Shrinking annuli mechanism and stage-dependent rate capability of thin-layer graphite electrodes for lithium-ion batteries

TL;DR

This study investigates the rate capability of thin-layer graphite electrodes in lithium-ion batteries, revealing stage-dependent limitations and proposing a shrinking annuli mechanism to explain charge-discharge asymmetry at high rates.

Contribution

It introduces a shrinking annuli mechanism and stage-dependent analysis to better understand graphite's rate performance in lithium-ion batteries.

Findings

Dense stage transitions limit charge/discharge rates.

Dilute stage transitions occur rapidly and compensate for diffusion limitations.

Graphite can be charged at ~6C and discharged at 600C while retaining 80% capacity.

Abstract

The kinetic performance of graphite particles is difficult to deconvolute from half-cell experiments, where the influences of the working electrode porosity and the counter electrode contribute nonlinearly to the electrochemical re-sponse. Therefore, thin-layer electrodes of circa 1 {\mu}m thickness were prepared with standard, highly crystalline graphite particles to evaluate their rate capability. The performance was evaluated based on the different stage transitions. We found that the tran-sitions towards the dense stages 1 and 2 with LiC6 in-plane densi-ty are one of the main rate limitations for charge and discharge. But surprisingly, the transitions towards the dilute stages 2L, 3L, 4L, and 1L progress very fast and can even compensate for the initial diffusion limitations of the dense stage transitions during discharge. We show the existence of a substantial difference between the diffusion coefficients of the liquid-like stages and the dense stages. We also demonstrate that graphite can be charged at a rate of ~6C (10 min) and discharged at 600C (6 s) while maintaining 80 % of the total specific charge for particles of 3.3 {\mu}m median diameter. Based on these findings, we propose a shrinking annuli mechanism which describes the propagation of the different stages in the particle at medium and high rates. Besides the limited applicable overpotential during charge, this mechanism can explain the long-known but as yet unexplained asymmetry between the charge and discharge rate performance of lithium intercalation in graphite.