Unveiling the critical role of interfacial ionic conductivity in all-solid-state lithium batteries

被引:73
作者
Wang, Changhong [1 ]
Liang, Jianwen [1 ]
Hwang, Sooyeon [2 ]
Li, Xiaona [1 ]
Zhao, Yang [1 ]
Adair, Keegan [1 ]
Zhao, Changtai [1 ]
Li, Xia [1 ]
Deng, Sixu [1 ]
Lin, Xiaoting [1 ]
Yang, Xiaofei [1 ]
Li, Ruying [1 ]
Huang, Huan [3 ]
Zhang, Li [4 ]
Lu, Shigang [4 ]
Su, Dong [2 ]
Sun, Xueliang [1 ]
机构
[1] Univ Western Ontario, Dept Mech & Mat Engn, 1151 Richmond St, London, ON N6A 3K7, Canada
[2] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[3] Glabat Solid State Battery Inc, 700 Collip Circle, London, ON N6G 4X8, Canada
[4] China Automot Battery Res Inst Co Ltd, 5th Floor,43 Min Bldg,North Sanhuan Middle Rd, Beijing 100088, Peoples R China
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
Interfacial ionic conductivity; Ion transport kinetics; Li+ diffusivity; All-solid-state batteries; LIQUID-PHASE TECHNIQUE; SUPERIONIC CONDUCTORS; LICOO2; CATHODES; ELECTROLYTES; ELECTRODES; STABILITY; TRANSPORT;
D O I
10.1016/j.nanoen.2020.104686
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
Advancement of all-solid-state lithium-ion (Li+) batteries (ASSLIBs) has been hindered by the large interfacial resistance mainly originating from interfacial reactions between oxide cathodes and solid-state sulfide electrolytes (SEs). To suppress the interfacial reactions, an interfacial coating layer between cathodes and SEs is indispensable. However, the kinetics of interfacial Li+ transport across the coating layer has not been well understood yet. Herein, we tune the interfacial ionic conductivity of the coating layer LiNb0.5Ta0.5O3 (LNTO) by manipulating post-annealing temperature. It is found that the interfacial ionic conductivity determines interfacial Li+ transport kinetics and enhancing the interfacial ionic conductivity can significantly boost the electrochemical performance of SE-based ASSLIBs. A representative cathode LiNi0.5Mn0.3Co0.2O2 coated by LNTO with the highest interfacial ionic conductivity exhibits a high initial capacity of 152 mAh.g(-1) at 0.1 C and 107.5 mAh. g(-1) at 1 C. This work highlights the importance of increasing interfacial ionic conductivity for high-performance SE-based ASSLIBs.
引用
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页数:6
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