Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userAlignment-dependent decay rate of an atomic dipole near an optical nanofiber
175
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
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.
rate research
Read More
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 study the strong coupling between photons and atoms that can be achieved in an optical nanofiber geometry when the interaction is dispersive. While the Purcell enhancement factor for spontaneous emission into the guided mode does not reach the strong-coupling regime for individual atoms, one can obtain high cooperativity for ensembles of a few thousand atoms due to the tight confinement of the guided modes and constructive interference over the entire chain of trapped atoms. We calculate the dyadic Greens function, which determines the scattering of light by atoms in the presence of the fiber, and thus the phase shift and polarization rotation induced on the guided light by the trapped atoms. The Greens function is related to a full Heisenberg-Langevin treatment of the dispersive response of the quantized field to tensor polarizable atoms. We apply our formalism to quantum nondemolition (QND) measurement of the atoms via polarimetry. We study shot-noise-limited detection of atom number for atoms in a completely mixed spin state and the squeezing of projection noise for atoms in clock states. Compared with squeezing of atomic ensembles in free space, we capitalize on unique features that arise in the nanofiber geometry including anisotropy of both the intensity and polarization of the guided modes. We use a first principles stochastic master equation to model the squeezing as function of time in the presence of decoherence due to optical pumping. We find a peak metrological squeezing of ~5 dB is achievable with current technology for ~2500 atoms trapped 180 nm from the surface of a nanofiber with radius a=225 nm.
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 is already achieved for moderately-sized ensembles, containing 10 to 15 atoms. 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 non-reciprocal photon devices or quantum information transfer channels.
It is shown that a circular dipole can deflect the focused laser beam that induces it, and will experience a corresponding transverse force. Quantitative expressions are derived for Gaussian and angular tophat beams, while the effects vanish in the plane-wave limit. The phenomena are analogous to the Magnus effect pushing a spinning ball onto a curved trajectory. The optical case originates in the coupling of spin and orbital angular momentum of the dipole and the light. In optical tweezers the force causes off-axis displacement of the trapping position of an atom by a spin-dependent amount up to $lambda/2pi$, set by the direction of a magnetic field. This suggests direct methods to demonstrate and explore these effects, for instance to induce spin-dependent motion.
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.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
