Helical copper-porphyrinic framework nanoarrays for highly efficient CO2 electroreduction

被引:21
作者
Xiao, Yi-Hong [1 ,3 ]
Zhang, Yu-Xiang [4 ]
Zhai, Rui [1 ]
Gu, Zhi-Gang [1 ,2 ,3 ]
Zhang, Jian [1 ,3 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[2] Fujian Sci & Technol Innovat Lab Optoelect Inform, Fuzhou 350108, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Fujian Normal Univ, Coll Phys & Energy, Fuzhou 350117, Peoples R China
基金
中国国家自然科学基金;
关键词
metal-organic framework; helical nanoarrays; CO2; electroreduction; METAL-ORGANIC FRAMEWORKS; ELECTROCHEMICAL REDUCTION; GROWTH; ELECTROCATALYSIS; CONVERSION; NANOSHEETS; NANOWIRES; ACETATE; FORMATE; DRIVEN;
D O I
10.1007/s40843-021-1835-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In recent years, metal-organic frameworks (MOFs) have been extensively investigated as electrocatalysts due to their highly efficient electroreduction of CO2. Herein, the electrocatalytic CO2 reduction reaction was investigated by growing helical Cu-porphyrinic MOF Cu meso-tetra(4-carboxyphenyl)porphyrin (TCPP) on Cu(OH)(2) nanoarrays (H-CuTCPP@Cu(OH)(2)) using a sacrificial template method. The electrocatalytic results showed that the H-CuTCPP@Cu(OH)(2) nanoarrays exhibited a high acetic acid Faradaic efficiency (FE) of 26.1% at -1.6 V vs. Ag/Ag+, which is much higher than the value of 19.8% obtained for non-helical CuTCPP@Cu(OH)(2) (nH-CuTCPP@Cu(OH)(2)). The higher efficiency may be because space was more effectively utilized in the helical MOF nanoarrays, resulting in a greater number of active catalytic sites. Furthermore, in situ diffuse reflectance infrared Fourier transform spectra showed that the H-CuTCPP@Cu(OH)(2) nanoarrays have much stronger CO linear adsorption, indicating a better selectivity of acetic acid than that of nH-CuTCPP@Cu(OH)(2). In this study, we develop new helical nanomaterials and propose a new route to enhance the reduction of CO2.
引用
收藏
页码:1269 / 1275
页数:7
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