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Random nucleation and growth of Pt nanoparticles at the polarized interface between two immiscible electrolyte solutions

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    SYSNO ASEP0081095
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleRandom nucleation and growth of Pt nanoparticles at the polarized interface between two immiscible electrolyte solutions
    TitleNáhodná nukleace a růst Pt nanočástic na polarizovaném rozhraní mezi nemísitelnými roztoky elektrolytů
    Author(s) Trojánek, Antonín (UFCH-W) RID
    Langmaier, Jan (UFCH-W) RID, ORCID, SAI
    Samec, Zdeněk (UFCH-W) RID, ORCID
    Source TitleJournal of the Electroanalytical Chemistry and Journal of Electroanalytical Chemistry and Interfacial Electrochemistry. - : Elsevier - ISSN 0022-0728
    Roč. 599, č. 2 (2007), s. 160-166
    Number of pages7 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordspolarized ITIES ; deposition ; platinum ; random nucleation and growth
    Subject RIVCG - Electrochemistry
    R&D ProjectsIAA4040407 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    AnnotationCyclic voltammetry and potential-step chronoamperometry are used to study the Pt deposition at the polarised water vertical bar 1,2-dichloro-ethane (DCE) interface through reduction of a Pt(II) chloro-complex in water by 1,1'-dimethylferrocene in DCE. Thermodynamic analysis suggests that the deposition is controlled by the interfacial kinetics, and that the activity of the metal particle at ITIES does not differ much from that of the bulk metal phase. It is shown that the shape of the experimental potential-step current transients could be described with the help of the available theory of nucleation and growth of a metal particle at a liquid-liquid interface. However, the repeated potential-step experiments on the bare interface reveal that the initial rate of the Pt deposition can attain a broad range of values that spans over two orders of magnitude.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2007
Number of the records: 1  

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