人体净化
吸附
共价有机骨架
共价键
多孔性
激进的
化学工程
材料科学
化学
氧化物
纳米技术
组合化学
有机化学
废物管理
工程类
作者
Chencheng Qin,Yi Yang,Xiaodong Wu,Long Chen,Zhaoli Liu,Lin Tang,Lai Lyu,Danlian Huang,Dongbo Wang,Chang Zhang,Xingzhong Yuan,Wen Liu,Hou Wang
标识
DOI:10.1038/s41467-023-42513-x
摘要
Abstract 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.
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