We investigate the Rydberg states generation of Hydrogen atoms with intense laser pulses, by solving the time-dependent Schrodinger equation and by means of classical trajectory monte-carlo simulations. Both linearly polarized multi-cycle pulses and
pairs of optical half cycle pulses are used. Comparisons between these methods show that both the Coulomb force and initial lateral momentum, which have effects on the $n$-distribution and $l$-distribution of the population of excited states, are important in the generation of Rydberg states.
We identify that both the dynamic core polarization and dynamic orbital deformation are important in the orientation-dependent high-harmonic generation of CO molecules subjected to intense few cycle laser fields. These polarization dynamics allow for
the observation of strong orientation effects and dynamic minimum in the harmonic spectra. The generated attosecond pulses can be greatly affected by these multielectron effects. This work sheds light on future development of dynamic orbital imaging on attosecond time scale.
The ionization of two-active-electron systems by intense laser fields is investigated theoretically. In comparison with time-dependent Hartree-Fock and exact two electron simulation, we show that the ionization rate is overestimated in SAE approximat
ion. A modified single-active-electron model is formulated by taking into account of the dynamical core polarization. Applying the new approach to Ca atoms, it is found that the polarization of the core can be considered instantaneous and the large polarizability of the cation suppresses the ionization by 50% while the photoelectron cut-off energy increases slightly. The existed tunneling ionization formulation can be corrected analytically by considering core polarization.
The orientation-dependent strong-field ionization of CO molecules is investigated using the fully propagated three-dimensional time-dependent Hartree-Fock theory. The full ionization results are in good agreement with recent experiments. The comparis
ons between the full method and single active orbital (SAO) method show that although the core electrons are generally more tightly bounded and contribute little to the total ionization yields, their dynamics cannot be ignored, which effectively modify the behaviors of electrons in the highest occupied molecular orbital. By incorporating it into the SAO method, we identify that the dynamic core polarization plays an important role in the strong-field tunneling ionization of CO molecules, which is helpful for future development of tunneling ionization theory of molecules beyond single active electron approximation.
