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arXiv:0707.3003 · Physical Review A

Energy dependence of scattering ground-state polar molecules

Christopher Ticknor

Published Nov 7, 2007• 22 citations

Abstract

We explore the total collisional cross section of ground-state polar molecules in an electric field at various energies, focusing on $\mathrm{RbCs}$ and $\mathrm{RbK}$. An external electric field polarizes the molecules and induces strong dipolar interactions, leading to nonzero partial waves contributing to the scattering even as the collision energy goes to zero. This results in the need to compute scattering problems with many different values of total $M$ to converge the total cross section. An accurate and efficient approximate total cross section is introduced and used to study the low-field temperature dependence. To understand the scattering of the polar molecules we compare a semiclassical cross section with the quantum unitarity limit. This comparison leads to the ability to characterize the scattering based on the value of the electric field and the collision energy. General and simple forms of the characteristic electric field and energy are given, enabling characterization of the scattering.

DOI: 10.1103/physreva.76.052703

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We explore the total collisional cross section of ground-state polar molecules in an electric field at various energies, focusing on

\mathrm{RbCs}

and

\mathrm{RbK}

. An external electric field polarizes the molecules and induces strong dipolar interactions, leading to nonzero partial waves contributing to the scattering even as the collision energy goes to zero. This results in the need to compute scattering problems with many different values of total

M

to converge the total cross section. An accurate and efficient approximate total cross section is introduced and used to study the low-field temperature dependence. To understand the scattering of the polar molecules we compare a semiclassical cross section with the quantum unitarity limit. This comparison leads to the ability to characterize the scattering based on the value of the electric field and the collision energy. General and simple forms of the characteristic electric field and energy are given, enabling characterization of the scattering.

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.

The dipolar collision between ultracold polar molecules is an important topic both by its own right from the fundamental point of view and for the successful exploration of many-body physics with strong and longrange dipolar interactions.Here, we report the investigation of collisions between ultracold ground-state sodium-rubidium molecules in electric fields with induced electric dipole moments as large as 0.7 D. We observe a stepwise enhancement of losses due to the coupling between different partial waves induced by the increasingly stronger anisotropic dipolar interactions.Varying the temperature of our sample, we find good agreement with theoretical loss rates assuming complex formation as the main loss process.Our results shed new light on the understanding of complex molecular collisions in the presence of strong dipolar interactions and also demonstrate the versatility of modifying molecular interactions with electric fields.

We present first steps toward understanding the ultracold scattering properties of polar molecules in strong electric field-seeking states. We have found that the elastic cross section displays a quasiregular set of potential resonances as a function of the electric field, which potentially offers intimate details about the intermolecular interaction. We illustrate these resonances in a ``toy'' model composed of pure dipoles, and in more physically realistic systems. To analyze these resonances, we use a simple WKB approximation to the eigenphase, which proves both reasonably accurate and meaningful. A general treatment of the Stark effect and dipolar interactions is also presented.

We investigate the scattering cross section of aligned dipolar molecules in low-temperature gases. Over a wide range of collision energies relevant to contemporary experiments, the cross section declines in inverse proportion to the collision speed, and is given nearly exactly by a simple semiclassical formula. At yet lower energies, the cross section becomes independent of energy, and is reproduced within the Born approximation to within corrections due to the s-wave scattering length. While these behaviors are universal for all polar molecules, nevertheless interesting deviations from universality are expected to occur in the intermediate energy range.

Cold molecules promise to reveal a rich set of novel collision dynamics in the low-energy regime. By combining for the first time the techniques of Stark deceleration, magnetic trapping, and cryogenic buffer gas cooling, we present the first experimental observation of cold collisions between two different species of state-selected neutral polar molecules. This has enabled an absolute measurement of the total trap loss cross sections between OH and ND(3) at a mean collision energy of 3.6 cm(-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 ab initio potential energy surfaces are in agreement with the measured value at zero external electric field. The theory presented here represents the first such analysis of collisions between a (2)Π radical and a closed-shell polyatomic molecule.