Positronium Laser Cooling via the 1

We report on laser cooling of a large fraction of positronium (Ps) in free flight by strongly saturating the 1^{3}S-2^{3}P transition with a broadband, long-pulsed 243 nm alexandrite laser. The ground state Ps cloud is produced in a magnetic and electric field-free environment. We observe two different laser-induced effects. The first effect is an increase in the number of atoms in the ground state after the time Ps has spent in the long-lived 2^{3}P states. The second effect is one-dimensional Doppler cooling of Ps, reducing the cloud's temperature from 380(20) to 170(20) K. We demonstrate a 58(9)% increase in the fraction of Ps atoms with v_{1D}<3.7×10^{4} ms^{-1}.

Experimental perspectives on the matter-antimatter asymmetry puzzle: developments in electron EDM and [Formula: see text] experiments.

In the search for clues to the matter-antimatter puzzle, experiments with atoms or molecules play a particular role. These systems allow measurements with very high precision, as demonstrated by the unprecedented limits down to [Formula: see text] e cm on electron EDM using molecular ions, and relative measurements at the level of [Formula: see text] in spectroscopy of antihydrogen atoms. Building on these impressive measurements, new experimental directions offer potential for drastic improvements. We review here some of the new perspectives in those fields and their associated prospects for new physics searches. This article is part of the theme issue 'The particle-gravity frontier'.

Determining a vibrational distribution with a broadband optical source.

This work presents an experimental protocol conceived to determine the vibrational distribution of barium monofluoride molecules seeded in a supersonic beam of argon. Here, as in many cases, the detection signal is related to the number of molecules by an efficiency involving several parameters that may be difficult to determine properly. In particular, this efficiency depends on the vibrational level of the detected molecules. Our approach avoids these complications by comparing different detection signals generated by different vibrational excitations. Such an excitation is made possible by the use of a broadband optical source that depletes a specific vibrational level whose population is redistributed in the other levels.

Watt-level narrow-linewidth fibered laser source at 852 nm for FIB application.

We realize a 1 W all-fibered polarized compact and robust laser source at 852 nm for laser cooling of cesium atoms. The architecture is based on the sum-frequency generation of 1540 and 1908 nm lasers, realized through a periodically poled lithium niobate waveguide with a conversion efficiency of 40%. A linewidth of 20 kHz is achieved with the development of a distributed feedback fiber laser at 1908 nm. The operation of this laser source is demonstrated on a focused ion beam (FIB) experiment based on cold cesium atoms.

AEgIS at ELENA: outlook for physics with a pulsed cold antihydrogen beam.

The efficient production of cold antihydrogen atoms in particle traps at CERN's Antiproton Decelerator has opened up the possibility of performing direct measurements of the Earth's gravitational acceleration on purely antimatter bodies. The goal of the AEgIS collaboration is to measure the value of g for antimatter using a pulsed source of cold antihydrogen and a Moiré deflectometer/Talbot-Lau interferometer. The same antihydrogen beam is also very well suited to measuring precisely the ground-state hyperfine splitting of the anti-atom. The antihydrogen formation mechanism chosen by AEgIS is resonant charge exchange between cold antiprotons and Rydberg positronium. A series of technical developments regarding positrons and positronium (Ps formation in a dedicated room-temperature target, spectroscopy of the n=1-3 and n=3-15 transitions in Ps, Ps formation in a target at 10 K inside the 1 T magnetic field of the experiment) as well as antiprotons (high-efficiency trapping of [Formula: see text], radial compression to sub-millimetre radii of mixed [Formula: see text] plasmas in 1 T field, high-efficiency transfer of [Formula: see text] to the antihydrogen production trap using an in-flight launch and recapture procedure) were successfully implemented. Two further critical steps that are germane mainly to charge exchange formation of antihydrogen-cooling of antiprotons and formation of a beam of antihydrogen-are being addressed in parallel. The coming of ELENA will allow, in the very near future, the number of trappable antiprotons to be increased by more than a factor of 50. For the antihydrogen production scheme chosen by AEgIS, this will be reflected in a corresponding increase of produced antihydrogen atoms, leading to a significant reduction of measurement times and providing a path towards high-precision measurements.This article is part of the Theo Murphy meeting issue 'Antiproton physics in the ELENA era'.

Ion microscopy based on laser-cooled cesium atoms.

We demonstrate a prototype of a Focused Ion Beam machine based on the ionization of a laser-cooled cesium beam and adapted for imaging and modifying different surfaces in the few-tens nanometer range. Efficient atomic ionization is obtained by laser promoting ground-state atoms into a target excited Rydberg state, then field-ionizing them in an electric field gradient. The method allows obtaining ion currents up to 130pA. Comparison with the standard direct photo-ionization of the atomic beam shows, in our conditions, a 40-times larger ion yield. Preliminary imaging results at ion energies in the 1-5keV range are obtained with a resolution around 40nm, in the present version of the prototype. Our ion beam is expected to be extremely monochromatic, with an energy spread of the order of the eV, offering great prospects for lithography, imaging and surface analysis.

A moiré deflectometer for antimatter.

The precise measurement of forces is one way to obtain deep insight into the fundamental interactions present in nature. In the context of neutral antimatter, the gravitational interaction is of high interest, potentially revealing new forces that violate the weak equivalence principle. Here we report on a successful extension of a tool from atom optics--the moiré deflectometer--for a measurement of the acceleration of slow antiprotons. The setup consists of two identical transmission gratings and a spatially resolving emulsion detector for antiproton annihilations. Absolute referencing of the observed antimatter pattern with a photon pattern experiencing no deflection allows the direct inference of forces present. The concept is also straightforwardly applicable to antihydrogen measurements as pursued by the AEgIS collaboration. The combination of these very different techniques from high energy and atomic physics opens a very promising route to the direct detection of the gravitational acceleration of neutral antimatter.

Efficient broadband composite optical isolator.

A new design of a broadband optical isolator, composed as a sequence of ordinary Faraday rotators and achromatic quarter-wave plates (QWPs), is presented. In particular, we demonstrate that by using four Faraday rotators and six achromatic QWPs, rotated at specific angles, optical isolation better than 15 dB over the range from 700 to 1000 nm can be achieved. The measured transmittance (corrected for absorption and reflection) in the forward direction over the same wavelength range shows broadening of the transmission spectrum compared with the one of a single Faraday rotator.

Rovibrational cooling of molecules by optical pumping.

We demonstrate rotational and vibrational cooling of cesium dimers by optical pumping techniques. We use two laser sources exciting all the populated rovibrational states, except a target state that thus behaves like a dark state where molecules pile up thanks to absorption-spontaneous emission cycles. We are able to accumulate photoassociated cold Cs(2) molecules in their absolute ground state (v = 0, J = 0) with up to 40% efficiency. Given its simplicity, the method could be extended to other molecules and molecular beams. It also opens up general perspectives in laser cooling the external degrees of freedom of molecules.

Observation of a resonant four-body interaction in cold cesium Rydberg atoms.

Cold Rydberg atoms subject to long-range dipole-dipole interactions represent a particularly interesting system for exploring few-body interactions and probing the transition from 2-body physics to the many-body regime. In this work we report the direct observation of a resonant 4-body Rydberg interaction. We exploit the occurrence of an accidental quasicoincidence of a 2-body and a 4-body resonant Stark-tuned Förster process in cesium to observe a resonant energy transfer requiring the simultaneous interaction of at least four neighboring atoms. These results are relevant for the implementation of quantum gates with Rydberg atoms and for further studies of many-body physics.

Deeply bound cold caesium molecules formed after 0(-)(g) resonant coupling.

Translationally cold caesium molecules are created by photoassociation below the 6s + 6p(1/2) excited state and selectively detected by resonance enhanced two photon ionization (RE2PI). A series of excited vibrational levels belonging to the 0(-)(g) symmetry is identified. The regular progression of the vibrational spacings and of the rotational constants of the 0(-)(g) (6s + 6p(1/2)) levels is strongly altered in two energy domains. These deviations are interpreted in terms of resonant coupling with deeply bound energy levels of two upper 0(-)(g) states dissociating into the 6s + 6p(3/2) and 6s + 5d(3/2) asymptotes. A theoretical model is proposed to explain the coupling and a quantum defect analysis of the perturbed level position is performed. Moreover, the resonant coupling changes dramatically the spontaneous decay products of the photoexcited molecules, strongly enhancing the decay into deeply bound levels of the a(3)Σ(+)(u) triplet state and of the X(1)Σ(+)(g) ground state. These results may be relevant when conceiving population transferring schemes in cold molecule systems.

Atom-molecule collisions in an optically trapped gas.

Cold inelastic collisions between confined cesium (Cs) atoms and Cs2 molecules are investigated inside a CO2 laser dipole trap. Inelastic atom-molecule collisions can be observed and measured with a rate coefficient of approximately 2.6 x 10(-11) cm3 s(-1), mainly independent of the molecular rovibrational state populated. Lifetimes of purely atomic and molecular samples are essentially limited by rest gas collisions. The pure molecular trap lifetime ranges 0.3-1 s, 4 times smaller than the atomic one, as is also observed in a pure magnetic trap. We give an estimation of the inelastic molecule-molecule collision rate to be approximately 10(-11) cm3 s(-1).

Photoassociative spectroscopy as a self-sufficient tool for the determination of the Cs triplet scattering length

In photoassociation spectroscopy, the line intensities of a given vibrational progression exhibit zero-signal modulation reflecting the node structure of the s-wave ground state wave function of two free colliding atoms. This leads to the determination of the scattering length. We performed photoassociation of cold Cs atoms polarized in the Zeeman sublevel f = 4, m(f) = 4. We analyzed the intensities of the lines associated with the Cs2 0(-)(g) state dissociating to the 6s(1/2)+6p(3/2) asymptote. This yields a value of the Cs triplet state scattering length, a(T) = -530a(0), while consistency requirements impose a value of the multipole ground state molecular coefficient, C6 = 6510 a.u.

Photoassociative Spectroscopy and Formation of Cold Molecules in Cold Cesium Vapor: Trap-Loss Spectrum versus Ion Spectrum.

We report on the experimental spectra of all the optically accessible long-range attractive molecular states of the Cs2 dimer below the 6s2S1/2 + 6p2P3/2 dissociation limit by molecular photoassociation of cold Cs atoms. The spectra are obtained by the usual trap-loss method as well as by pulsed-laser photoionization of Cs2 molecules into Cs+2 ions. The two spectra present markedly different features. While the 1g, 0(+)u, and 0(-)g vibrational progressions are present in the trap-loss spectrum, the Cs+2 ion spectrum presents only the 0(-)g and 1u vibrational progressions. Those states (0(-)g and 1u) lead to the formation of the translationally cold Cs2 ground state molecules at temperatures in the 100 µK range, to our knowledge the lowest molecular temperature reported up until now. The C3 asymptotic coefficients for the 0(+)u and 1g states are determined through a fit of the experimental energy levels. Copyright 1999 Academic Press.