Effect of the finite speed of light in ionization of extended molecular systems.

We study propagation effects due to the finite speed of light in ionization of extended molecular systems. We present a general quantitative theory of these effects and show under which conditions such effects should appear. The finite speed of light propagation effects are encoded in the non-dipole terms of the time-dependent Shrödinger equation and display themselves in the photoelectron momentum distribution projected on the molecular axis.

Attosecond Molecular Angular Streaking with All-Ionic Fragments Detection.

Attosecond angular streaking (or "attoclock") is an insightful technique for probing the ultrafast electron dynamics in strong laser fields. Up until recently, this technique relied solely on an accurate measurement of the photoelectron momentum distribution and has remained restricted to atomic targets. Here, we propose a novel attosecond angular streaking scheme applicable to molecules, for which the ionic fragments of dissociative ionization are detected in the polarization plane of a close-to-circular polarized laser light.

Author Correction: Attosecond angular streaking and tunnelling time in atomic hydrogen.

In this Letter, the statement 'I.I. and A.

Attosecond angular streaking and tunnelling time in atomic hydrogen.

The tunnelling of a particle through a potential barrier is a key feature of quantum mechanics that goes to the core of wave-particle duality. The phenomenon has no counterpart in classical physics, and there are no well constructed dynamical observables that could be used to determine 'tunnelling times'. The resulting debate about whether a tunnelling quantum particle spends a finite and measurable time under a potential barrier was reignited in recent years by the advent of ultrafast lasers and attosecond metrology.

Using a passively stable attosecond beamline for relative photoemission time delays at high XUV photon energies.

We present and demonstrate an experimental scheme that enables overlap-free reconstruction of attosecond beating by interference of two-photon transitions (RABBITT) measurements at high extreme-ultraviolet (XUV) photon energies. A compact passively-stabilized attosecond beamline employing a multilayer (ML) mirror allows us to obtain XUV pulses consisting of only two odd high-harmonic orders from an attosecond pulse train (APT). We compare our new technique to existing schemes that are used to perform RABBITT measurements and discuss how our scheme resolves the limitations imposed by spectral complexity of the harmonic comb at high photon energies.

Keldysh-Rutherford Model for the Attoclock.

We demonstrate a clear similarity between attoclock offset angles and Rutherford scattering angles taking the Keldysh tunneling width as the impact parameter and the vector potential of the driving pulse as the asymptotic velocity. This simple model is tested against the solution of the time-dependent Schrödinger equation using hydrogenic and screened (Yukawa) potentials of equal binding energy. We observe a smooth transition from a hydrogenic to "hard-zero" intensity dependence of the offset angle with variation of the Yukawa screening parameter.

Photoionization delays in xenon using single-shot referencing in the collinear back-focusing geometry.

Attosecond photoemission delays for all the valence (5p, 5p, 5s, 4d, 4d) subshells of xenon have been accessed using the interferometric RABBITT technique. The 4d subshell delays in Xe have been accessed for the first time, to the best of our knowledge, due to the high photon energy used. A novel technique of single-shot referencing in the collinear back-focusing geometry has been introduced.

Time delay in XUV/IR photoionization of HO.

We solve the time-dependent Schrödinger equation describing a water molecule driven by a superposition of the extreme ultraviolet and IR pulses typical for a reconstruction of attosecond beating by interference of two-photon transitions experiment. This solution is obtained by a combination of the time-dependent coordinate scaling and the density functional theory with self-interaction correction. Results of this solution are used to determine the time delay in photoionization of the water and hydrogen molecules.

Attosecond Time Delay in Photoemission and Electron Scattering near Threshold.

We study the time delay in the primary photoemission channel near the opening of an additional channel and compare it with the Wigner time delay in elastic scattering of the photoelectron near the corresponding inelastic threshold. The photoemission time delay near threshold is significantly enhanced, to a measurable 40 as, in comparison to the corresponding elastic scattering delay. The enhancement is due to the different lowest order of interelectron interaction coupling the primary and additional photoemission channels.

Spectral momentum densities in matter determined by electron scattering.

In electron momentum spectroscopy (EMS), an incoming energetic electron (50 keV in this work) ionizes the target and the scattered and ejected electrons are detected in coincidence (at energies near 25 keV). From the energy and momentum of the detected particles, the energy omega and momentum q transferred to the target can be inferred. The observed intensity distribution I(omega, q) is proportional to the spectral momentum density of the target and hence provides a direct challenge to many-body theoretical descriptions of condensed matter.