Insights into Adsorbate-Induced Dynamic Structures and Catalytic Microenvironments of Zeolite Acid Sites via Solid-State NMR

化学 催化作用 沸石 合理设计 吸附 核磁共振波谱 多相催化 纳米技术 分子 化学工程 光谱学 控制重构 组合化学 分子动力学 酸催化 计算化学 反应中间体 表征(材料科学) 分子筛 纳米结构 化学物理
作者
Youdong Xing,Xianfeng Yi,Yao Xiao,Guoliang Liu,Peng Peng,Anmin Zheng
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:148 (12): 12427-12446
标识
DOI:10.1021/jacs.6c01162
摘要

Zeolites are essential solid acid catalysts whose catalytic performance is determined by the nature of their acid sites. Conventionally, these sites are viewed as static, predetermined structural motifs, characterized by metrics such as acid type (Brønsted/Lewis), strength, and spatial distribution within a rigid framework. Emerging insights, however, reveal that acid sites are dynamic and adaptive entities. Their local structure and chemical properties can be continuously reshaped by guest molecules, particularly in working catalysts where pores are occupied by reactants, intermediates, and products. This adsorbate-induced structural reconfiguration governs key steps in catalysis, including reactant adsorption and activation, intermediate stabilization, and thus ultimate activity and selectivity. Solid-state nuclear magnetic resonance (SSNMR) spectroscopy stands out as a unique and powerful technique for resolving these dynamic processes by translating subtle host-guest interactions into atomic-scale observables. This Perspective highlights recent SSNMR advances that uncover dynamic coordination states, map adaptive catalytic microenvironments, and establish direct correlations between these dynamic features and catalytic performance. These insights are reshaping fundamental understanding in zeolite chemistry and opening new avenues for the rational design of zeolite catalysts. We conclude by outlining key challenges and future opportunities for SSNMR in advancing the molecular-level understanding and optimization of catalysts under realistic reaction conditions.
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