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Degradation of Carbon Supports in PEFC Cathode Investigated by Electrochemical STM: Effects of Platinum and Oxygen on Enhanced Carbon Corrosion

机译:电化学STM研究的PEFC阴极中碳载体的降解:铂和氧对增强的碳腐蚀的影响

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摘要

The corrosion of highly oriented pyrolytic graphite (HOPG) model electrodes' surfaces with Pt nanoparticles and oxygen molecules in an aqueous solution was investigated using electrochemical scanning tunneling microscopy in order to understand the degradation of carbon supports found in polymer electrolyte fuel cells (PEFCs) cathode. Structural changes of HOPG surfaces with Pt nanoparticles and oxygen due to the corrosion were observed directly at atomic levels under potentiostatic control between 0.6 to 1.2 V vs. RHE. The STM observations revealed that the graphite surface oxide formation due to corrosion of the HOPG surfaces with Pt nanoparticles occurred initially at step edge sites, i.e., at defect sites and then grew toward terraces. This indicates that Pt particles and oxygen on the HOPG surface accelerated the corrosion. Surface oxygen species formed through the partial oxidation of water and the dissociative adsorption of oxygen molecules likely enhance the oxidation rate of graphitic oxide species.
机译:使用电化学扫描隧道显微镜研究了高度定向的热解石墨(HOPG)模型电极表面在水溶液中的Pt纳米颗粒和氧分子的腐蚀,以了解聚合物电解质燃料电池(PEFC)阴极中碳载体的降解。在0.6至1.2 V vs. RHE的恒电位控制下,直接在原子水平上观察到由于腐蚀导致的具有Pt纳米颗粒和氧的HOPG表面的结构变化。 STM观察结果表明,由于HOPG表面被Pt纳米颗粒腐蚀而形成的石墨表面氧化物最初发生在台阶边缘部位,即缺陷部位,然后向平台生长。这表明HOPG表面上的Pt颗粒和氧气加速了腐蚀。通过水的部分氧化和氧分子的解离吸附形成的表面氧物种可能会增强石墨氧化物的氧化速率。

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  • 来源
  • 会议地点 HonoluluIL(US);HonoluluIL(US)
  • 作者

    M. Matsumoto; T. Manako; H. Imai;

  • 作者单位

    Nano Electronics Res. Labs., NEC Corporation 34, Miyukigaoka, Tsukuba, Ibaraki 305-8501, Japan;

    Nano Electronics Res. Labs., NEC Corporation 34, Miyukigaoka, Tsukuba, Ibaraki 305-8501, Japan;

    Nano Electronics Res. Labs., NEC Corporation 34, Miyukigaoka, Tsukuba, Ibaraki 305-8501, Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 表面处理 ;
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