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双色激光诱导无场分子取向的机制。

Mechanisms of two-color laser-induced field-free molecular orientation.

机构信息

Steacie Institute for Molecular Sciences, National Research Council of Canada, Ottawa, ON, Canada K1A 0R6.

出版信息

Phys Rev Lett. 2012 Sep 14;109(11):113001. doi: 10.1103/PhysRevLett.109.113001. Epub 2012 Sep 12.

Abstract

Two mechanisms of two-color (ω+2ω) laser-induced field-free molecular orientation, based on the hyperpolarizability and ionization depletion, are explored and compared. The CO molecule is used as a computational example. While the hyperpolarizability mechanism generates small amounts of orientation at intensities below the ionization threshold, ionization depletion quickly becomes the dominant mechanism as soon as ionizing intensities are reached. Only the ionization mechanism leads to substantial orientation (e.g., on the order of <cosθ> ≳0.1). For intensities typical of laser-induced molecular alignment and orientation experiments, the two mechanisms lead to robust, characteristic timings of the field-free orientation wave-packet revivals relative to the alignment revivals and the revival time. The revival timings can be used to detect the active orientation mechanism experimentally.

摘要

两种双色(ω+2ω)激光诱导无场分子取向的机制,基于极化率和离化耗竭,进行了探索和比较。以 CO 分子为例。虽然在低于离化阈值的强度下,极化率机制会产生少量的取向,但一旦达到离化强度,离化耗竭就会迅速成为主导机制。只有离化机制才会导致大量的取向(例如,<cosθ>≳0.1)。对于典型的激光诱导分子排列和取向实验强度,这两种机制导致无场取向波包相对于排列的复振和复振时间的稳健、特征定时。复振时间可用于实验检测活性取向机制。

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