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无机填料的表面正电荷修饰以优化锂金属电池复合聚合物电解质中的锂离子传导路径。

Surface positive-charged modification of inorganic fillers to optimize lithium ion conductive pathways in composite polymer electrolytes for lithium-metal batteries.

作者信息

Wang Meihuang, Tian Liying, Cao Yu, Su Zhe, Zhang Wanyu, Yi Shan, Zhang Yayun, Niu Bo, Long Donghui

机构信息

Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, East China University of Science and Technology, School of Chemical Engineering, Shanghai 200237, PR China.

Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, East China University of Science and Technology, School of Chemical Engineering, Shanghai 200237, PR China.

出版信息

J Colloid Interface Sci. 2023 Jan 15;630(Pt B):634-644. doi: 10.1016/j.jcis.2022.10.137. Epub 2022 Oct 31.

DOI:10.1016/j.jcis.2022.10.137
PMID:36343555
Abstract

The incorporation of inorganic fillers into composite polymer electrolytes (CPEs) is a common strategy to improve ionic conductivity. However, the high surface energy of inorganic fillers typically aggravates poor interfacial contact with polymer chains. Herein, we develop a surface positive-charge modification strategy for enhancing the intermolecular interaction of poly(ethylene oxide) (PEO) electrolytes with inorganic fillers and optimizing lithium ion (Li) conductive pathways in CPEs. The SiO nanoparticles are coated with a polydopamine adhesive layer and then functionalized with a branched polyethyleneimine positively charged functional layer. Such surface modification not only effectively induces more amorphous structure into the PEO matrix but also promotes the dissociation of lithium salts and activates more free Li in the PEO to accelerate Li transport. The CPEs achieved a superior ionic conductivity of 6.12 × 10 S cm at 30 °C. In addition, the modified fillers could induce the formation of a lithium fluoride (LiF)-rich solid-state interphase and correspondingly achieve excellent compatibility with Li metal. The Li symmetric battery using the as-prepared CPEs delivered stable Li plating/stripping performances over 3960 h under 0.2 mA cm. The resulting LiFePO|Li battery has an excellent capacity retention of 92.8 % after 260 cycles at 0.5C and 60 °C.

摘要

将无机填料掺入复合聚合物电解质(CPE)中是提高离子电导率的常用策略。然而,无机填料的高表面能通常会加剧与聚合物链的不良界面接触。在此,我们开发了一种表面正电荷修饰策略,以增强聚环氧乙烷(PEO)电解质与无机填料的分子间相互作用,并优化CPE中的锂离子(Li)传导途径。SiO纳米颗粒涂覆有聚多巴胺粘合剂层,然后用带正电荷的支化聚乙烯亚胺功能层进行功能化。这种表面修饰不仅有效地在PEO基体中诱导出更多的非晶结构,还促进了锂盐的解离并激活了PEO中更多的游离Li以加速Li传输。CPE在30℃时实现了6.12×10 S cm的优异离子电导率。此外,改性填料可诱导形成富含氟化锂(LiF)的固态界面,并相应地与锂金属实现优异的相容性。使用所制备的CPE的锂对称电池在0.2 mA cm下3960 h以上提供稳定的锂电镀/剥离性能。所得的LiFePO|Li电池在0.5C和60℃下260次循环后具有92.8%的优异容量保持率。

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