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

机译:可视化从分子到原子过渡期间的空间和时间电子重排

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摘要

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 ultra-short 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.
机译:在电子水平上对分子和材料中的反应进行成像和控制是科学上的巨大挑战,这与我们对化学,物理和生物学中的电荷转移过程以及材料动力学的理解有关。当电子在化学键原子之间共享或转移时,直接获得动态电子密度将大大改善我们对分子键和结构的理解。使用反应显微镜技术,我们显示出当键断裂时,我们可以捕获分子中整个价壳电子密度如何从分子状重新转换为原子状。强烈的超短激光脉冲用于在解离过程中的不同时间使溴分子电离,并且我们测量了总电离信号和电离产率的角度分布。使用这种技术,我们可以观察到令人惊讶的长时间和距离上的密度变化,从而使我们看到电子直到碎片彼此分开(约5.5Å),直到其势能范围内才定位在单个Br原子上。离解的能量曲线几乎是简并的。我们的观察与溴分子强场电离速率的计算非常吻合。

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