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Rotations of molecular photoelectron angular distributions with intense ultrashort circularly polarized attosecond laser pulses

机译:具有强超短圆偏振阿秒激光脉冲的分子光电子角分布的旋转

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Molecular photoelectron angular distributions (MPADs) by intense (I _0 ≥ 10~(14) W/cm~2) circularly polarized ultrashort, few cycle (attosecond) ultraviolet laser pulses are presented from numerical solutions of time dependent Schr?dinger equations. For the aligned molecular ion H_2 ~+, the MPADs exhibit rotations with respect to the polarization and molecular symmetry axes which are determined by the symmetry of the initial electronics states. It is also found that the rotation angle of MPADs is insensitive to the pulse intensity. We attribute these effects to the asymmetry between the parallel and perpendicular (to the molecular axis) polarization photoionization. Influence of the molecular alignment and ionizing pulse ellipticity on the rotation of MPADs is also shown to allow control of the nonsymmetric ionization.
机译:从随时间变化的薛定er方程的数值解给出了强(I _0≥10〜(14)W / cm〜2)圆极化的超短,极少周期(阿秒)的紫外激光脉冲的分子光电子角分布(MPAD)。对于对齐的分子离子H_2〜+,MPAD相对于极化和分子对称轴表现出旋转,而旋转和分子对称轴由初始电子态的对称性决定。还发现MPAD的旋转角度对脉冲强度不敏感。我们将这些效应归因于平行和垂直(相对于分子轴)极化光电离之间的不对称性。还显示了分子排列和电离脉冲椭圆度对MPAD旋转的影响,可以控制非对称电离。

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