HYSTERESIS EFFECTS AND LONG-PERIOD OSCILLATIONS OF THE D-2 NO REACTION ON RH(110)/

Citation
S. Heinze et al., HYSTERESIS EFFECTS AND LONG-PERIOD OSCILLATIONS OF THE D-2 NO REACTION ON RH(110)/, Surface science, 341(1-2), 1995, pp. 124-132
Citations number
25
Categorie Soggetti
Chemistry Physical
Journal title
ISSN journal
00396028
Volume
341
Issue
1-2
Year of publication
1995
Pages
124 - 132
Database
ISI
SICI code
0039-6028(1995)341:1-2<124:HEALOO>2.0.ZU;2-E
Abstract
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.