Bulletin of the American Physical Society
APS March Meeting 2011
Volume 56, Number 1
Monday–Friday, March 21–25, 2011; Dallas, Texas
Session H6: Ultracold Molecules and Quantum Many Body Physics |
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Sponsoring Units: DAMOP Chair: Lincoln Carr, Colorado School of Mines Room: Ballroom C2 |
Tuesday, March 22, 2011 8:00AM - 8:36AM |
H6.00001: Control of dipolar collisions of polar molecules in the quantum regime Invited Speaker: Ultracold polar molecular quantum gases promise to open new research directions ranging from the study of ultra-cold chemistry, precision measurements to novel quantum phase transitions. Based on the preparation of high-phase space density gases of polar KRb molecules, I will discuss the control of dipolar collisions and chemical reactions of polar molecules in a regime where quantum statistics, single scattering partial waves, and quantum threshold laws play a dominant role. In particular, I will discuss the crucial role of electric dipole-dipole interactions and external confinement in determining the chemical reaction rate. Finally, I will discuss prospects of reaching quantum degeneracy in bi-alkali samples of polar molecules and prospects for these systems as novel dipolar quantum many-body systems. [Preview Abstract] |
Tuesday, March 22, 2011 8:36AM - 9:12AM |
H6.00002: Ultracold high-density samples of rovibronic ground-state molecules in an optical lattice Invited Speaker: Ultracold molecules controlled at the level of single quantum states with respect to all internal and external degrees of freedom will enable a series of fundamental studies in physics and chemistry, ranging from novel quantum gas experiments and cold controlled chemistry to quantum information and quantum simulation. Ultracold molecules trapped in an optical lattice at high density and prepared in their lowest internal quantum state are an ideal starting point for these studies. We create ultracold and dense samples of molecules in a single hyperfine sublevel of the rovibronic ground state while each molecule is individually trapped in the motional ground state of an optical lattice well [1,2]. Starting from an atomic Mott-insulator state with optimized double-site occupancy, weakly bound Cs dimer molecules are efficiently formed on a Feshbach resonance and subsequently transferred to the rovibronic ground state by a stimulated 4-photon process with the Stimulated Raman Adiabatic Passage (STIRAP) technique. The molecules are trapped in the lattice with a lifetime of 8 s. We aim at producing Bose-Einstein condensates of ground-state molecules by adiabatically removing the lattice. Our results, when suitably generalized to heteronuclear molecules, present an important step towards the realization of dipolar quantum-gas phases in optical lattices. I will report on recent progress in Innsbruck on the formation of RbCs ground state molecules. \\[4pt] [1] Science \textbf{321}, 1062 (2008) \\[0pt] [2] Nature Physics \textbf{6}, 265 (2010) [Preview Abstract] |
Tuesday, March 22, 2011 9:12AM - 9:48AM |
H6.00003: Theory of ultracold heteronuclear polar molecules Invited Speaker: This abstract not available. [Preview Abstract] |
Tuesday, March 22, 2011 9:48AM - 10:24AM |
H6.00004: Laser Cooling of a Diatomic Molecule Invited Speaker: Laser cooling techniques to produce ultracold (T$<$1$\mu$K) atoms have lead to rapid advances in a wide array of fields. However, extending laser cooling to molecules has remained elusive. The primary problem is that laser cooling requires a large number ($>$104) of photon absorption/emission cycles. Molecules, however, have vibrational and rotational degrees of freedom, which typically lead to high branching probabilities into a large number of unwanted sublevels. Here we report on experiments demonstrating the laser cooling of a diatomic molecule which have overcome this problem. We use the molecule strontium monofluoride (SrF) where only three lasers and a magnetic field are necessary to scatter $>$105 photons. We have demonstrated 1-D transverse cooling of a beam of SrF, dominated by Doppler or Sisyphus-type cooling forces depending on experimental parameters. We observe a reduction in the velocity distribution by a factor of 3 or more, corresponding to final 1-D temperature T $<$ 1 mK. This transverse cooling may be useful for a variety of experiments; in addition, our results open a path to trapping and 3D cooling of SrF to the ultracold regime. [Preview Abstract] |
Tuesday, March 22, 2011 10:24AM - 11:00AM |
H6.00005: Meta-stable 1-D gases of polar molecules with attractive dipole forces Invited Speaker: The recent achievements in the formation and manipulation of ultracold polar molecules have opened the gate to exciting new studies in several fields of physical sciences. Polar molecules could find uses in quantum information science and in precision measurements, while dense samples could provide a fertile ground for novel quantum gases because of their long-range and anisotropic interactions. Until now, stable dipolar gases were thought to require a repulsive dipole-dipole interaction, such as provided by parallel dipoles aligned perpendicularly to a two-dimensional (2-D) trap. However, to observe interesting new correlations and condensed matter phases, attractive interactions are needed. Here, we explore how meta-stable one-dimensional (1-D) samples of ultracold polar molecules could be created with attractive long-range dipole-dipole interaction. We show that a repulsive barrier due to a strong quadrupole interaction can stabilize a gas of ultracold KRb molecules and even lead to long-range wells supporting bound states. The properties of these wells can be controlled by external electric fields, allowing the formation of long chains of KRb polymers, and the further study of Luttinger liquid transition. We also discuss the general molecular properties necessary for the existence of a repulsive barrier. [Preview Abstract] |
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