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- W4386797394 abstract "Artificial photoreduction of CO2 is considered an attractive solution for simultaneously achieving carbon neutrality goals and solving the energy shortage crisis. In this study, a donor–acceptor (D–A) covalent organic framework (COF), COF-BT, comprising (1,1′-biphenyl)-3,3′,5,5′-tetracarbaldehyde and 4,4′-(2,1,3-benzothiadiazole-4,7-diyl)bis[benzenamine] was prepared, and cheap CoO was introduced into COF-BT via a two-step impregnation-calcination process to obtain Co-COF-BT with immobilized transition metals. Photoelectrochemical experimental and theoretical results indicate that the D–A structure of Co-COF-BT reduces the band gap, enhances visible light absorption, inhibits electron–hole recombination, and prolongs the life of photogenerated carriers. The introduction of CoO provides additional active sites, and the Co-S bond in Co-COF-BT provides an additional channel for ultrafast electron migration from the COF-BT unit to the CoO active center, which increases charge mobility and reduces the energy barrier formed by *COOH intermediates. Thus, the excellent photocatalytic CO2 reduction activity of Co-COF-BT is achieved with a CO yield of 2423 μmol g−1h−1 and selectivity > 99% under visible light. The superior photocatalytic performance is attributed to the synergistic effect of D–A moieties and CoO in Co-COF-BT. This study not only presents a novel COF-based photocatalyst with high charge transfer efficiency and high catalytic activity in CO2 reduction but also provides a potential strategy to fine-tune photoelectronic properties by adjusting the functional building blocks and additional metal active sites." @default.
- W4386797394 created "2023-09-17" @default.
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- W4386797394 date "2023-11-01" @default.
- W4386797394 modified "2023-10-01" @default.
- W4386797394 title "Cheap transition metal reinforced donor–acceptor covalent organic frameworks for CO2 photoreduction" @default.
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- W4386797394 doi "https://doi.org/10.1016/j.cej.2023.146106" @default.
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