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arXiv:1409.5556 · New Journal of Physics

Polar molecule reactive collisions in quasi-1D systems

Andrea Simoni, S Srinivasan, J. M. Launay, Krzysztof Jachymski, Zbigniew Idziaszek, Paul S. Julienne

Published Jan 15, 2015• 19 citations
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Abstract

We study polar molecule scattering in quasi-one-dimensional geometries. Elastic and reactive collision rates are computed as a function of collision energy and electric dipole moment for different confinement strengths. The numerical results are interpreted in terms of first order scattering and of adiabatic models. Universal dipolar scattering is also discussed. Our results are relevant to experiments where control of the collision dynamics through one-dimensional confinement and an applied electric field is envisioned.

DOI
10.1088/1367-2630/17/1/013020

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We study polar molecule scattering in quasi-one-dimensional geometries. Elastic and reactive collision rates are computed as a function of collision energy and electric dipole moment for different confinement strengths. The numerical results are interpreted in terms of first order scattering and of adiabatic models. Universal dipolar scattering is also discussed. Our results are relevant to experiments where control of the collision dynamics through one-dimensional confinement and an applied electric field is envisioned.
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We investigate collisions of polar molecules in quasi-2D traps in the presence of an external electric field perpendicular to the collision plane. We use the quantum-defect model characterized by two dimensionless parameters: yyy and sss. The first of them is related to the probability of the reaction at short distances, whereas the latter one defines the wave function phase at short distances. For yyy close to unity we obtain universal collision rates determined by the quantum reflection process from the long-range part of the interaction potential that depends only on the van der Waals coefficient, dipole-dipole interaction and the trap frequency. For small short-range reaction probabilities collision rates are highly nonuniversal and trap induced shape resonances are visible. For high dipole moments we observe the damping of reactive collisions, which can stabilize the ultracold gas of polar molecules. The calculations were performed with help of multichannel wave funcion propagation by imposing short-range boundary condition derived from the quantum-defect model.
Recent experimental developments in the loading of ultracold KRb molecules into quasi-two-dimensional traps, combined with the ability to tune the ratio between elastic and loss (inelastic, reactive) collisions through application of an external electric field, are opening the door to achieving efficient evaporative cooling of reactive polar molecules. In this paper, we use Monte Carlo simulations and semianalytic models to study theoretically the experimental parameter regimes in which evaporative cooling is feasible under current trapping conditions. We investigate the effect of the anisotropic character of dipole-dipole collisions and reduced dimensionality on evaporative cooling. We also present an analysis of the experimentally relevant antievaporation effects that are induced by chemical reactions that take place when more than one axial vibrational state is populated.
We explore the impact of the short-range interaction on the scattering of ground state polar molecules and study the transition from a weak to strong dipolar scattering over an experimentally reasonable range of energies and electric field values. In the strong dipolar limit, the scattering scales with respect to a dimensionless quantity defined by mass, induced dipole moment, and collision energy. The scaling has implications for all quantum mechanical dipolar scattering. Furthermore the universal scattering regime will readily be achieved with polar molecules at ultracold temperatures.