材料科学
金属锂
电解质
锂(药物)
金属
高能
纳米技术
锂离子电池的纳米结构
快离子导体
能量密度
化学工程
工程物理
冶金
电化学
电极
物理化学
医学
化学
工程类
内分泌学
作者
L. Liu,Yongzheng Shi,Mengyue Liu,Qing Zhong,Yuqi Chen,Bingyang Li,Zhen Li,Tao Zhang,Hang Su,Jiaying Peng,Na Yang,Pengfei Wang,Adrian C. Fisher,Jin Niu,Feng Wang
标识
DOI:10.1002/adfm.202403154
摘要
Abstract Solid‐state electrolytes (SSEs) are key to unlocking the potential of lithium metal batteries (LMBs), but their high thickness (>100 µm) due to poor mechanical properties limits energy density improvements. Herein, an ultrathin (≈5 µm) polymer SSE with a high Young's modulus (10.6 GPa), made from a polyvinylidene fluoride‐hexafluoropropylene (PVDF‐HFP) matrix and an ethylene diamine tetraacetic acid (EDTA) additive is proposed. By virtue of the electron‐donating property, EDTA induces the conformation transformation of PVDF‐HFP, enhancing the mechanical strength by a fine‐grain strengthening mechanism. In addition, PVDF‐HFP with cis ‐conformation shortens the pathway for Li + , promotes the Li + dissociation and immobilizes the anions of lithium salt, thus increasing the ionic conductivity (2.47 × 10 −4 S cm −1 ) and transfer number (0.59) of the electrolyte. Moreover, the electrolyte also possesses a wide voltage window (4.7 V) and good heat/flame resistance. The half cells and full cells with the electrolytes show good cycling and rate performance. Notably, a pouch cell based on the electrolyte exhibits impressive energy densities of 516 Wh kg −1 and 1520 Wh L −1 (excluding packages), showing great potential for practical use in LMBs.
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