Steven Hoekstra
University of Groningen
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Featured researches published by Steven Hoekstra.
Science | 2006
Joop J. Gilijamse; Steven Hoekstra; Sebastiaan Y. T. van de Meerakker; Gerrit C. Groenenboom; Gerard Meijer
Molecular scattering behavior 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 absolute velocity by passing the beam through a Stark decelerator. 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, with an overall energy resolution of about 13 wavenumbers. The behavior 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.
Journal of Chemical Physics | 2007
Joop J. Gilijamse; Steven Hoekstra; Samuel A. Meek; Markus Metsala; Sebastiaan Y. T. van de Meerakker; Gerard Meijer; Gerrit C. Groenenboom
We present a combined experimental and theoretical study on the radiative lifetime of CO in the a (3)Pi(1,2), v=0 state. CO molecules in a beam are prepared in selected rotational levels of this metastable state, Stark-decelerated, and electrostatically trapped. From the phosphorescence decay in the trap, the radiative lifetime is measured to be 2.63+/-0.03 ms for the a (3)Pi(1), v=0, J=1 level. From the spin-orbit coupling between the a (3)Pi and the A (1)Pi states a 20% longer radiative lifetime of 3.16 ms is calculated for this level. It is concluded that coupling to other (1)Pi states contributes to the observed phosphorescence rate of metastable CO.
Physical Review A | 2010
T. A. Isaev; Steven Hoekstra; Robert Berger
The parameter W{sub a}, which characterizes nuclear-spin-dependent parity violation (PV) in the molecular spin-rotational Hamiltonian, was computed with a quasirelativistic Hartree-Fock approach for radium fluoride (RaF) and found to be one of the largest absolute values predicted so far. The peculiar electronic structure of RaF leads to highly diagonal Franck-Condon matrices between the energetically lowest two electronic states, which qualifies RaF for direct laser cooling. A subset of diatomic molecules with a wide range of internal structures suitable for this cooling technique is also indicated. As trapped cold molecules offer superior coherence times, RaF can be considered promising for high-precision experiments aimed at molecular PV.
Physical Review A | 2007
Steven Hoekstra; Markus Metsala; Peter C. Zieger; Ludwig Scharfenberg; Joop J. Gilijamse; Gerard Meijer; Sebastiaan Y. T. van de Meerakker
We report on the Stark deceleration and electrostatic trapping of
Journal of Physics B | 2006
Sebastiaan Y. T. van de Meerakker; Irena Labazan; Steven Hoekstra; Jochen Küpper; Gerard Meijer
^{14}\text{N}\text{H}
Physical Review Letters | 2013
Marina Quintero-Pérez; P.G.W. Jansen; Thomas E. Wall; Joost E. van der Berg; Steven Hoekstra; Hendrick L. Bethlem
arXiv: Nuclear Experiment | 2013
H. W. Wilschut; Elwin Dijck; Steven Hoekstra; Klaus-Peter Jungmann; S. Müller; J. P. Noordmans; C. J. G. Onderwater; C. Pijpker; A. Sytema; Robertus Timmermans; K. Keri Vos; Lorenz Willmann
(a^{1}\ensuremath{\Delta})
Physical Review A | 2006
Joop J. Gilijamse; Jochen Küpper; Steven Hoekstra; Nicolas Vanhaecke; Sebastiaan Y. T. van de Meerakker; Gerard Meijer
radicals. In the trap, the molecules are excited on the spin-forbidden
European Physical Journal D | 2010
Joop J. Gilijamse; Steven Hoekstra; Nicolas Vanhaecke; S.Y.T. van de Meerakker; Gerard Meijer
A^{3}\ensuremath{\Pi}\ensuremath{\leftarrow}a^{1}\ensuremath{\Delta}
Journal of Molecular Spectroscopy | 2014
Marina Quintero-Pérez; Thomas E. Wall; Steven Hoekstra; Hendrick L. Bethlem
transition and detected via their subsequent fluorescence to the