Ordered phases of reduced ceria as inverse model catalysts
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F19%3A10389483" target="_blank" >RIV/00216208:11320/19:10389483 - isvavai.cz</a>
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=udleIJhJoU" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=udleIJhJoU</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.apsusc.2018.09.068" target="_blank" >10.1016/j.apsusc.2018.09.068</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Ordered phases of reduced ceria as inverse model catalysts
Popis výsledku v původním jazyce
Inverse model catalysts represent valuable systems for studying metal-oxide interactions and finite size effects in heterogeneous catalysis. To maximize the potential of model catalytic studies, high level of control over model catalyst properties is desirable. Here we introduce experimental approaches for obtaining inverse ceria/copper model catalysts of well-defined crystallographic phases CeO2, iota-Ce7O12, CeO1.67, and c-Ce2O3 supported on Cu (1 1 1). The presented cerium oxide thin films are ultrathin (2 monolayers), discontinuous, and feature highly defined stoichiometry and crystallographic structure with characteristic (1x1), (root 7x root 7) R19 degrees, (3x3), or (4x4) electron diffraction patterns. Compared to thicker films and bulk ceria, the prepared ultrathin cerium oxides exhibit a distinctly different dependence of the lattice constant on the stoichiometry, and show activation barrier preventing their complete oxidation. These phenomena illustrate that metal-oxide interactions and finite size effects strongly influence the behavior of the presented inverse model catalysts indicating their prospective use in disentangling complex functionalities of ceria/copper catalytic systems.
Název v anglickém jazyce
Ordered phases of reduced ceria as inverse model catalysts
Popis výsledku anglicky
Inverse model catalysts represent valuable systems for studying metal-oxide interactions and finite size effects in heterogeneous catalysis. To maximize the potential of model catalytic studies, high level of control over model catalyst properties is desirable. Here we introduce experimental approaches for obtaining inverse ceria/copper model catalysts of well-defined crystallographic phases CeO2, iota-Ce7O12, CeO1.67, and c-Ce2O3 supported on Cu (1 1 1). The presented cerium oxide thin films are ultrathin (2 monolayers), discontinuous, and feature highly defined stoichiometry and crystallographic structure with characteristic (1x1), (root 7x root 7) R19 degrees, (3x3), or (4x4) electron diffraction patterns. Compared to thicker films and bulk ceria, the prepared ultrathin cerium oxides exhibit a distinctly different dependence of the lattice constant on the stoichiometry, and show activation barrier preventing their complete oxidation. These phenomena illustrate that metal-oxide interactions and finite size effects strongly influence the behavior of the presented inverse model catalysts indicating their prospective use in disentangling complex functionalities of ceria/copper catalytic systems.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10305 - Fluids and plasma physics (including surface physics)
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Applied Surface Science
ISSN
0169-4332
e-ISSN
—
Svazek periodika
465
Číslo periodika v rámci svazku
Jan
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
7
Strana od-do
557-563
Kód UT WoS článku
000449683100064
EID výsledku v databázi Scopus
2-s2.0-85054161888