电解质
材料科学
聚合物
电池(电)
化学工程
纤维素
锂(药物)
羟丙基纤维素
金属锂
锂电池
高分子化学
化学
复合材料
有机化学
电极
离子
离子键合
功率(物理)
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Hongbing Zhang,Sijie Wang,Yujie Wang,Shuhan Dong,Wen Chen,De Li,Feng Yu,Yong Chen
标识
DOI:10.1016/j.cclet.2022.108031
摘要
Gel polymer electrolytes (GPEs) are considered to be one most promising alternative to liquid electrolytes due to their suitability for creating safe and durable solid-state lithium-metal batteries. However, the mechanical properties of GPEs usually deteriorate dramatically when polymer matrices are plasticized by a liquid electrolyte, which leads to significant loss of battery performance. Therefore, the long-term structural integrity and good mechanical strength are critical characteristics of GPEs designed for high-performance batteries. Here, an ecologically compatible cellulose-based GPE with a crosslinked structure is synthesized via a facile and effective thiol-ene click chemistry method. The prepared thiol-ene crosslinked GPE possesses enhanced mechanical strength (10.95 MPa) and rigid structure, which enabled us to fabricate LiFePO4|Li batteries with ultra-long cycling performance. The capacity retention of the crosslinked cellulose-based GPE can be up to 84% at 0.5 C, even after 350 cycles, which is considerably higher than that of non-crosslinked GPE for which rapid decline in capacity occurs after 200 cycles. In addition, a GPE preparation method described in this work compares favorably well with existing commercial electrolytes for lithium metal batteries.
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