首页> 外文期刊>Journal of power sources >Hydrogen oxidation mechanisms on Ni/yttria stabilized zirconia anodes: Separation of reaction pathways by geometry variation of pattern electrodes
【24h】

Hydrogen oxidation mechanisms on Ni/yttria stabilized zirconia anodes: Separation of reaction pathways by geometry variation of pattern electrodes

机译:Ni /氧化钇稳定的氧化锆阳极上的氢氧化机理:通过图案电极的几何变化来分离反应路径

获取原文
获取原文并翻译 | 示例
       

摘要

Nickel/yttria stabilized zirconia (YSZ) electrodes are affecting the overall performance of solid oxide fuel cells (SOFCs) in general and strongly contribute to the cell resistance in case of novel metal supported SOFCs in particular. The electrochemical fuel conversion mechanisms in these electrodes are, however, still only partly understood. In this study, micro-structured Ni thin film electrodes on YSZ with 15 different geometries are utilized to investigate reaction pathways for the hydrogen electro-oxidation at Ni/YSZ anodes. From electrodes with constant area but varying triple phase boundary (TPB) length a contribution to the electro-catalytic activity is found that does not depend on the TPB length. This additional activity could clearly be attributed to a yet unknown reaction pathway scaling with the electrode area. It is shown that this area related pathway has significantly different electrochemical behavior compared to the TPB pathway regarding its thermal activation, sulfur poisoning behavior, and H-2/H2O partial pressure dependence. Moreover, possible reaction mechanisms of this reaction pathway are discussed, identifying either a pathway based on hydrogen diffusion through Ni with water release at the TPB or a path with oxygen diffusion through Ni to be a very likely explanation for the experimental results.
机译:镍/氧化钇稳定的氧化锆(YSZ)电极通常会影响固体氧化物燃料电池(SOFC)的整体性能,尤其是在新型金属负载的SOFC的情况下,它们对电池的电阻有很大贡献。然而,这些电极中的电化学燃料转化机理仍然仅被部分理解。在这项研究中,利用具有15种不同几何形状的YSZ上的微结构Ni薄膜电极来研究Ni / YSZ阳极上氢电氧化的反应途径。从具有恒定面积但变化的三相边界(TPB)长度的电极中发现了对电催化活性的贡献,它与TPB长度无关。这种额外的活性显然可以归因于未知的反应路径随电极面积的变化。结果表明,与TPB途径相比,该区域相关途径在热活化,硫中毒行为和H-2 / H2O分压依赖性方面具有明显不同的电化学行为。此外,讨论了该反应途径的可能的反应机理,确定基于氢通过Ni扩散而在TPB处释放水的途径或基于氧通过Ni扩散的途径是对实验结果的一种很有可能的解释。

著录项

  • 来源
    《Journal of power sources》 |2018年第15期|46-54|共9页
  • 作者单位

    Christian Doppler Lab Interfaces Met Supported El, Getreidemarkt 9-164 EC, A-1060 Vienna, Austria;

    TU Wien, Inst Chem Technol & Analyt, Getreidemarkt 9-164 EC, A-1060 Vienna, Austria;

    Christian Doppler Lab Interfaces Met Supported El, Getreidemarkt 9-164 EC, A-1060 Vienna, Austria;

    Christian Doppler Lab Interfaces Met Supported El, Getreidemarkt 9-164 EC, A-1060 Vienna, Austria;

  • 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

    Microelectrode; Metal/solid electrolyte interface; SOFC anode; Electrochemical reaction kinetics; Impedance spectroscopy;

    机译:微电极;金属/固体电解质界面;SOFC阳极;电化学反应动力学;阻抗谱;
  • 入库时间 2022-08-18 00:21:23

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号