Imaging and Localizing Individual Atoms Interfaced with a Nanophotonic Waveguide.

Single particle-resolved fluorescence imaging is an enabling technology in cold-atom physics. However, so far, this technique has not been available for nanophotonic atom-light interfaces. Here, we image single atoms that are trapped and optically interfaced using an optical nanofiber. Near-resonant light is scattered off the atoms and imaged while counteracting heating mechanisms via degenerate Raman cooling. We detect trapped atoms within 150 ms and record image sequences of given atoms. Building on our technique, we perform two experiments which are conditioned on the number and position of the nanofiber-trapped atoms. We measure the transmission of nanofiber-guided resonant light and verify its exponential scaling in the few-atom limit, in accordance with Beer-Lambert's law. Moreover, depending on the interatomic distance, we observe interference of the fields that two simultaneously trapped atoms emit into the nanofiber. The demonstrated technique enables postselection and possible feedback schemes and thereby opens the road toward a new generation of experiments in quantum nanophotonics.

Wavelength-scale errors in optical localization due to spin-orbit coupling of light.

Far-field optical imaging techniques allow the determination of the position of point-like emitters and scatterers [1-3]. 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 for example in the determination of stars position [4] or in optical super-resolution microscopy [5]. 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 [6-8]. 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 estimation 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. For certain settings, the expected shift can become arbitrarily large. Beyond optical imaging techniques, our findings could be relevant for 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.

Observation of Ultrastrong Spin-Motion Coupling for Cold Atoms in Optical Microtraps.

We realize a mechanical analogue of the Dicke model, achieved by coupling the spin of individual neutral atoms to their quantized motion in an optical trapping potential. The atomic spin states play the role of the electronic states of the atomic ensemble considered in the Dicke model, and the in-trap motional states of the atoms correspond to the states of the electromagnetic field mode. The coupling between spin and motion is induced by an inherent polarization gradient of the trapping light fields, which leads to a spatially varying vector light shift. We experimentally show that our system reaches the ultrastrong coupling regime; i.e., we obtain a coupling strength that is a significant fraction of the trap frequency. Moreover, with the help of an additional light field, we demonstrate the in situ tuning of the coupling strength. Beyond its fundamental interest, the demonstrated one-to-one mapping between the physics of optically trapped cold atoms and the Dicke model paves the way for implementing protocols and applications that exploit extreme coupling strengths.

Quantum state-controlled directional spontaneous emission of photons into a nanophotonic waveguide.

The spin of light in subwavelength-diameter waveguides can be orthogonal to the propagation direction of the photons because of the strong transverse confinement. This transverse spin changes sign when the direction of propagation is reversed. Using this effect, we demonstrate the directional spontaneous emission of photons by laser-trapped caesium atoms into an optical nanofibre and control their propagation direction by the excited state of the atomic emitters. In particular, we tune the spontaneous emission into the counter-propagating guided modes from symmetric to strongly asymmetric, where more than % of the optical power is launched into one or the other direction. We expect our results to have important implications for research in quantum nanophotonics and for implementations of integrated optical signal processing in the quantum regime.

Biprism electron interferometry with a single atom tip source.

Experiments with electron or ion matter waves require a coherent, monochromatic and long-term stable source with high brightness. These requirements are best fulfilled by single atom tip (SAT) field emitters. The performance of an iridium covered W(111) SAT is demonstrated and analyzed for electrons in a biprism interferometer. Furthermore we characterize the emission of the SAT in a separate field electron and field ion microscope and compare it with other emitter types. A new method is presented to fabricate the electrostatic charged biprism wire that separates and combines the matter wave. In contrast to other biprism interferometers the source and the biprism size are well defined within a few nanometers. The setup has direct applications in ion interferometry and Aharonov-Bohm physics.

Thermalization via heat radiation of an individual object thinner than the thermal wavelength.

Modeling and investigating the thermalization of microscopic objects with arbitrary shape from first principles is of fundamental interest and may lead to technical applications. Here, we study, over a large temperature range, the thermalization dynamics due to far-field heat radiation of an individual, deterministically produced silica fiber with a predetermined shape and a diameter smaller than the thermal wavelength. The temperature change of the subwavelength-diameter fiber is determined through a measurement of its optical path length in conjunction with an ab initio thermodynamic model of the fiber structure. Our results show excellent agreement with a theoretical model that considers heat radiation as a volumetric effect and takes the emitter shape and size relative to the emission wavelength into account.

Coherence properties of nanofiber-trapped cesium atoms.

We experimentally study the ground state coherence properties of cesium atoms in a nanofiber-based two-color dipole trap, localized ∼ 200 nm away from the fiber surface. Using microwave radiation to coherently drive the clock transition, we record Ramsey fringes as well as spin echo signals and infer a reversible dephasing time of T(2)(*) = 0.6 ms and an irreversible dephasing time of T(2)(') = 3.7 ms. By modeling the signals, we find that, for our experimental parameters, T(2)(*) and T(2)(') are limited by the finite initial temperature of the atomic ensemble and the heating rate, respectively. Our results represent a fundamental step towards establishing nanofiber-based traps for cold atoms as a building block in an optical fiber quantum network.

Nanofiber Fabry-Perot microresonator for nonlinear optics and cavity quantum electrodynamics.

We experimentally realize a Fabry-Perot-type optical microresonator near the cesium D2 line wavelength based on a tapered optical fiber, equipped with two fiber Bragg gratings that enclose a subwavelength diameter waist. Owing to the very low taper losses, the finesse of the resonator reaches F=86 while the on-resonance transmission is T=11%. The characteristics of our resonator fulfill the requirements of nonlinear optics and cavity quantum electrodynamics in the strong coupling regime. These characteristics, combined with the demonstrated ease of use and advantageous mode geometry, open a realm of applications.

Bottle microresonator with actively stabilized evanescent coupling.

The evanescent coupling of light between a whispering-gallery-mode bottle microresonator and a subwavelength-diameter coupling fiber is actively stabilized by means of the Pound-Drever-Hall technique. We demonstrate the stabilization of a critically coupled resonator with a control bandwidth of 0.1 Hz, yielding a residual transmission of (9±3)×10(-3) for more than an hour. Simultaneously, the frequency of the resonator mode is actively stabilized.

Dispersive optical interface based on nanofiber-trapped atoms.

We dispersively interface an ensemble of 1000 atoms trapped in the evanescent field surrounding a tapered optical nanofiber. This method relies on the azimuthally asymmetric coupling of the ensemble with the evanescent field of an off-resonant probe beam, transmitted through the nanofiber. The resulting birefringence and dispersion are significant; we observe a phase shift per atom of ∼1 mrad at a detuning of 6 times the natural linewidth, corresponding to an effective resonant optical density per atom of 0.027. Moreover, we utilize this strong dispersion to nondestructively determine the number of atoms.

Optical interface created by laser-cooled atoms trapped in the evanescent field surrounding an optical nanofiber.

Trapping and optically interfacing laser-cooled neutral atoms are essential requirements for their use in advanced quantum technologies. Here we simultaneously realize both of these tasks with cesium atoms interacting with a multicolor evanescent field surrounding an optical nanofiber. The atoms are localized in a one-dimensional optical lattice about 200 nm above the nanofiber surface and can be efficiently interrogated with a resonant light field sent through the nanofiber. Our technique opens the route towards the direct integration of laser-cooled atomic ensembles within fiber networks, an important prerequisite for large scale quantum communication schemes. Moreover, it is ideally suited to the realization of hybrid quantum systems that combine atoms with, e.g., solid state quantum devices.

Ultra-sensitive fluorescence spectroscopy of isolated surface-adsorbed molecules using an optical nanofiber.

The strong radial confinement and the pronounced evanescent field of the guided light in optical nanofibers yield favorable conditions for ultra-sensitive surface spectroscopy of molecules deposited on the fiber. Using the guided mode of the nanofiber for both excitation and fluorescence collection, we present spectroscopic measurements on 3,4,9,10-perylenetetracarboxylic dianhydride molecules (PTCDA) at ambient conditions. Surface coverages as small as 1 per thousand of a compact monolayer still give rise to fluorescence spectra with a good signal to noise ratio. Moreover, we analyze and quantify the self-absorption effects due to reabsorption of the emitted fluorescence light by circumjacent surface-adsorbed molecules distributed along the fiber waist.

Ultrahigh-Q tunable whispering-gallery-mode microresonator.

Typical microresonators exhibit a large frequency spacing between resonances and a limited tunability. This impedes their use in a large class of applications which require a resonance of the microresonator to coincide with a predetermined frequency. Here, we experimentally overcome this limitation with highly prolate-shaped whispering-gallery-mode "bottle microresonators" fabricated from standard optical glass fibers. Our resonators combine an ultrahigh quality factor of 3.6 x 10(8), a small mode volume, and near-lossless fiber coupling, characteristic of whispering-gallery-mode resonators, with a simple and customizable mode structure enabling full tunability.

Cold-atom physics using ultrathin optical fibers: light-induced dipole forces and surface interactions.

The strong evanescent field around ultrathin unclad optical fibers bears a high potential for detecting, trapping, and manipulating cold atoms. Introducing such a fiber into a cold-atom cloud, we investigate the interaction of a small number of cold cesium atoms with the guided fiber mode and with the fiber surface. Using high resolution spectroscopy, we observe and analyze light-induced dipole forces, van der Waals interaction, and a significant enhancement of the spontaneous emission rate of the atoms. The latter can be assigned to the modification of the vacuum modes by the fiber.

Ultra-sensitive surface absorption spectroscopy using sub-wavelength diameter optical fibers.

The guided modes of sub-wavelength diameter air-clad optical fibers exhibit a pronounced evanescent field. The absorption of particles on the fiber surface is therefore readily detected via the fiber transmission. We show that the resulting absorption for a given surface coverage can be orders of magnitude higher than for conventional surface spectroscopy. As a demonstration, we present measurements on sub-monolayers of 3,4,9,10-perylene-tetracarboxylic dianhydride (PTCDA) molecules at ambient conditions, revealing the agglomeration dynamics on a second to minutes timescale.

Inserting two atoms into a single optical micropotential.

We recently demonstrated that strings of trapped atoms inside a standing wave optical dipole trap can be rearranged using optical tweezers [Y. Miroshnychenko, Nature 442, 151 (2006)]. This technique allows us to actively set the interatomic separations on the scale of the individual trapping potential wells. Here, we use such a distance-control operation to insert two atoms into the same potential well. The detected success rate of this manipulation is 16(-3)(+4)%, in agreement with the predictions of a theoretical model based on our experimental parameters.

Submicrometer position control of single trapped neutral atoms.

We optically detect the positions of single neutral cesium atoms stored in a standing wave dipole trap with a subwavelength resolution of 143 nm rms. The distance between two simultaneously trapped atoms is measured with an even higher precision of 36 nm rms. We resolve the discreteness of the interatomic distances due to the 532 nm spatial period of the standing wave potential and infer the exact number of trapping potential wells separating the atoms. Finally, combining an initial position detection with a controlled transport, we place single atoms at a predetermined position along the trap axis to within 300 nm rms.

Neutral atom quantum register.

We demonstrate the realization of a quantum register using a string of single neutral atoms which are trapped in an optical dipole trap. The atoms are selectively and coherently manipulated in a magnetic field gradient using microwave radiation. Our addressing scheme operates with a high spatial resolution, and qubit rotations on individual atoms are performed with 99% contrast. In a final readout operation we analyze each individual atomic state. Finally, we have measured the coherence time and identified the predominant dephasing mechanism for our register.

Coherence properties and quantum state transportation in an optical conveyor belt.

We have prepared and detected quantum coherences of trapped cesium atoms with long dephasing times. Controlled transport by an "optical conveyor belt" over macroscopic distances preserves the atomic coherence with slight reduction of coherence time. The limiting dephasing effects are experimentally identified, and we present an analytical model of the reversible and irreversible dephasing mechanisms. Our experimental methods are applicable at the single-atom level. Coherent quantum bit operations along with quantum state transport open the route towards a "quantum shift register" of individual neutral atoms.

Continued imaging of the transport of a single neutral atom.

We have continuously imaged the controlled motion of a single atom as well as of a small number of distinguishable atoms with observation times exceeding one minute. The Cesium atoms are confined to potential wells of a standing wave optical dipole trap which allows to transport them over macroscopic distances. The atoms are imaged by an intensified CCD camera, and spatial resolution near the diffraction limit is obtained.