TY - JOUR
T1 - Ionic conductivity, sintering and thermal expansion behaviors of mixed ion conductor BaZr0.1Ce0.7Y0.1Yb 0.1O3-δ prepared by ethylene diamine tetraacetic acid assisted glycine nitrate process
AU - Zhou, Xiaoliang
AU - Liu, Limin
AU - Zhen, Jiangman
AU - Zhu, Shengcai
AU - Li, Baowen
AU - Sun, Kening
AU - Wang, Peng
N1 - Funding Information:
This project is financially supported by Project (HIT.NSRIF.2009085) Supported by Natural Scientific Research Innovation Foundation in Harbin Institute of Technology, Development Program for Outstanding Young Teachers in Harbin Institute of Technology (No. HITQNJS.2008.056 ), China Postdoctoral Science Foundation (No. 20070420865 ), and Natural Science Foundations of China (No. 90510006 and 50821002 ).
PY - 2011/6/1
Y1 - 2011/6/1
N2 - BaZr0.1Ce0.7Y0.1Yb0.1O 3-δ as a candidate electrolyte material is prepared by ethylene diamine tetraacetic acid assisted glycine-nitrate process. After calcining at 900 °C, the single-phase perovskite is obtained due to the better distribution of starting materials and the more feasible reaction kinetic conditions than solid state reaction method. The relative densities reach 96.8 and 98.4% respectively after sintering the pressed pellets at 1280 and 1400 °C for 10 h. In humidified oxygen the ionic conductivities are 0.015, 0.045, 0.101 and 0.207 S cm-1 at 500, 600, 700 and 800 °C, respectively. In air and humidified oxygen the activation energies for ionic conductivity are 66.1 and 68.9 kJ mol-1. In humidified hydrogen, however, different activation energies occur in low and high temperature ranges. The thermal expansion curve inflections at 500-800 °C with respect to possible phase changes are found. Zirconia aggregation possibly results in the higher activation energy and peculiar thermal expansion behavior. The results indicate the ethylene diamine tetraacetic acid assisted glycine-nitrate process is a very promising preparation method for solid oxide fuel cell practical application.
AB - BaZr0.1Ce0.7Y0.1Yb0.1O 3-δ as a candidate electrolyte material is prepared by ethylene diamine tetraacetic acid assisted glycine-nitrate process. After calcining at 900 °C, the single-phase perovskite is obtained due to the better distribution of starting materials and the more feasible reaction kinetic conditions than solid state reaction method. The relative densities reach 96.8 and 98.4% respectively after sintering the pressed pellets at 1280 and 1400 °C for 10 h. In humidified oxygen the ionic conductivities are 0.015, 0.045, 0.101 and 0.207 S cm-1 at 500, 600, 700 and 800 °C, respectively. In air and humidified oxygen the activation energies for ionic conductivity are 66.1 and 68.9 kJ mol-1. In humidified hydrogen, however, different activation energies occur in low and high temperature ranges. The thermal expansion curve inflections at 500-800 °C with respect to possible phase changes are found. Zirconia aggregation possibly results in the higher activation energy and peculiar thermal expansion behavior. The results indicate the ethylene diamine tetraacetic acid assisted glycine-nitrate process is a very promising preparation method for solid oxide fuel cell practical application.
KW - AC impedance
KW - Doped barium cerate
KW - Glycine-nitrate process
KW - Mixed ion conductor
KW - Solid oxide fuel cell
UR - http://www.scopus.com/inward/record.url?scp=79952994609&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2011.01.092
DO - 10.1016/j.jpowsour.2011.01.092
M3 - Article
AN - SCOPUS:79952994609
SN - 0378-7753
VL - 196
SP - 5000
EP - 5006
JO - Journal of Power Sources
JF - Journal of Power Sources
IS - 11
ER -