The dynamics of a collection of resonant atoms embedded inside an inhomogeneous nondispersive and lossless dielectric is described with a dipole Hamiltonian that is based on a canonical quantization theory. The dielectric is described macroscopically by a position-dependent dielectric function and the atoms as microscopic harmonic oscillators. We identify and discuss the role of several types of Green tensors that describe the spatio-temporal propagation of field operators. After integrating out the atomic degrees of freedom, a multiple-scattering formalism emerges in which an exact Lippmann-Schwinger equation for the electric field operator plays a central role. The equation describes atoms as point sources and point scatterers for light. First, single-atom properties are calculated such as position-dependent spontaneous-emission rates as well as differential cross sections for elastic scattering and for resonance fluorescence. Secondly, multiatom processes are studied. It is shown that the medium modifies both the resonant and the static parts of the dipole-dipole interactions. These interatomic interactions may cause the atoms to scatter and emit light cooperatively. Unlike in free space, differences in position-dependent emission rates and radiative line shifts influence cooperative decay in the dielectric. As a generic example, it is shown that near a partially reflecting plane there is a sharp transition from two-atom superradiance to single-atom emission as the atomic positions are varied.
The dynamics of a collection of resonant atoms embedded inside an inhomogeneous nondispersive and lossless dielectric is described with a dipole Hamiltonian that is based on a canonical quantization theory. The dielectric is described macroscopically by a position-dependent dielectric function and the atoms as microscopic harmonic oscillators. We identify and discuss the role of several types of Green tensors that describe the spatio-temporal propagation of field operators. After integrating out the atomic degrees of freedom, a multiple-scattering formalism emerges in which an exact Lippmann-Schwinger equation for the electric field operator plays a central role. The equation describes atoms as point sources and point scatterers for light. First, single-atom properties are calculated such as position-dependent spontaneous-emission rates as well as differential cross sections for elastic scattering and for resonance fluorescence. Secondly, multiatom processes are studied. It is shown that the medium modifies both the resonant and the static parts of the dipole-dipole interactions. These interatomic interactions may cause the atoms to scatter and emit light cooperatively. Unlike in free space, differences in position-dependent emission rates and radiative line shifts influence cooperative decay in the dielectric. As a generic example, it is shown that near a partially reflecting plane there is a sharp transition from two-atom superradiance to single-atom emission as the atomic positions are varied.
When atoms are coupled to a common electromagnetic environment, the exchange of photons through dipole-dipole interactions leads to the emergence of cooperative effects. As a particular example, superradiance arises from spontaneous emission when this exchange leads to constructive interference of the emitted photons. Here, we introduce an integrated method for studying cooperative radiation in many-body systems. This method, which allows to study extended systems with arbitrarily large number of particles, can be formulated by an effective, nonlinear, two-atom master equation that describes the dynamics using a closed form which treats single- and many-body terms on an equal footing. We apply this method to a homogeneous gas of initially inverted two-level atoms, and demonstrate the appearance of both superradiance and subradiance, identifying a many-body coherence term as the source of these cooperative effects. We describe the many-body induced broadening -- which is analytically found to scale with the optical depth of the system -- and light shifts, and distinguish spontaneous effects from induced ones. In addition, we theoretically predict the time-dependence of subradiance, and the phase change of the radiated field during the cooperative decay.
A reduced equation of motion that describes the excited-state dynamics of interacting two-level impurity molecules in a dielectric host crystal is derived starting from a microscopic model for the total system. Our theory generalizes the derivation of the conventional superradiance master equation for molecules in vacuum; the role of photons in the conventional theory is played by polaritons (mixed crystal-radiation excitations) in our approach. Our final equation thus contains dispersive and superradiant polariton-mediated intermolecular interactions. The effect of the dielectric host is completely contained within a rescaling of these interactions with the transverse dielectric function \ensuremath{\epsilon}(\ensuremath{\omega}) of the crystal taken at the impurity's transition frequency. Our theory yields all local field and screening factors for both the dispersive and the dissipative couplings from a single, unified starting point. Known scaling laws for the spontaneous-emission rate and the instantaneous dipole-dipole interaction are extended to the frequency region where the dispersion of \ensuremath{\epsilon}(\ensuremath{\omega}) is important.
We discuss the quantum fluctuations of the fields associated with a broad class of optical scattering and transmission problems by developing the quantum electrodynamics of an idealized linear, but nonuniform, dielectric medium. We present and compare two quantization schemes for this purpose. The first is based on the expansion of the field in terms of a set of single-frequency solutions of the Maxwell equations. The second involves expanding the field in the set of plane-wave solutions of the Maxwell equations in the vacuum. The relation between the two quantization schemes is discussed in the framework of the scattering theory that connects them. The methods presented are used to show that various field components within a dielectric medium may be either superfluctuant or subfluctuant relative to their fundamental uncertainties in the vacuum. These alterations of the fluctuation properties of the fields are shown to lead to changes in the spontaneous emission rates for both electric and magnetic dipole transitions of excited atoms within or near dielectric media. We also analyze the quantum properties of the transition radiation emitted by a fast charged particle in passing from one dielectric medium to another.
Spontaneous-radiation processes associated with a number of multiatom systems are studied. Green's-function techniques are used in conjunction with a model of N two-level atoms interacting with a quantized radiation field to investigate the assumption of the independence of the spontaneous-radiation properties of a given atom from the states of the other atoms in the system. It is shown that the natural linewidth of an excited atom in the presence of a deexcited atom is different from that of an isolated excited atom. For interatomic separations smaller than a critical separation, the two-atom system is best considered as a collective unit with regard to its spontaneous-radiation properties. The influence of these "radiative cooperative effects" is studied also for the systems of two initially excited atoms. Also the influence of radiative cooperative effects in the scattering of a photon by a system of two deexcited atoms is studied. It is shown that the frequency distribution of the scattered radiation exhibits a double-peak structure for interatomic separations smaller than $\frac{3}{4}\ensuremath{\lambda}$. The techniques of Green's functions are then applied to the study of radiative cooperative effects in several many-atom systems. It is shown that within the context of the model certain information is obtained exactly via the Green's-function techniques as applied to the manyatom problems of a single excited atom in the presence of $N\ensuremath{\gg}1$ deexcited atoms and the scattering of a photon by a system of $N\ensuremath{\gg}1$ deexcited atoms. The necessity of treating manyatom systems from a "collective" point of view is easily seen from our results.
This thesis concerns the theoretical investigation of interference phenomena related to elastic and inelastic scattering of quantized light. The presented work is naturally divided into two parts, the first is concerning elastic scattering while the second explores inelastic scattering. In the first part we use a scattering-matrix formalism combined with results from random-matrix theory to investigate the interference of quantum optical states on a multiple scattering medium. We investigate a single realization of a scattering medium thereby showing that it is possible to create entangled states by interference of squeezed beams. Mixing photon states on the single realization also shows that quantum interference naturally arises by interfering quantum states. We further investigate the ensemble averaged transmission properties of the quantized light and see that the induced quantum interference survives even after disorder averaging. The quantum interference manifests itself through increased photon correlations. Furthermore, the theoretical description of a measurement procedure is presented. In this work we relate the noise power spectrum of the total transmitted or reflected light to the photon correlations after ensemble averaging. This analysis enables us to describe an experimental observation of the quantum nature of light that survives the averaging over disorder. In the second part we investigate inelastic scattering. This we do by first treating the scattering of light on dipoles embedded in an arbitrary dielectric environment. By considering the two different models for dipole interaction known as the minimal-coupling and electric-dipole interaction Hamiltonians, we find exact relations between the electric field and the dipole operators in the Heisenberg picture, while keeping the model of the dipoles arbitrary. Due to the exact treatment of the electric-field operators, we obtain kernels known from classical scattering theory to describe the propagation of the field from the dipoles. Using the found electric field operators we derive the Heisenberg equations of motion for the dipoles while treating them as quantum two-level systems and using the Born–Markov and rotating-wave approximations. Postponing the rotating-wave approximation to the very end of the formal calculations allows us to identify the different physical parameters of the dipole evolution in terms of physical quantities known from optics. Finally, we use our Heisenberg picture formalism to treat a dilute cloud of two-level atoms, by simplifying the equations of motion using a single-scattering approximation for the interaction between the atoms. This enables us to derive expressions for the steady-state population and fluorescence spectrum, where we find cooperative effects in both the elastic and the inelastic spectra.
The interaction of light with an atomic sample containing a large number of particles gives rise to many collective (or cooperative) effects, such as multiple scattering, superradiance, and subradiance, even if the atomic density is low and the incident optical intensity weak (linear optics regime). Tracing over the degrees of freedom of the light field, the system can be well described by an effective atomic Hamiltonian, which contains the light-mediated dipole-dipole interaction between atoms. This long-range interaction is at the origin of the various collective effects, or of collective excitation modes of the system. Even though an analysis of the eigenvalues and eigenfunctions of these collective modes does allow distinguishing superradiant modes, for instance, from other collective modes, this is not sufficient to understand the dynamics of a driven system, as not all collective modes are significantly populated. Here, we study how the excitation parameters, i.e., the driving field, determines the population of the collective modes. We investigate in particular the role of the laser detuning from the atomic transition, and demonstrate a simple relation between the detuning and the steady-state population of the modes. This relation allows understanding several properties of cooperative scattering, such as why superradiance and subradiance become independent of the detuning at large enough detuning without vanishing, and why superradiance, but not subradiance, is suppressed near resonance. We also show that the spatial properties of the collective modes allow distinguishing diffusive modes, responsible for radiation trapping, from subradiant modes.