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arXiv:1908.02703 · Physical Review Letters

Singlet Pathway to the Ground State of Ultracold Polar Molecules

Anbang Yang, Sofia Botsi, Sunil Kumar, Sat Pal, M. M. Lam, Ieva Čepaitė, Andrew Laugharn, Kai Dieckmann

Published Apr 1, 2020• 23 citations
arXivHTMLPDF

Abstract

Starting from weakly bound Feshbach molecules, we demonstrate a two-photon pathway to the dipolar ground state of bi-alkali molecules that involves only singlet-to-singlet optical transitions. This pathway eliminates the search for a suitable intermediate state with sufficient singlet-triplet mixing and the exploration of its hyperfine structure, as is typical for pathways starting from triplet dominated Feshbach molecules. By selecting a Feshbach state with a stretched singlet hyperfine component and controlling the laser polarizations, we assure coupling to only single hyperfine components of the A^{1}Σ^{+} excited potential and the X^{1}Σ^{+} rovibrational ground state. In this way an ideal three level system is established, even if the hyperfine structure is not resolved. We demonstrate this pathway with ^{6}Li^{40}K molecules, and discuss its application to other important molecular species.

DOI
10.1103/physrevlett.124.133203

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Starting from weakly bound Feshbach molecules, we demonstrate a two-photon pathway to the dipolar ground state of bi-alkali molecules that involves only singlet-to-singlet optical transitions. This pathway eliminates the search for a suitable intermediate state with sufficient singlet-triplet mixing and the exploration of its hyperfine structure, as is typical for pathways starting from triplet dominated Feshbach molecules. By selecting a Feshbach state with a stretched singlet hyperfine component and controlling the laser polarizations, we assure coupling to only single hyperfine components of the A^{1}Σ^{+} excited potential and the X^{1}Σ^{+} rovibrational ground state. In this way an ideal three level system is established, even if the hyperfine structure is not resolved. We demonstrate this pathway with ^{6}Li^{40}K molecules, and discuss its application to other important molecular species.
We demonstrate a two-photon pathway to the ground state of 6 Li 40 K molecules that involves only singlet-to-singlet optical transitions.We start from a molecular state which contains a significant admixture from the singlet ground state potential by selecting the Feshbach resonance for molecule association.With the only contributing singlet state to the molecular state being fully stretched and with control over the lasers polarization we address a sole hyperfine component of the excited A 1 Σ + potential without resolving its hyperfine structure.This scheme ensures access to only one ground state hyperfine component with sufficient Franck-Condon factors and moderate laser powers for both coupling transitions.Its implementation results in large and balanced Rabi frequencies, a favourable condition for the coherent transfer to the ground state.We perform dark resonance spectroscopy to precisely determine the transition frequencies of the states involved.The strong dipolar nature of 6 Li 40 K is revealed by Stark spectroscopy, as it is necessary for the study of dipolar interactions in an optical lattice.
We report on high-resolution spectroscopy of ultracold fermionic 23 Na 40 K Feshbach molecules, and identify a two-photon pathway to the rovibrational singlet ground state via a resonantly mixed B 1 Π ∼ c 3 Σ + intermediate state.Photoassociation in a 23 Na-40 K atomic mixture and one-photon spectroscopy on 23 Na 40 K Feshbach molecules reveal about 20 vibrational levels of the electronically excited c 3 Σ + state.Two of these levels are found to be strongly perturbed by nearby B 1 Π levels via spinorbit coupling, resulting in additional lines of dominant singlet character in the perturbed complex. The dominantly singlet level is used to locate the absolute rovibrational singlet ground state v J X 0, 0via Autler-Townes spectroscopy.We demonstrate coherent two-photon coupling via dark state spectroscopy between the predominantly triplet Feshbach molecular state and the singlet ground state.Its binding energy is measured to be 5212.0447(1)cm -1 , a thousand-fold improvement in accuracy compared to previous determinations.In their absolute singlet ground state, 23 Na 40 K molecules are chemically stable under binary collisions and possess a large electric dipole moment of 2.72 Debye.Our work thus paves the way towards the creation of strongly dipolar Fermi gases of NaK molecules.
Ultracold bialkali polar molecules play a leading part at the frontline of quantum physics. They recently attract a lot of attention in the field of ultracold quantum chemistry, quantum many-body physics and quantum simulations. The key for their success is the rich internal level structure with rotational and vibrational degrees of freedom and their large electric dipole moments. Still, only a handful of molecular species are available at ultracold temperatures until now, although it is highly desirable to produce new molecular species to further expand the range of applications. Besides direct laser cooling methods for molecules, the assembly of heteronuclear ground-state molecules from ultracold atomic mixtures is the most promising approach for the creation of polar molecules. It includes the formation of weakly bound Feshbach molecules from the diatomic mixture and the subsequent two-photon stimulated Raman adiabatic passage (STIRAP) transfer to the rovibrational ground state. This creation strategy has been successfully demonstrated for the first time in the pioneering experiments at JILA with ultracold 40K87Rb molecules. Since then, only a few more molecular species from different alkali atoms have been created, namely 6Li23Na, 23Na40K, 23Na87Rb and 87Rb133Cs. In this thesis, I report the successful creation of a new species of ultracold polar ground-state molecules: 23Na39K. Starting from an ultracold mixture of bosonic 23Na and 39K atoms, weakly bound molecules are created. For this purpose, a Feshbach resonance in a high angular momentum scattering channel is chosen, experimentally identified and characterized. Close to this resonance the weakly bound Feshbach molecules are formed using resonant radio frequency radiation. For the two-photon ground-state transfer, a unique, highly specialized two-color laser system is designed and realized. It is used for one- and two-photon spectroscopy to identify the relevant transitions for the ground-state transfer. Based on the obtained data, a local model of the singlet-triplet mixed excited state manifolds is developed, with which the hyperfine structure and the magnetic field dependence is predicted with high accuracy. According to these findings, a suitable pathway to a single hyperfine ground state is chosen considering selection rules and experimental conditions such as laser polarization and beam alignment. To precisely determine the two-photon resonance condition for STIRAP, electromagnetically induced transparency measurements are performed. The ground-state transfer is then performed using STIRAP. The experimental findings regarding the STIRAP are successfully supported theoretically by a model based on a five-level master equation. The pure molecular gas shows evidence for two-body dominated loss mechanisms, such as sticky four-body collisions. The molecule-atom mixture of 23Na39K+39K reveals an unexpectedly low loss rate coefficient although sticky three-body collisions are assumed to occur. This behavior demands further investigations regarding different hyperfine collisional chan-nels and magnetic field regions.
Abstract We spectroscopically investigate a pathway for the conversion of 23Na39K Feshbach molecules into rovibronic ground state molecules via stimulated Raman adiabatic passage. Using photoassociation spectroscopy from the diatomic scattering threshold in the a 3Σ+ potential, we locate the resonantly mixed electronically excited intermediate states ∣ B 1 Π , v = 8 〉 and ∣ c 3 Σ + , v = 30 〉 which, due to their singlet–triplet admixture, serve as an ideal bridge between predominantly a 3Σ+ Feshbach molecules and pure X 1Σ+ ground state molecules. We investigate their hyperfine structure and present a simple model to determine the singlet–triplet coupling of these states. Using Autler–Townes spectroscopy, we locate the rovibronic ground state of the 23Na39K molecule ( ∣ X 1 Σ + , v = 0 , N = 0 〉 ) and the second rotationally excited state N = 2 to unambiguously identify the ground state. We also extract the effective transition dipole moment from the excited to the ground state. Our investigations result in a fully characterized scheme for the creation of ultracold bosonic 23Na39K ground state molecules.
We report on high-resolution spectroscopy of ultracold fermionic [superscript 23]Na[superscript 40]K Feshbach molecules, and identify a two-photon pathway to the rovibrational singlet ground state via a resonantly mixed B[superscript 1]Π ~ c[superscript 3]Σ[superscript +]intermediate state. Photoassociation in a [superscript 23]Na–[superscript 40]K atomic mixture and one-photon spectroscopy on [superscript 23]Na[superscript 40]K Feshbach molecules reveal about 20 vibrational levels of the electronically excited c[superscript 3]Σ[superscript +]state. Two of these levels are found to be strongly perturbed by nearby B[superscript 1]Π levels via spin–orbit coupling, resulting in additional lines of dominant singlet character in the perturbed complex B[superscript 1}Π |v = 4〉 ~ c[superscript 3]∑[superscript +] v = 25〉, or of resonantly mixed character in B[superscript 1}Π |v = 12〉 ~ c[superscript 3]∑[superscript +] v = 35〉. The dominantly singlet level is used to locate the absolute rovibrational singlet ground state X[superscript 1]∑[superscript +] |v = 0, J = 0〉 via Autler–Townes spectroscopy. We demonstrate coherent two-photon coupling via dark state spectroscopy between the predominantly triplet Feshbach molecular state and the singlet ground state. Its binding energy is measured to be 5212.0447(1) cm[superscript −1], a thousand-fold improvement in accuracy compared to previous determinations. In their absolute singlet ground state, [superscript 23]Na[superscript 40]K molecules are chemically stable under binary collisions and possess a large electric dipole moment of 2.72 Debye. Our work thus paves the way towards the creation of strongly dipolar Fermi gases of NaK molecules.
We report the creation of ultracold ground state ^{6}Li^{40}K polar molecules with high efficiency. Starting from weakly bound molecules, stimulated Raman adiabatic passage is adopted to coherently transfer the molecules to their singlet rovibrational ground state |X^{1}Σ^{+},v=0,J=0⟩. By employing a singlet stimulated Raman adiabatic passage pathway and low-phase-noise narrow-linewidth lasers, we observed a one-way transfer efficiency of 96(4)%. Held in an optical dipole trap, the lifetime of the ground state molecules is measured to be 5.0(3) ms. The large permanent dipole moment of LiK is confirmed by applying a dc electric field on the molecules and performing Stark shift spectroscopy of the ground state. With recent advances in the quantum control of collisions, our work paves the way for exploring quantum many-body physics with strongly interacting ^{6}Li^{40}K molecules.