Causal Relationship between Electrochemical Symmetry and Thermodynamic Overpotential

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Federico Calle-Vallejo
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引用次数: 0

Abstract

In general, not knowing the origin of a correlation restricts its applicability and prevents safe extrapolations. In particular, there are countless correlations in electrocatalysis nowadays, but their use is limited because the theory behind them is often unclear or nonexistent. This certainly encourages the search for the physics and chemistry beneath correlations. Here, on the example of the oxygen evolution reaction (OER), I show that there is a causal relationship between the thermodynamic overpotential (ηOER), a paramount concept in contemporary computational electrochemistry, and an energetic descriptor called electrochemical-step symmetry index (ESSI). Finally, I use an adsorption-energy database to illustrate the match between the parameters of the relationship predicted by theory and statistical analysis.

Abstract Image

电化学对称性与热力学过电位的因果关系
一般来说,不知道相关性的起源限制了它的适用性,并妨碍了安全的推断。特别是,如今电催化中有无数的相关性,但它们的使用受到限制,因为它们背后的理论往往不清楚或不存在。这当然鼓励了对相关性背后的物理和化学的探索。在这里,以析氧反应(OER)为例,我展示了热力学过电位(ηOER)(当代计算电化学中的一个重要概念)与称为电化学步骤对称指数(ESSI)的能量描述符之间存在因果关系。最后,利用吸附能数据库来说明理论预测的关系参数与统计分析之间的匹配。
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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