共 34 条
Cobalt-N4 macrocyclic complexes for heterogeneous electrocatalysis of the CO2 reduction reaction
被引:19
作者:

Lin, Zhichao
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Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China

Jiang, Zhan
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Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China

Yuan, Yubo
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Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China

Li, Huan
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Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China

Wang, Hongxuan
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Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China

Tang, Yirong
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Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China

Liu, Chunchen
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Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China

Liang, Yongye
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h-index: 0
机构:
Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China
Southern Univ Sci & Technol, Guangdong Prov Key Lab Energy Mat Elect Power, Shenzhen 518055, Guangdong, Peoples R China Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China
机构:
[1] Southern Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Guangdong Prov Key Lab Energy Mat Elect Power, Shenzhen 518055, Guangdong, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CO2;
reduction;
Cobalt phthalocyanine;
Cobalt corrole;
Cobalt porphyrin;
Heterogeneous electrocatalysis;
CARBON-DIOXIDE;
METAL PHTHALOCYANINES;
ELECTROREDUCTION;
IMMOBILIZATION;
ELECTRODES;
PORPHYRINS;
D O I:
10.1016/S1872-2067(21)63880-9
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Metal-N-4 (M-N-4) macrocyclic complexes are interesting electrocatalysts due to their well-defined structures and rich molecular tuning. Among them, metal phthalocyanines have been widely studied for the carbon dioxide reduction reaction (CO2RR) in heterogeneous systems and demonstrated good electrocatalytic performance. However, other complexes like metal corroles and metal porphyrins are much less explored, and often show inferior performances. In this study, three cobalt macrocyclic complexes, cobalt phthalocyanine, cobalt meso-tetraphenylporphyrin, and cobalt meso-triphenylcorrole (CoPc, CoTPP and CoTPC) are investigated in heterogeneous electrocatalysis of CO2RR. Although CoPc/carbon nanotube (CNT) hybrid exhibits high electrocatalytic activity, CNT hybridization does not work for CoTPC and CoTPP that hold weak interactions with CNTs. By the drop-dry method with a high molecular loading of 5.4 x 10(-7) mol cm(-2), CoTPC and CoTPP could deliver appreciable electrode activities. Poly(4-vinylpyridine) (PVP) introduction is further demonstrated as a facile method to afford enhanced activities for CoTPP at low molecular loadings through enhancing molecule-substrate interactions. The partial current density of carbon monoxide for CoTPP+CNT/PVP is around 8 times higher than the sample without PVP at -0.67 V versus reversible hydrogen electrode. This work provides solutions to enhance the electrode activities of molecular electrocatalysts with weak substrate interactions in heterogeneous systems. (C) 2022, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
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页码:104 / 109
页数:6
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