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界面电化学性质的建模:超越隐式溶剂化限制

modelling of interfacial electrochemical properties: beyond implicit solvation limitations.

作者信息

Hagopian Arthur, Falcone Aurélie, Ben Yahia Mouna, Filhol Jean-Sébastien

机构信息

ICGM, Université de Montpellier, CNRS, ENSCM, Montpellier, France.

RS2E French network on Electrochemical Energy Storage, FR5439, Amiens, France.

出版信息

J Phys Condens Matter. 2021 Jun 10;33(30). doi: 10.1088/1361-648X/ac0207.

Abstract

First-principles calculations are an important tool to investigate the complex processes occurring at solid/liquid interfaces which are at the heart of modern technologies. Currently, capturing the whole electrochemical environment at an interface, including the applied potential and solvation, still remains challenging as it necessitates to couple different approaches whose interactions are not fully understood. In this work, a grand canonical density functional theory approach is coupled with solvation models to investigate the electrochemical interfaces under applied potential. We show that a parametrized polarizable continuum model (PCM) which represent solvation in a mean field approach by a continuous polarizable media, possesses catastrophic limitations for the modelling of ionic and charged interfaces. We reveal the origin of PCM instabilities under chemical or electrochemical strong oxidation to be the consequence of a phase transition in the surface Li electronic structure. Thus, PCM undergoes an unphysical response to this phase transition by penetrating within the atomic radius of surface Li atoms. To recover a physical response, an explicit first solvation shell has to be included in addition to the PCM in order to properly describe the electrochemistry of the interface. The Fukui functions show that the first solvation shell becomes involved in the redox process as solvent electron doublet is transferred to the acidic Li. If another explicit solvent layer is added, the interface electrochemical properties become independent of the PCM parameters: in particular capacitance can then be computed from a parameter-free electrochemical approach. This is an important conclusion as the experimental electrochemical capacitance are not easily found and thus the parametrization of the PCM for electrochemical interface can be difficult. This approach can easily be applied to investigate electrochemical properties at the atomic scale and generalized to any electrochemical device for which interfaces play a crucial role.

摘要

第一性原理计算是研究发生在固/液界面的复杂过程的重要工具,而这些界面是现代技术的核心。目前,要捕捉界面处的整个电化学环境,包括外加电势和溶剂化作用,仍然具有挑战性,因为这需要将不同的方法结合起来,而这些方法之间的相互作用尚未完全理解。在这项工作中,一种巨正则密度泛函理论方法与溶剂化模型相结合,以研究外加电势下的电化学界面。我们表明,一种通过连续可极化介质以平均场方法表示溶剂化作用的参数化可极化连续介质模型(PCM),在模拟离子和带电界面时存在灾难性的局限性。我们揭示了在化学或电化学强氧化条件下PCM不稳定性的根源是表面锂电子结构中相变的结果。因此,PCM对这种相变会产生非物理响应,即渗透到表面锂原子的原子半径范围内。为了恢复物理响应,除了PCM之外,还必须包含明确的第一溶剂化层,以便正确描述界面的电化学性质。福井函数表明,随着溶剂电子对转移到酸性锂上,第一溶剂化层参与了氧化还原过程。如果添加另一个明确的溶剂层,界面的电化学性质将变得与PCM参数无关:特别是电容随后可以通过无参数的电化学方法计算得出。这是一个重要的结论,因为实验中的电化学电容不容易获得,因此PCM用于电化学界面的参数化可能会很困难。这种方法可以很容易地应用于研究原子尺度上的电化学性质,并推广到任何界面起关键作用的电化学器件。

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