Lin, Bin and Hu, Mingjun and Ma, Jianjun and Jiang, Yinzhu and Tao, Shanwen and Meng, Guangyao (2008) Stable, easily sintered BaCe0.5Zr0.3Y0.16Zn0.04O3-delta electrolyte-based protonic ceramic membrane fuel cells with Ba0.5Sr0.5Zn0.2Fe0.8O3-delta perovskite cathode. Journal of Power Sources, 183 (2). pp. 479-484. ISSN 0378-7753Full text not available in this repository. (Request a copy from the Strathclyde author)
A stable, easily sintered perovskite oxide BaCe0.5Zr0.3Y0.16Zn0.04O3-delta (BCZYZn) as an electrolyte for protonic ceramic mernbrane fuel cells (PCMFCs) with Ba0.5Sr0.5Zn0.2Fe0.8O3-delta (BSZF) perovskite cathode was investigated. The BCZYZn perovskite electrolyte synthesized by a modified Pechini method exhibited higher sinterability and reached 97.4% relative density at 1200 degrees C for 5 h in air, which is about 200 degrees C lower than that without Zn dopant. By fabricating thin membrane BCZYZn electrolyte (about 30 mu m in thickness) on NiO-BCZYZn anode support, PCMFCs were assembled and tested by selecting stable BSZF perovskite cathode. An open-circuit potential of 1.00V, a maximum power density of 236 mWcm(-2), and a low polarization resistance of the electrodes of 0.17 Omega cm(2) were achieved at 700 degrees C. This investigation indicated that proton conducting electrolyte BCZYZn with BSZF perovskite cathode is a promising material system for the next generation solid oxide fuel cells. (C) 2008 Elsevier B.V. All rights reserved.
|Keywords:||solid oxide fuel cells, BaCe0.5Zr0.3Y0.16Zn0.04O3-delta, Ba0.5Sr0.5Zn0.2Fe0.8O3-delta, Zn dopant, Pechini method, ELECTROCHEMICAL PROPERTIES, BACEO3 ELECTROLYTE, DOPED BACEO3, THIN-FILM, OXIDE, PERFORMANCE, CONDUCTIVITY, CONDUCTORS, Energy Engineering and Power Technology, Physical and Theoretical Chemistry, Electrical and Electronic Engineering, Renewable Energy, Sustainability and the Environment|
|Department:||Faculty of Engineering > Chemical and Process Engineering|
|Depositing user:||Pure Administrator|
|Date Deposited:||21 Oct 2011 08:34|
|Last modified:||04 Nov 2016 03:44|