Enhancing Interfacial Contact in Solid-State Batteries with a Gradient Composite Solid Electrolyte

被引:42
|
作者
Deng, Chenglong [1 ,2 ]
Chen, Nan [1 ,3 ]
Hou, Chuanyu [1 ]
Liu, Hanxiao [1 ]
Zhou, Zhiming [2 ]
Chen, Renjie [1 ,3 ,4 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing Key Lab Environm Sci & Engn, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing 100081, Peoples R China
[3] Beijing Inst Technol, Inst Adv Technol, Jinan 250300, Peoples R China
[4] Collaborat Innovat Ctr Elect Vehicles Beijing, Beijing 100081, Peoples R China
基金
美国国家科学基金会;
关键词
composite solid electrolyte; gradient; mechanical strength; uniform lithium deposition; LITHIUM; ANODE;
D O I
10.1002/smll.202006578
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state batteries promise to meet the challenges of high energy density and high safety for future energy storage. However, poor interfacial contact and complex manufacturing processes limit their practical applications. Herein, a simple strategy is proposed to enhance interfacial contact by introducing a gradient composite polymer solid electrolyte (GCPE), which is prepared by a facile UV-curing polymerization technique. The high-Li6.4La3Zr1.4Ta0.6O12 (LLZTO)-content side of the electrolyte exhibits high oxidation resistance (5.4 V versus Li+/Li), making it compatible with a high-voltage cathode material, whereas the LLZTO-deficient side achieves excellent interfacial contact with the Li metal anode, facilitating uniform Li deposition. Benefiting from the elaborate composition and structure of GCPE films, the symmetric Li//Li cell exhibits a low-voltage hysteresis potential of 42 mV and a long cycle life of >1900 h without short-circuiting. The Li//LiFePO4 solid-state batteries deliver a capacity of 161.0 mA h g(-1) at 60 degrees C and 0.1 C (82.4% capacity is retained after 200 cycles). Even at 80 degrees C, the cell still shows an outstanding capacity of 132.9 mAh g(-1) at 0.2 C after 100 cycles. The design principle of gradient electrolytes provides a new path for achieving enhanced interfacial contact in high-performance solid-state batteries.
引用
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页数:9
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