Perovskite oxides are promising electrodes for oxygen evolution and reduction reactions (OER/ORR), but it is difficult for a single material to catalyze both reactions efficiently. We investigated using first-principles calculations the K-doped Sr2Fe1.5Mo0.5O6-d mixed proton-electron conducting oxide. We found that aliovalent doping tunes the electronic features to be optimal for the ORR and lattice expansion-driven surface reconstruction stabilizes the key ∗OOH intermediate for the OER. The resulting ORR/OER overpotentials are very low (∼0.5 V), suggesting the application of this material as an air electrode in reversible solid oxide electrochemical cells.

K-doped Sr2Fe1.5Mo0.5O6-d predicted as a bifunctional catalyst for air electrodes in proton-conducting solid oxide electrochemical cells / MUNOZ GARCIA, ANA BELEN; Pavone, Michele. - In: JOURNAL OF MATERIALS CHEMISTRY. A. - ISSN 2050-7488. - 5:25(2017), pp. 12735-12739. [10.1039/c7ta03340k]

K-doped Sr2Fe1.5Mo0.5O6-d predicted as a bifunctional catalyst for air electrodes in proton-conducting solid oxide electrochemical cells

MUNOZ GARCIA, ANA BELEN;PAVONE, MICHELE
2017

Abstract

Perovskite oxides are promising electrodes for oxygen evolution and reduction reactions (OER/ORR), but it is difficult for a single material to catalyze both reactions efficiently. We investigated using first-principles calculations the K-doped Sr2Fe1.5Mo0.5O6-d mixed proton-electron conducting oxide. We found that aliovalent doping tunes the electronic features to be optimal for the ORR and lattice expansion-driven surface reconstruction stabilizes the key ∗OOH intermediate for the OER. The resulting ORR/OER overpotentials are very low (∼0.5 V), suggesting the application of this material as an air electrode in reversible solid oxide electrochemical cells.
2017
K-doped Sr2Fe1.5Mo0.5O6-d predicted as a bifunctional catalyst for air electrodes in proton-conducting solid oxide electrochemical cells / MUNOZ GARCIA, ANA BELEN; Pavone, Michele. - In: JOURNAL OF MATERIALS CHEMISTRY. A. - ISSN 2050-7488. - 5:25(2017), pp. 12735-12739. [10.1039/c7ta03340k]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/683562
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