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Journal of Optical Technology

Nonsteady-state anti-Stokes near-field spectroscopy in the optical superradiation regime

S. N. Andrianov, Yu. E. Pol’skii

Published May 1, 2006• 0 citations
Publisher

Abstract

This paper proposes a new form of nonsteady-state anti-Stokes near-field spectroscopy with high spatial resolution in Dicke's optical superradiation regime. A system of kinetic equations is constructed that describes collections of excited atoms and fluorescence photons in the far field. It is solved approximately, and a formula is obtained for the signal intensity of nonsteady-state anti-Stokes near-field spectroscopy. Possible ways of constructing a new method of high-spatial-resolution spectroscopy of atoms and molecules are discussed.

DOI
10.1364/jot.73.000305

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Saturation effects in coherent anti-Stokes Raman scattering

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Physical Review A•Mar 1, 1982•39 citations
This paper proposes a new form of nonsteady-state anti-Stokes near-field spectroscopy with high spatial resolution in Dicke's optical superradiation regime. A system of kinetic equations is constructed that describes collections of excited atoms and fluorescence photons in the far field. It is solved approximately, and a formula is obtained for the signal intensity of nonsteady-state anti-Stokes near-field spectroscopy. Possible ways of constructing a new method of high-spatial-resolution spectroscopy of atoms and molecules are discussed.
This paper is devoted to the study of the cooperative two-photon scattering processes between two resonator modes stimulated by an excited atomic beam. It has been proved that these collective scattering phenomena between the Stokes and anti-Stokes resonator modes are taking place due to the energy transfer between these fields. The statistical properties of the Stokes and anti-Stokes photons have been described using the photon correlation functions. The numerical solution of this equation describes the statistical transformation of n-Stokes photons into anti-Stokes photons.
A simple description of the stimulated Raman emission of Stokes radiation, and of the induced absorption found by Stoicheff at the anti-Stokes frequency, is based on the semiclassical theory of radiation. This theory gives the well-known formulas for absorption and stimulated emission when carried to the first order in the time-dependent perturbation due to the interaction of the light beam with the molecules. If there are two light beams of frequencies ωL and ω, the second-order perturbation may be associated with stimulated emission at the Stokes frequency ω=ω−1=ωL—ωR and with induced absorption at the anti-Stokes frequency ω=ω1=ωL+ωR, where ωL is the laser frequency and ωR a Raman-active vibrational frequency; in both cases, there is a molecular transition to the excited vibrational state. The highly directional and very sharp anti-Stokes emission at ω1 arises from the conversion by molecules in intense beams at ωL and ω−1 of two ωL photons into an ω−1, ω1 pair. Like spontaneous emission from excited states, the production of this anti-Stokes radiation requires the full quantum theory of radiation for an adequate description. The emission of ω1 and the observed directional absorption of ω−1 due to the reverse conversion ω−1+ω1→2ωL are explained. The anti-Stokes emission is proportional to the Stokes intensity and to the square of that of the laser, and to the square of the molecular number density; its sharpness is due to the absence of a molecular transition. The generation of photon pairs ω−n+ωn, where ωn=ωL+nωR, can occur for all values of n, but it is most efficient for n=1, due to resonance in the appropriate molecular hyperpolarizability and to the intensity of the Stokes beam at ω−1.
During the last half century, quantum coherence has been of great interest due to its own right and also due to its broad range of applications in many areas of physics. The reason for that is the technological progress made last century, specially, the invention of coherent light sources and their commercialization. Indeed, coherent laser sources allow us to coherently excite atoms and molecules, as a consequence, to study variety of coherent and collective phenomena in atomic physics, for instance, coherent optical spectroscopy, superradiance, superflourescence, lasing without inversion and so forth. Interestingly, recent studies in biological systems also seem to exhibit coherent processes, in particular, photosynthetic transport and avian compass.\n\nIn this dissertation, we present some of the theory and applications of the quantum coherence. This study considers (i) application of quantum coherence to enhance output signals of coherent anti-Stokes Raman spectroscopy of optically active media (chiral molecules), (ii) a way to find general formulas of single- and double-excited subradiant Dicke states using symmetry group theory, (iii) an impact of Fano-Agarwal coupling and other virtual processes arising from non-rotating wave approximation on the decay of super and subradiant timed Dicke states, and finally (iv) quantum coherence and collective phenomena of relativistically and uniformly accelerating atoms.\n\nApplications of the results presented in the dissertation may be a new method for resolving chirality of molecules using coherent anti-Stokes Raman spectroscopy - Raman optical activity, and a sidewise excitation method for single- and double-excited subradiant states. The obtained results also advance our theoretical understanding of quantum coherence specially theory of super and subradiance.
Saturation effects in coherent anti-Stokes Raman scattering (CARS) spectroscopy are discussed. The discussion is limited to Raman-resonant CARS (${\ensuremath{\omega}}_{l}\ensuremath{-}{\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{21}$, where ${\ensuremath{\omega}}_{l,s}$ are the frequencies of the pump fields with powers Pl,s{P}_{l,s}Pl,s​, and ${\ensuremath{\omega}}_{21}$ is the frequency of the Raman transition $|1〉\ensuremath{\rightarrow}|2〉$) with the possible addition of a one-photon resonance (${\ensuremath{\omega}}_{l}\ensuremath{\simeq}{\ensuremath{\omega}}_{31}$ is the frequency of the electronic transition $|1〉\ensuremath{\rightarrow}|3〉$). For these cases we show that the CARS polarization pCARS{\mathcal{p}}_{\mathrm{CARS}}pCARS​ is proportional to the off-diagonal density-matrix element ${\ensuremath{\rho}}_{21}$. In order to determine ${\ensuremath{\rho}}_{21}$, we use Laplace transforms to solve the Bloch equations for the effective two-level system ∣1〉|1〉∣1〉 and ∣2〉|2〉∣2〉 when ${\ensuremath{\omega}}_{l}$ is far from resonance, or for the three-level system ∣1〉,∣2〉|1〉,|2〉∣1〉,∣2〉, and ∣3〉|3〉∣3〉, when ${\ensuremath{\omega}}_{l}\ensuremath{\simeq}{\ensuremath{\omega}}_{31}$. The steady-state expression for pCARS{\mathcal{p}}_{\mathrm{CARS}}pCARS​ in the former case gives ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}{P}_{s}^{\frac{1}{2}}$ at low powers and ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}^{0}{P}_{s}^{\frac{\ensuremath{-}1}{2}}$ at high powers. In the three-level system, we show that when the pressure is low and at least one field is weak, the slow time dependence of ${\ensuremath{\rho}}_{21}$ must be considered. When one field is strong and the other weak, the CARS spectrum is Stark split. When Pl{P}_{l}Pl​ is high, for example, ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}^{0}{P}_{s}^{\frac{1}{2}}$ for ${\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{32}$ and ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{({P}_{l}{P}_{s})}^{\frac{1}{2}}$ when ${\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{32}\ifmmode\pm\else\textpm\fi{}{V}_{13}$ where V13{V}_{13}V13​ is the one-photon Rabi frequency for the $|1〉\ensuremath{\rightarrow}|3〉$ transition. The Wilcox-Lamb approximation is used to reduce the three-level Bloch equations to rate equations containing one- and two-photon terms. When the fields are so weak that both one- and two-photon terms are small compared to the decay terms, the usual expression for pCARS{\mathcal{p}}_{\mathrm{CARS}}pCARS​ is reproduced. If only the direct two-photon processes are important, the effective-two-system results are reproduced. When both fields are intense and nearly resonant, the steady state is rapidly achieved. The results for the case where one field is much stronger than the other are essentially the same as those for one strong and one weak field. When the fields are of comparable strength, ${\mathcal{p}}_{\mathrm{CARS}}\ensuremath{\propto}{P}_{l}^{\frac{1}{2}}{P}_{s}^{0}$ for ${\ensuremath{\omega}}_{l}\ensuremath{\simeq}{\ensuremath{\omega}}_{31}$ and ${\ensuremath{\omega}}_{s}\ensuremath{\simeq}{\ensuremath{\omega}}_{32}$, and the CARS spectrum is split into five components.