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arXiv:2605.14825

Stokes-anti-Stokes correlations of light propagating through weakly guiding optical fiber

Ivan V. Panyukov, E. S. Andrianov

Published May 14, 2026• 0 citations
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Abstract

Statistical properties of light produced in spontaneous Raman scattering on an ensemble of molecules indicate the quantum nature of this phenomenon. The scattered light is non-classical and has high non-classical intensity correlations between Stokes and anti-Stokes components. The temporal coherence of this light is well investigated, while many questions related to spatial coherence remain open. Recent experiments reveal two peculiar features of the spatial coherence of the Stokes and anti-Stokes light. First, the intensity correlations between Stokes and anti-Stokes light remain non-classical even for macroscopic samples containing many molecules. Second, these correlations decrease when signal propagates through a multi-mode optical fiber: the more propagating fiber modes at Stokes and anti-Stokes frequencies the less the correlations. Moreover, the second-order autocorrelation function of Stokes and anti-Stokes light also decreases with the number of propagating modes in multi-mode fiber. In this paper, we build a model of spontaneous Raman scattering correlations of light produced by an ensemble of molecules and propagating through weakly guiding optical fiber that quantitatively explains all these observations. We show that spacial orthogonality of the fiber modes makes the light propagating through these modes uncorrelated in the standard detection scheme. This leads to suppression of non-classical intensity correlations of the total field in the multi-mode fiber. We find the degree of non-classical correlations on fiber parameters. The obtained results pave the way for engineering of non-classical Stokes -- anti-Stokes correlations.

DOI
10.48550/arxiv.2605.14825

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Statistical properties of light produced in spontaneous Raman scattering on an ensemble of molecules indicate the quantum nature of this phenomenon. The scattered light is non-classical and has high non-classical intensity correlations between Stokes and anti-Stokes components. The temporal coherence of this light is well investigated, while many questions related to spatial coherence remain open. Recent experiments reveal two peculiar features of the spatial coherence of the Stokes and anti-Stokes light. First, the intensity correlations between Stokes and anti-Stokes light remain non-classical even for macroscopic samples containing many molecules. Second, these correlations decrease when signal propagates through a multi-mode optical fiber: the more propagating fiber modes at Stokes and anti-Stokes frequencies the less the correlations. Moreover, the second-order autocorrelation function of Stokes and anti-Stokes light also decreases with the number of propagating modes in multi-mode fiber. In this paper, we build a model of spontaneous Raman scattering correlations of light produced by an ensemble of molecules and propagating through weakly guiding optical fiber that quantitatively explains all these observations. We show that spacial orthogonality of the fiber modes makes the light propagating through these modes uncorrelated in the standard detection scheme. This leads to suppression of non-classical intensity correlations of the total field in the multi-mode fiber. We find the degree of non-classical correlations on fiber parameters. The obtained results pave the way for engineering of non-classical Stokes -- anti-Stokes correlations.
It is known that spontaneous Raman scattering is accompanied by the appearance of nonclassical cross correlations of photons at Stokes and anti-Stokes frequencies. Such correlations occur due to the internal nonlinear interaction between electronic and nuclear vibration degrees of freedom. Since the properties of a given media are unchangeable, the possibilities for controlling the cross correlations are limited. This, in turn, restricts the possible applications of the correlated light obtained during the spontaneous Raman scattering. In this work, we investigate the influence of statistical properties of an incident light on the cross correlations of Stokes and anti-Stokes light. We show that the incoherence of the incident light results not only in the incoherence of the scattered light but also in the enhancement of the interbeam coherence at different frequencies. We demonstrate that the cross correlations of Stokes and anti-Stokes light intensities are enhanced when the incident light with high second-order autocorrelation function is applied. Our results pave the way to control correlated light obtained in the process of spontaneous Raman scattering.
Spontaneous vibrational Raman scattering is a ubiquitous form of light-matter interaction whose description necessitates quantization of the electromagnetic field. It is usually considered as an incoherent process because the scattered field lacks any predictable phase relationship with the incoming field. When probing an ensemble of molecules, the question therefore arises: What quantum state should be used to describe the molecular ensemble following spontaneous Stokes scattering? We experimentally address this question by measuring time-resolved Stokes-anti-Stokes two-photon coincidences on a molecular liquid consisting of several sub-ensembles with slightly different vibrational frequencies. When spontaneously scattered Stokes photons and subsequent anti-Stokes photons are detected into a single spatiotemporal mode, the observed dynamics is inconsistent with a statistical mixture of individually excited molecules. Instead, we show that the data are reproduced if Stokes-anti-Stokes correlations are mediated by a collective vibrational quantum, i.e. a coherent superposition of all molecules interacting with light. Our results demonstrate that the degree of coherence in the vibrational state of the liquid is not an intrinsic property of the material system, but rather depends on the optical excitation and detection geometry.
In the coherent anti-Stokes Raman scattering process, the spectrum of the generated optical phonon depends on the degree of temporal correlation between the pump laser field and the Stokes field. When the two fields are strongly correlated, such as when the Stokes field is generated with stimulated Raman scattering (SRS), the spectral shape of the optical phonon is found experimentally and theoretically to be the same as the gain-narrowed Raman line shape because the laser phase fluctuations cancel out totally, leaving only the collisional noise in the SRS process. When the two fields are uncorrelated, the shape of the optical-phonon spectrum is found to be the same as the Raman line shape without gain narrowing. When two fields are partially correlated, then the two spectral components appear together. We provide a method to measure the degree of correlation between two optical fields that have different central frequencies. The theory developed to interpret the experimental results is an extension of the quantum theory of SRS to include anti-Stokes scattering. We show that only in the high-gain limit can the quantum fluctuations be thought of as arising from a classical noise process.
Stimulated Raman scattering is conventionally employed to probe vibrational dynamics by inducing a coherent oscillation within a molecular ensemble. In contrast, spontaneous Raman scattering is considered as an incoherent process because the scattered field lacks any predictable phase relationship with the incoming laser pulse. It raises questions about the nature of the quantum state of a molecular ensemble following spontaneous Stokes scattering: should it be described as a statistical mixture of vibrationally excited molecules, where collective coherence is absent? Here, we measure time-resolved Stokes--anti-Stokes two-photon coincidences on a molecular liquid and find that a coherent superposition of two collective vibrational modes from two isotopic sub-ensembles is generated under spontaneous Raman scattering. Our results confirm that a spatially extended vibrational coherence emerges when a single collective excitation is spontaneously scattered and detected in a single spatiotemporal mode.
By investigating the intensity correlation function, we study the temporal mode properties of spontaneous Raman photons generated in single mode fibers pumped by short pulses. We find that the intensity correlation function of the Raman photons is related to the dispersion induced temporal mismatch among the Raman photons generated in different subparts of the fiber. When no temporal mismatch exists, the intensity correlation function only depends on the ratio between the pulse width of the pump and the coherence time of the Raman photons. With the ratio decreasing, the intensity correlation function increase. Our study is helpful for easily creating high-quality true thermal light which will be a useful resource for second-order coherence based remote sensing.
Light with high mutual correlations at different frequencies can be used to create heralded single-photon sources, which may serve as the basic elements of existing quantum cryptography and quantum teleportation schemes. One of the important examples in natural systems of light with high mutual correlations is the light produced by spontaneous Raman scattering on an ensemble of molecules. In this paper, we investigate the possibility of using Raman light to create a heralded single-photon source. We show that when using Stokes scattered light for postselection of anti-Stokes scattered light, the latter may possess single-photon properties. We analyze the influence of various negative factors on the characteristics of such a heralded single-photon source, which include a time delay between Stokes and anti-Stokes photons, the finiteness of the correlation radius of an external source, and background radiation. We show that the low value of the second-order autocorrelation function of the single-photon source is preserved even when the flow of uncorrelated photons exceeds the flow of correlated photons in scattered Raman light by an order of magnitude.