Benzotrifuran-based donor-acceptor covalent organic frameworks for enhanced photocatalytic hydrogen generation

被引:19
|
作者
Yang, Chuanmeng [1 ]
Zhang, Zhenwei [1 ]
Li, Jiali [1 ]
Hou, Yuxin [1 ]
Zhang, Qi [2 ]
Li, Zhongping [4 ]
Yue, Huijuan [3 ]
Liu, Xiaoming [1 ]
机构
[1] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
[2] Univ Warwick, Sch Engn, Coventry CV4 7AL, England
[3] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
[4] Ulsan Natl Inst Sci & Technol UNIST, Ctr Dimens Controllable Organ Frameworks, Sch Energy & Chem Engn, Ulsan 44919, South Korea
基金
中国国家自然科学基金;
关键词
WATER;
D O I
10.1039/d3gc04972h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 mu mol 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.
引用
收藏
页码:2605 / 2612
页数:8
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