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Reaching high densities is a key step towards cold-collision experiments with polyatomic molecules. We use a cryofuge to load up to 2$\times10^7$ CH$_3$F molecules into a box-like electric trap, achieving densities up to 10$^7$/cm$^3$ at temperatures around 350 mK where the elastic dipolar cross-section exceeds 7$\times$10$^{-12}$cm$^2$. We measure inelastic rate constants below 4$\times$10$^{-8}$cm$^3$/s and control these by tuning a homogeneous electric field that covers a large fraction of the trap volume. Comparison to ab-initio calculations gives excellent agreement with dipolar relaxation. Our techniques and findings are generic and immediately relevant for other cold-molecule collision experiments., Comment: To be published in Physical Review Letters: https://journals.aps.org/prl/accepted/e5070Y42Cf013066f8871d5761f80f99fa8136ff5

Long-distance quantum communication requires quantum repeaters to overcome photon loss in optical fibers. Here we demonstrate a repeater node with two memory atoms in an optical cavity. Both atoms are individually and repeatedly entangled with photons that are distributed until each communication partner has independently received one of them. An atomic Bell-state measurement followed by classical communication serves to establish a key. We demonstrate scaling advantage of the key rate, increase the effective attenuation length by a factor of two, and beat the error-rate threshold of 11\% for unconditionally secure communication, the corner stones for repeater-based quantum networks.

Photonic qubits memories are essential ingredients of numerous quantum networking protocols. The ideal situation features quantum computing nodes that are efficiently connected to quantum communication channels via quantum interfaces. The nodes contain a set of long-lived matter qubits, the channels support the propagation of light qubits, and the interface couples light and matter qubits. Towards this vision, we here demonstrate a random-access multi-qubit write-read memory for photons using two rubidium atoms coupled to the same mode of an optical cavity, a setup which is known to feature quantum computing capabilities. We test the memory with more than ten independent photonic qubits, observe no noticeable cross talk, and find no need for re-initialization even after ten write-read attempts. The combined write-read efficiency is 26% and the coherence time approaches 1ms. With these features, the node constitutes a promising building block for a quantum repeater and ultimately a quantum internet.

Thorough control of the optical mode of a single photon is essential for quantum information applications. We present a comprehensive experimental and theoretical study of a light-matter interface based on cavity quantum electrodynamics. We identify key parameters like the phases of the involved light fields and demonstrate absolute, flexible, and accurate control of the time-dependent complex-valued wave function of a single photon over several orders of magnitude. This capability will be an important tool for the development of distributed quantum systems with multiple components that interact via photons., Comment: main text + supplementary material

The knowledge and thus characterization of the temporal modes of quantum light fields is important in many areas of quantum physics ranging from experimental setup diagnosis to fundamental-physics investigations. Recent results showed how the auto-correlation function computed from continuous-wave homodyne measurements can be a powerful way to access the temporal mode structure. Here, we push forward this method by providing a deeper understanding and by showing how to extract the amplitude and phase of the temporal mode function with reduced experimental resources. Moreover, a quantitative analysis allows us to identify a regime of parameters where the method provides a trustworthy reconstruction, which we illustrate experimentally.

We show an optical wave-mixing scheme that generates quantum light by means of a single three-level atom. The atom couples to an optical cavity and two laser fields that together drive a cycling current within the atom. Weak driving in combination with strong atom-cavity coupling induces transitions between the dark states of the system, accompanied by single-photon emission and suppression of atomic excitation by quantum interference. For strong driving, the system can generate coherent or Schr\"odinger cat-like fields with frequencies distinct from those of the applied lasers., Comment: 5 pages, 4 figures

We demonstrate a new feedback algorithm to cool a single neutral atom trapped inside a standing-wave optical cavity. The algorithm is based on parametric modulation of the confining potential at twice the natural oscillation frequency of the atom, in combination with fast and repetitive atomic position measurements. The latter serve to continuously adjust the modulation phase to a value for which parametric excitation of the atomic motion is avoided. Cooling is limited by the measurement back action which decoheres the atomic motion after only a few oscillations. Nonetheless, applying this feedback scheme to a ~ 5 kHz oscillation mode increases the average storage time of a single atom in the cavity by a factor of 60 to more than 2 seconds. In contrast to previous feedback schemes, our algorithm is also capable of cooling a much faster ~ 500 kHz oscillation mode within just microseconds. This demonstrates that parametric cooling is a powerful technique that can be applied in all experiments where optical access is limited., Comment: 7 pages, 5 figures

The long-lived, efficient storage and retrieval of a qubit encoded on a photon is an important ingredient for future quantum networks. Although systems with intrinsically long coherence times have been demonstrated, the combination with an efficient light-matter interface remains an outstanding challenge. In fact, the coherence times of memories for photonic qubits are currently limited to a few milliseconds. Here we report on a qubit memory based on a single atom coupled to a high-finesse optical resonator. By mapping and remapping the qubit between a basis used for light-matter interfacing and a basis which is less susceptible to decoherence, a coherence time exceeding 100 ms has been measured with a time-independant storage-and-retrieval efficiency of 22%. This demonstrates the first photonic qubit memory with a coherence time that exceeds the lower bound needed for teleporting qubits in a global quantum internet., Comment: 3 pages, 4 figures

We present a comprehensive characterization of cold molecular beams from a cryogenic buffer-gas cell, providing an insight into the physics of buffer-gas cooling. Cold molecular beams are extracted from a cryogenic cell by electrostatic guiding, which is also used to measure their velocity distribution. Molecules' rotational-state distribution is probed via radio-frequency resonant depletion spectroscopy. With the help of complete trajectory simulations, yielding the guiding efficiency for all of the thermally populated states, we are able to determine both the rotational and the translational temperature of the molecules at the output of the buffer-gas cell. This thermometry method is demonstrated for various regimes of buffer-gas cooling and beam formation as well as for molecular species of different sizes, $\rm{CH_3F}$ and $\rm{CF_3CCH}$. Comparison between the rotational and translational temperatures provides evidence of faster rotational thermalization for the $\rm{CH_3F-He}$ system in the limit of low He density. In addition, the relaxation rates for different rotational states appear to be different.

Producing large samples of slow molecules from thermal-velocity ensembles is a formidable challenge. Here we employ a centrifugal force to produce a continuous molecular beam with a high flux at near-zero velocities. We demonstrate deceleration of three electrically guided molecular species, CH$_3$F, CF$_3$H, and CF$_3$CCH, with input velocities of up to $200\,\rm{m\,s^{-1}}$ to obtain beams with velocities below $15\,\rm{m\,s^{-1}}$ and intensities of several $10^9\,\rm{mm^{-2}\,s^{-1}}$. The centrifuge decelerator is easy to operate and can, in principle, slow down any guidable particle. It has the potential to become a standard technique for continuous deceleration of molecules., Comment: 5 pages, 4 figures; version accepted for publication in PRL

We investigate phase shifts in the strong coupling regime of single-atom cavity quantum electrodynamics (QED). On the light transmitted through the system, we observe a phase shift associated with an antiresonance and show that both its frequency and width depend solely on the atom, despite the strong coupling to the cavity. This shift is optically controllable and reaches 140 degrees - the largest ever reported for a single emitter. Our result offers a new technique for the characterization of complex integrated quantum circuits., Comment: 5 pages, 5 figures

The rich internal structure and long-range dipole-dipole interactions establish polar molecules as unique instruments for quantum-controlled applications and fundamental investigations. Their potential fully unfolds at ultracold temperatures, where a plethora of effects is predicted in many-body physics, quantum information science, ultracold chemistry, and physics beyond the standard model. These objectives have inspired the development of a wide range of methods to produce cold molecular ensembles. However, cooling polyatomic molecules to ultracold temperatures has until now seemed intractable. Here we report on the experimental realization of opto-electrical cooling, a paradigm-changing cooling and accumulation method for polar molecules. Its key attribute is the removal of a large fraction of a molecule's kinetic energy in each step of the cooling cycle via a Sisyphus effect, allowing cooling with only few dissipative decay processes. We demonstrate its potential by reducing the temperature of about 10^6 trapped CH_3F molecules by a factor of 13.5, with the phase-space density increased by a factor of 29 or a factor of 70 discounting trap losses. In contrast to other cooling mechanisms, our scheme proceeds in a trap, cools in all three dimensions, and works for a large variety of polar molecules. With no fundamental temperature limit anticipated down to the photon-recoil temperature in the nanokelvin range, our method eliminates the primary hurdle in producing ultracold polyatomic molecules. The low temperatures, large molecule numbers and long trapping times up to 27 s will allow an interaction-dominated regime to be attained, enabling collision studies and investigation of evaporative cooling toward a BEC of polyatomic molecules.

We present a versatile electric trap for the exploration of a wide range of quantum phenomena in the interaction between polar molecules. The trap combines tunable fields, homogeneous over most of the trap volume, with steep gradient fields at the trap boundary. An initial sample of up to 10^8 CH3F molecules is trapped for as long as 60 seconds, with a 1/e storage time of 12 seconds. Adiabatic cooling down to 120 mK is achieved by slowly expanding the trap volume. The trap combines all ingredients for opto-electrical cooling, which, together with the extraordinarily long storage times, brings field-controlled quantum-mechanical collision and reaction experiments within reach.

Entanglement between stationary systems at remote locations is a key resource for quantum networks. We report on the experimental generation of remote entanglement between a single atom inside an optical cavity and a Bose-Einstein condensate (BEC). To produce this, a single photon is created in the atom-cavity system, thereby generating atom-photon entanglement. The photon is transported to the BEC and converted into a collective excitation in the BEC, thus establishing matter-matter entanglement. After a variable delay, this entanglement is converted into photon-photon entanglement. The matter-matter entanglement lifetime of 100 $\mu$s exceeds the photon duration by two orders of magnitude. The total fidelity of all concatenated operations is 95%. This hybrid system opens up promising perspectives in the field of quantum information.

While the phase of a coherent light field can be precisely known, the phase of the individual photons that create this field, considered individually, cannot. Phase changes within single-photon wave packets, however, have observable effects. In fact, actively controlling the phase of individual photons has been identified as a powerful resource for quantum communication protocols. Here we demonstrate the arbitrary phase control of a single photon. The phase modulation is applied without affecting the photon's amplitude profile and is verified via a two-photon quantum interference measurement, which can result in the fermionic spatial behaviour of photon pairs. Combined with previously demonstrated control of a single photon's amplitude, frequency, and polarisation, the fully deterministic phase shaping presented here allows for the complete control of single-photon wave packets., Comment: 4 pages, 4 figures

We present an opto-electrical cooling scheme for polar molecules based on a Sisyphus-type cooling cycle in suitably tailored electric trapping fields. Dissipation is provided by spontaneous vibrational decay in a closed level scheme found in symmetric-top rotors comprising six low-field-seeking rovibrational states. A generic trap design is presented. Suitable molecules are identified with vibrational decay rates on the order of 100Hz. A simulation of the cooling process shows that the molecular temperature can be reduced from 1K to 1mK in approximately 10s. The molecules remain electrically trapped during this time, indicating that the ultracold regime can be reached in an experimentally feasible scheme.

We use laser light near resonant with an optical bound-to-bound transition to shift the magnetic field at which a Feshbach resonance occurs. We operate in a regime of large detuning and large laser intensity. This reduces the light-induced atom-loss rate by one order of magnitude compared to our previous experiments [D.M. Bauer et al. Nature Phys. 5, 339 (2009)]. The experiments are performed in an optical lattice and include high-resolution spectroscopy of excited molecular states, reported here. In addition, we give a detailed account of a theoretical model that describes our experimental data.

The capability to tune the strength of the elastic interparticle interaction is crucial for many experiments with ultracold gases. Magnetic Feshbach resonances are a tool widely used for this purpose, but future experiments would benefit from additional flexibility such as spatial modulation of the interaction strength on short length scales. Optical Feshbach resonances offer this possibility in principle, but suffer from fast particle loss due to light-induced inelastic collisions. Here we show that light near-resonant with a molecular bound-to-bound transition can be used to shift the magnetic field at which a magnetic Feshbach resonance occurs. This makes it possible to tune the interaction strength with laser light and at the same time induce considerably less loss than an optical Feshbach resonance would do.

An experiment is performed where a single rubidium atom trapped within a high-finesse optical cavity emits two independently triggered entangled photons. The entanglement is mediated by the atom and is characterized both by a Bell inequality violation of S=2.5, as well as full quantum-state tomography, resulting in a fidelity exceeding F=90%. The combination of cavity-QED and trapped atom techniques makes our protocol inherently deterministic - an essential step for the generation of scalable entanglement between the nodes of a distributed quantum network., Comment: 5 pages, 4 figures

Single atoms absorb and emit light from a resonant laser beam photon by photon. We show that a single atom strongly coupled to an optical cavity can absorb and emit resonant photons in pairs. The effect is observed in a photon correlation experiment on the light transmitted through the cavity. We find that the atom-cavity system transforms a random stream of input photons into a correlated stream of output photons, thereby acting as a two-photon gateway. The phenomenon has its origin in the quantum anharmonicity of the energy structure of the atom-cavity system. Future applications could include the controlled interaction of two photons by means of one atom., Comment: PRL, 4 figures

Strongly correlated states in many-body systems are traditionally created using elastic interparticle interactions. Here we show that inelastic interactions between particles can also drive a system into the strongly correlated regime. This is shown by an experimental realization of a specific strongly correlated system, namely a one-dimensional molecular Tonks-Girardeau gas., Comment: To appear in "ATOMIC PHYSICS 21", proceedings of the XXI International Conference on Atomic Physics (ICAP 2008)

We show that strong inelastic interactions between bosons in one dimension create a Tonks-Girardeau gas, much as in the case of elastic interactions. We derive a Markovian master equation that describes the loss caused by the inelastic collisions. This yields a loss rate equation and a dissipative Lieb-Liniger model for short times. We obtain an analytic expression for the pair correlation function in the limit of strong dissipation. Numerical calculations show how a diverging dissipation strength leads to a vanishing of the actual loss rate and renders an additional elastic part of the interaction irrelevant.

We present a theoretical investigation of a lattice Tonks-gas that is created by inelastic, instead of elastic interactions. An analytical calculation shows that in the limit of strong two-body losses, the dynamics of the system is effectively that of a Tonks gas. We also derive an analytic expression for the effective loss rate. We find good agreement between these analytical results and results from a rigorous numerical calculation. The Tonks character of the gas is visible both in a reduced effective loss rate and in the momentum distribution of the gas.

Electrostatic velocity filtering and guiding is an established technique to produce high fluxes of cold polar molecules. In this paper we clarify different aspects of this technique by comparing experiments to detailed calculations. In the experiment, we produce cold guided beams of the three water isotopologs H2O, D2O and HDO. Their different rotational constants and orientations of electric dipole moments lead to remarkably different Stark shift properties, despite the molecules being very similar in a chemical sense. Therefore, the signals of the guided water isotopologs differ on an absolute scale and also exhibit characteristic electrode voltage dependencies. We find excellent agreement between the relative guided fractions and voltage dependencies of the investigated isotopologs and predictions made by our theoretical model of electrostatic velocity filtering., Comment: 14 pages, 13 figures; small changes to the text, updated references

Atomic quantum gases in the strong-correlation regime offer unique possibilities to explore a variety of many-body quantum phenomena. Reaching this regime has usually required both strong elastic and weak inelastic interactions, as the latter produce losses. We show that strong inelastic collisions can actually inhibit particle losses and drive a system into a strongly-correlated regime. Studying the dynamics of ultracold molecules in an optical lattice confined to one dimension, we show that the particle loss rate is reduced by a factor of 10. Adding a lattice along the one dimension increases the reduction to a factor of 2000. Our results open up the possibility to observe exotic quantum many-body phenomena with systems that suffer from strong inelastic collisions.

We report on the fast excitation of a single atom coupled to an optical cavity using laser pulses that are much shorter than all other relevant processes. The cavity frequency constitutes a control parameter that allows the creation of single photons in a superposition of two tunable frequencies. Each photon emitted from the cavity thus exhibits a pronounced amplitude modulation determined by the oscillatory energy exchange between the atom and the cavity. Our technique constitutes a versatile tool for future quantum networking experiments., Comment: 4 pages, 5 figures

We present a method which delivers a continuous, high-density beam of slow and internally cold polar molecules. In our source, warm molecules are first cooled by collisions with a cryogenic helium buffer gas. Cold molecules are then extracted by means of an electrostatic quadrupole guide. For ND$_3$ the source produces fluxes up to $(7 \pm ^{7}_{4}) \times 10^{10}$ molecules/s with peak densities up to $(1.0 \pm ^{1.0}_{0.6}) \times 10^9$ molecules/cm$^3$. For H$_2$CO the population of rovibrational states is monitored by depletion spectroscopy, resulting in single-state populations up to $(82 \pm 10)%$., Comment: 4 pages, 4 figures, changes to the text, updated figures and references

Optical nonlinearities typically require macroscopic media, thereby making their implementation at the quantum level an outstanding challenge. Here we demonstrate a nonlinearity for one atom enclosed by two highly reflecting mirrors. We send laser light through the input mirror and record the light from the output mirror of the cavity. For weak laser intensity, we find the vacuum-Rabi resonances. But for higher intensities, we find an additional resonance. It originates from the fact that the cavity can accommodate only an integer number of photons and that this photon number determines the characteristic frequencies of the coupled atom-cavity system. We selectively excite such a frequency by depositing at once two photons into the system and find a transmission which increases with the laser intensity squared. The nonlinearity differs from classical saturation nonlinearities and is direct spectroscopic proof of the quantum nature of the atom-cavity system. It provides a photon-photon interaction by means of one atom, and constitutes a step towards a two-photon gateway or a single-photon transistor., Comment: 7 figures, Nature Physics

We present measurements of the internal state distribution of electrostatically guided formaldehyde. Upon excitation with continuous tunable ultraviolet laser light the molecules dissociate, leading to a decrease in the molecular flux. The population of individual guided states is measured by addressing transitions originating from them. The measured populations of selected states show good agreement with theoretical calculations for different temperatures of the molecule source. The purity of the guided beam as deduced from the entropy of the guided sample using a source temperature of 150K corresponds to that of a thermal ensemble with a temperature of about 30 K.

Experimental observation of Doppler-free signals for weak transitions can be greatly facilitated by an estimate for their expected amplitudes. We derive an analytical model which allows the Doppler-free amplitude to be estimated for small Doppler-free signals. Application of this model to formaldehyde allows the amplitude of experimentally observed Doppler-free signals to be reproduced to within the experimental error., Comment: 7 pages, 7 figures, 1 table, v2: many small improvements + corrected line assignment

We trap neutral ground-state rubidium atoms in a macroscopic trap based on purely electric fields. For this, three electrostatic field configurations are alternated in a periodic manner. The rubidium is precooled in a magneto-optical trap, transferred into a magnetic trap and then translated into the electric trap. The electric trap consists of six rod-shaped electrodes in cubic arrangement, giving ample optical access. Up to 10^5 atoms have been trapped with an initial temperature of around 20 microkelvin in the three-phase electric trap. The observations are in good agreement with detailed numerical simulations., Comment: 4 pages, 4 figures

We observe large-amplitude Rabi oscillations between an atomic and a molecular state near a Feshbach resonance. The experiment uses 87Rb in an optical lattice and a Feshbach resonance near 414 G. The frequency and amplitude of the oscillations depend on magnetic field in a way that is well described by a two-level model. The observed density dependence of the oscillation frequency agrees with the theoretical expectation. We confirmed that the state produced after a half-cycle contains exactly one molecule at each lattice site. In addition, we show that for energies in a gap of the lattice band structure, the molecules cannot dissociate.

A single atom strongly coupled to a cavity mode is stored by three-dimensional confinement in blue-detuned cavity modes of different longitudinal and transverse order. The vanishing light intensity at the trap center reduces the light shift of all atomic energy levels. This is exploited to detect a single atom by means of a dispersive measurement with 95% confidence in 0.010 ms, limited by the photon-detection efficiency. As the atom switches resonant cavity transmission into cavity reflection, the atom can be detected while scattering about one photon.

Between mirrors, the density of electromagnetic modes differs from the one in free space. This changes the radiation properties of an atom as well as the light forces acting on an atom. It has profound consequences in the strong-coupling regime of cavity quantum electrodynamics. For a single atom trapped inside the cavity, we investigate the atom-cavity system by scanning the frequency of a probe laser for various atom-cavity detunings. The avoided crossing between atom and cavity resonance is visible in the transmission of the cavity. It is also visible in the loss rate of the atom from the intracavity dipole trap. On the normal-mode resonances, the dominant contribution to the loss rate originates from dipole-force fluctuations which are dramatically enhanced in the cavity. This conclusion is supported by Monte-Carlo simulations., Comment: 7 pages, 3 figures

We prepare a quantum state where each site of an optical lattice is occupied by exactly one molecule. This is the same quantum state as in a Mott insulator of molecules in the limit of negligible tunneling. Unlike previous Mott insulators, our system consists of molecules which can collide inelastically. In the absence of the optical lattice these collisions would lead to fast loss of the molecules from the sample. To prepare the state, we start from a Mott insulator of atomic 87Rb with a central region, where each lattice site is occupied by exactly two atoms. We then associate molecules using a Feshbach resonance. Remaining atoms can be removed using blast light. Our method does not rely on the molecule-molecule interaction properties and is therefore applicable to many systems., Comment: Proceedings of the 20th International Conference on Atomic Physics (ICAP 2006), edited by C. Roos, H. Haffner, and R. Blatt, AIP Conference Proceedings, Melville, 2006, Vol. 869, pp. 278-283

We present measurements of the loss-rate coefficients K_am and K_mm caused by inelastic atom-molecule and molecule-molecule collisions. A thermal cloud of atomic 87Rb is prepared in an optical dipole trap. A magnetic field is ramped across the Feshbach resonance at 1007.4 G. This associates atom pairs to molecules. A measurement of the molecule loss at 1005.8 G yields K_am=2 10^-10 cm^3/s. Additionally, the atoms can be removed with blast light. In this case, the measured molecule loss yields K_mm=3 10^-10 cm^3/s.

Vacuum-stimulated Raman transitions are driven between two magnetic substates of a rubidium-87 atom strongly coupled to an optical cavity. A magnetic field lifts the degeneracy of these states, and the atom is alternately exposed to laser pulses of two different frequencies. This produces a stream of single photons with alternating circular polarization in a predetermined spatio-temporal mode. MHz repetition rates are possible as no recycling of the atom between photon generations is required. Photon indistinguishability is tested by time-resolved two-photon interference., Comment: 4 pages, 3 figures

Ultracold gases in optical lattices are of great interest, because these systems bear a great potential for applications in quantum simulations and quantum information processing, in particular when using particles with a long-range dipole-dipole interaction, such as polar molecules. Here we show the preparation of a quantum state with exactly one molecule at each site of an optical lattice. The molecules are produced from an atomic Mott insulator with a density profile chosen such that the central region of the gas contains two atoms per lattice site. A Feshbach resonance is used to associate the atom pairs to molecules. Remaining atoms can be removed with blast light. The technique does not rely on the molecule-molecule interaction properties and is therefore applicable to many systems.

We predict the resonance enhanced magnetic field dependence of atom-dimer relaxation and three-body recombination rates in a $^{87}$Rb Bose-Einstein condensate (BEC) close to 1007 G. Our exact treatments of three-particle scattering explicitly include the dependence of the interactions on the atomic Zeeman levels. The Feshbach resonance distorts the entire diatomic energy spectrum causing interferences in both loss phenomena. Our two independent experiments confirm the predicted recombination loss over a range of rate constants that spans four orders of magnitude., Comment: 4 pages, 3 eps figures (updated references)

Single-photons of well-defined polarisation that are deterministically generated in a single spatio-temporal field mode are the key to the creation of multi-partite entangled states in photonic networks. Here, we present a novel scheme to produce such photons from a single atom in an optical cavity, by means of vacuum-stimulated Raman transitions between the Zeeman substates of a single hyperfine state. Upon each transition, a photon is emitted into the cavity, with a polarisation that depends on the direction of the Raman process., Comment: 7 pages, 4 figures

We report the creation of a confined slow beam of heavy-water (D2O) molecules with a translational temperature around 1 kelvin. This is achieved by filtering slow D2O from a thermal ensemble with inhomogeneous static electric fields exploiting the quadratic Stark shift of D2O. All previous demonstrations of electric field manipulation of cold dipolar molecules rely on a predominantly linear Stark shift. Further, on the basis of elementary molecular properties and our filtering technique we argue that our D2O beam contains molecules in only a few ro-vibrational states., Comment: 4 pages, 4 figures, 1 table

Adiabatic passage techniques allow the generation of single photons which are very long compared to the typical detector time resolution. Therefore the detection time of a photon can be measured within the duration of the single-photon wavepacket. As a consequence, two-photon interference can be investigated in a time-resolved manner, i.e., the coincidence rate can be measured as a function of the time between photodetections. The theoretical analysis shows that this method not only gives information about the duration of single photons, but also about their coherence time. Here we discuss how to use this method for a spectral or temporal characterization of a single-photon source., Comment: 17 pages, 12 figures

It is shown that the momentum diffusion of free-space laser cooling has a natural correspondence in optical cavities when the internal state of the atom is treated as a harmonic oscillator. We derive a general expression for the momentum diffusion which is valid for most configurations of interest: The atom or the cavity or both can be probed by lasers, with or without the presence of traps inducing local atomic frequency shifts. It is shown that, albeit the (possibly strong) coupling between atom and cavity, it is sufficient for deriving the momentum diffusion to consider that the atom couples to a mean cavity field, which gives a first contribution, and that the cavity mode couples to a mean atomic dipole, giving a second contribution. Both contributions have an intuitive form and present a clear symmetry. The total diffusion is the sum of these two contributions plus the diffusion originating from the fluctuations of the forces due to the coupling to the vacuum modes other than the cavity mode (the so called spontaneous emission term). Examples are given that help to evaluate the heating rates induced by an optical cavity for experiments operating at low atomic saturation. We also point out intriguing situations where the atom is heated although it cannot scatter light., Comment: More information added

A continuously operated electrostatic trap for polar molecules is demonstrated. The trap has a volume of ~0.6 cm^3 and holds molecules with a positive Stark shift. With deuterated ammonia from a quadrupole velocity filter, a trap density of ~10^8/cm^3 is achieved with an average lifetime of 130 ms and a motional temperature of ~300 mK. The trap offers good starting conditions for high-precision measurements, and can be used as a first stage in cooling schemes for molecules and as a "reaction vessel" in cold chemistry., Comment: 4 pages, 3 figures v2: several small improvements, new intro

The energy-level structure of a single atom strongly coupled to the mode of a high-finesse optical cavity is investigated. The atom is stored in an intracavity dipole trap and cavity cooling is used to compensate for inevitable heating. Two well-resolved normal modes are observed both in the cavity transmission and the trap lifetime. The experiment is in good agreement with a Monte Carlo simulation, demonstrating our ability to localize the atom to within $\lambda/10$ at a cavity antinode., Comment: 4 pages, 4 figures

The photon statistics of the light emitted from an atomic ensemble into a single field mode of an optical cavity is investigated as a function of the number of atoms. The light is produced in a Raman transition driven by a pump laser and the cavity vacuum [M.Hennrich et al., Phys. Rev. Lett. 85, 4672 (2000)], and a recycling laser is employed to repeat this process continuously. For weak driving, a smooth transition from antibunching to bunching is found for about one intra-cavity atom. Remarkably, the bunching peak develops within the antibunching dip. For saturated driving and a growing number of atoms, the bunching amplitude decreases and the bunching duration increases, indicating the onset of Raman lasing., Comment: 4 pages, 4 figures

We investigate the photon statistics of a single-photon source that operates under non-stationary conditions. The photons are emitted by shining a periodic sequence of laser pulses on single atoms falling randomly through a high-finesse optical cavity. Strong antibunching is found in the intensity correlation of the emitted light, demonstrating that a single atom emits photons one-by-one. However, the number of atoms interacting with the cavity follows a Poissonian statistics so that, on average, no sub-Poissonian photon statistics is obtained, unless the measurement is conditioned on the presence of single atoms., Comment: 9 pages, 5 figures

All conventional methods to laser-cool atoms rely on repeated cycles of optical pumping and spontaneous emission of a photon by the atom. Spontaneous emission in a random direction is the dissipative mechanism required to remove entropy from the atom. However, alternative cooling methods have been proposed for a single atom strongly coupled to a high-finesse cavity; the role of spontaneous emission is replaced by the escape of a photon from the cavity. Application of such cooling schemes would improve the performance of atom cavity systems for quantum information processing. Furthermore, as cavity cooling does not rely on spontaneous emission, it can be applied to systems that cannot be laser-cooled by conventional methods; these include molecules (which do not have a closed transition) and collective excitations of Bose condensates, which are destroyed by randomly directed recoil kicks. Here we demonstrate cavity cooling of single rubidium atoms stored in an intracavity dipole trap. The cooling mechanism results in extended storage times and improved localization of atoms. We estimate that the observed cooling rate is at least five times larger than that produced by free-space cooling methods, for comparable excitation of the atom.

Transits of single atoms through higher-order Hermite-Gaussian transverse modes of a high-finesse optical cavity are observed. Compared to the fundamental Gaussian mode, the use of higher-order modes increases the information on the atomic position. The experiment is a first experimental step towards the realisation of an atomic kaleidoscope., Comment: 6 pages, d figures

Simultaneous two-dimensional trapping of neutral dipolar molecules in low- and high-field seeking states is analyzed. A trapping potential of the order of 20 mK can be produced for molecules like ND3 with time-dependent electric fields. The analysis is in agreement with an experiment where slow molecules with longitudinal velocities of the order of 20 m/s are guided between four 50 cm long rods driven by an alternating electric potential at a frequency of a few kHz., Comment: 4 pages, 4 figures; some paragraphs rewritten and minor improvements throughout the paper