Synthesis, physical-chemical characterization and electrochemical performance of GdBaCo2-xNixO5+δ (x = 0-0.8) as cathode materials for IT-SOFC application

Y. Hu, C. Bogicevic, Y. Bouffanais, M. Giot, O. Hernandez, G. Dezanneau

Research output: Contribution to journalArticlepeer-review

Abstract

GdBaCo2-xNixO5+δ (x = 0-0.8) cathode materials have been synthesized by a citrate-gel modified chemical route, by which we have achieved a high level of substitution up to x = 0.8. Oxygen stoichiometry at room temperature has been determined by iodometry and the structural evolution as a function of Ni content has been extracted from XRD patterns analysis. All compounds are orthorhombic at room temperature and a DSC analysis reveals that the high-temperature orthorhombic-to-tetragonal phase transition is observed at lower temperature as Ni substitution increases. Three compositions, with x = 0, 0.3 and 0.6, were then chosen for further characterization: high-temperature XRD has been performed confirming the abovementioned structural evolution with temperature and allowing to determine that Ni doping diminishes slightly the thermal expansion coefficient. According to 4-probe measurements, we show that these compounds present a high electronic conductivity, suitable for cathode materials. Finally, electrochemical characterization has been performed by AC impedance spectroscopy with symmetric cells using composite electrode showing an improvement of performance at intermediate substitution levels.

Original languageEnglish
Pages (from-to)50-56
Number of pages7
JournalJournal of Power Sources
Volume242
DOIs
Publication statusPublished - 18 Jun 2013
Externally publishedYes

Keywords

  • Cathode
  • GdBaCoNiO
  • IT-SOFC
  • Impedance spectroscopy
  • Oxygen content
  • Phase transition

Fingerprint

Dive into the research topics of 'Synthesis, physical-chemical characterization and electrochemical performance of GdBaCo2-xNixO5+δ (x = 0-0.8) as cathode materials for IT-SOFC application'. Together they form a unique fingerprint.

Cite this