High-temperature CO2 electrolysis in solid oxide electrochemical cells offers one of the most efficient routes for carbon dioxide conversion, enabling the production of highly pure carbon monoxide due to favorable thermodynamics and fast kinetics above 600 degrees C. The emergence of CO:CO2 reversible solid oxide cells (rSOCs) further enhances system efficiency, promoting integration with CO2-rich and CO-rich industrial exhaust streams. However, reversible operation imposes stringent requirements on electrode materials, which must combine high catalytic activity, redox stability, and long-term durability under a wide range of oxygen partial pressures. Herein, we report a doubly B-site-substituted perovskite, La0.eSr0.4Fe0.eMn0.2M0.2O3_ delta (M = Cu, Ni), as a multifunctional electrode platform for rSOCs. Both La0.eSr0.4Fe0.eMn0.2Cu0.2O3_ delta (LSFMC) and La0.eSr0.4Fe0. eMn0.2Ni0.2O3_ delta (LSFMN) are synthesized as single-phase perovskites, with rhombohedral symmetry (R-3c). When evaluated as oxygen electrodes in symmetric cell configurations, LSFMC and LSFMN exhibit significantly enhanced oxygen electrocatalysis, achieving a decrease in area-specific resistance by 51% and 38%, respectively, compared to the unsubstituted material. Under reducing conditions, LSFMN undergoes controlled and homogeneous exsolution of Fe-Ni nanoparticles, generating catalytically active metallic domains while preserving structural integrity. A quasi-symmetric electrolyte-supported cell based on La0.8Sr0.2Ga0.8Mg0.2O3_ delta (LSGM) electrolyte, employing LSFMN as fuel electrode and LSFMC as air electrode, demonstrates excellent performance and durability in both CO-fuelled solid oxide fuel cell mode and CO2 electrolysis mode. Stable and reversible operation is maintained for over 150 h in a 50:50 CO:CO2 mixture. Targeted B-site substitution of Mn-stabilized ferrites enables the design of high-performance, cobalt-free and reversible electrodes, offering a promising strategy for next-generation rSOCs.

(2026). Double substituted Co-free perovskite oxides for quasi-symmetric reversible solid oxide cells (rSOCs) [journal article - articolo]. In CHEMICAL ENGINEERING JOURNAL. Retrieved from https://hdl.handle.net/10446/325485

Double substituted Co-free perovskite oxides for quasi-symmetric reversible solid oxide cells (rSOCs)

Natali Sora I.;Pelosato R.;Bertolotti B.;
2026-01-01

Abstract

High-temperature CO2 electrolysis in solid oxide electrochemical cells offers one of the most efficient routes for carbon dioxide conversion, enabling the production of highly pure carbon monoxide due to favorable thermodynamics and fast kinetics above 600 degrees C. The emergence of CO:CO2 reversible solid oxide cells (rSOCs) further enhances system efficiency, promoting integration with CO2-rich and CO-rich industrial exhaust streams. However, reversible operation imposes stringent requirements on electrode materials, which must combine high catalytic activity, redox stability, and long-term durability under a wide range of oxygen partial pressures. Herein, we report a doubly B-site-substituted perovskite, La0.eSr0.4Fe0.eMn0.2M0.2O3_ delta (M = Cu, Ni), as a multifunctional electrode platform for rSOCs. Both La0.eSr0.4Fe0.eMn0.2Cu0.2O3_ delta (LSFMC) and La0.eSr0.4Fe0. eMn0.2Ni0.2O3_ delta (LSFMN) are synthesized as single-phase perovskites, with rhombohedral symmetry (R-3c). When evaluated as oxygen electrodes in symmetric cell configurations, LSFMC and LSFMN exhibit significantly enhanced oxygen electrocatalysis, achieving a decrease in area-specific resistance by 51% and 38%, respectively, compared to the unsubstituted material. Under reducing conditions, LSFMN undergoes controlled and homogeneous exsolution of Fe-Ni nanoparticles, generating catalytically active metallic domains while preserving structural integrity. A quasi-symmetric electrolyte-supported cell based on La0.8Sr0.2Ga0.8Mg0.2O3_ delta (LSGM) electrolyte, employing LSFMN as fuel electrode and LSFMC as air electrode, demonstrates excellent performance and durability in both CO-fuelled solid oxide fuel cell mode and CO2 electrolysis mode. Stable and reversible operation is maintained for over 150 h in a 50:50 CO:CO2 mixture. Targeted B-site substitution of Mn-stabilized ferrites enables the design of high-performance, cobalt-free and reversible electrodes, offering a promising strategy for next-generation rSOCs.
articolo
2026
Panunzi, A. P.; Duranti, L.; Natali Sora, Isabella; Pelosato, Renato; Bertolotti, Benedetta; Laverdura, U. P.; Grilli, M. L.; Di Bartolomeo, E....espandi
(2026). Double substituted Co-free perovskite oxides for quasi-symmetric reversible solid oxide cells (rSOCs) [journal article - articolo]. In CHEMICAL ENGINEERING JOURNAL. Retrieved from https://hdl.handle.net/10446/325485
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10446/325485
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