Abstract A general approach to the discussion of optical birefringence phenomena is presented. It is based on the S-matrix approach to photon scattering in a nonrelativistic quantum field theoretical formalism and the Stokes operator description of polarization. The use of a canonically transformed interaction Hamiltonian in combination with diagrammatic perturbation theory enables the response of a system to electromagnetic radiation to be calculated in a straightforward and consistent manner to any order in the perturbation, and the effect of static fields is included easily. As an illustration, the angle of rotation of a beam of plane-polarized light by a solution of optically active molecules is calculated and the intensity dependence of the angle determined. The latter phenomenon should become apparent at high photon flux densities particularly when ω, the frequency of the incident light, or 2ω are similar to electronic excitation frequencies in the optically active molecules.
Abstract A general approach to the discussion of optical birefringence phenomena is presented. It is based on the S-matrix approach to photon scattering in a nonrelativistic quantum field theoretical formalism and the Stokes operator description of polarization. The use of a canonically transformed interaction Hamiltonian in combination with diagrammatic perturbation theory enables the response of a system to electromagnetic radiation to be calculated in a straightforward and consistent manner to any order in the perturbation, and the effect of static fields is included easily. As an illustration, the angle of rotation of a beam of plane-polarized light by a solution of optically active molecules is calculated and the intensity dependence of the angle determined. The latter phenomenon should become apparent at high photon flux densities particularly when ω, the frequency of the incident light, or 2ω are similar to electronic excitation frequencies in the optically active molecules.
The theory of optical birefringence is discussed from the point of view of the scattering of polarized photons by molecules using the framework of formal scattering theory and quantum electrodynamics. In Part One, those features from noncovariant quantum electrodynamics relevant to the molecular scattering of photons are reviewed. Chapter One contains an outline of classical electrodynamics in the Coulomb gauge, including the Stokes parameter and density matrix formulations of polarization. Chapter Two deals with the quantization of the radiation field, and the occupation number representation is defined. The quantum mechanical description of polarized light is outlined in Chapter Three: operator equivalents of the density matrix and Stokes parameters are invoked, the parameters themselves being obtained from the expectation values of the Stokes operators with the state vector of the photon. The Stokes parameter and density matrix are then applied to the polarization of a general beam containing an arbitrary number of photons, and some new methods are developed. The interaction of the electromagnetic field with bound electrons is formulated in Chapter Four in terms of a canonically transformed interaction Hamiltonian in which the multipole terms are explicit. Since each term is then gauge-invariant, this Hamiltonian is particularly suited to the application of diagrammatic perturbation theory which follows from the iteration of the scattering matrix in the interaction representation (Chapter Five). Also the extension of the theory to multiphoton processes is facilitated "because the field strength is explicit in the transformed Hamiltonian. The S-matrix connects the initial and final asymptotic states of the scattering system, and in Chapter Six the state vector and density operator of the scattered photon beam are obtained from those of the incident beam. Part Two contains the application of the above methods to a variety of linear and nonlinear optical birefringence effects in the absence or presence of external fields. In Chapter Seven, general equations are obtained for the polarization changes imposed on a forward scattered photon in terms of matrix elements of the reaction operator between plane polarized photon base states; whereas Chapter Eight extends this treatment to an n-photon beam, thereby encompassing the hyperpolarizability contributions to the polarization changes of the forward scattered beam. It is then demonstrated that the fundamental process in optical birefringence can be interpreted as an infinitesimal unitary transformation of the polarization spinor. Also the S-matrix approach to birefringence is compared with the methods used in crystal optics, and with the classical treatments of the scattering of polarized light by molecules. The general equations obtained for the polarization changes of the forward scattered beam are subsequently interpreted in the light of the physical circumstances appropriate to the bire- fringence effect of interest. In Chapters Nine, Ten, and Eleven, diagrammatic perturbation theory is used to obtain explicit expressions, in terms of molecular polarizability and rotation tensors, for the linear and nonlinear contributions to the polarization changes involved in natural optical activity, and in birefringence phenomena induced by static and optical electric and magnetic fields. The nonforward scattering of polarized photons by molecules is discussed in Part Three. General equations are calculated in Chapter Twelve for the azimuth, ellipticity, and depolarization ratio of the Rayleigh beam at any scattering angle and for any polarization of the incident beam. Explicit expressions in terms of molecular quantities are then obtained for the polarization at scattering angles of 90° and almost zero from both optically inactive and optically active molecules. It is demonstrated that a determination of the precise polarization state of the scattered beam can provide useful molecular information additional to that obtained from depolarization ratios alone. This is because the depolarization ratio depends on only the diagonal elements of the polarization density matrix and so does not convey all the information about the system. Raman scattering processes are contained in the formulation and the polarization of the Raman light at any scattering angle can be obtained. This is shown to be particularly useful for predicting the polarization of stimulated Raman light for any Raman-active liquid placed within a laser cavity. By extending the nonforward scattering formulation to incorporate multiphoton processes, equations are obtained in Chapter Thirteen for the ellipticity, azimuth, and depolarization ratio of the second harmonic wave at any scattering angle as a function of the incident polarization. Several specific situations are subsequently investigated. Finally, it is shown in Chapter Fourteen that the near-forw- ard Rayleigh and Raman scattering formulations provide an explanation for the observed polarization, as a function of the initial polarization, of the self-trapped filaments that arise from the self-focusing of an intense laser beam.
A general description of linear optical birefringence effects is presented in terms of the effect of forward scattering on the photon polarization density matrix. The approach enables explicit statements to be given for the polarization changes involved in any linear birefringence phenomenon in terms of R matrix elements between plane-polarized base states. Expressions in terms of molecular quantities are listed for the R matrix elements involved in some typical natural and induced birefringence effects. This description of birefringence is related to the infinitestimal unitary transformations of the density matrix and rotations in Poincaré space.
The theoretical dependence of optical birefringence phenomena on the statistical nature of the light is investigated. Photon S-matrix calculations lead to expressions relating the change induced in the statistical nature of the beam to the molecular properties of the target sample. A hypothetical generalized optical birefringence experiment is analysed: in the experiment the coincidences of photons arriving at spatially separated detectors sensitive to different polarizations are observed with and without the sample in the beam, and the difference in the photon correlations depend on the initial statistical composition and polarization of the beam and the molecular properties of the sample. When the beam is generated by a thermal source the difference of the signals (with and without the sample) depends on the product of the polarizability and optical rotation tensors. When the light is generated by a single-mode coherent source the statistical properties of the light are such as to eliminate the second-order interaction terms, and so the experiment yields the hyperpolarizability and hyper-rotation tensors automatically and with the explicit exclusion of the polarization and rotation tensor contributions.
ABSTRACT It is shown that the phenomena of double refraction—optical activity, Faraday rotation, Kerr effect, etc.—may be treated as scattering problems in quantum field theory. An expression for the scattering cross-section of an atom or molecule for photons may be easily obtained and from this expression using the idea of Stokes operators, equating their expectation values to the classical Stokes parameters, the usual quantum mechanical expressions for optical activity, etc. may be obtained. This approach does not require the ideas of refractive index or polarization of the medium, and emphasizes what are the actual observables in these experiments.
A treatment of nonlinear optical phenomena beginning with a microscopically correct Hamiltonian containing the Bose operators of the light field and the Fermi operators for the optically active electrons in the medium is presented. Using techniques recently developed, a nonperturbative solution to the Schrodinger equation is possible. No linearization or semiclassical approximations are introduced. Two photon emission and absorption including both the degenerate and nondegenerate cases are considered. Parametric amplification and frequency conversion are investigated as examples of multiphoton processes. Atomic cooperation is shown to enhance the above phenomena. A formal treatment of a model illustrating super and subradiance is included.
Classically, light is an electromagnetic phenomenon, described by Maxwell's equations. However, under certain conditions, such as low intensity or in the presence of certain nonlinear optical materials, light starts to behave differently, and we have to construct a ‘quantum theory of light’. We can exploit this quantum behaviour of light for quantum information processing, which is the subject of this book. In this chapter, we develop the quantum theory of the free electromagnetic quantum field. This means that we do not yet consider the interaction between light and matter; we postpone that to Chapter 7. We start from first principles, using the canonical quantization procedure in the Coulomb gauge: we derive the field equations of motion from the classical Lagrangian density for the vector potential, and promote the field and its canonical momentum to operators and impose the canonical commutation relations. This will lead to the well-known creation and annihilation operators, and ultimately to the concept of the photon. After quantization of the free electromagnetic field we consider transformations of the mode functions of the field. We will demonstrate the intimate relation between these linear mode transformations and the effect of beam splitters, phase shifters, and polarization rotations, and show how they naturally give rise to the concept of squeezing. Finally, we introduce coherent and squeezed states.