期刊
NATURE
卷 607, 期 7920, 页码 703-+出版社
NATURE PORTFOLIO
DOI: 10.1038/s41586-022-04876-x
关键词
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资金
- National Key Research and Development Program of China [2020YFB0606401]
- National Natural Science Foundation of China [22005170, 21771029, 202013981]
- National Key R&D Program of China [2017YFB0602204]
- Suzhou Key Laboratory of Functional Nano & Soft Materials, Collaborative Innovation Center of Suzhou Nano Science Technology
- 111 Project
This study presents a method of directly observing single molecule behaviors in porous materials using low-dose electron microscopy. The researchers successfully observed the adsorption and desorption behaviors of single pyridine and thiophene molecules in the channels of zeolite, and studied the strong interactions between molecules and acid sites through real-space images.
Single-molecule imaging with atomic resolution is a notable method to study various molecular behaviours and interactions(1-5). Although low-dose electron microscopy has been proved effective in observing small molecules(6-13), it has not yet helped us achieve an atomic understanding ofthe basic physics and chemistry of single molecules in porous materials, such as zeolites(14-16.) The configurations of small molecules interacting with acid sites determine the wide applications of zeolites in catalysis, adsorption, gas separation and energy storage(17-21). Here we report the atomic imaging of single pyridine and thiophene confined in the channel of zeolite ZSM-5 (ref.(22)). On the basis of integrated differential phase contrast scanning transmission electron microscopy (i DPC-STEM)(23-25), we directly observe the adsorption and desorption behaviours of pyridines in ZSM-5 underthe in situ atmosphere. The adsorption configuration of single pyridine is atomically resolved and the S atoms in thiophenes are located after comparing imaging results with calculations. The strong interactions between molecules and acid sites can be visually studied in real-space images. This work provides a general strategy to directly observe these molecular structures and interactions in both the static image and the in situ experiment, expanding the applications of electron microscopy to the further study ofvarious single-molecule behaviours with high resolution.
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