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Benzotrifuran-based donor-acceptor covalent organic frameworks for enhanced photocatalytic hydrogen generation
Visible-light-driven hydrogen evolution from water represents a green and sustainable technology to convert solar energy into chemical energy. Covalent organic frameworks (COFs) are the most competitive platforms among the variety of photocatalysts. Herein, a novel benzotrifuran-based donor-acceptor...
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Published in: | Green chemistry : an international journal and green chemistry resource : GC 2024-03, Vol.26 (5), p.265-2612 |
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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: | Visible-light-driven hydrogen evolution from water represents a green and sustainable technology to convert solar energy into chemical energy. Covalent organic frameworks (COFs) are the most competitive platforms among the variety of photocatalysts. Herein, a novel benzotrifuran-based donor-acceptor material (COF-JLU42) was constructed using a Schiff base polycondensation reaction by introducing electron-rich benzotrifuran and deficient triazine moieties into the framework. The new COF features high crystallinity and permanent porosity with a large surface area and proves to be a photoactive semiconductor with efficient visible-light harvesting capacity. Importantly, COF-JLU42 exhibits a superior photocatalytic activity with a hydrogen evolution rate of over 40 000 μmol g
−1
h
−1
under visible-light illumination, which is 2.5 times higher than that of the isomorphic benzotrithiophene-based COFs under the same conditions. These findings suggest the huge application prospect of benzotrifuran-based framework materials as metal-free and solid photocatalysts in solar-energy conversion and storage.
A novel benzotrifuranyl COF with excellent photovoltaic properties and low exciton binding energy was successfully constructed and used for efficient photolysis of water. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/d3gc04972h |