Atomically Dispersed Pd, Ni, and Pt Species in Ceria-Based Catalysts: Principal Differences in Stability and Reactivity
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F16%3A10334198" target="_blank" >RIV/00216208:11320/16:10334198 - isvavai.cz</a>
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Dqh0EN-UfD" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Dqh0EN-UfD</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jpcc.6b02264" target="_blank" >10.1021/acs.jpcc.6b02264</a>
Alternative languages
Result language
angličtina
Original language name
Atomically Dispersed Pd, Ni, and Pt Species in Ceria-Based Catalysts: Principal Differences in Stability and Reactivity
Original language description
We have investigated the stability and the reactivity of atomically dispersed Pt, Pd, and Ni species on nanostructured CeO2 films by means of synchrotron radiation photoelectron spectroscopy and resonant photoemission spectroscopy in combination with density functional calculations. All three metals reveal specific similarities associated with the high adsorption energy of atomically dispersed Pt2+, Pd2+, and Ni2+ species that exceeds the corresponding cohesive energies of the bulk metals. The corresponding Pt-CeO2, Pd-CeO2, and Ni-CeO2 model catalysts have been prepared in the form of thin films on CeO2(111)/Cu(111) substrates and investigated experimentally under ultrahigh vacuum conditions. The atomically dispersed Pt2+, Pd2+, and Ni-2 species were formed exclusively at low concentrations of the corresponding metals. High concentrations resulted in the presence of additional metal oxide phases and emergence of metallic particles. We found that under the employed experimental conditions the Pd-CeO2 films closely resemble the Pt-CeO2 system with respect to the redox behavior upon reaction with hydrogen. Unlike Pt-CeO2, the Pd-CeO2 system shows a strong tendency to stabilize Pd2+ not only at the surface but also in the ceria bulk. In sharp contrast to both Pt-CeO2 and Pd-CeO2, the Ni-CeO2 system does not exhibit the redox functionality required for hydrogen activation due to the remarkably high stability of Ni2+ species.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10305 - Fluids and plasma physics (including surface physics)
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2016
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 Physical Chemistry C
ISSN
1932-7447
e-ISSN
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Volume of the periodical
120
Issue of the periodical within the volume
18
Country of publishing house
US - UNITED STATES
Number of pages
11
Pages from-to
9852-9862
UT code for WoS article
000375969000035
EID of the result in the Scopus database
2-s2.0-84971255027