La2O3 Filler's Stabilization of Residual Solvent in Polymer Electrolyte for Advanced Solid‐State Lithium‐Metal Batteries

Author:

Zeng Yaping1,Zhao Le1,Zhang Jiaming1,Li Qiuping1,Sun Dan1,Ren Yu2,Tang Yougen1,Jin Guanhua3,Wang Haiyan1ORCID

Affiliation:

1. Hunan Provincial Key Laboratory of Chemical Power Sources College of Chemistry and Chemical Engineering Central South University Changsha 410083 P. R. China

2. Jiangsu Yeeli Technology Co., Ltd. Wuxi 214200 P. R. China

3. College of Energy and Chemical Engineering Xinjiang Institute of Technology Aksu 843100 P. R. China

Abstract

Polymer solid electrolytes (SEs) with high safety and flexibility are ideal for advanced lithium‐metal solid‐state batteries (SSBs). Among various polymer SEs, polyvinylidene fluoride‐co‐hexafluoropropylene (PVDF‐HFP) polymer SEs have gained increased attention for their high dielectric constants, high ionic conductivity, and excellent flexibility. However, severe side reactions at the interface caused by the decomposition of residual DMF solvent significantly reduce the cycle life of PVDF‐HFP‐based SSBs. Herein, La2O3 nanoparticles are used as new inorganic fillers to form a PVDF‐HFP/LiFSI/La2O3‐40% composite polymer electrolyte (PVDF‐HFP/La2O3 CPE). Benefiting from the interaction between La2O3 and N,N‐dimethylformamide (DMF) solvent molecules, the cell cycling stability is greatly improved. In addition, the PVDF‐HFP/LiFSI solid electrolyte (PVDF‐HFP SE) containing 40 wt% La2O3 has the highest ionic conductivity of 1.33 × 10−3 S cm−1 at 25 °C. It also exhibits a higher lithium‐ion transference number of 0.52 and lower polarization. The PVDF‐HFP/La2O3 CPE here ensures high ionic conductivity and stable interface chemistry in SSB, demonstrating a promising application potential.

Funder

National Nature Science Foundation of China

Hunan Provincial Science and Technology Department

Publisher

Wiley

Subject

General Earth and Planetary Sciences,General Environmental Science

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