2008 APS March Meeting
Volume 53, Number 2
Monday–Friday, March 10–14, 2008;
New Orleans, Louisiana
Session B26: Focus Session: Photophysics of Cold Molecules II
11:15 AM–2:15 PM,
Monday, March 10, 2008
Morial Convention Center
Room: 218
Sponsoring
Unit:
DCP
Chair: Roland Wester, University of Freiburg
Abstract ID: BAPS.2008.MAR.B26.1
Abstract: B26.00001 : Molecular collision studies with Stark-decelerated beams
11:15 AM–11:51 AM
Preview Abstract
Abstract
Author:
Gerard Meijer
(Fritz Haber Institute of the Max Planck Society, Faradayweg 4-6, D-14195 Berlin, Germany)
Molecular scattering behaviour has generally proven difficult to
study at low collision energies. We formed a molecular beam of
OH radicals with a narrow velocity distribution and a tunable
velocity by passing the beam through a Stark decelerator [1].
The transition probabilities for inelastic scattering of the OH
radicals with Xe atoms were measured as a function of the
collision energy in the range of 50 to 400 wavenumbers. The
behaviour of the cross-sections for inelastic scattering near
the energetic thresholds was accurately measured, and excellent
agreement was obtained with cross-sections derived from coupled-
channel calculations on ab initio computed potential energy
surfaces [2].
For collision studies at lower energies, the decelerated beams
of molecules can be loaded into a variety of traps. In these
traps, electric fields are used to keep the molecules confined
in a region of space where they can be studied in complete
isolation from the (hot) environment. Typically, 10$^5$ state-
selected molecules can be trapped for times up to several
seconds at a density of 10$^7$ mol/cm$^3$ and at a temperature
of several tens of mK [3]. The long interaction time afforded by
the trap has been exploited to measure the infrared radiative
lifetime of vibrationally excited OH radicals, for instance, as
well as to study the far-infrared optical pumping of these polar
molecules due to blackbody radiation [4].
As an alternative to these traps, we have demonstrated an
electrostatic storage ring for neutral molecules. In its
simplest form, a storage ring is a trap in which the molecules -
rather than having a minimum potential energy at a single
location in space - have a minimum potential energy on a circle.
To fully exploit the possibilities offered by a ring structure,
it is imperative that the molecules remain in a bunch as they
revolve around the ring. This ensures a high density of stored
molecules, moreover, this makes it possible to inject multiple -
either co-linear or counter propagating - packets into the ring
without affecting the packet(s) already stored. We have recently
demonstrated a prototype molecular synchrotron, which will be
used as a low-energy collider for neutral molecules in the
future [5].\newline
[1] H.L. Bethlem, G. Berden, and G. Meijer, Phys. Rev. Lett. 83,
(1999) 1558-1561.\newline
[2] J.J. Gilijamse, S. Hoekstra, S.Y.T. van de
Meerakker, G.C. Groenenboom, and G. Meijer, Science 313, (2006)
1617-1620.\newline
[3] S.Y.T. van de Meerakker, P.H.M. Smeets, N.
Vanhaecke, R.T. Jongma, and G. Meijer, Phys. Rev. Lett. 94,
(2005) Artn. 023004.\newline
[4] S. Hoekstra, J.J. Gilijamse, B.
Sartakov, N. Vanhaecke, L. Scharfenberg, S.Y.T. van de
Meerakker, and G. Meijer, Phys. Rev. Lett. 98, (2007) Artn.
133001.\newline
[5] C.E. Heiner, D. Carty, G. Meijer, and H.L. Bethlem,
Nature Physics 3, (2007) 115-118.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2008.MAR.B26.1