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本文引用的文献

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Time-resolved molecular frame dynamics of fixed-in-space CS2 molecules.固定在空间中的二硫化碳(CS₂)分子的时间分辨分子框架动力学
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Direct measurement of the angular dependence of the single-photon ionization of aligned N2 and CO2.对齐的N₂和CO₂单光子电离角依赖性的直接测量。
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Direct measurement of the angular dependence of ionization for N2, O2, and CO2 in intense laser fields.在强激光场中对N2、O2和CO2电离角依赖性的直接测量。
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在分子到原子的转变过程中,可视化电子在空间和时间上的重排。

Visualizing electron rearrangement in space and time during the transition from a molecule to atoms.

机构信息

JILA and Department of Physics, University of Colorado, Boulder, CO 80309, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Nov 23;107(47):20219-22. doi: 10.1073/pnas.1014723107. Epub 2010 Nov 8.

DOI:10.1073/pnas.1014723107
PMID:21059945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2996685/
Abstract

Imaging and controlling reactions in molecules and materials at the level of electrons is a grand challenge in science, relevant to our understanding of charge transfer processes in chemistry, physics, and biology, as well as material dynamics. Direct access to the dynamic electron density as electrons are shared or transferred between atoms in a chemical bond would greatly improve our understanding of molecular bonding and structure. Using reaction microscope techniques, we show that we can capture how the entire valence shell electron density in a molecule rearranges, from molecular-like to atomic-like, as a bond breaks. An intense ultrashort laser pulse is used to ionize a bromine molecule at different times during dissociation, and we measure the total ionization signal and the angular distribution of the ionization yield. Using this technique, we can observe density changes over a surprisingly long time and distance, allowing us to see that the electrons do not localize onto the individual Br atoms until the fragments are far apart (∼5.5 Å), in a region where the potential energy curves for the dissociation are nearly degenerate. Our observations agree well with calculations of the strong-field ionization rates of the bromine molecule.

摘要

在分子和材料的电子水平上对反应进行成像和控制是科学上的一大挑战,这与我们对化学、物理和生物学中电荷转移过程以及材料动力学的理解有关。直接获取电子在化学键中共享或转移时的动态电子密度,将极大地增进我们对分子键合和结构的理解。使用反应显微镜技术,我们展示了如何在化学键断裂时捕捉分子中整个价壳层电子密度从分子态到原子态的重排。利用强度极高的超短激光脉冲在不同时间对溴分子进行离解,我们测量了总离化信号和离化产额的角分布。使用这种技术,我们可以观察到令人惊讶的长时间和长距离的密度变化,从而可以看到电子直到碎片相距很远(约 5.5 Å)时才会定位到各个 Br 原子上,而在这个区域,离解的势能曲线几乎简并。我们的观察结果与溴分子的强场离化率的计算结果吻合得很好。