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

Negative nonlinear susceptibility of cesium vapor around 1.06 μm

Robert H. Lehmberg, John F. Reintjes, Robert C Eckardt

Published Mar 1, 1976• 25 citations
Publisher

Abstract

We outline a complete theory of the nonlinear susceptibility of cesium around 1.06 \ensuremath{\mu}m, and present the first measurements of the negative nonlinear refractive index ${n}_{2}$ primarily responsible for the self-defocusing that is observed. For linearly polarized light, our measured value of ${n}_{2}$ is $\ensuremath{-}(1.4\ifmmode\pm\else\textpm\fi{}0.2)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N$ esu, where $N$ is the atomic density. This is in reasonable agreement with our calculated value of $\ensuremath{-}2.62\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N$. The main portion of ${n}_{2}$ comes from a two-photon resonance between the $6s$ and $7s$ levels, and an additional negative term arises from induced population changes between $6s$ and $6p$. For circular polarization, ${n}_{2}$ arises mainly from the induced population changes, giving the measured and calculated values of $\ensuremath{-}(0.26\ifmmode\pm\else\textpm\fi{}0.03)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N$ and $\ensuremath{-}0.525\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N$, respectively. In our experiments where the 35-psec pulses were shorter than the $6s\ensuremath{-}6p$ inverse linewidth, the nonlinear susceptibility depends mainly on the instantaneous intensity; however, for longer pulses, one would obtain additional contributions proportional to time integrals over the intensity. Since the useful output power from large Nd laser systems is limited by self-focusing due to the laser glass, our results suggest the possibility of increasing this power by using Cs vapor for compensation.

DOI
10.1103/physreva.13.1095

Related papers

Two-photon resonantly enhanced self-defocusing in Cs vapor at 1.06 μ

Robert H. Lehmberg, John F. Reintjes, Robert C Eckardt

The electronic nonlinear refractive index in Cs vapor at 1.06 μ is shown to be negative and to consist of two distinct contributions. One of these contributions arises from a two-photon resonance in the susceptibility and can be made comparable in magnitude to the positive n2 in laser glass. The other term arises from population redistributions between the ground and first excited state. We present measurements of self-defocusing of a single pulse from a Nd: YAG mode-locked laser that are in agreement with the theoretical predictions.

Applied Physics Letters•Oct 1, 1974•31 citations

Complete compensation of self-phase modulation in cesium vapor at 1.06 μ

Robert H. Lehmberg, John F. Reintjes, Robert C Eckardt

We have observed a complete cancellation of self-phase modulation in 1.06-μ pulses propagating through cesium vapor. The negative nonlinear refractive index responsible for this is measured as n2/N=−(2.5±0.5) ×10−30 esu, in good agreement with the theoretical value −2.62×10−30 esu.

Applied Physics Letters•May 1, 1977•9 citations

Two photon resonantly enhanced self-defocusing in Cs Vapor at 1.06µ

Robert H. Lehmberg, John F. Reintjes, Robert C Eckardt

The electronic nonlinear refractive index in Cs Vapor at 1.06μ is shown to be negative and to consist of two distinct contributions. One of these arises from a two-photon resonance in the susceptibility, and can be made comparable in magnitude to the positive n2in laser glass. The other term arises from population redistribution between the ground and the first excited state. We present preliminary measurements of self defocusing of a single pulse from a Nd:YAG mode locked laser which are in agreement with the theoretical predictions.

Technical digest - International Electron Devices Meeting/Technical digest•Dec 1, 1974•0 citations

Resonant nonlinear refraction of 4–5−μm light in CO and CO2 gas

J. J. Pigeon, D. Tovey, Sergei Ya. Tochitsky +7 more

The resonant nonlinear refraction of $4\text{--}5\text{\ensuremath{-}}\ensuremath{\mu}\text{m}$ light in CO and $\mathrm{C}{\mathrm{O}}_{2}$ gas at a peak intensity of $15\phantom{\rule{0.16em}{0ex}}\mathrm{MW}/\mathrm{c}{\mathrm{m}}^{2}$ was demonstrated using time- and frequency-resolved measurements of self-focusing and self-defocusing. The nonlinearity of these molecular gases exhibits intensity-dependent sign reversals and a $<4\text{\ensuremath{-}}\mathrm{ns}$ response time. A change from self-focusing to self-defocusing or vice versa was observed to occur for Rabi frequencies that are comparable to the collisional linewidth. A density matrix model for the nonlinear susceptibility of a strongly driven two-level system provides a qualitative explanation for these results.

arXiv:2106.11131•Physical Review A•Oct 21, 2021•2 citations

Three Laser Experiments in Gases.

Michael Toubert Myers

This thesis describes three experiments performed in gases. Chapter 2 describes the first observation of four wave degenerate mixing in cesium vapor. Its basis in nonlinear optics is explained and a simple set of equations are derived which predict the resonant behavior, density dependence, and the power dependence of the signal. Experimental results are then compared to those predicted and reasonable agreement is obtained. A value of (chi)(,zxxz) is measured as (DIAGRAM, TABLE OR GRAPHIC OMITTED...PLEASE SEE DAI) compared to the value calculated of 2.8(.)10('-30) esu/atom. The agreement is satisfactory considering the competing processes involved such as photoionization, two-photon absorption, etc. which would tend to reduce the signal observed. The experimental difficulties encountered, i.e., large background and absorption of the laser, limit the usefulness of the process as a probe of the nonlinear optics of cesium. In the third chapter, results are given for measurements of inelastic scattering cross-sections for the 9D and 10D states of cesium. The cross-sections measured (in units of 10('-13)cm('2)) for the fine structure-changing collisions (sigma)(,21) Cs(n('2)D(,5/2)) + Cs(6('2)S(,1/2)) Cs(n('2)D(,3/2)) + Cs(6('2)S(,1/2)) (sigma)(,12) for n = 9 and n = 10 are 1.50 (+OR-) 0.3 and 2.01 (+OR-) 0.4, for (sigma)(,t1) respectively. The cross sections for nonradiative relaxation (sigma)(,t2) Cs(n('2)D(,5/2)) + Cs(6('2)S(,1/2)) out of D states (sigma)(,t1) Cs(n('2)D(,3/2) )+(, )Cs(6('2)S(,1/2)) out of D states for n = 9 and n = 10 are 0.66 (+OR-) 0.3 and 1.4 (+OR-) 0.4 for (sigma)(,t1) and 1.1 (+OR-) 0.4 and 1.7 (+OR-) 0.4 for (sigma)(,t2), respectively. The cross-sections agree well with previously measured values, where available, and represented the first experimental verification that the cross-sections (sigma)(,t1) and (sigma)(,t2) are the same within our experimental uncertainties. In chapter 4 we report the observation of cancellation of rotational e-fects in the intensity of ultraviolet b and s of OH. The b and oscillator strength for transition in the (1,0) b and of OH has been measured and found to be independent of rotational excitation. This independence is explained in terms of the cancellation of a rotationally induced increase in the Franck-Condon factor by an equivalent decrease in the electronic transition moment. We have also remeasured the (0,0) b and oscillator strength as a function of rotational energy and obtained a value for (rho) = 0.75 (+OR-) 0.02A('-1). This value is used along with spectroscopic data to fit a simple model for explaining rotationally induced effects. Very good agreement is found with our data and previous calculations.

•Jan 1, 1981•0 citations

Two-photon resonant, optical third-harmonic generation in cesium vapor

K. M. Leung, John Francis Ward, Brian J. Orr

Resonant enhancement of optical third-harmonic generation in cesium vapor has been observed when twice the energy of the fundamental photon becomes equal to the energy difference between the $9d^{2}D_{\frac{3}{2}}$ level and the ground state of the cesium atom. The measured, effective coefficient is ${10}^{\ensuremath{-}30}$ esu/atom, which is more than a factor ${10}^{8}$ larger than the corresponding coefficient for the helium atom. An effective coefficient is synthesized by first calculating the coefficient for a single cesium atom at rest and then including the effects of Doppler broadening and the fundamental laser spectrum. The calculated value is in satisfactory agreement with experiment.

Physical Review A•Jun 1, 1974•59 citations
We outline a complete theory of the nonlinear susceptibility of cesium around 1.06 \ensuremath{\mu}m, and present the first measurements of the negative nonlinear refractive index n2{n}_{2}n2​ primarily responsible for the self-defocusing that is observed. For linearly polarized light, our measured value of n2{n}_{2}n2​ is \ensuremath−(1.4\ifmmode±\else\textpm\fi0.2)\ifmmode×\else\texttimes\fi10\ensuremath−30N\ensuremath{-}(1.4\ifmmode\pm\else\textpm\fi{}0.2)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N\ensuremath−(1.4\ifmmode±\else\textpm\fi0.2)\ifmmode×\else\texttimes\fi10\ensuremath−30N esu, where NNN is the atomic density. This is in reasonable agreement with our calculated value of \ensuremath−2.62\ifmmode×\else\texttimes\fi10\ensuremath−30N\ensuremath{-}2.62\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N\ensuremath−2.62\ifmmode×\else\texttimes\fi10\ensuremath−30N. The main portion of n2{n}_{2}n2​ comes from a two-photon resonance between the 6s6s6s and 7s7s7s levels, and an additional negative term arises from induced population changes between 6s6s6s and 6p6p6p. For circular polarization, n2{n}_{2}n2​ arises mainly from the induced population changes, giving the measured and calculated values of \ensuremath−(0.26\ifmmode±\else\textpm\fi0.03)\ifmmode×\else\texttimes\fi10\ensuremath−30N\ensuremath{-}(0.26\ifmmode\pm\else\textpm\fi{}0.03)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N\ensuremath−(0.26\ifmmode±\else\textpm\fi0.03)\ifmmode×\else\texttimes\fi10\ensuremath−30N and \ensuremath−0.525\ifmmode×\else\texttimes\fi10\ensuremath−30N\ensuremath{-}0.525\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}30}N\ensuremath−0.525\ifmmode×\else\texttimes\fi10\ensuremath−30N, respectively. In our experiments where the 35-psec pulses were shorter than the 6s\ensuremath−6p6s\ensuremath{-}6p6s\ensuremath−6p inverse linewidth, the nonlinear susceptibility depends mainly on the instantaneous intensity; however, for longer pulses, one would obtain additional contributions proportional to time integrals over the intensity. Since the useful output power from large Nd laser systems is limited by self-focusing due to the laser glass, our results suggest the possibility of increasing this power by using Cs vapor for compensation.
The electronic nonlinear refractive index in Cs vapor at 1.06 μ is shown to be negative and to consist of two distinct contributions. One of these contributions arises from a two-photon resonance in the susceptibility and can be made comparable in magnitude to the positive n2 in laser glass. The other term arises from population redistributions between the ground and first excited state. We present measurements of self-defocusing of a single pulse from a Nd: YAG mode-locked laser that are in agreement with the theoretical predictions.
The electronic nonlinear refractive index in Cs Vapor at 1.06μ is shown to be negative and to consist of two distinct contributions. One of these arises from a two-photon resonance in the susceptibility, and can be made comparable in magnitude to the positive n2in laser glass. The other term arises from population redistribution between the ground and the first excited state. We present preliminary measurements of self defocusing of a single pulse from a Nd:YAG mode locked laser which are in agreement with the theoretical predictions.
The resonant nonlinear refraction of $4\text{--}5\text{\ensuremath{-}}\ensuremath{\mu}\text{m}$ light in CO and CO2\mathrm{C}{\mathrm{O}}_{2}CO2​ gas at a peak intensity of 15MW/cm215\phantom{\rule{0.16em}{0ex}}\mathrm{MW}/\mathrm{c}{\mathrm{m}}^{2}15MW/cm2 was demonstrated using time- and frequency-resolved measurements of self-focusing and self-defocusing. The nonlinearity of these molecular gases exhibits intensity-dependent sign reversals and a $<4\text{\ensuremath{-}}\mathrm{ns}$ response time. A change from self-focusing to self-defocusing or vice versa was observed to occur for Rabi frequencies that are comparable to the collisional linewidth. A density matrix model for the nonlinear susceptibility of a strongly driven two-level system provides a qualitative explanation for these results.
This thesis describes three experiments performed in gases. Chapter 2 describes the first observation of four wave degenerate mixing in cesium vapor. Its basis in nonlinear optics is explained and a simple set of equations are derived which predict the resonant behavior, density dependence, and the power dependence of the signal. Experimental results are then compared to those predicted and reasonable agreement is obtained. A value of (chi)(,zxxz) is measured as (DIAGRAM, TABLE OR GRAPHIC OMITTED...PLEASE SEE DAI) compared to the value calculated of 2.8(.)10('-30) esu/atom. The agreement is satisfactory considering the competing processes involved such as photoionization, two-photon absorption, etc. which would tend to reduce the signal observed. The experimental difficulties encountered, i.e., large background and absorption of the laser, limit the usefulness of the process as a probe of the nonlinear optics of cesium. In the third chapter, results are given for measurements of inelastic scattering cross-sections for the 9D and 10D states of cesium. The cross-sections measured (in units of 10('-13)cm('2)) for the fine structure-changing collisions (sigma)(,21) Cs(n('2)D(,5/2)) + Cs(6('2)S(,1/2)) Cs(n('2)D(,3/2)) + Cs(6('2)S(,1/2)) (sigma)(,12) for n = 9 and n = 10 are 1.50 (+OR-) 0.3 and 2.01 (+OR-) 0.4, for (sigma)(,t1) respectively. The cross sections for nonradiative relaxation (sigma)(,t2) Cs(n('2)D(,5/2)) + Cs(6('2)S(,1/2)) out of D states (sigma)(,t1) Cs(n('2)D(,3/2) )+(, )Cs(6('2)S(,1/2)) out of D states for n = 9 and n = 10 are 0.66 (+OR-) 0.3 and 1.4 (+OR-) 0.4 for (sigma)(,t1) and 1.1 (+OR-) 0.4 and 1.7 (+OR-) 0.4 for (sigma)(,t2), respectively. The cross-sections agree well with previously measured values, where available, and represented the first experimental verification that the cross-sections (sigma)(,t1) and (sigma)(,t2) are the same within our experimental uncertainties. In chapter 4 we report the observation of cancellation of rotational e-fects in the intensity of ultraviolet b and s of OH. The b and oscillator strength for transition in the (1,0) b and of OH has been measured and found to be independent of rotational excitation. This independence is explained in terms of the cancellation of a rotationally induced increase in the Franck-Condon factor by an equivalent decrease in the electronic transition moment. We have also remeasured the (0,0) b and oscillator strength as a function of rotational energy and obtained a value for (rho) = 0.75 (+OR-) 0.02A('-1). This value is used along with spectroscopic data to fit a simple model for explaining rotationally induced effects. Very good agreement is found with our data and previous calculations.
Resonant enhancement of optical third-harmonic generation in cesium vapor has been observed when twice the energy of the fundamental photon becomes equal to the energy difference between the 9d2D329d^{2}D_{\frac{3}{2}}9d2D23​​ level and the ground state of the cesium atom. The measured, effective coefficient is ${10}^{\ensuremath{-}30}$ esu/atom, which is more than a factor 108{10}^{8}108 larger than the corresponding coefficient for the helium atom. An effective coefficient is synthesized by first calculating the coefficient for a single cesium atom at rest and then including the effects of Doppler broadening and the fundamental laser spectrum. The calculated value is in satisfactory agreement with experiment.