Electrical characterization of ruddlesden-popper phases with preferred orientations and tunable composition [La,Sr][Al,Ga,Mg,Na]O4-δ

Marino, C; Serafini, D; Troncoso, L

Keywords: ionic conductivity, impedance spectroscopy, xrd, SOFC electrolyte, K2NiF4-type structure, Ruddlesden popper phases, DRT

Abstract

This work investigates the structural, morphological, and electrical properties of a Ruddlesden-Popper phase LaSrAl0.4Ga0.4Mg0.1Na0.1O4-delta, synthesized via the Pechini method, with potential applications as a solid electrolyte in solid oxide fuel cells (SOFCs). For the first time, this phase exhibits a preferred crystallographic orientation and a plate-like microstructure with 45 degrees alignments around the compression axis. X-ray diffraction (XRD) and Rietveld refinement confirm a strong orientation of the (004) and (105) Miller planes and a proper Ga/Al cation distribution at the Wyckoff 2a site. Scanning electron microscopy (SEM) reveals a dense (similar to 96 %) plate-like microstructure. Electrical characterization demonstrates a significant three-order-of-magnitude improvement in conductivity compared to undoped samples, with values of 28.9 mS/m at 845 degrees C and 13 mS/m at 749 degrees C. The oxygen ion activation energy is reduced by 22 % (1.28 eV) due to Mg and Na dopants, which enhance oxygen vacancy formation and ion mobility. Additionally, a distribution of relaxation times (DRT) analysis was performed using DRT Tools software, distinguishing contributions from intergranular conduction (0.2-1.2 mu S), grain boundary conduction (3.9-29 mu S), and electrode-electrolyte interface processes (78-500 mu S) at 507 degrees C-592 degrees C. These findings highlight the potential of this material for SOFC applications, offering enhanced ionic transport properties and improved densification.

Más información

Título según WOS: Electrical characterization of ruddlesden-popper phases with preferred orientations and tunable composition [La,Sr][Al,Ga,Mg,Na]O4-δ
Volumen: 51
Número: 17
Fecha de publicación: 2025
Página de inicio: 23383
Página final: 23391
Idioma: English
DOI:

10.1016/j.ceramint.2025.03.027

Notas: ISI