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arXiv:1705.01422 · Physical Review A

Efficient production of long-lived ultracold Sr2 molecules

A. Ciamei, Alex Bayerle, Chun-Chia Chen, Benjamin Pasquiou, Florian Schreck

Published Jul 7, 2017• 38 citations
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Abstract

Ultracold ground-state diatomic molecules are produced from pairs of ${}^{84}$Sr atoms in a Mott insulator. Even in the absence of a Feshbach resonance, the improved stimulated Raman adiabatic passage (STIRAP) technique used in the state-transferring process leads to a production efficiency above 80%.

DOI
10.1103/physreva.96.013406

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Ultracold ground-state diatomic molecules are produced from pairs of 84{}^{84}84Sr atoms in a Mott insulator. Even in the absence of a Feshbach resonance, the improved stimulated Raman adiabatic passage (STIRAP) technique used in the state-transferring process leads to a production efficiency above 80%.
We report on the creation of ultracold (84)Sr(2) molecules in the electronic ground state. The molecules are formed from atom pairs on sites of an optical lattice using stimulated Raman adiabatic passage (STIRAP). We achieve a transfer efficiency of 30% and obtain 4×10(4) molecules with full control over the external and internal quantum state. STIRAP is performed near the narrow (1)S(0)-(3)P(1) intercombination transition, using a vibrational level of the 1(0(u)(+)) potential as an intermediate state. In preparation of our molecule association scheme, we have determined the binding energies of the last vibrational levels of the 1(0(u)(+)), 1(1(u)) excited-state and the X (1)Σ(g)(+) ground-state potentials. Our work overcomes the previous limitation of STIRAP schemes to systems with magnetic Feshbach resonances, thereby establishing a route that is applicable to many systems beyond alkali-metal dimers.
We produce 84 Sr 2 molecules using Bose-enhanced Raman photoassociation. We apply the stimulated Raman adiabatic passage (STIRAP) technique on a Bose-Einstein condensate (BEC) to produce more than 8 × 10 3 ultracold molecules. This chemical reaction is only made possible because of the Bose enhancement of the optical transition dipole moment between the initial atomic state and an intermediate molecular state. We study the effect of Bose enhancement by measuring the transition Rabi frequency in a BEC and by comparing it with measurements for two atoms in sites of a Mott insulator. By breaking the dimers' bond and directly observing the separated atoms, we measure the molecular inelastic collision rate parameters. We discuss the possibility of applying Bose-enhanced STIRAP to convert a BEC of atoms into a BEC of molecules, and argue that the required efficiency for STIRAP is within experimental reach.
One possibility for the creation of ultracold, high phase space density quantum gases of molecules in the rovibronic ground state relies on first associating weakly-bound molecules from quantum-degenerate atomic gases on a Feshbach resonance and then transferring the molecules via several steps of coherent two-photon stimulated Raman adiabatic passage (STIRAP) into the rovibronic ground state. Here, in ultracold samples of Cs2 Feshbach molecules produced out of ultracold samples of Cs atoms, we observe several optical transitions to deeply-bound rovibrational levels of the excited 0(u)+ molecular potentials with high resolution. At least one of these transitions, although rather weak, allows efficient STIRAP transfer into the deeply-bound vibrational level (see text for symbols)v = 73 > of the singlet X1 sigma(g)+ ground state potential, as recently demonstrated (J. G. Danzl, E. Haller, M. Gustavsson, M. J. Mark, R. Hart, N. Bouloufa, O. Dulieu, H. Ritsch, and H.-C. Nägerl, Science, 2008, 321, 1062). From this level, the rovibrational ground state (see text for symbols)v = 0, J = 0 > can be reached with one more transfer step. In total, our results show that coherent ground state transfer for Cs2 is possible using a maximum of two successive two-photon STIRAP processes or one single four-photon STIRAP process.
We develop a theoretical description of photoassociative stimulated Raman adiabatic passage (STIRAP) near a Feshbach resonance in a thermal atomic gas. We show that it is possible to use low-intensity laser pulses to directly excite pairs of atoms in the continuum near a Feshbach resonance and to transfer most of the atomic cloud to the lowest rovibrational level of the molecular ground state. For a broad resonance, commonly found in several mixtures of alkali atoms, our model predicts a transfer efficiency up to 97% for a given atom pair, and up to 70% when averaged over an atomic ensemble. The laser intensities and pulse durations needed for such an optimal transfer, 10 2 –10 3 W cm −2 and several microseconds, are easily achievable experimentally. A single pair of STIRAP pulses converts an estimated fraction f ∼10 −6 –10 −4 of atoms in an atomic ensemble, leading to the production of 10–1000 molecules in a large sample of 10 7 atoms. A total of ∼10 4 –10 6 pulse pairs are thus required to transfer most atoms into molecules. Such an efficiency compares with or surpasses currently available techniques for creating stable diatomic molecules, and the versatility of this approach simplifies its potential use for many molecular species.
Ultracold fermionic 23{}^{23}23Na40{}^{40}40K polar molecules are produced in their ground rovibrational state. A multilevel stimulated Raman adiabatic passage (STIRAP) state-transfer process is employed with an intermediate state having an unresolved hyperfine structure, which can be a situation commonly encountered in performing the state transfer.
Using the technique of stimulated Raman adiabatic passage (STIRAP) we have coherently transferred ultracold (87)Rb(2) Feshbach molecules into a more deeply bound vibrational quantum level. Our measurements indicate a high transfer efficiency of up to 87%. Because the molecules are held in an optical lattice with not more than a single molecule per lattice site, inelastic collisions between the molecules are suppressed and we observe long molecular lifetimes of about 1 s. Using STIRAP we have created quantum superpositions of the two molecular states and tested their coherence interferometrically. These results represent an important step towards Bose-Einstein condensation of molecules in the vibrational ground state.