We investigate how laser-driven, cooperative dipole-dipole interactions in weakly trapped atomic arrays give rise to self-organized configurations. Starting from an analytically tractable two-emitter system, we identify the possible steady-state spatial arrangements accessible to the atoms. We then extend this analysis to larger ensembles in both linear and ring geometries. In linear chains, we demonstrate the emergence of topologically nontrivial dimerized configurations across a range of initial interatomic spacings. In ring geometries, we find that the system undergoes self-organized contraction and expansion, enabling access to length scales below those set by the trapping lattice. Our results demonstrate that collective light-matter interactions in free space can spontaneously generate modified ordered geometries, even when the emitters are initially separated by distances larger than their transition wavelength.
We investigate how laser-driven, cooperative dipole-dipole interactions in weakly trapped atomic arrays give rise to self-organized configurations. Starting from an analytically tractable two-emitter system, we identify the possible steady-state spatial arrangements accessible to the atoms. We then extend this analysis to larger ensembles in both linear and ring geometries. In linear chains, we demonstrate the emergence of topologically nontrivial dimerized configurations across a range of initial interatomic spacings. In ring geometries, we find that the system undergoes self-organized contraction and expansion, enabling access to length scales below those set by the trapping lattice. Our results demonstrate that collective light-matter interactions in free space can spontaneously generate modified ordered geometries, even when the emitters are initially separated by distances larger than their transition wavelength.
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.
Collective behavior in many-body systems, where the dynamics of an individual element depend on the state of the entire ensemble, play an important role in both basic science research and applied technologies. Over the last twenty years, studies of such effects in cold atomic vapors have lead to breakthroughs in areas such as quantum information science and atomic and condensed matter physics. Nevertheless, in order to generate photon-mediated atom-atom coupling strengths that are large enough to produce collective behavior, these studies employ techniques that intrinsically limit their applicability. In this thesis, I describe a novel nonlinear optical process that enables me to overcome these limitations and realize a new regime of collective light-matter interaction. My experiment involves an anisotropic cloud of cold rubidium atoms illuminated by a pair of counterpropagating optical (pump) fields propagating at an angle to the trap's long axis. When the pump beam intensities exceed a threshold value, a collective instability occurs in which new beams of light are generated spontaneously and counterpropagate along the trap's long axis. In order to understand the physical mechanism responsible for this behavior, I study first the system's nonlinear optical response when driven below the instability threshold. I find that the incident optical fields produce an optical lattice that causes the atoms to become spatially organized on the sub-wavelength length scale. This organization corresponds to the formation of an atomic density grating, which effectively couples the involved fields to one another and enables the transfer of energy between them. The loading of atoms into this grating is enhanced by my choice of field polarizations, which simultaneously results in cooling of the atoms from T~30 μK to T~3 μK via the Sisyphus effect. As a result, I observe a fifth-order nonlinear susceptibility χ^{(5)}=1.9x10^-12 (m/V)^4 that is 7 orders of magnitude larger than previously observed. In addition, because of the unique scaling of the resulting nonlinear response with material parameters, the magnitude of the nonlinearity can be large for small pump intensities (\\ie, below the resonant electronic saturation intensity 1.6 mW/cm^2) while simultaneously suffering little linear absorption. I confirm my interpretation of the nonlinearity by developing a theoretical model that agrees quantitatively with my experimental observations with no free parameters. The collective instability therefore corresponds to the situation where the cold vapor transitions spontaneously from a spatially-homogeneous state to an ordered one. This emergent organization leads to the simultaneous emission of new optical fields in a process that one can interpret either in terms of mirrorless parametric self-oscillation or superradiance. By mapping out the phase diagram for this transition, I find that the instability can occur for pump intensities as low as 1 mW/cm^2, which is approximately 50 times smaller than previous observations of similar phenomena. The intensity of the emitted light can be up to 20% of the pump beam intensity and depends superlinearly on the number of atoms, which is a clear signature of collective behavior. In addition, the generated light demonstrates temporal correlations between the counterpropagating modes of up to 0.987 and is nearly coherent over several hundred μs. The most significant attributes of the light, though, are that it consists of multiple transverse spatial modes and persists in steady-state. This result represents the first observation of such dynamics, which have been shown theoretically to lead to a rich array of new phenomena and possible applications.
When quantum emitters couple indistinguishably to light, they can synchronize into a collective light matter system with radiative properties profoundly different from those of independent particles. To date, the resulting collective effects have largely been confined to point like or homogeneous ensembles. Here, we open access to a qualitatively new collective regime by realizing geometrically ordered, spatially extended atom arrays with subwavelength spacing. This establishes a fundamentally new platform in which collective emission is no longer confined to a single Dicke mode but instead emerges from an ordered network of photon mediated interactions. We find that 2D atom arrays undergo strong super and subradiant emission. Despite subwavelength spacing, we achieve site resolved imaging and directly observe the buildup of spatial correlations, demonstrating the transformation of cooperative decay into a strongly correlated many-body process. We observe extensive scaling of superradiance, uncover superradiant revivals, and reveal the ferromagnetic nature of superradiance and the antiferromagnetic nature of subradiance. Our results realize a novel programmable platform for exploring and utilizing dissipative many-body quantum physics, opening new possibilities for photon capture, storage, and atom photon entanglement.
Quantum cooperativity is evident in light-matter platforms where quantum emitter ensembles are interfaced with confined optical modes and are coupled via the ubiquitous electromagnetic quantum vacuum. Cooperative aspects such as dipole-dipole interactions and subradiance find applications in the design of nanoscale coherent light sources and highly-reflective quantum metasurfaces made up of hundreds of optically trapped atoms, in the implementation of topological quantum optics on subwavelength arrays of emitters, in quantum metrology and quantum information. The quick bursts of radiation from a collection of quasi-indistiguishable emitters provides an alternative approach to standard lasers by introducing superradiant lasers operating at extremely low intracavity power. This tutorial provides a set of theoretical tools to tackle the behavior responsible for the onset of cooperativity in light-matter systems by extending open quantum system dynamics methods, such as the master equation and quantum Langevin equations, to electron-photon interactions in strongly coupled and correlated quantum emitters ensembles. These analytical approaches are then also extended to frequency disordered or vibronically coupled quantum emitter ensembles with wide relevance ranging from atoms in optical lattices, quantum dots in solid state environments or molecular quantum systems.
Coupling between quantum emitters and modes of light is foundational to studies of quantum systems. Coherent interactions between matter and light have greatly advanced the development of quantum technologies. When an ensemble of atoms interacts with light that is confined within a cavity---a resonator for photons---light also mediates atom-atom interactions, leading to collective phenomena that cannot be extrapolated from microscopic behaviors. Understanding how interactions among quantum particles lead to macroscopic phenomena, such as phase transitions and breaking of symmetries, remains a challenge in modern physics. In this dissertation, I present results addressing this challenge in the context of mesoscopic arrays of optical-tweezer-trapped atoms interfaced with a high-finesse optical cavity. In particular, the physics we investigate arises from the collective scattering of light. Utilizing the ability to place atoms with nanometer-scale precision, we engineer superradiant and subradiant states, where control over interference of the emission from multiple atoms leads to collectively enhanced or suppressed amounts of scattered light. Building on this work, we investigate the emergence of optomechanical self-organization, mediated by superradiance in the cavity electromagnetic field. By coupling atoms to the same cavity mode, the atoms exert forces on one another through the exchange of photons, leading them to autonomously order themselves spatially. We characterize mesoscopic fluctuations and their effect on symmetry-breaking dynamics associated with self-organization. Finally, we extend this framework to theoretically investigate how the phase of the atom-cavity coupling can be altered to generate higher symmetries. Our analysis reveals first-order phase transitions and instabilities induced by non-reciprocal forces. Altogether, this work establishes a path towards realizing mesoscopic systems of complex phases of matter in cavity quantum electrodynamics with unprecedented programmability.
Coherent and efficient light-matter interfaces between an atom and a single mode of the electromagnetic field are essential for quantum technologies. Traditionally, these systems employ optical cavities or waveguides to isolate a specific mode of light, but a more recent approach is to engineer antennas from ordered configurations of trapped ultracold atoms that exhibit controllable and directed scattering. In this work, we propose a method to engineer an antenna from the center-of-mass wavefunction of a single atom, which can produce directed emission and thereby exhibit strong coupling to a target mode of light in free space. We predict that the resulting single-atom cooperativity can be comparable to the current state of the art in optical cavity and waveguide QED experiments. Building on this approach, we show that a wavepacket antenna becomes a single-atom mirror in the linear response regime. We study the modified dipole-dipole interactions and band structure of chains of such emitters, which can exhibit sub- and superradiance at spacings much larger than the wavelength of the light. Extending our approach to multi-level atoms, we propose a method to achieve arbitrary spatial scattering from a single atom, including uni-directional spontaneous emission. Finally, we elucidate how our approach can enhance cooperative scattering in conventional arrays of tightly trapped atoms.