电解质
金属锂
锂(药物)
材料科学
融合
金属
聚合物
化学工程
聚合物电解质
复合材料
冶金
电极
化学
离子电导率
物理化学
工程类
内分泌学
哲学
医学
语言学
作者
Yi Qu,Xue Hong,Peng Huang,Chuying Ouyang,Wen Yan,Chao Lai
标识
DOI:10.1016/j.jechem.2024.06.032
摘要
In the pursuit of ultrathin polymer electrolyte (< 20 μm) for lithium metal batteries, achieving a balance between mechanical strength and interfacial stability is crucial for the longevity of the electrolytes. Herein, 11 μm-thick gel polymer electrolyte is designed via an integrated electrode/electrolyte structure supported by lithium metal anode. Benefiting from an exemplary superiority of excellent mechanical property, high ionic conductivity, and robust interfacial adhesion, the in-situ formed polymer electrolyte reinforced by titanosiloxane networks (ISPTS) embodies multifunctional roles of physical barrier, ionic carrier, and artificial protective layer at the interface. The potent interfacial interactions foster a seamless fusion of the electrode/electrolyte interfaces and enable continuous ion transport. Moreover, the built-in ISPTS electrolyte participates in the formation of gradient solid-electrolyte interphase (SEI) layer, which enhances the SEI's structural integrity against the strain induced by volume fluctuations of lithium anode. Consequently, the resultant 11 μm-thick ISPTS electrolyte enables lithium symmetric cells with cycling stability over 600 h and LiFePO4 cells with remarkable capacity retention of 96.6% after 800 cycles. This study provides a new avenue for designing ultrathin polymer electrolytes towards stable, safe, and high-energy-density lithium metal batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI