Performance and Degradation of LiFePO4/Graphite Cells: The Impact of Water Contamination and an Evaluation of Common Electrolyte Additives

被引:57
作者
Logan, E. R. [1 ]
Hebecker, Helena [1 ]
Eldesoky, A. [2 ]
Luscombe, Aidan [1 ]
Johnson, Michel B. [1 ]
Dahn, J. R. [1 ,2 ]
机构
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada
[2] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CAPACITY FADING MECHANISM; HIGH-PRECISION COULOMETRY; LITHIUM-ION BATTERIES; LIFEPO4; CATHODE; TEMPERATURE STORAGE; GRAPHITE ANODES; HIGH-POWER; BEHAVIOR; STABILITY; CARBONATE;
D O I
10.1149/1945-7111/abbbbe
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
LiFePO4(LFP) is an appealing cathode material for Li-ion batteries. Its superior safety and lack of expensive transition metals make LFP attractive even with the commercialization of higher specific capacity materials. In this work the performance of LFP/graphite cells is tested at various temperatures and cycling protocols. The amount of water contamination is controlled to study the impact of water on capacity fade in LFP. Further, several additive systems that have been effective in NMC/graphite chemistries are tested in LFP/graphite cells. The presence of excess water impacts cell performance severely when no electrolyte additives are used, or when the electrodes are poorly passivated. When effective additive systems are used, the existence of up to 500 ppm excess water in the cell is does not strongly affect cycle life and storage performance. Fe dissolution is studied in LFP with micro X-ray fluorescence spectroscopy (mu XRF), and most electrolyte additives virtually eliminate Fe dissolution, even at high temperature and with water contamination. Removing excess water contamination suppresses Fe dissolution in cells without electrolyte additives. Finally, the capacity retention of LFP/graphite cells at high temperature is compared with long lifetime NMC/graphite cells, demonstrating challenges for LFP/graphite cells.
引用
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页数:16
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