Influence of alkaline-earth metal substitution on structure, electrical conductivity and oxygen transport properties of perovskite-type oxides La0.6A0.4FeO3−δ(A = Ca, Sr and Ba)

Jia Song, De Ning, Henny J.M. Bouwmeester*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

25 Citations (Scopus)
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Abstract

Structural evolution, electrical conductivity, oxygen nonstoichiometry and oxygen transport properties of perovskite-type oxides La0.6A0.4FeO3−δ(A = Ca, Sr, and Ba) were investigated. La0.6Ca0.4FeO3−δ(LCF64) and La0.6Sr0.4FeO3−δ(LSF64) show a phase transformation in air at elevated temperature,i.e., from orthorhombic (Pnma) to rhombohedral (R3̄c) and from rhombohedral to cubic (Pm3̄m), respectively, while La0.6Ba0.4FeO3−δ(LBF64) remains cubic over the entire temperature range from room temperature to 1000 °C. The different phase behaviour of the solids is interpreted to reflect the decreased tendency for octahedral tilting with increasing alkaline-earth-metal dopant ion radius. The electrical conductivity of LSF64 is 191 S cm−1in air at 800 °C, decreasing to a value of 114 S cm−1at apO2of 0.01 atm, and found over thispO2range roughly twice as high as those of LCF64 and LBF64. Failure to describe the data of electrical conductivity using Holstein's small polaron theory is briefly discussed. Chemical diffusion coefficients and surface exchange coefficients of the materials in the range 650-900 °C were extracted from data of electrical conductivity relaxation. Data of oxygen nonstoichiometry was used to calculate the vacancy diffusion coefficients from the measured chemical diffusion coefficients. The calculated migration enthalpies are found to decrease in the order LCF64 (1.08 ± 0.04 eV) > LSF64 (0.95 ± 0.01 eV) > LBF64 (0.81 ± 0.01 eV). The estimated ionic conductivities of the materials, at 900 °C, are within a factor of 1.4.

Original languageEnglish
Pages (from-to)11984-11995
Number of pages12
JournalPhysical chemistry chemical physics
Volume22
Issue number21
DOIs
Publication statusPublished - 7 May 2020

Keywords

  • UT-Hybrid-D

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