High entropy oxides (HEOs) are an emerging class of materials constituted by multicomponent systems that are receiving special interest as candidates for obtaining novel and desirable properties. In this study we present a detailed investigation of the relevant intermediates arising at the surface of the prototypical HEO Mg0.2Co0.2Ni0.2Cu0.2Zn0.2O during low-Temperature CO oxidation. By combining Cu L2,3-edge operando soft X-ray absorption spectroscopy (soft-XAS) with density functional theory simulations and in situ FT-IR spectroscopy, we propose that upon HEO exposure to CO at 235 °C reduced Cu(i) sites arise mostly coordinated to activated CO molecules and partly to bidentate carbonate species. When the HEO surface is then exposed to a stoichiometric mixture of CO + 1/2O2 at 250 °C, CO2 is produced while bidentate carbonate moieties remain interacting with the Cu(i) sites. We structurally characterize the carbonate and CO preferential adsorption geometries on the Cu(i) surface metal centers, and find that CO adopts a bent conformation that may energetically favor its subsequent oxidation. The unique surface, structural and electronic sensitivity of soft-XAS coupled with the developed data analysis work-flow and supported by FT-IR spectroscopy may be beneficial to characterize often elusive surface properties of systems of catalytic interest.

Structural and mechanistic insights into low-Temperature CO oxidation over a prototypical high entropy oxide by Cu L-edge operando soft X-ray absorption spectroscopy

Braglia L.;Morandi S.;Manzoli M.;
2021-01-01

Abstract

High entropy oxides (HEOs) are an emerging class of materials constituted by multicomponent systems that are receiving special interest as candidates for obtaining novel and desirable properties. In this study we present a detailed investigation of the relevant intermediates arising at the surface of the prototypical HEO Mg0.2Co0.2Ni0.2Cu0.2Zn0.2O during low-Temperature CO oxidation. By combining Cu L2,3-edge operando soft X-ray absorption spectroscopy (soft-XAS) with density functional theory simulations and in situ FT-IR spectroscopy, we propose that upon HEO exposure to CO at 235 °C reduced Cu(i) sites arise mostly coordinated to activated CO molecules and partly to bidentate carbonate species. When the HEO surface is then exposed to a stoichiometric mixture of CO + 1/2O2 at 250 °C, CO2 is produced while bidentate carbonate moieties remain interacting with the Cu(i) sites. We structurally characterize the carbonate and CO preferential adsorption geometries on the Cu(i) surface metal centers, and find that CO adopts a bent conformation that may energetically favor its subsequent oxidation. The unique surface, structural and electronic sensitivity of soft-XAS coupled with the developed data analysis work-flow and supported by FT-IR spectroscopy may be beneficial to characterize often elusive surface properties of systems of catalytic interest.
2021
23
46
26575
26584
Tavani F.; Fracchia M.; Tofoni A.; Braglia L.; Jouve A.; Morandi S.; Manzoli M.; Torelli P.; Ghigna P.; D'Angelo P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1831223
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