Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userWavelength-scale errors in optical localization due to spin-orbit coupling of light
134
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
The precise determination of the position of point-like emitters and scatterers using far-field optical imaging techniques is of utmost importance for a wide range of applications in medicine, biology, astronomy, and physics. Although the optical wavelength sets a fundamental limit to the image resolution of unknown objects, the position of an individual emitter can in principle be estimated from the image with arbitrary precision. This is used, e.g., in stars position determination and in optical super-resolution microscopy. Furthermore, precise position determination is an experimental prerequisite for the manipulation and measurement of individual quantum systems, such as atoms, ions, and solid state-based quantum emitters. Here we demonstrate that spin-orbit coupling of light in the emission of elliptically polarized emitters can lead to systematic, wavelength-scale errors in the estimate of the emitters position. Imaging a single trapped atom as well as a single sub-wavelength-diameter gold nanoparticle, we demonstrate a shift between the emitters measured and actual positions which is comparable to the optical wavelength. Remarkably, for certain settings, the expected shift can become arbitrarily large. Beyond their relevance for optical imaging techniques, our findings apply to the localization of objects using any type of wave that carries orbital angular momentum relative to the emitters position with a component orthogonal to the direction of observation.
rate research
Read More
Calibrating the strength of the light-matter interaction is an important experimental task in quantum information and quantum state engineering protocols. The strength of the off-resonant light-matter interaction in multi-atom spin oscillators can be characterized by the coupling rate $Gamma_text{S}$. Here we utilize the Coherently Induced Faraday Rotation (CIFAR) signal for determining the coupling rate. The method is suited for both continuous and pulsed readout of the spin oscillator, relying only on applying a known polarization modulation to the probe laser beam and detecting a known optical polarization component. Importantly, the method does not require changes to the optical and magnetic fields performing the state preparation and probing. The CIFAR signal is also independent of the probe beam photo-detection quantum efficiency, and allows direct extraction of other parameters of the interaction, such as the tensor coupling $zeta_text{S}$, and the damping rate $gamma_text{S}$. We verify this method in the continuous wave regime, probing a strongly coupled spin oscillator prepared in a warm cesium atomic vapour.
Optical waveguides in the form of glass fibers are the backbone of global telecommunication networks. In such optical fibers, the light is guided over long distances by continuous total internal reflection which occurs at the interface between the fiber core with a higher refractive index and the lower index cladding. Although this mechanism ensures that no light escapes from the waveguide, it gives rise to an evanescent field in the cladding. While this field is protected from interacting with the environment in standard optical fibers, it is routinely employed in air- or vacuum-clad fibers in order to efficiently couple light fields to optical components or emitters using, e.g., tapered optical fiber couplers. Remarkably, the strong confinement imposed by the latter can lead to significant coupling of the lights spin and orbital angular momentum. Taking advantage of this effect, we demonstrate the controlled directional spontaneous emission of light by quantum emitters into a sub-wavelength-diameter waveguide. The effect is investigated in a paradigmatic setting, comprising cesium atoms which are located in the vicinity of a vacuum-clad silica nanofiber. We experimentally observe an asymmetry higher than 10:1 in the emission rates into the counterpropagating fundamental guided modes of the nanofiber. Moreover, we demonstrate that this asymmetry can be tailored by state preparation and suitable excitation of the quantum emitters. We expect our results to have important implications for research in nanophotonics and quantum optics and for implementations of integrated optical signal processing in the classical as well as in the quantum regime.
Contemporary experiments in cavity quantum electrodynamics (cavity QED) with gas-phase neutral atoms rely increasingly on laser cooling and optical, magneto-optical or magnetostatic trapping methods to provide atomic localization with sub-micron uncertainty. Difficult to achieve in free space, this goal is further frustrated by atom-surface interactions if the desired atomic placement approaches within several hundred nanometers of a solid surface, as can be the case in setups incorporating monolithic dielectric optical resonators such as microspheres, microtoroids, microdisks or photonic crystal defect cavities. Typically in such scenarios, the smallest atom-surface separation at which the van der Waals interaction can be neglected is taken to be the optimal localization point for associated trapping schemes, but this sort of conservative strategy generally compromises the achievable cavity QED coupling strength. Here we suggest a new approach to the design of optical dipole traps for atom confinement near surfaces that exploits strong surface interactions, rather than avoiding them, and present the results of a numerical study based on $^{39}$K atoms and indium tin oxide (ITO). Our theoretical framework points to the possibility of utilizing nanopatterning methods to engineer novel modifications of atom-surface interactions.
We investigate the spatio-temporal evolution of a Gaussian probe pulse propagating through a four-level $N$-type atomic medium. At two-photon resonance of probe-and control fields, weaker probe pulses may propagate through the medium with low absorption and pulse shape distortion. In contrast, we find that increasing the probe pulse intensity leads to a splitting of the initially Gaussian pulse into a sequence of subpulses in the time domain. The number of subpulses arising throughout the propagation can be controlled via a suitable choice of the probe and control field parameters. Employing a simple theoretical model for the nonlinear pulse propagation, we conclude that the splitting occurs due to an interplay of Kerr nonlinearity and group velocity dispersion.
Photon-based quantum information processing promises new technologies including optical quantum computing, quantum cryptography, and distributed quantum networks. Polarization-encoded photons at telecommunication wavelengths provide a compelling platform for practical realization of these technologies. However, despite important success towards building elementary components compatible with this platform, including sources of entangled photons, efficient single photon detectors, and on-chip quantum circuits, a missing element has been atomic quantum memory that directly allows for reversible mapping of quantum states encoded in the polarization degree of a telecom-wavelength photon. Here we demonstrate the quantum storage and retrieval of polarization states of heralded single-photons at telecom-wavelength by implementing the atomic frequency comb protocol in an ensemble of erbium atoms doped into an optical fiber. Despite remaining limitations in our proof-of-principle demonstration such as small storage efficiency and storage time, our broadband light-matter interface reveals the potential for use in future quantum information processing.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
