Oxygen-ionic conductivity of perovskite-type La1-xSrxGa1-yMgyM0.20O3-delta (M = Fe, Co, Ni)

authors	Yaremchenko, AA; Shaula, AL; Logvinovich, DI; Kharton, VV; Kovalevsky, A; Naumovich, EN; Frade, JR; Marques, FMB
nationality	International
journal	MATERIALS CHEMISTRY AND PHYSICS
author keywords	ceramics; electrochemical techniques; electrical conductivity; diffusion
keywords	OXIDE FUEL-CELLS; LANTHANUM GALLATE; DOPED LAGAO3; ELECTRICAL-PROPERTIES; LACO(M)O-3 M; ELECTROLYTE; TRANSPORT; CR; TEMPERATURE; MAGNESIUM
abstract	The oxygen-ionic conductivity of perovskite-type La1-xSrxGa0.80-yMgyM0.2O3-delta (x = 0-0.20, y = 0.15-0.20, M = Fe, Co, Ni) and La0.50Pr0.50Ga0.65Mg0.15Ni0.2O3-delta in air, determined by the measurements of total conductivity, faradaic efficiency and oxygen permeability at 973-1223 K, increases with increasing concentration of the acceptor-type dopants, within the solid solution formation limits. The level of ionic conduction in these phases is, however, lower than that in parent compounds, La1-xSrxGa1-yMgyO3-delta, probably due to partial oxygen-vacancy ordering and a higher average cation-anion bond energy in transition metal-containing gallates. The activation energy for ionic transport in La1-xSrxGa0.80-gammaMgyM0.20O3-delta varies in the range of 126-171 kJ mol(-1). For compositions containing different transition metal cations, the ionic transport increases in the sequence M = Co < Fe < Ni, with the maximum ionic conductivity observed for La0.90Sr0.10Ga0.65Mg0.15Ni0.20O3-delta perovskite. (C) 2003 Elsevier B.V. All rights reserved.
publisher	ELSEVIER SCIENCE SA
issn	0254-0584
year published	2003
volume	82
issue	3
beginning page	684
ending page	690
digital object identifier (doi)	10.1016/S0254-0584(03)00329-8
web of science category	Materials Science, Multidisciplinary
subject category	Materials Science
unique article identifier	WOS:000187239300031