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Water interaction with CeO2(1 1 1)/Cu(1 1 1) model catalyst surface

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F12%3A10129681" target="_blank" >RIV/00216208:11320/12:10129681 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.cattod.2011.05.032" target="_blank" >http://dx.doi.org/10.1016/j.cattod.2011.05.032</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.cattod.2011.05.032" target="_blank" >10.1016/j.cattod.2011.05.032</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Water interaction with CeO2(1 1 1)/Cu(1 1 1) model catalyst surface

  • Original language description

    Interaction of water with fully oxidized and partially reduced CeO2(1 1 1) thin film model catalyst grown on a Cu(1 1 1) surface was investigated by photoelectron spectroscopy (PES), scanning tunneling microscopy (STM) and temperature programmed desorption (TPD). On the stoichiometric surface water adsorbs molecularly at low temperatures ({= 120 K) while on the reduced surface the adsorption is partially dissociative with formation of OH groups. STM indicates no morphology variation and a very sensitiveCe 4d-4f resonant photoelectron spectroscopy (RPES) no noticeable change of the oxidation state of ceria upon water adsorption and subsequent complete desorption. Formation of co-adsorbed phase of residual water with OH during molecular water desorption, on the other hand, leads to a substantial resonance of the Ce3+ photoemission state around 170 K. We propose that this behaviour indicating ceria reduction is in this case an electronic effect of the Ce 4f charge accumulation and Ce 5d

  • 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

    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)<br>S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2012

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Catalysis Today

  • ISSN

    0920-5861

  • e-ISSN

  • Volume of the periodical

    181

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    9

  • Pages from-to

    124-132

  • UT code for WoS article

    000299315100020

  • EID of the result in the Scopus database