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Behaviour of the adsorbed chloride intermediate in electrocatalysis of anodic chlorine evolution at oxide film surfaces at platinum and ruthenium.

机译:在铂和钌的氧化膜表面上的阳极氯析出的电催化中,吸附的氯化物中间体的行为。

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摘要

In this thesis, the investigation of the mechanism of chlorine evolution reaction at (i) both freshly reduced and pre-oxidized Pt electrodes; (ii) RuO;As described in Chapter V, the influence of co-deposited OH and O species in the surface oxidation process on the extent of chemisorption of the Cl;In Chapter VI, some exploratory experiments at other noble metal (e.g., Pd, Ir, Ru, and Rh) electrodes in non-aqueous TFA solution have shown very interesting interfacial capacitance information, which must be interpreted probably in terms of more than one adsorbed reaction intermediate being present.;In Chapter VII, a possible mechanism of recombination kinetically control has been proposed for the Cl;Some of the results in this work have been published or in press, as listed below: (1) "Surface electrochemistry of the anodic chlorine evolution reaction at Pt influence of co-deposition of the Cl
机译:本文研究了(i)新还原的和预氧化的Pt电极上的氯放出反应的机理。 (ii)RuO;如第五章所述,在表面氧化过程中共沉积的OH和O物种对Cl的化学吸附程度的影响;在第六章中,对其他贵金属(例如Pd)进行了一些探索性实验非水性TFA溶液中的,Ir,Ru和Rh)电极显示了非常有趣的界面电容信息,这可能必须以存在多个吸附反应中间体的方式来解释。;在第七章中,可能的重组机理已经提出了对Cl进行动力学控制的方法;该工作的一些结果已经发表或在印刷中,如下所示:(1)“在Cl共同沉积的Pt影响下,阳极氯析出反应的表面电化学

著录项

  • 作者

    Gu, Ping.;

  • 作者单位

    University of Ottawa (Canada).;

  • 授予单位 University of Ottawa (Canada).;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 1990
  • 页码 273 p.
  • 总页数 273
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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