Preparation of compact Li-doped Y2Ti2O7 solid electrolyte

被引:10
作者
Wen, L. C. [1 ]
Hsieh, H. Y. [1 ]
Lee, Y. H. [1 ]
Chang, S. C. [1 ]
Kao, H. -C. I. [1 ]
Sheu, H. S. [2 ]
Lin, I. N. [3 ]
Chang, J. C. [4 ]
Lee, M. C. [5 ]
Lee, Y. S. [5 ]
机构
[1] Tamkang Univ, Dept Chem, Tamsui 25137, Taiwan
[2] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
[3] Tamkang Univ, Dept Phys, Tamsui 25137, Taiwan
[4] Solar Technol Inc, Tainan 70955, Taiwan
[5] Atom Energy Council, Inst Nucl Energy Res, Langton 32546, Taiwan
关键词
(Y2-xLix)Ti2O7-x; Pyrochlore; Titanate; Li2O; Oxygen ion conductor; ELECTRICAL-CONDUCTIVITY; CONSTITUENT OXIDES; ION CONDUCTIVITY; PYROCHLORE; GD; CERIA; TEMPERATURE; CERAMICS; SYSTEM; SOFC;
D O I
10.1016/j.ssi.2011.10.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Three series of solid electrolytes were prepared with the nominal compositions of (Y2 - xLi3x)Ti2O7 (Y3LT), (Y2 - xLix)Ti2O7 - x (YLT) and Y2 - xTi2O7 - 3x/2 (YT) with x = 0.040 - 0.11. Comparing the unit cell a-axis of the YLT with that of YT, the latter is shorter with the same amount of x. This indicates a successful substitution of the Li ion into the Y site of Y2Ti2O7. However, both Y3LTand YLT have exactly the same unit cell a-axis length with the same amount of x so that the solid solution formed probably has the same formula, (Y2 - xLix)Ti2O7 - x, in which only one Li ion is substituted into the Y site. Extra Li2O added in the Y3LT is probably acting as a self flux to lower the melting point of the mixture. As a result, materials become more compact and grains grow bigger. One compound of Y3LT with x = 0.060 has a total conductivity of 4.3 (4) x 10(-4) S.cm(-1) at 700 degrees C. Adding Li2O as a flux and carefully controlling the heat treatment history, compact sample of Y3LT with a relative density higher than 90% was obtained at a temperature as low as 1150 degrees C. Its ionic conductivity is comparable to one Y2Ti2O7 prepared at 1600 degrees C with a conductivity reported as 2.30 x 10(-4) S.cm(-1). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 44
页数:6
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