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H3PO3 electrochemical behaviour on a bulk Pt electrode: adsorption and oxidation kinetics

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F16%3A43901998" target="_blank" >RIV/60461373:22310/16:43901998 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.electacta.2016.07.045" target="_blank" >http://dx.doi.org/10.1016/j.electacta.2016.07.045</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.electacta.2016.07.045" target="_blank" >10.1016/j.electacta.2016.07.045</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    H3PO3 electrochemical behaviour on a bulk Pt electrode: adsorption and oxidation kinetics

  • Original language description

    Polybenzimidazole-type polymer doped with H3PO4 is commonly used as the proton-conductive phase in high-temperature proton-exchange membrane fuel cells. However, H3PO4 is not stable during fuel cell operation and undergoes reduction by hydrogen on a Pt surface to phosphorus compounds in a lower oxidation state, such as H3PO3. In this work the kinetics of H3PO3 oxidation on Pt electrode was studied, including an investigation of H4P2O6 as a possible oxidation intermediate. H3PO3 adsorption in hydrogen underpotential deposition region was described by a triple Langmuir isotherm corresponding to adsorption on specific Pt crystalline planes. Co-adsorption of hydrogen as well as SO42MINUS SIGN , HSO4MINUS SIGN ions decreased the total amount of adsorbed H3PO3. The determined apparent charge transfer coefficients of H3PO3 anodic oxidation on a metallic Pt surface were found to be concentration and temperature-dependent, indicating that the nature of the anodic process is complex. From chronopotentiometric measurements of H3PO3 and H4P2O6 oxidation on a preoxidised Pt surface it was concluded that, while H3PO3 is oxidised by means of a chemical reaction with PtOx, H4P2O6 undegoes anodic oxidation on the PtOx surface. According to voltammetry and bulk electrolysis experiments H4P2O6 is not formed as an intermediate product during electrochemical oxidation of H3PO3 on a metallic Pt surface.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CG - Electrochemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/7HX13002" target="_blank" >7HX13002: Understanding the Degradation Mechanisms of a High Temperature PEMFC Stack and Optimization of the Individual Components</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

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

    Electrochimica Acta

  • ISSN

    0013-4686

  • e-ISSN

  • Volume of the periodical

    212

  • Issue of the periodical within the volume

    10 September 2016

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    "465?472"

  • UT code for WoS article

    000382250200053

  • EID of the result in the Scopus database