Fluorinated Covalent Organic Frameworks Coupled with Molecular Cobalt Cocatalysts for Efficient Photocatalytic CO2 Reduction



Fu, Zhiwei, Shu, Chang, Wang, Xiaoyan, Chen, Linjiang, Wang, Xue, Liu, Lunjie, Wang, Kewei, Clowes, Rob, Chong, Samantha Y ORCID: 0000-0002-3095-875X, Wu, Xiaofeng ORCID: 0000-0001-5549-8836
et al (show 1 more authors) (2023) Fluorinated Covalent Organic Frameworks Coupled with Molecular Cobalt Cocatalysts for Efficient Photocatalytic CO2 Reduction. CCS CHEMISTRY, 5 (10). pp. 2290-2300.

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Abstract

The combination of covalent organic framework (COF) photosensitizers with molecular cocatalysts is a promising avenue for photocatalytic carbon dioxide (CO2) reduction. Here, a series of isostructural COFs was synthesized using linkers of different lengths, with or without partial fluorination. These COFs were investigated for photocatalytic CO2 reduction under visible-light irradiation when combined with cobalt(II) bipyridine complexes as a cocatalyst. Fluorination was found to enhance both CO2 affinity and catalytic activity, and a partially fluorinated COF, FBP-COF, achieved the highest CO2-to-CO conversion efficiency, showing a carbon monoxide (CO) generation rate of 2.08 mmol h−1 g−1 and a 90% CO selectivity. FBP-COF also showed good stability under sacrificial conditions, generating CO for 50 h with a turnover number of 91.5. This activity is much higher than a homogeneous system using ruthenium bipyridine complexes as the photosensitizer combined with the same cobalt bipyridine complexes.

Item Type: Article
Uncontrolled Keywords: sis, covalent organic frameworks, fluorinated, solar, energy conversion
Divisions: Faculty of Science and Engineering > School of Physical Sciences
Depositing User: Symplectic Admin
Date Deposited: 29 Sep 2023 15:33
Last Modified: 15 Mar 2024 08:33
DOI: 10.31635/ccschem.023.202202688
Open Access URL: https://doi.org/10.31635/ccschem.023.202202688
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3173236