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A comparative study of RuO2 and Ru reveals the role of oxygen vacancies in electrocatalytic nitrogen reduction to ammonia under ambient conditions

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23640%2F23%3A43972902" target="_blank" >RIV/49777513:23640/23:43972902 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1016/j.apcata.2023.119375" target="_blank" >https://doi.org/10.1016/j.apcata.2023.119375</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.apcata.2023.119375" target="_blank" >10.1016/j.apcata.2023.119375</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A comparative study of RuO2 and Ru reveals the role of oxygen vacancies in electrocatalytic nitrogen reduction to ammonia under ambient conditions

  • Original language description

    Nitrogen molecule reduction to ammonia requires adsorption and hydrogenation sites. In this study, the nitrogen reduction reaction (NRR) activity of RuO2 and metallic Ru catalysts was studied to explore the role of oxides and metallic dual active sites. Ruthenium oxide nanoparticles displayed an ammonia production rate of 16.5 &amp; mu;g h-1 cm- 2 with a Faradaic efficiency (FE) of 0.26% at - 0.15 V vs. RHE in N2-saturated 0.1 M KOH which is 58% higher compared to Ru black (6.8 &amp; mu;g h-1 cm- 2 with 0.19% FE at -0.15 Vvs.RHE). This is attributed to the formation of oxygen vacancies (Vo) on the RuO2 surface during cathodic potential polarization, which provides a facile adsorption site for N2 in addition to the Ru4+ active site while the proton supplied via hydrogen spillover from the metal hydride site to the adsorbed Vo-N2 site. This assumption was validated by detailed XPS, XRD, and N2 TPD analysis.Nitrogen molecule reduction to ammonia requires adsorption and hydrogenation sites. In this study, the nitrogen reduction reaction (NRR) activity of RuO2 and metallic Ru catalysts was studied to explore the role of oxides and metallic dual active sites. Ruthenium oxide nanoparticles displayed an ammonia production rate of 16.5 &amp; mu;g h-1 cm- 2 with a Faradaic efficiency (FE) of 0.26% at - 0.15 V vs. RHE in N2-saturated 0.1 M KOH which is 58% higher compared to Ru black (6.8 &amp; mu;g h-1 cm- 2 with 0.19% FE at -0.15 Vvs.RHE). This is attributed to the formation of oxygen vacancies (Vo) on the RuO2 surface during cathodic potential polarization, which provides a facile adsorption site for N2 in addition to the Ru4+ active site while the proton supplied via hydrogen spillover from the metal hydride site to the adsorbed Vo-N2 site. This assumption was validated by detailed XPS, XRD, and N2 TPD analysis.

  • 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

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    APPLIED CATALYSIS A-GENERAL

  • ISSN

    0926-860X

  • e-ISSN

    1873-3875

  • Volume of the periodical

    665

  • Issue of the periodical within the volume

    SEP 5 2023

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

  • UT code for WoS article

    001068500900001

  • EID of the result in the Scopus database

    2-s2.0-85168081468