Tracing the origins of an asymmetric momentum distribution for polar molecules in strong linearly polarized laser fields

Shang Wang, J. Che, C. Chen, G. Xin, Yan-jun Chen
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引用次数: 12

Abstract

We study the ionization dynamics of oriented HeH$^+$ in strong linearly-polarized laser fields by numerically solving the time-dependent Schr\"{o}dinger equation. The calculated photoelectron momentum distributions for parallel orientation show a striking asymmetric structure. With a developed model pertinent to polar molecules, we trace the electron motion in real time. We show that this asymmetric structure arises from the interplay of the Coulomb effect and the permanent dipole in strong laser fields. This structure can be used to probe the degree of orientation which is important in ultrafast experiments for polar molecules. we also check our results for other polar molecules such as CO and BF.
强线偏振激光场中极性分子不对称动量分布的溯源
通过数值求解随时间变化的薛定谔方程,研究了强线偏振激光场中定向HeH$^+$的电离动力学。计算得到的平行方向的光电子动量分布具有明显的不对称结构。我们开发了一个与极性分子相关的模型,实时跟踪电子运动。我们证明了这种不对称结构是由强激光场中的库仑效应和永久偶极子相互作用引起的。这种结构可以用来探测极性分子的取向程度,这在极性分子的超快实验中是很重要的。我们还检查了其他极性分子(如CO和BF)的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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