Article ID Journal Published Year Pages File Type
5391075 Chemical Physics Letters 2006 5 Pages PDF
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 → 360° sphere. This produces a better separation of different reaction mechanisms than previous θ = 0  → 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
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
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