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通过原位力学测量探究磷酸铁锂阴极上阴极-电解质界面的形成

Probing the Formation of Cathode-Electrolyte Interphase on Lithium Iron Phosphate Cathodes via Operando Mechanical Measurements.

作者信息

Bal Batuhan, Ozdogru Bertan, Nguyen Dan Thien, Li Zheng, Murugesan Vijayakumar, Çapraz Ömer Özgür

机构信息

The School of Chemical Engineering, Oklahoma State University, Stillwater, Oklahoma 74078, United States.

Center for Energy Conversion & Storage Systems, National Renewable Energy Laboratory, Golden, Colorado 80401, United States.

出版信息

ACS Appl Mater Interfaces. 2023 Sep 13;15(36):42449-42459. doi: 10.1021/acsami.3c05749. Epub 2023 Sep 2.

Abstract

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 LiFePO cathodes during charge/discharge by utilizing operando digital image correlation, impedance spectroscopy, and cryo X-ray photoelectron spectroscopy. LiFePO cathodes were cycled in either LiPF, LiClO, 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 LiPF-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 LiPOF 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.

摘要

电极中的界面不稳定性控制着锂离子电池的性能和寿命。虽然阳极上固体电解质界面(SEI)的形成受到了广泛关注,但对于阴极上阴极电解质界面(CEI)的形成仍缺乏了解。为了填补这一空白,我们通过使用原位数字图像相关、阻抗谱和低温X射线光电子能谱,报告了LiFePO4阴极在充电/放电过程中的动态变形。LiFePO4阴极在含LiPF6、LiClO4或LiTFSI的有机液体电解质中循环。在第一个循环之后,锂离子嵌入导致电化学应变与(脱)充电状态之间几乎呈线性相关,而与电解质化学性质无关。然而,在含LiPF6的电解质中首次充电期间,在阳极电流上升开始时以及在约4.0 V处的电流衰减时,存在明显的不可逆正应变演变。阻抗研究表明在相同电位窗口中表面电阻增加,表明在阴极上形成了CEI层。通过X射线光电子能谱对CEI层的化学性质进行了表征。在首次充电期间,早在3.4 V时就在CEI层中检测到LiF,并且在高于4.0 V的电压下出现LiPOF。我们的方法为阴极电极上CEI层的形成机制提供了见解,这对于开发用于高性能电池的坚固阴极和电解质化学至关重要。

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