Insight into cathode surface to boost the performance of solid-state batteries

被引:72
作者
Deng, Sixu [1 ]
Sun, Qian [1 ]
Li, Minsi [1 ]
Adair, Keegan [1 ]
Yu, Chuang [1 ]
Li, Junjie [1 ]
Li, Weihan [1 ]
Fu, Jiamin [1 ]
Li, Xia [1 ]
Li, Ruying [1 ]
Hu, Yongfeng [2 ]
Chen, Ning [2 ]
Huang, Huan [4 ]
Zhang, Li [3 ]
Zhao, Shangqian [3 ]
Lu, Shigang [3 ]
Sun, Xueliang [1 ]
机构
[1] Univ Western Ontario, Dept Mech & Mat Engn, London, ON N6A 5B9, Canada
[2] Canadian Light Source, 44 Innovat Blvd, Saskatoon, SK S7N 2V3, Canada
[3] China Automot Battery Res Inst Co Ltd, Fifth Floor,43,Min Bldg,North Sanhuan Middle Rd, Beijing 100088, Peoples R China
[4] Glabat Solid State Battery Inc, 700 Collip Circle, London, ON N6G 4X8, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
Ni-rich NMC; Sulfide electrolyte; Cathode interface; Degradation mechanism; ELECTROCHEMICAL PERFORMANCE; EDGE XANES; EVOLUTION; STORAGE; SULFUR;
D O I
10.1016/j.ensm.2020.12.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cathode interface instability is a significant obstacle for the practical application of sulfide-based all-solid-state lithium-ion batteries (ASSLIBs). However, the origin of cathode interface degradation is lack of comprehensive understanding. In this paper, X-ray characterizations combined with electrochemical analysis are adopted to investigate the underlying degradation mechanism at cathode interface. The results indicate that residual lithium compounds on the surface of Ni-rich LiNi0.8Mn0.1Co0.1O2 (NMC811) are the main reason that triggering the oxidation of sulfide solid-state electrolytes (SSEs), therefore inducing severe side-reactions at cathode interface and structural degradation of NMC811. The degradation of the cathode interface can be significantly suppressed when the cathode surface is cleaned. As a result, the surface cleaned NMC811 without coating demonstrates significantly improved electrochemical performance in both Li5.5PS4.5Cl1.5 (LPSCl) and Li10GeP2S12 (LGPS) based ASSLIBs, proving the universal application of this strategy.
引用
收藏
页码:661 / 668
页数:8
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