Covalent organic framework photocatalysts for green and efficient photochemical transformations

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Covalent organic framework photocatalysts for green and efficient photochemical transformations
Title:
Covalent organic framework photocatalysts for green and efficient photochemical transformations
Journal Title:
Nature Communications
Publication Date:
14 July 2025
Citation:
Chen, Y., Guo, Y., Wang, T., Ji, S., Shao, H., Lin, M., Seki, S., Yan, N., & Jiang, D. (2025). Covalent organic framework photocatalysts for green and efficient photochemical transformations. Nature Communications, 16(1). https://doi.org/10.1038/s41467-025-61853-4
Abstract:
Artificial photosynthesis is impeded by rapid charge recombination and inefficient use of photogenerated carriers. Here we present covalent organic frameworks with systematically tailored skeletons and pores for green yet efficient photosynthesis with water and air. The hexavalent frameworks with non-conjugated photocatalytic skeletons enable water oxidation at knot corners and oxygen reduction at linker edges, while orientated triangular micropores timely supply water and air. Noteworthily, the framework with the highest π density and smallest supermicropores exhibits optimal charge separation and utilization and achieves rapid, efficient and cyclable hydrogen peroxide production in both batch and membrane reactors. Remarkably, the supermicroporous framework instantly removes organic dye contaminants from water and fully degrades these dyes under visible light. Our findings enable a paradigm shift to the systematic design of both electron/hole flow and mass transport for constructing photocatalysts, which are not only scientifically important but also technologically key to shaping sustainable society and future.
License type:
Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
Funding Info:
This research / project is supported by the Ministry of Education - Academic Research Fund Tier 1
Grant Reference no. : A-8003573-00-00

This research / project is supported by the Ministry of Education - Academic Research Fund Tier 2
Grant Reference no. : T2EP10221-0012

This research / project is supported by the A*STAR - NA
Grant Reference no. : U2102d2004
Description:
ISSN:
2041-1723
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