Structural, morphological, and electrical properties of doped ceria as a solid electrolyte for intermediate-temperature solid oxide fuel cells

The solid solutions of CeO 2 with one or more rare-earth oxides among Yb 2 O 3 , Sm 2 O 3 , and Gd 2 O 3 are synthesized by either modified glycine nitrate procedure (MGNP) or self-propagating reaction at room temperature (SPRT). The overall mole fraction of rare-earth oxide dopants was x  = 0.2. Th...

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Veröffentlicht in:Journal of materials science 2015-05, Vol.50 (10), p.3781-3794
Hauptverfasser: Stojmenović, M., Žunić, M., Gulicovski, J., Bajuk-Bogdanović, D., Holclajtner-Antunović, I., Dodevski, V., Mentus, S.
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Sprache:eng
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Zusammenfassung:The solid solutions of CeO 2 with one or more rare-earth oxides among Yb 2 O 3 , Sm 2 O 3 , and Gd 2 O 3 are synthesized by either modified glycine nitrate procedure (MGNP) or self-propagating reaction at room temperature (SPRT). The overall mole fraction of rare-earth oxide dopants was x  = 0.2. The characterization was committed by XRPD, TEM, BET, and Raman Spectroscopy methods. According to XRPD and Raman spectroscopy, the obtained products presented the single-phase solid solutions with basic fluorite-type CeO 2 structure, regardless on the number and the concentration of dopants. Both XRPD and TEM analysis evidenced the nanometer particle dimensions. The defect model was applied to calculate lattice parameters of single-, co-, and multi-doped solids. The sintering of the sample nanopowders was performed at 1550 °C, in air atmosphere. The sintered samples were characterized by XRPD, SEM, and complex impedance methods. The sintering did not affect the concentration ratios of the constituents. The highest conductivity at 700 °C amounting to 2.14 × 10 −2 and 1.92 × 10 −2  Ω −1  cm −1 was measured for the sample Ce 0.8 Sm 0.08 Gd 0.12 O 2−δ , synthesized by SPRT and MGNP methods, respectively. The corresponding activation energies of conductivity, measured in the temperature range 500–700 °C, amounted to 0.24 and 0.23 eV.
ISSN:0022-2461
1573-4803
DOI:10.1007/s10853-015-8943-y