Abstract

In this study, a phase-field model is developed to simulate the microstructure morphology evolution that occurs during solid electrolyte interphase (SEI) growth. Compared with other simulation methodologies, the phase-field method has been widely applied in the solidification modeling that has great relevance to SEI formation. The developed model can simulate SEI structure and morphology evolution, and can predict SEI thickness growth rate. X-ray photoelectron spectroscopy (XPS) experiments are performed to confirm the major SEI species as LiF, Li2O, ROLi, and ROCO2Li. Transmission electron microscopy (TEM) experiment is performed to present the SEI layer structures. The experiments reduce the complexity of the model development and provide validation to some extent. Fick's law and mass balance are applied to investigate lithium-ion concentration distributions and diffusion coefficients in different types of SEI layers predicted by the phase-field simulations. Simulation results show that lithium-ion diffusion coefficients between 298 K and 318 K are 1.340–7.328(10−16) cm2/s, 1.734–3.405(10−12) cm2/s, and 2.611–2.389(10−15) cm2/s in the compact, porous, and multilayered structures of SEI layer, respectively. The resistances between 298 K and 318 K are 0.740–1.693 Ω⋅cm2, 2.827–5.517 Ω⋅cm2, and 3.726–5.839 Ω⋅cm2 in the compact, porous, and multilayered structures of SEI layer, respectively.

Highlights

  • The phase-field model developed in the previous section is applied to capture solid electrolyte interphase (SEI) formation and morphology evolution

  • Focus is placed on the evolution of SEI microstructure that is related to the electrochemical properties of interest

  • The shape of the SEI species is determined by minimizing the total free energy density of the two-phase system to reach a state of equilibrium

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Summary

Introduction

Many researchers have investigated SEI in LIBs in terms of structure,[7,8,29,31,32,33] formation and composition,[20,22,27] and thickness growth prediction and measurement.[15,16,34,35] SEI is believed to have a multilayered structure: a compact layer of inorganic components (e.g., LiF, Li2O) close to graphite electrode followed by a porous organic layer (e.g., ROLi, ROCO2Li) close to the electrolyte solution phase.[22,29,31,32,33] The composition of SEI depends on the electrode materials and electrolyte composition.[27] Broussely et al investigated the mechanism of lithium loss in LIBs during storage, and their developed diffusion-limited SEI growth model revealed that the rate of lithium loss is proportional to the SEI electronic conductance.[28] The work by Borodin et al showed that the nature of the electrolyte has a fundamental impact on the formation and composition of SEI.[27] Kim et al carried out simulations to study the effect of the electrolyte on the composition of SEI. A diffusion model based on Fick’s law and mass balance is developed to investigate the lithium-ion diffusion in different types of SEI layers predicted by the phase-field simualtions

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