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

Electron angular correlation in nonsequential double ionization of molecules by counter-rotating two-color circularly polarized fields.
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DOI:
10.1364/oe.439864
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发表时间:
2021-08
期刊:
影响因子:
3.8
通讯作者:
Zhen-Cheng Chen;Jie Su;X. Zeng;Xuefei Huang;Yingbin Li;Cheng Huang
Zhen-Cheng Chen;Jie Su;X. Zeng;Xuefei Huang;Yingbin Li;Cheng Huang
中科院分区:
物理与天体物理2区
文献类型:
--
作者:
Zhen-Cheng Chen;Jie Su;X. Zeng;Xuefei Huang;Yingbin Li;Cheng Huang

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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.