Key factors in semi-generic coarse-grained modeling of solid polymer electrolytes

YH Zhang and LM Hall, JOURNAL OF CHEMICAL PHYSICS, 163, 194905 (2025).

DOI: 10.1063/5.0295871

Given the long length and time scales of interest and strong interactions present in solid polymer electrolytes, coarse-grained molecular models can be useful in understanding the molecular basis of their structure and transport properties. Rather than representing atoms individually, coarse-grained models use beads representing groups of atoms, making the system simpler and more efficient. Generic coarse- grained models, which are not built based on matching a particular atomistic system, can provide insight into the important physical considerations that apply across different chemical systems, though it can be unclear how to best match experimental systems and capture relevant experimental behaviors with as simple a model as possible. Here, we build on generic bead-spring models but use stiff angle potentials, set different bead properties for different polymer types, and include additional ion parameters, creating a semi-generic coarse- grained model that can map more specifically to polymers and copolymers with different chain architectures, component glass transition temperatures, and ion solvation behaviors. We set most parameters with basic homopolymer data, such as glass transition temperatures, Kuhn length, density, and dielectric constant, with further adjustment based on data from the polymer electrolyte system. We specifically model polystyrene-block-poly(oligo-oxyethylene methyl ether methacrylate) (PS- b-POEM) with lithium triflate salt, considering the POEM to be made of a poly(methylmethacrylate) backbone with poly(ethylene oxide) side chains. Solvation of ions is accounted for by additional polymer-ion interactions of the form -S/r(4), plus additional lithium-polymer Lennard-Jones interactions. We find that these potentials have different effects and discuss strategies for setting these parameters.

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