Structural behavior and thermoelectric properties of the brownmillerite system Ca2(ZnxFe2-x)O5

被引:15
作者
Asenath-Smith, Emily [1 ]
Misture, Scott T. [1 ]
Edwards, Doreen D. [1 ]
机构
[1] Alfred Univ, Kazuo Inamori Sch Engn Mat Sci & Engn, Alfred, NY 14802 USA
基金
美国国家科学基金会;
关键词
Structure modulation; Browmillerite; Seebeck coefficient; Thermal properties; Electrical conductivity; High-temperature X-ray diffraction; X-RAY-DIFFRACTION; TRANSITION-METAL OXIDES; TETRAHEDRAL CHAINS; IRREVERSIBLE-PROCESSES; ELECTRONIC PROPERTIES; RECIPROCAL RELATIONS; NEEL TEMPERATURE; PHASE-TRANSITION; CALCIUM FERRITE; CA2FE2O5;
D O I
10.1016/j.jssc.2011.06.009
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The Ca-2(ZnxFe2-x)O-5 series was synthesized and characterized to determine the influence of zinc dopant on the brownmillerite structure for thermoelectric applications. All single-phase compounds exhibited Pnma symmetry at room temperature up to the solubility limit at x=0.10. High-temperature X-ray powder diffraction was used to show that the nature of the Pnma-Imma(0 0 gamma)s00 transition in Ca2Fe2O5 is modified by the presence of zinc. While the Zn-free composition transitions to an incommensurate phase, the Zn-containing phases transition instead to a commensurate phase, Imma(0 0 gamma)s00 with gamma=1/2. Both the Neel temperature and the onset temperature of the Pnma-Imma(0 0 gamma)s00 phase transition decreased with increasing zinc concentration. Rietveld analysis of the in situ diffraction pattern for the x=0 sample at 1300 degrees C demonstrates that the structure contains statistically disordered chain orientations as described by space group Imma. Thermoelectric properties were analyzed in air from 100 to 800 degrees C. The positive Seebeck coefficient revealed hole-type conduction for all compositions. Doped samples exhibited electrical conductivities up to 3.4 S/cm and thermal conductivity of 1.5 W/mK Transport analysis revealed thermally activated mobility consistent with polaron conduction behavior for all compositions. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:2167 / 2177
页数:11
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