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Dynamics of chemical reactions at cold and ultracold temperatures

P F Weck and N Balakrishnan

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The main characteristics of cold and ultracold chemical reactions are reviewed through the illustrative study of the O(3P) + H2 reaction dynamics. Using separate analytic representations of the lowest H2O(3A'') electronic state which differ essentially by their descriptions of long-range forces, quantum-mechanical scattering calculations show the crucial role played by the van der Waals interaction potential in chemical reactions at low temperatures. Furthermore, the presence of zero-energy resonances is found to significantly enhance chemical reactivity in the ultracold regime. At translational energies comparable to the well depth of the van der Waals potential, initial-state-selected probabilities and excitation functions are characterized by Feshbach resonances arising from the decay of quasibound states supported by the van der Waals well in the entrance channel of the reaction.


PACS

82.30.Cf Atom and radical reactions; chain reactions; molecule-molecule reactions

34.20.Gj Intermolecular and atom-molecule potentials and forces

82.20.Kh Potential energy surfaces for chemical reactions

82.60.-s Chemical thermodynamics

82.20.Xr Quantum effects in rate constants (tunneling, resonances, etc.)

82.20.Bc State selected dynamics and product distribution

Subjects

Atomic and molecular physics

Chemical physics and physical chemistry

Dates

Issue 19 (14 October 2006)

Received 27 March 2006

Published 25 September 2006


A Corrigendum for this article has been published in 2006 J. Phys. B: At. Mol. Opt. Phys. 39 5023


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