用于高压锂电池的离子-偶极相互作用调节的固体聚合物电解质

IF 5.4 1区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY GIANT Pub Date : 2024-06-19 DOI:10.1016/j.giant.2024.100310
Tao Chen , Yuncong Liu , Zhekai Jin , Lin Sun , Zeyu Liu , Hao Xu , Zhiguo Zhao , Chao Wang
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摘要

高能量密度锂电池需要具有宽电化学稳定窗口和高锂离子转移数(tLi+)的固体聚合物电解质(SPE)。在这里,我们通过原位聚合构建了一种带有醚酯双官能团的共聚物电解质(PDA),它具有较低的最高占据分子轨道(HOMO)能级。与聚(1,3-二氧戊环)(PDOL)纯聚醚电解质相比,PDA 电解质中锂盐与聚合物之间的离子-偶极相互作用减弱,促进了 "弱溶解 "结构的形成。因此,该电解质实现了高氧化稳定性(对 Li+/ Li 的电压为 4.6 V,标准泄漏电流为 10 μA)和高 Li+ 转移数(0.60),更重要的是,在高压阴极表面形成了稳定的富含 LiF 的成分。这项研究为设计抗氧化固相萃取物以实现高能量密度锂电池提供了基本认识。
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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Solid polymer electrolytes regulated by ion-dipole interactions for high voltage lithium batteries

Solid polymer electrolytes (SPEs) with wide electrochemically stable window and high lithium-ion transference number (tLi+) are a requirement for high energy density lithium batteries. Here, we construct a copolymer electrolyte (PDA) with ether-ester bifunctional groups that exhibits a low highest occupied molecular orbital (HOMO) energy level by in situ polymerization. Compared to the poly(1,3-dioxolane) (PDOL) pure polyether electrolyte, the weakening of the ion-dipole interaction between lithium salt and polymer in the PDA electrolyte promotes the formation of a “weak solvation” structure. Therefore, the electrolyte achieves high oxidative stability (4.6 V vs. Li+/ Li with a standard leakage current of 10 μA), high Li+ transference number (0.60), and importantly, derives a stable LiF-rich composition on high voltage cathode surface. Which ultimately enables stable cycling of Li||LiNi0.5Co0.2Mn0.3O2 (NCM523) batteries at a range of 3.0–4.3 V. This work provides a fundamental understanding of the design of antioxidant SPEs to achieve high energy density lithium batteries.

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来源期刊
GIANT
GIANT Multiple-
CiteScore
8.50
自引率
8.60%
发文量
46
审稿时长
42 days
期刊介绍: Giant is an interdisciplinary title focusing on fundamental and applied macromolecular science spanning all chemistry, physics, biology, and materials aspects of the field in the broadest sense. Key areas covered include macromolecular chemistry, supramolecular assembly, multiscale and multifunctional materials, organic-inorganic hybrid materials, biophysics, biomimetics and surface science. Core topics range from developments in synthesis, characterisation and assembly towards creating uniformly sized precision macromolecules with tailored properties, to the design and assembly of nanostructured materials in multiple dimensions, and further to the study of smart or living designer materials with tuneable multiscale properties.
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