Electron angular correlation in nonsequential double ionization of molecules by counter-rotating two-color circularly polarized fields

  • Chen Z
  • Su J
  • Zeng X
  • et al.
13Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Electron correlation in nonsequential double ionization (NSDI) of molecules by counter-rotating two-color circularly polarized (TCCP) fields is investigated with a three-dimensional classical ensemble model. Numerical results indicate that the two electrons from NSDI of molecules in counter-rotating TCCP fields show strong angular correlation and the angular correlation behavior sensitively depends on the internuclear distance. With the internuclear distance increasing, the dominant behavior of electron pairs evolves from correlation to anti-correlation. It leaves a clear imprint on the ion momentum distributions, which exhibit an inverted Y-shape distribution at a small internuclear distance and a triangle-shape distribution at a large internuclear distance. Back analysis indicates that the asymmetric electron energy sharing by soft recollision and longer time delay of double ionization are responsible for more anti-correlated emissions at large internuclear distances.

Cite

CITATION STYLE

APA

Chen, Z., Su, J., Zeng, X., Huang, X., Li, Y., & Huang, C. (2021). Electron angular correlation in nonsequential double ionization of molecules by counter-rotating two-color circularly polarized fields. Optics Express, 29(18), 29576. https://doi.org/10.1364/oe.439864

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free