共价键
光催化
亚胺
离域电子
材料科学
共轭体系
降级(电信)
化学
纳米技术
光化学
有机化学
催化作用
聚合物
计算机科学
电信
作者
Xiaorong Chen,Wei‐Rong Cui,Ru‐Ping Liang,Shouxin Zhang,Rui‐Han Xu,Wei Jiang,Jian‐Ding Qiu
出处
期刊:ACS applied bio materials
[American Chemical Society]
日期:2021-08-01
卷期号:4 (8): 6502-6511
被引量:29
标识
DOI:10.1021/acsabm.1c00621
摘要
Photocatalysis is regarded as one of the most promising technologies to remove organic contaminants. At present, most of the covalent organic frameworks (COFs) used as photocatalysts are connected by imine or borate bonds, which have relatively low stability and relatively poor π-delocalization. Herein, we report, for the first time, vinylene-linked COFs constructed by various diacetylene and triazine moieties for photocatalytic degradation of organic contaminants and disinfection of bacteria. The pioneering introduction of diacetylene moieties not only enhances conjugated π-electrons delocalization but also optimizes the electronic band structures that significantly improve photocatalytic activity. Therefore, the vinylene-bridged COFs have excellent photocatalytic activity with ultrahigh stability and great π-electron delocalization, thus exhibiting ultrafast photocatalytic degradation efficiency for phenol and norfloxacin (>96%, within 15 min). Our work provides a strong basis for the rational regulation of the chemical structure of COFs to enhance their photocatalytic activity, thus broadening the application of COFs in photocatalysis.
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