离子
钠
电压
材料科学
环境科学
计算机科学
电气工程
化学
冶金
工程类
有机化学
作者
Tengfei Song,Brij Kishore,Yazid Lakhdar,Lin Chen,Peter R. Slater,Emma Kendrick
出处
期刊:Batteries
[Multidisciplinary Digital Publishing Institute]
日期:2024-10-11
卷期号:10 (10): 361-361
标识
DOI:10.3390/batteries10100361
摘要
Sodium-ion batteries (SIBs) are gaining attention as a safer, more cost-effective alternative to lithium-ion batteries (LIBs) due to their use of abundant and non-critical materials. A notable feature of SIBs is their ability to utilize aluminum current collectors, which are resistant to oxidation, allowing for safer storage at 0 V. However, the long-term impacts of such storage on their electrochemical performance remain poorly understood. This study systematically investigates how storage conditions at various states of charge (SOCs) affect open circuit voltage (OCV) decay, internal resistance, and post-storage cycling stability in two different Na-ion chemistries: Prussian white//hard carbon and layered oxide//hard carbon. Electrochemical Impedance Spectroscopy before and after storage shows a pronounced increase in internal resistance and a corresponding decline in cycling performance when SIBs are stored in a fully discharged state (0 V), particularly for layered oxide-based cells, illustrating the sensitivity of different SIB chemistries to storage conditions. Additionally, a novel reformation protocol is proposed that reactivates cell capacity by rebuilding the solid electrolyte interphase (SEI) layer, offering a recovery path after prolonged storage. These insights into the long-term storage effects on SIBs provide new guidelines for optimizing storage and transport conditions to minimize performance degradation, making them more viable for commercial applications.
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