电解质
阴极
材料科学
X射线光电子能谱
介电谱
阳极
锂(药物)
电化学
电极
分析化学(期刊)
化学工程
化学
物理化学
有机化学
医学
工程类
内分泌学
作者
Batuhan Bal,Bertan Özdoğru,Dan Thien Nguyen,Zheng Li,Vijayakumar Murugesan,Ömer Özgür Çapraz
标识
DOI:10.1021/acsami.3c05749
摘要
Interfacial instabilities in electrodes control the performance and lifetime of Li-ion batteries. While the formation of the solid-electrolyte interphase (SEI) on anodes has received much attention, there is still a lack of understanding the formation of the cathode-electrolyte interphase (CEI) on the cathodes. To fill this gap, we report on dynamic deformations on LiFePO4 cathodes during charge/discharge by utilizing operando digital image correlation, impedance spectroscopy, and cryo X-ray photoelectron spectroscopy. LiFePO4 cathodes were cycled in either LiPF6, LiClO4, or LiTFSI-containing organic liquid electrolytes. Beyond the first cycle, Li-ion intercalation results in a nearly linear correlation between electrochemical strains and the state of (dis)-charge, regardless of the electrolyte chemistry. However, during the first charge in the LiPF6-containing electrolyte, there is a distinct irreversible positive strain evolution at the onset of anodic current rise as well as current decay at around 4.0 V. Impedance studies show an increase in surface resistance in the same potential window, suggesting the formation of CEI layers on the cathode. The chemistry of the CEI layer was characterized by X-ray photoelectron spectroscopy. LiF is detected in the CEI layer starting as early as 3.4 V and LixPOyFz appeared at voltages higher than 4.0 V during the first charge. Our approach offers insights into the formation mechanism of CEI layers on the cathode electrodes, which is crucial for the development of robust cathodes and electrolyte chemistries for higher-performance batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI