Combustion synthesis and characterization of Cu-Sm co-doped CeO2 electrolytes

被引:18
作者
Dong, Yingchao [1 ]
Hampshire, Stuart [1 ]
Zhou, Jian-er [2 ]
Dong, Xinfa [4 ]
Lin, Bin [3 ]
Meng, Guangyao [3 ]
机构
[1] Univ Limerick, MSSI, Limerick, Ireland
[2] Jingdezhen Ceram Univ, Key Lab, Jiangxi Univ Inorgan Membranes, Jingdezhen, Peoples R China
[3] Univ Sci & Technol China, USTC Lab Solid State Chem & Inorgan Membranes, Hefei, Peoples R China
[4] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou, Guangdong, Peoples R China
关键词
Solid oxide fuel cell; Ceria electrolyte; Combustion synthesis; Co-doping; Low-temperature sintering; Mechanical and electrical properties; MECHANICAL-PROPERTIES; ELECTRICAL-PROPERTIES; HYDROTHERMAL SYNTHESIS; IONIC-CONDUCTIVITY; SOLID-SOLUTIONS; NANOPARTICLES; POWDERS; CERAMICS; SOFC; PVA;
D O I
10.1016/j.jeurceramsoc.2011.04.037
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nano-sized CSO (Ce0.80Sm0.20O2-delta) and CSCO (Ce0.79Sm0.20Cu0.01O2-delta) were synthesized by the PVA-assisted combustion method, and then characterized by the structure of PVA-cation complexes and nano-powders, as well as mechanical and electrical performance after sintering. The results indicate that the PVA-cation complexes (PVA-(Ce3+,Sm3+) and PVA-(Ce3+,Sm3+,Cu2+)) were formed by coordinating metal cations to hydroxyl groups, as well as the COO-1 group derived from the oxidation of PVA with NO3-1. Low temperatures (around 200 degrees C) caused intense combustion reactions, resulting in the direct crystallization of cubic fluorite nano-CSO (10-20 nm) and nano-CSCO (10-15 nm) crystals with homogeneous element distribution. This slight compositional modification of CSO by co-doping with 1 mol% CuO resulted in a significantly lowered densification temperature, as well as enhanced mechanical and electrical property. The strength improvement can be ascribed to the dense and fine-grained microstructure without normal grain coarsening, resulting in a transgranular-dominant fracture mode during strength testing. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2365 / 2376
页数:12
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