Correlated two-electron momentum spectra for strong-field nonsequential double ionization of He at 800 nm.

We report on a kinematically complete experiment on nonsequential double ionization of He by 25 fs 800 nm laser pulses at 1.5 PW/cm;{2}. The suppression of the recollision-induced excitation at this high intensity allows us to address in a clean way direct (e,2e) ionization by the recolliding electron. In contrast with earlier experimental results, but in agreement with various theoretical predictions, the two-electron momentum distributions along the laser polarization axis exhibit a pronounced V-shaped structure, which can be explained by the role of Coulomb repulsion and typical (e,2e) kinematics.

Complete characterization of molecular dynamics in ultrashort laser fields.

Reaction Microscope-based, complete, and time-resolved Coulomb explosion imaging of vibrating and dissociating D(2)(+) molecules with femtosecond time-resolution allowed us to perform an internuclear distance (R-)dependent Fourier analysis of the corresponding wave packets. Calculations demonstrate that the obtained two-dimensional R-dependent frequency spectra enable the complete characterization of the wave packet dynamics and directly visualize the field-modified molecular potential curves in intense, ultrashort laser pulses.

Few-photon multiple ionization of ne and ar by strong free-electron-laser pulses.

Few-photon multiple ionization of Ne and Ar atoms by strong vacuum ultraviolet laser pulses from the free-electron laser at Hamburg was investigated differentially with the Heidelberg reaction microscope. The light-intensity dependence of Ne2+ production reveals the dominance of nonsequential two-photon double ionization at intensities of I<6x10(12) W/cm2 and significant contributions of three-photon ionization as I increases. Ne2+ recoil-ion-momentum distributions suggest that two electrons absorbing "instantaneously" two photons are ejected most likely into opposite hemispheres with similar energies.

Spatiotemporal imaging of ultrafast molecular motion: collapse and revival of the D+2 nuclear wave packet.

We report on a real-time imaging of the ultrafast D(+)2 rovibrational nuclear wave-packet motion performed using a combination of a pump-probe setup with 7 fs laser pulses and a "reaction-microscope" spectrometer. We observe fast dephasing (collapse) of the vibrational wave packet and its subsequent revival and prove rotational excitation in ultrashort laser pulses. Channel-selective Fourier analysis of the wave packet's long-term (approximately 3000 fs) evolution allows us to resolve its individual constituents, revealing unique information on the mechanisms of strong-field ionization and dissociation.

Quantum-phase resolved mapping of ground-state vibrational D2 wave packets via selective depletion in intense laser pulses.

Applying 7 fs pump-probe pulses (780 nm, 4 x 10(14) W/cm2) we observe electronic ground-state vibrational wave packets in neutral D2 with a period of T=11.101(70) fs by following the internuclear separation (R-)dependent ionization with a sensitivity of Delta

Time-resolved imaging and manipulation of H2 fragmentation in intense laser fields.

We report on the experimental realization of time-resolved coincident Coulomb explosion imaging of H2 fragmentation in 10(14) W/cm(2) laser fields. Combining a high-resolution "reaction microscope" and a fs pump-probe setup, we map the motion of wave packets dissociating via one- or two-photon channels, respectively, and observe a new region of enhanced ionization. The long-term interferometric stability of our system allows us to extend pump-probe experiments into the region of overlapping pulses, which offers new possibilities for the manipulation of ultrafast molecular fragmentation dynamics.

Correlated multielectron dynamics in ultrafast laser pulse interactions with atoms.

We present the results of the detailed experimental study of multiple ionization of Ne and Ar by 25 and 7 fs laser pulses. Whereas in multiple ionization of Ar different mechanisms, involving field ionization steps and recollision-induced excitations, play a role, for Ne only one channel, where the highly correlated instantaneous emission of up to four electrons is triggered by a recollisional electron impact, is found to be important. Using few-cycle pulses we are able to suppress those processes that occur on time scales longer than one laser cycle.

Evidence for rescattering in intense, femtosecond laser interactions with a negative ion.

It is now well established that energetic electron emission, nonsequential ionization, and high harmonic generation, produced during the interaction of intense, femtosecond laser pulses with atoms (and atomic positive ions), can be explained by invoking rescattering of the active electron in the laser field, the so-called rescattering mechanism. In contrast for negative ions, the role of rescattering has not been established experimentally. By irradiating F- ions with ultrashort laser pulses, F+ ion yields as a function of intensity for both linearly and circularly polarized light have been measured. We find that, at intensities well below saturation for F+ production by sequential ionization, there is a small but significant enhancement in the yield for the case of linearly polarized light, providing the first clear experimental evidence for the existence of the rescattering mechanism in negative ions.