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Journal of Physics B Atomic Molecular and Optical Physics

An electrostatic mirror for neutral polar molecules

Steven J. Wark, G. I. Opat

Published Oct 28, 1992• 18 citations
Publisher

Abstract

An electrostatic mirror for neutral polar molecules has been constructed using an array of electrodes of alternating polarity between which a high potential was applied. This configuration produces an exponentially evanescing electric field that interacts with polar molecules by the Stark effect. The spatial gradients of the Stark energies produce forces which were used to reflect a pulsed beam of chloromethane (CH 3 Cl) molecules with a reflectivity of 25% at grazing angles of incidence of around 5 mrad. Reflections have also been produced with applied voltages as low as 100 V or with grazing angles greater than 20 mrad. This type of device could be useful for the manipulation of slow molecular beams and would permit the construction of optical elements for the de Broglie waves of molecules.

DOI
10.1088/0953-4075/25/20/018

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An electrostatic mirror for neutral polar molecules has been constructed using an array of electrodes of alternating polarity between which a high potential was applied. This configuration produces an exponentially evanescing electric field that interacts with polar molecules by the Stark effect. The spatial gradients of the Stark energies produce forces which were used to reflect a pulsed beam of chloromethane (CH 3 Cl) molecules with a reflectivity of 25% at grazing angles of incidence of around 5 mrad. Reflections have also been produced with applied voltages as low as 100 V or with grazing angles greater than 20 mrad. This type of device could be useful for the manipulation of slow molecular beams and would permit the construction of optical elements for the de Broglie waves of molecules.
Focusing optics for neutral molecules finds application in shaping and steering molecular beams. Here we present an electrostatic elliptical mirror for polar molecules consisting of an array of microstructured gold electrodes deposited on a glass substrate. Alternating positive and negative voltages applied to the electrodes create a repulsive potential for molecules in low-field-seeking states. The equipotential lines are parallel to the substrate surface, which is bent in an elliptical shape. The mirror is characterized by focusing a beam of metastable CO molecules and the results are compared to the outcome of trajectory simulations.
Focusing optics for neutral molecules finds application in shaping and steering molecular beams. Here we present an electrostatic elliptical mirror for polar molecules consisting of an array of microstructured gold electrodes deposited on a glass substrate. Alternating positive and negative voltages applied to the electrodes create a repulsive potential for molecules in low-field-seeking states. The equipotential lines are parallel to the substrate surface, which is bent in an elliptical shape. The mirror is characterized by focusing a beam of metastable CO molecules and the results are compared to the outcome of trajectory simulations.
By miniaturizing electrode geometries high electric fields can be produced using modest voltages. A planar array of $20\text{ }\ensuremath{\mu}\mathrm{m}$ wide gold electrodes, spaced $20\text{ }\ensuremath{\mu}\mathrm{m}$ apart, is made on a sapphire substrate. A voltage difference of up to 350 V is applied to adjacent electrodes, generating an electric field that decreases exponentially with distance from the substrate. This microstructured array can be used as a mirror for polar molecules and can be rapidly switched on and off. This is demonstrated by retro\penalty1000\-\allowhyphens{}reflecting a beam of state-selected ammonia molecules with a forward velocity of about 30  m/s30\text{ }\text{ }\mathrm{m}/\mathrm{s}30  m/s.
Summary form only given. Acceleration of molecules within a time varying electric field produced by an optical traveling wave has been proposed as a means to accelerate neutral particles to high velocity. This technique is attractive because extremely large Stark forces can be produced by the high electric field gradients that can be created within an optical traveling wave. The electrodeless electric field gradient produced by focused laser beams can be orders of magnitude greater than electrostatic gradients, allowing acceleration of polar as well as polarizable molecules and atoms. This concept has already been used to accelerate ultracold atoms in a very weak optical periodic potentials, or lattices, and acceleration up to the velocities in the m/s velocity was observed. We report on the study of acceleration of polarizable particles to velocities in excess of 10 km/s range in an accelerated optical lattice, using high intensity pulsed fields.
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.
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.