General framework for enzyme-photo-coupled catalytic toward carbon dioxide conversion

被引:12
|
作者
Sun, Yiying [1 ,3 ]
Li, Wenping [1 ,3 ]
Wang, Zhuo [2 ,3 ]
Shi, Jiafu [2 ,3 ,4 ,5 ]
Jiang, Zhongyi [1 ,3 ,4 ,5 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Minist Educ, 92 Weijin Rd, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Environm Sci & Engn, 92 Weijin Rd, Tianjin 300072, Peoples R China
[3] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[4] Joint Sch Natl Univ Singapore, Singapore, Singapore
[5] Tianjin Univ, Int Campus, Fuzhou 350207, Peoples R China
关键词
NADH REGENERATION; ORGANIC FRAMEWORK; ELECTRON-TRANSFER; CHARGE-TRANSFER; CO2; REDUCTION; SOLAR-ENERGY; FORMIC-ACID; PHOTOCATALYST; FIXATION; SYSTEM;
D O I
10.1016/j.copbio.2021.07.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High emission of carbon dioxide (CO2) has aroused global concern due to the 'greenhouse effect'. The conversion of CO2 to valuable chemicals/materials is an indispensable route toward 'carbon neutrality'. Enzyme-photo-coupled catalytic systems (EPCCSs), integrating synthetic library of semiconductor photocatalyst and natural database of enzyme, have emerged as a green and powerful platform toward CO2 conversion. Herein, we discuss the recent progress in design and application of EPCCSs for CO2 conversion from the perspective of pathway engineering, reaction engineering and system engineering. We firstly summarize the explored pathways of EPCCSs for converting CO2 to C-1 and C2+ products. Secondly, we discuss the matching of kinetics between photocatalytic and enzymatic reactions in EPCCSs. Thirdly, we unveil the complex interplay between photocatalytic and enzymatic modules, and further demonstrate the strategy of compartmentalization to eliminate the negative interactions. Lastly, we conclude with the perspective on the opportunities and challenges of EPCCSs for CO2 conversion.
引用
收藏
页码:67 / 73
页数:7
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