4.8 Review

Progress in understanding and development of Ba0.5Sr0.5Co0.8Fe0.2O3-δ-based cathodes for intermediate-temperature solid-oxide fuel cells: A review

Journal

JOURNAL OF POWER SOURCES
Volume 192, Issue 2, Pages 231-246

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2009.02.069

Keywords

Intermediate-temperature solid-oxide fuel cell; Ba0.5Sr0.5Co0.8Fe0.2O3-delta; Cathode; Oxygen reduction reaction; Perovskite

Funding

  1. National Natural Science Foundation of China [20703024, 20676061]
  2. National 863 [2007AA05Z133]
  3. National Basic Research Program of China [2007CB209704]

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Solid-oxide fuel cells (SOFCs) convert chemical energy directly into electric power in a highly efficient way. Lowering the operating temperature of SOFCs to around 500-800 degrees C is one of the main goals in current SOFC research. The associated benefits include reducing the difficulties associated with sealing and thermal degradation, allowing the use of low-cost metallic interconnectors and suppressing reactions between the cell components. However, the electrochemical activity of the cathode deteriorates dramatically with decreasing temperature for the typical La0.8Sr0.2MnO3-based electrodes. The cathode becomes the limiting factor in determining the overall cell performance. Therefore, the development of new electrodes with high electrocatalytic activity for oxygen reduction becomes a critical issue for intermediate-temperature (IT)-SOFCs. Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) perovskite oxide was first reported as a potential IT-SOFC cathode material in 2004 by Shao and Haile. After that, the BSCF cathode has attracted considerable attention. This paper reviews the current research activities on BSCF-based cathodes for IT-SOFCs. Emphasis will be placed on the understanding and optimization of BSCF-based materials. The issues raised by the BSCF cathode are also presented and analyzed to provide some guidelines in the search for the new generation of cathode materials for IT-SOFCs. (C) 2009 Elsevier B.V. All rights reserved.

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