Study of the Failure Mechanisms of LiNi0.8Mn0.1Co0.1O2Cathode Material for Lithium Ion Batteries

电解质 锂(药物) 阴极 电化学 材料科学 扫描电子显微镜 电极 离子 化学工程 等温微量热法 分析化学(期刊) 化学 复合材料 热力学 物理化学 色谱法 医学 物理 工程类 内分泌学 有机化学
作者
Jing Li,Laura E. Downie,Lin Ma,Wen-Da Qiu,J. R. Dahn
出处
期刊:Journal of The Electrochemical Society [Institute of Physics]
卷期号:162 (7): A1401-A1408 被引量:494
标识
DOI:10.1149/2.1011507jes
摘要

LiNi0.8Mn0.1Co0.1O2 (NMC811) can deliver a high capacity of ∼200 mAh/g with an average discharge potential of ∼3.8 V (vs. Li+/Li), making it a promising positive electrode material for high energy density lithium ion batteries. However, electrochemical tests from half cells and full cells show poor cycling performance when charged to potentials above 4.2 V. The calendar and cycle lifetimes of cells are affected by the structural stability of the active electrode materials as well as the parasitic reactions that occur in lithium ion batteries. In order to explore the major failure mechanisms of the material, half cells (coin cells) with control electrolyte and full cells (pouch cells) with control electrolyte and with selected electrolyte additives were tested over four different potential ranges. Isothermal microcalorimetry was used to explore the parasitic reactions and their potential dependence. In-situ and ex-situ X-ray diffraction and scanning electron microscopy were used to investigate the structural and morphological degradation of the materials over cycling. It was found that the dramatic c-axis change of the active material during charge and discharge may not be the major problem for cells that are cycled to higher potentials. The parasitic reactions that arise from the interactions between the electrolyte and the highly reactive delithiated cathode surface at high potentials are suggested as the main reason for the failure of cells cycled above 4.2 V. It should be possible to further improve the performance of NMC811 at high potentials by modifying the cathode surface and/or identifying and using electrolyte blends which reduce parasitic reactions.
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