Zhang Tianjun, Chen Ziyi, Walsh Andrew G, Li Yi, Zhang Peng
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun, 130012, P. R. China.
Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, B3H 4R2, Canada.
Adv Mater. 2020 Nov;32(44):e2002910. doi: 10.1002/adma.202002910. Epub 2020 Jul 12.
Single-atom catalysts (SACs) have recently emerged as an exciting system in heterogeneous catalysis showing outstanding performance in many catalytic reactions. Single-atom catalytic sites alone are not stable and thus require stabilization from substrates. Crystalline porous materials such as zeolites and metal-organic frameworks (MOFs) are excellent substrates for SACs, offering high stability with the potential to further enhance their performance due to synergistic effects. This review features recent work on the structure, electronic, and catalytic properties of zeolite and MOF-protected SACs, offering atomic-scale views from the "inside" thanks to the subatomic resolution of synchrotron X-ray absorption spectroscopy (XAS). The extended X-ray absorption fine structure and associated methods will be shown to be powerful tools in identifying the single-atom site and can provide details into the coordination environment and bonding disorder of SACs. The X-ray absorption near-edge structure will be demonstrated as a valuable method in probing the electronic properties of SACs by analyzing the white line intensity, absorption edge shift, and pre-/postedge features. Emphasis is also placed on in situ/operando XAS using state-of-the-art equipment, which can unveil the changes in structure and properties of SACs during the dynamic catalytic processes in a highly sensitive and time-resolved manner.
单原子催化剂(SACs)最近已成为多相催化领域中一个令人兴奋的体系,在许多催化反应中表现出卓越的性能。仅单原子催化位点并不稳定,因此需要来自基底的稳定作用。诸如沸石和金属有机框架(MOFs)之类的晶体多孔材料是SACs的优良基底,它们具有高稳定性,并且由于协同效应而具有进一步提升其性能的潜力。本综述重点介绍了近期关于沸石和MOF保护的SACs的结构、电子和催化性质的研究工作,借助同步加速器X射线吸收光谱(XAS)的亚原子分辨率,从“内部”提供了原子尺度的观点。扩展X射线吸收精细结构及相关方法将被证明是识别单原子位点的有力工具,并且可以提供有关SACs配位环境和键合无序的详细信息。通过分析白线强度、吸收边位移和边前/边后特征,X射线吸收近边结构将被证明是探测SACs电子性质的一种有价值的方法。还重点介绍了使用先进设备进行的原位/ operando XAS,它能够以高度灵敏和时间分辨的方式揭示SACs在动态催化过程中的结构和性质变化。