Abstract
The
reactive and inelastic scattering dynamics of
ground-state atomic and molecular oxygen from a carbon fiber network at 1023-1823 K was
investigated with a molecular beam-surface scattering technique. A molecular beam containing hyperthermal O and O2
with a mole ratio of 0.92:0.08 and nominal velocity of 8 km s-1 was
directed at the network, and time-of-flight distributions of the scattered
products were collected at various angles with the use of a rotatable mass
spectrometer detector. O atoms exhibited both impulsive scattering (IS)
and thermal desorption (TD) dynamics, where the TD O-atom flux
increased with surface temperature and the IS O-atom flux remained relatively constant. While the
majority of the TD O atoms desorbed promptly after the beam pulse struck the
network, signatures of thermal processes occurring over long residence times
were also observed. Evidence of O2 reactions was not observed, and
the behavior of the inelastically scattered O2 was invariant to the
temperature of the network and showed both IS and TD dynamics. The dominant reactive product was CO, whereas CO2
was a minor product. Both these products showed only TD dynamics. The observed
flux of CO initially increased with temperature and then reached a plateau
above which the flux no longer increased with temperature, over the temperature
range studied. Thermally desorbed CO products exited the network promptly or
after relatively long residence times, and two populations of CO with long
residence times were distinguished. Hysteresis was observed in the
temperature-dependent flux of thermally desorbed O and CO, with opposing trends
for the two products. This work follows similar studies in our
laboratory where the target materials were vitreous carbon and highly oriented
pyrolytic graphite. The data suggest that the chemical reactivity of the three
forms of sp2 carbon surfaces
is similar and that the differences arise from the variations of the
morphology.