催化作用
Atom(片上系统)
纳米技术
氧化还原
氧化态
化学
量子点
材料科学
组合化学
化学物理
光化学
有机化学
计算机科学
嵌入式系统
作者
Akif Zeb,Shafaq Sahar,Sheng‐Yao Lv,Ammar Bin Yousaf,Peter Kasák,Xiaoming Lin,Zhilie Tang,Yongbo Wu,Guoliang Li,An‐Wu Xu
出处
期刊:Small
[Wiley]
日期:2022-07-27
卷期号:18 (34)
被引量:9
标识
DOI:10.1002/smll.202202522
摘要
Abstract Regulating the catalytic pathways of single‐atom sites in single atom catalysts (SACs) is an exciting debate at the moment, which has redirected the research towards understanding and modifying the single‐atom catalytic sites through various strategies including altering the coordination environment of single atom for desirable outcomes as well as increasing their number. One useful aspect concerning the tunability of the catalytic pathways of SACs, which has been overlooked, is the oxidation state dynamics of the single atoms. In this study, iron single‐atoms (FeSA) with variable oxidation states, dependent on the precursors, are harnessed inside a nitrogen‐rich functionalized carbon quantum dots (CQDs) matrix via a facile one‐step and low‐temperature synthesis process. Dynamic electronic properties are imparted to the FeSAs by the simpler carbon dots matrix of CQDs in order to achieve the desired catalytic pathways of reactive oxygen species (ROS) generation in different environments, which are explored experimentally and theoretically for an in‐depth understanding of the redox chemistry that drives the alternative catalytic pathways in FeSA@CQDs. These alternative and oxidation state‐dependent catalytic pathways are employed for specific as well as cascade‐like activities simulating natural enzymes as well as biomarkers for the detection of cancerous cells.
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