Reaction-diffusion front propagation across stepped surfaces during catalytic oxidation of CO on Pt(100)

verfasst von: M. Tammaro, J. W. Evans, C. S. Rastomjee, W. Swiech, A. M. Bradshaw, R. Imbihl
Abstract: High-resolution microscopy studies of the removal of CO-adlayers on Pt(100) by exposure to oxygen reveal that reaction-diffusion front propagation is impeded both by mesoscopic step bunches and by monoatomic steps. The resulting "stop-and-go" nature to front propagation can be characterized in terms of a time delay for crossing each step bunch or step, at least when the separation of these defects is comparable to or exceeds the width of the front. Here, we quantify this time delay in terms of the reduced diffusion coefficient for CO in step bunch regions and the width of these regions, or in terms of the reduced hop rate for CO across monoatomic steps. We also briefly examine front propagation across arrays of more closely spaced steps. Results facilitate assessment of terrace diffusivities from average or macroscopic front propagation velocities across multiply stepped surfaces.
Organisationseinheit(en): Institut für Physikalische Chemie und Elektrochemie
Externe Organisation(en): University of Rhode Island
Fritz-Haber-Institut der Max-Planck-Gesellschaft
University of Illinois Urbana-Champaign (UIUC)
Iowa State University
Typ: Artikel
Journal: Surface science
Band: 407
Seiten: 162-170
Anzahl der Seiten: 9
ISSN: 0039-6028
Publikationsdatum: 30.11.1998
Publikationsstatus: Veröffentlicht
Peer-reviewed: Ja
ASJC Scopus Sachgebiete: Physik der kondensierten Materie, Oberflächen und Grenzflächen, Oberflächen, Beschichtungen und Folien, Werkstoffchemie
Elektronische Version(en): https://doi.org/10.1016/S0039-6028(98)00168-X (Zugang: Geschlossen)

BibTeX

@article{ab3ff6c8274d49179dcd283156238cd0,
title = "Reaction-diffusion front propagation across stepped surfaces during catalytic oxidation of CO on Pt(100)",
abstract = "High-resolution microscopy studies of the removal of CO-adlayers on Pt(100) by exposure to oxygen reveal that reaction-diffusion front propagation is impeded both by mesoscopic step bunches and by monoatomic steps. The resulting {"}stop-and-go{"} nature to front propagation can be characterized in terms of a time delay for crossing each step bunch or step, at least when the separation of these defects is comparable to or exceeds the width of the front. Here, we quantify this time delay in terms of the reduced diffusion coefficient for CO in step bunch regions and the width of these regions, or in terms of the reduced hop rate for CO across monoatomic steps. We also briefly examine front propagation across arrays of more closely spaced steps. Results facilitate assessment of terrace diffusivities from average or macroscopic front propagation velocities across multiply stepped surfaces.",
keywords = "CO-oxidation, Pt(100), Reaction-diffusion fronts, Steps, Surface diffusion",
author = "M. Tammaro and Evans, {J. W.} and Rastomjee, {C. S.} and W. Swiech and Bradshaw, {A. M.} and R. Imbihl",
note = "Funding Information: The work of M.T. and J.W.E. was supported by the Division of Chemical Sciences, Basic Energy Sciences, USDOE. It was performed at Ames Laboratory, which is operated for the USDOE by Iowa State University under Contract No. W-7405-Eng-82.",
year = "1998",
month = nov,
day = "30",
doi = "10.1016/S0039-6028(98)00168-X",
language = "English",
volume = "407",
pages = "162--170",
journal = "Surface science",
issn = "0039-6028",
publisher = "Elsevier",
number = "1-3",
}