Qin Chencheng, Yang Yi, Wu Xiaodong, Chen Long, Liu Zhaoli, Tang Lin, Lyu Lai, Huang Danlian, Wang Dongbo, Zhang Chang, Yuan Xingzhong, Liu Wen, Wang Hou
College of Environmental Science and Engineering and Key Laboratory of Environmental Biology and Pollution Control (Ministry of Education), Hunan University, 410082, Changsha, China.
College of Materials Science and Engineering, Nanjing Tech University, 210009, Nanjing, China.
Nat Commun. 2023 Oct 24;14(1):6740. doi: 10.1038/s41467-023-42513-x.
The pre-designable structure and unique architectures of covalent organic frameworks (COFs) render them attractive as active and porous medium for water crisis. However, the effect of functional basis with different metrics on the regulation of interfacial behavior in advanced oxidation decontamination remains a significant challenge. In this study, we pre-design and fabricate different molecular interfaces by creating ordered π skeletons, incorporating different pore sizes, and engineering hydrophilic or hydrophobic channels. These synergically break through the adsorption energy barrier and promote inner-surface renewal, achieving a high removal rate for typical antibiotic contaminants (like levofloxacin) by BTT-DATP-COF, compared with BTT-DADP-COF and BTT-DAB-COF. The experimental and theoretical calculations reveal that such functional basis engineering enable the hole-driven levofloxacin oxidation at the interface of BTT fragments to occur, accompanying with electron-mediated oxygen reduction on terphenyl motif to active radicals, endowing it facilitate the balanced extraction of holes and electrons.
共价有机框架(COF)的可预设计结构和独特架构使其成为解决水危机的活性多孔介质的理想选择。然而,不同指标的功能基团对高级氧化去污中界面行为调控的影响仍是一项重大挑战。在本研究中,我们通过构建有序的π骨架、引入不同孔径以及设计亲水性或疏水性通道来预设计和制备不同的分子界面。这些措施协同突破吸附能垒并促进内表面更新,与BTT-DADP-COF和BTT-DAB-COF相比,BTT-DATP-COF对典型抗生素污染物(如左氧氟沙星)实现了高去除率。实验和理论计算表明,这种功能基团工程使BTT片段界面处的空穴驱动左氧氟沙星氧化得以发生,同时三联苯基序上电子介导的氧还原为活性自由基,使其便于空穴和电子的平衡提取。