电解质
材料科学
化学工程
离子电导率
电池(电)
锂(药物)
陶瓷
膜
锂电池
聚合物
阴极
快离子导体
原位聚合
电极
离子
离子键合
聚合
复合材料
化学
物理化学
有机化学
热力学
医学
功率(物理)
物理
生物化学
工程类
内分泌学
作者
Qixin Gai,Tianyu Zhao,Junwei Ma,Chuangsheng Wang,Hongtao Gao,Li Li
标识
DOI:10.1016/j.est.2023.110150
摘要
The utilization of ceramic-polymer hybrid electrolytes has gained popularity in the development of all-solid-state lithium batteries that are capable of high-energy and long-lasting performance. This research presents a novel dual hybrid in-situ solid electrolyte membrane (iHSE) that is tailored for high-performance Li-ion batteries, consisting of LATP and PVDF-HFP. The hybrid membrane is comprised of LATP particles and PVDF-HFP with PEG polymer matrix (HSE), and the migration of Li+ ions in LATP particles was simulated through molecular dynamics. At a temperature of 40 °C, the hybrid membrane demonstrates an ionic conductivity of 7.36 × 10−4 S·cm−1 and a lithium-ion migration number of 0.61. The interface between the cathode and electrolyte membrane is effectively enhanced through in situ polymerization with the resulting all-solid-state lithium battery exhibits a reversible discharge capacity of 160 mAh·g−1 at a current density of 0.1C multiplier at ambient temperature and can function normally for over 1000 cycles of charge and discharge at 1C multiplier. Moreover, the discharge capacity trend exhibits greater uniformity in comparison to a battery lacking interface enhancement.
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