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Register a new userSpontaneous emission and energy shifts of a Rydberg rubidium atom close to an optical nanofiber
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In this paper, we report on numerical calculations of the spontaneous emission rates and Lamb shifts of a $^{87}text{Rb}$ atom in a Rydberg-excited state $left(nleq30right)$ located close to a silica optical nanofiber. We investigate how these quantities depend on the fibers radius, the distance of the atom to the fiber, the direction of the atomic angular momentum polarization as well as the different atomic quantum numbers. We also study the contribution of quadrupolar transitions, which may be substantial for highly polarizable Rydberg states. Our calculations are performed in the macroscopic quantum electrodynamics formalism, based on the dyadic Greens function method. This allows us to take dispersive and absorptive characteristics of silica into account; this is of major importance since Rydberg atoms emit along many different transitions whose frequencies cover a wide range of the electromagnetic spectrum. Our work is an important initial step towards building a Rydberg atom-nanofiber interface for quantum optics and quantum information purposes.
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We study the spontaneous emission of an excited atom close to an optical nanofiber and the resulting scattering forces. For a suitably chosen orientation of the atomic dipole, the spontaneous emission pattern becomes asymmetric and a resonant Casimir--Polder force parallel to the fiber axis arises. For a simple model case, we show that the such a lateral force is due to the interaction of the circularly oscillating atomic dipole moment with its image inside the material. With the Casimir--Polder energy being constant in the lateral direction, the predicted lateral force does not derive from a potential in the usual way. Our results have implications for optical force measurements on a substrate as well as for laser cooling of atoms in nanophotonic traps.
We propose a novel platform for the investigation of quantum wave packet dynamics, offering a complementary approach to existing theoretical models and experimental systems. It relies on laser-cooled neutral atoms which orbit around an optical nanofiber in an optical potential produced by a red-detuned guided light field. We show that the atomic center-of-mass motion exhibits genuine quantum effects like collapse and revival of the atomic wave packet. As distinctive advantages, our approach features a tunable dispersion relation as well as straightforward readout for the wave packet dynamics and can be implemented using existing quantum optics techniques.
We calculate analytically and numerically the axial orbital and spin torques of guided light on a two-level atom near an optical nanofiber. We show that the generation of these torques is governed by the angular momentum conservation law in the Minkowski formulation. The orbital torque on the atom near the fiber has a contribution from the average recoil of spontaneously emitted photons. Photon angular momentum and atomic spin angular momentum can be converted into atomic orbital angular momentum. The orbital and spin angular momenta of the guided field are not transferred separately to the orbital and spin angular momenta of the atom.
We theoretically investigate measurement-based feedback control of a laser-driven one-dimensional atomic chain interfaced with a nanofiber. The interfacing leads to all-to-all interactions among the atomic emitters and induces chirality, i.e. the directional emission of photons into a preferred guided mode of the nanofiber. In the setting we consider, the measurement of guided light -- conducted either by photon counting or through homodyne detection of the photocurrent quadratures -- is fed back into the system through a modulation of the driving laser field. We investigate how this feedback scheme influences the photon counting rate and the quadratures of the guided light field. Moreover, we analyse how feedback alters the many-body steady state of the atom chain. Our results provide some insights on how to control and engineer dynamics in light-matter networks realizable with state-of-the-art experimental setups.
Non dispersive electronic Rydberg wave packets may be created in atoms illuminated by a microwave field of circular polarization. We discuss the spontaneous emission from such states and show that the elastic incoherent component (occuring at the frequency of the driving field) dominates the spectrum in the semiclassical limit, contrary to earlier predictions. We calculate the frequencies of single photon emissions and the associated rates in the harmonic approximation, i.e. when the wave packet has approximately a Gaussian shape. The results agree well with exact quantum mechanical calculations, which validates the analytical approach.
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