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首页> 外文期刊>Journal of power sources >Direct methane solid oxide fuel cells based on catalytic partial oxidation enabling complete coking tolerance of Ni-based anodes
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Direct methane solid oxide fuel cells based on catalytic partial oxidation enabling complete coking tolerance of Ni-based anodes

机译:基于催化部分氧化的直接甲烷固体氧化物燃料电池,可实现镍基阳极的完全焦化耐受性

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摘要

Solid oxide fuel cells (SOFCs) can oxidize diverse fuels by harnessing oxygen ions. Benefited by this feature, direct utilization of hydrocarbon fuels without external reformers allows for cost-effective realization of SOFC systems. Superior hydrocarbon reforming catalysts such as nickel are required for this application. However, carbon coking on nickel-based anodes and the low efficiency associated with hydrocarbon fueling relegate these systems to immature technologies. Herein, we present methane fueled SOFCs operated under conditions of catalytic partial oxidation (CPDX). Utilizing CPDX eliminates carbon coking on Ni and facilitates the oxidation of methane. Ni-gadolinium-doped ceria (GDC) anode-based cells exhibit exceptional power densities of 1.35 W cm(-2) at 650 C and 0.74 W cm(-2) at 550 degrees C, with stable operation over 500 h, while the similarly prepared Ni-yttria stabilized zirconia anode based cells exhibit a power density of 0.27 W cm(-2) at 650 degrees C, showing gradual degradation. Chemical analyses suggest that combining GDC with the Ni anode prevents the oxidation of Ni due to the oxygen exchange ability of GDC. In addition, CPDX operation allows the usage of stainless steel current collectors. Our results demonstrate that high-performance SOFCs utilizing methane CPDX can be realized without deterioration of Ni-based anodes using cost-effective current collectors. (C) 2017 Elsevier B.V. All rights reserved.
机译:固体氧化物燃料电池(SOFC)可以通过利用氧离子来氧化多种燃料。受益于此功能,无需外部重整器即可直接利用烃类燃料,从而可以经济高效地实现SOFC系统。该应用需要高级烃重整催化剂,例如镍。但是,镍基阳极上的碳焦化以及与碳氢化合物燃料供应相关的低效率使这些系统成为了不成熟的技术。本文中,我们介绍了在催化部分氧化(CPDX)条件下运行的以甲烷为燃料的SOFC。利用CPDX消除了Ni上的碳焦化并促进了甲烷的氧化。镍ga掺杂的二氧化铈(GDC)阳极电池在650 C时表现出1.35 W cm(-2)的高功率密度,在550 C时表现出0.74 W cm(-2)的出色功率密度,在500 h内稳定运行,而同样制备的Ni-氧化钇稳定的氧化锆阳极基电池在650摄氏度下显示出0.27 W cm(-2)的功率密度,显示出逐渐降解。化学分析表明,由于GDC的氧交换能力,将GDC与Ni阳极结合可防止Ni的氧化。另外,CPDX操作允许使用不锈钢集电器。我们的结果表明,使用具有成本效益的集电器,可以实现利用甲烷CPDX的高性能SOFC,而不会降低镍基阳极的性能。 (C)2017 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Journal of power sources》 |2017年第31期|30-40|共11页
  • 作者单位

    Yonsei Univ, Dept Mat Sci & Engn, 50 Yonsei Seodaemun, Seoul 03722, South Korea;

    Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland;

    Yonsei Univ, Dept Mat Sci & Engn, 50 Yonsei Seodaemun, Seoul 03722, South Korea;

    Yonsei Univ, Dept Mat Sci & Engn, 50 Yonsei Seodaemun, Seoul 03722, South Korea;

    Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland;

    Korea Inst Sci & Technol, High Temp Energy Mat Res Ctr, Seoul 02792, South Korea;

    Yonsei Univ, Dept Mat Sci & Engn, 50 Yonsei Seodaemun, Seoul 03722, South Korea;

  • 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
  • 中图分类
  • 关键词

    Solid oxide fuel cell; Methane fueling; Ni catalyst; Catalytic partial oxidation; Oxygen exchange kinetics;

    机译:固体氧化物燃料电池甲烷燃料镍催化剂催化部分氧化氧交换动力学;

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