Modeling Solid-Liquid Interfaces in MARTINI 3

05 November 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The MARTINI force field has become increasingly popular in material science by virtue of its versatility and its building block approach. However, force field parametrization is primarily based on reproducing structural and thermodynamic properties of the building blocks in solution, which may not be the most suitable strategy for regular, extended surfaces at solid-liquid interfaces, e.g., the planar facets of nanoparticles. In this study, we propose a novel strategy for parametrizing MARTINI planar surfaces in contact with liquids. While the choice of bead types in MARTINI models for molecules and ions in solution is often dictated by their chemistry, we suggest that surface-liquid interactions can be refined through a top-down approach. Specifically, we propose tuning the density of particles in the model surface to reproduce available experimental data on contact angles. In addition, we suggest several possible solutions to mitigate an artifact of the force field, that is, the excessive ordering of the liquid in contact with regular surfaces. Our findings demonstrate that water ordering can be reduced by tuning surface roughness and the level of coarse-graining of water. Eventually, we validate our approach on silica surfaces functionalized by alkyl chains.

Keywords

Surface
Martini
Simulations
Molecular Dynamics
Solid-liquid interfaces
Coarse-grained
Contact angle
Water layering

Supplementary materials

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