4.7 Article

A comparative study of Sm0.5Sr0.5MO3-δ (M = Co and Mn) as oxygen reduction electrodes for solid oxide fuel cells

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 37, 期 5, 页码 4377-4387

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2011.11.150

关键词

Solid oxide fuel cells; Perovskite; Sm0.5Sr0.5CoO3-delta; Sm0.5Sr0.5MnO3-delta; Cathode

资金

  1. National Science Foundation for Distinguished Young Scholars of China [51025209]
  2. program for New Century Excellent Talents
  3. Fok Ying Tung Education Foundation [111073]

向作者/读者索取更多资源

Sm0.5Sr0.5MO3-delta (M = Co and Mn) materials are synthesized, and their properties and performance as cathodes for solid oxide fuel cells (SOFCs) on Sm0.2Ce0.8O1.9 (SDC) and Y0.16Zr0.92O2.08 (YSZ) electrolytes are comparatively studied. The phase structure, thermal expansion behavior, oxygen mobility, oxygen vacancy concentration and electrical conductivity of the oxides are systematically investigated. Sm0.5Sr0.5CoO3-delta (SSC) has a much larger oxygen vacancy concentration, electrical conductivity and TEC than Sm0.5Sr0.5MnO3-delta (SSM). A powder reaction demonstrates that SSM is more chemically compatible with the YSZ electrolyte than SSC, while both are compatible with the SDC electrolyte. EIS results indicate that the performances of SSC and SSM electrodes depend on the electrolyte that they are deposited on. SSC is suitable for the SDC electrolyte, while SSM is preferred for the YSZ electrolyte. A peak power density as high as 690 mW cm(-2) at 600 degrees C is observed for a thin-film SDC electrolyte with SSC cathode, while a similar cell with YSZ electrolyte performs poorly. However, SSM performs well on YSZ electrolyte at an operation temperature of higher than 700 degrees C, and a fuel cell with SSM cathode and a thin-film YSZ electrolyte delivers a peak power density of similar to 590 mW cm(-2) at 800 degrees C. The poor performances of SSM cathode on both YSZ and SDC electrolytes are obtained at a temperature of lower than 650 degrees C. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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