共聚物
固态
锂电池
电解质
材料科学
锂(药物)
网络结构
电池(电)
化学工程
快离子导体
高分子化学
化学
聚合物
计算机科学
有机化学
工程类
复合材料
物理化学
离子
电极
物理
机器学习
功率(物理)
量子力学
离子键合
内分泌学
医学
作者
Bo Chen,Qiang Xu,Zhen Huang,Yanran Zhao,Shaojie Chen,Xiaoxiong Xu
标识
DOI:10.1016/j.jpowsour.2016.09.063
摘要
A new class of copolymer electrolytes with tunable network structure is successfully designed and prepared via a facile one-pot reaction. The trimethylolpropane triglycidyl ether (TMPEG) is cross-linked with poly (ethylene glycol) diamine (NPEG) to create well-defined solid network polymer electrolyte (SNPE). The network structure could be tuned by changing the molar ratio of TMPEG and NPEG or the molecular weight of NPEG. The effects of molecular weight of NPEG and molar ratio of EO/Li+ on the ionic conductivity are systematically investigated. The optimal electrolyte TMPEG-NPEG4K[2:1]-16:1 presents a maximum conductivity of 1.10 × 10−4 S cm−1 under 30 °C, and an 18-fold ionic conductivity enhancement in that of PEO-based electrolyte. Furthermore, it also exhibits wide electrochemical window (0–5.4 V), excellent compatibility with metallic Li, and superior mechanical properties. The all-solid-state lithium batteries LiFePO4/Li are assembled with TMPEG-NPEG4K[2:1]-16:1 electrolyte, and present good cycling and rate performance under 60 °C. The initial discharge specific capacities of the batteries are 161.7 mAh g−1 at 0.2 C and 132.7 mAh g−1 at 1 C, and the capacity retention ratio can be retained at 90.6% and 90.5% after 100 cycles. This new copolymer electrolyte may become a promising candidate for applications in all-solid-state lithium battery.
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