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Extracting an electron's angle of return from shifted interference patterns in macroscopic high-harmonic spectra of diatomic molecules

机译:从移位的干扰中提取电子的返回角   双原子分子的宏观高次谐波谱中的模式

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摘要

We investigate high-order harmonic spectra from aligned diatomic molecules inintense driving fields whose components have orthogonal polarizations. We focuson how the driving-field ellipticity influences structural interferencepatterns in a macroscopic medium. In a previous publication [Phys. Rev. A 88,023404 (2013)] we have shown that the non-vanishing ellipticity introduces aneffective dynamic shift in the angle for which the two-center interferencemaxima and minima occur, with regard to the existing condition for linearlypolarized fields. In this work we show through simulation that it is stillpossible to observe this shift in harmonic spectra that have undergonemacroscopic propagation, and discuss the parameter range for doing so. Thesefeatures are investigated for $H_2$ in a bichromatic field composed of twoorthogonally polarized waves. The shift is visible both in the near- and in thefar-field regime, so that, in principle, it can be observed in experiments.
机译:我们研究了来自排列成双极性的强烈驱动场中排列的双原子分子的高阶谐波谱。我们关注驱动场椭圆率如何影响宏观介质中的结构干涉图样。在以前的出版物[Phys。 Rev. A 88,023404(2013)]我们已经证明,相对于线性极化场的现有条件,不消失的椭圆率会引入有效的动态位移,即出现两个中心干扰最大值和最小值的角度。在这项工作中,我们通过仿真表明,仍然有可能观察到经过宏观传播的谐波频谱中的这种偏移,并讨论了这样做的参数范围。在由两个正交极化波组成的双色场中针对$ H_2 $研究了这些特征。这种变化在近场和远场都可见,因此,原则上可以在实验中观察到。

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