Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5391075 | Chemical Physics Letters | 2006 | 5 Pages |
Abstract
The plane wave packet (PWP) and nearside-farside approaches are combined, in order to obtain time-dependent differential cross-sections (DCSs) describing the scattering of a plane wave packet over the full θ = 0 â 360° sphere. This produces a better separation of different reaction mechanisms than previous θ = 0  â 180° PWP calculations. Application to the He+H2+ reaction separates clearly the direct and time-delayed mechanisms, showing that the latter (caused by decay of HeH2+ scattering resonances) does not begin until the HeH2+ complex has rotated by over half a revolution, and then continues until the HeH2+ has described almost an entire revolution. The resulting nearside-farside interference from this decay dominates the (energy-domain) DCS.
Related Topics
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Physical and Theoretical Chemistry
Authors
Aditya N. Panda, Stuart C. Althorpe,