A study has been made on the scattering of light by the hydrodynamical and statistical atom model. Bloch's treatment of the hydrodynamical equations of motion for this model is supplemented here by inclusion of the interaction with the electromagnetic field. We limited attention to oscillations of small amplitude. By correspondence principle arguments, general expressions were derived for the cross sections for absorption, coherent and incoherent scattering. The energy can be expressed—following Bloch—as the energy of a Thomas-Fermi atom plus a Hamiltonian which is associated with departures from the Thomas-Fermi distribution. Using Bloch's quantization of this Hamiltonian and applying the method of quantum field theory, we rederived the correspondence principle results for elementary cross sections. Then applying the correspondence theoretical argument to the matrix element, we rederived Heisenberg's result for the total intensity of the Compton scattering. We also apply the method of stationary phase to the hydrodynamical treatment and show that this method gives the same result as does the linear term in the momentum transfer in Heisenberg's expression, except for a numerical factor 3½/2—a point that was discussed by Bloch many years ago. Application of the general formulas given here for angular distribution of Rayleigh and Compton scattering will require electronic machine calculations of higher modes of oscillation of the gas model of the atom analogous to those made by Wheeler and Fireman for l=1.
A study has been made on the scattering of light by the hydrodynamical and statistical atom model. Bloch's treatment of the hydrodynamical equations of motion for this model is supplemented here by inclusion of the interaction with the electromagnetic field. We limited attention to oscillations of small amplitude. By correspondence principle arguments, general expressions were derived for the cross sections for absorption, coherent and incoherent scattering. The energy can be expressed—following Bloch—as the energy of a Thomas-Fermi atom plus a Hamiltonian which is associated with departures from the Thomas-Fermi distribution. Using Bloch's quantization of this Hamiltonian and applying the method of quantum field theory, we rederived the correspondence principle results for elementary cross sections. Then applying the correspondence theoretical argument to the matrix element, we rederived Heisenberg's result for the total intensity of the Compton scattering. We also apply the method of stationary phase to the hydrodynamical treatment and show that this method gives the same result as does the linear term in the momentum transfer in Heisenberg's expression, except for a numerical factor 3½/2—a point that was discussed by Bloch many years ago. Application of the general formulas given here for angular distribution of Rayleigh and Compton scattering will require electronic machine calculations of higher modes of oscillation of the gas model of the atom analogous to those made by Wheeler and Fireman for l=1.
Quantum stochastic differential equations have been used to describe the dynamics of an atom interacting with the electromagnetic field via absorption/emission processes. Here, by using the full quantum stochastic Schrödinger equation proposed by Hudson and Parthasarathy, we show that such models can be generalized to include other processes into the interaction. In the case of a two-level atom we construct a model on the basis of some physical requirements, the main being a balance equation on the fluxes of the ingoing and outgoing photons; in this model the atom-field interaction turns out to be due either to absorption/emission processes either to direct scattering processes, which simulate the interaction due to virtual transitions to the levels which have been eliminated from the description. To see the effects of the new terms, we consider both direct and heterodyne detection of the fluorescence light emitted by an atom stimulated by a monochromatic coherent laser and we deduce from these two detection schemes the expressions of the total, elastic and inelastic electromagnetic cross sections and the spectral distribution of the fluorescence light. The total cross section, as a function of the frequency of the stimulating laser, can present not only a Lorentzian shape, but the full variety of Fano profiles; intensity dependent widths and shifts are obtained. The fluorescence spectrum can present complicated shapes, according to the values of the various parameters; when the direct scattering is not important the usual symmetric triplet structure of the Mollow spectrum appears (for high intensity of the stimulating laser), while a strong contribution of the direct scattering process can distort such a triplet structure or can even make it to disappear.
A fully quantum-mechanical treatment of resonant light scattering is presented. The incident field is assumed to be described by a coherent state, and is allowed to be intense enough to cause saturation. Complete solutions are obtained for the correlated atom-field pure state vector, including multiphoton contributions of arbitrary order. The frequency spectrum of the scattered field is evaluated and is found to agree exactly with the result previously obtained by means of the quantum fluctuation-regression theorem. A derivation of the fluctuation-regression theorem and of the optical Bloch equations is given which is fully quantum mechanical and which relies upon no assumption of statistical factorization of atom and field states. The accuracy of the result found for the scattered - field spectrum is thus shown to be limited only by the assumption of the smallness of the saturated linewidth compared to the (optical) atomic resonance frequency. The one-photon approximation is analyzed in some detail. The method of adding an imaginary term to the upper-atomic-state energy is clarified, and it is shown how the vacuum and one-photon amplitudes thereby obtained may be used, within a simple and plausible iteration scheme, to construct the complete multiphoton spectrum. A variety of commonly used injection schemes and methods of representing atomic relaxation are discussed, and comparisons are made with results found by other authors. The entire analysis is performed with the aid of a canonical transformation which replaces the applied field by a c number. It is thus proved quite rigorously and generally that the use of a c-number applied field is a fully quantum-mechanical procedure, provided only that radiation-reaction terms are retained.
We study interactions of light with a sample of two-level atoms. Quantum statistical effects of degenerate boson and fermion gases are described by using the quantum field theory of atom-photon interactions, fully including the angular momentum degeneracies. Coupled propagation equations are given for light and matter fields, and plausible general simplifications are enumerated.^ In the limit of large atom-field detuning, multiple scattering of light and QED linewidths and line shifts may be ignored, and the propagation equations of light and matter fields may be decoupled. A general expression for the spectrum of the scattered light is derived, complete with the dependence on atomic level scheme, on various light polarizations, and on the geometry of the experiment. With these simplifications we are able to find distinct qualitative features in the spectrum of the scattered light in the case of both fermions and bosons that depend on the statistics of atoms. This is because for bosons (fermions), those scattering events in which an atom recoils to an already occupied state are enhanced (inhibited).^ As the driving light gets closer to the atomic resonance, multiple scattering and vacuum fluctuations of the electromagnetic fields should also be taken into account. We write the equations of motion for the excited state field operators by eliminating the vacuum electromagnetic field. It is always assumed that the driving external laser field is in the coherent state. We find in the limit of low light intensity, a hierarchy of equations of motion for correlation functions that contain one excited-atom field and one, two, three, etc., ground state atom fields. It is conjectured that the entire linear hierarchy may be solved by solving numerically the classical equations for the coupled system of electromagnetic fields and charged harmonic oscillators. We discuss the emergence of resonant dipole-dipole interactions and collective linewidths, and delineate the limits of validity of the column density approach in terms of non-cooperative atoms by presenting a mathematical example in which this approach is exact. ^
Quantum-mechanical expressions for nonresonance-dipole light-scattering cross sections are related to corresponding expressions for oscillator strengths and refractive indices. In particular, Rayleigh and Raman cross sections for atoms are expressed in terms of oscillator strengths and vector-coupling coefficients. Several of our results, including the relationship between Rayleigh scattering and refractive index, differ in general from the corresponding results of classical dispersion theory. We show that these differences arise from antisymmetric components Ckja = (Ckj − Cjk)/2 of the polarizability tensor, which have been neglected in the classical analyses. Calculated Rayleigh cross sections for cesium and aluminum atoms, and Raman cross sections for aluminum atoms are presented to illustrate our results. The antisymmetric contribution is found to be substantial in all of these cross sections; its most obvious effect is to cause the depolarization (for linearly polarized incident light) to exceed 34 over extended wavelength ranges away from resonance. On the other hand, for atoms initially in states of zero angular momentum, and molecules under conditions which allow the use of Placzek’s polarizability approximation, our results agree with those of classical dispersion theory.
Correspondence theorem for frequencies.---It is well known that the frequency emitted by a hydrogen atom as it falls from one of its quantized states to another may be expressed as a mean value of the frequency of motion of the electron (or overtone thereof) when averaged in the proper manner over orbits intermediate between the initial and final states. In the present paper it is proved that, similarly, the Compton shift is a properly taken mean of the classical Doppler shift. The quantum frequency actually scattered is thus a properly taken average of the frequency which would be scattered on the classical theory as the electron is accelerated from its state of rest to its final recoil condition.Correspondence principle for intensities.---In like manner, the amount of light scattered in various directions may be determined if it is assumed that the intensity in the quantum theory equals a proper average of the intensities scattered according to the classical theory. A comparison is made with observed data on the scattering of $\ensuremath{\gamma}$-rays.The characteristic feature of the present paper is that the corresponding classical electron is assumed to have the same direction of motion as the scattered quantum, whereas an actual classical electron would from symmetry recoil straight forward in the direction of the incident beam, as in Compton's and Woo's theories of intensities. This new point of view eliminates the difficulty of a constant correction-factor which has been encountered by Compton and Woo in their explanation of intensity relations.
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.