范德瓦尔斯力
分子间力
化学物理
分子
物理
纳米技术
原子单位
范德瓦尔斯曲面
范德瓦尔斯半径
化学
材料科学
量子力学
有机化学
作者
Boyuan Shen,Xiao Chen,Huiqiu Wang,Hao Xiong,Eric Bosch,Ivan Lazić,Dali Cai,Weizhong Qian,Shifeng Jin,Xin Liu,Yu Han,Fei Wei
出处
期刊:Nature
[Nature Portfolio]
日期:2021-04-21
卷期号:592 (7855): 541-544
被引量:133
标识
DOI:10.1038/s41586-021-03429-y
摘要
Single-molecule imaging is challenging but highly beneficial for investigating intermolecular interactions at the molecular level1–6. Van der Waals interactions at the sub-nanometre scale strongly influence various molecular behaviours under confinement conditions7–11. Inspired by the traditional compass12, here we use a para-xylene molecule as a rotating pointer to detect the host–guest van der Waals interactions in the straight channel of the MFI-type zeolite framework. We use integrated differential phase contrast scanning transmission electron microscopy13–15 to achieve real-space imaging of a single para-xylene molecule in each channel. A good correlation between the orientation of the single-molecule pointer and the atomic structure of the channel is established by combining the results of calculations and imaging studies. The orientations of para-xylene help us to identify changes in the van der Waals interactions, which are related to the channel geometry in both spatial and temporal dimensions. This work not only provides a visible and sensitive means to investigate host–guest van der Waals interactions in porous materials at the molecular level, but also encourages the further study of other single-molecule behaviours using electron microscopy techniques. The orientation of a rotating para-xylene molecule in the nanochannel of a zeolite framework can be visualised by electron microscopy to determine the host–guest van der Waals interaction inside the channel.
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