Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:1107.5476 · Review of Scientific Instruments

A traveling wave decelerator for neutral polar molecules

Samuel A. Meek, Maxwell F. Parsons, Georg Heyne, Viktor Platschkowski, Henrik Haak, Gerard Meijer, Andreas Osterwalder

Published Sep 1, 2011• 34 citations
arXivHTMLPDF

Abstract

Recently, a decelerator for neutral polar molecules has been presented that operates on the basis of macroscopic, three-dimensional, traveling electrostatic traps [A. Osterwalder, S. A. Meek, G. Hammer, H. Haak, and G. Meijer, Phys. Rev. A 81, 051401 (2010)]. In the present paper, a complete description of this decelerator is given, with emphasis on the electronics and the mechanical design. Experimental results showing the transverse velocity distributions of guided molecules are shown and compared to trajectory simulations. An assessment of non-adiabatic losses is made by comparing the deceleration signals from (13)CO with those from (12)CO and with simulated signals.

DOI
10.1063/1.3640413

Related papers

Deceleration of neutral molecules in macroscopic traveling traps

Andreas Osterwalder, Samuel A. Meek, Georg Hammer +2 more

A decelerator is presented where polar neutral molecules are guided and decelerated using the principle of traveling electric potential wells, such that molecules are confined in stable three-dimensional traps throughout. We compare this decelerator with that of Scharfenberg et al. [Phys. Rev. A 79, 023410 (2009)] and we show that the current decelerator provides a substantially larger phase-space acceptance, even at higher acceleration. The mode of operation is described and experimentally demonstrated by guiding and decelerating CO molecules.

arXiv:0911.3324•Physical Review A•May 10, 2010•100 citations

Non-adiabatic losses in a traveling-wave Stark decelerator

M. Buisman

Traveling-wave Stark deceleration is a wonderful tool to slow down polar molecules. Once the molecules are slowed down, the molecules can be interrogated by means of spectroscopy and information can be extracted which might lead to new discoveries. Before that can happen, the deceleration process needs to be optimized and losses such as non-adiabatic transitions must be minimized. A computer simulation can help to assist, predict and analyze particle behaviour. The simulation that was previously developed has been extended with a new non-adiabatic transition mechanism based on energy difference between energy states. With the new loss mechanism in place, results have shown that the losses can have a great impact on the spatial particle distribution within the confinement zone.

•Jan 1, 2017•0 citations

A new design for a traveling-wave Zeeman decelerator: II. Experiment

Tomislav Damjanović, Stefan Willitsch, Nicolas Vanhaecke +4 more

A novel traveling-wave Zeeman decelerator based on a double-helix coil geometry capable of decelerating paramagnetic molecules with high efficiency is presented. Moving magnetic traps are generated by applying time-dependent currents through the decelerator coils. Paramagnetic molecules in low-field-seeking Zeeman states are confined inside the moving traps which are decelerated to lower forward velocities. As a prototypical example, we demonstrate the deceleration of OH radicals from an initial velocity of 445 m s −1 down to various final velocities. The experimental results are analyzed and numerically reproduced with the help of trajectory simulations confirming the phase-space stability and efficiency of the deceleration of the molecules in the new device.

arXiv:2108.02593•New Journal of Physics•Oct 1, 2021•11 citations

Static Trapping of Polar Molecules in a Traveling Wave Decelerator

Marina Quintero‐Pérez, Paul Jansen, Thomas E. Wall +3 more

We present experiments on decelerating and trapping ammonia molecules using a combination of a Stark decelerator and a traveling wave decelerator. In the traveling wave decelerator, a moving potential is created by a series of ring-shaped electrodes to which oscillating high voltages (HV) are applied. By lowering the frequency of the applied voltages, the molecules confined in the moving trap are decelerated and brought to a standstill. As the molecules are confined in a true 3D well, this kind of deceleration has practically no losses, resulting in a great improvement on the usual Stark deceleration techniques. The necessary voltages are generated by amplifying the output of an arbitrary wave generator using fast HV amplifiers, giving us great control over the trapped molecules. We illustrate this by experiments in which we adiabatically cool trapped NH3 and ND3 molecules and resonantly excite their motion.

arXiv:1301.2113•Physical Review Letters•Mar 27, 2013•56 citations

Deceleration and trapping of ammonia molecules in a traveling-wave decelerator

Paul Jansen, Marina Quintero‐Pérez, Thomas E. Wall +3 more

We have recently demonstrated static trapping of ammonia isotopologues in a decelerator that consists of a series of ring-shaped electrodes to which oscillating high voltages are applied [Quintero-P\'erez et al., Phys. Rev. Lett. 110, 133003 (2013)]. In this paper we provide further details about this traveling-wave decelerator and present new experimental data that illustrate the control over molecules that it offers. We analyze the performance of our setup under different deceleration conditions and demonstrate phase-space manipulation of the trapped molecular sample.

arXiv:1306.0397•Physical Review A•Oct 21, 2013•23 citations

Deceleration and Trapping of SrF Molecules

Parul Aggarwal, Y. Yin, Kevin Esajas +12 more

We report on the electrostatic trapping of neutral SrF molecules. The molecules are captured from a cryogenic buffer-gas beam source into the moving traps of a 4.5-m-long traveling-wave Stark decelerator. The SrF molecules in X^{2}Σ^{+}(v=0,N=1) state are brought to rest as the velocity of the moving traps is gradually reduced from 190 m/s to zero. The molecules are held for up to 50 ms in multiple electric traps of the decelerator. The trapped packets have a volume (FWHM) of 1 mm^{3} and a velocity spread of 5(1) m/s, which corresponds to a temperature of 60(20) mK. Our result demonstrates a factor 3 increase in the molecular mass that has been Stark decelerated and trapped. Heavy molecules (mass>100 amu) offer a highly increased sensitivity to probe physics beyond the standard model. This work significantly extends the species of neutral molecules of which slow beams can be created for collision studies, precision measurement, and trapping experiments.

arXiv:2103.07968•Physical Review Letters•Oct 21, 2021•30 citations
Recently, a decelerator for neutral polar molecules has been presented that operates on the basis of macroscopic, three-dimensional, traveling electrostatic traps [A. Osterwalder, S. A. Meek, G. Hammer, H. Haak, and G. Meijer, Phys. Rev. A 81, 051401 (2010)]. In the present paper, a complete description of this decelerator is given, with emphasis on the electronics and the mechanical design. Experimental results showing the transverse velocity distributions of guided molecules are shown and compared to trajectory simulations. An assessment of non-adiabatic losses is made by comparing the deceleration signals from (13)CO with those from (12)CO and with simulated signals.
A decelerator is presented where polar neutral molecules are guided and decelerated using the principle of traveling electric potential wells, such that molecules are confined in stable three-dimensional traps throughout. We compare this decelerator with that of Scharfenberg et al. [Phys. Rev. A 79, 023410 (2009)] and we show that the current decelerator provides a substantially larger phase-space acceptance, even at higher acceleration. The mode of operation is described and experimentally demonstrated by guiding and decelerating CO molecules.
Traveling-wave Stark deceleration is a wonderful tool to slow down polar molecules. Once the molecules are slowed down, the molecules can be interrogated by means of spectroscopy and information can be extracted which might lead to new discoveries. Before that can happen, the deceleration process needs to be optimized and losses such as non-adiabatic transitions must be minimized. A computer simulation can help to assist, predict and analyze particle behaviour. The simulation that was previously developed has been extended with a new non-adiabatic transition mechanism based on energy difference between energy states. With the new loss mechanism in place, results have shown that the losses can have a great impact on the spatial particle distribution within the confinement zone.
A novel traveling-wave Zeeman decelerator based on a double-helix coil geometry capable of decelerating paramagnetic molecules with high efficiency is presented. Moving magnetic traps are generated by applying time-dependent currents through the decelerator coils. Paramagnetic molecules in low-field-seeking Zeeman states are confined inside the moving traps which are decelerated to lower forward velocities. As a prototypical example, we demonstrate the deceleration of OH radicals from an initial velocity of 445 m s −1 down to various final velocities. The experimental results are analyzed and numerically reproduced with the help of trajectory simulations confirming the phase-space stability and efficiency of the deceleration of the molecules in the new device.
We present experiments on decelerating and trapping ammonia molecules using a combination of a Stark decelerator and a traveling wave decelerator. In the traveling wave decelerator, a moving potential is created by a series of ring-shaped electrodes to which oscillating high voltages (HV) are applied. By lowering the frequency of the applied voltages, the molecules confined in the moving trap are decelerated and brought to a standstill. As the molecules are confined in a true 3D well, this kind of deceleration has practically no losses, resulting in a great improvement on the usual Stark deceleration techniques. The necessary voltages are generated by amplifying the output of an arbitrary wave generator using fast HV amplifiers, giving us great control over the trapped molecules. We illustrate this by experiments in which we adiabatically cool trapped NH3 and ND3 molecules and resonantly excite their motion.
We have recently demonstrated static trapping of ammonia isotopologues in a decelerator that consists of a series of ring-shaped electrodes to which oscillating high voltages are applied [Quintero-P\'erez et al., Phys. Rev. Lett. 110, 133003 (2013)]. In this paper we provide further details about this traveling-wave decelerator and present new experimental data that illustrate the control over molecules that it offers. We analyze the performance of our setup under different deceleration conditions and demonstrate phase-space manipulation of the trapped molecular sample.
We report on the electrostatic trapping of neutral SrF molecules. The molecules are captured from a cryogenic buffer-gas beam source into the moving traps of a 4.5-m-long traveling-wave Stark decelerator. The SrF molecules in X^{2}Σ^{+}(v=0,N=1) state are brought to rest as the velocity of the moving traps is gradually reduced from 190 m/s to zero. The molecules are held for up to 50 ms in multiple electric traps of the decelerator. The trapped packets have a volume (FWHM) of 1 mm^{3} and a velocity spread of 5(1) m/s, which corresponds to a temperature of 60(20) mK. Our result demonstrates a factor 3 increase in the molecular mass that has been Stark decelerated and trapped. Heavy molecules (mass>100 amu) offer a highly increased sensitivity to probe physics beyond the standard model. This work significantly extends the species of neutral molecules of which slow beams can be created for collision studies, precision measurement, and trapping experiments.