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Spontaneous and Photoinduced Conversion of CO2 on TiO2 Anatase

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    SYSNO ASEP0506996
    Document TypeC - Proceedings Paper (int. conf.)
    R&D Document TypeConference Paper
    TitleSpontaneous and Photoinduced Conversion of CO2 on TiO2 Anatase
    Author(s) Civiš, Svatopluk (UFCH-W) RID, ORCID, SAI
    Ferus, Martin (UFCH-W) ORCID, RID
    Article number7193632
    Source Title17TH INTERNATIONAL CONFERENCE ON TRANSPARENT OPTICAL NETWORKS (ICTON). - New York : IEEE, 2015 - ISSN 2162-7339 - ISBN 978-1-4673-7880-2
    Pages(2015)
    SeriesInternational Conference on Transparent Optical Networks-ICTON
    Number of pages5 s.
    Publication formPrint - P
    ActionInternational Conference on Transparent Optical Networks (ICTON 2015) /17./
    Event date05.07.2015 - 09.07.2015
    VEvent locationBudapest
    CountryHU - Hungary
    Event typeWRD
    Languageeng - English
    CountryUS - United States
    Keywordssurface defect ; 1st step ; laser ; spectroscopy ; decomposition ; nanocrystal ; formamide ; structure and reactions of adsorbates
    Subject RIVCF - Physical ; Theoretical Chemistry
    OECD categoryPhysical chemistry
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000380506700347
    EID SCOPUS84940931343
    DOI10.1109/ICTON.2015.7193632
    AnnotationSpontaneous isotopic exchange of oxygen atoms between gaseous (CO2)-O-18 and (TiO2)-O-16 nanoparticles has been studied using high-resolution Fourier transform infrared absorption and first principles density functional theory calculations. The rate of formation of gaseous (CO2)-O-16 is found to be highly dependent on the nature of the titania sample, growing with increasing calcination temperature for both amorphous and crystalline nanoparticles. This is attributed to an increase in the population of oxygen atom defects and for uncoordinated sites at higher calcination temperatures. Additional support for the experimental observations is provided by calculations of the activation barriers for oxygen exchange on crystalline anatase and on a (TiO2)(10) cluster.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2020
Number of the records: 1  

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