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

被引:18
作者
Chen, Zhenhao [1 ,2 ]
Su, Jie [1 ,2 ]
Zeng, Xue [1 ,2 ]
Huang, Xuefei [1 ,2 ]
Li, Yingbin [3 ]
Huang, Cheng [1 ,2 ]
机构
[1] Southwest Univ, Sch Phys Sci & Technol, Chongqing 400715, Peoples R China
[2] Southwest Univ, Chongqing Key Lab Micro & Nano Struct Optoelect, Chongqing 400715, Peoples R China
[3] Xinyang Normal Univ, Coll Phys & Elect Engn, Xinyang 464000, Peoples R China
基金
中国国家自然科学基金;
关键词
RESCATTERING; EMISSION; DYNAMICS; HELIUM; DRIVEN;
D O I
10.1364/OE.439864
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
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. (C) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:29576 / 29586
页数:11
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