Improving Ionic Conductivity with Bimodal-Sized Li7La3Zr2O12 Fillers for Composite Polymer Electrolytes

被引:123
作者
Sun, Yan [1 ,2 ]
Zhan, Xiaowen [2 ]
Hu, Jiazhi [2 ]
Wang, Yikai [2 ]
Gao, Shuang [2 ]
Shen, Yuhua [1 ]
Cheng, Yang-Tse [2 ]
机构
[1] Anhui Univ, Coll Chem & Chem Engn, Lab Clean Energy & Green Catalysis, Hefei 230601, Anhui, Peoples R China
[2] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
基金
美国国家科学基金会;
关键词
lithium batteries; Li7La3Zr2O12; composite polymer electrolytes; ionic conductivity; ceramic-polymer interactions; POLY(VINYLIDENE FLUORIDE); SOLID-ELECTROLYTE; ELASTIC-MODULUS; LITHIUM; INDENTATION; BATTERIES; MEMBRANES; SPECTROSCOPY; TRANSPORT; HARDNESS;
D O I
10.1021/acsami.8b21770
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ceramic-polymer composite electrolytes (CPEs) are being explored to achieve both high ionic conductivity and mechanical flexibility. Here, we show that, by incorporating 10 wt % (3 vol %) mixed-sized fillers of Li7La3Zr2O12 (LLZO) doped with Nb/Al, the room-temperature ionic conductivity of a polyvinylidene fluoride (PVDF)-LiClO4-based composite can be as high as 2.6 x 10(-4) S/cm, which is 1 order of magnitude higher than that with nano- or micrometer-sized LLZO particles as fillers. The CPE also shows a high lithium-ion transference number of 0.682, a stable and low Li/CPE interfacial resistance, and good mechanical properties favorable for all-solid-state lithium-ion battery applications. X-ray photoelectron spectroscopy and Raman analysis demonstrate that the LLZO fillers of all sizes interact with PVDF and LiClO4. High packing density (i.e., lower porosity) and long conducting pathways are believed responsible for the excellent performance of the composite electrolyte filled with mixed-sized ionically conducting ceramic particles.
引用
收藏
页码:12467 / 12475
页数:9
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