Construction of Azobenzene Covalent Organic Frameworks as High-Performance Heterogeneous Photocatalyst

光催化 偶氮苯 化学 共价键 偶氮化合物 降级(电信) 结晶度 化学工程 催化作用 分子 有机化学 结晶学 聚合物 工程类 电信 计算机科学
作者
Qin Tong,Bowei Wang,Xiangdi Zhang,Shanglong Yang,Ligong Chen,Yang Li,Guoyi Bai,Xilong Yan
出处
期刊:Catalysis Letters [Springer Nature]
卷期号:152 (11): 3233-3242 被引量:5
标识
DOI:10.1007/s10562-021-03887-z
摘要

Photocatalytic performances of covalent organic frameworks (COFs) have attracted intensive attention by virtue of their regular pore structure, high specific surface area, excellent crystallinity and periodic π bonds. Herein, COF Tp-Azo was simply synthesized from 2,4,6-triformylphloroglucinol (Tp) and 4,4′-diaminoazobenzene (Azo); and incorporation of copper salt into Tp-Azo yielded a novel COF Cu-Tp-Azo. XRD, SEM and TEM results indicated that the skeleton structure of Tp-Azo was retained in Cu-Tp-Azo. Subsequently, they were applied in the photocatalytic degradation of tetracycline, the results showed that both COFs exhibited excellent photocatalytic performance and Cu-Tp-Azo showed better degradation efficiency compared with Tp-Azo, indicating that the advantages of azo-based COFs with great potential for photocatalytic applications, and the modification of copper ions did make a difference as it can not only facilitate the separation and migration of photo-generated electron–hole pairs, but decrease their recombination, further improved the photocatalytic activity of Tp-Azo.Graphical AbstractCOF Tp-Azo was simply synthesized from 2,4,6-triformylphloroglucinol (Tp) and 4,4′-diaminoazobenzene (Azo); and incorporation of copper salt into Tp-Azo yielded a novel COF Cu-Tp-Azo. Both COFs exhibited excellent photocatalytic performance and Cu-Tp-Azo was even better compared with Tp-Azo, indicating that the advantages of azo-based COFs with great potential for photocatalytic applications, and the modification of copper ions can not only facilitate the separation and migration of photo-generated electron-hole pairs, but decrease their recombination, further improved the photocatalytic activity of Tp-Azo.
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