X射线光电子能谱
材料科学
聚合物
电极
化学工程
反应性(心理学)
氧化物
压延
化学稳定性
锂(药物)
二氟
热稳定性
锂电池
复合材料
化学状态
金属
光谱学
电池(电)
聚偏氟乙烯
氧化锂
无机化学
作者
Rabeb Grissa,Alla Abramova,S. J. Tambio,Margaud Lécuyer,Marc Deschamps,Vincent Fernandez,Jean‐Marc Grenèche,Dominique Guyomard,Bernard Lestriez,Philippe Moreau
标识
DOI:10.1021/acsami.9b01761
摘要
The lithium and lithium-ion battery electrode chemical stability in the pristine state has rarely been considered as a function of the binder choice and the electrode processing. In this work, X-ray photoelectron spectroscopy (XPS) and XPS imaging analyses associated with complementary Mössbauer spectroscopy are used in order to study the chemical stability of two pristine positive electrodes: (i) an extruded LiFePO4-based electrode formulated with different polymer matrices [polyethylene oxide and a polyvinylidene difluoride (PVdF)] and processed at different temperatures (90 and 130 °C, respectively) and (ii) a Li[Ni0.5Mn0.3Co0.2]O2 (NMC)-based electrode processed by tape-casting, followed by a mild or heavy calendering treatment. These analyses have allowed the identification of reactivity mechanisms at the interface of the active material and the polymer in the case of PVdF-based electrodes.
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