Key Laboratory for Energy Conversion and Storage, Key Laboratory of Theoretical Chemistry of Environment, School of Chemistry, South China Normal University, Guangzhou, 510006, P. R. China.
Guangdong Provincial Key Laboratory of Quantum Engineering and Quantum Materials, National Demonstration Center for Experimental Physics Education, School of Physics and Telecommunications Engineering, South China Normal University, Guangzhou, 510006, P. R. China.
Small. 2022 Aug;18(34):e2202522. doi: 10.1002/smll.202202522. Epub 2022 Jul 27.
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.
调控单原子催化剂(SACs)中单原子位点的催化途径是目前一个令人兴奋的争论点,该争论促使研究人员通过各种策略来理解和修饰单原子催化位点,包括改变单原子的配位环境以实现理想的结果,以及增加单原子的数量。在 SACs 的催化途径的可调谐性方面,有一个被忽视的有用方面,那就是单原子的氧化态动力学。在这项研究中,通过简便的一步低温合成工艺,在富含氮的功能化碳量子点(CQDs)基质内利用依赖于前体的具有可变氧化态的铁单原子(FeSA)。通过更简单的 CQDs 碳点基质赋予 FeSAs 动态电子特性,以实现不同环境中活性氧(ROS)生成的所需催化途径,从实验和理论两方面深入探索驱动 FeSA@CQDs 中替代催化途径的氧化还原化学。这些替代的和氧化态依赖的催化途径被用于特定的和级联样的活性,模拟天然酶以及用于癌细胞检测的生物标志物。