Electrochemical CO2 reduction on heterogeneous cobalt phthalocyanine catalysts with different carbon supports

被引:29
作者
Huai, Mingming [1 ]
Yin, Zhenglei [1 ]
Wei, Fengyuan [1 ]
Wang, Gongwei [1 ]
Xiao, Li [1 ]
Lu, Juntao [1 ]
Zhuang, Lin [1 ,2 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan 430072, Hubei, Peoples R China
[2] Wuhan Univ, Inst Adv Studies, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; reduction; Cobalt phthalocyanine; Carbon support; Durability; pi-pi interaction; ORGANIC FRAMEWORKS; ELECTROREDUCTION; DIOXIDE; COMPLEXES;
D O I
10.1016/j.cplett.2020.137655
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Supporting materials have a significant impact on heterogeneous molecular catalysts. Herein, we have studied the electrochemical CO2 reduction on cobalt phthalocyanine (CoPc) with Vulcan XC-72 and carbon nanotubes (CNTs) supports, respectively. Compared with pure CoPc, the resulting CoPc/XC-72 and CoPc/CNTs exhibits a notable improvement in catalytic activity. The CoPc/XC-72 maintains a stable polarization just for 15 h with a turnover number (TON) of 48,600, whereas the CoPc/CNTs lasts over 45 h with a high TON of 180,000 and CO Faraday efficiency of 88%. The excellent catalytic stability of CoPc/CNTs is attributed to a strong pi-pi interaction between CoPc and CNTs.
引用
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页数:5
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