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Stability of multifunctional Pd-Rh electrocatalysts supported on Co3O4(111) in alkaline environment: impact of the electronic metal-support interaction

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F25%3A10501148" target="_blank" >RIV/00216208:11320/25:10501148 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=qyvAmr98Xq" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=qyvAmr98Xq</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d5nr00413f" target="_blank" >10.1039/d5nr00413f</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Stability of multifunctional Pd-Rh electrocatalysts supported on Co3O4(111) in alkaline environment: impact of the electronic metal-support interaction

  • Original language description

    The stabilities of monometallic Rh and Pd nanoparticles and bimetallic Pd-Rh core-shell nanoparticles supported on Co3O4(111) thin films grown on Ir(100) were investigated with respect to the oxidation state and dissolution in alkaline electrolyte under the conditions relevant for electrochemical ethanol oxidation. Towards this aim, the well-defined model systems were characterized by means of synchrotron radiation photoelectron spectroscopy coupled with an ex situ emersion electrochemical cell (EC-SRPES) and scanning tunneling microscopy (STM). We found that the electronic metal-support interaction (EMSI) has a strong influence on the oxidation state of Rh, resulting in a strong oxidation and anchoring of the oxidized Rh3+ species on the surface of Co3O4(111). Consequently, the EMSI prevents the dissolution of Rh into the electrolyte regardless of the potential range. In contrast, it has no effect on the oxidation state and dissolution of Pd in the potential range of 0.3-1.1 VRHE. However, extending the potential range to 0.3-1.5 VRHE results in a stronger dissolution of Pd due to the reversible oxidation/reduction of Pd, which is enhanced in the presence of the EMSI. Most importantly, the magnitude of the EMSI and, thus, the extent of noble metal oxidation, can be effectively controlled by the nature of the metal/Co3O4(111) interface in the bimetallic Pd-Rh core-shell nanoparticles.

  • 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

    10305 - Fluids and plasma physics (including surface physics)

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)

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Nanoscale

  • ISSN

    2040-3364

  • e-ISSN

    2040-3372

  • Volume of the periodical

    17

  • Issue of the periodical within the volume

    18

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    11679-11690

  • UT code for WoS article

    001471747300001

  • EID of the result in the Scopus database

    2-s2.0-105003750746