Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:1410.0970 · Physical Review A

Field-ionization threshold and its induced ionization-window phenomenon for Rydberg atoms in a short single-cycle pulse

B. C. Yang, F. Robicheaux

Published Dec 5, 2014• 23 citations
arXivHTMLPDF

Abstract

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.

DOI
10.1103/physreva.90.063413

Related papers

Basic Energy Sciences, under Award number DE-SC0012193.

Baochun Yang, F. Robicheaux

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.

•Jan 1, 2015•0 citations

Field ionization of Rydberg atoms in a single-cycle pulse

Baozhu Yang, F. Robicheaux

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.

Physical Review A•Apr 13, 2015•18 citations

Scaling properties of field ionization of Rydberg atoms in single-cycle THz pulses: 1D considerations

Hicham Agueny, M Chovancova, J. P. Hansen +1 more

Abstract In recent experiments of single-cycle field ionization of excited Na( nd ) atoms with principal quantum number n ∈ [ 6 , 15 ] (Li and Jones 2014 Phys. Rev. Lett. 112 143006 ) it was shown that the maximum field intensity necessary to ionize 10% of the atoms decreases with increasing n according to an n − 3 power law dependence. This scaling property at the same ionization probability was confirmed in classical trajectory Monte Carlo calculations. In this work we note that the scaling relation in the experiment is much more general, it is in fact valid for all ionization probabilities. When applied to the emitted electron energies it places a very wide distribution of electron momenta from different initial states onto a narrow range. These aspects are investigated in a one-dimensional model with a 3D hydrogen-like spectrum. Calculations confirm the general n − 3 scaling relation for the ionization probability and that this particular scaling of the kinetic emission spectrum puts the ejected electron momenta on a narrow common scale. The ionization mechanism itself is identified as quantum mechanical tunneling and the nature of the tunneling process is the direct origin of the scaling law.

Journal of Physics B Atomic Molecular and Optical Physics•Nov 25, 2016•8 citations

Ionization of Rydberg atoms by half-cycle pulses

Carlos O Reinhold, Michael Melles, Hai Shao +1 more

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.

Journal of Physics B Atomic Molecular and Optical Physics•Oct 14, 1993•83 citations

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

P. H. Bucksbaum, D. You, Douglas R. Dykaar +1 more

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.

AIP conference proceedings•Jan 1, 1993•0 citations

Short-pulse microwave ionization of Na Rydberg atoms

M. Gatzke, Bernard Broers, Lambertus D. Noordam +2 more

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.

Physical Review A•Sep 1, 1994•18 citations
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 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.
Abstract In recent experiments of single-cycle field ionization of excited Na( nd ) atoms with principal quantum number n ∈ [ 6 , 15 ] (Li and Jones 2014 Phys. Rev. Lett. 112 143006 ) it was shown that the maximum field intensity necessary to ionize 10% of the atoms decreases with increasing n according to an n − 3 power law dependence. This scaling property at the same ionization probability was confirmed in classical trajectory Monte Carlo calculations. In this work we note that the scaling relation in the experiment is much more general, it is in fact valid for all ionization probabilities. When applied to the emitted electron energies it places a very wide distribution of electron momenta from different initial states onto a narrow range. These aspects are investigated in a one-dimensional model with a 3D hydrogen-like spectrum. Calculations confirm the general n − 3 scaling relation for the ionization probability and that this particular scaling of the kinetic emission spectrum puts the ejected electron momenta on a narrow common scale. The ionization mechanism itself is identified as quantum mechanical tunneling and the nature of the tunneling process is the direct origin of the scaling law.
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 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 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.