Abstract

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. Furthermore, we propose a method allowing for manipulating the returning trajectories with the initial direction of the tunneled electrons almost unchanged.

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