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Journal of Physics B Atomic and Molecular Physics

Polarization effects in stimulated Raman scattering and related phenomena

Laurence David Barron

Published Nov 1, 1970• 5 citations
Publisher

Abstract

Polarization effects in stimulated Raman and stimulated Rayleigh scattering and self focusing are investigated from the viewpoint of the scattering of polarized photons by molecules. Both stimulated vibrational Raman scattering in liquids and stimulated rotational Raman scattering in gases are considered, and it is demonstrated that the polarization changes and relative power thresholds for different laser polarizations should be somewhat different to those predicted in other theories. For example, the ellipticity eta 0 of the stimulated rotational Raman photons in the forward direction from Delta J=+or-2 transitions in gaseous symmetric top molecules is given in terms of the initial ellipticity eta 1 by sin 2 eta 0 = - 5 / 7 sin 2 eta 1 , whereas conventional theories predict that eta 0 and eta 1 are equal in magnitude and opposite in sign. Furthermore it is shown that deviations from this relation could provide a measure of the degree of optical orientation of the molecules.

DOI
10.1088/0022-3700/3/11/017

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Stimulated Raman Scattering

Raman scattering is a two-photon process [1]. As illustrated in Fig. la, an incident photon is annihilated and a new photon of a different frequency is created. This implies that the scattering is inelastic, and the medium is left in a different energy state. When the scattered photon is lower in energy, or frequency, it is said to be Stokes shifted. The shift in frequency of the Stokes photon is related to a characteristic frequency of the medium. This is illustrated in Fig. 2a. Calling this characteristic material excitation frequency ω)v, the Stokes frequency is then ωs = ΩL — ωv, where ωL is the incident laser frequency. Thus, Raman (Stokes) scattering results in an excitation from the ground state of the medium to an excited state mediated by a two-photon inelastic scattering. The internal material excitation can involve the creation of an excited electronic state, an excited vibrational-rotational state, a lattice vibration, a spin flip in semiconductors, or electron waves in plasmas [2]. The phenomenon occurs in gases, liquids, solids, and plasmas.

CRC Press eBooks•Apr 22, 2003•1 citation
Polarization effects in stimulated Raman and stimulated Rayleigh scattering and self focusing are investigated from the viewpoint of the scattering of polarized photons by molecules. Both stimulated vibrational Raman scattering in liquids and stimulated rotational Raman scattering in gases are considered, and it is demonstrated that the polarization changes and relative power thresholds for different laser polarizations should be somewhat different to those predicted in other theories. For example, the ellipticity eta 0 of the stimulated rotational Raman photons in the forward direction from Delta J=+or-2 transitions in gaseous symmetric top molecules is given in terms of the initial ellipticity eta 1 by sin 2 eta 0 = - 5 / 7 sin 2 eta 1 , whereas conventional theories predict that eta 0 and eta 1 are equal in magnitude and opposite in sign. Furthermore it is shown that deviations from this relation could provide a measure of the degree of optical orientation of the molecules.
A theoretical study of the polarization dependence of stimulated Rayleigh-wing scattering and the optical-frequency Kerr effect has been undertaken. When the incident light is circularly polarized, a striking difference in gain is found for the co- and counter-rotating senses of polarization of the scattered light---the former being suppressed and the latter being exceptionally favored. The analysis begins with a model for the Kerr effect, which involves the alignment of anisotropic molecules in an electric field, but the results can be immediately generalized to any light scattering process of tensor symmetry. The nonlinear problem of the propagation of an intense elliptically polarized light wave in a Kerr-active medium is shown to have a solution in which the vibrational ellipse undergoes self-precession and self-retardation. The stimulated scatterings or instabilities of such a self-precessing and self-retarding light wave are obtained for the backward and forward directions. Birefringence, optical activity, and linear and circular dichroisms are some of the phenomena which result, but the forward direction yields substantially different results from the backward direction because of Stokes-anti-Stokes coupling.
The phenomenon of stimulated Rayleigh-wing scattering in anisotropic molecular liquids is analyzed. Representative combinations of polarization for the incident and scattered light are considered. It is shown that in regions where the focused laser beam is intense, saturation occurs in the molecular response to external optical fields, in that perfect alignment of the individual liquid molecules in the optical fields is approached. Accordingly, the nonlinear amplification associated with the stimulated radiation is reduced. The results of the analysis qualitatively explain several important recent observations which are in conflict with previous theroretical predictions. For example, it is shown that the nonlinear gain is considerably greater when the incident light is circularly polarized (the stimulated radiation being circularly polarized in the reverse sense) than it is when the incident light is linearly polarized. Despite saturation, sufficient amplification exists in the former case to allow the efficient conversion of incident to stimulated Rayleigh light at moderate power levels.
An investigation was made of the influence of different excitation conditions on the self-focusing of stimulated Raman-scattered light. It was found that the dimensions of self-focusing filaments and their number depended on the energy of the exciting radiation and the thickness of the scattering layer. In the situation in which self-focusing points were observed at both ends of a Dewar flask, the anti-Stokes scattering included (in addition to rings of class 1) scattering along the axis. Estimates were obtained of the self-focusing threshold power related to the Kerr effect and to the increase in the polarizability of molecules due to excitation. It was found that the first of these mechanisms could not give rise to self-focusing of the Raman-scattered light, whereas the threshold of the second mechanism was close to the excitation energy at which such self-focusing was observed.
Transient stimulated rotational Raman scattering induced by a polarization-modulated femtosecond pulse whose polarization varies with time is reported. The peak intensity of the polarization-modulated pulse produced in this study is low compared to that of a pulse without polarization variation, and this leads to the low efficiency of self-phase-modulation and thus the high efficiency of stimulated Raman scattering compared to the case of a pump pulse without polarization modulation. The scattering process is unique in terms of the high peak ratio of the anti-Stokes to Stokes emissions compared to the ratio in the case of the scattering induced by linearly, circularly, and elliptically polarized pump pulses. Under optimum conditions, the ratio approaches 1, which is not realized in the general case of stimulated rotational Raman scattering.
Raman scattering is a two-photon process [1]. As illustrated in Fig. la, an incident photon is annihilated and a new photon of a different frequency is created. This implies that the scattering is inelastic, and the medium is left in a different energy state. When the scattered photon is lower in energy, or frequency, it is said to be Stokes shifted. The shift in frequency of the Stokes photon is related to a characteristic frequency of the medium. This is illustrated in Fig. 2a. Calling this characteristic material excitation frequency ω)v, the Stokes frequency is then ωs = ΩL — ωv, where ωL is the incident laser frequency. Thus, Raman (Stokes) scattering results in an excitation from the ground state of the medium to an excited state mediated by a two-photon inelastic scattering. The internal material excitation can involve the creation of an excited electronic state, an excited vibrational-rotational state, a lattice vibration, a spin flip in semiconductors, or electron waves in plasmas [2]. The phenomenon occurs in gases, liquids, solids, and plasmas.