Subradiant states of a finite subwavelength atomic chain in free space offer a powerful resource for photon storage. Yet their preparation and control remain challenging experimentally. A standard technique is to drive the atoms by a laser and observe the florescence light of the long-lived subradiant modes of excitation after the laser is switched off. However, these modes are highly degenerate and form an almost continuous band in the subradiant manifold. Here we propose a new method of exciting a given subradiant state by coupling atoms to a surface plasmon wave propagating along the interface with a metallic film. By controlling the chain/surface distance we may load, store and release photons in the atoms, making them a promising tool for future quantum memories.
Subradiant states of a finite subwavelength atomic chain in free space offer a powerful resource for photon storage. Yet their preparation and control remain challenging experimentally. A standard technique is to drive the atoms by a laser and observe the florescence light of the long-lived subradiant modes of excitation after the laser is switched off. However, these modes are highly degenerate and form an almost continuous band in the subradiant manifold. Here we propose a new method of exciting a given subradiant state by coupling atoms to a surface plasmon wave propagating along the interface with a metallic film. By controlling the chain/surface distance we may load, store and release photons in the atoms, making them a promising tool for future quantum memories.
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.
Abstract We explore excitation transport within a one-dimensional chain of atoms where the atomic transition dipoles are coupled to the free radiation field. When the atoms are separated by distances smaller or comparable to the wavelength of the transition, the exchange of virtual photons leads to the transport of the excitation through the lattice. Even though this is a strongly dissipative system, we find that the transport is subradiant, that is, the excitation lifetime is orders of magnitude longer than the one of an individual atom. In particular, we show that a subspace of the spectrum is formed by subradiant states with a linear dispersion relation, which allows for the dispersionless transport of wave packets over long distances with virtually zero decay rate. Moreover, the group velocity and direction of the transport can be controlled via an external uniform magnetic field while preserving its subradiant character. The simplicity and versatility of this system, together with the robustness of subradiance against disorder, makes it relevant for a range of applications such as lossless energy transport and long-time light storage.
Plasmonic nanocavities are known for their extreme field enhancement and subwavelength light confinement in gaps of just a few nanometers. Pairing this with the ability to host quantum emitters, they form highly promising platforms to control or engineer quantum states at room temperature. Here, we use the lossy nature of plasmonic nanocavities to form subradiant entangled states between two or more quantum emitters, that persist for ∼ 100 times longer than the plasmonic excitation. We develop a theoretical description that directly links quantum variables to experimentally measurable quantities, such as the extinction cross section, and unlike previous studies includes plasmonic excitations necessary to resonantly form subradiant states. This work paves the way towards engineering quantum entangled states in ambient conditions with plasmonic nanocavities.
In recent years, there has been an increasing interest in subradiance in ordered atomic arrays, both for its rich phenomenology and its potential importance in realizing robust quantum optical applications. However, the weak interaction of subradiant states with light makes it challenging to observe and measure these states. Recently, an experimental technique was demonstrated, which allows for efficient and coherent manipulation of the wavevector associated with atomic spin- wave excitations. We propose that this can be a useful tool to unlock subradiant phenomena. In particular, we theoretically analyze how this technique can be used to map the subradiant dynamics of a highly excited atomic array onto the properties of the emitted light.
We develop a microscopic quantum theory of surface plasmon polaritons valid for arbitrary metal-dielectric geometries. Our framework is based on the Power-Zienau-Woolley representation of quantum electrodynamics, which provides an optimal separation between electronic and photonic degrees of freedom and is therefore particularly well suited for constructing quantum descriptions of polaritonic excitations in strongly dispersive media. Within this formulation, the fundamental electronic oscillator is identified as the bulk plasmon mode, which is nonperturbatively coupled to the radiative continuum of free photon modes. This coupling induces a geometry-dependent renormalization of the bulk plasma frequency, giving rise to confined plasmonic resonances. As specific applications, we recover the localized surface plasmon modes of metallic nanoparticles, including radiative frequency shifts and decay, as well as the exact dispersion relation of propagating surface plasmon polaritons at planar interfaces. Our quantum treatment further reveals that light-matter interactions at metal-dielectric interfaces are inherently in the ultrastrong coupling regime. As a result, in the quasistatic limit, the system exhibits unconventional ground-state quantum fluctuations that can be controlled through the refractive index. These results open new intriguing perspectives in the field of quantum plasmonics.
Recent experimental advances in preparing regular defect-free 2D arrays of atoms with optical traps have offered new opportunities to engineer strong collective couplings between light and atoms as quantum optical dipoles. Applications of such collective light-matter interactions include the realization of atom-thick mirrors, retrieval of quantum memories with high efficiency, or the implementation of topological quantum optics. I will present novel applications in the context of quantum networking. First, I will discuss the design of a chiral photonic quantum link, where distant single atoms interact by exchanging photons propagating in a unique direction in free space. This is achieved by coupling both single atoms, representing qubits implemented using a pair of Rydberg states, to bi-layer atomic arrays which act as quantum phased-array antennas. Exploiting the combination of a “Rydberg-dressing” laser and a control laser driving the atomic arrays, an effective Rydberg dipole-dipole interaction can be engineered between atoms and atomic arrays as quantum emitters, allowing to match the spatial modes of spontaneously emitted and absorbed photons to a Gaussian mode of interest. In this way, we realize a chiral quantum interface, i.e., where atoms couple to photonic modes with a unique direction of propagation. This setup provides a basic building block of a novel platform for quantum networks in free space, i.e., without requiring coupling atoms to modes of cavities or nanostructures, which I will illustrate with the deterministic coherent transfer of quantum states between single atoms with high fidelity. Second, I will discuss the collective radiation properties of two distant single-layer atomic arrays acting as quantum memories. This system can support a long-lived non-local superposition state of atomic excitations exhibiting strong subradiance. This “dark” mode consists of an atomic excitation which is delocalized between the two distant atomic arrays, in such a way that the overall radiation is strongly suppressed by quantum interference. I will describe the preparation of these states and their application as resource of non-local entanglement. In particular, by weakly driving the arrays, the state of the quantum memories, localized in each array, can be transferred to this “non-local” subradiant state, allowing again for a deterministic coherent quantum state transfer with high fidelity between the memories. Finally, I will discuss experimental realizations using cold atoms in optical trap arrays, and the effect of experimental imperfections in the arrays, such as finite defect probability, temperature, and depth of the optical traps.