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Turnover Numbers, Turnover Frequencies, and Overpotential in Molecular Catalysis of Electrochemical Reactions. Cyclic Voltammetry and Preparative-Scale Electrolysis

机译:电化学反应的分子催化中的周转数,周转频率和超电势。循环伏安法和制备级电解

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摘要

The search for efficient catalysts to face modern energy challenges requires evaluation and comparison through reliable methods. Catalytic current efficiencies may be the combination of many factors besides the intrinsic chemical properties of the catalyst. Defining turnover number and turnover frequency (TOF) as reflecting these intrinsic chemical properties, it is shown that catalysts are not characterized by their TOF and their overpotential {η) as separate parameters but rather that the parameters are linked together by a definite relationship. The log TOF-η relationship can often be linearized, giving rise to a Tafel law, which allows the characterization of the catalyst by the value of the TOF at zero overpotential (TOF_0). Foot-of-the-wave analysis of the cyclic voltammetric catalytic responses allows the determination of the TOF, log TOF-η relationship, and TOF_0, regardless of the side-phenomena that interfere at high current densities, preventing the expected catalytic current plateau from being reached. Strategies for optimized preparative-scale electrolyses may then be devised on these bases. The validity of this methodology is established on theoretical grounds and checked experimentally with examples taken from the catalytic reduction of CO_2 by iron(0) porphyrins.
机译:寻找有效催化剂以应对现代能源挑战,需要通过可靠的方法进行评估和比较。除催化剂的固有化学性质外,催化电流效率可能是许多因素的组合。将周转数和周转频率(TOF)定义为反映这些内在的化学性质,结果表明,催化剂的特征不是以它们的TOF和其超电势(η)作为单独的参数,而是通过确定的关系将这些参数链接在一起。对数TOF-η关系通常可以线性化,从而产生塔菲尔定律,该定律允许通过零超电势(TOF_0)处的TOF值表征催化剂。循环伏安催化响应的波峰分析可以确定TOF,logTOF-η关系和TOF_0,而无需考虑在高电流密度下发生干扰的侧面现象,从而防止了预期的催化电流平稳被达到。然后可以在这些基础上设计优化制备规模的电解的策略。这种方法的有效性是建立在理论基础上的,并通过实例证明了铁(0)卟啉​​催化还原CO_2的有效性。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第27期|p.11235-11242|共8页
  • 作者单位

    Laboratoire d'Electrochimie Moleculaire, Unite Mixte de Recherche Universite-CNRS No. 7591, Universite Paris Diderot, Sorbonne Paris Cite, Batiment Lavoisier, 15 rue Jean de Balf, 75205 Paris Cedex 13, France;

    Laboratoire d'Electrochimie Moleculaire, Unite Mixte de Recherche Universite-CNRS No. 7591, Universite Paris Diderot, Sorbonne Paris Cite, Batiment Lavoisier, 15 rue Jean de Balf, 75205 Paris Cedex 13, France;

    Laboratoire d'Electrochimie Moleculaire, Unite Mixte de Recherche Universite-CNRS No. 7591, Universite Paris Diderot, Sorbonne Paris Cite, Batiment Lavoisier, 15 rue Jean de Balf, 75205 Paris Cedex 13, France;

    Laboratoire d'Electrochimie Moleculaire, Unite Mixte de Recherche Universite-CNRS No. 7591, Universite Paris Diderot, Sorbonne Paris Cite, Batiment Lavoisier, 15 rue Jean de Balf, 75205 Paris Cedex 13, France;

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