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arXiv:1408.0410 · Journal of Physics B Atomic Molecular and Optical Physics

Slow ground state molecules from matrix isolation sublimation

A N Oliveira, R L Sacramento, B X Alves, B A Silva, W. Wolff, Claudio Lenz Cesar

Published Dec 3, 2014• 6 citations
arXivHTMLPDF

Abstract

We describe the generation and properties of a cryogenic beam of $^7$Li$_2$ dimers from sublimation of a neon matrix where lithium atoms have been implanted via laser ablation of solid precursors of metallic lithium or lithium hydride (LiH). Different sublimation regimes lead to pulsed molecular beams with different temperatures, densities and forward velocities. With laser absorption spectroscopy these parameters were measured using the molecular $^7$Li$_2$ (R) transitions A$^1Σ_u^+(v'=4,J'=J''+1)\leftarrow $X$^1Σ_g^+ (v''=0,J''=0,1,3)$. In a typical regime, sublimating a matrix at 16 K, translational temperatures of 6--8 K with a drift velocity of 130 m$\,$s$^{-1}$ in a free expanding pulsed beam with molecular density of 10$^9$ cm$^{-3}$, averaged along the laser axis, were observed. Rotational temperatures around 5--7 K were obtained. In recent experiments we were able to monitor the atomic Li signal -- in the D2 line -- concomitantly with the molecular signal in order to compare them as a function of the number of ablation pulses. Based on the data and a simple model, we discuss the possibility that a fraction of these molecules are being formed in the matrix, by mating atoms from different ablation pulses, which would open up the way to formation of other more interesting and difficult molecules to be studied at low temperatures. Such a source of cryogenic molecules have possible applications encompassing fundamental physics tests, quantum information studies, cold collisions, chemistry, and trapping.

DOI
10.1088/0953-4075/47/24/245302

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We describe the production of cold, slow-moving LiH molecules. The molecules are produced in the ground state using laser ablation and supersonic expansion, and 68% of the population is transferred to the rotationally excited state using narrowband radiation at the rotational frequency of 444 GHz. The molecules are then decelerated from 420 to 53 m s −1 using a 100 stage Stark decelerator. We demonstrate and compare two different deceleration modes, one where every stage is used for deceleration, and another where every third stage decelerates and the intervening stages are used to focus the molecules more effectively. We compare our experimental data to the results of simulations and find good agreement. These simulations include the velocity dependence of the detection efficiency and the probability of transitions between the weak-field seeking and strong-field seeking quantum states. Together, the experimental and simulated data provide information about the spatial extent of the source of molecules. We consider the prospects for future trapping and sympathetic cooling experiments.
Cold molecules are an invaluable tool for modern physics. Cold atoms have already revolutionized precision metrology, allowed for spectacular findings in quantum physics and opened the door for the creation and observation of novel states of matter. Cold molecules bring with them additional degrees of freedom which give rise to unique properties that enable new kinds of experiments. For these experiments it is of vital importance to start with a sufficiently large number of cold molecules. There are multiple paths for the slowing and cooling of atoms and most of the slowing techniques utilizing lasers for direct cooling have been transferred to the molecular case with its specific requirements. The Zeeman slowing technique is advantageous for loading a trap with cold particles but had not yet been transferred from atoms to the molecular case. In this thesis I will show the first realization of the Zeeman slowing technique for diatomic molecules. This thesis will discuss several preparatory steps: Our group has had some ideas to collimate the molecular beam with a conical nozzle outlet at the buffer gas cell which I investigated on potassium atoms generated by the ablation of 39K35Cl inside the buffer gas cell. I also realized a fluorescence spectroscopy of the |XΣ1/2, N = 1, v = 0⟩ → |AΠ1/2, N = 0, v = 0⟩ transition in magnetic fields up to 300 G and confirmed simulations regarding our two laser cycling scheme in the Paschen-Back regime by measuring the scattering rate of light on one molecule. Finally, I created pre-cooled 40Ca19F with a forward velocity of around 150 m s−1 from a 40Ca19F2 target with laser ablation inside a cryogenic buffer gas cell. With the Zeeman slowing technique I slowed the molecules down to 25 m s−1, a velocity where trapping can be possible. I have also shown the characteristic compression into specific velocity classes for not yet trappable velocities. Together these two findings demonstrate that molecular Zeeman slowing is possible and a real promising tool for future experiments.