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arXiv:1203.2989 · Physical Review Letters

Controlled Production of Subradiant States of a Diatomic Molecule in an Optical Lattice

Yosuke Takasu, Yutaka Saito, Yoshiro Takahashi, Mateusz Borkowski, R. Ciuryło, Paul S. Julienne

Published Apr 23, 2012• 50 citations
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Abstract

We report the successful production of subradiant states of a two-atom system in a three-dimensional optical lattice starting from doubly occupied sites in a Mott insulator phase of a quantum gas of atomic ytterbium. We can selectively produce either a subradiant 1(g) state or a superradiant 0(u) state by choosing the excitation laser frequency. The inherent weak excitation rate for the subradiant 1(g) state is overcome by the increased atomic density due to the tight confinement in a three-dimensional optical lattice. Our experimental measurements of binding energies, linewidth, and Zeeman shift confirm the observation of subradiant levels of the 1(g) state of the Yb(2) molecule.

DOI
10.1103/physrevlett.108.173002

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We report the successful production of subradiant states of a two-atom system in a three-dimensional optical lattice starting from doubly occupied sites in a Mott insulator phase of a quantum gas of atomic ytterbium. We can selectively produce either a subradiant 1(g) state or a superradiant 0(u) state by choosing the excitation laser frequency. The inherent weak excitation rate for the subradiant 1(g) state is overcome by the increased atomic density due to the tight confinement in a three-dimensional optical lattice. Our experimental measurements of binding energies, linewidth, and Zeeman shift confirm the observation of subradiant levels of the 1(g) state of the Yb(2) molecule.
We demonstrate quantum control over both internal and external quantum degrees of freedom in a high number of identical "chemical reactions," carried out in an array of microtraps in a 3D optical lattice. Starting from a Mott insulating phase of an ultracold atomic quantum gas, we use two-photon Raman transitions to create molecules on lattice sites occupied by two atoms. In the atom-molecule conversion process, we can control both the internal rovibronic and external center of mass quantum state of the molecules. The lattice isolates the microscopic chemical reactions from each other, thereby allowing photoassociation spectra without collisional broadening even at high densities of up to 2 x 10(15) cm(-3).
We observe long-lived tightly bound van der Waals molecules of ytterbium in a three-dimensional optical lattice with a lifetime of 8.0 s. The molecules, state-selectively produced by a photoassociation technique from a Bose-Einstein condensate or an atomic Mott insulator, are successfully detected with a photodissociation method where the molecules are photodissociated into two atoms and the atoms are captured by a magneto-optical trap or optical molasses, for the fluorescence detection. This work will open up various possibilities of research with van der Waals molecules in an optical lattice.
We observe magnetic Feshbach resonances in a collision between the ground and metastable states of two-electron atoms of ytterbium (Yb). We measure the on-site interaction of doubly occupied sites of an atomic Mott-insulator state in a three-dimensional optical lattice as a collisional frequency shift in a high-resolution laser spectroscopy. The observed spectra are well fitted by a simple theoretical formula, in which two particles with an s-wave contact interaction are confined in a harmonic trap. This analysis reveals a wide variation of the interaction with a resonance behavior around a magnetic field of about 1.1 G for the energetically lowest magnetic sublevel of 170Yb, as well as around 360 mG for the energetically highest magnetic sublevel of 174Yb. The observed Feshbach resonance can only be induced by an anisotropic interatomic interaction. This scheme will open the door to a variety of studies using two-electron atoms with tunable interaction.
We demonstrated high-sensitivity optical spectral imaging of a single layer of a quantum gas of ytterbium atoms in a two-dimensional optical lattice using the ultranarrow 1S0{}^{1}{S}_{0}1S0​-3P2{}^{3}{P}_{2}3P2​ transition. We successfully obtained a set of excitation-frequency-dependent fluorescence images with an excitation laser of the linewidth of 1 kHz (FWHM), and the overall features were well explained by considering the inhomogeneous light shift originating from the Gaussian beam shape of the optical lattice potential which provided the steepest potential gradient of 3.6 kHz/$\ensuremath{\mu}$m. This result is also the successful demonstration of the tunable local atom addressing along the equipotential contour depending on the excitation laser frequency with the frequency resolution of 8 kHz and the spatial resolution of approximately 2 $\ensuremath{\mu}$m. The demonstrated technique will be useful for many purposes including the measurement of interaction shift in the study of a quantum gas and quantum information processing.
We produce an ultracold and dense sample of rovibronic ground state Cs 2 molecules close to the regime of quantum degeneracy, in a single hyperfine level, in the presence of an optical lattice. The molecules are individually trapped, in the motional ground state of an optical lattice well, with a lifetime of 8 s. For preparation, we start with a zero-temperature atomic Mott-insulator state with optimized double-site occupancy and efficiently associate weakly-bound dimer molecules on a Feshbach resonance. Despite extremely weak Franck-Condon wavefunction overlap, the molecules are subsequently transferred with >50% efficiency to the rovibronic ground state by a stimulated four-photon process. Our results present a crucial step towards the generation of Bose-Einstein condensates of ground-state molecules and, when suitably generalized to polar heteronuclear molecules such as RbCs, the realization of dipolar many-body quantum-gas phases in periodic potentials.