No Arabic abstract
An ionization-induced plasma grating can be formed by spatially selective ionization of gases by the interference of two intersecting ultra-short laser pulses. The density modulation of a plasma grating can approach unity since the plasma is produced only where the two pulses constructively interfere and ionization does not occur in destructive interference regions. Such a large density modulation leads to efficient Thomson scattering of a second ultra-short probe pulse once the Bragg condition is satisfied. By measuring the scattering efficiency, it is possible to determine the absolute electron density in the plasma grating and thereby deduce the ionization degree for a given neutral gas density. In this paper, we demonstrate the usefulness of this concept by showing two applications: ionization degree measurement of strong-field ionization of atoms and molecules and characterization of extremely low-density gas jets. The former application is of particular interest for ionization physics studies in dense gases where the collision of the ionized electron with neighboring neutrals may become important-sometimes referred to as many-body ionization, and the latter is useful for plasma-based acceleration that requires extremely low-density plasmas.
An improved formula is proposed for field ionization rate covering tunnel and barrier suppression regime. In contrast to the previous formula obtained recently in [I. Yu. Kostyukov and A. A. Golovanov, Phys. Rev. A 98, 043407 (2018)], it more accurately describes the transitional regime (between the tunnel regime and the barrier suppression regime). In the proposed approximation, the rate is mainly governed by two parameters: by the atom ionization potentials and by the external electric field, which makes it perfectly suitable for particle-in-cell (PIC) codes dedicated to modeling of intense laser-matter interactions.
We report on the unambiguous observation of the sub-cycle ionization bursts in sequential strong-field double ionization of H$_2$ and their disentanglement in molecular frame photoelectron angular distributions. This observation was made possible by the use of few-cycle laser pulses with a known carrier-envelope phase in combination with multi-particle coincidence momentum imaging. The approach demonstrated here will allow sampling of the intramolecular electron dynamics and the investigation of charge-state specific Coulomb-distortions on emitted electrons in polyatomic molecules.
Several recent attoclock experiments have investigated the fundamental question of a quantum mechanically induced time delay in tunneling ionization via extremely precise photoelectron momentum spectroscopy. The interpretations of those attoclock experimental results were controversially discussed, because the entanglement of the laser and Coulomb field did not allow for theoretical treatments without undisputed approximations. The method of semiclassical propagation matched with the tunneled wavefunction, the quasistatic Wigner theory, the analytical R-matrix theory, the backpropagation method, and the under-the-barrier recollision theory are the leading conceptual approaches put forward to treat this problem, however, with seemingly conflicting conclusions on the existence of a tunneling time delay. To resolve the contradicting conclusions of the different approaches, we consider a very simple tunneling scenario which is not plagued with complications stemming from the Coulomb potential of the atomic core, avoids consequent controversial approximations and, therefore, allows us to unequivocally identify the origin of the tunneling time delay as well as to confirm it with the backpropagation method being most known for predicting vanishing tunneling time.
We investigate the role of nuclear motion and strong-field-induced electronic couplings during the double ionization of deuterated water using momentum-resolved coincidence spectroscopy. By examining the three-body dicationic dissociation channel, D$^{+}$/D$^{+}$/O, for both few- and multi-cycle laser pulses, strong evidence for intra-pulse dynamics is observed. The extracted angle- and energy-resolved double ionization yields are compared to classical trajectory simulations of the dissociation dynamics occurring from different electronic states of the dication. In contrast with measurements of single photon double ionization, pronounced departure from the expectations for vertical ionization is observed, even for pulses as short as 10~fs in duration. We outline numerous mechanisms by which the strong laser field can modify the nuclear wavefunction en-route to final states of the dication where molecular fragmentation occurs. Specifically, we consider the possibility of a coordinate-dependence to the strong-field ionization rate, intermediate nuclear motion in monocation states prior to double ionization, and near-resonant laser-induced dipole couplings in the ion. These results highlight the fact that, for small and light molecules such as D$_2$O, a vertical-transition treatment of the ionization dynamics is not sufficient to reproduce the features seen experimentally in the strong field coincidence double-ionization data.
Strong-field ionization of atoms by circularly polarized femtosecond laser pulses produces a donut-shaped electron momentum distribution. Within the dipole approximation this distribution is symmetric with respect to the polarization plane. The magnetic component of the light field is known to shift this distribution forward. Here, we show that this magnetic non-dipole effect is not the only non-dipole effect in strong-field ionization. We find that an electric non-dipole effect arises that is due to the position dependence of the electric field and which can be understood in analogy to the Doppler effect. This electric non-dipole effect manifests as an increase of the radius of the donut-shaped photoelectron momentum distribution for forward-directed momenta and as a decrease of this radius for backwards-directed electrons. We present experimental data showing this fingerprint of the electric non-dipole effect and compare our findings with a classical model and quantum calculations.