电解质
材料科学
化学工程
离子电导率
电化学
膜
锂(药物)
电池(电)
聚合物
电化学窗口
电导率
化学
电极
复合材料
医学
物理
工程类
内分泌学
量子力学
物理化学
功率(物理)
生物化学
作者
Jiangchao Chen,Guisheng Zhu,Kunpeng Jiang,Huarui Xu,Yunyun Zhao,Hu Wang,Pengfei Pang,Yiran Bai,Peipei Wang,Haining Wu
标识
DOI:10.1016/j.cej.2023.147761
摘要
Safety concerns such as lithium dendrite growth, leakage and volatilization regularly plague conventional liquid lithium metal batteries. However, solid polymer electrolytes can mitigate these issues due to their chemical and electrochemical stability. In this paper, we show that the construction of porous structures gives PVDF-HFP based polymers excellent solution retention, quick Li+ transport channels, and ultra-long Li-symmetric cycle stability. PVDF-HFP based electrolyte membrane with porous structure exhibits excellent electrolyte retention (129.5 %) and superior ionic conductivity (2.4 × 10-3 S cm−1 at 20 ℃). In addition, Lithium-symmetric half battery uses the DPH250 porous electrolyte film to stably last more than 2000 h during the lithium plating/stripping process. DI regulation of PVDF-HFP electrolyte membrane is beneficial to achieve uniform lithium deposition, and better solve the interface problems existing in solid state batteries. LiFePO4/DPH250-LiPF6/Li batteries exhibit stable cycling performance and reversible specific discharge capacity, suggesting a potential strategy for stabilizing lithium metal batteries.
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