详细信息

Self-Healing Interfacial Cross-Links Enable Supertough Solid Polymer Electrolytes with Eliminating-Dendrite Lithium Metal Battery  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Self-Healing Interfacial Cross-Links Enable Supertough Solid Polymer Electrolytes with Eliminating-Dendrite Lithium Metal Battery

作者:Fang, Biao[1];Wang, Lei[1];Wang, Zhangyuan[1];Su, Zhipeng[1];Zou, Feng[1];Mo, Runwei[1]

机构:[1]East China Univ Sci & Technol, Sch Mech & Power Engn, Shanghai 200037, Peoples R China

年份:2025

卷号:7

期号:10

起止页码:3292

外文期刊名:ACS MATERIALS LETTERS

收录:;EI(收录号:20253919236969);WOS:【SCI-EXPANDED(收录号:WOS:001562804400001)】;

基金:This work is financially supported by Shanghai pilot Program for Basic Research (No. 22TQ1400100-8), Shanghai Pujiang Program (No. 20PJ1402500), Natural Science Foundation of Shanghai (No. 22ZR1416600), and the Fundamental Research Funds for the Central Universities.

语种:英文

外文关键词:Crosslinking - Dynamics - Fillers - Fluorine compounds - Interface states - Lithium - Lithium batteries - Lithium compounds - Self-healing materials - Solid electrolytes - Solid state devices - Solid-State Batteries

摘要:The integration of solid-state inorganic fillers into polymer matrices can improve the performance of solid lithium metal batteries. However, there is poor interface interaction between the polymer matrix and solid-state inorganic fillers, which has led to the performance of solid lithium metal batteries falling far short of expectations. Here, we constructed a bridging interaction based on borate ester dynamic cross-linking to prepare a supertough and self-healing poly(vinylidene fluoride)-hexafluoropropylene/graphene oxide/borate bonds/Li6.5La3Zr1.5Ta0.5O12 solid polymer electrolyte. The electrolyte exhibits a wide electrochemical window (4.84 V), high elongation at break (205%), outstanding thermal stability (200 degrees C), and high-capacity retention (90.3% after 900 cycles under 2C). We further revealed the influence of borate ester dynamic cross-linking on the performance of solid polymer electrolyte through density functional theory calculations. This work offers insight into designing high-performance solid polymer electrolytes for solid-state batteries.

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