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Photoelectrochemical, photocatalytic and electrocatalytic behavior of titania films modified by nitrogen and platinum species

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27710%2F21%3A10246778" target="_blank" >RIV/61989100:27710/21:10246778 - isvavai.cz</a>

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s13204-021-01690-1#citeas" target="_blank" >https://link.springer.com/article/10.1007/s13204-021-01690-1#citeas</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s13204-021-01690-1" target="_blank" >10.1007/s13204-021-01690-1</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Photoelectrochemical, photocatalytic and electrocatalytic behavior of titania films modified by nitrogen and platinum species

  • Original language description

    Co-doping of titania by N and Pt species was employed to tune the electronic structure and enhance the electrocatalytic and photocatalytic activity of the films. Herein, the different approaches of synthesis procedure of Pt- and Pt,N-TiO2 films were used to investigate their effect on the platinum oxidation states. The resulting different species of Pt led to the changes in the electronic structure of TiO2, with consequent bandgap narrowing, anodic shift of the flat band potential, and cathodic shift of the valence band The quantum yield efficiency was correlated with Pt0 atomic content and the relative atomic content of Ptn+-O-Ti fragments, whereas its decrease for some samples can be caused by the presence of N and Ptn+. The highest response for N2O photocatalytic decomposition was observed over Pt,N-TiO2 films. The presence of metal and non-metal species in TiO2 structure resulted in synergistic effect including (1) inhibition of recombination of the electrons and holes and (2) narrowing of the bandgap. Electrocatalytic properties in hydrogen and oxygen evolution reactions were improved by Pt doping. The formed Pt2+-O-Ti bonds rather than Pt nanoparticles are suggested to be responsible for the highest electrocatalytic activity. The additional UV exposure of the electrodes led to Pt NPs aggregation as a result of photodeposition of Pt ions. The mechanism of the Pt2+ photoreduction in TiO2 structure is proposed.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10400 - Chemical sciences

Result continuities

  • Project

    <a href="/en/project/EF16_019%2F0000853" target="_blank" >EF16_019/0000853: Institute of Environmental Technology - Excellent Research</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Applied Nanoscience

  • ISSN

    2190-5509

  • e-ISSN

  • Volume of the periodical

    neuveden

  • Issue of the periodical within the volume

    February

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    13

  • Pages from-to

    1-13

  • UT code for WoS article

    000616042300001

  • EID of the result in the Scopus database