共价键
光催化
噻唑
化学工程
材料科学
光化学
催化作用
化学
氧气
组合化学
有机化学
工程类
作者
Yanghui Hou,Peng Zhou,Fuyang Liu,Ke Tong,Yanyu Lü,Zhengmao Li,Jialiang Liang,Meiping Tong
标识
DOI:10.1038/s41467-024-51878-6
摘要
Owing to their capability to produce reactive oxygen species (ROS) under solar irradiation, covalent organic frameworks (COFs) with pre-designable structure and unique architectures show great potentials for water purification. However, the sluggish charge separation, inefficient oxygen activation and poor structure stability in COFs restrict their practical applications to decontaminate water. Herein, via a facile one-pot synthetic strategy, we show the direct conversion of reversible imine linkage into rigid thiazole linkage can adjust the π-conjugation and local charge polarization of skeleton to boost the exciton dissociation on COFs. The rigid linkage can also improve the robustness of skeleton and the stability of COFs during the consecutive utilization process. More importantly, the thiazole linkage in COFs with optimal C 2p states (COF-S) effectively increases the activities of neighboring benzene unit to directly modulate the O2-adsorption energy barrier and improve the ROS production efficiency, resulting in the excellent photocatalytic degradation efficiency of seven toxic emerging contaminants (e.g. degrading ~99% of 5 mg L−1 paracetamol in only 7 min) and effective bacterial/algal inactivation performance. Besides, COF-S can be immobilized in continuous-flow reactor and in enlarged reactor to efficiently eliminate pollutants under natural sunlight irradiation, demonstrating the feasibility for practical application. Linking COFs by rigid thiazole linkages can simultaneously enhance the stability, charge separation efficiency, and oxygen activation capability of COFs, resulting in the excellent photocatalytic degradation performance towards micropollutants in water.
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