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arXiv:2405.09427 · Physical Review Research

Laser cooling of barium monofluoride molecules using synthesized optical spectra

Marian Rockenhäuser, Felix Kogel, Tatsam Garg, Sebastián A. Morales-Ramírez, Tim Langen

Published Nov 18, 2024• 13 citations
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Abstract

We demonstrate laser cooling of barium monofluoride ( BaF 138 ) molecules. We use serrodynes to synthesize time-sequenced optical spectra that can be precisely tailored to the hyperfine structure of this heaviest nonradioactive alkaline earth monofluoride. By optimizing these optical spectra, we realize strong Sisyphus cooling forces that efficiently collimate a molecular beam. Our technique is an important step toward using intense beams of barium monofluoride for precision measurement applications, and will be useful for cooling other molecular species with complex level structure. Published by the American Physical Society 2024

DOI
10.1103/physrevresearch.6.043161

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We demonstrate laser cooling of barium monofluoride ( BaF 138 ) molecules. We use serrodynes to synthesize time-sequenced optical spectra that can be precisely tailored to the hyperfine structure of this heaviest nonradioactive alkaline earth monofluoride. By optimizing these optical spectra, we realize strong Sisyphus cooling forces that efficiently collimate a molecular beam. Our technique is an important step toward using intense beams of barium monofluoride for precision measurement applications, and will be useful for cooling other molecular species with complex level structure. Published by the American Physical Society 2024
Abstract An important effort is currently underway to extend optical cycling and laser cooling to more molecular species. Significant challenges arise in particular when multiple nuclear spins give rise to complex, resolved hyperfine spectra, as is the case for several molecular species relevant to precision tests of fundamental symmetries. We provide a detailed introduction to the use of optical spectra generated via serrodyne waveforms to address this complexity. We discuss our experimental implementation of these serrodynes, characterize their properties, and outline procedures to find optimized sideband configurations that generate strong laser cooling forces. We demonstrate the application of these techniques to barium monofluoride molecules and explore their prospects for the cooling of other species relevant to the study of fundamental physics.
Currently, there is great interest in laser cooling of barium monofluoride (BaF) molecules for precision tests of fundamental symmetries. We use high-resolution absorption spectroscopy to characterize several as yet imprecisely known transition frequencies required to realize such cooling. We extract an improved set of molecular constants for the bosonic 138Ba19F^{138}\mathrm{Ba}^{19}\mathrm{F}138Ba19F and 136Ba19F^{136}\mathrm{Ba}^{19}\mathrm{F}136Ba19F isotopologues, confirm the existence of a significant hyperfine splitting in the excited state of the laser cooling cycle, and investigate the effects of this splitting on the achievable cooling forces. As a direct application of our spectroscopic insights, we experimentally demonstrate nearly background-free fluorescence imaging of a BaF molecular beam in a glass cell vacuum chamber. We expect such high-fidelity detection to be useful for various types of precision measurement scenarios.
We theoretically investigate the laser cooling of fermionic barium monofluoride (137BaF) molecules, which are promising candidates for precision studies of weak parity violation and nuclear anapole moments. This molecular species features two nuclear spins, resulting in a hyperfine structure that is considerably more complicated than the one found in the usual laser-cooled diatomics. We use optical Bloch equations and rate equations to show that optical cycling, sub-Doppler cooling and bichromatic forces can all be realized under realistically achievable experimental conditions.
Abstract Direct laser cooling of molecules has made significant progress in recent years. However, the selective cooling and manipulation of generic molecular samples based on their isotopic composition, which is ubiquitous in atomic laser cooling, has not yet been achieved. Here, we demonstrate such isotopologue-selective laser cooling and near-arbitrary control over the isotopic composition of a molecular beam, using barium monofluoride (BaF) as an example. The manipulation of the rare and previously uncooled 136 BaF is achieved in the presence of several isotopologues of significantly higher natural abundance. Our results enable intense molecular beams, high fidelity detection and manipulation of select low-abundance isotopologues or isotopic mixtures. Such beams are a first step towards isotopologue-selective molecular trapping and will be useful for applications in trace gas analysis, cold collisions and precision tests of fundamental symmetries.
Abstract We theoretically investigate the laser cooling of fermionic barium monofluoride (137BaF) molecules, which are promising candidates for precision studies of weak parity violation and nuclear anapole moments. This molecular species features two nuclear spins, resulting in a hyperfine structure that is considerably more complicated than the one found in the usual laser-cooled diatomics. We use optical Bloch equations and rate equations to show that optical cycling, sub-Doppler cooling and bichromatic forces can all be realized under realistically achievable experimental conditions.
We demonstrate buffer-gas cooling, high-resolution spectroscopy, and cycling fluorescence of cold barium monofluoride (BaF) molecules. Our source produces an intense and internally cold molecular beam containing the different BaF isotopologues with a mean forward velocity of 190m/s190\phantom{\rule{0.16em}{0ex}}\mathrm{m}/\mathrm{s}190m/s. For a well-collimated beam of 138Ba19F^{138}\mathrm{Ba}\phantom{\rule{0.16em}{0ex}}^{19}\mathrm{F}138Ba19F we observe a flux of >1010>{10}^{10}>1010 molecules ${\mathrm{sr}}^{\ensuremath{-}1}\phantom{\rule{0.16em}{0ex}}{\mathrm{pulse}}^{\ensuremath{-}1}$ in the $X{\phantom{\rule{0.16em}{0ex}}}^{2}\mathrm{\ensuremath{\Sigma}}$, N=1N=1N=1 state in our downstream detection region. Studying the absorption line strength of the intermediate ${A}^{\ensuremath{'}}\mathrm{\ensuremath{\Delta}}$ state we infer a lifetime of ${\ensuremath{\tau}}_{\mathrm{\ensuremath{\Delta}}}=790\ifmmode\pm\else\textpm\fi{}346\phantom{\rule{0.16em}{0ex}}\mathrm{ns}$, significantly longer than previously estimated. Finally, highly diagonal Franck-Condon factors and magnetic remixing of dark states allow us to realize a quasicycling transition in 138Ba19F^{138}\mathrm{Ba}\phantom{\rule{0.16em}{0ex}}^{19}\mathrm{F}138Ba19F that is suitable for future laser cooling of this heavy diatomic molecule.