Molecular high-order harmonic generation in a nonlinear two-electron molecule: the equilateral H3+

被引:24
作者
Tchitchekova, Deyana S. [1 ]
Lu, Huizhong [1 ]
Chelkowski, Szczepan [1 ]
Bandrauk, Andre D. [1 ]
机构
[1] Univ Sherbrooke, Fac Sci, Dept Chim, Sherbrooke, PQ J1K 2R1, Canada
关键词
FIELDS ENHANCED IONIZATION; LASER FIELDS; SINGLE; MODEL; IONS;
D O I
10.1088/0953-4075/44/6/065601
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Molecular high-order harmonic generation (MHOHG) is studied from appropriate time-dependent Schrodinger equation (TDSE) solutions of a 2D equilateral two-electron H-3(+) molecular ion in interaction with an intense (5 x 10(14) W cm(-2)) few-cycle 800 nm linearly polarized laser pulse. The nonperturbative time-dependent Born-Oppenheimer (static nuclei) two-electron wavefunction is used to calculate the MHOHG spectrum as a function of the laser-molecule orientation and internuclear distance R. Three-centre interferences in the MHOHG spectrum are shown to be sensitive functions of the laser-molecule orientation and R. A comparison is made of the MHOHG spectrum at the ground state equilibrium distance, R-e, at an intermediate R where a three-photon transition ((1)A(1)' -> E-1') occurs, and finally at internuclear distance R-c where enhanced ionization can occur due to the nonlinear electron-laser interaction. Analytic expressions for MHOHG spectra interferences are derived based on a recollision model and are compared to the exact 2D TDSE simulations.
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页数:9
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