催化作用
选择性
单线态氧
合理设计
化学
材料科学
电子结构
氧气
降级(电信)
过程(计算)
电子效应
计算机科学
化学物理
氧化法
计算化学
组合化学
分子氧
密度泛函理论
生物系统
光化学
化学工程
纳米技术
多相催化
电子舌
氧原子
作者
Yifei Wang,Xuedi Sun,Hao Wang,Yiyang Wu,Yuqing Ma,Ze Wang,Tingting Zhu,Jinshan Wei,Yang Huo,Meng Sun,Jae‐Hong Kim
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-08-14
卷期号:12 (33): eaeg4626-eaeg4626
标识
DOI:10.1126/sciadv.aeg4626
摘要
The activation of peroxymonosulfate (PMS) for selective oxidant generation in advanced oxidation process is a sought objective when using single-atom catalysts (SACs) over conventional nanomaterials. However, challenges in controlling atomic-level morphology and understanding the intricate interplay between electronic and geometric properties that affect catalytic selectivity hinder rational material design. To address this issue, we developed a library of iron single-atom catalysts (FeSACs) featuring tunable interatomic distances ranging from 2.6 to 10.5 angstroms, facilitating the independent investigation of electronic and geometric effects. We propose a complementary descriptor (CD) integrating electronic effect index ( I EE ) and geometric effect index ( I GE ) in a weighted predictive framework. The CD strongly correlates with singlet oxygen ( 1 O 2 ) production in selective PMS activation by the FeSAC series. Specifically, the optimized FeSAC 5.0 delivers 94.2% 1 O 2 selectivity and nearly complete degradation of electron-rich micropollutants. This CD framework offers a universal strategy for the rational design of high-performance SACs grounded in electronic and geometric criteria.
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