Analytical approximations for the higher energy structure in strong field ionization with inhomogeneous electric fields

Recently, the emergence of a higher energy structure (HES) due to a spatial inhomogeneity in the laser electric field, as is typically found close to a nano tip, was reported in Phys.~Rev. Letter {\bf 119}, 053204 (2017). For practical applications, such as the characterization of near-fields or the creation of localized sources of monoenergetic electron beams with tunable energies, further insight into the nature of this higher energy structure is needed. Here, we give a closed form analytical approximation to describe the movement of the electron in the inhomogeneous electric field. In particular, we derive a simple scaling law for the location of the HES peak and give a scheme to analytically tune the width of the peak, both of which will prove useful in optimizing the nanostructure size or geometry for creating the HES in experimental settings

Intensity dependence of Rydberg states

We investigate numerically and analytically the intensity dependence of the fraction of electrons that end up in a Rydberg state after strong-field ionization with linearly polarized light. We find that including the intensity dependent distribution of ionization times and non-adiabatic effects leads to a better understanding of experimental results. Furthermore, we observe using Classical Trajectory Monte Carlo simulations that the intensity dependence of the Rydberg yield changes with wavelength and that the previously observed power-law dependence breaks down at longer wavelengths. Our work suggests that Rydberg yield measurements can be used as an independent test for non-adiabaticity in strong field ionization

Controlling the quantum number distribution and yield of Rydberg states via the duration of the laser pulse

We show that the distribution of quantum numbers of Rydberg states does not only depend on the field strength and wavelength of the laser which the atom is exposed to, but that it also changes significantly with the duration of the laser pulse. We provide an intuitive explanation for the underlying mechanism and derive a scaling law for the position of the peak in the quantum number distribution on the pulse duration. The new analytic description for the electron's movement in the superposed laser and Coulomb field (applied in the study of quantum numbers) is then used to explain the decrease of the Rydberg yield with longer pulse durations. This description stands in contrast to the concepts that explained the decrease so far and also reveals that approximations which neglect Coulomb effects during propagation are not sufficient in cases such as this.Comment: 8 pages, 8 figure

Instantaneous ionization rate as a functional derivative

We describe an approach defining instantaneous ionization rate (IIR) as a functional derivative of the total ionization probability. The definition is based on physical quantities which are directly measurable, such as the total ionization probability and the waveform of the pulse. The definition is, therefore, unambiguous and does not suffer from gauge non-invariance. We compute IIR by solving numerically the time-dependent Schrodinger equation for the hydrogen atom in a strong laser field. We find that the IIR lags behind the electric field, but this lag is entirely due to the long tail effect of the Coulomb field. In agreement with the previous results using attoclock methodology, therefore, the IIR we define does not show measurable delay in strong field tunnel ionization