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Possible influence of the non-classical nature of light on biological systems

James Kevin Koga

Published Dec 4, 2019• 0 citations
OpenAlex

Abstract

It has been shown that laser sight shown in water can convert some of the light into nonclassical photon pairs. Also, photonic counterparts of Cooper pairs have been shown to occur when light scatters off of various media. Here, we consider the effects of non-classical light produced by such interactions on biological systems and whether there could be an influence.

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It has been shown that laser sight shown in water can convert some of the light into nonclassical photon pairs. Also, photonic counterparts of Cooper pairs have been shown to occur when light scatters off of various media. Here, we consider the effects of non-classical light produced by such interactions on biological systems and whether there could be an influence.
The generation of nonclassical light has recently received a great deal of attention because three forms of it have now been observed in the laboratory: antibunched light, photon-number-squeezed (or sub-Poisson) light, and quadrature-squeezed light. These characteristics may, but need not, accompany each other in any given light source. Nonclassical light has been produced in experiments using resonance fluorescence, the Franck-Hertz effect, parametric interact ions, and semiconductor light sources. It is likely to be useful in providing new insights in various physical and biological processes, and in applications such as lightwave communications. Some of the characteristics, methods of generation, and expected uses of squeezed light will be addressed.
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.
The microscopic theory of superconductivity raised the disruptive idea that electrons couple through the elusive exchange of virtual phonons, overcoming the strong Coulomb repulsion to form Cooper pairs. Light is also known to interact with atomic vibrations, as, for example, in the Raman effect. We show that photon pairs exchange virtual vibrations in transparent media, leading to an effective photon-photon interaction identical to that for electrons in the BCS theory of superconductivity, in spite of the fact that photons are bosons. In this scenario, photons may exchange energy without matching a quantum of vibration of the medium. As a result, pair correlations for photons scattered away from the Raman resonances are expected to be enhanced. An experimental demonstration of this effect is provided here by time-correlated Raman measurements in different media. The experimental data confirm our theoretical interpretation of a photonic Cooper pairing, without the need for any fitting parameters.