Soft-Hard Synergistic Solid All-Polymer Electrolyte Inspired by Musculoskeletal Structure for High-Temperature Lithium Metal Batteries

IF 18.5 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Guo-Rui Zhu, Qin Zhang, Ying-Ying Zhang, Xiu-Li Wang, Gang Wu, Yu-Zhong Wang
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Abstract

Robust structures are essential for extending the application of shapeless soft polymer electrolytes and maintaining the self-supporting of solid-state all-polymer electrolytes (SPEs) at elevated temperatures. Common strategies of introducing additional separators or cross-linking can significantly increase the manufacturing complexity of SPEs, thus limiting their commercialization. Herein, inspired by the musculoskeletal structure, a “soft-hard synergy” enhanced SPE (named PPH-SPE) is successfully designed and manufactured by a simple one-step in situ microphase separation strategy for high-temperature lithium–metal batteries. In the bicontinuous PPH-SPE, the “soft” polyphosphazene liquid polymer electrolyte (PPZ-LPE) phase provides excellent electrochemical properties, interfacial compatibility, and high-temperature stable Li3N/Li3PO4-rich hybrid interfaces. PVDF-HFP crystals are skillfully used to build a 3D continuous, high-strength (0.32 ± 0.02 MPa at 90 °C), thermotolerant “hard” skeleton. In the synergy of two phases, Li//Li cell can maintain continuous electrodeposition over 4500 h of the plating/stripping process at 0.25 mA cm−2 and 0.25 mAh cm−2. Furthermore, LiFePO4//Li coin and pouch cells achieve an ultra-long lifetime of over 1000 (1 C) and 1800 (0.5 C) cycles at 90 °C, respectively. This strategy provides new ideas for large-scale fabrication and enhancement of solid all-polymer electrolytes.

Abstract Image

基于肌肉骨骼结构的高温锂金属电池软硬协同固体全聚合物电解质
坚固的结构对于扩大非定型软聚合物电解质的应用范围和保持固态全聚合物电解质(spe)在高温下的自支撑性至关重要。引入额外分离器或交联的常见策略会显著增加spe的制造复杂性,从而限制其商业化。在此,受肌肉骨骼结构的启发,通过简单的一步原位微相分离策略,成功设计并制造了一种“软硬协同”增强的SPE(命名为PPH-SPE),用于高温锂金属电池。在双连续的PPH-SPE中,“软”聚磷腈液态聚合物电解质(PPZ-LPE)相具有优异的电化学性能、界面相容性和高温稳定的Li3N/ li3po4富杂化界面。PVDF-HFP晶体被巧妙地用于构建3D连续,高强度(90°C时0.32±0.02 MPa),耐热的“硬”骨架。在两相的协同作用下,Li//Li电池可以在0.25 mA cm - 2和0.25 mAh cm - 2的条件下保持超过4500 h的电镀/剥离过程。此外,LiFePO4//Li硬币电池和袋状电池在90°C下分别实现了超过1000(1℃)和1800(0.5℃)循环的超长寿命。该策略为固体全聚合物电解质的大规模制造和增强提供了新的思路。
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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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