电化学中内球/外球术语的使用-六氰高铁酸盐II/III案例研究

J. Cassidy, Rafaela C de Carvalho, A. Betts
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引用次数: 1

摘要

六氰高铁酸盐II/III阴离子已被广泛用作氧化还原偶探针分子来测定电极表面的特性。例子包括用于能源应用的电催化剂的评估和用于检测生物或化学物种的电催化剂,以及电化学活性表面积的确定。对电化学文献的研究,主要基于循环伏安研究,揭示了广泛的峰分离和/或异质电子转移速率常数,有时被分类为内球或外球电子转移过程。最初是为溶液中无机过渡金属化合物的机理解释而发展起来的,这个术语已经扩展到解释发生在电极上的非均相电子转移。在六氰高铁离子II/III阴离子的情况下,有许多原因可以解释为什么它有时表现为外球探针,而在其他时候表现为内球电子转移特征。在检查了六氰高铁酸盐II/III种的一些结构和化学性质之后,描述了用于确定此类分类的方法。最常用的方法是在循环伏安图中测量峰对峰分离,以确定非均质速率常数,但它有固有的缺陷。本文综述了分类差异的原因,包括各种氧表面种类的影响,有机表面膜的影响,阳离子反离子的性质,表面吸附和表面亲疏水性。其他的表面相互作用也可能发生,例如金腐蚀或pH效应。这些可以影响电双层,从而可能影响电子转移过程。因此,建议将六氰高铁酸盐II/III视为多球或表面敏感的电子转移物质。
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Use of Inner/Outer Sphere Terminology in Electrochemistry—A Hexacyanoferrate II/III Case Study
Salts of hexacyanoferrate II/III anions have been widely used as redox couple probe molecules to determine the characteristics of electrode surfaces. Examples include the assessment of electrocatalysts for energy applications and electrocatalysts for the detection of biological or chemical species, as well as the determination of electrochemically active surface areas. An examination of the electrochemical literature, based largely on cyclic voltammetric investigations, reveals a wide range of peak separation and/or heterogeneous electron transfer rate constants, classified sometimes as inner or outer sphere electron transfer processes. Originally developed for the mechanistic interpretation of inorganic transition metal compounds in solution, this terminology has since been extended to account for heterogeneous electron transfer occurring at electrodes. In the case of the hexacyanoferrate II/III anions, there can be a number of reasons why it sometimes behaves as an outer sphere probe and at other times displays inner sphere electron transfer characteristics. After examining some of the structural and chemical properties of the hexacyanoferrate II/III species, the methods used to determine such classifications are described. The most common method involves measuring peak-to-peak separation in a cyclic voltammogram to ascertain a heterogeneous rate constant, but it has inherent flaws. This paper reviews the reasons for the classification disparity, including the effects of various oxygen surface species, the influence of organic surface films, the nature of the cation counter-ion, surface adsorption and surface hydrophilicity/hydrophobicity. Other surface interactions may also take place, such as those occurring with Au corrosion or pH effects. These can impact the electrical double layer and thus may affect the electron transfer process. Consequently, it is recommended that hexacyanoferrate II/III should be considered a multi-sphere or alternatively a surface-sensitive electron transfer species.
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