Abstract
Lithium-ion batteries (LIBs) are pivotal for energy storage in electric vehicles and renewable systems, but how to effectively monitor their conditions and ensure their operational reliability is still a concern today. This study employs electrochemical impedance spectroscopy (EIS) to systematically investigate the evolution of impedance characteristics in nickelβcobaltβmanganese oxide (NCM) lithium-ion batteries (LIBs) under varying states of charge (SOCs), states of health (SOHs), temperatures, and mechanical compression displacements. Results reveal that higher SOC and temperature reduce impedance by enhancing ion kinetics and interfacial activity, with π
πβ’π‘ (charge transfer resistance) exhibiting a U-shaped dependence on SOC, minimized at 40β60%. As SOH declines from 100% to 80%, π
πβ’πΈβ’πΌ (SEI film resistance) and π
πβ’π‘ increase progressively, reflecting SEI thickening and electrode degradation. Mechanical compression (0β8 mm) elevates all resistances, particularly π
πβ’π‘ at high SOC, due to structural deformation and hindered diffusion. DRT (distribution of relaxation times) spectra highlight amplified low-frequency peaks with aging and low SOC, underscoring diffusion limitations. These findings elucidate multi-scale failure mechanisms, from interfacial polarization to structural instability, providing a framework for non-invasive health monitoring and lifetime prediction.
| Original language | English |
|---|---|
| Article number | 1048 |
| Number of pages | 21 |
| Journal | Molecules |
| Volume | 31 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 22 Mar 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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