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Surface Interrogation of CoP_i Water Oxidation Catalyst by Scanning Electrochemical Microscopy

机译:扫描电化学显微镜对CoP_i水氧化催化剂的表面询问

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摘要

Despite exhaustive spectroscopic investigations on the CoP_i oxygen-evolving catalyst over the past several years, little is known about the surface cobalt sites and intermediates in direct contact with water that are responsible for the actual catalysis. Many studies thus far have been limited to ex situ characterizations or bulk film measurements, often in the absence of solvent. Here we describe an investigation of the CoP_i catalyst by surface interrogation scanning electrochemical microscopy (SI-SECM). This method should allow us to selectively study surface atoms separately from the bulk in a solvent-filled environment. By SI-SECM, independent titrations of surface Co~Ⅲ and Co~Ⅳ were performed, yielding a direct measurement of the surface active-site density of a CoP_i electrode (11 Com~2). The pseudo-first-order reaction rate constants of Co~Ⅲ and Co~Ⅳ with water Were determined to be 0.19 and >2 s~(-1), respectively, through time-dependent titration measurements.
机译:尽管在过去的几年中对CoP_i析氧催化剂进行了详尽的光谱研究,但对于负责实际催化作用的表面钴位点和与水直接接触的中间体知之甚少。迄今为止,许多研究通常仅限于在没有溶剂的情况下进行异位表征或体膜测量。在这里,我们描述了通过表面询问扫描电化学显微镜(SI-SECM)对CoP_i催化剂的研究。这种方法应使我们能够在充满溶剂的环境中有选择地研究表面原子与本体原子。通过SI-SECM,对Co〜Ⅲ和Co〜Ⅳ的表面进行了独立的滴定,直接测量了CoP_i电极的表面活性位密度(11 Co / nm〜2)。通过时间依赖性滴定法测得Co〜Ⅲ和Co〜Ⅳ与水的拟一级反应速率常数分别为0.19和> 2 s〜(-1)。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2015年第2期|612-615|共4页
  • 作者

    Hyun S. Ahn; Allen J. Bard;

  • 作者单位

    Center for Electrochemistry, Department of Chemistry, The University of Texas at Austin, Austin, Texas 78712, United States;

    Center for Electrochemistry, Department of Chemistry, The University of Texas at Austin, Austin, Texas 78712, United States;

  • 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);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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