Synthesis and sintering of Gd-doped CeO2 electrolytes with and without 1 at.% CuO dopping for solid oxide fuel cell applications

被引:38
|
作者
Dong, Yingchao [1 ,2 ]
Hampshire, Stuart [1 ]
Zhou, Jian-er
Meng, Guangyao [2 ]
机构
[1] Univ Limerick, MSSI, Limerick, Ireland
[2] USTC, USTC Lab Solid State Chem & Inorgan Membranes, Hefei, Peoples R China
关键词
Solid oxide fuel cell; Ceria electrolyte; Sintering aid CuO; Combustion synthesis; Low temperature sintering; ELECTRICAL-CONDUCTIVITY; THIN-FILMS; CERIA; COMBUSTION; POWDERS; MICROSTRUCTURE; SOFC; AIDS;
D O I
10.1016/j.ijhydene.2011.01.030
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
Nano-sized Ce0.8Gd0.2O2-delta and ce(0.79)Gd(0.2)Cu(0.01)O(2-delta) electrolyte powders were synthesized by the polyvinyl alcohol assisted combustion method, and then characterized by powder characteristics, sintering behaviors and electrical properties. The results demonstrate that the as-synthesized Ce0.8Gd0.2O2-delta and ce(0.79)Gd(0.2)Cu(0.01)O(2-delta) possessed similar powder characteristics, including cubic fluorite crystalline structure, porous foamy morphology and agglomerated secondary particles composed of gas cavities and primary nano crystals. Nevertheless, after ball-milling these two powders exhibited quite different sintering abilities. A significant reduction of about 400 degrees C in densification temperature of ce(0.79)Gd(0.2)Cu(0.01)O(2-delta) was obtained when compared with Ce0.8Gd0.2O2-delta. The ce(0.79)Gd(0.2)Cu(0.01)O(2-delta) pellets sintered at 1000 degrees C and the Ce0.8Gd0.2O2-delta sintered at 1400 degrees C exhibited relative densities of 96.33% and 95.7%, respectively. The sintering of ce(0.79)Gd(0.2)Cu(0.01)O(2-delta) was dominated by the liquid phase process, followed by the evaporation-condensation process, Moreover, ce(0.79)Gd(0.2)Cu(0.01)O(2-delta) shows much higher conductivity of 0.026 S cm(-1) than Ce0.8Gd0.2O2-delta (0.0065 S cm(-1)) at a testing temperature of 600 degrees C. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5054 / 5066
页数:13
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