Li3PO4-added garnet-type Li6.5La3Zr1.5Ta0.5O12 for Li-dendrite suppression

被引:162
|
作者
Xu, Biyi [1 ]
Li, Wenlong [2 ,3 ]
Duan, Huanan [1 ]
Wang, Haojing [2 ,3 ]
Guo, Yiping [1 ]
Li, Hua [1 ]
Liu, Hezhou [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[2] Chinese Acad Sci, Xian Inst Opt & Precis Mech, State Key Lab Transient Opt & Photon, Xian 710119, Shaanxi, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
Lithium garnet; Li3PO4; Lithium dendrite suppression; Lithium anode; Symmetric cells; SOLID-ELECTROLYTE; DOPED LI7LA3ZR2O12; LITHIUM METAL; INTERFACE MODIFICATION; IONIC-CONDUCTIVITY; AIR STABILITY; BATTERIES; DEPOSITION; COMPOSITE; KINETICS;
D O I
10.1016/j.jpowsour.2017.04.026
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
This paper proposes a strategy to stabilize the garnet/Li interface by introducing Li3PO4 as an additive in garnet-type Li6.5La3Zr1.5Ta0.5O12. The Li3PO4-added Li6.5La3Zr1.5Ta0.5O12 electrolyte exhibits a room temperature Li-ion conductivity of 1.4 x 10(-4) S cm(-1), which is less than that of the Li3PO4-free counterparts (4.6 x 10(-4) S cm(-1)). However, the presence of Li3PO4 improves the interfacial compatibility and suppresses Li-dendrite formation during Li-metal plating/stripping. The symmetric Li/garnet/Li cells with Li3PO4-added Li6.3La3Zr1.5Ta0.5O12 have been successfully cycled at a current density of 0.1 mA cm(-2) at 60 degrees C for 60 h; on contrast, the control cells with Li3PO4-free Li6.5La3Zr1.5Ta0.5O12 display noisy potential with large voltage polarization and get short-circuited completely after 33-h cycling under the same operating condition. The outstanding interface stability can be attributed to the in situ reaction of the Li flux with Li3PO4 to form a self-limiting and ion-conducting interphase, Li3P, which is confirmed experimentally. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 73
页数:6
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