中国物理B ›› 2024, Vol. 33 ›› Issue (12): 123401-123401.doi: 10.1088/1674-1056/ad7c2b

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Momentum distributions of symmetric (H2+) and asymmetric (HeH2+) molecular ions in a circularly polarized laser field under different ionization mechanisms

Xin-Yu Hao(郝欣宇), Shu-Juan Yan(闫淑娟), Ying Guo(郭颖), and Jing Guo(郭静)†   

  1. Institute of Atomic and Molecular Physics, Jilin University, Changchun 130012, China
  • 收稿日期:2024-05-13 修回日期:2024-09-11 接受日期:2024-09-18 发布日期:2024-11-12
  • 通讯作者: Jing Guo E-mail:gjing@jlu.edu.cn
  • 基金资助:
    Project supported by the Natural Science Foundation of Jilin Province (Grant No. 20220101010JC) and the National Natural Science Foundation of China (Grant No. 12074146).

Momentum distributions of symmetric (H2+) and asymmetric (HeH2+) molecular ions in a circularly polarized laser field under different ionization mechanisms

Xin-Yu Hao(郝欣宇), Shu-Juan Yan(闫淑娟), Ying Guo(郭颖), and Jing Guo(郭静)†   

  1. Institute of Atomic and Molecular Physics, Jilin University, Changchun 130012, China
  • Received:2024-05-13 Revised:2024-09-11 Accepted:2024-09-18 Published:2024-11-12
  • Contact: Jing Guo E-mail:gjing@jlu.edu.cn
  • Supported by:
    Project supported by the Natural Science Foundation of Jilin Province (Grant No. 20220101010JC) and the National Natural Science Foundation of China (Grant No. 12074146).

摘要: By numerically solving the two-dimensional (2D) time-dependent Schrödinger equation (TDSE), we present photoelectron momentum distributions (PMDs) and photoelectron angular distributions (PADs) of symmetric (${{\rm H}_{2}^{+}}$) and asymmetric (${{\rm HeH}^{2+}}$) molecular ions in circularly polarized (CP) laser pulses. By adjusting the laser wavelength, two circumstances of resonance excitation and direct ionization were considered. The ionization mechanism of the resonance excitation was mainly investigated. The results show that the PMDs of ${{\rm H}_{2}^{+}}$ and ${{\rm HeH}^{2+}}$ in the $y$-direction gradually increase with increasing intensity, and the number of PMDs lobes is in good agreement with the results predicted by the ultrafast ionization model. In the resonance excitation scenario, the PMDs of ${{\rm H}_{2}^{+}}$ are dominated by two-photon ionization, whereas the PMDs of HeH$^{2+}$ are dominated by three-photon ionization. Furthermore, the PMDs of ${{\rm HeH}^{2+}}$ are stronger in the resonance excitation scenario than those of ${{\rm H}_{2}^{+}}$, which can be explained by the time-dependent population of electrons. In addition, the molecular structure is clearly imprinted onto the PMDs.

关键词: resonance excitation, time-dependent Schrödinger equation, ultrafast ionization model, photoelectron momentum distributions

Abstract: By numerically solving the two-dimensional (2D) time-dependent Schrödinger equation (TDSE), we present photoelectron momentum distributions (PMDs) and photoelectron angular distributions (PADs) of symmetric (${{\rm H}_{2}^{+}}$) and asymmetric (${{\rm HeH}^{2+}}$) molecular ions in circularly polarized (CP) laser pulses. By adjusting the laser wavelength, two circumstances of resonance excitation and direct ionization were considered. The ionization mechanism of the resonance excitation was mainly investigated. The results show that the PMDs of ${{\rm H}_{2}^{+}}$ and ${{\rm HeH}^{2+}}$ in the $y$-direction gradually increase with increasing intensity, and the number of PMDs lobes is in good agreement with the results predicted by the ultrafast ionization model. In the resonance excitation scenario, the PMDs of ${{\rm H}_{2}^{+}}$ are dominated by two-photon ionization, whereas the PMDs of HeH$^{2+}$ are dominated by three-photon ionization. Furthermore, the PMDs of ${{\rm HeH}^{2+}}$ are stronger in the resonance excitation scenario than those of ${{\rm H}_{2}^{+}}$, which can be explained by the time-dependent population of electrons. In addition, the molecular structure is clearly imprinted onto the PMDs.

Key words: resonance excitation, time-dependent Schrödinger equation, ultrafast ionization model, photoelectron momentum distributions

中图分类号:  (Molecular excitation and ionization)

  • 34.80.Gs
32.80.-t (Photoionization and excitation) 31.15.xv (Molecular dynamics and other numerical methods) 42.65.Re (Ultrafast processes; optical pulse generation and pulse compression)