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Physical Review A

Stimulated Raman scattering: Unified treatment of spontaneous initiation and spatial propagation

Michael G. Raymer, Jan Mostowski

Published Oct 1, 1981• 358 citations
Publisher

Abstract

A theory of stimulated Raman scattering (SRS) is presented which treats in a unified manner the buildup of SRS from spontaneous Raman scattering and the spatial propagation which leads to gain. Maxwell-Bloch equations describe the coupling between the Stokes field operator and the collective atomic operators, which are driven by a classical laser field under low-signal-gain conditions, where the atomic ground states and laser field remain undepleted. An analytic expression is derived for the forward-propagating Stokes field operator in a one-dimensional spatial approximation when the Fresnel number of the excited medium is unity. Steady-state and transient Stokes intensities are evaluated under low-gain (spontaneous) and high-gain (stimulated) conditions. The Stokes intensity is found to be exactly independent of a laser bandwidth arising solely from phase fluctuations. The power spectrum of steady-state SRS is evaluated, giving a gain-narrowed spectral profile when the laser is narrow band, and a spectrum identical to the laser spectrum when the laser is broad band. A strong analogy between SRS and two-level superfluorescence is found; in both cases the macroscopic, collective dipole moment is initiated by quantum fluctuations.

DOI
10.1103/physreva.24.1980

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A pencil shaped region of a Raman-active medium forms a source for Stokes-shifted light via stimulated Raman Scattering (SRS) when driven by an intense laser pulse. Stokes photons are scattered spontaneously at first, and then amplified during propagation through the medium. Since the scattering is initiated by quantum noise, the actual number of photons produced in any given pulse will be highly uncertain, even if the pulse energy of the driving laser is constant1. As the Stokes light propagates through such an extended region, it's coherence properties will be changed. The spatial coherence is determined by the size and shape of the region, which may be characterized by its Fresnel number F, defined as F= A/λSL, where A is the cross-sectional area of the interaction region, which has length L, and λS is the Stokes wavelength. The rate at which the microscopic scatterers (atoms or molecules) are dephased by collisions affects the temporal coherence of the Stokes light, characterised by the temporal coherence parameter Γτ /gL, where Γ is the collisional dephasing rate, τ is the laser pulse duration and g is the steady-state Raman gain coefficient.

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Molecular cooperation in the transient regime of stimulated Raman scattering

Michael G. Raymer, Ian A. Walmsley

The nonlinear regime of stimulated Raman scattering (SRS) may be reached in two ways. The best known is that of depletion of the pump laser as a large number of photons are scattered into the Stokes field. There is, however, another way in which gain saturation can occur, that is, by depletion of the atomic population while the laser remains undepleted. The equations which describe SRS, including damping and population inversion,1 are remarkably similar to those of well-known theories of two-level superfluorescence, and it is possible by analogy to define a delay time τ D for cooperative Raman scattering (CRS). This delay time is inversely proportional to the spontaneous scattering rate, which depends on the pump laser intensity. A sufficient condition for CRS is that the spontaneous Stokes linewidth Γ is very much greater than τ D − 1 . The only other requirement is that there be more laser photons than scatterers, so that τ D is independent of the number of scatterers. The S(1) transition in molecular hydrogen, when excited by a short (≅ 100-ps) laser pulse, provides a possible system for observing pure CRS. Similar studies have been carried out previously2 for Γ ≅ τ D − 1 .

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Quantum Fluctuations in Picosecond Transient Stimulated Raman Scattering

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From a classical point of view the generation of Stokes light by stimulated Raman scattering (SRS) is not possible unless a Stokes input signal is supplied. On the other hand, the gain in SRS can be so large that without input the spontaneous build-up of strong Stokes waves can be observed. A proper quantum theoretical description1 shows that this spontaneous initiation of Stokes generation is due to microscopic random fluctuations originating from quantum noise associated with the dynamical variable Q(t) which is active in the Raman process, e.g., a molecular normal mode coordinate. In highly transient SRS -when the duration of the excitation pulse is shorter than the dephasing time- the Stokes field is proportional to the initial Heisenberg operator Q(0) describing the state of the system just before the excitation pulse is turned on (t=0). In this case the statistics of the final Stokes pulse energy is determined by quantum mechanical uncertainties associated with the random Raman polarization of the initial state2. On the other hand, in a steady state situation the Stokes pulse fluctuations are substantially reduced and the Stokes pulse energy is stabilized as a result of damping processes.

International Conference on Ultrafast Phenomena•Jan 1, 1984•0 citations
A theory of stimulated Raman scattering (SRS) is presented which treats in a unified manner the buildup of SRS from spontaneous Raman scattering and the spatial propagation which leads to gain. Maxwell-Bloch equations describe the coupling between the Stokes field operator and the collective atomic operators, which are driven by a classical laser field under low-signal-gain conditions, where the atomic ground states and laser field remain undepleted. An analytic expression is derived for the forward-propagating Stokes field operator in a one-dimensional spatial approximation when the Fresnel number of the excited medium is unity. Steady-state and transient Stokes intensities are evaluated under low-gain (spontaneous) and high-gain (stimulated) conditions. The Stokes intensity is found to be exactly independent of a laser bandwidth arising solely from phase fluctuations. The power spectrum of steady-state SRS is evaluated, giving a gain-narrowed spectral profile when the laser is narrow band, and a spectrum identical to the laser spectrum when the laser is broad band. A strong analogy between SRS and two-level superfluorescence is found; in both cases the macroscopic, collective dipole moment is initiated by quantum fluctuations.
The authors have extended the theory of stimulated Raman scattering to include the effects of laser bandwidths, in both the transient and steady-state regimes. The case of two interacting laser beams, a pump laser and a probe (Stokes) laser, is treated. Using the phase-diffusion model for laser bandwidth, the authors demonstrate that in the absence of dispersion, the forward Raman gain is essentially independent of the laser bandwidths in the high-gain limit, while in the low-gain limit the gain coefficient is inversely proportional to the sum of the bandwidths. It is further shown that when the pump-laser bandwidth is much larger than the linewidth of the Raman medium, the stimulated Stokes output assumes the same spectrum as the pump laser in the high-gain limit. A possible interpretation of these results is discussed assuming a "phase-locking" of the Stokes phase to the fluctuations in the pump-laser phase, due to the nonlinear interaction of the two beams through the Raman medium.
A quantum theory of stimulated Raman scattering is presented that takes into account three-dimensional propagation and collisional dephasing, allowing the study of the spatial and temporal coherence properties of the generated Stokes light. Maxwell-Bloch equations for the Stokes field operator and the collective atomic operators are solved analytically under low-signal-gain conditions, where the laser field and the atomic ground states remain undepleted. The intensity and the space-time autocorrelation function of the Stokes field are calculated. The Stokes field is expanded into a set of statistically independent ``coherence modes,'' which are determined explicitly for the case of a cylindrically shaped pumped volume. The Stokes pulse energy W is found to fluctuate from pulse to pulse. The probability distribution function for pulse energies P(W) is calculated for a range of Fresnel numbers of the excited volume and collisional dephasing rates. For small values of Fresnel number and dephasing rate, P(W) is a negative exponential distribution. For large values of either, P(W) narrows and approaches a Gaussian-shaped distribution. This occurs because many independent modes contribute to the Stokes emission, making it spatially and/or temporally incoherent.
We present a three-dimensional theory of stimulated Raman scattering (SRS) or super-radiance. In particular we address how the spatial and temporal properties of the generated SRS beam or Stokes beam of radiation depends on the spatial properties of the gain medium. Maxwell equations for the Stokes field operators and of the atomic operators are solved analytically and a correlation function for the Stokes field is derived. In the analysis we identify a super-radiating part of the Stokes radiation that exhibit beam characteristics. We show how the intensity in this beam builds up in time and at some point largely dominates the total Stokes radiation of the gain medium. We show how the SRS depends on the Fresnel number and the optical depth and that in fact these two factors are the only factors describing the coherent radiation.
A pencil shaped region of a Raman-active medium forms a source for Stokes-shifted light via stimulated Raman Scattering (SRS) when driven by an intense laser pulse. Stokes photons are scattered spontaneously at first, and then amplified during propagation through the medium. Since the scattering is initiated by quantum noise, the actual number of photons produced in any given pulse will be highly uncertain, even if the pulse energy of the driving laser is constant1. As the Stokes light propagates through such an extended region, it's coherence properties will be changed. The spatial coherence is determined by the size and shape of the region, which may be characterized by its Fresnel number F, defined as F= A/λSL, where A is the cross-sectional area of the interaction region, which has length L, and λS is the Stokes wavelength. The rate at which the microscopic scatterers (atoms or molecules) are dephased by collisions affects the temporal coherence of the Stokes light, characterised by the temporal coherence parameter Γτ /gL, where Γ is the collisional dephasing rate, τ is the laser pulse duration and g is the steady-state Raman gain coefficient.
The nonlinear regime of stimulated Raman scattering (SRS) may be reached in two ways. The best known is that of depletion of the pump laser as a large number of photons are scattered into the Stokes field. There is, however, another way in which gain saturation can occur, that is, by depletion of the atomic population while the laser remains undepleted. The equations which describe SRS, including damping and population inversion,1 are remarkably similar to those of well-known theories of two-level superfluorescence, and it is possible by analogy to define a delay time τ D for cooperative Raman scattering (CRS). This delay time is inversely proportional to the spontaneous scattering rate, which depends on the pump laser intensity. A sufficient condition for CRS is that the spontaneous Stokes linewidth Γ is very much greater than τ D − 1 . The only other requirement is that there be more laser photons than scatterers, so that τ D is independent of the number of scatterers. The S(1) transition in molecular hydrogen, when excited by a short (≅ 100-ps) laser pulse, provides a possible system for observing pure CRS. Similar studies have been carried out previously2 for Γ ≅ τ D − 1 .
From a classical point of view the generation of Stokes light by stimulated Raman scattering (SRS) is not possible unless a Stokes input signal is supplied. On the other hand, the gain in SRS can be so large that without input the spontaneous build-up of strong Stokes waves can be observed. A proper quantum theoretical description1 shows that this spontaneous initiation of Stokes generation is due to microscopic random fluctuations originating from quantum noise associated with the dynamical variable Q(t) which is active in the Raman process, e.g., a molecular normal mode coordinate. In highly transient SRS -when the duration of the excitation pulse is shorter than the dephasing time- the Stokes field is proportional to the initial Heisenberg operator Q(0) describing the state of the system just before the excitation pulse is turned on (t=0). In this case the statistics of the final Stokes pulse energy is determined by quantum mechanical uncertainties associated with the random Raman polarization of the initial state2. On the other hand, in a steady state situation the Stokes pulse fluctuations are substantially reduced and the Stokes pulse energy is stabilized as a result of damping processes.