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Identification of the activity source of CO2 electroreduction by strategic catalytic site distribution in stable supramolecular structure system
Authors:Sheng-Nan Sun  Ning Li  Jiang Liu  Wen-Xin Ji  Long-Zhang Dong  Yi-Rong Wang  Ya-Qian Lan
Institution:Jiangsu Collaborative Innovation Centre of Biomedical Functional Materials, Jiangsu Key Laboratory of New Power Batteries, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China;School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China;State Key Laboratory of High-efficiency Coal Utilization and Green Chemical Engineering, Ningxia University, Yinchuan 750021, China
Abstract:Identification of the real catalytic site in CO2 reduction reaction (CO2RR) is critical for the rational design of catalysts and the understanding of reactive mechanisms. In this study, the catalytic activity of pyridine-containing materials was for the first time structurally demonstrated in CO2RR by crystalline supramolecular coordination compounds model system. The system consists of three stable supramolecular coordination compounds (Ni-TPYP, Ni-TPYP-1 and Ni-TPP) with different numbers (4, 2 and 0) of active pyridine groups (i.e. uncoordinated pyridine nitrogen atoms). The electrocatalytic test results show that with the decrease of the number of active pyridine groups, the CO2RR performance is gradually reduced, mainly showing the reduction of highest FECO (99.8%, 83.7% and 25.6%, respectively). The crystallographic, experimental and theoretical evidences prove that the CO2RR activity is more likely derived from uncoordinated pyridine nitrogen than the electrocatalytic inert metal nickel in porphyrin center. This work serves as an important case study for the identification of electrocatalytic activity of pyridine-containing materials in CO2RR by simple supramolecular model system.
Keywords:strategic catalytic site distribution  supramolecular structure system  active source  CO2 electroreduction
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