Degradation Mechanism of LiNi0.82Co0.15Al0.03O2 Positive Electrodes of a Lithium-Ion Battery by a Long-Term Cycling Test

被引:44
作者
Hayashi, Tetsutaro [1 ,2 ]
Okada, Jiro [3 ]
Toda, Eiji [1 ]
Kuzuo, Ryuichi [1 ]
Oshimura, Nobumitsu [3 ]
Kuwata, Naoaki [2 ]
Kawamura, Junichi [2 ]
机构
[1] Sumitomo Met Min Co Ltd, Battery Res Labs, Niihama, Ehime 792008, Japan
[2] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Sendai, Miyagi 9808577, Japan
[3] Sumitomo Met Min Co Ltd, Ichikawa Res Labs, Ichikawa, Chiba 2728588, Japan
关键词
CAPACITY-FADING MECHANISMS; R(3)OVER-BAR-M; PERFORMANCE; MICROSCOPY; PARTICLES; LINIO2;
D O I
10.1149/2.056406jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We conducted a long-term cycling test of a commercial 18650-type lithium-ion battery with a capacity of 3100 mA.h at room temperature and investigated the degradation mechanism of the battery's LiNi0.82Co0.15Al0.03O2 positive electrode. Spherical-aberration-corrected scanning transmission electron microscopy (Cs-STEM) revealed the presence of a thick degraded surface layer on the surface of the positive active material after the cycling test, and electron energy loss spectroscopy (EELS) revealed that the degraded surface layer continuously evolved from a LiNiO2 layered structure to a NiO structure, in the direction from the bulk toward the surface. Hard X-ray photoemission spectroscopy (HX-PES) indicated that the majority of low-valence Ni existed on the surface of the positive active material, which was charged after the cycling test, and that the degraded surface layer was inactive against charge reaction. The results suggest that the degraded surface layer was responsible for battery degradation during the cycling test. X-ray photoemission spectroscopy (XPS) indicated that Li2CO3 increased on the surface of the positive electrode after the cycling test. The phenomena would contribute to the formation of the degraded surface layer on the surface of the positive active material. (C) 2014 The Electrochemical Society. All rights reserved.
引用
收藏
页码:A1007 / A1011
页数:5
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