鸟嘌呤
催化作用
基因
Atom(片上系统)
化学
抗生素耐药性
按需
抗生素
组合化学
业务
生物化学
计算机科学
商业
嵌入式系统
核苷酸
作者
Zhiyu Pan,Xun‐Heng Jiang,Xia Feng,Yi Liu,Wenhua Dong,Yue Chen,Can Li,Bijun Yang,Jie Hou,Jianying Zhang,Lizhong Zhu,Daohui Lin,Jiang Xu
标识
DOI:10.1021/acs.est.4c13667
摘要
Nonradical Fenton-like catalysis offers an opportunity to degrade extracellular antibiotic resistance genes (eARGs). However, high-loading single-atom catalysts (SACs) with controllable configurations are urgently required to selectively generate high-yield nonradicals. Herein, we constructed high-loading Fe SACs (5.4-34.2 wt %) with uniform Fe-N4 sites via an optimized coordination balance of supermolecular assembly for peroxymonosulfate activation. The selectivity of singlet oxygen (1O2) generation and its contribution to eARGs degradation were both >98%. This targeting strategy of oxidizing guanines with low ionization potentials by 1O2 allowed 7 log eARGs degradation within 10 min and eliminated their transformation within 2 min, outperforming most reported advanced oxidation processes. Relevant interactions between 1O2 and guanines were revealed at a single-molecule resolution. The high-loading Fe SACs exhibited excellent universality and stability for different eARGs and water matrices. These findings provide a promising route for constructing high-loading SACs for efficient and selective Fenton-like water treatment.
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