Safety characteristics of Li(Ni0.8Co0.15Al0.05)O2 and Li(Ni1/3CO1/3Mn1/3)O2

被引:252
|
作者
Belharouak, I [1 ]
Lu, WQ [1 ]
Vissers, D [1 ]
Amine, K [1 ]
机构
[1] Argonne Natl Lab, Div Chem Engn, Electrochem Technol Program, Argonne, IL 60439 USA
关键词
lithium-ion batteries; cathode; thermal stability; high power; HEV;
D O I
10.1016/j.elecom.2005.12.007
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Layered Li-0.45(Ni0.8Co0.15Al0.05)O-2 and Li-0.55(Ni1/3Co1/3Mn1/3)O-2 materials have been, respectively, prepared by a chemical delithiation of layered Li(Ni0.8Co0.15Al0.05)O-2 and Li(Ni1/3Co1/3Mn1/3)O-2 compounds using NO2BF4 oxidizer in ail acetonitrile medium. The thermal gravimetric results show that both Li-0.45(Ni0.8Co0.15Al0.05)O-2 and Li-0.55(Ni1/3Co1/3Mn1/3)O-2 powders release oxygen starting from 190 and 250 degrees C with an overall oxygen loss of 11 and 9 wt% at 900 degrees C, respectively. The results show that the oxygen release from these delithiated powders was associated with the occurrence of several structural transformations, ranging from a R (3) over barm -> Fd3m (layered -> spinel) transition to a Fd3m -> Fm3m (spinel -> NiO-type) transition. The 3 wt% weight gain, solely observed for Li-0.55(Ni1/3Co1/3Mn1/3)O-2 between 800 degrees C and room temperature, involved a reversible Fd3m reversible arrow Fm3m (spinel reversible arrow NiO-type) structural transition. The reactivity of these delithiated powders with electrolytes was investigated by a differential scanning calorimetry (DSC) between room temperature and 375 degrees C. In the case of Li-0.55(Ni1/3Co1/3Mn1/3)O-2 powder, the DSC result shows that the oxidation of the electrolyte was delayed by 50 'C toward high temperatures with the generation of lower heat when compared to Li-0.45(Ni0.8Co0.15Al0.05)O-2 powder. The relationship between the safety characteristics of Li-0.45(Ni0.8Co0.15Al0.05)O-2 and Li-0.55(Ni1/3Co1/3Mn1/3)O-2 powders and their thermal stability was discussed in the light of their structural rearrangement during the thermal heating processes. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:329 / 335
页数:7
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