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arXiv:1905.00508 · New Journal of Physics

Subradiance-protected excitation transport

Jemma A Needham, Igor Lesanovsky, Beatriz Olmos

Published Jul 1, 2019• 75 citations
arXivHTMLPDF

Abstract

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.

DOI
10.1088/1367-2630/ab31e8

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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.
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.
In contrast to free space, in waveguides the dispersive and dissipative dipole–dipole interactions among quantum emitters exhibit a periodic behavior over remarkably long distances. We propose a novel setup, to our knowledge, exploiting this long-range periodicity in order to create highly excited subradiant states and facilitate fast controlled collective energy transport among far-apart ensembles coupled to a waveguide. For sufficiently large ensembles, collective superradiant emission into the fiber modes dominates over its free space counterpart. We show that, for a large number of emitters, a fast transverse coherent pulse can create almost perfect subradiant states with up to 50% excitation. On the other hand, for a coherent excitation of one sub-ensemble above an overall excitation fraction of 50% we find a nearly lossless and fast energy transfer to the ground state sub-ensemble. This transport can be enhanced or suppressed by controlling the positions of the ensembles relative to each other, while it can also be realized with a random position distribution. In the optimally enhanced case this fast transfer appears as superradiant emission with subsequent superabsorption, yet, without a superradiant decay after the absorption. The highly excited subradiant states, as well as the superradiant excitation transfer, appear as suitable building blocks in applications such as active atomic clocks, quantum batteries, quantum information protocols, and quantum metrology procedures such as fiber-based Ramsey schemes.
Atomic arrays provide an important quantum optical platform with photon-mediated dipole–dipole interactions that can be engineered to realize key applications in quantum information processing. A major obstacle for such applications is the fast decay of the excited states. By controlling two-band Bloch oscillations of single excitation in an atomic array under an external magnetic field, here we show that exotic subradiance can be realized and maintained with orders of magnitude longer than the spontaneous decay time in atomic arrays with the finite size. The key finding is to show a way for preventing the wavepacket of excited states scattering into the dissipative zone inside the free space light cone, which therefore leads to the excitation staying at a subradiant state for an extremely long decay time. We show that such operation can be achieved by introducing a spatially linear potential from the external magnetic field in the atomic arrays and then manipulating interconnected two-band Bloch oscillations along opposite directions. Our results also point out the possibility of controllable switching between superradiant and subradiant states, which leads to potential applications in quantum storage.
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.
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.