| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5392106 | Chemical Physics Letters | 2006 | 6 Pages |
Abstract
A theoretical approach used for studying the multiphoton ionization of NO molecule in two-color strong femtosecond pulse laser fields is proposed. Time- and energy-resolved photoelectron energy spectra are calculated for describing the photionization process. The NO molecule is first excited to the D2Σ+ Rydberg state. The pump and probe pulses then couple the D2Σ+ with M2Σ+ states via a two-photon Raman coupling and a laser-induced continuum structure state. Three channels from the D2Σ+ and M2Σ+ states to ionization state are described. The population transfers through the continuum state and the Raman coupling passage are also calculated.
Related Topics
Physical Sciences and Engineering
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Physical and Theoretical Chemistry
Authors
Sen-Ming Wang, Shu-Lin Cong, Kai-Jun Yuan, Ying-Yu Niu,