Theoretical Study on Electroreduction of CO2 to C3+ Catalyzed by Polymetallic Phthalocyanine Covalent Organic Frameworks (COFs) in Tandem

被引:4
作者
Du, Jinping [1 ]
Guo, Ling [1 ]
机构
[1] Shanxi Normal Univ, Sch Chem & Mat Sci, Key Lab Magnet Mol & Magnet Informat Mat, Minist Educ, Taiyuan 030000, Peoples R China
关键词
CO2RR; Tandem catalysis; n-propanol; COFs; DFT; SINGLE-ATOM CATALYSTS; ELECTROCHEMICAL REDUCTION; OXYGEN REDUCTION; CARBON-DIOXIDE; HIGHLY EFFICIENT; METAL; PERFORMANCE; OXIDATION; PERCHLOROPHTHALOCYANINE; CYCLOHEXANE;
D O I
10.1007/s10562-022-04229-3
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
In CO2RR, CO2 can be changed into a wide succession of premium chemicals and fuels, amid which C3+ products such as n-propanol, n-propanol is of great economic value. To improve the selectivity of C-3 products, the idea of tandem catalysis is proposed in this paper through the reduction of CO2 to CO, followed by the electrochemical reduction reaction of CO to n-propanol, we screen out Fe-Co-Pc-Ni-O-COFs catalyst that was the most promising catalyst by DFT calculation method, NiO4 and Fe-Co-Pc can work independently that the CO generated on NiO4 can spontaneously and rapidly migrate to the active sites of Fe-Co-Pc catalyst that C-1-C-1 coupling can be carried out to obtain C-2 intermediates and C-2 intermediates can be coupled with CO (C-1-C-2 coupling) to obtain C-3 products. Finally, it is concluded that *CO-*CHO coupling is the most critical steps in the formation of C-2 products, the coupling of *CH3CHO with *CO to form *CH3CHOCO is a key step to generate the n-propanol, an optimal way to form C-3 is also screened out. [GRAPHICS] .
引用
收藏
页码:3270 / 3283
页数:14
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