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.
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.
Controllable generation of photon pairs is essential for the utilization of quantum pair states for quantum applications such as quantum communication, quantum cryptography, teleportation, and linear optics quantum computing. Raman scattering is one of the most fundamental light-matter interactions and can be used to generate photon pairs. Using the spontaneous Stokes Raman interaction, a photon from a strong pump laser pulse is annihilated, and a Stokes photon and Raman-mediated collective excitation are created. This excitation can then be read out deterministically as an anti-Stokes photon with the application of a second laser pulse within the excitation lifetime, creating a photon pair. The heralding capability of the Stokes photon and lifetime of the excitation makes this source quasi-deterministic, where the anti-Stokes photon can be created at a later time than the Stokes. This gives additional advantages and uses over traditional photon-pair sources using nonlinear interactions of light in a transparent medium, which generate the pair of photons simultaneously. In this thesis, we study the correlations of photon pairs generated via spontaneous Raman interactions and demonstrate how these interactions can be used for quantum applications. First, we develop a model to study the spectral correlations between the Raman generated Stokes and anti-Stokes photons. This model is used to calculate the spectral single-photon purity of the photons in a generic material system ignoring the effects of material dispersion. We calculate how various parameters effect the purity including pump spectral bandwidth, excitation linewidth, and time delay between pump pulses. We then introduced an experimental realization of a Raman-mediated photon-pair source in an integrated quantum photonic circuit platform. Interstitial N2 molecules inherently trapped in silicon nitride thin films during the deposition process possess a sharp Raman mission corresponding to the vibrational mode of the molecules, which can be used as a Raman-mediated photon-pair source. We present evidence of N2 defects in silicon nitride thin films and estimate the defect density and excitation lifetime. By patterning the films into waveguide structures, the photon-matter interaction is enhanced. We perform finite-element simulation of light propagation in our fabricated waveguides and use the results to examine effects from the waveguide on ultrafast optical pulses and phase-matching requirements for efficient photon-pair generation. We then present experimental progress towards detecting Stokes and anti-Stokes photon-pair generation from N2 defects in silicon nitride waveguides. We show results from degenerate and non-degenerate wavelength optical pump pulses. We discuss limitations of the experimental methods and study in detail the sources of noise arising from the silicon nitride waveguide, and conclude by discussing future extensions on the results presented here.
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.
We propose a scheme of heralded storages of single photons via spontaneous Raman scattering (SRS) enhanced by a chiral standing-wave cavity, which creates a non-classically correlated pair of a spin wave and a Stokes photon (heralded photon) when a single-photon “write” pulse is applied to an atomic ensemble. In this scheme, to decrease the power of the write pulse for SRS, the write laser and the Stokes fields are aligned to propagate near-collinearly through the atoms. The short storage lifetime remains a challenge in standing-wave cavity-enhanced SRS. To prolong the storage lifetime, we achieve a long-wavelength spin-wave memory by removing the backward-scattering Stokes field from the cavity, which is realized by using non-reciprocal couplings between the Stokes fields and the atoms. In the experiment, the memory lifetime is demonstrated up to ∼100 μs, which is beyond the limitation (∼350 ns) of the storage in the atomic ensembles coupled to standing-wave cavities. We achieve a spin-wave memory for the write pulse containing a mean photon number of ∼4. The quantum correlation of the Stokes-spin-wave pairs is beyond 2, which gives strong evidence of non-classical behavior.
Single photon sources are fundamental elements for quantum information science, mainly for quantum key distribution (QKD) applications. Nevertheless, on-demand single photon sources are difficult to obtain, and their implementation in a practical application, such as QKD, demands further developments. A different approach to a single photon source is based on the generation of quantum correlated photon-pairs. In that case, the detection of one photon of the pair heralds the presence of the second photon. In this work, we present a heralded single photon source based on the spontaneous four-wave mixing (FWM) process in optical fibers. We characterize theoretically the heralded photon source by means of the conditional second-order coherence function, gc(2) , with gc(2) = 0 for a perfect single photon source. We observe the nonclassical nature of the source, with gc(2) ≪ 1 far below the classical limit. Our results also show that the Raman scattering in general degrades the quality of the source, due to the generation of uncorrelated photons. However, our findings show that in some frequency regimes we are able to observe a gc(2) ≈ 10−3. Moreover, our analysis shows that the propagation of the photons in a standard single mode fiber (SSMF) does not change significantly the value of gc(2), for distances of L < 25/α, with α the loss coefficient of the SSMF. This results can help to guide the development of single photon sources for quantum information applications.