Search

The interfacial debonding between the active layer and the current collector has been recognized as a critical mechanism for battery fading, and thus has attracted great efforts focused on the related analyses. However, much still remains to be studied regarding practical methods for suppressing electrode debonding, especially from the perspective of mechanics. In this paper, a pre-strain strategy of current collectors to alleviate electrode debonding is proposed. An analytical model for a symmetric electrode with a deformable and limited-thickness current collector is developed to analyze the debonding behavior involving both a pre-strain of the current collector and an eigen-strain of the active layers. The results reveal that the well-designed pre-strain can significantly delay the debonding onset (by up to 100%) and considerably reduce the debonding size. The critical values of the pre-strain are identified, and the pre-strain design principles are also provided. Based on these findings, this work sheds light on the mechanical design to suppress electrode degradation. [ABSTRACT FROM AUTHOR]

Prelithiation has been intensively investigated in high-capacity lithium-ion batteries (LIBs). However, the optimization of prelithiation degrees for long service life of LIBs still remains a challenge. The positive efffect of prelithiation on suppressing degradation of LIBs, besides directly pursuing the high first Coulomb efficiency which has been widely reported in the literature, is revealed and discussed based on an analytical model focusing on the interfacial delamination in electrodes. For full charge-discharge cycling, well-designed prelithiation can effectively suppress the delamination and reduce the debonding size by approximately 25%, compared with the case without prelithiation. For the strategy combining partial charge-discharge cycling and prelithiation, the largest reversible capacity without debonding can be significantly improved by approximately 100% with well-designed prelithiation. This work is expected to provide a prelithiation design principle and further improve the mechanical stability of LIB electrodes. [ABSTRACT FROM AUTHOR]

A fully coupling model for the diffusion induced finite elastoplastic bending of bilayer electrodes in lithium-ion batteries is proposed. The effect of the mechanical stress on the lithium diffusion is accounted for by the mechanical part of the chemical potential derived from the Gibbs free energy along with the logarithmic stress and strain. Eight dimensionless parameters, governing the stress-assisted diffusion and the diffusion induced elastoplastic bending, are identified. It is found that the finite plasticity starting from the interface of the bilayer increases the chemical potential gradient and thereby facilitates the lithium diffusion. The full plastic flow makes the abnormal lithium concentration distribution possible, i.e., the concentration at the lithium inlet can be lower than the concentration at the interface (downstream). The increase in the thickness of the active layer during charging is much larger than the eigen-stretch due to lithiation, and this excess thickening is found to be caused by the lithiation induced plastic yield. [ABSTRACT FROM AUTHOR]