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

Physical Review A

Role of counter-rotating wave dynamics in near-threshold photoionization of atomic hydrogen

Bernard Piraux, P. L. Knight

Published Jul 1, 1989• 18 citations
Publisher

Abstract

We consider the excitation of atomic hydrogen in its ground state by an intense radiation field tuned close to the ionization threshold. Results are presented for the ac Stark shift of the 1s and 2s states, the width of the 1s state, and the photoelectron energy spectrum. In the first instance, our nonperturbative approach includes the 1s state, the p series of excited states, and the p continuum: we demonstrate that the p Rydberg states generate a rich structure in the photoelectron energy spectrum through the action of the counter-rotating wave dynamics when the laser frequency is tuned below the ionization threshold. We then go on to analyze in detail how the interaction of the p states with the other Rydberg series and continua increases the width of the p states; it is shown, however, that at the field intensities considered here (\ensuremath{\approxeq}${10}^{13}$ W ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}2}$), this effect is not sufficient to smear out the structure in the photoelectron energy spectrum.

DOI
10.1103/physreva.40.712

Related papers

Nonadiabatic transitions between degenerate opposite-parity states of hydrogen in an intense field

Thomas Millack, Bernard Piraux, P. L. Knight

We analyze the photoelectron energy spectrum that results from near-threshold ionization of atomic hydrogen, initially in the 2s state, by a sharply turned on intense field. We demonstrate the existence of resonance structure close to threshold. The structure derives from transitions between degenerate ns and np states; opposite parity, degenerate states in the hydrogen atom are mixed by the nonadiabatic turn-on; at higher energies further structures in the photoelectron energy spectrum are generated through the action of counterrotating terms in the atom-laser coupling. We confirm the existence of a Rydberg series structure and investigate the possibility of q reversals in the line shapes.

Physical Review A•May 1, 1990•6 citations

Nonperturbative resonant strong field ionization of atomic hydrogen

M G Girju, K. Hristov, Oleg Kidun +1 more

We investigate resonant strong field ionization of atomic hydrogen with respect to the 1s–2p transition. By 'strong' we understand that Rabi periods are executed on a femtosecond time scale. Ionization and AC Stark shifts modify the bound state dynamics severely, leading to nonperturbative signatures in the photoelectron spectra. We introduce an analytical model, capable of predicting qualitative features in the photoelectron spectra such as the positions of the Autler–Townes peaks for modest field strengths. Ab initio solutions of the time-dependent Schrödinger equation show a pronounced shift and broadening of the left Autler–Townes peak as the field strength is increased. The right peak remains rather narrow and shifts less. This result is analysed and explained with the help of exact AC Stark shifts and ionization rates obtained from Floquet theory. Finally, it is demonstrated that in the case of finite pulses as short as 20 fs the Autler–Townes duplet can still be resolved. The fourth generation light sources under construction worldwide will provide bright, coherent radiation with photon energies ranging from a tenth of an meV up to tens of keV, hence covering the regime studied in the paper so that measurements of nonperturbative, relative AC Stark shifts should become feasible with these new light sources.

arXiv:0707.3111•Journal of Physics B Atomic Molecular and Optical Physics•Oct 17, 2007•31 citations

Two-frequency above threshold ionization with pulses

L. Wang, J. W. Haus, K. Rzazewski

We solve a model with one bound state and two continua.1 Two lasers are used to study the above threshold ionization process. The first laser couples the electron in a bound state to a continuum state. The photons are assumed to be energetic enough to promote the electron directly into the continuum far from the threshold; this avoids complications due to the Rydberg levels and the ponderomotive shifts of the threshold. The second laser mixes the electron wavefunction between two continuum states (C—C transitions); since we avoid the rotating wave approximation, multiple transitions between these continua are allowed. We find that the ionization rate is unaffected by the C—C transitions. Our model of hydrogenic atoms allows redistribution among the continua only during the ionization process and the photoelectron spectra exhibits peak suppression; i.e., the population is not the strongest at the energy of the ionization laser.

Annual Meeting Optical Society of America•Jan 1, 1989•0 citations

Photoionization of the hydrogen atom near the ionization limit in strong electric fields

H. Rottke, K. H. Welge

The Stark spectroscopy of the hydrogen atom has been investigated near the ionization threshold in static homogeneous external electric fields from \ensuremath{\sim}1000 to \ensuremath{\sim}8000 V/cm with use of a two-step excitation H(n=1)+\ensuremath{\Elzxh}${\ensuremath{\omega}}_{\mathrm{vuv}\ensuremath{\rightarrow}}$H(n=2)+\ensuremath{\Elzxh}\ensuremath{\omega} $_{\mathrm{uv}\ensuremath{\rightarrow}}$${\mathrm{H}}^{\mathrm{*}}$ with vuv and uv laser radiation, independently tunable and linearly polarized either parallel (\ensuremath{\pi}) or perpendicular (\ensuremath{\sigma}) with respect to the external field. Different from other, nonhydrogenic atoms, the hydrogen atom is a peculiar case insofar as the initial states of H(n=2), from which excitation takes place, are essentially of parabolic character at the field strengths employed in this study.Individual sublevels (${n}_{1}$,${n}_{2}$,\ensuremath{\Vert}${m}_{l}$\ensuremath{\Vert}) have been prepared in the n=2 state with sub-Doppler resolution. Photoionization spectra have been obtained with \ensuremath{\pi}- and \ensuremath{\sigma}-polarized uv radiation from the four possible sublevels of the n=2 Stark manifold: \ensuremath{\Vert}1,0,0〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉, \ensuremath{\Vert}0,1,0〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉, \ensuremath{\Vert}0,0,\ifmmode\pm\else\textpm\fi{}1〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉, and \ensuremath{\Vert}0,0,\ensuremath{\mp}1〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉. All spectra show sharp line structures of quasistable field-ionizing states superimposed on continua in the energy region between the classical saddle point, ${E}_{\mathrm{SP}=\mathrm{\ensuremath{-}}2\phantom{\rule{0ex}{0ex}}\mathrm{\ensuremath{\surd}}\mathrm{F}}$ a.u., and the zero-field ionization threshold E=0 a.u. Employing existing theoretical treatments, the quasistable spectral structures are quantitatively completely analyzed and accounted for, as long as their field ionization rate is less than \ensuremath{\sim}5\ifmmode\times\else\texttimes\fi{}${10}^{11}$ ${\mathrm{sec}}^{\mathrm{\ensuremath{-}}1}$. Field-ionization rates of quasistable states have been measured and are compared with theory. Oscillatory resonance structures of the ionization cross section near the zero-field threshold are observed with pronounced modulation degree only in the spectrum from the \ensuremath{\Vert}1,0,0〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉 sublevel excited with the uv \ensuremath{\pi}-polarized. The energy spacing of the oscillations has been measured as a function of the electric field strength F and found to be nearly proportional to ${F}^{3/4}$, with slight but definite deviations. Theoretical analysis of the oscillations yields quantitative agreement with the experiment.

Physical Review A•Jan 1, 1986•102 citations

Resonant multiphoton ionization of the 1s state of a hydrogen atom in a strong laser field

Ekaterina A. Volkova, A. M. Popov, Olga V. Tikhonova

The process of resonant multiphoton ionization of a hydrogen atom in the ground 1 s state is studied by direct numerical integration of the nonstationary Schrödinger equation for a quantum system in an electromagnetic field. The dependence of photoionization probability on the radiation intensity is found to be nonmonotonic. It is established that the minima of ionization correspond to multiphoton resonances between the ground state and one of the excited (Rydberg) atomic states perturbed by the laser field. It is shown that ionization is suppressed due to rearrangement of Rydberg states in a strong electromagnetic field and is accompanied by efficient Raman Λ transitions, which connect a set of closely lying Rydberg states via the continuum.

Optics and Spectroscopy•Jan 1, 2000•8 citations

Near-threshold photoelectron spectrum in resonant two-photon ionization of atoms

Andrzej Raczyński, Jarosław Zaremba

The near-threshold photoelectron spectrum in a resonant two-photon ionization process is investigated using a nonperturbative method. The hydrogen atom is represented by a realistic model including an infinite number of Rydberg states converging at the threshold. When the threshold is crossed a typical two-peak structure of the spectrum is modified by cutting off part of the spectrum which may include one or even two peaks.

Physical Review A•Nov 1, 1987•8 citations
We consider the excitation of atomic hydrogen in its ground state by an intense radiation field tuned close to the ionization threshold. Results are presented for the ac Stark shift of the 1s and 2s states, the width of the 1s state, and the photoelectron energy spectrum. In the first instance, our nonperturbative approach includes the 1s state, the p series of excited states, and the p continuum: we demonstrate that the p Rydberg states generate a rich structure in the photoelectron energy spectrum through the action of the counter-rotating wave dynamics when the laser frequency is tuned below the ionization threshold. We then go on to analyze in detail how the interaction of the p states with the other Rydberg series and continua increases the width of the p states; it is shown, however, that at the field intensities considered here (\ensuremath{\approxeq}1013{10}^{13}1013 W cm\ensuremath−2{\mathrm{cm}}^{\mathrm{\ensuremath{-}}2}cm\ensuremath−2), this effect is not sufficient to smear out the structure in the photoelectron energy spectrum.
We analyze the photoelectron energy spectrum that results from near-threshold ionization of atomic hydrogen, initially in the 2s state, by a sharply turned on intense field. We demonstrate the existence of resonance structure close to threshold. The structure derives from transitions between degenerate ns and np states; opposite parity, degenerate states in the hydrogen atom are mixed by the nonadiabatic turn-on; at higher energies further structures in the photoelectron energy spectrum are generated through the action of counterrotating terms in the atom-laser coupling. We confirm the existence of a Rydberg series structure and investigate the possibility of q reversals in the line shapes.
We investigate resonant strong field ionization of atomic hydrogen with respect to the 1s–2p transition. By 'strong' we understand that Rabi periods are executed on a femtosecond time scale. Ionization and AC Stark shifts modify the bound state dynamics severely, leading to nonperturbative signatures in the photoelectron spectra. We introduce an analytical model, capable of predicting qualitative features in the photoelectron spectra such as the positions of the Autler–Townes peaks for modest field strengths. Ab initio solutions of the time-dependent Schrödinger equation show a pronounced shift and broadening of the left Autler–Townes peak as the field strength is increased. The right peak remains rather narrow and shifts less. This result is analysed and explained with the help of exact AC Stark shifts and ionization rates obtained from Floquet theory. Finally, it is demonstrated that in the case of finite pulses as short as 20 fs the Autler–Townes duplet can still be resolved. The fourth generation light sources under construction worldwide will provide bright, coherent radiation with photon energies ranging from a tenth of an meV up to tens of keV, hence covering the regime studied in the paper so that measurements of nonperturbative, relative AC Stark shifts should become feasible with these new light sources.
We solve a model with one bound state and two continua.1 Two lasers are used to study the above threshold ionization process. The first laser couples the electron in a bound state to a continuum state. The photons are assumed to be energetic enough to promote the electron directly into the continuum far from the threshold; this avoids complications due to the Rydberg levels and the ponderomotive shifts of the threshold. The second laser mixes the electron wavefunction between two continuum states (C—C transitions); since we avoid the rotating wave approximation, multiple transitions between these continua are allowed. We find that the ionization rate is unaffected by the C—C transitions. Our model of hydrogenic atoms allows redistribution among the continua only during the ionization process and the photoelectron spectra exhibits peak suppression; i.e., the population is not the strongest at the energy of the ionization laser.
The Stark spectroscopy of the hydrogen atom has been investigated near the ionization threshold in static homogeneous external electric fields from \ensuremath{\sim}1000 to \ensuremath{\sim}8000 V/cm with use of a two-step excitation H(n=1)+\ensuremath{\Elzxh}${\ensuremath{\omega}}_{\mathrm{vuv}\ensuremath{\rightarrow}}$H(n=2)+\ensuremath{\Elzxh}\ensuremath{\omega} $_{\mathrm{uv}\ensuremath{\rightarrow}}$H∗{\mathrm{H}}^{\mathrm{*}}H∗ with vuv and uv laser radiation, independently tunable and linearly polarized either parallel (\ensuremath{\pi}) or perpendicular (\ensuremath{\sigma}) with respect to the external field. Different from other, nonhydrogenic atoms, the hydrogen atom is a peculiar case insofar as the initial states of H(n=2), from which excitation takes place, are essentially of parabolic character at the field strengths employed in this study.Individual sublevels (n1{n}_{1}n1​,n2{n}_{2}n2​,\ensuremath{\Vert}ml{m}_{l}ml​\ensuremath{\Vert}) have been prepared in the n=2 state with sub-Doppler resolution. Photoionization spectra have been obtained with \ensuremath{\pi}- and \ensuremath{\sigma}-polarized uv radiation from the four possible sublevels of the n=2 Stark manifold: \ensuremath{\Vert}1,0,0〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉, \ensuremath{\Vert}0,1,0〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉, \ensuremath{\Vert}0,0,\ifmmode\pm\else\textpm\fi{}1〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉, and \ensuremath{\Vert}0,0,\ensuremath{\mp}1〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉. All spectra show sharp line structures of quasistable field-ionizing states superimposed on continua in the energy region between the classical saddle point, ${E}_{\mathrm{SP}=\mathrm{\ensuremath{-}}2\phantom{\rule{0ex}{0ex}}\mathrm{\ensuremath{\surd}}\mathrm{F}}$ a.u., and the zero-field ionization threshold E=0 a.u. Employing existing theoretical treatments, the quasistable spectral structures are quantitatively completely analyzed and accounted for, as long as their field ionization rate is less than \ensuremath{\sim}5\ifmmode\times\else\texttimes\fi{}1011{10}^{11}1011 ${\mathrm{sec}}^{\mathrm{\ensuremath{-}}1}$. Field-ionization rates of quasistable states have been measured and are compared with theory. Oscillatory resonance structures of the ionization cross section near the zero-field threshold are observed with pronounced modulation degree only in the spectrum from the \ensuremath{\Vert}1,0,0〉 \ensuremath{\Vert}\ifmmode\pm\else\textpm\fi{}1/2〉 sublevel excited with the uv \ensuremath{\pi}-polarized. The energy spacing of the oscillations has been measured as a function of the electric field strength F and found to be nearly proportional to F3/4{F}^{3/4}F3/4, with slight but definite deviations. Theoretical analysis of the oscillations yields quantitative agreement with the experiment.
The process of resonant multiphoton ionization of a hydrogen atom in the ground 1 s state is studied by direct numerical integration of the nonstationary Schrödinger equation for a quantum system in an electromagnetic field. The dependence of photoionization probability on the radiation intensity is found to be nonmonotonic. It is established that the minima of ionization correspond to multiphoton resonances between the ground state and one of the excited (Rydberg) atomic states perturbed by the laser field. It is shown that ionization is suppressed due to rearrangement of Rydberg states in a strong electromagnetic field and is accompanied by efficient Raman Λ transitions, which connect a set of closely lying Rydberg states via the continuum.