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 & 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 & 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 & 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 & 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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)
Result continuities
Project
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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
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UT code for WoS article
001068500900001
EID of the result in the Scopus database
2-s2.0-85168081468