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ChemSusChem ; 10(3): 600-611, 2017 02 08.
Article in English | MEDLINE | ID: mdl-27860352

ABSTRACT

Perovskite-related (La1-x Srx )2 NiO4-δ (x=0.5-0.8) phases were explored for possible use as oxygen electrodes in solid electrolyte cells with a main focus on the effect of oxygen deficiency on the electrocatalytic activity. (La1-x Srx )2 NiO4-δ solid solutions were demonstrated to preserve the K2 NiF4 -type tetragonal structure under oxidizing conditions. Acceptor-type substitution by Sr is compensated by the formation of oxygen vacancies and electron holes and progressively increases high-temperature oxygen nonstoichiometry, which reaches as high as δ=0.40 for x=0.8 at 950 °C in air. The electrical conductivity of (La1-x Srx )2 NiO4-δ ceramics at 500-1000 °C and p(O2 )≥10-3  atm is p-type metallic-like. The highest conductivity, 300 S cm-1 at 800 °C in air, is observed for x=0.6. The average thermal expansion coefficients, (14.0-15.4)×10-6  K-1 at 25-900 °C in air, are sufficiently low to ensure the thermomechanical compatibility with common solid electrolytes. The polarization resistance of porous (La1-x Srx )2 NiO4-δ electrodes applied on a Ce0.9 Gd0.1 O2-δ solid electrolyte decreases with increasing Sr concentration in correlation with the concentration of oxygen vacancies in the nickelate lattice and the anticipated level of mixed ionic-electronic conduction. However, this is accompanied by increasing reactivity between the cell components and necessitates the microstructural optimization of the electrode materials to reduce the electrode fabrication temperature.


Subject(s)
Calcium Compounds/chemistry , Oxides/chemistry , Oxygen/chemistry , Temperature , Titanium/chemistry , Electric Conductivity , Electrochemistry , Electrodes
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