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Bulletin of the American Physical Society

Decelerating and Trapping Larger Polar Molecules

David Patterson

Published Jun 11, 2015• 0 citations
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Decelerating and Trapping Large Polar Molecules

David Patterson

Abstract Manipulating the motion of large polyatomic molecules, such as benzonitrile (C6H5CN), presents significant difficulties compared to the manipulation of diatomic molecules. Although recent impressive results have demonstrated manipulation, trapping, and cooling of molecules as large as CH3F, no general technique for trapping such molecules has been demonstrated, and cold neutral molecules larger than 5 atoms have not been trapped (M. Zeppenfeld, B. G. U. Englert, R. Glöckner, A. Prehn, M. Mielenz, C. Sommer, L. D. van Buuren, M. Motsch, G. Rempe, Nature 2012, 491, 570–573 ). In particular, extending Stark deceleration and electrostatic trapping to such species remains challenging. Here, we propose to combine a novel “asymmetric doublet state” Stark decelerator with recently demonstrated slow, cold, buffer‐gas‐cooled beams of closed‐shell volatile molecules to realize a general system for decelerating and trapping samples of a broad range of volatile neutral polar prolate asymmetric top molecules. The technique is applicable to most stable volatile molecules in the 100–500 AMU range, and would be capable of producing trapped samples in a single rotational state and at a motional temperature of hundreds of mK. Such samples would immediately allow for spectroscopy of unprecedented resolution, and extensions would allow for further cooling and direct observation of slow intramolecular processes such as vibrational relaxation and Hertz‐level tunneling dynamics.

ChemPhysChem•Jul 25, 2016•3 citations
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.
Abstract Manipulating the motion of large polyatomic molecules, such as benzonitrile (C6H5CN), presents significant difficulties compared to the manipulation of diatomic molecules. Although recent impressive results have demonstrated manipulation, trapping, and cooling of molecules as large as CH3F, no general technique for trapping such molecules has been demonstrated, and cold neutral molecules larger than 5 atoms have not been trapped (M. Zeppenfeld, B. G. U. Englert, R. Glöckner, A. Prehn, M. Mielenz, C. Sommer, L. D. van Buuren, M. Motsch, G. Rempe, Nature 2012, 491, 570–573 ). In particular, extending Stark deceleration and electrostatic trapping to such species remains challenging. Here, we propose to combine a novel “asymmetric doublet state” Stark decelerator with recently demonstrated slow, cold, buffer‐gas‐cooled beams of closed‐shell volatile molecules to realize a general system for decelerating and trapping samples of a broad range of volatile neutral polar prolate asymmetric top molecules. The technique is applicable to most stable volatile molecules in the 100–500 AMU range, and would be capable of producing trapped samples in a single rotational state and at a motional temperature of hundreds of mK. Such samples would immediately allow for spectroscopy of unprecedented resolution, and extensions would allow for further cooling and direct observation of slow intramolecular processes such as vibrational relaxation and Hertz‐level tunneling dynamics.