18 research outputs found
Linking Ultracold Polar Molecules
We predict that pairs of polar molecules can be weakly bound together in an
ultracold environment, provided that a dc electric field is present. The field
that links the molecules together also strongly influences the basic properties
of the resulting dimer, such as its binding energy and predissociation
lifetime. Because of their long-range character these dimers will be useful in
disentangling cold collision dynamics of polar molecules. As an example, we
estimate the microwave photoassociation yield for OH-OH cold collisions.Comment: 4 pages 2 figure
Field-linked States of Ultracold Polar Molecules
We explore the character of a novel set of ``field-linked'' states that were
predicted in [A. V. Avdeenkov and J. L. Bohn, Phys. Rev. Lett. 90, 043006
(2003)]. These states exist at ultralow temperatures in the presence of an
electrostatic field, and their properties are strongly dependent on the field's
strength. We clarify the nature of these quasi-bound states by constructing
their wave functions and determining their approximate quantum numbers. As the
properties of field-linked states are strongly defined by anisotropic dipolar
and Stark interactions, we construct adiabatic surfaces as functions of both
the intermolecular distance and the angle that the intermolecular axis makes
with the electric field. Within an adiabatic approximation we solve the 2-D
Schrodinger equation to find bound states, whose energies correlate well with
resonance features found in fully-converged multichannel scattering
calculations
Molecular excitation in the Interstellar Medium: recent advances in collisional, radiative and chemical processes
We review the different excitation processes in the interstellar mediumComment: Accepted in Chem. Re
Scattering of Stark-decelerated OH radicals with rare-gas atoms
We present a combined experimental and theoretical study on the rotationally
inelastic scattering of OH (X\,^2\Pi_{3/2}, J=3/2, f) radicals with the
collision partners He, Ne, Ar, Kr, Xe, and D as a function of the collision
energy between cm and 400~cm. The OH radicals are state
selected and velocity tuned prior to the collision using a Stark decelerator,
and field-free parity-resolved state-to-state inelastic relative scattering
cross sections are measured in a crossed molecular beam configuration. For all
OH-rare gas atom systems excellent agreement is obtained with the cross
sections predicted by close-coupling scattering calculations based on accurate
\emph{ab initio} potential energy surfaces. This series of experiments
complements recent studies on the scattering of OH radicals with Xe [Gilijamse
\emph{et al.}, Science {\bf 313}, 1617 (2006)], Ar [Scharfenberg \emph{et al.},
Phys. Chem. Chem. Phys. {\bf 12}, 10660 (2010)], He, and D [Kirste \emph{et
al.}, Phys. Rev. A {\bf 82}, 042717 (2010)]. A comparison of the relative
scattering cross sections for this set of collision partners reveals
interesting trends in the scattering behavior.Comment: 10 pages, 5 figure
State-to-state scattering of oriented OH
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Determination of Lambda-doublet resolved cross-sections for inelastic scattering of OH by para- and normal-H-2
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