Time-dependent density-functional study of the alignment-dependent ionization of acetylene and ethylene by strong laser pulses

被引:26
作者
Russakoff, Arthur [1 ]
Bubin, Sergiy [2 ]
Xie, Xinhua [3 ]
Erattupuzha, Sonia [3 ]
Kitzler, Markus [3 ]
Varga, Kalman [1 ]
机构
[1] Vanderbilt Univ, Dept Phys & Astron, Nashville, TN 37235 USA
[2] Nazarbayev Univ, Sch Sci & Technol, Dept Phys, Astana 010000, Kazakhstan
[3] Vienna Univ Technol, Photon Inst, A-1040 Vienna, Austria
来源
PHYSICAL REVIEW A | 2015年 / 91卷 / 02期
基金
美国国家科学基金会; 奥地利科学基金会;
关键词
HIGH HARMONIC-GENERATION; MULTIPLE ORBITALS; ELECTRON LOCALIZATION; ENHANCED IONIZATION; DIATOMIC-MOLECULES; TUNNEL IONIZATION; ALIGNED MOLECULES; COULOMB EXPLOSION; FIELD-IONIZATION; DYNAMICS;
D O I
10.1103/PhysRevA.91.023422
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The alignment-dependent ionization of acetylene and ethylene in short laser pulses is investigated in the framework of the time-dependent density-functional theory coupled with Ehrenfest dynamics. The molecular alignment is found to have a substantial effect on the total ionization. Bond stretching is shown to cause an increase of the ionization efficiency, i.e., enhanced ionization, in qualitative agreement with previous theoretical investigations. It is also demonstrated that the enhanced ionization mechanism greatly enhances the ionization from the inner valence orbitals, and the ionization of the inner orbitals is primarily due to their extended weakly bound density tails.
引用
收藏
页数:11
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