Wave-particle duality is an inherent peculiarity of the quantum world. The double-slit experiment has been frequently used for understanding different aspects of this fundamental concept. The occurrence of interference rests on the lack of which-way information and on the absence of decoherence mechanisms, which could scramble the wave fronts. Here, we report on the observation of two-center interference in the molecular-frame photoelectron momentum distribution upon ionization of the neon dimer by a strong laser field. Postselection of ions, which are measured in coincidence with electrons, allows choosing the symmetry of the residual ion, leading to observation of both, gerade and ungerade, types of interference.

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We report on the non-adiabatic offset of the initial electron momentum distribution in the plane of polarization upon single ionization of argon by strong field tunneling and show how to experimentally control the degree of non-adiabaticity. Two-color counter-and co-rotating fields (390 and 780 nm) are compared to show that the non-adiabatic offset strongly depends on the temporal evolution of the laser electric field. We introduce a simple method for the direct access to the non-adiabatic offset using two-color counter-and co-rotating fields. Further, for a single-color circularly polarized field at 780 nm we show that the radius of the experimentally observed donut-like distribution increases for increasing momentum in the light propagation direction. Our observed initial momentum offsets are well reproduced by the strong-field approximation (SFA). A mechanistic picture is introduced that links the measured non-adiabatic offset to the magnetic quantum number of virtually populated intermediate states.

The attoclock technique which maps the emission time of a photoelectron to its detection angle is an important tool in strong-field physics. Previously, it was implemented only with circularly or elliptically polarized laser fields. Here, we show how counter-rotating bicircular laser fields can be used as an attoclock to investigate the ionization dynamics in quasilinear polarization. This is achieved by choosing the ratio of the two field strengths in a way such that the vector potential has aspects of the attoclock and time is mapped directly to the photoelectron momentum, but the shape of the electric field corresponds to approximately linear polarization during three intervals per optical cycle. We report momentum distributions calculated by solving the time-dependent Schrödinger equation for a model helium atom and obtain the mapping from photoelectron momentum to ionization time using a trajectory-free method. Unlike circular polarization where the time of maximal ionization rate typically deviates less than 5 attoseconds from the maximium of the electric field, we find positive ionization times of more than 10 attoseconds in the quasilinear case.

Compton scattering is one of the fundamental interaction processes of light with matter. When discovered [1], it was described as a billiard-type collision of a photon 'kicking' a quasi-free electron. With decreasing photon energy, the maximum possible momentum transfer becomes so small that the corresponding energy falls below the binding energy of the electron. In this regime, ionization by Compton scattering becomes an intriguing quantum phenomenon. Here, we report on a kinematically complete experiment studying Compton scattering o helium atoms in that regime. We determine the momentum correlations of the electron, the recoiling ion and the scattered photon in a coincidence experiment based on cold target recoil ion momentum spectroscopy, nding that electrons are not only emitted in the direction of the momentum transfer, but that there is a second peak of ejection to the backward direction. This nding links Compton scattering to processes such as ionization by ultrashort optical pulses [2], electron impact ionization [3,4], ion impact ionization [5,6], and neutron scattering [7], where similar momentum patterns occur.