Single-molecule observation of diffusion and catalysis in nanoporous solids

被引:33
|
作者
Maris, J. J. Erik [1 ]
Fu, Donglong [1 ]
Meirer, Florian [1 ]
Weckhuysen, Bert M. [1 ]
机构
[1] Univ Utrecht, Inorgan Chem & Catalysis, Debye Inst Nanomat Sci, Univ Weg 99, NL-3584 CG Utrecht, Netherlands
基金
欧洲研究理事会;
关键词
Diffusion; Zeolites; Catalysis; Spectroscopy; Microscopy;
D O I
10.1007/s10450-020-00292-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanoporous solids, including microporous, mesoporous and hierarchically structured porous materials, are of scientific and technological interest because of their high surface-to-volume ratio and ability to impose shape- and size-selectivity on molecules diffusing through them. Enormous efforts have been put in the mechanistic understanding of diffusion-reaction relationships of nanoporous solids, with the ultimate goal of developing materials with improved catalytic performance. Single-molecule localization microscopy can be used to explore the pore space via the trajectories of individual molecules. This ensemble-free perspective directly reveals heterogeneities in diffusion and diffusion-related reactivity of individual molecules, which would have been obscured in bulk measurements. In this article, we review developments in the spatial and temporal characterization of nanoporous solids using single-molecule localization microscopy. We illustrate various aspects of this approach, and showcase how it can be used to follow molecular diffusion and reaction behaviors in nanoporous solids.
引用
收藏
页码:423 / 452
页数:30
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