An ensemble of atoms coupled to the radiation field exhibits collective behaviours when the interatomic separation is comparable to the wavelength of photons emitted by the atoms. The collective coupling of the atoms with the electromagnetic field gives rise to coherent exchange interactions between the atoms. In addition, the spontaneous decay of photons from the ensemble becomes a collective process that can happen at a much faster (superradiant) or slower (subradiant) rate than that of a single atom. These processes affect the way that fluorescence light is scattered from the system when it is driven by a laser. However, little is known about the response of a dense atomic gas beyond the linear regime of very weak driving, due to the involved complexity of the problem. The first part of this thesis investigates how the presence of strong laser driving affects properties of the far-field fluorescence light emitted by the ensemble, such as the power spectrum and second order coherence. Depending on the strength of the driving laser and the particular arrangement of the atoms, the laser can modify considerably how the collective behaviours of the atomic ensemble are manifested in the fluorescence. The relative strengths of the coherent interaction and collective decay process are intrinsically linked to the way that the atoms couple to the radiation field; one cannot be changed without modifying the other. Altering the environment by, for example, placing the atoms near a surface or a waveguide, can change this relation significantly from that for atoms in free space. Therefore, modified environments represent a platform for the generation of otherwise inaccessible regimes of collective behaviour, with potential applications in quantum state engineering. The second part of this thesis provides a numerical investigation into how the collective properties of a dense atomic system can be manipulated by placing the atoms close to planar surfaces or an optical nanofiber. These structures modify the light-matter coupling by altering the electric field experienced by the atoms. It is shown that surfaces of metallic and dielectric materials can be used to either enhance or suppress the collective behaviours, depending on the particular system arrangement. In particular, the coupling of atoms with bound surface modes, such as the surface plasmon polaritons that are formed at an air-metal interface, is demonstrated to have a strong effect on the interactions. An optical nanofiber supports a set of fundamental guided modes, that propagate along the fiber. If the atoms are suitably polarised, then they will emit primarily into the guided modes travelling in one direction. By calculating and analysing the collective decay states of a chain of atoms placed near a nanofiber, it is demonstrated that the atom-fiber coupling leads to the formation of a superradiant mode that is preserved at large atomic separations. The presence of chiral emission is shown to introduce phase gradients to the collective modes.
An ensemble of atoms coupled to the radiation field exhibits collective behaviours when the interatomic separation is comparable to the wavelength of photons emitted by the atoms. The collective coupling of the atoms with the electromagnetic field gives rise to coherent exchange interactions between the atoms. In addition, the spontaneous decay of photons from the ensemble becomes a collective process that can happen at a much faster (superradiant) or slower (subradiant) rate than that of a single atom. These processes affect the way that fluorescence light is scattered from the system when it is driven by a laser. However, little is known about the response of a dense atomic gas beyond the linear regime of very weak driving, due to the involved complexity of the problem. The first part of this thesis investigates how the presence of strong laser driving affects properties of the far-field fluorescence light emitted by the ensemble, such as the power spectrum and second order coherence. Depending on the strength of the driving laser and the particular arrangement of the atoms, the laser can modify considerably how the collective behaviours of the atomic ensemble are manifested in the fluorescence. The relative strengths of the coherent interaction and collective decay process are intrinsically linked to the way that the atoms couple to the radiation field; one cannot be changed without modifying the other. Altering the environment by, for example, placing the atoms near a surface or a waveguide, can change this relation significantly from that for atoms in free space. Therefore, modified environments represent a platform for the generation of otherwise inaccessible regimes of collective behaviour, with potential applications in quantum state engineering. The second part of this thesis provides a numerical investigation into how the collective properties of a dense atomic system can be manipulated by placing the atoms close to planar surfaces or an optical nanofiber. These structures modify the light-matter coupling by altering the electric field experienced by the atoms. It is shown that surfaces of metallic and dielectric materials can be used to either enhance or suppress the collective behaviours, depending on the particular system arrangement. In particular, the coupling of atoms with bound surface modes, such as the surface plasmon polaritons that are formed at an air-metal interface, is demonstrated to have a strong effect on the interactions. An optical nanofiber supports a set of fundamental guided modes, that propagate along the fiber. If the atoms are suitably polarised, then they will emit primarily into the guided modes travelling in one direction. By calculating and analysing the collective decay states of a chain of atoms placed near a nanofiber, it is demonstrated that the atom-fiber coupling leads to the formation of a superradiant mode that is preserved at large atomic separations. The presence of chiral emission is shown to introduce phase gradients to the collective modes.
We study how the radiative properties of a dense ensemble of atoms can be modified when they are placed near or between metallic or dielectric surfaces. If the average separation between the atoms is comparable or smaller than the wavelength of the scattered photons, the coupling to the radiation field induces long-range coherent interactions based on the interatomic exchange of virtual photons. Moreover, the incoherent scattering of photons back to the electromagnetic field is known to be a many-body process, characterized by the appearance of superradiant and subradiant emission modes. By changing the radiation field properties, in this case by considering a layered medium where the atoms are near metallic or dielectric surfaces, these scattering properties can be dramatically modified. We perform a detailed study of these effects, with focus on experimentally relevant parameter regimes. We finish with a specific application in the context of quantum information storage, where the presence of a nearby surface is shown to increase the storage time of an atomic excitation that is transported across a one-dimensional chain.
Surface plasmon polaritons are charge density waves of electrons in a metal, which are coupled to an electromagnetic field at a metal-dielectric interface. The electro- magnetic field associated with surface plasmons is confined, resulting in increased field intensities near the interface. Optical emitters placed near a metal film interact strongly with the surface plasmon modes present, not only modifying the radiation rates, but also the radiation profile. These emitters may be used to store and process information, and understanding their behaviour in the presence of a lossy metal film is important in determining the advantages and limitations of using surface plasmons. In this thesis, we wish to understand how we can optically control atoms by exploring two physical phenomena: first, the influence of surface plasmons on collective effects in an ensemble of emitters. Secondly, the single photon excitation of an emitter near a metal film. In the first case, we analyze the collective radiative behaviour of multiple classical emitters near a metal film that radiatively couple to the far-field through surface plasmon modes. We demonstrate that the contributions of dipolar image charges within the metal film significantly affect the cooperative emission of nearby sources, generating sub- and super-radiant emission that can be controlled with a suitably detuned external driving field. In the second case, we determine the excitation probability of an atom near a metal film by a single photon pulse that is time reversed. Using a quantum electro- dynamic description of absorbing dielectrics, we show that non-radiative decay will limit the excitation probability to about half of the maximum that could be achieved in the absence of losses.
The study of atom-light interaction is a key element of quantum optics and a central part of atomic physics. Systems composed of atoms interacting with each other through the electromagnetic field can be used for studies from fundamental research to practical applications. Experimental realizations of these systems benefit from three distinct attributes: large atom-light coupling, trapping and control of atomic ensembles, and engineering and manipulation of the electromagnetic field. Optical waveguides provide a platform that achieves these three goals. In particular, optical nanofibers are an excellent candidate. They produce a high confinement of the electromagnetic field that improves atom-light coupling, guiding the field that mediates the interactions between atoms, while allowing trapping of the atoms close to it. This thesis describes the uses of an optical nanofiber for quantum optics experiments, demonstrating its possibilities for enabling special atom-light interactions. We trap atoms near the optical nanofiber surface, and characterize the trap in a non-destructive manner. We show how the presence of the nanofiber modifies the fundamental atomic property of spontaneous emission, by altering the electromagnetic environment of the atom. Finally, we use the nanofiber to prepare collective states of atoms around it. These states can radiate faster or slower than a single atom (superradiance and subradiance). The observation of subradiance of a few atoms, a rather elusive effect, evidences nanofibers as a strong candidate for future quantum optics experiments. Moreover, we show how the guided field mediates interaction between atoms hundreds of wavelengths apart, creating macroscopically delocalized collective states.
The objective of this thesis is to expand our understanding of collective light-scattering phenomena, which manifest themselves in the strong suppression of radiation from the scattering medium. In particular, we are interested in subradiance, a collective effect in spontaneous emission which, as a result of the dissipative coupling of atoms through common electromagnetic modes, creates long-lived excitation modes in an ensemble of cold atoms, with lifetimes much longer than those of individual, isolated atoms. Previously, subradiance had been well-characterized for dilute cold-atom scattering media and the low-intensity limit of the driving laser (linear-optics regime). In this thesis, we study this collective phenomenon beyond the linear-optics and dilute regimes.To study experimentally subradiance beyond the linear-optics regime, we varied the saturation parameter of the excitation laser up to relatively large values and we have observed the increase of the subradiant population with increasing saturation parameter. More importantly, we have identified the super-linear scaling of the subradiant population beyond the linear-optics regime, due to a process similar to optical pumping via multi-excitation superradiant states. This study showed that the increase in the intensity of the driving laser beyond the linear-optics regime can overcome the weak coupling of subradiant modes with the external world.Moreover, we have numerically studied subradiance using the vectorial coupled-dipole model, with a focus on understanding the effect of the near-field dipole-dipole interaction. For that, we extensively compared the vectorial and scalar (which does not contain near-field interaction terms) models and studied the subradiant lifetime as a function of the density and optical thickness of the cold-atom cloud. We observed that the near-field terms are detrimental for subradiance, which was seen in the reduction of the subradiant lifetimes with increasing density. This detrimental character of near-field terms can be interpreted as being due to an effective inhomogeneous broadening induced by the near-field interaction, which reduces the subradiant lifetimes as the density increases.The detrimental character of near-field interaction has also been previously numerically identified for Anderson localization of light waves (Anderson localization is a coherent multiple-scattering wave phenomenon in a strongly scattering medium that results in a cessation of a diffusive wave transport; it also yields long-lived modes): the scalar coupled-dipole model predicts Anderson localization of light waves, but not the vectorial one. However, adding a strong magnetic field allows one to recover localized modes for vectorial light. In this context, we numerically studied a possible signature of Anderson localization of light in cold atoms, based on the measurement of intensity fluctuations of the scattered light. We have shown that at the transition to the localized regime, the fluctuations are enhanced. In particular, for vectorial light, we have demonstrated the absence and recovery of enhanced intensity fluctuations without and with the applied magnetic field, which further corroborates that the intensity fluctuations could serve as an experimental way to probe the localized states.
We analyze the temporal response of the fluorescence light that is emitted from a dense gas of cold atoms driven by a laser. When the average interatomic distance is comparable to the wavelength of the photons scattered by the atoms, the system exhibits strong dipolar interactions and collective dissipation. We solve the exact dynamics of small systems with different geometries and show how these collective features are manifest in the scattered light properties such as the photon emission rate, the power spectrum and the second-order correlation function. By calculating these quantities beyond the weak (linear) driving limit, we make progress in understanding the signatures of collective behavior in these many-body systems. Furthermore, we shed light on the role of disorder and averaging on the resonance fluorescence, of direct relevance for recent experimental efforts that aim at the exploration of many-body effects in dipole–dipole interacting gases of atoms.
The interaction between light and matter has captivated physicists for centuries, from early studies of vision and refraction in ancient Greece to the development of quantum mechanics and quantum electrodynamics in the past century. While the response of a single quantum emitter to light is well understood, the radiative properties of an ensemble of closely spaced emitters are far more intricate. Coupling to a shared electromagnetic environment induces coherent and dissipative interactions between emitters, giving rise to a collective response that cannot be captured by treating them independently. In the regime of few excitations, the system hosts delocalized subradiant states, that is, coherent superpositions that are largely decoupled from the electromagnetic field and thus decay at suppressed rates. While this weak coupling makes subradiant states attractive for quantum technologies, it also renders them difficult to manipulate. At higher excitation densities, the intrinsic nonlinearity of emitters and the exponential growth of the Hilbert space make theoretical and numerical descriptions of the system and its dynamics increasingly challenging. This thesis explores two fundamental questions: How can subradiant and dark states be selectively accessed and harnessed for practical applications in quantum technologies? And how can interacting ensembles of quantum emitters be efficiently simulated to uncover their many-body physics? The first part of the thesis develops protocols for controlling and addressing dark states in free-space and waveguide-coupled atomic arrays, demonstrating their utility in quantum storage and the deterministic generation of entangled photonic states. Incorporating atomic motion, we further show that collective subradiant states can enhance cooling in dense atomic arrays, offering new avenues for controlling motional dynamics. In the second part, we introduce cumulant expansions of the equations of motion as a powerful tool to analytically and numerically investigate collective decay in the many-body regime. We first examine the collective decay of fully excited atomic arrays in free space, characterizing the onset and scaling of the superradiant burst across different geometries. In collaboration with experiments on ultracold erbium atoms in optical lattices, we provide the first direct observations of many-body collective effects in free-space ordered arrays, including early-time superradiant bursts, late-time subradiant tails, and the emergence of atomic correlations throughout the dynamics. Finally, we theoretically and numerically explore the transient formation of multi-excitation subradiant states, and demonstrate how the existence of multiple dissipation channels suppresses steady-state superradiance in extended arrays.