Ab initio modelling of interfacial electrochemical properties: beyond implicit solvation limitations

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.

Keywords: capacitance; density functional theory; electrochemical interface; explicit solvation; grand canonical; implicit solvent; polarizable continuum model.