The Influence of the Conditions of Synthesis and Consolidation of Nanopowders on the Physicochemical Properties of Solid Solutions in the (CeO2)1 – x(Dy2O3)x System as Electrolytes for Medium-Temperature Fuel Cells
M. V. Kalininaa, S. V. Mjakinb, *, M. A. Teplonogovac, I. A. Drozdovaa, N. V. Farafonova, b, and N. R. Loktyushkina, b
aKonstantinov St. Petersburg Institute of Nuclear Physics–Grebenshchikov Institute of Silicate Chemistry, National Research Centre “Kurchatov Institute”, St. Petersburg, 199155 Russia
bSt. Petersburg State Technological Institute (Technical University), St. Petersburg, 190013 Russia
cKurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow, 117901 Russia
email: *svmjakin@technolog.edu.ru
Received 25 October, 2024
Abstract— Using liquid-phase methods of coprecipitation of hydroxides and cocrystallization of nitrate salts, highly dispersed powders of the (CeO2)1 – x(Dy2O3)x (x = 0.05, 0.10, 0.15, 0.20) composition are synthesized. On their basis, ceramics, which are cubic solid solutions of the fluorite type with a coherent scattering region (CSR) of ~90 nm (1300°С) with open porosity in the range of 2–14% and apparent density of 6–7 g/cm3, are obtained. The influence of methods of synthesis and sintering additives on the physicochemical and electrophysical properties of ceramics is studied. It is established that the obtained ceramics have a predominantly ionic type of electrical conductivity (ion transport numbers ti = 0.78–0.96 in the range of 300–700°С). Electrical conductivity in solid solutions is realized by the vacancy mechanism and reaches the value of σ700°С = 0.43 × 10–2 S/cm. Based on their physical and chemical properties (density, open porosity, type and mechanism of specific electrical conductivity), the obtained ceramic materials are promising as solid oxide electrolytes for medium-temperature fuel cells.
Keywords:
coprecipitation of hydroxides,
joint crystallization of salts,
solid solutions,
highly dispersed powders,
density,
porosity,
electrolyte materials
DOI: 10.1134/S1087659624601114