MOLECULAR-BOND HARDENING AND DYNAMICS OF MOLECULAR STABILIZATION AND TRAPPING IN INTENSE LASER-PULSES

被引:61
作者
YAO, GH
CHU, SI
机构
[1] Department of Chemistry, University of Kansas, Lawrence
来源
PHYSICAL REVIEW A | 1993年 / 48卷 / 01期
关键词
D O I
10.1103/PhysRevA.48.485
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We extend our previous study [Chem. Phys. Lett. 197, 413 (1992)] of the molecular stabilization in intense laser fields by considering the dynamical behavior of the H-2+ molecules in intense femtosecond short laser pulses at 775 nm. Significant stabilization and population trapping of high-lying vibrational states and chemical bond hardening are predicted for both continuous-wave (cw) lasers and short laser pulses. While the intensity dependences of the laser-induced stabilization are essentially the same for both cases, the detailed wave-packet localization dynamics is quite different. The correlation of the time-dependent dynamics with the time-independent Floquet complex quasienergy results, the probability for localization, the pulse-width dependence of molecular stabilization, the proton kinetic-energy spectrum, as well as the contrary dynamical response of low- and high-lying states, are studied at length for intense short laser pulses. In addition, the dynamic origin of ''bond-softening'' (for low-lying vibrational states) and ''bond-hardening'' (for high-lying vibrational states) effects in intense laser fields are explored.
引用
收藏
页码:485 / 494
页数:10
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