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Vincent Barbé

Publications and source records attributed to Vincent Barbé.

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An Al$^+$ clock with $1.6\times10^{-18}$ systematic uncertainty and its frequency ratios

Advances in optical clocks motivate a redefinition of the second, requiring rigorous evaluations of systematic uncertainties and robust consistency among the clocks. Here, we report the full evaluation of the systematic frequency shifts of an $^{27}\mathrm{Al}^+$ single-ion clock, and the measurement of its absolute frequency and frequency ratio with a $^{87}$Sr optical lattice clock at PTB. The evaluated total systematic fractional frequency uncertainty is $1.6\times10^{-18}$, mainly limited by the accuracy of the relevant atomic coefficients and by background gas collisions. The absolute frequency of the clock has been measured to be $ν_{\mathrm{Al}^+}=1 121 015 393 207 859.19(24)\,$Hz, obtained by comparison with two primary caesium fountain clocks at PTB. The frequency ratio between the Al and Sr optical clocks has been determined to be $ν_{\mathrm{Al}^+}/ν_{^{87}\mathrm{Sr}}=2.611 701 431 781 462 668(36)$, limited by the accuracy of the Sr clock. This ratio differs by $8.6σ$ and $1.2σ$ from the 2021 and 2025 frequency ratio published by the BACON collaboration, respectively. These results represent an important contribution toward a future redefinition of the second using optical clocks, and underscore the importance of independent measurements of clock-candidate frequency ratios across different institutions.

physics.atom-ph

Laser Excitation of the 1S-2S Transition in Singly-Ionized Helium

Precision laser spectroscopy in the extreme ultraviolet of the 1S-2S two-photon transition in singly-ionized helium is a promising route for tests of fundamental physics. We demonstrate laser excitation of this transition in an atomic beam of $^3$He, based on an amplified frequency comb pulse at 790 nm combined with its 25$^{\text{th}}$ harmonic at 32 nm. A clear resonance is observed with a maximum excitation probability of close to 10$^{-4}$ per pulse, and the results are well described by our simulations. This paves the way for high-precision Ramsey-comb spectroscopy of a single helium ion in a Paul trap.

physics.atom-ph

Active stabilization of kilogauss magnetic fields to the ppm level for magnetoassociation on ultranarrow Feshbach resonances

Feshbach association of ultracold molecules using narrow resonances requires exquisite control of the applied magnetic field. Here we present a magnetic field control system to deliver magnetic fields of over 1000 G with ppm-level precision integrated into an ultracold-atom experimental setup. We combine a battery-powered current-stabilized power supply with active feedback stabilization of the magnetic field using fluxgate magnetic field sensors. As a real-world test we perform microwave spectroscopy of ultracold Rb atoms and demonstrate an upper limit on our magnetic field stability of 2.4(3) mG at 1050 G [2.3(3) ppm relative] as determined from the spectral feature.

physics.atom-ph

The RbSr $^2Σ^+$ ground state investigated via spectroscopy of hot & ultracold molecules

We report on spectroscopic studies of hot and ultracold RbSr molecules, and combine the results in an analysis that allows us to fit a potential energy curve (PEC) for the X(1)$^2Σ^+$ ground state bridging the short-to-long-range domains. The ultracold RbSr molecules are created in a $μ$K sample of Rb and Sr atoms and probed by two-colour photoassociation spectroscopy. The data yield the long-range dispersion coefficients $C_6$ and $C_8$, along with the total number of supported bound levels. The hot RbSr molecules are created in a $1000 \,$K gas mixture of Rb and Sr in a heat-pipe oven and probed by thermoluminescence and laser-induced fluorescence spectroscopy. We compare the hot molecule data with spectra we simulated using previously published PECs determined by three different ab-initio theoretical methods. We identify several band heads corresponding to radiative decay from the B(2)$^2Σ^+$ state to the deepest bound levels of X(1)$^2Σ^+$. We determine a mass-scaled high-precision model for X(1)$^2Σ^+$ by fitting all data using a single fit procedure. The corresponding PEC is consistent with all data, thus spanning short-to-long internuclear distances and bridging an energy gap of about 75% of the potential well depth, still uncharted by any experiment. We benchmark ab-initio PECs against our results, and give the PEC fit parameters for both X(1)$^2Σ^+$ and B(2)$^2Σ^+$ states. As first outcomes of our analysis, we calculate the $s$-wave scattering properties for all stable isotopic combinations and corroborate the locations of Fano-Feshbach resonances between alkali Rb and closed-shell Sr atoms recently observed [Barbé et al., Nat. Phys., 2018, DOI:10.1038/s41567-018-0169-x]. These results should greatly contribute to the generation of ultracold alkali$-$alkaline-earth dimers, whose applications range from quantum simulation to quantum chemistry.

physics.atom-ph

Observation of Feshbach resonances between alkali and closed-shell atoms

Magnetic Feshbach resonances are an invaluable tool for controlling ultracold atoms and molecules. They can be used to tune atomic interactions and have been used extensively to explore few- and many-body phenomena. They can also be used for magnetoassociation, in which pairs of atoms are converted into molecules by ramping an applied magnetic field across a resonance. Pairs of open-shell atoms, such as the alkalis, chromium, and some lanthanides, exhibit broad resonances because the corresponding molecule has multiple electronic states. However, molecules formed between alkali and closed-shell atoms have only one electronic state and no broad resonances. Narrow resonances have been predicted in such systems, but until now have eluded observation. Here we present the first observation of magnetic Feshbach resonances in a system containing a closed-shell atom, Sr, interacting with an alkali atom, Rb. These resonances pave the way to creating an ultracold gas of strongly polar, open-shell molecules, which will open up new possibilities for designing quantum many-body systems and for tests of fundamental symmetries.

physics.atom-ph