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Zirconium oxide-based compound as new cathode without platinum group metals for PEFC

机译:基于氧化锆的化合物作为PEFC的不含铂族金属的新型阴极

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摘要

Partially oxidized zirconium carbonitrides (Zr-CNO) powders were evaluated as a non-precious cathode for polymer electrolyte fuel cells (PEFCs). Zr-CNO powders were prepared from zirconium carbonitrides (Zr-CN) with heat-treatment under 0.25%O_2/2%H_2/N_2 at 1000 - 1400℃. The slow scan voltammetry was performed to evaluate the catalytic activity for the oxygen reduction reaction (ORR) under nitrogen and oxygen in 0.1 mol dm~(-3) H_2SO_4 at 30℃. Although the onset potential of ORR for untreated Zr-CN is 0.55 V vs. reversible hydrogen electrode (RHE), the onset potential of the appropriate oxidized Zr-CNO reached 0.97 V vs. RHE. XRD and XPS data suggested that the surface of the Zr-CNO was oxidized to ZrO_2 and Zr-CN remained in the inner part of the each particle. The existence of tetragonal and/or cubic ZrO_2 in the XRD patterns of the Zr-CNO suggested that the vacancies on the surface of the Zr-CNO might affect the catalytic activity for the ORR.
机译:评价了部分氧化的碳氮化锆(Zr-CNO)粉末作为聚合物电解质燃料电池(PEFC)的非贵金属阴极。由碳氮化锆(Zr-CN)制备,在0.25%O_2 / 2%H_2 / N_2和1000-1400℃的温度下进行热处理,制得Zr-CNO粉。采用慢扫描伏安法在30℃下于0.1 mol dm〜(-3)H_2SO_4中在氮气和氧气下评估氧还原反应(ORR)的催化活性。尽管未处理的Zr-CN的ORR起始电势相对于可逆氢电极(RHE)为0.55 V,但适当的氧化Zr-CNO的起始电势相对于RHE达到0.97V。 XRD和XPS数据表明,Zr-CNO的表面被氧化为ZrO_2,Zr-CN保留在每个颗粒的内部。 Zr-CNO的XRD图谱中存在四方和/或立方ZrO_2,表明Zr-CNO表面的空位可能会影响ORR的催化活性。

著录项

  • 来源
    《》|2009年|129-139|共11页
  • 会议地点 Vienna(AT);Vienna(AT);Vienna(AT)
  • 作者单位

    Chemical Energy Laboratory, Yokohama National University, Yokohama 240-8501, Japan;

    Chemical Energy Laboratory, Yokohama National University, Yokohama 240-8501, Japan;

    Chemical Energy Laboratory, Yokohama National University, Yokohama 240-8501, Japan;

    Chemical Energy Laboratory, Yokohama National University, Yokohama 240-8501, Japan;

    Chemical Energy Laboratory, Yokohama National University, Yokohama 240-8501, Japan;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学电源、电池、燃料电池;
  • 关键词

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