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用于过氧化氢人工光合作用的介孔sp碳共轭苯并噻二唑共价有机框架的设计合成

Designed Synthesis of Mesoporous sp Carbon-Conjugated Benzothiadiazole Covalent Organic Frameworks for Artificial Photosynthesis of Hydrogen Peroxide.

作者信息

Zhang Fulin, Wang Yuexin, Zhao Qi, Zhao Hongxiang, Dong Xiaoyun, Gu Xiang-Kui, Sheng Hua, Sarina Sarina, Lang Xianjun

机构信息

Hubei Key Lab on Organic and Polymeric Optoelectronic Materials, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.

Key Laboratory of Photochemistry, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

ACS Appl Mater Interfaces. 2025 Jan 8;17(1):1097-1109. doi: 10.1021/acsami.4c16707. Epub 2024 Dec 25.

Abstract

Artificial photosynthesis of hydrogen peroxide (HO) from ambient air, water, and sunlight has attracted considerable attention recently. Despite being extremely challenging to synthesis, sp carbon-conjugated covalent organic frameworks (COFs) can be powerful and efficient materials for the photosynthesis of HO due to desirable properties. Herein, we report the designed synthesis of an sp carbon-conjugated COF, BTD-spc-COF, from benzothiadiazole and triazine units with high crystallinity and ultralarge mesopores (∼4 nm). The sp carbon-conjugated skeletons guarantee BTD-spc-COF superior optoelectronic properties and chemical stability. BTD-spc-COF exhibits an exceptional efficiency of 3066 μmol g h from pure water and air, much better than that of BTD-imine-COF. In contrast, the resilience of BTD-imine-COF is compromised due to the participation of imine linkages in the oxygen reduction reaction. Importantly, in situ characterization and theoretical calculation results reveal that both benzothiadiazole and triazine units serve as oxygen reduction reaction centers for HO photosynthesis through a sequential electron transfer pathway, while the vinylene bridged phenyls serve as water oxidation reaction centers. The sp carbon-conjugated COFs pave the way for potent artificial photosynthesis.

摘要

近期,利用环境空气、水和阳光通过人工光合作用制备过氧化氢(HO)已引起广泛关注。尽管合成极具挑战性,但由于具有理想的特性,sp 碳共轭共价有机框架(COF)有望成为高效的 HO 光合作用材料。在此,我们报道了一种由苯并噻二唑和三嗪单元设计合成的 sp 碳共轭 COF,即 BTD-spc-COF,它具有高结晶度和超大介孔(约 4 纳米)。sp 碳共轭骨架确保了 BTD-spc-COF 具有优异的光电性能和化学稳定性。BTD-spc-COF 在纯水和空气中表现出 3066 μmol g h 的卓越效率,远优于 BTD-亚胺-COF。相比之下,由于亚胺键参与氧还原反应,BTD-亚胺-COF 的稳定性受到影响。重要的是,原位表征和理论计算结果表明,苯并噻二唑和三嗪单元均通过连续电子转移途径作为 HO 光合作用的氧还原反应中心,而亚乙烯基桥连的苯基则作为水氧化反应中心。sp 碳共轭 COF 为高效人工光合作用开辟了道路。

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