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分子中与取向相关的立体威格纳时移和电子局域化。

Orientation-dependent stereo Wigner time delay and electron localization in a small molecule.

机构信息

Department of Physics, ETH Zurich, 8093 Zurich, Switzerland.

Max Born Institute, 12489 Berlin, Germany.

出版信息

Science. 2018 Jun 22;360(6395):1326-1330. doi: 10.1126/science.aao4731.

Abstract

Attosecond metrology of atoms has accessed the time scale of the most fundamental processes in quantum mechanics. Transferring the time-resolved photoelectric effect from atoms to molecules considerably increases experimental and theoretical challenges. Here we show that orientation- and energy-resolved measurements characterize the molecular stereo Wigner time delay. This observable provides direct information on the localization of the excited electron wave packet within the molecular potential. Furthermore, we demonstrate that photoelectrons resulting from the dissociative ionization process of the CO molecule are preferentially emitted from the carbon end for dissociative Σ states and from the center and oxygen end for the Π states of the molecular ion. Supported by comprehensive theoretical calculations, this work constitutes a complete spatially and temporally resolved reconstruction of the molecular photoelectric effect.

摘要

原子的阿秒计量学已经进入了量子力学中最基本过程的时间尺度。将时间分辨光电效应从原子转移到分子会极大地增加实验和理论上的挑战。在这里,我们展示了取向和能量分辨测量可以描述分子的 Wigner 时间延迟。这个可观测量提供了关于分子势能中激发电子波包定位的直接信息。此外,我们还证明了 CO 分子的离解电离过程产生的光电子,优先从碳端被发射出来,对于分子离子的∑态,优先从碳端和氧端被发射出来,对于Π态,则优先从中心端被发射出来。这项工作得到了全面的理论计算的支持,它构成了分子光电效应的完整的空间和时间分辨的重建。

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