Abstract
Several full-dimensional potential energy
surfaces (PESs) are reported for vibrating CO adsorbates at two coverages on a
rigid NaCl(100) surface based on first principles calculations. These PESs
reveal a rather flat energy landscape for physisorption of vibrationless CO on
NaCl(100), evidenced by various C-down adsorption patterns within a small
energy range. Agreement with available
experimental results is satisfactory, although quantitative differences exist.
These PESs are used to explore isomerization pathways between the C-down and
higher energy O-down configurations, which reveal a significant isomerization
barrier. As CO vibration is excited, however, the energy order of the two
isomer changes, which helps to explain the experimental observed flipping of
vibrationally excited CO adsorbates.