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Synthesis of Ce0.8Sm0.2O1.9 solid electrolyte by a proteic sol-gel green method

The present study reports the synthesis of Ce0.8Sm0.2O1.9 solid electrolyte by a novel proteic sol‐gel method which uses gelatin as polymerizing agent. The as‐synthesized powder material was calcined at 700 °C for 2 h, with X‐ray diffraction revealing a single cubic phase with lattice parameter a =...

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Bibliographic Details
Published in:Crystal research and technology (1979) 2016-06, Vol.51 (6), p.400-404
Main Authors: Macedo, Daniel A., Dutra, Ricardo P. S., Nascimento, Rubens M., Sasaki, José M., Cesário, Moisés R., Rajesh, Surendran, Figueiredo, Filipe L., Marques, Fernando M. B.
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Language:English
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Summary:The present study reports the synthesis of Ce0.8Sm0.2O1.9 solid electrolyte by a novel proteic sol‐gel method which uses gelatin as polymerizing agent. The as‐synthesized powder material was calcined at 700 °C for 2 h, with X‐ray diffraction revealing a single cubic phase with lattice parameter a = 0.5435 nm and theoretical density of 7.144 gcm‐3. The average crystallite size is 12 nm, as determined by the Scherrer equation. Impedance spectroscopy revealed a larger resistive contribution of the grain boundaries than that from grain bulk, which, due to its lower activation energy, tends to dominate the total conductivity above 650 °C. The total conductivity is in line with literature data for ceramics of the same composition prepared by various methods, thus confirming the potential of the proteic sol‐gel method as a green, low cost alternative synthetic route to prepare ceria‐based solid electrolytes. This study describes an environmentally friendly proteic sol‐gel route to produce ceria‐based nanopowders using natural gelatin as a polymeric precursor. The powder calcined at 700 °C presents crystallite size of 12 nm and theoretical density of 7.144 gcm−3. The properties of the obtained ceramics are comparable to most literature data, thus confirming the potential of the proposed method as a green alternative to produce fuel cell materials.
ISSN:0232-1300
1521-4079
DOI:10.1002/crat.201600052