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Ion-molecule chemistry at very low temperatures : cold chemical reactions between Coulomb-crystallized ions and velocity-selected neutral molecules

Bell, Martin T. and Gingell, Alexander D. and Oldham, James M. and Softley, Timothy P. and Willitsch, Stefan. (2009) Ion-molecule chemistry at very low temperatures : cold chemical reactions between Coulomb-crystallized ions and velocity-selected neutral molecules. In: Faraday Discussions, 142. London, pp. 73-91.

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Official URL: http://edoc.unibas.ch/dok/A5251873

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Abstract

The recent development of a range of techniques for producing cold atoms and molecules at very low translational temperatures T >= 1 K has provided the opportunity to investigate collisional processes in a new physical regime. We have recently presented a new experimental method to study low-temperature reactive collisions between translationally cold ions and neutral molecules (S. Willitsch et al., Phys. Rev. Lett. 2008, 100, 043203). Our technique relies on the combination of a quadrupole-guide velocity selector for the generation of translationally cold neutral molecules with a facility to produce ordered structures of cold ions (Coulomb crystals) by laser cooling in a linear quadrupole ion trap. The strong localisation of the ions in the trap in combination with the high sensitivity of laser-induced-fluorescence detection enabled us to study chemical reactions on the single-particle level, down to temperatures of T approximate to 1 K. In the current paper, we present a detailed characterisation of the scope and limitations of this method based on our study of the reaction between laser-cooled Ca+ ions and velocity-selected CH3F molecules. The properties of our cold-neutrals source and the dependence of the measured rate constant on the shape of the Coulomb crystals, trapping and laser-cooling parameters are discussed. An extension of our technique for the study of low-temperature reactions with sympathetically cooled molecular ions (translational temperature T < 10 mK) i s presented and first results on the charge-transfer reaction between OCS+ and ND3 are discussed. Finally, perspectives for further developments of our method are explored.
Faculties and Departments:05 Faculty of Science > Departement Chemie > Chemie > Chemische Physik (Willitsch)
UniBasel Contributors:Willitsch, Stefan
Item Type:Conference or Workshop Item, refereed
Conference or workshop item Subtype:Conference Paper
Publisher:Royal Society of Chemistry
ISSN:1359-6640
e-ISSN:1364-5498
Note:Publication type according to Uni Basel Research Database: Conference paper
Identification Number:
Last Modified:03 May 2017 13:04
Deposited On:22 Mar 2012 14:01

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