电解质
离子电导率
材料科学
化学工程
电化学
聚合物
电导率
电池(电)
聚合
高分子化学
化学
复合材料
电极
物理化学
量子力学
物理
工程类
功率(物理)
作者
Chaoran Xu,Zexin Wang,Wenbin Jiao,Qifang Sun,Qing Zhang,Chen Li,Su Wang,Yue Ma,Zhaocheng He,Dawei Song,Hongzhou Zhang,Xixi Shi,Chunliang Li,Lianqi Zhang
标识
DOI:10.1016/j.jallcom.2023.171548
摘要
A dual network solid polymer electrolyte is prepared, the cross-linked part is constructed using ring-opening polymerization reaction, in which SiO2 particles connect with polyethylene glycol diglycidyl ether (PEGDE) and polyetheramine (PEA) as cross-linking point. The introduction of SiO2 is conducive to reduce the crystallization of polymer matrix, improve the strength and promote the fast migration of Li ions. The abundant C-O segments in PEGDE and PEA are advantageous to the hopping behavior of Li ions and improve the ionic conductivity of electrolyte. Poly (vinylidenefluoride-hexaflouropropylene) (PVDF-HFP) is selected as linear part due to its robust mechanical behavior and outstanding electrochemical property. The obtained SiO2 functionalized PEGDE and PEA-PVDF-HFP solid polymer electrolyte (referred to as SGPP-ASPE) demonstrates excellent ionic conductivity of 2.4 × 10−4 S cm−1, high lithium-ion transference number of 0.54 and minor interfacial polarization of 0.09 V after 1000 h using Li//Li symmetrical cell. After assembling Li/LiFePO4 cell, a favorable cycling stability with the capacity retention of 93.8% after 100 cycles at 0.2 C is delivered. The reasonable design of advanced polymer electrolytes with dual network opens up a new path for the development of solid high-performance LMBs.
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