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Shifts in Redox Formal Potentials Accompanying the Incorporation of Cationic Complexes in Perfluoro Polycarboxylate and Polysulfonate Coatings on Graphite Electrodes

机译:石墨电极上全氟聚羧酸盐和聚磺酸盐涂层中阳离子配合物的结合,氧化还原形式电位的变化

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摘要

The formal potentials of several redox couples incorporated in coatings of a perfluoropolycarboxylate on graphite electrodes were measured and compared with the formal potentials of the same couples in homogeneous solution. The differences observed agreed with those calculated from the Nernst equation with the independently measured incorporationcoefficients for both halves of the redox couples. The dependences of the shifts in formal potentials on the nature of theincorporating complex ion, the ionic strength, and the temperature were determined and indicated that the incorporationequilibrium is governed by electrostatic and hydrophobic interactions that act in opposite directions. The incorporation ofmost cations examined was driven by large increases in entropy which overcame the usually unfavorable enthalpy changes.
机译:测量了在石墨电极上全氟聚羧酸盐涂层中掺入的几种氧化还原对的形式电位,并将其与均质溶液中相同对的形式电位进行比较。观察到的差异与由能斯特方程计算得到的差异一致,其中独立测量了氧化还原对的两半的结合系数。确定了形式势的变化对掺入复合离子的性质,离子强度和温度的依赖性,并表明掺入平衡受作用于相反方向的静电和疏水相互作用控制。所检查的大多数阳离子的掺入是由熵的大幅度增加驱动的,这种熵克服了通常不利的焓变。

著录项

  • 作者

    Tsou Yu-Min; Anson Fred C.;

  • 作者单位
  • 年度 1984
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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