Stereocontrol of attosecond time-scale electron dynamics in ABCU using ultrafast laser pulses: a computational study

被引:29
|
作者
Mignolet, B. [2 ]
Gijsbertsen, A. [1 ]
Vrakking, M. J. J. [1 ,3 ]
Levine, R. D. [4 ,5 ,6 ,7 ]
Remacle, F. [2 ,4 ]
机构
[1] FOM Inst AMOLF, NL-1098 XG Amsterdam, Netherlands
[2] Univ Liege, Dept Chem, B-4000 Liege, Belgium
[3] Max Born Inst, D-12489 Berlin, Germany
[4] Hebrew Univ Jerusalem, Fritz Haber Ctr Mol Dynam, IL-91904 Jerusalem, Israel
[5] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, Crump Inst Mol Imaging, Los Angeles, CA 90095 USA
关键词
MULTIPLE ORBITALS; LINEAR-MOLECULES; IONIZATION; GENERATION; LOCALIZATION; SPECTROSCOPY; TRANSITION; ALIGNMENT;
D O I
10.1039/c1cp20094a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The attosecond time-scale electronic dynamics induced by an ultrashort laser pulse is computed using a multi configuration time dependent approach in ABCU (C10H19N), a medium size polyatomic molecule with a rigid cage geometry. The coupling between the electronic states induced by the strong pulse is included in the many electron Hamiltonian used to compute the electron dynamics. We show that it is possible to implement control of the electron density stereodynamics in this medium size molecule by varying the characteristics of the laser pulse, for example by polarizing the electric field either along the N-C axis of the cage, or in the plane perpendicular to it. The excitation produces an oscillatory, non-stationary, electronic state that exhibits localization of the electron density in different parts of the molecule both during and after the pulse. The coherent oscillations of the non-stationary electronic state are also demonstrated through the alternation of the dipole moment of the molecule.
引用
收藏
页码:8331 / 8344
页数:14
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