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 study the force of light on a two-level atom near an ultrathin optical fiber using the mode function method and the Green tensor technique. We show that the total force consists of the driving-field force, the spontaneous-emission recoil force, and the fiber-induced van der Waals potential force. Due to the existence of a nonzero axial component of the field in a guided mode, the Rabi frequency and, hence, the magnitude of the force of the guided driving field may depend on the propagation direction. When the atomic dipole rotates in the meridional plane, the spontaneous-emission recoil force may arise as a result of the asymmetric spontaneous emission with respect to opposite propagation directions. The van der Waals potential for the atom in the ground state is off-resonant and opposite to the off-resonant part of the van der Waals potential for the atom in the excited state. Unlike the potential for the ground state, the potential for the excited state may oscillate depending on the distance from the atom to the fiber surface.
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 the force of a near-resonant guided light field of an ultrathin optical fiber on a two-level atom. We show that, if the atomic dipole rotates in the meridional plane, the magnitude of the force of the guided light depends on the field propagation direction. The chirality of the force arises as a consequence of the directional dependencies of the Rabi frequency of the guided driving field and the spontaneous emission from the atom. This provides a unique method for controlling atomic motion in the vicinity of an ultrathin fiber.
We study the modification of the atomic spontaneous emission rate, i.e. Purcell effect, of $^{87}$Rb in the vicinity of an optical nanofiber ($sim$500 nm diameter). We observe enhancement and inhibition of the atomic decay rate depending on the alignment of the induced atomic dipole relative to the nanofiber. Finite-difference time-domain simulations are in quantitative agreement with the measurements when considering the atoms as simple oscillating linear dipoles. This is surprising since the multi-level nature of the atoms should produce a different radiation pattern, predicting smaller modification of the lifetime than the measured ones. This work is a step towards characterizing and controlling atomic properties near optical waveguides, fundamental tools for the development of quantum photonics.
A single atom in free space can have a strong influence on a light beam and a single photon can have a strong effect on a single atom in free space. Regarding this interaction, two conceptually different questions can be asked: can a single atom fully absorb a single photon and can a single atom fully reflect a light beam. The conditions for achieving the full effect in either case are different. Here we discuss related questions in the context of an optical resonator. When shaping a laser pulse properly it will be fully absorbed by an optical resonator, i.e., no light will be reflected and all the pulse energy will accumulate inside the resonator before it starts leaking out. We show in detail that in this case the temporal pulse shape has to match the time-reversed pulse obtained by the cavitys free decay. On the other hand a resonator, made of highly reflecting mirrors which normally reflect a large portion of any incident light, may fully transmit the light, as long as the light is narrow band and resonant with the cavity. The analogy is the single atom - normally letting most of the light pass - which under special conditions may fully reflect the incident light beam. Using this analogy we are able to study the effects of practical experimental limitations in the atom-photon coupling, such as finite pulses, bandwidths, and solid angle coverage, and to use the optical resonator as a test bed for the implementation of the quantum experiment.