Microdomain texture and microstructures of Fe4+-containing CaTi0.4Fe0.6O3-δ

被引:8
作者
Canales-Vázquez, J
Figueiredo, FM [1 ]
Waerenborgh, JC
Zhou, WZ
Frade, JR
Irvine, JTS
机构
[1] Univ Aveiro, Ceram & Glass Engn Dept, CICECO, P-3810193 Aveiro, Portugal
[2] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[3] U Aberta, Sci & Technol Dept, P-1269001 Lisbon, Portugal
[4] Inst Tecnol & Nucl, Dept Chem, P-2686953 Sacavem, Portugal
关键词
titanates; structure; microdomains; HRTEM; image simulation; Mossbauer spectroscopy;
D O I
10.1016/j.jssc.2004.05.029
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A study of the structure of Fe-1V CaTi0.4Fe0.6O3-delta is presented and compared to data on the Fe-III counterparts. The powder XRD pattern was dominated by a simple cubic perovskite unit cell;, however, some small peaks indicated an orthorhombic distortion. All peaks could be indexed using a space group analogous to the Fe-III phase Ca3TiFe2O8. From HRTEM the strong cubic peaks are well explained by the Superposition of three equivalent and mutually perpendicular orthorhombic unit cells. TEM analysis further revealed a microdomain structure consisting of disordered intergrowths of CaTiO3- and Ca3TiFe2O8-like phases. Mossbauer spectra show that ca. 4% of the Fe cations are in the 4+ oxidation state. Results suggest that the Fe 4+ cations are associated with octahedral coordination and hence are associated with the CaTiO3-like regions, transition regions between the CaTiO3- and Ca3TiFe2O8 intergrown phases and the domain boundaries. Structural models for the intergrowths are proposed based on HRTEM image simulations. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:3105 / 3113
页数:9
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