SrCo0.50Fe0.40Ir0.10O3−δ decorated with Pd and La0.8Sr0.2Ga0.83Mg0.17O3−δ: a cleaner electrode for intermediate-temperature solid oxide fuel cells with reduced cobalt content

Recent studies related to cathode materials for solid oxide fuel cells (SOFCs) have showcased the feasibility of stabilizing cubic or tetragonal perovskite phases in the SrCoO3−δ system at room temperature. This achievement has been facilitated by partially substituting Co atoms with small amounts o...

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Detalles Bibliográficos
Autores: Chivite-Lacaba, Mónica, Prado Gonjal, Jesús de la Paz, Troncoso, Loreto, Cascos Jiménez, Vanessa Amelia
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/101885
Acceso en línea:https://hdl.handle.net/20.500.14352/101885
Access Level:acceso abierto
Palabra clave:546
Pilas de combustible de óxido solido
Energía
Difracción de neutrones
Cátodos
Química inorgánica (Química)
Cristalografía (Química)
Física del estado sólido
2303 Química Inorgánica
2210.28-1 Preparación y Caracterización de Materiales Inorgánicos
2207.09 Conversión de Energía
Descripción
Sumario:Recent studies related to cathode materials for solid oxide fuel cells (SOFCs) have showcased the feasibility of stabilizing cubic or tetragonal perovskite phases in the SrCoO3−δ system at room temperature. This achievement has been facilitated by partially substituting Co atoms with small amounts of highly charged cations such as Ir4+ in SrCo0.90Ir0.10O3−δ. This specific material exhibits exceptional performance as a cathode for SOFCs operating at intermediate temperatures (800−850 °C). However, it contains a high amount of cobalt, which is both costly and toxic. In this study, our focus has been on further improving this material by reducing its cobalt content, resulting in a cleaner and more cost-effective cathode for SOFCs. The resulting SrCo0.50Fe0.40Ir0.10O3−δ perovskite, synthesized by the citrate method, introduces a 40% composition of Fe in the sites of Co and Ir, effectively decreasing the amount of Co in the material. The crystal structure of this perovskite oxide has been analyzed using X-ray diffraction (XRD) and neutron powder diffraction (NPD), allowing us to establish correlations with its mechanical and electrical properties. In the single-cell test, this material gave reasonable performances as a cathode at intermediate temperatures (800−850 °C), with La0.8Sr0.2Ga0.83Mg0.17O3−δ (LSGM) as the electrolyte. An analysis of the chemical compatibility between the cathode and the electrolyte, LSGM, demonstrated no interaction at elevated temperatures. Thermal expansion coefficient (TEC) measurements exhibited consistent linear expansion across the entire temperature range. Lastly, the perovskite displayed commendable electrical conductivity along with a promising power density measurement of 384 mW/cm2 at 850 °C. These findings collectively suggest the potential of this material as a viable cleaner cathode option for intermediate-temperature SOFCs. Moreover, the cathode was further optimized and the performance of the cell improved, by either infiltrating SrCo0.50Fe0.40Ir0.10O3−δ with a Pd(NO3)2 solution or mixing it with 30% of LSGM electrolyte, resulting in higher power densities (568 and 675 mW/cm2, respectively) in test cells fed with pure H2 as a fuel.