Vibrational Relaxation of Highly Vibrationally Excited CO Scattered from Au(111): Evidence for CO^– Formation

Abstract

Electronically nonadiabatic dynamics can be important in collisions of molecules at surfaces; for example, when vibrational degrees of freedom of molecules are coupled to electron-hole-pair (EHP) excitation of a metal. Such dynamics have been inferred from a host of observations involving multiquantum relaxation of NO molecules scattered from metal surfaces. Electron transfer forming transient NO^- is thought to be essential to the nonadiabatic coupling. The question remains: is this behavior usual? Here, we present final vibrational state distributions resulting from the scattering of CO(v_i = 17) from Au(111), which exhibits significantly less vibrational relaxation than NO(v_i = 16). We explain this observation in terms of the lower electron affinity of CO compared to NO, a result that is consistent with the formation of a transient CO^- ion being important to CO vibrational relaxation.