Effect of sintering temperature on the microstructure and ionic conductivity of Ce0.8Sm0.1Ba0.1O2-δ electrolyte
This study investigated the effects of sintering temperature on the microstructure and ionic conductivity of codoped ceria electrolyte with barium and samarium as dopants. The electrolyte (Ce0.8Sm0.1Ba0.1O2-δ) powder was synthesized using the citric acid-nitrate combustion method and calcined at 900...
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
University of Novi Sad
2017-03-01
|
| Series: | Processing and Application of Ceramics |
| Subjects: | |
| Online Access: | http://www.tf.uns.ac.rs/publikacije/PAC/pdf/PAC%2035%2010.pdf |
| Summary: | This study investigated the effects of sintering temperature on the microstructure and ionic conductivity of codoped ceria electrolyte with barium and samarium as dopants. The electrolyte (Ce0.8Sm0.1Ba0.1O2-δ) powder was synthesized using the citric acid-nitrate combustion method and calcined at 900 °C for 5 h. The calcined electrolyte exhibited a cubic fluorite crystal structure with some impurity phases. The calcined powder was then pressed into cylindrical pellets using uniaxial die-pressing. The pellets were sintered at three different temperatures, i.e., 1200, 1300 and 1400 °C for 5 h. Microstructural analysis of the pellets showed that the average grain size increased with the increase in sintering temperature. The sintered densities of the pellets were measured by Archimedes’ method, and the relative density values were within the range of 78 %TD to 87 %TD as the sintering temperature increased from 1200 to 1400 °C. Electrochemical impedance spectroscopy analysis showed that conductivity increased with the increase in sintering temperature, but no considerable change in conductivity was observed for the pellets sintered at 1300 and 1400 °C. The results revealed that the electrolyte pellet sintered at 1300 °C exhibited the ionic conductivity of 0.005 S/cm with lowest activation energy of 0.7275 eV. |
|---|---|
| ISSN: | 1820-6131 2406-1034 |