We introduce a protocol for dynamical dispersion engineering in an atomic chain formed by an ordered array of multilevel atoms with subwavelength lattice constant. This chain supports dark states that are protected from dissipation and can be understood as spin waves traveling along the array. By using an external control field with a spatially varying elliptical polarization we correlate internal and external degrees of freedom of the array in a controllable way. The coherent control over atomic states translates into control over the group velocity of the spin waves. A traveling excitation can be stored and released without dissipation by adiabatically changing the control field amplitude. This protocol is an alternative to the more conventional electromagnetically induced transparency and exemplifies the rich physics born of the interplay between coherent control and correlated decay.
We introduce a protocol for dynamical dispersion engineering in an atomic chain formed by an ordered array of multilevel atoms with subwavelength lattice constant. This chain supports dark states that are protected from dissipation and can be understood as spin waves traveling along the array. By using an external control field with a spatially varying elliptical polarization we correlate internal and external degrees of freedom of the array in a controllable way. The coherent control over atomic states translates into control over the group velocity of the spin waves. A traveling excitation can be stored and released without dissipation by adiabatically changing the control field amplitude. This protocol is an alternative to the more conventional electromagnetically induced transparency and exemplifies the rich physics born of the interplay between coherent control and correlated decay.
Collective excitations in ordered subwavelength atomic arrays can exhibit strongly suppressed radiative decay due to interference between light scattered by neighboring emitters. These so-called subradiant states make these systems a promising platform for storing and manipulating photonic excitations. The external geometry of the array, combined with dynamical control of the atomic dipole orientation, enables localized trapping and coherent transport of these subradiant excitations. Here, we theoretically demonstrate these capabilities in ring-shaped atomic arrays. Specifically, we show adiabatic transport of a localized excitation around a single ring, coherent transfer of a single excitation between two neighboring rings with geometry-controlled selectivity, and interaction-induced conditional phase shifts between two simultaneously trapped excitations in neighboring rings. The latter can be interpreted as effective controlled-phase operations between stored excitations. Together, these results demonstrate the potential of ordered atomic arrays as a platform for coherent photonic quantum information processing with dissipation-protected collective excitations.
Ordered atomic arrays with subwavelength spacing have emerged as an efficient and versatile light-matter interface, where collective interactions give rise to sets of super- and subradiant lattice states. Here, we demonstrate that highly subradiant states, so-called lattice dark states, can be individually addressed and manipulated by applying a spatial modulation of the atomic detuning. More specifically, we show that lattice dark states can be used to store and retrieve single photons with near-unit efficiency, as well as to control the temporal, frequency, and spatial degrees of freedom of the emitted electromagnetic field. Furthermore, we demonstrate how to engineer arbitrary coherent interactions between multiple dark states and thereby manipulate information stored in the lattice. These results pave the way towards quantum optics and information processing using atomic arrays.
We identify form-stable coupled excitations of light and matter ("dark-state polaritons") associated with the propagation of quantum fields in electromagnetically induced transparency. The properties of dark-state polaritons such as the group velocity are determined by the mixing angle between light and matter components and can be controlled by an external coherent field as the pulse propagates. In particular, light pulses can be decelerated and "trapped" in which case their shape and quantum state are mapped onto metastable collective states of matter. Possible applications of this reversible coherent-control technique are discussed.
We investigate collective behaviour that appears in open, many-body systems of two- and four-level atoms. Here, ``open" refers to the system interacting with an external environment that causes dissipation. We derive a general open quantum master equation to describe the system dynamics only, independent of this environment. We identify processes such as coherent exchange of virtual photons and modified decay rates caused by long-range interactions between all pairs of atoms that scale with distance by inverse power laws. 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 interatomic spacing is smaller than or comparable to the wavelength of light associated with the photon emitted from a given transition, virtual photon exchange interactions facilitate excitation transport through the chain. Atomic systems coupled to an environment display dissipative dynamics, however subradiant transport is exhibited from a variety of initial states; spontaneous emission from the chain occurs at a rate much slower than that for an individual atom. In particular, we find a region within the decay spectrum that consists entirely of subradiant states with a corresponding linear dispersion relation in the interaction energy. Identifying this subspace allows for the dispersionless transport of wave packets over long distances with near-zero decay. Moreover, the group velocity of the wave packet and direction of the transport can be controlled via an external uniform magnetic field while preserving its subradiant character. We discuss a number of experimental considerations to justify the feasibility and robustness of this protocol. Initial state preparation is outlined, utilising external laser driving to excite the system into the single excitation sector. Furthermore, we consider positional disorder by explicitly accounting for the external atomic degrees of freedom -- position and momentum -- which allows us to model the positions of all atoms by a motional state representing the occupation of a lattice well with a given width. These discussions are made in the low-temperature limit, where the atomic motion is essentially frozen, and we identify that subradiant transport is indeed robust. Finally, we explore the experimental limits of interatomic spacing and imperfect filling within an experimentally achievable optical lattice. We calculate the photon emission rate -- an experimentally measurable quantity -- and compare the emission spectra to our analysis. By limiting parameters to those achieved experimentally, we observe a reduction, yet not an absence, of collective behaviour. 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. The lifetime of an atomic excitation could be increased by a factor of thousands to millions for a chain of atoms under the conditions that we explore in this thesis.
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.
In dense and ordered atomic arrays, destructive interference in photon emission leads to the emergence of subradiant states, which are protected from radiative decay and are characterized by long lifetimes. Within linear optics, subradiant states of one-dimensional chains can be interpreted as guided modes. Collective interactions in arrays have attracted a lot of interest recently, with work showing that collective emission can be used to realize improved quantum memories [1, 2] as well as almost-perfect atomic mirrors [3, 4], among other exciting applications. While tantalizing, these ideas strongly rely on one assumption: that atoms are two-level systems and only have a unique electronic ground state. However, most atoms exhibit a rich and complex internal structure. In this talk, I will discuss the properties of subradiant states of two-level and multilevel atoms. In particular, I will present a new mechanism for subradiance and atomic wave-guiding in atoms with hyperfine structure, which crucially depends on many-body correlations, a radical departure from conventional subradiant states found in classical-dipole lattices or two-level-atom arrays [5].