IFISUR   23398
INSTITUTO DE FISICA DEL SUR
Unidad Ejecutora - UE
artículos
Título:
Stabilization of the cubic perovskite in the system La1-xBaxCo1-yFeyO3-d (0.7 < x < 0.9) and its electrochemical performance as cathode materials for intermediate-temperature solid oxide fuel cells
Autor/es:
C. F. MARTINEZ SETEVICH; F. D. PRADO; D. Z. DE FLORIO; A. CANEIRO
Revista:
JOURNAL OF POWER SOURCES
Editorial:
ELSEVIER SCIENCE BV
Referencias:
Lugar: Amsterdam; Año: 2014 vol. 247 p. 264 - 272
ISSN:
0378-7753
Resumen:
The effects of the substitution of Co by Fe on the crystal chemistry and electrode reaction of the system La1?xBaxCo1?yFeyO3?δ (0.7 ≤ x ≤ 0.9), are investigated. The incorporation of Fe stabilizes the cubic perovskite and suppresses the structural transformation of La1?xBaxCoO3?δ from a metastable cubic perovskite to a hexagonal phase below 900 °C. The linear expansion decreases with the replacement of Co by Fe. The lowest expansion coefficient value, α ∼ 20.5 × 10−6 K−1, was obtained for the samples with Fe content y = 0.6. AC impedance spectroscopy measurements on symmetrical cells reveal the presence of an intermediate (IF) and a low (LF) frequency contributions at T ≥ 600 °C. The LF arc varies with the pO2, at 700 °C, according to a power law with exponent n = −1, indicating oxygen diffusion through the porous of the electrode. The minimum Rp value (0.6 Ω cm2 at 600°C) was obtained for La0.3Ba0.7Co0.6Fe0.4O3−δ. At constant temperature, T = 750 °C, only the IF contribution varies at a rate of 3 × 10−4Ω cm2 h−1, while the LF contribution remains constant. Experimental data suggest the growth of the IF arc is caused by the mismatch in the expansion coefficients of the electrode and electrolyte.