Highly selective and active CO2 reduction electro-catalysts based on cobalt phthalocyanine/carbon nanotube hybrid structures

被引:1221
作者
Zhang, Xing [1 ]
Wu, Zishan [2 ,3 ]
Zhang, Xiao [1 ]
Li, Liewu [1 ]
Li, Yanyan [1 ]
Xu, Haomin [1 ]
Li, Xiaoxiao [1 ]
Yu, Xiaolu [1 ]
Zhang, Zisheng [1 ]
Liang, Yongye [1 ]
Wang, Hailiang [2 ,3 ]
机构
[1] South Univ Sci & Technol China, Dept Mat Sci & Engn, Shenzhen 518055, Peoples R China
[2] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[3] Yale Univ, Energy Sci Inst, West Haven, CT 06516 USA
关键词
CARBON-DIOXIDE REDUCTION; ELECTROCHEMICAL REDUCTION; ELECTROCATALYTIC REDUCTION; ORGANIC FRAMEWORKS; EFFICIENT; NANOPARTICLES; ELECTROREDUCTION; CONVERSION; HYDROCARBONS; PORPHYRINS;
D O I
10.1038/ncomms14675
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Electrochemical reduction of carbon dioxide with renewable energy is a sustainable way of producing carbon-neutral fuels. However, developing active, selective and stable electrocatalysts is challenging and entails material structure design and tailoring across a range of length scales. Here we report a cobalt-phthalocyanine-based high-performance carbon dioxide reduction electrocatalyst material developed with a combined nanoscale and molecular approach. On the nanoscale, cobalt phthalocyanine (CoPc) molecules are uniformly anchored on carbon nanotubes to afford substantially increased current density, improved selectivity for carbon monoxide, and enhanced durability. On the molecular level, the catalytic performance is further enhanced by introducing cyano groups to the CoPc molecule. The resulting hybrid catalyst exhibits 495% Faradaic efficiency for carbon monoxide production in a wide potential range and extraordinary catalytic activity with a current density of 15.0mAcm(-2) and a turnover frequency of 4.1 s(-1) at the overpotential of 0.52V in a near-neutral aqueous solution.
引用
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页数:8
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