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

Sov. J. Plasma Phys. (Engl. Transl.); (United States)

Experimental study of the perturbation of the cesium-atom spectrum by a multiphoton-ionization method

V. A. Grinchuk, G. A. Delone, K. B. Petrosian

Published Jan 1, 1975• 0 citations
OpenAlex

Abstract

An experimental study has been made of the perturbation of an atomic spectrum in a 10/sup 6/-V/cm laser field for the case of the 6S--6F transition in cesium. The 6S--6F transition energy was found to be a linear function of the intensity (a quadratic function of the field strength). The dynamic polarizability of this transition was determined. The experimental results are compared with perturbation-theory calculations.

Related papers

Resonant multiphoton ionization of caesium atoms by ultra-short laser pulses at 1.06 μm

Louis A. Lompre, G. Mainfray, C. Manus +1 more

This paper reports the four-photon ionization of caesium atoms when the laser frequency is tuned through the resonant three-photon transition 6S → 6F. This experiment was performed by using a tunable-wavelength bandwidth-limited subnanosecond laser pulse at 1.06 μm, in the 108-109 W.cm-2 laser intensity range. Pulse widths of 1.5 ns, 50 ps, and 15 ps were used. The resonant character of the multiphoton ionization process was observed, even with the shortest pulse of 15 ps. Nevertheless the influence of a temporal effect is demonstrated according to theoretical predictions. The resonance shift ΔE of the 6S → 6F transition energy was found to be linear with the laser intensity I within the range 108-109 W.cm-2. ΔE = α I, with α = 2 cm-1/GW.cm-2. This result confirms previous measurements performed with single-mode 35 ns laser pulses and is in very good agreement with calculated resonance shifts.

Journal de physique•Jan 1, 1978•39 citations

Resonance shifts in the multiphoton ionization of cesium atoms

J. Morellec, Didier Normand, G. Petite

This work reports the multiphoton ionization of cesium atoms, via resonance with the $6F$ level, by interaction with a single transverse and longitudinal mode neodymium-glass laser beam. At a low rate of ion production, when the laser frequency is tuned through resonance, the laser intensity necessary to create a constant number of ions passes through a minimum, as expected, for a three-photon energy equal to the unperturbed $6S\ensuremath{\rightarrow}6F$ transition energy. But for a higher ionization rate, involving larger laser intensities, a departure from expectation is observed which is interpreted as a consequence of an energy shift of the transition. The level shifts are demonstrated in another way by their strong effect on the experimental order of nonlinearity of the interaction, ${K}_{\mathrm{expt}}$. A sharp variation of ${K}_{\mathrm{expt}}$ is observed when the energy shift of the $6S\ensuremath{\rightarrow}6F$ transition exactly compensates the wavelength detuning of the laser. The latter method gives shift values which are found to be independent of the large variations of the interaction volume under conditions of resonance. Both methods give a linear dependence of the shifts on the laser intensity. Identification of these shifts with energy shifts of the $6S\ensuremath{\rightarrow}6F$ transition is subject to theoretical reservations and needs further experimentation.

Physical Review A•Jul 1, 1976•107 citations

The multiphoton ionization of caesium and the perturbation of bound states

R. G. Evans, Peter C. Thonemann

Orer a small range of light intensity the three-photon ionization rate of caesium atoms by ruby laser light decreases when the incident photon flux is increased. This result may be quantitatively explained by an induced energy shift of the 913 levels of the caesium atom proportional to the square of the light intensity. Thus perturbations of bound electron states by an intense light beam can be of importance in determining the multiphoton ionization rate. In this paper the functional dependence of the ionization rate on the photon flux is calculated for caesium, using a perturbation theory somewhat different from that usually employed.

Philosophical magazine•Jun 1, 1973•6 citations

Experimental multiphoton ionization of cesium atoms through the 9D 3/2 resonant level

G. Brincourt

In this letter we report the results of an experiment concerning the multiphoton ionization of cesium atoms through the 9D3/2 resonant level, using a ruby laser. The experimental dispersion curve of the resonance obtained is compared to the theoretical shape of the resonant multiphoton ionization profile for cesium deduced from the calculations of B. L. Beers and L. Armstrong [1].

Journal de Physique Lettres•Jan 1, 1977•3 citations

Theory of resonant multiphoton processes

C. S. Chang

The present paper applies the method of high-intensity quantum electrodynamics developed earlier to several problems of current experimental interest. In this paper the intensitydependent shifts and widths of atomic levels are calculated and applied to a given transition near resonance. The technique is demonstrated with three examples: the multiphoton ionization of atomic cesium and hydrogen in atomic beams and third-harmonic production in an atomic vapor. It is found that the multiphoton-ionization rate in a relatively weak laser beam (of order ${10}^{8}$ W/${\mathrm{cm}}^{2}$) is determined by the intensity-dependent level width ($6f$ configuration) as well as the interference of the fine-structure states, and that the rates for hydrogen, in a much more intense beam (of order ${10}^{12}$ W/${\mathrm{cm}}^{2}$) are determined by both the intensity-dependent widths and shifts a$\stackrel{\mathrm{`}}{\mathrm{s}}$ well as the wave-function renormalization constants. The agreement of these two examples of calculations with the experiments done recently is satisfactory. For third-harmonic production the role of two-photon resonance is emphasized, and the dependence of the generated third-harmonic intensity on the intensity and frequency of the fundamental is discussed. Near resonance, the ratio of third-harmonic intensity to fundamental intensity saturates.

Physical Review A•May 1, 1974•14 citations

Theoretical and experimental study of the 6S-8S two-photon absorption cross-section in cesium atoms

Michael Caracas Núñez, Miguel A. Gonzalez, Mayerlin Núñez Portela

The probability of a two-photon absorption (TPA) process is quantified by means of the TPA cross-section. In this work the TPA cross-section for the 6 S 1/2 → 8 S 1/2 transition in cesium (Cs) atoms is obtained from a theoretical and experimental approach. It is calculated using second order perturbation theory including hyperfine structure and Doppler broadening for a thermal atomic vapor. The theoretical values for the TPA cross-sections of the two allowed hyperfine transitions are σ ~ 3,3 =3.10×10 −24 cm 4 /W and σ ~ 4,4 =3.65×10 −24 cm 4 /W. An experiment is set up to measure these cross-sections based on the quadratic dependence between the TPA transition rate and the intensity of the laser light. Values of σ ~ 3,3 =(3.6±1.1)×10 −24 cm 4 /W and σ ~ 4,4 =(4.6±1.1)×10 −24 cm 4 /W are obtained from the measurements. The results show an agreement between theory and experiment. To the best of our knowledge, this is the first time that these cross-sections are reported.

Optics Express•Aug 14, 2023•4 citations
An experimental study has been made of the perturbation of an atomic spectrum in a 10/sup 6/-V/cm laser field for the case of the 6S--6F transition in cesium. The 6S--6F transition energy was found to be a linear function of the intensity (a quadratic function of the field strength). The dynamic polarizability of this transition was determined. The experimental results are compared with perturbation-theory calculations.
This paper reports the four-photon ionization of caesium atoms when the laser frequency is tuned through the resonant three-photon transition 6S → 6F. This experiment was performed by using a tunable-wavelength bandwidth-limited subnanosecond laser pulse at 1.06 μm, in the 108-109 W.cm-2 laser intensity range. Pulse widths of 1.5 ns, 50 ps, and 15 ps were used. The resonant character of the multiphoton ionization process was observed, even with the shortest pulse of 15 ps. Nevertheless the influence of a temporal effect is demonstrated according to theoretical predictions. The resonance shift ΔE of the 6S → 6F transition energy was found to be linear with the laser intensity I within the range 108-109 W.cm-2. ΔE = α I, with α = 2 cm-1/GW.cm-2. This result confirms previous measurements performed with single-mode 35 ns laser pulses and is in very good agreement with calculated resonance shifts.
This work reports the multiphoton ionization of cesium atoms, via resonance with the 6F6F6F level, by interaction with a single transverse and longitudinal mode neodymium-glass laser beam. At a low rate of ion production, when the laser frequency is tuned through resonance, the laser intensity necessary to create a constant number of ions passes through a minimum, as expected, for a three-photon energy equal to the unperturbed $6S\ensuremath{\rightarrow}6F$ transition energy. But for a higher ionization rate, involving larger laser intensities, a departure from expectation is observed which is interpreted as a consequence of an energy shift of the transition. The level shifts are demonstrated in another way by their strong effect on the experimental order of nonlinearity of the interaction, Kexpt{K}_{\mathrm{expt}}Kexpt​. A sharp variation of Kexpt{K}_{\mathrm{expt}}Kexpt​ is observed when the energy shift of the $6S\ensuremath{\rightarrow}6F$ transition exactly compensates the wavelength detuning of the laser. The latter method gives shift values which are found to be independent of the large variations of the interaction volume under conditions of resonance. Both methods give a linear dependence of the shifts on the laser intensity. Identification of these shifts with energy shifts of the $6S\ensuremath{\rightarrow}6F$ transition is subject to theoretical reservations and needs further experimentation.
Orer a small range of light intensity the three-photon ionization rate of caesium atoms by ruby laser light decreases when the incident photon flux is increased. This result may be quantitatively explained by an induced energy shift of the 913 levels of the caesium atom proportional to the square of the light intensity. Thus perturbations of bound electron states by an intense light beam can be of importance in determining the multiphoton ionization rate. In this paper the functional dependence of the ionization rate on the photon flux is calculated for caesium, using a perturbation theory somewhat different from that usually employed.
The present paper applies the method of high-intensity quantum electrodynamics developed earlier to several problems of current experimental interest. In this paper the intensitydependent shifts and widths of atomic levels are calculated and applied to a given transition near resonance. The technique is demonstrated with three examples: the multiphoton ionization of atomic cesium and hydrogen in atomic beams and third-harmonic production in an atomic vapor. It is found that the multiphoton-ionization rate in a relatively weak laser beam (of order 108{10}^{8}108 W/cm2{\mathrm{cm}}^{2}cm2) is determined by the intensity-dependent level width (6f6f6f configuration) as well as the interference of the fine-structure states, and that the rates for hydrogen, in a much more intense beam (of order 1012{10}^{12}1012 W/cm2{\mathrm{cm}}^{2}cm2) are determined by both the intensity-dependent widths and shifts as‘\stackrel{\mathrm{`}}{\mathrm{s}}s‘ well as the wave-function renormalization constants. The agreement of these two examples of calculations with the experiments done recently is satisfactory. For third-harmonic production the role of two-photon resonance is emphasized, and the dependence of the generated third-harmonic intensity on the intensity and frequency of the fundamental is discussed. Near resonance, the ratio of third-harmonic intensity to fundamental intensity saturates.
The probability of a two-photon absorption (TPA) process is quantified by means of the TPA cross-section. In this work the TPA cross-section for the 6 S 1/2 → 8 S 1/2 transition in cesium (Cs) atoms is obtained from a theoretical and experimental approach. It is calculated using second order perturbation theory including hyperfine structure and Doppler broadening for a thermal atomic vapor. The theoretical values for the TPA cross-sections of the two allowed hyperfine transitions are σ ~ 3,3 =3.10×10 −24 cm 4 /W and σ ~ 4,4 =3.65×10 −24 cm 4 /W. An experiment is set up to measure these cross-sections based on the quadratic dependence between the TPA transition rate and the intensity of the laser light. Values of σ ~ 3,3 =(3.6±1.1)×10 −24 cm 4 /W and σ ~ 4,4 =(4.6±1.1)×10 −24 cm 4 /W are obtained from the measurements. The results show an agreement between theory and experiment. To the best of our knowledge, this is the first time that these cross-sections are reported.