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Composite ceramic materials as anodes for solid oxide fuel cells.

机译:复合陶瓷材料可作为固体氧化物燃料电池的阳极。

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摘要

In this thesis, a composite material of La0.8Sr0.2Cr 1-yXyO3 (LSC), Ce0.9Gd0.1O 1.95 (GDC) and Ni was proposed to replace the standard solid oxide fuel cell (SOFC) composite anode of Ni metal with Zr0.92Y0.08O 2 (YSZ). Ni-YSZ cermet anodes provide high performance for SOFCs operating on humidified hydrogen as a fuel. The anode performance degrades irreversibly, however, during reduction-oxidation (redox) cycling and due to carbon deposition on the anode when operating on hydrocarbon fuels without the addition of a reforming species (e.g., H2O, CO2). The LSC-GDC-Ni anode has the potential to avoid these drawbacks due to the very low Ni content, which is achieved by replacing the majority of the nickel with LSC, a ceramic electronic conductor.; SOFCs were tested from 500-800°C using GDC electrolyte-supported cells with LSCF-GDC cathodes. Current-voltage and impedance measurements were used to characterize the anode performance in hydrogen, methane and propane fuels. The anode atmosphere was cycled between hydrogen and air during operation to test the redox stability of the anode. Power densities of ≈150 mW/cm 2 were achieved in H2 at 750°C, and switching to methane or propane resulted in a ∼25% decrease in power density. The power density in H2 was comparable to an identically prepared Ni-GDC anode on GDC. No carbon deposition was observed for an LSC-GDC-Ni anode after > 3h operation in propane, while the Ni-GDC anode rapidly failed. Seven redox cycles at 750°C resulted in only minimal performance loss for an SOFC with an LSC-GDC-Ni anode.; Several studies were conducted to determine favorable compositions and processing parameters to obtain more active LSC-GDC-Ni anodes. The addition of 5 wt.% NiO to the anode was sufficient to catalyze the anode reaction for fine microstructures formed at 1100°C. The results agree well with a proposed reaction mechanism where adsorption/dissociation of H2 on the anode surface is co-limiting with surface diffusion of hydrogen species. The addition of Ni catalyzes both of these limiting reactions.; These results indicate the composite ceramic material LSC-GDC-Ni has promise as a high performance, redox-stable, direct hydrocarbon SOFC anode.
机译:本文提出了一种La0.8Sr0.2Cr 1-yXyO3(LSC),Ce0.9Gd0.1O 1.95(GDC)和Ni的复合材料,以取代标准的Ni金属固体氧化物燃料电池(SOFC)复合阳极。 Zr0.92Y0.08O 2(YSZ)。 Ni-YSZ金属陶瓷阳极为以湿化氢为燃料的SOFC提供了高性能。然而,在还原-氧化(氧化还原)循环期间以及由于在不添加重整物质(例如,H 2 O,CO 2)的烃类燃料上操作时,阳极上的碳沉积会导致阳极性能不可逆地降低。 LSC-GDC-Ni阳极由于镍含量极低而具有避免这些缺陷的潜力,这是通过用陶瓷电子导体LSC代替大部分镍来实现的。使用具有LSCF-GDC阴极的GDC电解质支持的电池,在500-800°C下测试了SOFC。使用电流-电压和阻抗测量来表征氢,甲烷和丙烷燃料中的阳极性能。在操作过程中,阳极气氛在氢气和空气之间循环,以测试阳极的氧化还原稳定性。在750°C的H2中获得的功率密度约为150 mW / cm 2,并且转换为甲烷或丙烷会导致功率密度降低约25%。 H2中的功率密度与GDC上相同制备的Ni-GDC阳极相当。 LSC-GDC-Ni阳极在丙烷中运行> 3h后未观察到碳沉积,而Ni-GDC阳极迅速失效。在750°C的七个氧化还原循环中,只有带有LSC-GDC-Ni阳极的SOFC的性能损失最小。进行了一些研究,以确定有利的成分和工艺参数,以获得更具活性的LSC-GDC-Ni阳极。向阳极添加5重量%的NiO足以催化在1100℃下形成的精细微结构的阳极反应。结果与提出的反应机理非常吻合,在反应机理中,H2在阳极表面的吸附/解离与氢物种的表面扩散共同受到限制。 Ni的添加催化了这两个限制性反应。这些结果表明,复合陶瓷材料LSC-GDC-Ni具有作为高性能,氧化还原稳定的直接烃类SOFC阳极的前景。

著录项

  • 作者

    Madsen, Brian Douglas.;

  • 作者单位

    Northwestern University.;

  • 授予单位 Northwestern University.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 212 p.
  • 总页数 212
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

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