Effects of lanthanide doping on the electrode properties and exsolution behavior of A-site deficient Sr 1.9 Fe 1.3 Ni 0.2 Mo 0.5 O 6-8 double perovskites

[EN] Double perovskite oxides of the Sr 2 Fe 1.5 Mo 0.5 O 6-8 class are promising electrodes for Solid Oxide Fuel Cells (SOFCs) and Electrolyzers (SOECs) due to their outstanding electrochemical properties and durability. Additionally, their physicochemical properties can be tuned by B-site cation d...

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Detalles Bibliográficos
Autores: Delgado-Galicia, Blanca, López-García, Andrés, Carrillo-Del Teso, Alfonso Juan, Serra Alfaro, José Manuel|||0000-0002-1515-1106
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/207841
Acceso en línea:https://riunet.upv.es/handle/10251/207841
Access Level:acceso embargado
Palabra clave:Exsolution
Double perovskites
A-site deficiency
A-site doping
Solid oxide electrochemical cells
Nickel
Descripción
Sumario:[EN] Double perovskite oxides of the Sr 2 Fe 1.5 Mo 0.5 O 6-8 class are promising electrodes for Solid Oxide Fuel Cells (SOFCs) and Electrolyzers (SOECs) due to their outstanding electrochemical properties and durability. Additionally, their physicochemical properties can be tuned by B-site cation doping, namely, by partially substituting Fe cations with other transition metals such as Ni, Co, Mn, or Cu. This also allows the grain-surface functionalization with metallic alloyed nanocatalysts upon reduction driven by the exsolution phenomena, leading to higher electrocatalytic activity and resistance against sintering and coking. Traditionally, A-site deficiency has been employed to improve the amount of exsolved nanoparticles and, thereby, increase the number of Triple Phase Boundaries in the electrode. However, in Ni-doped non-stoichiometric double perovskite materials (e.g., Sr 1.9 Fe 1.3 Ni 0.2 Mo 0.5 O 6-8 ), A-site deficiency results in undesired NiO phase segregations. This, in turn, lowers the number of exsolvable cations, decreasing the number of metallic nanocatalysts compared to the stoichiometric compound. In this work, the impact of A-site doping with lanthanides (viz. Gd, La, Nd, and Pr) on the exsolution ability and electrochemical properties of non-stoichiometric Sr 1.9 Fe 1.3 Ni 0.2 Mo 0.5 O 6-8 was evaluated. The results indicate that lanthanide doping enhances the conductivity of the double perovskites both in oxidizing and reducing atmospheres. In addition, lanthanide dopants that slightly destabilize the cubic structure also improve the exsolution dispersion, which decreases with increasing the double perovskite cell volume. These results illustrate how to design more efficient and durable electrocatalysts by modifying the double perovskite structure with A-site dopants.