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http://hdl.handle.net/10773/19688
Título: | Synthesis of Sr0.9K0.1FeO3-delta electrocatalysts by mechanical activation |
Autor: | Monteiro, J. F. Waerenborgh, J. C. Kovalevsky, A. V. Yaremchenko, A. A. Frade, J. R. |
Palavras-chave: | OXIDE FUEL-CELLS OXYGEN STOICHIOMETRY CATHODE MATERIALS SRFEO3-DELTA CONDUCTIVITY PEROVSKITES PERMEATION STABILITY CERAMICS SIZE |
Data: | 2013 |
Editora: | ACADEMIC PRESS INC ELSEVIER SCIENCE |
Resumo: | Potassium-substituted SrFeO3-delta for possible application as oxygen evolution electrode in alkaline or molten salt media was prepared by mechanical activation and characterized by X-ray diffraction, dilatometric and thermogravimetric analysis, Mossbauer spectroscopy, and electrical conductivity measurements. Room temperature mechanical activation of a mixture of oxide precursors with subsequent thermal treatments at 700-900 degrees C results in the formation of Sr(0.9)Ka(0.1)FeO(3-delta) with tetragonal perovskite-like structure. Such allows to decrease the synthesis temperature, if compared to the conventional solid-state route, and to prevent possible volatilization of potassium. The results of Mossbauer spectroscopy studies indicate that the oxygen nonstoichiometry in the samples annealed in air at 900-1100 degrees C with subsequent rapid cooling vary in the range delta=0.30-0.32. The electrical conductivity in air exhibits a metal-like behaviour at temperatures above 400 degrees C and semiconductor behaviour in the low-temperature range, reaching 13-30 S/cm under prospective operation conditions for alkaline electrolyzers (<= 90 degrees C). (C) 2012 Elsevier Inc. All rights reserved. |
Peer review: | yes |
URI: | http://hdl.handle.net/10773/19688 |
DOI: | 10.1016/j.jssc.2012.10.009 |
ISSN: | 0022-4596 |
Versão do Editor: | 10.1016/j.jssc.2012.10.009 |
Aparece nas coleções: | CICECO - Artigos |
Ficheiros deste registo:
Ficheiro | Descrição | Tamanho | Formato | |
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Synthesis of Sr0.9K0.1FeO3-δ electrocatalysts by mechanical activation_10.1016j.jssc.2012.10.009.pdf | 627.61 kB | Adobe PDF |
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