We find that Coulomb focusing persists even when the Coulomb field is barely noticeable compared with the laser field. Delayed recollisions proliferate in this regime and bring back energy slightly above the 3.17 U_p high-harmonic cutoff, in stark co
ntradiction with the Strong Field Approximation. We investigate the nonlinear-dynamical phase space structures which underlie this dynamics. It is found that the energetic delayed recollisions are organized by a reduced number of periodic orbits and their invariant manifolds.
We revisit the stabilization of ionization of atoms subjected to a superintense laser pulse using nonlinear dynamics. We provide an explanation for the lack of complete ionization at high intensity and for the decrease of the ionization probability a
s intensity is increased. We investigate the role of each part of the laser pulse (ramp-up, plateau, ramp-down) in this process. We emphasize the role of the choice for the ionization criterion, energy versus distance criterion.
The uncorrelated (``sequential) and correlated (``nonsequential) double ionization of the H2 molecule in strong laser pulses is investigated using the tools of nonlinear dynamics. We focus on the phase-space dynamics of this system, specifically by f
inding the dynamical structures that regulate these ionization processes. The emerging picture complements the recollision scenario by clarifying the distinct roles played by the recolliding and core electrons. Our analysis leads to verifiable predictions of the intensities where qualitative changes in ionization occur. We also show how these findings depend on the internuclear distance.
Both uncorrelated (sequential) and correlated (nonsequential) processes contribute to the double ionization of the helium atom in strong laser pulses. The double ionization probability has a characteristic knee shape as a function of the intensity of
the pulse. We investigate the phase-space dynamics of this system, specifically by finding the dynamical structures that regulate the ionization processes. The emerging picture complements the recollision scenario by clarifying the distinct roles played by the recolliding and core electrons. Our analysis leads to verifiable predictions of the intensities where qualitiative changes in ionization occur, leading to the hallmark knee shape.
Finding the causes for the nonstatistical vibrational energy relaxation in the planar carbonyl sulfide (OCS) molecule is a longstanding problem in chemical physics: Not only is the relaxation incomplete long past the predicted statistical relaxation
time, but it also consists of a sequence of abrupt transitions between long-lived regions of localized energy modes. We report on the phase space bottlenecks responsible for this slow and uneven vibrational energy flow in this Hamiltonian system with three degrees of freedom. They belong to a particular class of two-dimensional invariant tori which are organized around elliptic periodic orbits. We relate the trapping and transition mechanisms with the linear stability of these structures.
We investigate the response of two three-body Coulomb systems when driven by attosecond half-cycle pulses: The hydrogen molecular ion and the helium atom. Using very short half-cycle pulses (HCPs) which effectively deliver ``kicks to the electrons, w
e first study how a carefully chosen sequence of HCPs can be used to control to which of one of the two fixed atomic centers the electron gets re-attached. Moving from one electron in two atomic centers to two electrons in one atomic center we then study the double ionization from the ground state of He by a sequence of attosecond time-scale HCPs, with each electron receiving effectively a ``kick from each HCP. We investigate how the net electric field of the sequence of HCPs affects the total and differential ionization probabilities.
We discuss the influence of periodic orbits on the dissociation of a model diatomic molecule driven by a strong bichromatic laser fields. Through the stability of periodic orbits we analyze the dissociation probability when parameters like the two am
plitudes and the phase lag between the laser fields, are varied. We find that qualitative features of dissociation can be reproduced by considering a small set of short periodic orbits. The good agreement with direct simulations demonstrates the importance of bifurcations of short periodic orbits in the dissociation dynamics of diatomic molecules.
We investigate the multiphoton ionization of hydrogen driven by a strong bichromatic microwave field. In a regime where classical and quantum simulations agree, periodic orbit analysis captures the mechanism: Through the linear stability of periodic
orbits we match qualitatively the variation of experimental ionization rates with control parameters such as the amplitudes of the two modes of the field or their relative phases. Moreover, we discuss an empirical formula which reproduces quantum simulations to a high degree of accuracy. This quantitative agreement shows the mechanism by which short periodic orbits organize the dynamics in multiphoton ionization. We also analyze the effect of longer pulse durations. Finally we compare our results with those based on the peak amplitude rule. Both qualitative and quantitative analyses are implemented for different mode locked fields. In parameter space, the localization of the period doubling and halving allows one to predict the set of parameters (amplitudes and phase lag) where ionization occurs.
Vibrational energy flows unevenly in molecules, repeatedly going back and forth between trapping and roaming. We identify bottlenecks between diffusive and chaotic behavior, and describe generic mechanisms of these transitions, taking the carbonyl su
lphide molecule OCS as a case study. The bottlenecks are found to be lower-dimensional tori; their bifurcations and unstable manifolds govern the transition mechanisms.
