An ultrathin all-in-one free-standing polymer electrolyte realizing 400 Wh kg−1 lithium metal batteries via a dual anion-binding strategy

IF 9.8 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jinping Zhang, Yansong Liu, Xingchen Song, Guolin Sun, Nuo Xu, Peiran Bian, Xiangjian Wan, Chenxi Li, Hongtao Zhang, Yongsheng Chen
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引用次数: 0

Abstract

Solid polymer electrolytes hold significant promise for high-energy-density and safety batteries, particularly given their compatibility with scalable manufacturing. However, their practical development is currently impeded by limitations including insufficient mechanical robustness, excessive electrolyte thickness, and interfacial instability. Herein, an ultrathin (18 µm), all-in one, free-standing single-ion conducting polymer electrolyte (PBFG) is designed using a dual Lewis-acid anion-binding strategy and a new designed fluorinated tetraglyme plasticizer. Incorporating boron nitride and borate ester units, the dual Lewis-acid polymer framework effectively immobilizes anions to enhance lithium salt dissociation, resulting in a high Li+ transference number (\(t_{\rm Li^{+}} = 0.86\)). Concurrently, the fluorinated tetraglyme plasticizer promotes the formation of a stable, LiF-rich solid electrolyte interphase. This synergistic design imparts the PBFG with a high ionic conductivity of 1.0 × 10−3 S cm−1 at 25 °C. Impressively, by replacing the conventional separator with this ultrathin all-in-one electrolyte, we achieve 0.46 Ah Li-metal pouch cells that deliver exceptional gravimetric and volumetric energy densities of 403 Wh kg−1 and 1190 Wh L−1, respectively, while passing industry-standard nail penetration tests. These results underscore the tremendous potential of replacing separators with ultrathin all-in-one electrolytes for practical, high-energy lithium metal batteries.

一种超薄一体化独立聚合物电解质,通过双阴离子结合策略实现400wh kg - 1锂金属电池
固体聚合物电解质在高能量密度和安全电池方面具有重要的前景,特别是考虑到它们与可扩展制造的兼容性。然而,它们的实际发展目前受到包括机械稳健性不足、电解质厚度过大和界面不稳定性等限制的阻碍。本文采用双路易斯酸阴离子结合策略和新设计的氟化四酶增塑剂,设计了一种超薄(18µm)、一体化、独立的单离子导电聚合物电解质(PBFG)。结合氮化硼和硼酸酯单元,双刘易斯酸聚合物框架有效地固定阴离子,增强锂盐解离,从而获得高Li+转移数(\(t_{\rm Li^{+}} = 0.86\))。同时,氟化四烯酰胺增塑剂促进了稳定的富锂固体电解质界面的形成。这种协同设计使PBFG在25°C时具有1.0 × 10−3 S cm−1的高离子电导率。令人印象深刻的是,通过用这种超薄的一体化电解质取代传统的分离器,我们实现了0.46 Ah的锂金属袋状电池,其重量和体积能量密度分别为403 Wh kg - 1和1190 Wh L - 1,同时通过了行业标准的钉子穿透测试。这些结果强调了用超薄一体化电解质代替隔板用于实用的高能锂金属电池的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Science China Chemistry
Science China Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
7.30%
发文量
3787
审稿时长
2.2 months
期刊介绍: Science China Chemistry, co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China and published by Science China Press, publishes high-quality original research in both basic and applied chemistry. Indexed by Science Citation Index, it is a premier academic journal in the field. Categories of articles include: Highlights. Brief summaries and scholarly comments on recent research achievements in any field of chemistry. Perspectives. Concise reports on thelatest chemistry trends of interest to scientists worldwide, including discussions of research breakthroughs and interpretations of important science and funding policies. Reviews. In-depth summaries of representative results and achievements of the past 5–10 years in selected topics based on or closely related to the research expertise of the authors, providing a thorough assessment of the significance, current status, and future research directions of the field.
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