No Arabic abstract
We study the vacuum-induced degradation of high-finesse optical cavities with mirror coatings composed of SiO$_2$-Ta$_{2}$O$_{5}$ dielectric stacks, and present methods to protect these coatings and to recover their initial quality factor. For separate coatings with reflectivities centered at 370 nm and 422 nm, a vacuum-induced continuous increase in optical loss occurs if the surface-layer coating is made of Ta$_{2}$O$_{5}$, while it does not occur if it is made of SiO$_2$. The incurred optical loss can be reversed by filling the vacuum chamber with oxygen at atmospheric pressure, and the recovery rate can be strongly accelerated by continuous laser illumination at 422 nm. Both the degradation and the recovery processes depend strongly on temperature. We find that a 1 nm-thick layer of SiO$_2$ passivating the Ta$_{2}$O$_{5}$ surface layer is sufficient to reduce the degradation rate by more than a factor of 10, strongly supporting surface oxygen depletion as the primary degradation mechanism.
A novel approach to optics integration in ion traps is demonstrated based on a surface electrode ion trap that is microfabricated on top of a dielectric mirror. Additional optical losses due to fabrication are found to be as low as 80 ppm for light at 422 nm. The integrated mirror is used to demonstrate light collection from, and imaging of, a single 88 Sr+ ion trapped $169pm4 mu$m above the mirror.
A theoretical study is carried out for the cavity cooling of a $Lambda$-type three level atom in a high-finesse optical cavity with a weakly driven field. Analytical expressions for the friction, diffusion coefficients and the equilibrium temperatures are obtained by using the Heisenberg equations, then they are calculated numerically and shown graphically as a function of controlling parameters. For a suitable choice of these parameters, the dynamics of the cavity field interaction with the $Lambda$-type three-level atom introduces a sisyphus cooling mechanism yielding lower temperatures below the Doppler limit and allowing larger cooling rate, avoiding the problems induced by spontaneous emission.
Optical high-finesse cavities are a well-known mean to enhance light-matter interactions. Despite large progress in the realization of strongly coupled light-matter systems, the controlled positioning of single solid emitters in cavity modes remains a challenge. We pursue the idea to use nanofibers with sub-wavelength diameter as a substrate for such emitters. This paper addresses the question how strongly optical nanofibers influence the cavity modes. We analyze the influence of the fiber position for various fiber diameters on the finesse of the cavity and on the shape of the modes.
Confining a laser field between two high reflectivity mirrors of a high-finesse cavity can increase the probability of a given cavity photon to be scattered by an atom traversing the confined photon mode. This enhanced coupling between light and atoms is successfully employed in cavity quantum electrodynamics experiments and led to a very prolific research in quantum optics. The idea of extending such experiments to sub-wavelength sized nanomechanical systems has been recently proposed in the context of optical cavity cooling. Here we present an experiment involving a single nanorod consisting of about 10^9 atoms precisely positioned to plunge into the confined mode of a miniature high finesse Fabry-Perot cavity. We show that the optical transmission of the cavity is affected not only by the static position of the nanorod but also by its vibrational fluctuation. While an imprint of the vibration dynamics is directly detected in the optical transmission, back-action of the light field is also anticipated to quench the nanorod Brownian motion. This experiment shows the first step towards optical cavity controlled dynamics of mechanical nanostructures and opens up new perspectives for sensing and manipulation of optomechanical nanosystems.
We demonstrate the superior performance of fluoride coated versus oxide coated mirrors in long term vacuum operation of a high power deep-ultraviolet enhancement cavity. In high vacuum ($10^{-8}$ mbar), the fluoride optics can maintain up to a record-high 10 w of stable intracavity power on one hour time scales, whereas for the oxide optics, we observe rapid degradation at lower intracavity powers with a rate that increases with power. After observing degradation in high vacuum, we can recover the fluoride and oxide optics with oxygen; however, this recovery process becomes ineffective after several applications. For fluoride coatings, we see that initial UV conditioning in an oxygen environment helps to improve the performances of the optics. In oxygen-rich environments from $sim 10^{-4}$ mbar to 1 mbar, the fluoride optics can stably maintain up to 20 W of intracavity power on several-hour time scales whereas for the oxide optics there is immediate degradation with a rate that increases with decreasing oxygen pressure.