4.8 Article

Ionic conductivity, sintering and thermal expansion behaviors of mixed ion conductor BaZr0.1Ce0.7Y0.1Yb0.1O3-δ prepared by ethylene diamine tetraacetic acid assisted glycine nitrate process

Journal

JOURNAL OF POWER SOURCES
Volume 196, Issue 11, Pages 5000-5006

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2011.01.092

Keywords

Solid oxide fuel cell; Doped barium cerate; Mixed ion conductor; Glycine-nitrate process; AC impedance

Funding

  1. Natural Scientific Research Innovation Foundation in Harbin Institute of Technology [HIT.NSRIF.2009085]
  2. Development Program for Outstanding Young Teachers in Harbin Institute of Technology [HITQNJS.2008.056]
  3. China Postdoctoral Science Foundation [20070420865]
  4. Natural Science Foundations of China [90510006, 50821002]

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BaZr0.1Ce0.7Y0.1Yb0.1O3-delta as a candidate electrolyte material is prepared by ethylene diamine tetraacetic acid assisted glycine-nitrate process. After calcining at 900 degrees 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 degrees 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 degrees 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 degrees 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. (C) 2011 Elsevier B.V. All rights reserved.

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