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      Spin squeezing an ultracold molecule

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          Abstract

          In this article we present a concrete proposal for spin squeezing the ultracold ground state polar paramagnetic molecule OH, a system currently under fine control in the laboratory. In contrast to existing work, we consider a single, non-interacting molecule with angular momentum greater than \(1/2\). Starting from an experimentally relevant effective Hamiltonian, we identify a parameter regime where different combinations of static electric and magnetic fields can be used to realize the single-axis twisting Hamiltonian of Kitagawa and Ueda [M. Kitagawa and M. Ueda, Phys. Rev. A 47, 5138 (1993)], the uniform field Hamiltonian proposed by Law et al. [C. K. Law, H. T Ng and P. T. Leung, Phys. Rev. A 63, 055601 (2001)], and a model of field propagation in a Kerr medium considered by Agarwal and Puri [G. S. Agarwal and R. R. Puri, Phys. Rev. A 39, 2969 (1989)]. To support our conclusions, we provide analytical expressions as well as numerical calculations, including optimization of field strengths and accounting for the effects of field misalignment. Our results have consequences for applications such as precision spectroscopy, techniques such as magnetometry, and stereochemical effects such as the orientation-to-alignment transition.

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          Nonlinear atom interferometer surpasses classical precision limit

          Interference is fundamental to wave dynamics and quantum mechanics. The quantum wave properties of particles are exploited in metrology using atom interferometers, allowing for high-precision inertia measurements [1, 2]. Furthermore, the state-of-the-art time standard is based on an interferometric technique known as Ramsey spectroscopy. However, the precision of an interferometer is limited by classical statistics owing to the finite number of atoms used to deduce the quantity of interest [3]. Here we show experimentally that the classical precision limit can be surpassed using nonlinear atom interferometry with a Bose-Einstein condensate. Controlled interactions between the atoms lead to non-classical entangled states within the interferometer; this represents an alternative approach to the use of non-classical input states [4-8]. Extending quantum interferometry [9] to the regime of large atom number, we find that phase sensitivity is enhanced by 15 per cent relative to that in an ideal classical measurement. Our nonlinear atomic beam splitter follows the "one-axis-twisting" scheme [10] and implements interaction control using a narrow Feshbach resonance. We perform noise tomography of the quantum state within the interferometer and detect coherent spin squeezing with a squeezing factor of -8.2dB [11-15]. The results provide information on the many-particle quantum state, and imply the entanglement of 170 atoms [16].
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            Squeezing and entanglement in a Bose-Einstein condensate

            Entanglement, a key feature of quantum mechanics, is a resource that allows the improvement of precision measurements beyond the conventional bound reachable by classical means. This is known as the standard quantum limit, already defining the accuracy of the best available sensors for various quantities such as time or position. Many of these sensors are interferometers in which the standard quantum limit can be overcome by feeding their two input ports with quantum-entangled states, in particular spin squeezed states. For atomic interferometers, Bose-Einstein condensates of ultracold atoms are considered good candidates to provide such states involving a large number of particles. In this letter, we demonstrate their experimental realization by splitting a condensate in a few parts using a lattice potential. Site resolved detection of the atoms allows the measurement of the conjugated variables atom number difference and relative phase. The observed fluctuations imply entanglement between the particles, a resource that would allow a precision gain of 3.8 dB over the standard quantum limit for interferometric measurements.
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              Evaporative cooling of the dipolar radical OH

              Atomic physics was revolutionized by the development of forced evaporative cooling: it led directly to the observation of Bose-Einstein condensation, quantum-degenerate Fermi gases, and ultracold optical lattice simulations of condensed matter phenomena. More recently, great progress has been made in the production of cold molecular gases, whose permanent electric dipole moment is expected to generate rich, novel, and controllable phases, dynamics, and chemistry in these ultracold systems. However, while many strides have been made in both direct cooling and cold-association techniques, evaporative cooling has not yet been achieved due to unfavorable elastic-to-inelastic ratios and impractically slow thermalization rates in the available trapped species. We now report the observation of microwave-forced evaporative cooling of hydroxyl (OH) molecules loaded from a Stark-decelerated beam into an extremely high-gradient magnetic quadrupole trap. We demonstrate cooling by at least an order of magnitude in temperature and three orders in phase-space density, limited only by the low-temperature sensitivity of our spectroscopic thermometry technique. With evaporative cooling and sufficiently large initial populations, much colder temperatures are possible, and even a quantum-degenerate gas of this dipolar radical -- or anything else it can sympathetically cool -- may now be in reach.
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                Author and article information

                Journal
                2015-09-12
                2015-09-18
                Article
                10.1103/PhysRevA.92.063823
                1509.03707
                59d24c56-ebe8-47d3-aa99-f10d9a25f4a0

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

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                Custom metadata
                10 pages, 5 figures, updated references
                quant-ph physics.atom-ph

                Quantum physics & Field theory,Atomic & Molecular physics
                Quantum physics & Field theory, Atomic & Molecular physics

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