Vector momentum distributions of Ne(n+) (n = 1,2,3) ions created by 30 fs, approximately 1 PW/cm(2) laser pulses at 795 nm have been measured using recoil-ion momentum spectroscopy. Distinct maxima along the light polarization axis are observed at 4.0 and 7.5 a.u. for Ne2+ and Ne3+ production, respectively. Hence, mechanisms based on an instantaneous release of two (or more) electrons can be ruled out as a dominant contribution to nonsequential strong-field multiple ionization. The positions of the maxima are in accord with kinematical constraints set by the classical "rescattering model."

Vector momentum distributions of two electrons created in double ionization of Ar by 25 fs, 0.25 PW/cm(2) laser pulses at 795 nm have been measured using a "reaction microscope." At this intensity, where nonsequential ionization dominates, distinct correlation patterns are observed in the two-electron momentum distributions. A kinematical analysis of these spectra within the classical "recollision model" revealed an (e,2e)-like process and excitation with subsequent tunneling of the second electron as two different ionization mechanisms. This allows a qualitative separation of the two mechanisms demonstrating that excitation-tunneling is the dominant contribution to the total double ionization yield.

We observe fragmentation of H2 molecules exposed to strong laser fields into excited neutral atoms. The measured excited neutral fragment spectrum resembles the ionic fragmentation spectrum including peaks due to bond softening and Coulomb explosion. To explain the occurrence of excited neutral fragments and their high kinetic energy, we argue that the recently investigated phenomenon of frustrated tunnel ionization is also at work in the neutralization of H+ ions into excited H atoms. In this process the tunneled electron does not gain enough drift energy from the laser field to escape the Coulomb potential and is recaptured. Calculation of classical trajectories as well as a correlated detection measurement of neutral excited H and H+ ions support the mechanism.

A method is proposed for the calculation of the S matrix for many-electron processes in intense-laser atom physics, in close analogy to the strong-field approximation for one-electron processes. Given a scenario of how some process evolves, corresponding approximations to the classical action are made which allow for the evaluation of the quantum-mechanical S matrix. The method is applied to the distribution of the total electronic momentum in nonsequential double ionization, and the results are compared to recent measurements. Good agreement is obtained for neon for a rescattering scenario. There is no comparable agreement for helium and argon, and possible alternative scenarios are discussed.

A charged particle exposed to an oscillating electric field experiences a force proportional to the cycle-averaged intensity gradient. This so-called ponderomotive force plays a major part in a variety of physical situations such as Paul traps for charged particles, electron diffraction in strong (standing) laser fields (the Kapitza-Dirac effect) and laser-based particle acceleration. Comparably weak forces on neutral atoms in inhomogeneous light fields may arise from the dynamical polarization of an atom; these are physically similar to the cycle-averaged forces. Here we observe previously unconsidered extremely strong kinematic forces on neutral atoms in short-pulse laser fields. We identify the ponderomotive force on electrons as the driving mechanism, leading to ultrastrong acceleration of neutral atoms with a magnitude as high as approximately 10(14) times the Earth's gravitational acceleration, g. To our knowledge, this is by far the highest observed acceleration on neutral atoms in external fields and may lead to new applications in both fundamental and applied physics.

By the employment of "constant-scaled-energy spectroscopy" as a novel spectroscopic technique, the quasi-Landau resonance system of the diamagnetic H atom in even-partity m=0 magnetic final states is observed for the first time in its entirety from the regular \/n into the chaotic quasi-Landau regime. It evolves, fully unexpectedly, into a systematically structured hierarchy of generations of resonances, correlated to three physically different types of closed classical orbits.PACS numbers: 32.80. -t, 05.45.+b, 32.60.+i The physics of the highly excited diamagnetic hydrogen atom has recently attracted much attention, 1 " 8 largely because this simple nonseparable quantum system turns classically chaotic as it approaches the ionization limit. 6,9 In this context the quasi-Landau (QL) oscillations and their correlation to classical periodic orbits are of particular interest. 10 Until recently, it was accepted that only one QL resonance type, discovered by Garton and Tomkins, n exists. Experiments with the H atom 3 " 5 and theoretical studies 7,8,12,13 have uncovered further, basically new resonances correlated with threedimensional orbits. Nevertheless, the central question as to the entire set of QL resonances resulting from final states with a given m quantum number and parity evolving from the regular into the chaotic QL regime has remained open.We have addressed this basic problem and studied the H-atom Balmer spectrum with even-parity m=0 magnetic final states as a function of both the excitation energy E and the magnetic field B y employing for the first time "constant-scaled-energy spectroscopy." Different from previous experiments at constant Z?, 3 " 5 this technique makes a systematic search for, in principal, all possible QL resonances associated with closed classical orbits. 12 In analogy to theoretical work, it is based on the scaling property of the classical Hamiltonian 14

We report differential measurements of Ar++ ion momentum distributions from nonsequential double ionization in phase-stabilized few-cycle laser pulses. The distributions depend strongly on the carrier-envelope (CE) phase. Via control over the CE phase one is able to direct the nonsequential double-ionization dynamics. Data analysis through a classical model calculation reveals that the influence of the optical phase enters via (i) the cycle dependent electric field ionization rate, (ii) the electron recollision time, and (iii) the accessible phase space for inelastic collisions. Our model indicates that the combination of these effects allows a look into single cycle dynamics already for few-cycle pulses.

Abstract. We use correlated electron-ion momentum measurement to investigate laser induced non-sequential double ionization of Ar and Ne. Light intensities are chosen in a regime at and below the threshold where, within the rescattering model, electron impact ionization of the singly charged ion core is expected to become energetically forbidden. Yet, we find Ar ++ ion momentum distributions and an electron-electron momentum correlation indicative of direct impact ionization. Within the quasistatic model this may be understood by assuming that the electric field of the light wave reduces the ionization potential of the singly charged ion core at the instant of scattering. The width of the projection of the ion momentum distribution onto an axis perpendicular to the light beam polarization vector is found to scale with the square root of the peak electric field strength in the light pulse. A scaling like this is not expected from the phase space available after electron impact ionization. It may indicate that the electric field at the instant of scattering is usually different from zero and determines the transverse momentum distribution. A comparison of our experimental results with several theoretical results is given.