Timing Correlated-Electron Emission from Strong Field Atomic Double Ionization with Polarization-Gated Attoclock.

Attoclock provides a powerful tool for probing the ultrafast electron dynamics in strong laser fields. However, this technique has remained restricted to single electron or sequential double ionized electron dynamics. Here, we propose a novel attoclock scheme with a polarization-gated few-cycle laser pulse and demonstrate its application in timing the correlated-electron emission in strong field double ionization of argon.

Manipulating polarization effect in nonsequential double ionization.

We report on a theoretical study of nonsequential double ionization (NSDI) of magnesium atoms by using combined linearly and circularly polarized fields. By employing a concise model including the dynamic ionic dipole potential, we show that the polarization effects can be controlled by tuning the subcycle waveform of the electric field of the two-color pulses. We demonstrate that the influence of the dipole potential on NSDI depends on the symmetry of two-color laser fields by tracing back the electron trajectories.

Nonsequential double ionization of alkaline-earth metal atoms by intense mid-infrared femtosecond pulses.

A systematic study of nonsequential double ionization (NSDI) of alkaline-earth metal atoms with mid-infrared femtosecond pulses is reported. We find that the measured NSDI yield shows a strong target dependence and it is more suppressed for alkaline-earth metal with higher ionization potential. The observation is attributed to the differences in the recollision induced excitation and ionization cross sections of alkaline-earth metals.

Ionization suppression of diatomic molecules in an intense midinfrared laser field.

Diatomic molecules (e.g., O(2)) in an intense laser field exhibit a peculiar suppressed ionization behavior compared to their companion atoms.