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Sr 2 FeNi 0.4 Mo 0.6 O 6−δ Evolution for SOFC and SOEC Applications
Solid Oxide Cell electrode engineering is of paramount importance to obtain high performing, versatile and reliable devices. In this work, the structural and morphological evolution of Sr 2 FeNi 0.4 Mo 0.6 O 6- δ (SFNM) is investigated and fully characterized over subsequent temperature programmed r...
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Published in: | Journal of the Electrochemical Society 2023-11, Vol.170 (11), p.114511 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Solid Oxide Cell electrode engineering is of paramount importance to obtain high performing, versatile and reliable devices. In this work, the structural and morphological evolution of Sr
2
FeNi
0.4
Mo
0.6
O
6-
δ
(SFNM) is investigated and fully characterized over subsequent temperature programmed reductions. Comparison of the results of X-ray diffraction, high transmission electron microscopy and electrochemical impedance spectroscopy analyses confirms how metallic phase exsolution upon reduction endows the perovskite with highly active Ni-Fe-based catalytic sites for applications in hydrogen-fueled SOFCs. As a novelty, this study presents voltage-induced reduction of SFNM at 1.6 V as a fast and reliable way to induce morphological and structural changes of the SFMN-derivate exsolved-perovskite. This enhances its catalytic activity towards CO
2
electrolysis in SOEC configuration, providing SFNM with a high versatility in solid oxide cells applications.
Structural evolution of Sr
2
FeMo
0.6
Ni
0.4
O
6
(SFNM) is studied in various reduction conditions.
XRD and TPR characterizations provides insights into the redox behavior of SFMN.
Metals exsolution and the formation of a Ruddlesden-Popper (RP) are interdependent phenomena.
Cathodic polarization causes metal nanoparticles to be covered by the RP phase.
This unusual morphology increases the CO
2
electroreduction activity into SOEC. |
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ISSN: | 0013-4651 1945-7111 |
DOI: | 10.1149/1945-7111/ad06e7 |