摘要
Molecular complexes with active metal centers exhibit high activity and selectivity for electrochemical CO 2 reduction reaction (CO 2 RR), which represents a promising method for transforming greenhouse gas into valuable chemicals and feedstock. Using metal–organic frameworks (MOFs) to load the active molecular complexes then employing the combination with the carbonic conducting material may exhibit a beneficial effect for CO 2 RR. Herein, we obtained a composite catalyst named PCN-222(Fe)/CNTs, which was in situ synthesized through the solvothermal method that loads iron porphyrin-centered PCN-222(Fe) molecules onto CNTs. The catalyst PCN-222(Fe)/CNTs exhibits excellent electrocatalytic performance for CO 2 RR with a FE CO of 95.5% (m(Fe-TCPP):m(CNTs) = 1:30, written as PCN-222(Fe)/CNTs-30) and an overpotential ( η ) of 494 mV. In addition, the turnover frequency (TOF) is high as 448.76 h −1 (3.011 site −1 s −1 ) and the hydrogen evolution reaction (HER) is indistinctive. After long-term electrocatalysis of 10 h at −0.6 V vs. RHE, PCN-222(Fe)/CNTs-30 remained its high catalytic performance with average FE CO = 90%. This work provides a solid foundation for further research in the high-efficiency transformation of CO 2 to CO. Graphical abstract
危险品化学品经营许可证(带存储)