Room temperature epoxidation of ethylene over delafossite-based AgNiO 2 nanoparticles
A mixed oxide of silver and nickel AgNiO was obtained co-precipitation in alkaline medium. This oxide demonstrates room temperature activity in the reaction of ethylene epoxidation with a high selectivity (up to 70%). Using the PDF method, it was found that the initial structure of AgNiO contains st...
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Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2023-08, Vol.25 (31), p.20892-20902 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A mixed oxide of silver and nickel AgNiO
was obtained
co-precipitation in alkaline medium. This oxide demonstrates room temperature activity in the reaction of ethylene epoxidation with a high selectivity (up to 70%). Using the PDF method, it was found that the initial structure of AgNiO
contains stacking faults and silver vacancies, which cause the nonstoichiometry of the oxide (Ag/Ni < 1). It has been established that on the initial surface of AgNiO
oxide, silver state can be considered as an intermediate between Ag
O and Ag
(
Ag
-like), while nickel is characterized by signs of a deeply oxidized state (Ni
-like). The interaction of AgNiO
with C
H
at room temperature leads to the simultaneous removal of two oxygen species with
(O 1s) = 529.0 eV and 530.5 eV considered as nucleophilic and electrophilic oxygen states, respectively. Nucleophilic oxygen was attributed to the lattice oxygen (Ag-O-Ni), while the electrophilic species with epoxidation activity was associated with the weakly bound oxygen stabilized on the surface. According to the TPR-C
H
data, a large number of weakly bound oxygen species were found on the pristine AgNiO
surface. The removal of such species at room temperature didn't result in noticeable structural transformation of delafossite. As the temperature of ethylene oxidation over AgNiO
increased, the appearance of Ag
particles was first observed below 200 °C followed by the complete destruction of the delafossite structure at higher temperatures. |
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ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/D3CP01701J |