The oxidation kinetics of the Ni(111) surface have been quantitatively exam
ined utilizing kinetic energy selected supersonic beams of molecular oxygen
. Using in-situ high-resolution electron-energy-loss spectroscopy, we have
observed notable differences in the oxidation mechanism for this interface
asa function of incident-beam kinetic energy. Exposure of a 300-K surface t
o a relatively low-energy 60 meV O-2 beam leads to oxidation kinetics that
follow an island growth model, qualitatively similar to what is seen with s
imple ambient gas dosing. In contrast to this, exposure to a relatively hig
h-energy 600 meV O-2 beam yielded a fundamentally different oxidation behav
ior: the kinetics of oxidation no longer follow an island growth model but
rather behave with a Langmuir-like sticking model, implying key differences
in the nucleation stage for interface oxidation. Cryogenically cooled Ni(l
ll) could not be oxidized using either of these incident-beam conditions, i
ndicating that the energetic constraints needed to move from oxygen chemiso
rption to actual metallic oxidation cannot be simply overcome using inciden
t O-2 kinetic energy. (C) 1998 Published by Elsevier Science B.V. All right
s reserved.