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Boosting CO2 electroreduction performance over fullerene-modified MOF-545-Co promoted by π–π interaction
Metal-organic frameworks (MOFs) have showed high promise in CO2-electroreduction, yet their generally insufficient conductivity or low electron-transfer efficiency have largely restricted the wide-spread applications. Herein, fullerene molecules (i.e., C60 and C70) have been successfully introduced...
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Published in: | Chinese chemical letters 2023-04, Vol.34 (4), p.107459, Article 107459 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Metal-organic frameworks (MOFs) have showed high promise in CO2-electroreduction, yet their generally insufficient conductivity or low electron-transfer efficiency have largely restricted the wide-spread applications. Herein, fullerene molecules (i.e., C60 and C70) have been successfully introduced into the pore-channels of a Co-porphyrin based MOF through a facile strategy. Thus-obtained hybrid materials present higher electron-transfer ability, enhanced CO2 adsorption-enthalpy and CO2 electroreduction activity. Notably, the charge transfer resistance (Rct) of C60@MOF-545-Co is almost 5 times lower of than that of MOF-545-Co, as well as 1.5 times increased for the CO2 adsorption enthalpy. As expect, the FECO of C60@MOF-545-Co (97.0%) is largely higher than MOF-545-Co (70.2%), C60@MOF-545 (19.4%), C60 (11.5%) and physical mixture (70.3%) and presented as one of the best CO2 electroreduction catalysts reported in H-cell system. The facile strategy would give rise to new insight into the exploration of powerful MOF-based hybrid materials in high-efficiency CO2 electroreduction.
Fullerene is successfully introduced into the channels of MOF-545-Co through an impregnation method and the introducing of C60 largely increases the electrocatalytic performance of MOF material for CO2RR. [Display omitted] |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2022.04.057 |