Enhanced Electrocatalytic Activity of a Zinc Porphyrin for CO2 Reduction: Cooperative Effects of Triazole Units in the Second Coordination Sphere

被引:19
|
作者
Lashgari, Amir [1 ]
Williams, Caroline K. [1 ]
Glover, Jenna L. [1 ]
Wu, Yueshen [2 ]
Chai, Jingchao [1 ]
Jiang, Jianbing Jimmy [1 ]
机构
[1] Univ Cincinnati, Dept Chem, POB 210172, Cincinnati, OH 45221 USA
[2] Yale Univ, Dept Chem, 225 Prospect St, New Haven, CT 06520 USA
关键词
carbon-dioxide fixation; homogeneous catalysis; porphyrin; second coordination sphere; triazole; COUPLED ELECTRON-TRANSFER; CARBON-DIOXIDE; HYDROGEN EVOLUTION; COBALT COMPLEXES; PENDANT AMINES; PROTON; OXIDATION; ELECTROREDUCTION; CATALYSTS; LIGANDS;
D O I
10.1002/chem.202002813
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The control of the second coordination sphere in a coordination complex plays an important role in improving catalytic efficiency. Herein, we report a zinc porphyrin complex ZnPor8T with multiple flexible triazole units comprising the second coordination sphere, as an electrocatalyst for the highly selective electrochemical reduction of carbon dioxide (CO2) to carbon monoxide (CO). This electrocatalyst converted CO2 to CO with a Faradaic efficiency of 99 % and a current density of -6.2 mA cm(-2) at -2.4 V vs. Fc/Fc(+) in N,N-dimethylformamide using water as the proton source. Structure-function relationship studies were carried out on ZnPor8T analogs containing different numbers of triazole units and distinct triazole geometries; these unveiled that the triazole units function cooperatively to stabilize the CO2-catalyst adduct in order to facilitate intramolecular proton transfer. Our findings demonstrate that incorporating triazole units that function in a cooperative manner is a versatile strategy to enhance the activity of electrocatalytic CO2 conversion.
引用
收藏
页码:16774 / 16781
页数:8
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