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Angle-dependent electron-electron correlation in the single ionization of H2 in strong laser fields

机译:在强激光场中H2的单电离中依赖于角度的电子电子相关性

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摘要

The one-photon ionization and tunneling ionization of H2 exposed to strong XUV and infrared laser pulses are studied by numerically simulating the four-dimensional time-dependent Schrödinger equation, which includes two-electron dynamics for arbitrary angle between the molecular axis and the laser polarization direction. In the one-photon single ionization of H2, one electron escapes fast and the other bound electron is not disturbed but remains in coherent superposition of two electronic states of H2+. In another case, under the irradiation of strong infrared laser pulses, one electron tunnels through the laser-dressed Coulomb barrier, and the other bound electron has enough time to adapt to the potential of H2+ and thus is prone to transfer to the ground electronic state of H2+. In the intermediate regime, between the one photon and tunneling regimes, this electron-electron correlation depends strongly on the laser frequency, laser intensity and on the angle between laser polarization and the molecular axis.
机译:通过数值模拟与时间有关的四维Schrödinger方程,研究了在强XUV和红外激光脉冲作用下的H2的单光子电离和隧穿电离,该方程包括分子轴与激光偏振之间任意角度的两电子动力学方向。在H2的单光子电离中,一个电子快速逃逸,另一个电子不受干扰,但保留在 H 2 + 。在另一种情况下,在强红外激光脉冲的照射下,一个电子隧穿经过激光修饰的库仑势垒,而另一个被束缚的电子有足够的时间适应 H 2 + ,因此易于转移到 H 2 + 。在中间状态下,在一个光子和隧穿状态之间,这种电子电子相关性在很大程度上取决于激光频率,激光强度以及激光偏振与分子轴之间的夹角。

著录项

  • 期刊名称 Scientific Reports
  • 作者

    Wan-Yang Wu; Feng He;

  • 作者单位
  • 年(卷),期 -1(8),-1
  • 年度 -1
  • 页码 14933
  • 总页数 9
  • 原文格式 PDF
  • 正文语种
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