Poly(ethylene oxide)-based composite solid electrolyte modified by Li7La3Zr2O12 inorganic filler with grafted imidazolium-based ionic liquids functional groups

被引:0
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作者
Zhang, Yanhua [1 ,2 ]
Xiao, Yumei [1 ]
Tang, Zijun [1 ]
Zou, Liuli [1 ]
Liu, Qingting [1 ,2 ]
Fu, Xudong [1 ]
Xiang, Xing [1 ]
Deng, Jiadong [3 ]
机构
[1] Hubei Provincial Key Laboratory of Green Materials for Light Industry, Hubei University of Technology, Wuhan,430068, China
[2] Collaborative Innovation Center of Green Light-weight Materials and Processing, Hubei University of Technology, Wuhan,430068, China
[3] Hubei Key Laboratory of Advanced Technology for Automotive Components, Wuhan University of Technology, Wuhan,430070, China
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基金
中国国家自然科学基金;
关键词
All-solid-state lithium battery - Composite solid electrolytes - Functionals - Imidazolium-based ionic liquid - Inorganic-fillers - Li + - Lithium-ion conductivity - Poly(ethylene oxide) - Poly(ethylene) oxide - Surface grafting;
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学科分类号
摘要
High lithium-ion conductivity of poly(ethylene oxide)-based (PEO) composite solid electrolyte is one of the critical indicators for the development of all-solid-state lithium batteries. Herein, imidazolium-based ionic liquid (IL) functional groups are grafted on the surface of coral-like Li7La3Zr2O12 (LLZO@IL) to construct a rapid Li+ transmission channel at the PEO/LLZO interface. Results show that the IL groups are chemical bonded with LLZO and the N elemetal ratio of anion and cation is close to the theoretical equivalent in IL, suggesting that IL are successfully grafted. The lithium-ion conductivity with IL grafting is significantly improved from 6.43 × 10-6 S cm−1 to 3.41 × 10-4 S cm−1. XPS show that the grafted imidazolium cation has a fixation effect on the TFSI- anion, thus hindering the accumulation of TFSI- anions at the interface to occur decomposition. Moreover, an obvious new complex state of interface Li(TFSI)2- appears in the cycle, which indicates that the grafted IL groups form a rapid channel for Li+ transmission. The great enhancement of conductivity is ascribed to that LLZO@IL can not only promote the movement of PEO segment by reducing the crystallinity, increase the Li+ free number, but also improve the effective Li+ transmission by forming rapid channels at PEO/LLZO interface. © 2024
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