The dynamics of dissociative chemisorption of oxygen on Cu(110) and Cu(100) has been studied using a time-dependent quantum wave-packet approach. Dissociation probabilities for O2 on both (110) and (100) surfaces of copper are calculated for ground state as well as rovibrationally excited oxygen molecules. The present calculation simulates O2 dissociation on nascent copper surfaces with no consideration for surface reconstruction. The dynamics calculation is based on a flat-surface model in which three molecular degrees of freedom are explicitly included while the lateral coordinates of the molecule are neglected. The interaction potential energy surface (PES) for the dynamics calculation is constructed using the LEPS (London-Erying-Polyni-Sato) PES form with potential parameters fitted to some available experimental and theoretical data. The barrier of the LEPS PES for oxygen dissociation on copper is 0.11 eV for Cu(110) and 0.08 eV for Cu(100). Relatively speaking, the saddle point of the O2/Cu(110) PES is located near the entrance channel, while that of the O2/Cu(100) is near the product channel. This feature is primarily responsible for the difference in calculated dissociation probabilities of oxygen on two surfaces. Specifically, the dissociation probability of O2 on Cu(110) is large and less sensitive to the vibrational excitation of the molecule, while that of O2 on Cu(100) is much smaller and more sensitive to vibrational excitation of the molecule.
|Original language||English (US)|
|Number of pages||6|
|Journal||Journal of Physical Chemistry|
|Publication status||Published - Jul 4 1996|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry