We report the first theoretical study of the structure of laser-induced vibrational quasi-energy (VQE) resonance states of D: in intense one-and two-color (fundamental and its third harmonic) laser fields by means of the complex-scaling generalized Fourier-grid Floquet Hamiltonian technique. Stabili
Laser-induced molecular stabilization and trapping and chemical bond hardening in intense laser fields
✍ Scribed by Guanhua Yao; Shih-I Chu
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 542 KB
- Volume
- 197
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
We study the intensity-dependent behavior of laser-induced vibrational quasi-energy (VQE) resonance structure and photodissociation rates of H: molecular ions in intense laser fields at 775 nm and report a novel new high-intensity phenomenon. At strong fields, the vibrational levels are shifted and broadened substantially and break into several separate VQE resonance groups. distortion of the internuclear potential by the fields leads to the formation of various (field-dressed) adiabatic potential wells near multiphoton resonances which can support long-lived resonance states. The most striking finding is that high-lying VQE resonance states can in fact become more stabilized and longer lived at higher laser intensities, a phenomenon which may be termed as "bond hardening". Time-dependent calculations confirm the laser-induced stabilization phenomenon and reveals that molecular population may be trapped simultaneously in different potential wells, at different internuclear separations (multiple well trapping).
📜 SIMILAR VOLUMES
The time-dependent Schrodinger equation for the 1-D H q molecule ¨2 Ž . with both nuclear and electronic degrees of freedom included was solved numerically. A wave᎐function splitting technique was used, which allows one to circumvent the problem of lost information due to commonly used absorbing bou