Xue Qi, Zhang Zixuan, Ng Bryan K Y, Zhao Pu, Lo Benedict T W
The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen Hi-tech Industrial Park, Shenzhen, 518000, China.
State Key Laboratory of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, China.
Top Curr Chem (Cham). 2021 Feb 5;379(2):11. doi: 10.1007/s41061-021-00324-y.
This mini-review highlights some recent progress in the engineering of single-atom catalysts (SACs) through metal-organic frameworks (MOFs) and derivatives. The inherent molecular and chemical specificities within the MOFs and derivatives can offer stabilisation of the SACs with high atomic isolation and dispersion. As MOFs are often considered an infinite array of self-assembled molecular catalysts, specifically designed structures can provide further functionalities to suit the needs of different catalytic applications. In brief, we can divide the preparation approaches into three main categories: (1) fabrication onto functional groups of the ligands, (2) fabrication onto Lewis acid sites of nodal centres, and (3) synthesis via a pyrolysis-mediated technique. Through these approaches, strong metal-support interactions can be established to aid the fine-tuning of the catalytic properties. We also discuss how recent progress in the development of state-of-the-art microscopic, spectroscopic, and crystallographic techniques has enabled scientists to elucidate the structure-activity relationship.
本综述重点介绍了通过金属有机框架(MOF)及其衍生物制备单原子催化剂(SAC)的一些最新进展。MOF及其衍生物固有的分子和化学特异性能够以高原子隔离和分散度实现SAC的稳定化。由于MOF通常被认为是自组装分子催化剂的无限阵列,经过特殊设计的结构可以提供更多功能,以满足不同催化应用的需求。简而言之,我们可以将制备方法分为三大类:(1)在配体的官能团上制备;(2)在节点中心的路易斯酸位点上制备;(3)通过热解介导技术合成。通过这些方法,可以建立强大的金属-载体相互作用,以辅助催化性能的微调。我们还讨论了最新的先进微观、光谱和晶体学技术的发展如何使科学家能够阐明结构-活性关系。