The photon-wave-function formalism provides an alternative description of some quantum optical phenomena in a more intuitive way. We use this formalism to describe the process of correlated Stokes--anti-Stokes Raman scattering. In this process, two photons from a laser beam are inelastically scattered by a phonon created by the first photon (Stokes processes) and annihilated by the second photon (anti-Stokes process), producing a Stokes--anti-Sokes (SaS) photon pair. We arrive at an expression for the two-photon wave function of the scattered SaS photon pair, which is in agreement with a number of experimental results.
The photon-wave-function formalism provides an alternative description of some quantum optical phenomena in a more intuitive way. We use this formalism to describe the process of correlated Stokes--anti-Stokes Raman scattering. In this process, two photons from a laser beam are inelastically scattered by a phonon created by the first photon (Stokes processes) and annihilated by the second photon (anti-Stokes process), producing a Stokes--anti-Sokes (SaS) photon pair. We arrive at an expression for the two-photon wave function of the scattered SaS photon pair, which is in agreement with a number of experimental results.
The photon wave function formalism provides an alternative description of some quantum optical phenomena in a more intuitive way. We use this formalism to describe the Stokesanti-Stokes (SaS) correlated scattering process present in Raman scattering. In this process, two photons from a laser beam are inelastically scattered by a phonon created by the first photon (Stokes processes) and annihilated by the second photon (anti-Stokes process), producing a pair of Stokes–anti-Sokes (SaS) photons. . We arrive at an expression for the two-photon wavefunction, in the time and frequency domains, of the scattered SaS photon pair, which is in agreement with a number of experimental results. It was shown, from the phase matching analysis, that the scattering pattern is compatible with the experiments. It was seen that, in the application for Pump-and-probe experiments, it was possible to generate the correct curves for the decay of the population of phonons in the sample. Finally, it was verified that, through the analysis of the joint spectrum of the pairs, information was obtained about the entanglement in frequency of the scattered photons. Thus, it is concluded that, from the results, the photon wave function formalism provides an intuitive and robust way to calculate the SaS scattering properties.
The correlated Raman scattering, referred to here as the SaS process, occurs with the annihilation, within a material, of two photons of an excitation laser and the creation of a quantum correlated Stokes (S) and anti-Soktes (aS) photon pair where the phonon created in the S process is annihilated in the aS scattering. We found that, in addition to real SaS process where the energy exchange coincides with the energy of a vibrational state of the material, there is also the virtual SaS process, whose the exchange of energy and momentum between the photons of the laser, generating the S-aS photon pair, is mediated by a virtual vibrational excitation, setting up a photon-photon interaction similar to the electron-electron attraction responsible for the creation of Cooper pairs of the BCS theory of superconductivity. We observed the SaS process in transparent media in general, by measuring non-classical values of the normalized second-order cross-correlation function of the Stokes and anti-Stokes fields, 2(0). In diamond, we characterize the intensity of the virtual SaS scattering ( ) as a function of the virtual phonon energy, proving that the SaS process occurs only when the photon-photon interaction is attractive, as in the BCS theory for the Cooper pairs. We show that photons S and aS from the SaS process are scattered predominantly in the same polarization as the excitation laser of the sample and, with this, we implemented the pump-probe technique to study the lifetime of the real phonon (obtained in the diamond order 2.8 ps ) and the lifetime of the virtual excitation, which proved to be inferior to the temporal resolution of the measurement’s, characterizing one of the main differences between the two processes. We also observed that, due to the relations of energy and momentum conservation, have the same spatial intensity profile of the non-interacting laser that crosses the sample, different from the behavior observed for uncorrelated Raman scattering which spreads photons in all directions. We observed that the efficiency of the SaS scattering is proportional to the Raman scattering cross-section when we compare the process in different hydrocarbons and we generalize the observations made in the diamond to the sample of liquid decane. In water, the values of 2(0), predicted by the theoretical description of the process, corroborate the experimental data, validating the BCS theory for virtual SaS scattering, setting the pair of Stokes and anti-Stokes photons as counterparts of the Cooper pairs.
In this work we study the correlated Stokes and anti-Stokes Raman scattering, called here SaS. The SaS is an event where the same phonon participates in the of Stokes and anti-Stokes scattering processes. This process is not considered in current treatments of Raman scattering and can bring changes in the use of Raman spectroscopy for localtemperature measurements. Furthermore, these photons emerge as an important source of correlated photons pairs, widely used in quantum information, for example in implementing a quantum memory. We checked, by measurements of coincidence counting, that the Stokes and anti-Stokes photons generated in the Raman scattering from water, morespecifically the bands at }1644 1 concerning the angle variation mode between the H atoms, are quantum correlated. We get a value of 2(0) 517, much higher than what has been measured in others materials, as reported in the literature. We found that theintensity of the anti-Stokes signal has a quadratic dependence on the laser power, being another indication of the SaS occurrence. The value of 2(0) decays to high power values, in agreement with theoretical predictions. We have also obtained evidences that the SaScorrelation exhibits a dependence on the S and aS photon polarizations and can thus be exploited in future entanglement experiments.
In the correlated Stokes--anti-Stokes scattering (SAS) an incident photon interacts with a Raman-active material, creating a Stokes photon and exciting a quantum vibrational mode in the medium, which is posteriorly annihilated on contact with a second incident photon, producing in turn an anti-Stokes photon. This can be accomplished by real and virtual processes. In the real process the quantum mode shared between the Stokes and anti-Stokes events is a real particle, whereas in virtual processes the pair formation is mediated by the exchange of virtual particles. Here, we introduce a Hamiltonian to describe the pair production in SAS scattering, for both types of process, when stimulated by two orthogonally polarized laser pulses in a pump-and-probe configuration. We also model the effect of the natural decay of the vibration created in the Stokes event and compute the probability of producing SAS pairs. Additionally, we follow the dynamics of the vibration by considering the Stokes and anti-Stokes fields as external reservoirs, obtaining thus a master equation for the reduced density matrix for the vibrational population. Finally, we compare our theoretical results to recently published experimental data.
The process in which Raman scattering produces correlated Stokes and anti‐Stokes radiation is known as Stokes–anti‐Stokes (SaS) scattering. It has been shown recently that this process can generate entangled photon pairs, making it a promising tool for quantum optical technologies, but a proper quantum theoretical description was lacking. In this article, a fully quantum derivation of the electric polarization in a medium with vibrational Raman response, with quantized electromagnetic fields, is developed. Using quantum perturbation theory for Heisenberg operators, the solution for the material electric polarization is found and it is shown that a four‐wave mixing‐like correlated SaS scattering appears in the first order of perturbation and completely characterizes the nonresonant SaS photon pair production. It is also discussed how to construct the third‐order nonlinear optical susceptibility for the SaS scattering from the quantum formalism and show that it coincides with the one derived for classical fields in stimulated Raman.
A quantum model of the Raman process with the independent Stokes and anti-Stokes nonlinear interactions is developed to study nonclassical correlations between the photons in the Stokes and anti-Stokes fields. The role of the laser pump amplitude, the ratio of the Stokes and anti-Stokes coupling constants, and the population and losses of the vibrational mode in forming the correlations is elucidated. The g(2) intensity cross-correlation function, noise-reduction factor, two-mode principal squeezing variance, logarithmic negativity, nonclassicality depth, steering parameter, and the Bell parameter are analyzed side by side to shed light to the correlations between the Stokes and anti-Stokes fields. Conditions for having the Stokes and anti-Stokes fields composed of only photon pairs, similarly as it occurs in twin beams in parametric down-conversion, are revealed. They allow for nonzero mean thermal phonon numbers.