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AIP conference proceedings

Interactions of atoms with high-field single-cycle infrared radiation

P. H. Bucksbaum, D. You, Douglas R. Dykaar, R. R. Jones

Published Jan 1, 1993• 0 citations
Publisher

Abstract

We have studied ionization and excitation of Rydberg atoms by intense sub‐picosecond electromagnetic field pulses of less than one cycle duration. The ionization threshold electric field scales as the binding energy (i.e., n*−2, rather than the n*−4 threshold scaling characteristic of static field ionization and high order multiphoton ionization. This altered behavior is due to the short duration and the subcycle nature of the field. We also find a wide distribution of final states produced by these pulses, which are effectively ‘‘in resonance’’ for dozens of transitions simultaneously.

DOI
10.1063/1.45045

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•Jan 1, 1993•1 citation
We have studied ionization and excitation of Rydberg atoms by intense sub‐picosecond electromagnetic field pulses of less than one cycle duration. The ionization threshold electric field scales as the binding energy (i.e., n*−2, rather than the n*−4 threshold scaling characteristic of static field ionization and high order multiphoton ionization. This altered behavior is due to the short duration and the subcycle nature of the field. We also find a wide distribution of final states produced by these pulses, which are effectively ‘‘in resonance’’ for dozens of transitions simultaneously.
We have ionized Rydberg atoms using subpicosecond half-cycle electromagnetic pulses. The threshold electric field required to ionize a Rydberg state with effective quantum number n∗{\mathit{n}}^{\mathrm{*}}n∗ is found to scale as ${\mathit{n}}^{\mathrm{*}\mathrm{\ensuremath{-}}2}$ for states with n∗{\mathit{n}}^{\mathrm{*}}n∗>13 in contradistinction to the ${\mathit{n}}^{\mathrm{*}\mathrm{\ensuremath{-}}4}$ threshold scaling for static field ionization and high order multiphoton ionization. This novel result is explained using a classical model.
We study the field-ionization threshold behavior when a Rydberg atom is ionized by a short single-cycle pulse field. Both hydrogen and sodium atoms are considered. The required threshold field amplitude is found to scale inversely with the binding energy when the pulse duration becomes shorter than the classical Rydberg period, and, thus, more weakly bound electrons require larger fields for ionization. This threshold scaling behavior is confirmed by both three-dimensional classical trajectory Monte Carlo simulations and numerically solving the time-dependent Schr\"odinger equation. More surprisingly, the same scaling behavior in the short pulse limit is also followed by the ionization thresholds for much lower bound states, including the hydrogen ground state. An empirical formula is obtained from a simple model, and the dominant ionization mechanism is identified as a nonzero spatial displacement of the electron. This displacement ionization should be another important mechanism beyond the tunneling ionization and the multiphoton ionization. In addition, an ``ionization window'' is shown to exist for the ionization of Rydberg states, which may have potential applications to selectively modify and control the Rydberg-state population of atoms and molecules.
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.
We study the ionization of Rydberg atoms by half-cycle electromagnetic pulses as a function of the duration of the pulses covering a broad range of time intervals connecting the adiabatic and sudden regimes. The threshold fields for ionization lie on a universal classical scaling invariant curve. We present quantum mechanical results which agree well with the universal curve. The n -2 threshold field scaling found experimentally is a linear approximation to the universal curve by the tangent in the region where the pulse duration is of the order of the orbital period of the atom. We predict the existence of an ultrashort pulse limit in which the threshold field scales as n -1 . Effects due to the non-hydrogenic core are negligible.
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.
Theoretical analysis of the recently observed ionization of Rydberg atoms by ultra-short half-cycle single-polarity electromagnetic pulses is presented. It is shown that the observations are consistent with the general classical scaling for the hydrogen atom in a microwave field, but the quantitative explanation of the results is possible only within the framework of quantum mechanics. In other words, the photonic basis approach for quantum dynamics and the multiphoton ionization theory yield the measured threshold fields. This is an example of classical scaling of a non-classical effect. 1.