Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 4319-4326 |
| Seitenumfang | 8 |
| Fachzeitschrift | Journal of Chemical Physics |
| Jahrgang | 106 |
| Ausgabenummer | 10 |
| Publikationsstatus | Veröffentlicht - 8 März 1997 |
Abstract
Previous investigations have demonstrated that the formation of chemical waves in the NO+H2 reaction on Rh(110) involves a cyclic transformation of the surface structure via various N,O-induced reconstructions, i.e., starting form the c(2×6)-O a cycle is initiated comprising the formation of a (2×3)/(3×1)-N and a mixed c(2×4)-2O,N structure. The stability and reactivity of these structures has been investigated in titration experiments as well as under stationary reaction conditions employing LEED, work function, rate measurements, and thermal desorption spectroscopy. It was shown that the c(2×6)-O and c(2×4)-2O,N structures exhibit a low reactivity whereas the (2×1)/(2×1)-N displays only a small to moderate decrease in catalytic activity (≈20%-30%) compared to the clean surface. On the basis of these results, an excitation mechanism for pulses in the NO+H2 reaction on Rh(110) was constructed consisting of the sequence c(2×6)-O, (2×1)/(3×1)-N c(2×4)-2O,N, c(2×6)-O.
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in: Journal of Chemical Physics, Jahrgang 106, Nr. 10, 08.03.1997, S. 4319-4326.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - The role of structural changes in the excitation of chemical waves in the system Rh(110)/NO+H2
AU - Mertens, F.
AU - Schwegmann, S.
AU - Imbihl, R.
PY - 1997/3/8
Y1 - 1997/3/8
N2 - Previous investigations have demonstrated that the formation of chemical waves in the NO+H2 reaction on Rh(110) involves a cyclic transformation of the surface structure via various N,O-induced reconstructions, i.e., starting form the c(2×6)-O a cycle is initiated comprising the formation of a (2×3)/(3×1)-N and a mixed c(2×4)-2O,N structure. The stability and reactivity of these structures has been investigated in titration experiments as well as under stationary reaction conditions employing LEED, work function, rate measurements, and thermal desorption spectroscopy. It was shown that the c(2×6)-O and c(2×4)-2O,N structures exhibit a low reactivity whereas the (2×1)/(2×1)-N displays only a small to moderate decrease in catalytic activity (≈20%-30%) compared to the clean surface. On the basis of these results, an excitation mechanism for pulses in the NO+H2 reaction on Rh(110) was constructed consisting of the sequence c(2×6)-O, (2×1)/(3×1)-N c(2×4)-2O,N, c(2×6)-O.
AB - Previous investigations have demonstrated that the formation of chemical waves in the NO+H2 reaction on Rh(110) involves a cyclic transformation of the surface structure via various N,O-induced reconstructions, i.e., starting form the c(2×6)-O a cycle is initiated comprising the formation of a (2×3)/(3×1)-N and a mixed c(2×4)-2O,N structure. The stability and reactivity of these structures has been investigated in titration experiments as well as under stationary reaction conditions employing LEED, work function, rate measurements, and thermal desorption spectroscopy. It was shown that the c(2×6)-O and c(2×4)-2O,N structures exhibit a low reactivity whereas the (2×1)/(2×1)-N displays only a small to moderate decrease in catalytic activity (≈20%-30%) compared to the clean surface. On the basis of these results, an excitation mechanism for pulses in the NO+H2 reaction on Rh(110) was constructed consisting of the sequence c(2×6)-O, (2×1)/(3×1)-N c(2×4)-2O,N, c(2×6)-O.
UR - http://www.scopus.com/inward/record.url?scp=0000402141&partnerID=8YFLogxK
U2 - 10.1063/1.473133
DO - 10.1063/1.473133
M3 - Article
AN - SCOPUS:0000402141
VL - 106
SP - 4319
EP - 4326
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
SN - 0021-9606
IS - 10
ER -