| نویسندگان | عزیزمراد کوشکی,R Sadighi-Bonabi,محسن محسن نیا,ایرانی |
| نشریه | The Journal of Chemical Physics |
| شماره صفحات | 144306 |
| شماره مجلد | 148 |
| ضریب تاثیر (IF) | 2.997 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2018-04-13 |
| رتبه نشریه | علمی - پژوهشی |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
| نمایه نشریه | SCOPUS ,JCR |
چکیده مقاله
In the present work, an efficient method is theoretically investigated for extending high-order harmonics and ultrashort attosecond pulse generation in N2 and CO molecules by using the time-dependent density functional theory approach. Our results show that by utilizing chirped laser field in the presence of a low frequency field, not only is the harmonic cutoff extended remarkably but also the single short quantum trajectory is selected to contribute to the harmonic spectra. When a low frequency field is added to the two-color chirped laser field, the long quantum trajectories are suppressed and only the short quantum trajectories contribute to the higher harmonic emission mechanism. As a result, the spectral modulation is significantly decreased and an intense ultrashort pulse can be generated from the supercontinuum region of high harmonics. With such a scheme, the isolated ultrashort attosecond pulses can be generated in length, velocity, and acceleration gauges. Furthermore, these results are explained by using the classical and quantum time-frequency analyses.