Abstract

The cross section for charge transfer to fully stripped carbon ions in collision with ground-state hydrogen atoms is calculated in an adiabatic molecular-orbital basis. In contrast to previous work by Salop and Olson (1976), the cross section obtained by retaining only the dominant 4f sigma -5g sigma radial coupling is oscillatory. The inclusion of rotational coupling to other close-lying states damps out these oscillations to provide a smoothly varying cross section whose magnitude is considerably enhanced over that obtained from the two-state calculation.

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