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