A semi-classical model is utilized to explain the dissociation control of the hydrogen molecular ion （H^-）. By ana- lyzing the curve of the dissociation asymmetry parameter as a function of the time delay between the exciting and steering pulses, we find that the dissociation control is dependent not only on the peak intensity and direction of the electric field of the steering pulse, but also on the peak intensity of the exciting pulse.
The molecular dissociation with a two-laser-pulse scheme is theoretically investigated for the hydrogen molecular ion（H2^＋） and its isotopes（HD^＋and HT^＋）. The terahertz pulse is used to steer the electron motion after it has been excited by an ultrashort ultraviolet laser pulse and an unprecedented electron localization ratio can be achieved. With the coupled equations, the mass effect of the nuclei on the effective time of the electron localization control is discussed.
The influence of the carrier-envelope phase on high-harmonic generation is investigated, both experimentally and theoretically, for three different interaction gas media, driven by mid-infrared, few-cycle and CEP-stabiUzed laser pulses. Different patterns of harmonic spectra with varying CEP for the three interaction gas media are observed. Furthermore, in comparing our experiment results to the previous works driven by near-infrared laser pulses, different phenomena are found. Through numerical simulation, we find that for the two different kinds of driving fields, i.e. mid-infrared and near-infrared laser pulses, different kinds of electron trajectories contribute to the generation of high harmonics.
We experimentally and theoretically demonstrate that ＊~he property （odd or even） of generated harmonics can be selected by manipulating the macroscopic phase-matching conditions based on a three-color laser field. Only odd or even harmonics can be made dominant by changing the focal position and adjusting the gas pressure. These results indicate that the odd-even property of the generated harmonics can be controlled by using the mult i-color laser field with macroscopic phase-matching.
We report on a systematic experimental study on the fluorescence spectra produced from a femtosecond laser filament in air under a high electric field. The electric field alone was strong enough to create corona discharge(CD). Fluorescence spectra from neutral and ionic air molecules were measured and compared with pure high-voltage CD and pure laser filamentation(FIL). Among them, high electric field assisted laser FIL produced nitrogen fluorescence more efficiently than either pure CD or pure FIL processes. The nonlinear enhancement of fluorescence from the interaction of the laser filament and corona discharging electric field resulted in a more efficient ionization along the laser filament zone, which was confirmed by the spectroscopic measurement of both ionization-induced fluorescence and plasma-scattered 800 nm laser pulses. This is believed to be the key precursor process for filament-guided discharge.
Using a nonperturbative quantum electrodynamics theory of high-order harmonic generation （HHG）, a scaling law of HHG is established. The scaling law states that when the atomic binding energy Eb, the wavelength ）, and the intensity I of the laser field change simultaneously to kEb, λ/k, and k3I, respectively. The characteristics of the HHG spectrum remain unchanged, while the harmonic yield is enhanced k3 times. That HHG obeys the same scaling law with above-threshold ionization is a solid proof of the fact that the two physical processes have similar physical mechanisms. The variation of integrated harmonic yields is also discussed.
