Attosecond molecular spectroscopy -: The one-electron H2+ system

被引:1
作者
Bandrauk, AD [1 ]
Nguyen, HS
机构
[1] Univ Sherbrooke, Chim Theor Lab, Fac Sci, Sherbrooke, PQ J1K 2R1, Canada
[2] Univ Sherbrooke, Canada Res Chair Computat Chem & Photon, Sherbrooke, PQ J1K 2R1, Canada
关键词
attosecond spectroscopy; attosecond photoionization;
D O I
10.1139/V04-080
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Numerical solutions of the time-dependent Schrodinger equation for a 1-D model non-Born-Oppenheimer H-2(+) are used to illustrate the nonlinear, nonperturbative response of molecules to intense (I greater than or equal to 10(13) W/cm(2)), ultrashort (t < 10 fs) laser pulses. Molecular high-order harmonic generation (MHOHG) is shown to be an example of such response, and the resulting nonlinear photon emission spectrum is shown to lead to the synthesis of single attosecond (10(-18) s) pulses. Application of such ultrashort pulses to the H-2(+) system results in localized electron wave packets whose motion can be detected by asymmetry in the photoelectron spectrum generated by a subsequent probe attosecond pulse, thus leading to measurement of electron motion in molecules on an attosecond time scale.
引用
收藏
页码:831 / 836
页数:6
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