The reaction of D-2 with NO on Rh(110) was studied by means of quadrup
ole mass spectrometry in combination with work function measurements (
Delta Phi) and low-energy electron diffraction (LEED). A strong hyster
esis of the D2O production was found in the temperature range between
650 and 1050 K. This effect was most pronounced for a partial pressure
ratio D-2/NO = 1.2 at a total pressure in the 10(-6) mbar range. The
different reactivities of the hysteresis loop were found to be correla
ted with variable oxygen coverages, Theta(0). This was concluded from
the observation of specific LEED patterns, i.e. from the occurrence of
an oxygen-induced c(2 X 8) pattern (Theta(0) similar to 0.85 monolaye
r) in the low-reactivity branch and, respectively, of a (1 X 1) Rh pat
tern with insignificant oxygen coverages in the high-reactivity branch
. The change from low to high reactivity was found to involve transien
t c(2 X 6) and np(2 X 2) LEED patterns. Rate oscillations were found t
o occur with long periods, typically between 23 and 33 min, at 850-950
K. These oscillations could only be induced by a rapid change in the
D-2/NO ratio from 1.2 to 0.85 (at a total pressure of 6.5 X 10(-6) mba
r) and were stable for several hours with only slight variations in am
plitude and frequency. Simultaneous measurements of the work function
revealed a strong correlation with the D2O production rate, i.e. Delta
Phi was high when the reaction rate was low and vice versa, indicatin
g that the oscillations were associated with variations of the oxygen
surface coverage. The results are discussed within a kinetic model of
the catalytic cycle.