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arXiv:2506.16909

Collective emission of atomic nanorings around an optical nanofiber

Juliette Jiménez Jaimes, Síle Nic Chormaic, E. Brion

Published Jun 20, 2025• 0 citations
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Abstract

We theoretically investigate the collective emission of one and two circular arrays of two-level atoms surrounding an optical nanofiber. We show that the radiation eigenmodes of a single ring selectively couple to specific guided modes of the fiber, according to their symmetry, and study how the physical parameters of the system control their nature. In particular, we identify situations in which the emission toward radiation modes is highly suppressed with respect to fiber-guided modes while the lifetime of the atomic excitation is enhanced. We further address the case of two identical nanorings positioned at a distance from each other along the nanofiber. By contrast to free-space configurations, the rings can exchange excitations even at large separation through nanofiber guided modes resulting in enhanced sub- and super-radiance with respect to the single-ring case. Our findings suggest that the ring configuration is promising for the implementation of efficient and versatile light-matter nanofiber-based interfaces and the achievement of waveguide quantum electrodynamics.

DOI
10.48550/arxiv.2506.16909

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We theoretically investigate the collective emission of one and two circular arrays of two-level atoms surrounding an optical nanofiber. We show that the radiation eigenmodes of a single ring selectively couple to specific guided modes of the fiber, according to their symmetry, and study how the physical parameters of the system control their nature. In particular, we identify situations in which the emission toward radiation modes is highly suppressed with respect to fiber-guided modes while the lifetime of the atomic excitation is enhanced. We further address the case of two identical nanorings positioned at a distance from each other along the nanofiber. By contrast to free-space configurations, the rings can exchange excitations even at large separation through nanofiber guided modes resulting in enhanced sub- and super-radiance with respect to the single-ring case. Our findings suggest that the ring configuration is promising for the implementation of efficient and versatile light-matter nanofiber-based interfaces and the achievement of waveguide quantum electrodynamics.
We theoretically investigate the collective emission of one and two circular arrays of two-level atoms surrounding an optical nanofiber. We show that the radiation eigenmodes of a single ring selectively couple to specific guided modes of the fiber, according to their symmetry, and study how the physical parameters of the system control their nature. In particular, we identify situations in which the emission toward radiation modes is highly suppressed with respect to fiber guided modes while the lifetime of the atomic excitation is enhanced. We further address the case of two identical rings positioned at a distance from each other along the nanofiber. By contrast to free-space configurations, the rings can exchange an excitation even at large separation through nanofiber guided modes resulting in enhanced sub- and supper-radiance with respect to the single-ring case. Our findings suggest that the ring configuration is promising for the implementation of efficient and versatile light-matter nanofiber-based interfaces and the achievement of waveguide quantum electrodynamics.
We theoretically investigate the collective emission of one and two circular arrays of two-level atoms surrounding an optical nanofiber (ONF). Our study reveals that the radiation eigenmodes (REMs) of a single ring selectively couple to specific guided modes of the fiber, depending on their symmetry. By tuning the physical parameters of the system, we demonstrate that the emission towards radiation modes can be highly suppressed, thereby enhancing the lifetime of the atomic excitation. Two identical rings positioned at a distance from each other along the nanofiber can exchange an excitation even at large separations through nanofiber guided modes. This results in enhanced sub-and super-radiance compared to the single-ring case. The selective coupling of REMs to specific guided modes and the enhanced sub-and super-radiance in a two-ring system suggest that the ring configuration is promising for implementing efficient and versatile light-matter nanofiber-based interfaces and achieving waveguide quantum electrodynamics (WQED).
We experimentally and theoretically investigate collective radiative effects in an ensemble of cold atoms coupled to a single-mode optical nanofiber. Our analysis unveils the microscopic dynamics of the system, showing that collective interactions between the atoms and a single guided photon gradually build up along the atomic array in the direction of propagation of light. These results are supported by time-resolved measurements of the light transmitted and reflected by the ensemble after excitation via nanofiber-guided laser pulses, whose rise and fall times are shorter than the atomic lifetime. Superradiant decays more than 1 order of magnitude faster than the single-atom free-space decay rate are observed for emission in the forward-propagating guided mode, while at the same time, no speed-up of the decay rate is measured in the backward direction. In addition, position-resolved measurements of the light that is transmitted past the atoms are performed by inserting the nanofiber-coupled atomic array in a 45-m-long fiber ring resonator, which allow us to experimentally reveal the progressive growth of the collective response of the atomic ensemble. Our results highlight the unique opportunities offered by nanophotonic cold atom systems for the experimental investigation of collective light-matter interaction.
Emitter ensembles interact collectively with the radiation field. In the case of a one-dimensional array of atoms near a nanofiber, this collective light-matter interaction does not only lead to an increased photon coupling to the guided modes within the fiber, but also to a drastic enhancement of the chirality in the photon emission. We show that near-perfect chirality can be achieved already for moderately sized ensembles, containing 10 to 15 atoms, by phase matching a superradiant collective guided emission mode via an external laser field. This is of importance for developing an efficient interface between atoms and waveguide structures with unidirectional coupling, with applications in quantum computing and communication such as the development of nonreciprocal photon devices or quantum information transfer channels.
We investigate the radiative coupling between two two-level atoms with arbitrarily polarized dipoles in the vicinity of a nanofiber. We present a systematic derivation for the master equation, the single- and cross-atom decay coefficients, and the dipole-dipole interaction coefficients for the atoms interacting with the vacuum of the field in the guided and radiation modes of the nanofiber. We study numerically the case where the atomic dipoles are circularly polarized. In this case, the rate of emission depends on the propagation direction along the fiber axis and, hence, the radiative interaction between the atoms is chiral. We examine the time evolution of the atoms for different initial states. We calculate the fluxes and mean numbers of photons spontaneously emitted into guided modes in the positive and negative directions of the fiber axis. We show that the chiral radiative coupling modifies the collective emission of the atoms. We observe that the modifications strongly depend on the initial state of the atomic system, the radiative transfer direction, the distance between the atoms, and the distance from the atoms to the fiber surface.
We investigate the radiative coupling between two two-level atoms with arbitrarily polarized dipoles in the vicinity of a nanofiber. We present a systematic derivation for the master equation, the single- and cross-atom decay coefficients, and the dipole-dipole interaction coefficients for the atoms interacting with the vacuum of the field in the guided and radiation modes of the nanofiber. We study numerically the case where the atomic dipoles are circularly polarized. In this case, the rate of emission depends on the propagation direction, that is, the radiative interaction between the atoms is chiral. We examine the time evolution of the atoms for different initial states. We calculate the fluxes and mean numbers of photons spontaneously emitted into guided modes in the positive and negative directions of the fiber axis. We show that the chiral radiative coupling modifies the collective emission of the atoms. We observe that the modifications strongly depend on the initial state of the atomic system, the radiative transfer direction, the distance between the atoms, and the distance from the atoms to the fiber surface.