Ceria reoxidation by CO2: A model study
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F10%3A10071608" target="_blank" >RIV/00216208:11320/10:10071608 - isvavai.cz</a>
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Ceria reoxidation by CO2: A model study
Original language description
The activation of CO2 on ceria-based catalysts opens chemical routes to the use of CO2 as an oxidizing agent. Toward a better understanding of the underlying surface reactions, we have performed a model study on well-defined CeO2-x thin films on Cu(1 1 1) under ultra-high-vacuum conditions. Resonant photoelectron spectroscopy is used as a highly sensitive tool to monitor changes in the oxidation state of cerium as a function of CO2 exposure and thermal treatment. It is shown that partial reoxidation ofCeO2-x by CO2 occurs with high reaction probabilities (i) even at temperatures as low as room temperature, (ii) on pure CeO2-x in the complete absence of any noble metal co-catalysts, and (iii) in the absence of surface hydroxyl groups or water. In contrast to previous studies on ceria powders, the findings clearly demonstrate the high activity of pure hydroxyl- and metal-free ceria surfaces for CO2 activation, even at low reaction temperatures.
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
BM - Solid-state physics and magnetism
OECD FORD branch
—
Result continuities
Project
<a href="/en/project/LA08022" target="_blank" >LA08022: Participation of Czech scientists in synchrotron radiation experiments at Elettra</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2010
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Catalysis
ISSN
0021-9517
e-ISSN
—
Volume of the periodical
275
Issue of the periodical within the volume
1
Country of publishing house
US - UNITED STATES
Number of pages
5
Pages from-to
—
UT code for WoS article
000283409900018
EID of the result in the Scopus database
—