Internal collision induced strong-field nonsequential double ionization in molecules.

Using the classical ensemble method, we have investigated the alignment dependence of the correlated electron dynamics in strong-field nonsequential double ionization (NSDI) of diatomic molecules driven by linearly polarized laser pulses. Our numerical results show that the correlated electron pairs are more likely to emit into the same hemisphere (side-by-side emission) for the parallel aligned molecules at the small internuclear distance, in agreement with previous experimental results. Surprisingly, as the internuclear distance increases, this side-by-side emission is more prevalent for the perpendicularly aligned molecules. Back analyzing of the classical trajectories shows that a considerable part of the NSDI events for the parallel aligned molecules at the large internuclear distances occur through an internal collision, not the well-known recollision. In the internal collision induced NSDI, the first electron tunnels through the inner barrier from the up-field core, moves directly towards the other core, and kicks out the second electron. For this type of NSDI events, the electron pairs are more likely to emit into the opposite hemispheres and thus the correlated electron momentum spectrum exhibits a more dominant back-to-back behavior in the parallel aligned molecules.

Dissection of electron correlation in strong-field sequential double ionization using a classical model.

Recent experiments on strong-field sequential double ionization (SDI) have reported several observations which are regarded as evidence of electron correlation, querying the validity of the standard independent electron approximation for SDI. Here we theoretically study SDI with a classical ensemble model. The experimental results are well reproduced with this model. Back tracing of the ionization process shows that these results are ascribed to the subcycle ionization dynamics of the two electrons, not the evidences of the electron correlation in SDI. Thus, the previously reported observations are not enough to claim the breakdown of the independent electron approximation in SDI.

Transition of recollision trajectories from linear to elliptical polarization.

Using a classical ensemble method, we revisit the topic of recollision and nonsequential double ionization with elliptically polarized laser fields. We focus on how the recollision mechanism transitions from short trajectories with linear polarization to long trajectories with elliptical polarization. We propose how this transition can be observed by meansuring the carrier-envelop-phase dependence of the correlated electron momentum spectra using currently available few-cycle laser pulses.

Resolving subcycle electron emission in strong-field sequential double ionization.

Using a fully classical model, we have studied sequential double ionization (SDI) of argon driven by elliptically polarized laser pulses at intensities well in the over-barrier ionization region. The results show that ion momentum distributions evolve from the two-band structure to the four-band, six-band structure and finally to the previously obtained four-band structure as the pulse duration increases. Our analysis shows that the evolution of these band structures originates from the pulse-duration-dependent multiple ionization bursts of the second electron. These band structures unambiguously indicate the subcycle electron emission in SDI.

Electron dynamics of molecular double ionization by circularly polarized laser pulses.

Using the classical ensemble method, we have investigated double ionization (DI) of diatomic molecules driven by circularly polarized laser pulses with different internuclear distances (R). The results show that the DI mechanism changes from sequential double ionization (SDI) to nonsequential double ionization (NSDI) as the internuclear distance increases. In SDI range, the structure of the electron momentum distribution changes seriously as R increases, which indicates the sensitive dependence of the release times of the two electrons on R. For NSDI, because of the circular polarization, the ionization of the second electron is not through the well-known recollision process but through a process where the first electron ionizes over the inner potential barrier of the molecule, moves directly towards the other nucleus, and kicks out the second electron.

Correlated electron dynamics in nonsequential double ionization by orthogonal two-color laser pulses.

We have investigated the correlated electron dynamics in nonsequential double ionization (NSDI) of helium by the orthogonally polarized two-color pulses that consisted of an 800-nm and a 400-nm laser fields using the classical ensemble model. Depending on the relative phase of the two-color field, the electron momentum distributions along the polarization direction of the 800-nm field exhibit a surprisingly strong anticorrelated or correlated behavior. Back analysis reveals that recollisions eventually leading to NSDI are concentrated in a time window as short as several hundreds attoseconds with this scheme. By changing the relative phase of the two-color field, the revisit time of recolliding electron wave packet has been controlled with attosecond precision, which is responsible for the various correlated behaviors of the two electrons. Our results reveal that the orthogonally polarized two-color field can serve as a powerful tool to control the correlated electron dynamics in NSDI.

The effect of molecular alignment on correlated electron dynamics in nonsequential double ionization.

The electron-electron correlation in nonsequential double ionization (NSDI) from aligned molecules by linearly polarized 800 nm laser pulses has been investigated with the three-dimensional classical ensemble model. The result shows that for the perpendicular alignment the two electrons involved in NSDI more likely exit the molecule into the opposite hemispheres as compared to the parallel alignment, which agrees well with the experimental result [Phys. Rev. Lett. 95, 203003 (2005)]. This alignment effect is qualitatively explained based on the suppressed potential barriers which are different for parallel molecules and perpendicular molecules. Additionally, the intensity dependence of the alignment effect is also explored.

Internuclear-distance dependence of electron correlation in nonsequential double ionization of H(2).

Using three-dimensional classical ensembles, we have investigated the internuclear distance dependence of nonsequential double ionization (NSDI) of H(2) molecules by an 800 nm, 1x10(14) W/cm(2) laser pulse. For the internuclear distance R ranging from 2 to 12 a.u., the NSDI of H(2) provides rich correlation patterns in the two-electron momentum distributions. These correlation patterns essentially reveal different microscopic dynamics in NSDI process. Moreover, our calculations show that R approximately 4 a.u. is the critical distance for double ionization yield of H(2). These results are qualitatively explained based on the classical barrier expression model and back analysis.