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Physical Review A

Ionization and recombination in attosecond electric field pulses

Darko Dimitrovski, Eugene A. Solov’ev, J S Briggs

Published Oct 31, 2005• 63 citations
Publisher

Abstract

Based on the results of a previous communication [Dimitrovski et al., Phys. Rev. Lett. 93, 083003 (2004)], we study ionization and excitation of a hydrogenic atom from the ground and first excited states in short electric field pulses of several cycles. A process of ionization and recombination which occurs periodically in time is identified, for both small and extremely large peak electric field strengths. In the limit of large electric peak fields closed-form analytic expressions for the population of the initial state after single- and few-cycle pulses are derived. These formulas, strictly valid for asymptotically large momentum transfer from the field, give excellent agreement with fully numerical calculations for all momentum transfers.

DOI
10.1103/physreva.72.043411

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Based on the results of a previous communication [Dimitrovski et al., Phys. Rev. Lett. 93, 083003 (2004)], we study ionization and excitation of a hydrogenic atom from the ground and first excited states in short electric field pulses of several cycles. A process of ionization and recombination which occurs periodically in time is identified, for both small and extremely large peak electric field strengths. In the limit of large electric peak fields closed-form analytic expressions for the population of the initial state after single- and few-cycle pulses are derived. These formulas, strictly valid for asymptotically large momentum transfer from the field, give excellent agreement with fully numerical calculations for all momentum transfers.
We study the ionization of Rydberg atoms in a single-cycle-pulse electric field based on both classical and quantum calculations. The ionization-probability curve exhibits a ``ripple'' structure as a function of the pulse duration and the field amplitude. These ripple structures are found to be dependent on the angular distribution of the initial state. A large electron-emission asymmetry is observed, and the ionized electron is almost completely emitted to one side of the atom except when the pulse length is roughly one Rydberg period. In both the long-pulse and the short-pulse regimes, larger electron energy can be expected from the ionization of lower-lying Rydberg states, matching the observation in a recent experiment [S. Li and R. R. Jones, Phys. Rev. Lett. 112, 143006 (2014)]. This trend is closely related to the electron-emission asymmetry associated with the field-direction change in a single-cycle pulse. The possible implications of the different energy transfer in a single-cycle pulse from that in a multicycle pulse are also discussed briefly for the strong-field ionization of the ground atomic state.
ization of Rydberg atoms by a single-cycle pulse, and also its implications for the strong field ionization of ground state. The required threshold field amplitude (for 10% ionization probability) scales inversely with the binding energy of initial states and also the pulse-duration square when the pulse duration becomes much shorter than the classical Rydberg period. A simple model is introduced to understand this threshold behavior, where the nonzero displacement induced by a single-cycle pulse plays a critical role. By combining with the adiabatic-ionization threshold in the low-frequency limit, an ionization window is expected for the ionization of different states. The ionization-probability curve exhibits a “ripple” structure as a function of the pulse duration and the field amplitude, which is sensitive to the angular distribution of initial states. The observation of larger emitted-electron energy for the ionization of lower-lying Rydberg states in a recent experiment [S Li and R. R. Jones, Phys. Rev. Lett. 112, 143006 (2014)] is confirmed in our calculations for both sodium and hydrogen atoms. The differences between the ionization dynamics in a single-cycle pulse and that in a multi-cycle pulse are also discussed and presented.
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.
We have measured the microwave ionization threshold electric fields for ns-state Na Rydberg atoms from n=24--33 as a function of the duration of the ionizing microwave pulse. Pulses as short as 2.8 ns were used, containing fewer than 25 cycles of 8.55-GHz radiation. While the fields required to produce the onset of ionization were independent of pulse duration and exhibited the ${\mathit{n}}^{\mathrm{\ensuremath{-}}5}$ scaling characteristic of ionization by diffusion through higher-energy states, the fields required to produce nearly complete ionization increased dramatically as the pulse was shortened. Additional measurements of the populations of bound states after the shortest microwave pulses showed that up to \ensuremath{\sim}10% of the atoms were excited to states above the initially populated ns state and the adjacent (n-1) manifold of higher angular momentum states, while most either ionized or remained in these states. From this observation we conclude that the rate-limiting process for ionization is the transition from the initially populated ns states or the adjacent manifold to the next higher manifold, not the diffusion through higher-lying states.