Details
Originalsprache | Englisch |
---|---|
Seiten (von - bis) | 22539-22546 |
Seitenumfang | 8 |
Fachzeitschrift | Journal of Physical Chemistry C |
Jahrgang | 125 |
Ausgabenummer | 41 |
Frühes Online-Datum | 12 Okt. 2021 |
Publikationsstatus | Veröffentlicht - 21 Okt. 2021 |
Abstract
With LEEM (low-energy electron microscopy) and micro-LEED as in situ techniques we have studied the structural transitions in the excitation of traveling interface pulses (TIPs) in bistable methanol oxidation on a bare Rh(110) and on a Rh(110) surface covered with a 0.1 monolayer of V oxide in the 10-4 mbar range. Close to equistability, a (1×1) structure coexists with O-induced reconstructions of the "missing row"type at the interface. An oxidation pulse traveling along the interface exhibits a substructure consisting of various reconstructions of the "missing row"type; on the reduced surface, the slow development of a c(2×2) structure is accompanied by a strong loss of the (0,0)-beam intensity. The addition of 0.1 monolayer of V oxide increases structural disorder but causes no qualitative changes in the structural transitions.
ASJC Scopus Sachgebiete
- Werkstoffwissenschaften (insg.)
- Elektronische, optische und magnetische Materialien
- Energie (insg.)
- Chemie (insg.)
- Physikalische und Theoretische Chemie
- Werkstoffwissenschaften (insg.)
- Oberflächen, Beschichtungen und Folien
Zitieren
- Standard
- Harvard
- Apa
- Vancouver
- BibTex
- RIS
in: Journal of Physical Chemistry C, Jahrgang 125, Nr. 41, 21.10.2021, S. 22539-22546.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Structural Transitions Driving Interface Pulses in Methanol Oxidation on Rh(110) and VOx/Rh(110)
T2 - A LEEM Study
AU - von Boehn, Bernhard
AU - Krisponeit, Jon-Olaf
AU - Falta, Jens
AU - Imbihl, Ronald
N1 - Funding Information: The authors are indebted to the Deutsche Forschungsgemeinschaft (DFG) for financial support through projects: 409299786 and 408002857. B.v.B. would like to thank the Department of Inorganic Chemistry of the Fritz Haber Institute of the Max Planck Society for financial support.
PY - 2021/10/21
Y1 - 2021/10/21
N2 - With LEEM (low-energy electron microscopy) and micro-LEED as in situ techniques we have studied the structural transitions in the excitation of traveling interface pulses (TIPs) in bistable methanol oxidation on a bare Rh(110) and on a Rh(110) surface covered with a 0.1 monolayer of V oxide in the 10-4 mbar range. Close to equistability, a (1×1) structure coexists with O-induced reconstructions of the "missing row"type at the interface. An oxidation pulse traveling along the interface exhibits a substructure consisting of various reconstructions of the "missing row"type; on the reduced surface, the slow development of a c(2×2) structure is accompanied by a strong loss of the (0,0)-beam intensity. The addition of 0.1 monolayer of V oxide increases structural disorder but causes no qualitative changes in the structural transitions.
AB - With LEEM (low-energy electron microscopy) and micro-LEED as in situ techniques we have studied the structural transitions in the excitation of traveling interface pulses (TIPs) in bistable methanol oxidation on a bare Rh(110) and on a Rh(110) surface covered with a 0.1 monolayer of V oxide in the 10-4 mbar range. Close to equistability, a (1×1) structure coexists with O-induced reconstructions of the "missing row"type at the interface. An oxidation pulse traveling along the interface exhibits a substructure consisting of various reconstructions of the "missing row"type; on the reduced surface, the slow development of a c(2×2) structure is accompanied by a strong loss of the (0,0)-beam intensity. The addition of 0.1 monolayer of V oxide increases structural disorder but causes no qualitative changes in the structural transitions.
UR - http://www.scopus.com/inward/record.url?scp=85118214079&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.1c06106
DO - 10.1021/acs.jpcc.1c06106
M3 - Article
AN - SCOPUS:85118214079
VL - 125
SP - 22539
EP - 22546
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
SN - 1932-7447
IS - 41
ER -