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arXiv:physics/0604020 · Journal of Physics B Atomic Molecular and Optical Physics

Alternating gradient focusing and deceleration of polar molecules

Hendrick L. Bethlem, Michael R. Tarbutt, Jochen Küpper, David Carty, Kirstin Wohlfart, E. A. Hinds, Gerard Meijer

Published Aug 8, 2006• 86 citations
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Abstract

Beams of polar molecules can be focused using an array of electrostatic lenses in alternating gradient (AG) configuration. They can also be accelerated or decelerated by applying an appropriate high-voltage switching sequence to the lenses. AG focusing is applicable to molecules in both low-field- and high-field-seeking states and is particularly well suited to the problem of decelerating heavy molecules and those in their ground rotational state. We describe the principles of AG deceleration and set out criteria to be followed in decelerator design, construction and operation. We calculate the longitudinal and transverse focusing properties of a decelerator, and exemplify this by 2D-imaging studies of a decelerated beam of metastable CO molecules.

DOI
10.1088/0953-4075/39/16/r01

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Beams of polar molecules can be focused using an array of electrostatic lenses in alternating gradient (AG) configuration. They can also be accelerated or decelerated by applying an appropriate high-voltage switching sequence to the lenses. AG focusing is applicable to molecules in both low-field- and high-field-seeking states and is particularly well suited to the problem of decelerating heavy molecules and those in their ground rotational state. We describe the principles of AG deceleration and set out criteria to be followed in decelerator design, construction and operation. We calculate the longitudinal and transverse focusing properties of a decelerator, and exemplify this by 2D-imaging studies of a decelerated beam of metastable CO molecules.
Neutral dipolar molecules can be decelerated and trapped using time-varying inhomogeneous electric fields. This has been demonstrated only for molecules in low-field seeking states, but can, in principle, be performed on molecules in high-field seeking states as well. Transverse stability is then much more difficult to obtain, however, since molecules in high-field seeking states always experience a force towards the electrodes. Here we demonstrate that an array of dipole lenses in alternate gradient configuration can be used to maintain transverse stability. A pulsed beam of metastable CO in high-field seeking states is accelerated from 275 to 289 m/s as well as decelerated from 275 to 260 m/s.
We have decelerated a supersonic beam of 174YbF molecules using a switched sequence of electrostatic field gradients. These molecules are 7 times heavier than any previously decelerated. An alternating gradient structure allows us to decelerate and focus the molecules in their ground state. We show that the decelerator exhibits the axial and transverse stability required to bring the molecules to rest. Our work significantly extends the range of molecules amenable to this powerful method of cooling and trapping.
We have focused and decelerated benzonitrile (C7H5N)({\mathrm{C}}_{7}{\mathrm{H}}_{5}\mathrm{N})(C7​H5​N) molecules from a molecular beam, using an array of time-varying inhomogeneous electric fields in alternating-gradient configuration. Benzonitrile is prototypical for large asymmetric top molecules that exhibit rich rotational structure and a high density of states. At the rotational temperature of 3.5K3.5\phantom{\rule{0.3em}{0ex}}\mathrm{K}3.5K in the pulsed molecular beam, many rotational states are populated. Benzonitrile molecules in their absolute ground state are decelerated from 320to289m∕s320\phantom{\rule{0.3em}{0ex}}\text{to}\phantom{\rule{0.3em}{0ex}}289\phantom{\rule{0.3em}{0ex}}\mathrm{m}∕\mathrm{s}320to289m∕s, and similar changes in velocity are obtained for excited rotational states. All measurements agree well with the outcome of trajectory calculations. These experiments demonstrate that such large polyatomic molecules are amenable to the powerful method of Stark deceleration.
We report on the experimental realization of a microwave decelerator for neutral polar molecules, suitable for decelerating and focusing molecules in high-field-seeking states. The multistage decelerator consists of a cylindrical microwave cavity oscillating in the TE11n{}_{\mathit{11}\mathit{n}}11n​ mode, with n=12n=12n=12 electric field maxima along the symmetry axis. By switching the microwave field on and off at the appropriate times, a beam of state-selected ammonia molecules with an incident mean velocity of 25 m/s is guided while being spatially focused in the transverse direction and bunched in the forward direction. Deceleration from 20.0 to 16.9 m/s and acceleration from 20.0 to 22.7 m/s are demonstrated.
Inspired by the spectacular successes in the field of cold atoms, there is currently great interest in cold molecules. Cooling molecules is useful for various fundamental physics studies and gives access to an exotic regime in chemistry where the wave property of the molecules becomes important. Although cooling molecules has turned out to be considerably more difficult than cooling atoms, a number of methods to produce samples of cold molecules have been demonstrated over the last few years. This paper aims to review the application of cold molecules and the methods to produce them. Emphasis is put on the deceleration of polar molecules using time-varying electric fields. The operation principle of the array of electrodes that is used to decelerate polar molecules is described in analogy with, and using terminology from, charged-particle accelerators. It is shown that, by applying an appropriately timed high voltage burst, molecules can be decelerated while the phase-space density, i.e. the number of molecules per position-velocity interval, remains constant. In this way the high density and low temperature in the moving frame of a pulsed molecular beam can be transferred to the laboratory frame. Experiments on metastable CO in states that are either repelled by or attracted to high electric fields are presented. Loading of slow molecules into traps and storage rings is discussed.