A designer fast Li-ion conductor Li6.25PS5.25Cl0.75 and its contribution to the polyethylene oxide based electrolyte

被引:27
|
作者
Li, Dabing [1 ,2 ,3 ]
Cao, Liuyang [1 ,2 ,3 ]
Liu, Chaodeng [1 ,2 ]
Cao, Guoqin [1 ,2 ]
Hu, Junhua [1 ,2 ]
Chen, Jingbo [1 ]
Shao, Guosheng [1 ,2 ,3 ]
机构
[1] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, State Ctr Int Cooperat Designer Low Carbon & Envi, 100 Kexue Ave, Zhengzhou 450001, Henan, Peoples R China
[3] ZMGI, Xingyang 450100, Peoples R China
基金
中国国家自然科学基金;
关键词
Argyrodite Li6PS5X sulfide; All solid-state battery; Small angle X-ray scattering; Structure evolution; Polyethylene oxide; COMPOSITE SOLID-ELECTROLYTE; STATE LITHIUM BATTERIES; POLYMER ELECTROLYTE; HIGH-VOLTAGE; PERFORMANCE; ANODE; PATH; FILM;
D O I
10.1016/j.apsusc.2019.07.041
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
The composite polymer electrolytes, consisting of a flexible matrix and superb fast ion conductor are promising for large-scale practical application in safer lithium metal batteries. The quantification of polymer structure evolution induced by the inorganic filler was rarely reported. Here, a designer cubic argyrodite Li6PS5X sulfide electrolyte was fabricated by a solid reaction. A stoichiometry deviation by increasing S and Li, reducing Cl contents, leads to a novel electrolyte of Li6.25PS5.25Cl0.75 with high conductivity of 1.0 mS cm(-1) and low activation energy of 0.14 eV at room temperature. The off-stoichiometry Li6PS5X sulfide electrolyte Li6.25PS5.25Cl0.75 was used as active filler for polyethylene oxide. Small angle X-ray scattering experiment indicates that theLi(6.25)PS(5.25)Cl(0.75) triggers a pronounced structure evolution in the matrix. As a result, Li-ion diffusion pathway is expanded significantly by the Li6.25PS5.25Cl0.75 additives. An optimum ionic conductivity of 1.4 mS cm(-1) at 70 degrees C for CPEs-1 was obtained, and a LFP/Li demo battery delivers a high capacity retention of 91.1% for 100 cycles at 0.2 C.
引用
收藏
页码:1326 / 1333
页数:8
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