Non-sequential double ionization of CO_2 molecule and Kr atom in linearly polarized laser fields

Kai-Li Song, Yanshan Tian, S. Ben, Tong-Tong Xu, Hong-Dan Zhang, Xue-shen Liu, Jing Guo
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引用次数: 1

Abstract

Using two-dimensional classical ensemble method, a theoretical study of non-sequential double ionization (NSDI) with Krypton (Kr) and carbon dioxide (CO2) is presented at different laser intensities. The numerical results show that the probability for NSDI of Kr atom is higher than that of CO2 molecule. Moreover, for the same laser intensity, the momentum correlation spectrum of CO2 molecule is drastically different from Kr atom. For example, for the laser intensities I = 0.065 PW/cm 2 and I =0.15 PW/cm 2 , the correlation spectrum of CO2 molecule tends to distribute in the first and third quadrants, and presents a "finger-like" structure. However, for Kr atom at I = 0.065 PW/cm 2 , the emitted electrons pairs tend to distribute in the second and fourth quadrants; When the laser intensity increases to 0.15PW/cm 2 , the two electrons mainly distribute in the first and third quadrants and along two distinct lines being paralleled to the diagonal. In addition, our numerical calculations reveal that this different phenomenon is closely related to the Coulomb focusing effect: Coulomb potential will attract the returning electron more dramatically when it moves near the atomic or molecular core. For CO2 molecule, the returning electron is dramatically attracted by three cores, so the returned electron of CO2 molecule possesses higher energy than Kr atom does.
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线偏振激光场中CO_2分子和Kr原子的非顺序双电离
利用二维经典系综方法,研究了氪(Kr)和二氧化碳(CO2)在不同激光强度下的非顺序双电离(NSDI)。数值结果表明,Kr原子发生NSDI的概率高于CO2分子。而且,在相同的激光强度下,CO2分子的动量相关谱与Kr原子的动量相关谱有很大的不同。例如,当激光强度I = 0.065 PW/cm 2和I =0.15 PW/cm 2时,CO2分子的相关谱倾向于分布在第一象限和第三象限,呈“指状”结构。而对于I = 0.065 PW/ cm2的Kr原子,发射电子对倾向于分布在第二象限和第四象限;当激光强度增加到0.15PW/ cm2时,两个电子主要分布在第一象限和第三象限,沿平行于对角线的两条不同的线分布。此外,我们的数值计算表明,这种不同的现象与库仑聚焦效应密切相关:当电子靠近原子或分子核心时,库仑势会更强烈地吸引返回的电子。对于CO2分子来说,返回的电子被三核显著吸引,因此CO2分子的返回电子比Kr原子具有更高的能量。
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Journal of Atomic and Molecular Sciences
Journal of Atomic and Molecular Sciences PHYSICS, ATOMIC, MOLECULAR & CHEMICAL-
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