228 research outputs found

    Microwave state transfer and adiabatic dynamics of magnetically trapped polar molecules

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    Cold and ultracold polar molecules with nonzero electronic angular momentum are of great interest for studies in quantum chemistry and control, investigations of novel quantum systems, and precision measurement. However, in mixed electric and magnetic fields, these molecules are generically subject to a large set of avoided crossings among their Zeeman sublevels; in magnetic traps, these crossings lead to distorted potentials and trap loss from electric bias fields. We have characterized these crossings in OH by microwave-transferring trapped OH molecules from the upper |f; M = +3/2> parity state to the lower |e; +3/2> state and observing their trap dynamics under an applied electric bias field. Our observations are very well described by a simple Landau-Zener model, yielding insight to the rich spectra and dynamics of polar radicals in mixed external fields.Comment: 5 pages, 4 figures plus supplementary materia

    Low-energy molecular collisions in a permanent magnetic trap

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    Cold, neutral hydroxyl radicals are Stark decelerated and confined within a magnetic trap consisting of two permanent ring magnets. The OH molecules are trapped in the ro-vibrational ground state at a density of 106\sim10^{6} cm3^{-3} and temperature of 70 mK. Collisions between the trapped OH sample and supersonic beams of atomic He and molecular D2_{2} are observed and absolute collision cross sections measured. The He--OH and D2_{2}--OH center-of-mass collision energies are tuned from 60 cm1^{-1} to 230 cm1^{-1} and 145 cm1^{-1} to 510 cm1^{-1}, respectively, yielding evidence of reduced He--OH inelastic cross sections at energies below 84 cm1^{-1}, the OH ground rotational level spacing.Comment: 4 pages, 4 figure

    Magneto-electrostatic trapping of ground state OH molecules

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    We report the magnetic confinement of neutral, ground state hydroxyl radicals (OH) at a density of 3×103\sim3\times10^{3} cm3^{-3} and temperature of \sim30 mK. An adjustable electric field of sufficient magnitude to polarize the OH is superimposed on the trap in either a quadrupole or homogenous field geometry. The OH is confined by an overall potential established via molecular state mixing induced by the combined electric and magnetic fields acting on the molecule's electric dipole and magnetic dipole moments, respectively. An effective molecular Hamiltonian including Stark and Zeeman terms has been constructed to describe single molecule dynamics inside the trap. Monte Carlo simulation using this Hamiltonian accurately models the observed trap dynamics in various trap configurations. Confinement of cold polar molecules in a magnetic trap, leaving large, adjustable electric fields for control, is an important step towards the study of low energy dipole-dipole collisions.Comment: 4 pages, 4 figure

    Cold heteromolecular dipolar collisions

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    We present the first experimental observation of cold collisions between two different species of neutral polar molecules, each prepared in a single internal quantum state. Combining for the first time the techniques of Stark deceleration, magnetic trapping, and cryogenic buffer gas cooling allows the enhancement of molecular interaction time by 105^5. This has enabled an absolute measurement of the total trap loss cross sections between OH and ND3_3 at a mean collision energy of 3.6 cm1^{-1} (5 K). Due to the dipolar interaction, the total cross section increases upon application of an external polarizing electric field. Cross sections computed from \emph{ab initio} potential energy surfaces are in excellent agreement with the measured value at zero external electric field. The theory presented here represents the first such analysis of collisions between a 2Π^2\Pi radical and a closed-shell polyatomic molecule.Comment: 7 pages, 5 figure

    Magneto-Optical Trap for Polar Molecules

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    We propose a method for laser cooling and trapping a substantial class of polar molecules, and in particular titanium (II) oxide (TiO). This method uses pulsed electric fields to nonadiabatically remix the ground-state magnetic sublevels of the molecule, allowing us to build a magneto-optical trap (MOT) based on a quasi-cycling J=J"1J'=J"-1 transition. Monte-Carlo simulations of this electrostatically remixed MOT (ER-MOT) demonstrate the feasibility of cooling TiO to a temperature of 10 μK\mathrm{\mu}K and trapping it with a radiation-pumping-limited lifetime on the order of 80 ms.Comment: 4 pages, 4 figures, 1 table v2: updated to final published text and figure

    Quantum-limited optical time transfer for future geosynchronous links

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    The combination of optical time transfer and optical clocks opens up the possibility of large-scale free-space networks that connect both ground-based optical clocks and future space-based optical clocks. Such networks promise better tests of general relativity, dark matter searches, and gravitational wave detection. The ability to connect optical clocks to a distant satellite could enable space-based very long baseline interferometry (VLBI), advanced satellite navigation, clock-based geodesy, and thousand-fold improvements in intercontinental time dissemination. Thus far, only optical clocks have pushed towards quantum-limited performance. In contrast, optical time transfer has not operated at the analogous quantum limit set by the number of received photons. Here, we demonstrate time transfer with near quantum-limited acquisition and timing at 10,000 times lower received power than previous approaches. Over 300 km between mountaintops in Hawaii with launched powers as low as 40 μ\muW, distant timescales are synchronized to 320 attoseconds. This nearly quantum-limited operation is critical for long-distance free-space links where photons are few and amplification costly -- at 4.0 mW transmit power, this approach can support 102 dB link loss, more than sufficient for future time transfer to geosynchronous orbits

    Characterization of Large Volume 3.5 x 8 inches LaBr3:Ce Detectors

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    The properties of large volume cylindrical 3.5 x 8 inches (89 mm x 203 mm) LaBr3:Ce scintillation detectors coupled to the Hamamatsu R10233-100SEL photo-multiplier tube were investigated. These crystals are among the largest ones ever produced and still need to be fully characterized to determine how these detectors can be utilized and in which applications. We tested the detectors using monochromatic gamma-ray sources and in-beam reactions producing gamma rays up to 22.6 MeV; we acquired PMT signal pulses and calculated detector energy resolution and response linearity as a function of gamma-ray energy. Two different voltage dividers were coupled to the Hamamatsu R10233-100SEL PMT: the Hamamatsu E1198-26, based on straightforward resistive network design, and the LABRVD, specifically designed for our large volume LaBr3:Ce scintillation detectors, which also includes active semiconductor devices. Because of the extremely high light yield of LaBr3:Ce crystals we observed that, depending on the choice of PMT, voltage divider and applied voltage, some significant deviation from the ideally proportional response of the detector and some pulse shape deformation appear. In addition, crystal non-homogeneities and PMT gain drifts affect the (measured) energy resolution especially in case of high-energy gamma rays. We also measured the time resolution of detectors with different sizes (from 1x1 inches up to 3.5x8 inches), correlating the results with both the intrinsic properties of PMTs and GEANT simulations of the scintillation light collection process. The detector absolute full energy efficiency was measured and simulated up to gamma-rays of 30 Me

    Resonance phenomena in ultracold dipole-dipole scattering

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    Elastic scattering resonances occurring in ultracold collisions of either bosonic or fermionic polar molecules are investigated. The Born-Oppenheimer adiabatic representation of the two-bodydynamics provides both a qualitative classification scheme and a quantitative WKB quantization condition that predicts several sequences of resonant states. It is found that the near-threshold energy dependence of ultracold collision cross sections varies significantly with the particle exchange symmetry, with bosonic systems showing much smoother energy variations than their fermionic counterparts. Resonant variations of the angular distributions in ultracold collisions are also described.Comment: 19 pages, 6 figures, revtex4, submitted to J. Phys.
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