N together with characterization. The in situ DRIFTS revealed *CH2 and *C2H4 as key reaction intermediates to form CH4 and C2H4, respectively. The synergy effect in Cu single-atoms and CMP contributed greatly to C-C coupling and interfacial charge transfer, thus achieving excellent activity for conversion of CO2 to C-1/C-2. This work highlights the potential for constructing Cu single atoms on CMP to produce highly selective C2H4.
引用
收藏
页数:9
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