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      Laser cooling of a diatomic molecule

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          Abstract

          It has been roughly three decades since laser cooling techniques produced ultracold atoms, leading to rapid advances in a vast array of fields. Unfortunately laser cooling has not yet been extended to molecules because of their complex internal structure. However, this complexity makes molecules potentially useful for many applications. For example, heteronuclear molecules possess permanent electric dipole moments which lead to long-range, tunable, anisotropic dipole-dipole interactions. The combination of the dipole-dipole interaction and the precise control over molecular degrees of freedom possible at ultracold temperatures make ultracold molecules attractive candidates for use in quantum simulation of condensed matter systems and quantum computation. Also ultracold molecules may provide unique opportunities for studying chemical dynamics and for tests of fundamental symmetries. Here we experimentally demonstrate laser cooling of the molecule strontium monofluoride (SrF). Using an optical cycling scheme requiring only three lasers, we have observed both Sisyphus and Doppler cooling forces which have substantially reduced the transverse temperature of a SrF molecular beam. Currently the only technique for producing ultracold molecules is by binding together ultracold alkali atoms through Feshbach resonance or photoassociation. By contrast, different proposed applications for ultracold molecules require a variety of molecular energy-level structures. Our method provides a new route to ultracold temperatures for molecules. In particular it bridges the gap between ultracold temperatures and the ~1 K temperatures attainable with directly cooled molecules (e.g. cryogenic buffer gas cooling or decelerated supersonic beams). Ultimately our technique should enable the production of large samples of molecules at ultracold temperatures for species that are chemically distinct from bialkalis.

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          Most cited references14

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          A High Phase-Space-Density Gas of Polar Molecules

          A quantum gas of ultracold polar molecules, with long-range and anisotropic interactions, would not only enable explorations of a large class of many-body physics phenomena, but could also be used for quantum information processing. We report on the creation of an ultracold dense gas of 40K87Rb polar molecules. Using a single step of STIRAP (STImulated Raman Adiabatic Passage) via two-frequency laser irradiation, we coherently transfer extremely weakly bound KRb molecules to the rovibrational ground state of either the triplet or the singlet electronic ground molecular potential. The polar molecular gas has a peak density of 10^12 cm^-3, and an expansion-determined translational temperature of 350 nK. The polar molecules have a permanent electric dipole moment, which we measure via Stark spectroscopy to be 0.052(2) Debye for the triplet rovibrational ground state and 0.566(17) Debye for the singlet rovibrational ground state. (1 Debye= 3.336*10^-30 C m)
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            Nobel Lecture: Laser cooling and trapping of neutral atoms

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              Cold controlled chemistry.

              Collisions of molecules in a thermal gas are difficult to control. Thermal motion randomizes molecular encounters and diminishes the effects of external radiation or static electromagnetic fields on intermolecular interactions. The effects of the thermal motion can be reduced by cooling molecular gases to low temperatures. At temperatures near or below 1 K, the collision energy of molecules becomes less significant than perturbations due to external fields. At the same time, inelastic scattering and chemical reactions may be very efficient in low-temperature molecular gases. The purpose of this article is to demonstrate that collisions of molecules at temperatures below 1 K can be manipulated by external electromagnetic fields and to discuss possible applications of cold controlled chemistry. The discussion focuses on molecular interactions at cold (0.001-2 K) and ultracold (<0.001 K) temperatures and is based on both recent theoretical and experimental work. The article concludes with a summary of current challenges for theory and experiment in the research of cold molecules and cold chemistry.
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                Author and article information

                Journal
                30 March 2011
                2011-07-19
                Article
                10.1038/nature09443
                20852614
                1103.6004
                adae3963-9edc-44fb-9436-6cb86ed03f1c

                http://arxiv.org/licenses/nonexclusive-distrib/1.0/

                History
                Custom metadata
                Nature 467, 820-823 (2010)
                10 pages, 7 figures
                physics.atom-ph physics.chem-ph

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