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Physical Review A

Nonlinear spectroscopy by multiresonant four-wave mixing

J. L. Oudar, Y. Ron Shen

Published Sep 1, 1980• 144 citations
Publisher

Abstract

Four-wave mixing processes with double and triple resonances are discussed in detail. Explicit expressions for the resonant nonlinear susceptibilities of various cases are derived. It is shown that in some cases, four-wave mixing can yield a spectrum with reduced inhomogeneous broadening. Possible applications of multiresonant four-wave mixing as a spectroscopic technique are considered. They include high-resolution spectroscopy, deduction of transition matrix elements, study of transitions between excited states, measurement of longitudinal relaxation times, distinction between resonant Raman scattering and resonant fluorescence, etc. Selective polarization arrangement allows us to suppress the nonresonant background, separately measure the real and imaginary parts of the resonant nonlinear susceptibility, minimize the effects of absorption and laser intensity fluctuations, and greatly enhance the signal-to-noise ratio.

DOI
10.1103/physreva.22.1141

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We explain the utility of third-order nonlinear susceptibility, χ (3) (ω 2 ; ±ω 1 , \({\mp}\omega_{1}\), ω 2 ), for the observation of resonances with homogeneous widths from inhomogeneously broadened distributions in three-level systems related to Raman or two-photon allowed electronic transitions. The line narrowing and high resolution capabilities are demonstrated theoretically using a model for inhomogeneous distributions of transitions in which we regard an absorption spectrum as the composition of some inhomogeneously broadened substructures. The experimental methods to separate a signal having frequency ω 2 from ingoing beam at the same frequency are outlined.

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Raman-resonant four-wave mixing and energy transfer

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When nonlinear four-wave mixing (FWM) is resonant with a Raman transition, it causes coupling between lightwaves separated by two Raman frequency shifts. This coupling is manifested in effects such as Raman gain suppression, higher-order Stokes generation, and coherent Raman spectroscopies (e.g., CARS). An understanding of these effects, however, has been impeded by a widespread misconception that Raman-resonant FWM does not transfer energy between the lightwaves and the medium. The equations for the photon densities at each light frequency show that, in actuality, two medium excitations are created or destroyed for each photon produced by FWM. This point may be further clarified by consideration of the driving nonlinear polarization and by comparisons with broadband Raman conversion and nonresonant FWM. The Raman gain suppression effect may be understood qualitatively in terms of destructive interference between FWM and the usual stimulated Raman process.

Annual Meeting Optical Society of America•Jan 1, 1987•0 citations
Four-wave mixing processes with double and triple resonances are discussed in detail. Explicit expressions for the resonant nonlinear susceptibilities of various cases are derived. It is shown that in some cases, four-wave mixing can yield a spectrum with reduced inhomogeneous broadening. Possible applications of multiresonant four-wave mixing as a spectroscopic technique are considered. They include high-resolution spectroscopy, deduction of transition matrix elements, study of transitions between excited states, measurement of longitudinal relaxation times, distinction between resonant Raman scattering and resonant fluorescence, etc. Selective polarization arrangement allows us to suppress the nonresonant background, separately measure the real and imaginary parts of the resonant nonlinear susceptibility, minimize the effects of absorption and laser intensity fluctuations, and greatly enhance the signal-to-noise ratio.
We explain the utility of third-order nonlinear susceptibility, χ (3) (ω 2 ; ±ω 1 , ∓ω1{\mp}\omega_{1}∓ω1​, ω 2 ), for the observation of resonances with homogeneous widths from inhomogeneously broadened distributions in three-level systems related to Raman or two-photon allowed electronic transitions. The line narrowing and high resolution capabilities are demonstrated theoretically using a model for inhomogeneous distributions of transitions in which we regard an absorption spectrum as the composition of some inhomogeneously broadened substructures. The experimental methods to separate a signal having frequency ω 2 from ingoing beam at the same frequency are outlined.
We treat the problem of four-wave resonant mixing of ultrashort laser pulses in gaseous media. We show that for some transitions, for example, quadrupole transitions, the polarization effects can be strongly manifested. For four-wave two-photon resonant mixing we find that the signal-wave plane rotation depends on the parameters of the resonant medium and the pulses mixed. We show that for long pump pulses and short signal pulses in the ultrashort-pulse time domain the angle of rotation of the plane of polarization of the signal plane can reach several dozen degrees. We show that the effect of altering the state of polarization of the short signal pulse can be used for measuring its shape and duration. Since the polarization measurements are precise and the proposed regimes of four-wave mixing do not depend on phase and amplitude fluctuations of the measuring pulse, the polarization four-wave mixing technique can be more accurate than the technique widely used for such purposes, measurement of the second-order intensity correlation function. We also discuss new nonlinear spectroscopy for measuring fast resonant susceptibilities (in particular, second-order polarizabilities) of the medium, based on the rotation of the polarization plane or the polarization ellipse of the signal pulse.
Recent research has expanded the capabilities of four-wave mixing by providing it with component selectivity, site selectivity, and mode selectivity. The selectivity is achieved by taking advantage of the three resonance enhancements that occur in a four-wave mixing process. New spectral scanning strategies allow one to scan a single resonance while maintaining the other two resonances at constant values. The constant resonances can be used to select a specific component, a specific site within an inhomogeneously broadened envelope of a component, and/or a specific vibrational or vibronic mode of that site. The scanned resonance will then contain enhanced features corresponding to the particular component, site, and/or mode that was chosen by the constant resonances. These component and site selective capabilities of the four-wave mixing complement the single vibronic level fluorescence methods. The relative transition intensities from a specific component or site reflect the mode coupling between the vibrational and vibronic modes. Since the four-wave mixing is fully resonant in these experiments, saturation effects play a dominant role and cannot be ignored. This review presents a complete discussion of the theoretical and experimental factors that control the fully resonant four-wave mixing. It shows examples of the component selectivity and the line narrowing capabilities. It also provides examples of how mode selection can identify mode coupling through the relative intensities of different vibrational features.
An influence of nonlinear interference processes at quantum transitions in strong resonance electromagnetic fields on absorption, amplification and refractive indices as well as on four-wave mixing processes is investigated. Doppler broadening of the coupled transitions, incoherent excitation, relaxation processes, as well as power saturation processes associated with the coupled levels are taken into account. Both closed (ground state is involved) and open (only excited states are involved) energy level configurations are considered. Common expressions are obtained which allow to analyze the optical characteristics (including gain without inversion and enhanced refractive index at vanishing absorption) for various V, (Lambda) and H configurations of interfering transitions by a simple substitution of parameters. Similar expressions for resonant four-wave mixing (FWM) in Raman configurations are derived too. Crucial role of Doppler broadening is shown. Theory is applied for numerical analysis of some recent and potential experiments.
When nonlinear four-wave mixing (FWM) is resonant with a Raman transition, it causes coupling between lightwaves separated by two Raman frequency shifts. This coupling is manifested in effects such as Raman gain suppression, higher-order Stokes generation, and coherent Raman spectroscopies (e.g., CARS). An understanding of these effects, however, has been impeded by a widespread misconception that Raman-resonant FWM does not transfer energy between the lightwaves and the medium. The equations for the photon densities at each light frequency show that, in actuality, two medium excitations are created or destroyed for each photon produced by FWM. This point may be further clarified by consideration of the driving nonlinear polarization and by comparisons with broadband Raman conversion and nonresonant FWM. The Raman gain suppression effect may be understood qualitatively in terms of destructive interference between FWM and the usual stimulated Raman process.