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Two photon above threshold ionization in a relativistic framework : Attosecond delays in high Z elements

Jimmy Vinbladh

Published Jan 1, 2018• 1 citation
OpenAlex

Abstract

Recent advances in experimental physics opens up for improved time resolution on measurements of ionizing processes in atoms caused by an EM-field. There exist non-relativistic models that describe ...

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Tunneling and tunneling time are hot debated and very interesting issues because of their fundamental role in the quantum mechanics. The measurement of the tunneling time in today's attosecond and strong field (low-frequency) experiments, despite its controversial discussion offers a fruitful opportunity to understand the time measurement and the role of time in quantum mechanics. In previous work Kullie (2015 Phys. Rev. A 92 , 052118), we suggested a model and derived a simple relation to calculate the tunneling time, which showed a good agreement with the experimental result for He-atom. In the present work we analyze and discuss our model considering the experimental result for H-atom, which is obtained recently by Satya Sainadh et al (2017 arXiv: 1707.05445 ). In the tunneling region, we find that our model shows a good agreement with their experimental result (similar to the He-atom in our previous work), and with the accompanied time-dependent Schrödiger equation simulations. However, Sainadh et al use a different picture of the tunneling, in which tunneling time becomes an imaginary quantity. Whereas our model represents a real tunneling time picture, precisely a delay time with respect to the ionization time at the atomic field strength. Moreover, even though the above-threshold-ionization is beyond the tunneling regime, we still see that the actual ionization time is related to our model. However, crucial points arise and keep some questions open especially on the experimental side.
The advent of the ultrafast laser pulse provides the powerful and efficient tool for probing the ultrafast electron dynamics in atoms and molecules. The various nonlinear process induced by the laser-matter interaction allows one to obtain the electron motion information on the sub-femtosecond time scale. A series of the ultrafast spectroscopic technique, such as attosecond streak camera, attosecond transient absorption spectrum, and etc., have been successfully applied to the probe of electron dynamics in atoms, molecules, and solids. Using two-color field is one of the significant methods to achieve the coherent control and exploring of the electron motion. This paper summarizes recent research activities in the field of the atomic and molecular ultrafast process investigated in State Key Laboratory of High Field Laser Physics, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, including the detection of the electron dynamics of the multi-bound states, measurement of the carrier envelope phase (CEP) and the phase of the attosecond pulse, and the ultrafast electron control with the THz/UV and MIR/IR field. To measure the dynamics of the multi-bound states, a broadband attosecond pulse can be used to ionize the electrons after it is excited by the pump laser. By changing the delay between the pump laser and the attosecond pulse, the measured electrons ionized by the broadband xuv attosecond pulse can present the multi-bound states dynamics simultaneously. The XUV/IR scheme is popularly used in attosecond dynamics measurement. But usually, the IR field is not very strong. We find that, if the IR field is strong enough to induce the above threshold ionization (ATI), the interference between the ATI electron and the electron from XUV pulse can be used to measure the CEP of the attosecond XUV pulse. Besides, if the electron ionized by attosecond pulse can be pushed back to the nuclei, the emission from the recombination can be used to determine the spectral phase of the attosecond pulse, which is an all-optical measurement. We also investigate the two color scheme of THz/UV and MIR/IR fields. With THz/UV two color scheme, very high electron localization can be achieved duration molecular dissociation when we use the UV pulse to excite the electron and the THz pulse to control the following electron movement. When we use the MIR/IR field to control the electron motion during the high harmonic generation, the recollision can be greatly decreased and the single attosecond pulse can be produced with multi-cycle MIR laser field.
A model which describes the time evolution of strong-field photoionization of atoms is presented. Based on the numerical solution of the non-stationary Schrodinger equation, the model allows one to predict and to interpret the results of experiments on double photoionization of atoms by a combined action of a very short (attosecond) XUV pulse and a few-cycle IR pulse of a powerful laser at various delay times between the two pulses. Depending on the binding energy of the ionized electron, two types of processes are considered. If the electron is tightly bound (Ne case), the XUV pulse ionizes the atom and shakes up another (outer) electron to an excited state, which is subsequently ionized by the strong IR field. For an atom with a weakly bound outer electron (Li case), the IR field ionizes the latter, while the XUV pulse, ionizing the inner shell, terminates (or suppresses) the strong-field ionization. In both cases the yield of doubly ionized ions strongly depends on the delay time between the two pulses, revealing 'steps', oscillations and other features which characterize the time evolution of the ionization process. The presented model describes qualitatively the results of recent experiments on Ne.