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Journal of Physics B Atomic Molecular and Optical Physics

Abnormal anti-Stokes Raman emission as a coherent anti-Stokes Raman scattering-like process in disordered media

Ioan Baltog, Mihaela A. Baibarac, Ion Smaranda, S. Lefrant

Published Apr 19, 2011• 1 citation
Publisher

Abstract

In this paper, we demonstrate that, by continuous single beam excitation, one can generate an abnormal anti-Stokes Raman emission (AASRE) whose properties are similar to a coherent anti-Stokes Raman scattering (CARS). The effect has been observed in materials which possess intrinsically nonlinear properties (LiNbO3 and CdS), which have the electric susceptibility of third order different from zero, χ(3) ≠ 0, as well as in materials that become nonlinear under resonant optical excitation. In the latter case, we used poly-3,4-ethylendioxythiophene (PEDOT) in its undoped state deposited electrochemically on Au support. Raman studies corroborated with images of optical microscopy demonstrate that the production of AASRE is conditioned by the existence of a particular morphology of the sample able to ensure efficient transport of the light inside the sample through a multiple light scattering mechanism. In this context, it was found that LiNbO3 and CdS in powder form as well as the PEDOT films layered on a rough Au substrate are suitable morphological forms. We explain AASRE as resulting from a wave-mixing mechanism of the incident laser light ωl with a Stokes-shifted Raman light ωS produced by a spontaneous Raman light scattering process, both strongly scattered inside the sample. As a CARS process, AASRE is conditioned by the achievement of phase-matching requirements, which makes the difference between the wave vectors of mixing light close to zero, Δk =/2kl − kS − kCARS/≈ 0. In condensed media, the small dispersion of the refractive index makes Δk ≈ 0 so that the formation of a favourable phase-matching geometry may be accomplished even at a crossing angle θ of travelling scattered light ωl and ωS. For tightly focused beams, the requirement of phase matching relaxes; it is no longer sensitive to the Raman shift, so that a wide intense anti-Stokes Raman spectrum is observed at an angle larger than the Stokes Raman spectrum.

DOI
10.1088/0953-4075/44/9/095401

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In this paper, we demonstrate that, by continuous single beam excitation, one can generate an abnormal anti-Stokes Raman emission (AASRE) whose properties are similar to a coherent anti-Stokes Raman scattering (CARS). The effect has been observed in materials which possess intrinsically nonlinear properties (LiNbO3 and CdS), which have the electric susceptibility of third order different from zero, χ(3) ≠ 0, as well as in materials that become nonlinear under resonant optical excitation. In the latter case, we used poly-3,4-ethylendioxythiophene (PEDOT) in its undoped state deposited electrochemically on Au support. Raman studies corroborated with images of optical microscopy demonstrate that the production of AASRE is conditioned by the existence of a particular morphology of the sample able to ensure efficient transport of the light inside the sample through a multiple light scattering mechanism. In this context, it was found that LiNbO3 and CdS in powder form as well as the PEDOT films layered on a rough Au substrate are suitable morphological forms. We explain AASRE as resulting from a wave-mixing mechanism of the incident laser light ωl with a Stokes-shifted Raman light ωS produced by a spontaneous Raman light scattering process, both strongly scattered inside the sample. As a CARS process, AASRE is conditioned by the achievement of phase-matching requirements, which makes the difference between the wave vectors of mixing light close to zero, Δk =/2kl − kS − kCARS/≈ 0. In condensed media, the small dispersion of the refractive index makes Δk ≈ 0 so that the formation of a favourable phase-matching geometry may be accomplished even at a crossing angle θ of travelling scattered light ωl and ωS. For tightly focused beams, the requirement of phase matching relaxes; it is no longer sensitive to the Raman shift, so that a wide intense anti-Stokes Raman spectrum is observed at an angle larger than the Stokes Raman spectrum.
We demonstrate that under continuous single-beam excitation, one can generate an abnormal anti-Stokes Raman emission (AASRE) whose properties are similar to a coherent anti-Stokes Raman scattering. The effect has been observed in mesoscopic materials, which possess intrinsically nonlinear properties [lithium niobate (LiNbO3), bismuth germanium oxide (Bi12GeO20; BGO), bismuth silicon oxide (Bi12GeO20; BSO)], which have a nonzero electric susceptibility of the third order, χ(3)≠0. Corroborated Raman and coherent backscattering studies demonstrate that the occurrence of both effects is conditioned by the existence of a mesoscopic morphology of the sample, which is able to ensure efficient transport of the light inside the sample through a multiple light scattering mechanism. In this context, both AASRE and coherent backscattering effects are because of the Anderson localization of the light.
In theoretical investigations, we review several nonlinear optical approaches towards subdiffraction-limited resolution in label-free imaging via coherent anti-Stokes Raman scattering (CARS). Using a density matrix model and numerical integration, we investigate various level schemes and combinations of the light fields that induce CARS along with additional control laser fields. As the key to techniques that gain far-field resolution below the diffraction limit, we identify the inhibition of the buildup of vibrational molecular coherence via saturation or depletion of population (Beeker et al. Opt Express 17:22632–22638, 2009) or the generation of Stark broadening and spatially dependent Rabi sideband generation (Beeker et al. Phys Rev A 81(1), 2010). Depending on the coherence and population decay rates offered by a particular molecular energy level scheme, we identify various different regimes. In the first case, where an additional state (called the control state) and a vibrational state are able to rapidly exchange population via incoherent processes, a prepopulation of the upper vibrational state inhibits the buildup of vibrational coherence. With increasing control laser intensity, this suppresses CARS emission via an incoherent, saturation type of nonlinear process. Using an intense, donut-shaped control laser beam, similar to stimulated emission depletion (STED) microscopy, this can suppress CARS emission from all sample locations except within a subdiffraction-sized range around the central node. Scanning the control beams across the sample provides subdiffraction-limited resolution imaging. An alternative, which does not require a rapid exchange of population with the control state, applies a control beam that only partially depletes the vibrational ground state. Thereby, a CARS point spread function containing a subdiffraction-limited component is generated. Subdiffraction images can then be retrieved through deconvolution. Further approaches are based on the coherent, nonlinear, resonant response of the sample. In this case, CARS signal depletion by Stark splitting of the weakly populated upper vibrational state or the observation of spatially dependent Rabi oscillation may increase the resolution beyond the diffraction limit.
We present a theoretical investigation of stimulated emission pumping to achieve sub-diffraction-limited spatial resolution in coherent anti-Stokes Raman scattering (CARS) microscopy. A pair of control light fields is used to prepopulate the Raman state involved in the CARS process prior to the CARS signal generation. Efficient prepopulation is achieved by employing a path via an electronic or vibrational state. Thereby, the buildup of a coherence between the ground and Raman state during irradiation by the light fields for CARS signal generation is prevented, resulting in the suppression of the CARS intensity by more than 99.8%. Two-dimensional spatial excitation profiles have been calculated using donut-shaped spatial profiles for the control light fields, thus, an intensity-dependent narrowing of the CARS excitation profiles below the diffraction limit. Using computer-generated test images we demonstrate a resolution beyond the diffraction limit for CARS microscopy, which is scalable by the control light field intensity, similar to stimulated emission depletion microscopy.
The optical mixing of sufficiently coherent radiations of frequency (omega) 1 and (omega) 2 inside a suitable molecular medium can result coherent radiation at new frequency (omega) 3 equals [(omega) 1 + ((omega) 1 - (omega) 2)]. If (omega) 1 is kept fixed and (omega) 2 is varied so that a condition (omega) 1 - (omega) 2 equals (omega) is reached where (omega) is a molecular frequency of the medium, then (omega) 3 equals (omega) 1 + (omega) equals 2(omega) 1 - (omega) 2. In this case (omega) 3 coincides with the anti- Stokes Raman frequency associated with the molecular frequency (omega) . This process of coherent anti-Stokes Raman Scattering (CARS) is an important nonlinear optical process which provides intense collimated signal beams and is also an excellent spectroscopic tool. CARS being a four-wave mixing process, it is of interest to study the process in multi-level system to obtain a better insight into the problem. In the current paper we investigate the different quantum statistical properties of CARS in a inhomogeneously broadened three-level system based on density-matrix formalism where both the atomic system and the radiation fields are quantised. The photon-statistics, coherence characteristics and the occurrence of anti-bunching of the CARS field, in the steady state, are investigated.
We theoretically investigate a scheme in which backward coherent anti-Stokes Raman scattering (CARS) is significantly enhanced by using slow light. Specifically, we reduce the group velocity of the Stokes excitation pulse by introducing a coupling laser that causes electromagnetically induced transparency (EIT). When the Stokes pulse has a spatial length shorter than the CARS wavelength, the backward CARS emission is significantly enhanced. We also investigated the possibility of applying this scheme as a CARS lidar with O2 or N2 as the EIT medium. We found that if nanosecond laser with large pulse energy (>1 J) and a telescope with large aperture (~10 m) are equipped in the lidar system, a CARS lidar could become much more sensitive than a spontaneous Raman lidar.
Coherent anti-Stokes Raman scattering (CARS) is a well-known Raman scattering process that occurs when Stokes, anti-Stokes and pump waves are properly phase-matched. Using a quantum-field approach with Langevin noise sources, we calculate the noise figure for wavelength conversion between the Stokes and anti-Stokes waves in CARS and show its dependence on phase mismatch. Under phase matched conditions, the minimum noise figure is approximately 3 dB, with a correction that depends on the pump frequency, Stokes shift, refractive indices, and nonlinear susceptibilities. We calculate the photon statistics of CARS and show that the photon number distribution is non-Gaussian. Our findings may be significant for currently pursued applications of CARS including wavelength conversion in data transmission and spectroscopic detection of dilute biochemical species.