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Potentials of electrochemical reactions and nature of singularities in electrode polarization dependences

机译:电极极化依赖性中电化学反应的电势和奇异性

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The conditions of transition of the electrochemical polarization mode to a faradaic process are studied on the metal electrode within the framework of the microscopic approach when the value of polarization potential reaches the threshold value of the potential of the electrochemical reaction. It is suggested that the elementary act of electron transfer between the metal and redox electrolyte occurs at the interface under polarization bringing the local electron level of the reagent to the Fermi level of electrons of the metal. Discharge through the Helmholtz layer limited by electrons occurs due to resonance "lightening" of the potential barrier between the metal and localized redox state of the reagent. Estimates are obtained for the values of threshold potential and exchange current of the faradaic process. A method is suggested for consideration of the elementary act of the electrochemical reaction on the basis of the Hamiltonian describing the microscopic mechanism of Fermi edge singularities. Application of the known solutions allows the appearance of threshold singularities of polarization dependences in electrochemistry to be explained.
机译:当极化电位的值达到电化学反应电位的阈值时,在微观方法的框架内,对金属电极上电化学极化模式转变为法拉第过程的条件进行了研究。建议在极化下的界面处发生金属与氧化还原电解质之间电子转移的基本行为,从而使试剂的局部电子能级达到金属电子的费米能级。通过电子限制的亥姆霍兹层的放电是由于金属与试剂的局部氧化还原状态之间的势垒共振“变亮”而发生的。获得关于法拉第过程的阈值电势和交换电流的值的估计。建议使用一种基于哈密顿量描述费米边缘奇点微观机理的方法来考虑电化学反应的基本作用。已知解决方案的应用使得可以解释电化学中极化依赖性的阈值奇异性的出现。

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