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首页> 外文期刊>Journal of Materials Research >New buffer layer material La(Pr)CrO_3 for intermediate temperature solid oxide fuel cell using LaGaO_3-based electrolyte film
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New buffer layer material La(Pr)CrO_3 for intermediate temperature solid oxide fuel cell using LaGaO_3-based electrolyte film

机译:使用基于LaGaO_3的电解质膜的中温固体氧化物燃料电池的新型缓冲层材料La(Pr)CrO_3

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摘要

A metal-supported solid oxide fuel cell (SOFC) using Ce_(0.8)Sm_(0.2)O_2 (Sin-doped ceria, SDC) buffer layer and La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_3 (LSGM) electrolyte films showed a small degradation in the cell performance after a long-term operation because of La migration from the electrolyte to the buffer layer, resulted in a formation of a less conductive phase. Thus, various ceramic materials such as doped ceria and perovskite-related oxides were investigated for an effective buffer layer with respect to fabricating reliable metal-supported SOFCs using a LSGM electrolyte film. In particular, La-doped CeO_2 (LDC) and Pr-doped LaCrO_3 (LPCr) were investigated as buffer layer material since the materials showed chemical compatibility with the LSGM and anode materials. The cell using a LDC buffer layer showed a prior stability during the operation for 100 h at 973 K, while the power density of the cell was slightly low owing to the low electrical conductivity of LDC compared with that of SDC or LPCr. In contrast, the cell using a LPCr buffer layer revealed significantly low open circuit voltage (OCV) and power density, which were attributed to Pr decomposition in the LPCr caused by the reactivity with water vapor. However, the metal-supported cell with a multilayer electrolyte film including LSGM/LPCr/SDC layers showed an almost theoretical OCV and reasonably high power density with no degradation after a long-term operation for 100 h at 973 K, suggesting that the LPCr layer effectively prevented La migration and the SDC layer led to avoid the Pr decomposition. Thus, a LPCr is an effective buffer layer material for reliable metal-supported SOFCs using a LSGM electrolyte thin film.
机译:使用Ce_(0.8)Sm_(0.2)O_2(Sin掺杂的二氧化铈,SDC)缓冲层和La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_3的金属支撑固体氧化物燃料电池(SOFC)( LSGM)电解质膜在长期运行后由于La从电解质向缓冲层的迁移而表现出较小的电池性能下降,导致形成导电性较低的相。因此,对于使用LSGM电解质膜制造可靠的金属负载的SOFC,对于有效的缓冲层,研究了各种陶瓷材料,例如掺杂的二氧化铈和钙钛矿相关的氧化物。特别地,研究了掺La的CeO_2(LDC)和掺Pr的LaCrO_3(LPCr)作为缓冲层材料,因为该材料显示出与LSGM和阳极材料的化学相容性。使用LDC缓冲层的电池在973 K下运行100 h时表现出先验的稳定性,而与SDC或LPCr相比,由于LDC的电导率低,因此电池的功率密度略低。相反,使用LPCr缓冲层的电池的开路电压(OCV)和功率密度明显较低,这归因于LPCr中与水蒸气的反应性引起的Pr分解。然而,带有多层电解质膜的金属支撑电池(包括LSGM / LPCr / SDC层)在973 K下长期运行100 h后,显示出几乎理论上的OCV和相当高的功率密度,并且没有降解,这表明LPCr层有效地防止了La迁移和SDC层导致避免了Pr的分解。因此,LPCr是用于使用LSGM电解质薄膜的可靠的金属负载的SOFC的有效缓冲层材料。

著录项

  • 来源
    《Journal of Materials Research 》 |2012年第15期| p.1906-1914| 共9页
  • 作者单位

    Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Nishi-Ku, Fukuoka 819-0395, Japan;

    Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Nishi-Ku, Fukuoka 819-0395, Japan;

    Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Nishi-Ku, Fukuoka 819-0395, Japan;

    The Kansai Electric Power Co., Inc., Amagasaki, Hyogo 661-0974, Japan;

    Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Nishi-Ku, Fukuoka 819-0395, Japan;

    Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Nishi-Ku, Fukuoka 819-0395, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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