The laser-field-modified dipole response of the first ionization threshold of helium is studied by means of attosecond transient absorption spectroscopy. We resolve light-induced time-dependent structures in the photoabsorption spectrum both below and above the ionization threshold. By comparing the measured results to a quantum-dynamical model, we isolate the contributions of the unbound electron to these structures. They originate from light-induced couplings of near-threshold bound and continuum states and light-induced energy shifts of the free electron. The ponderomotive energy, at low laser intensities, is identified as a good approximation for the perturbed continuum response.

Two-electron dynamics of an excited model atom interacting with moderately strong laser fields is analyzed in the time domain. We solve the time-dependent Schrödinger equation (TDSE) for two electrons confined to the same one-dimensional configuration space, accounting also for the electronelectron interaction. The computational method allows direct access to the time-dependent population of the relevant atomic states during and right after the interaction with a near-infrared (NIR) laser pulse. We compare the ionization dynamics of singly excited states and doubly excited states. We find that doubly-excited initial states exhibit enhanced double ionization yield, with non-trivial dynamics including contributions from direct and sequential processes, while the electrons leave the atom either back-to-back or in the same direction.

We present a compact velocity-map imaging (VMI) spectrometer for photoelectron imaging at 100 MHz repetition rate. Ultrashort pulses from a near-infrared frequency comb laser are amplified in a polarization-insensitive passive femtosecond enhancement cavity. In the focus, multi-photon ionization (MPI) of gas-phase atoms is studied tomographically by rotating the laser polarization. We demonstrate the functioning of the VMI spectrometer by reconstructing photoelectron angular momentum distributions from xenon MPI. Our intra-cavity VMI setup collects electron energy spectra at high rates, with the advantage of transferring the coherence of the cavity-stabilized femtosecond pulses to the electrons. In addition, the setup will allow studies of strong-field effects in nanometric tips.

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