Suppr超能文献

通过弱溶剂化电解质调控锂离子电池中的界面化学*

Regulating Interfacial Chemistry in Lithium-Ion Batteries by a Weakly Solvating Electrolyte*.

作者信息

Yao Yu-Xing, Chen Xiang, Yan Chong, Zhang Xue-Qiang, Cai Wen-Long, Huang Jia-Qi, Zhang Qiang

机构信息

Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.

Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, China.

出版信息

Angew Chem Int Ed Engl. 2021 Feb 19;60(8):4090-4097. doi: 10.1002/anie.202011482. Epub 2020 Nov 19.

Abstract

The performance of Li-ion batteries (LIBs) is highly dependent on their interfacial chemistry, which is regulated by electrolytes. Conventional electrolyte typically contains polar solvents to dissociate Li salts. Herein we report a weakly solvating electrolyte (WSE) that consists of a pure non-polar solvent, which leads to a peculiar solvation structure where ion pairs and aggregates prevail under a low salt concentration of 1.0 M. Importantly, WSE forms unique anion-derived interphases on graphite electrodes that exhibit fast-charging and long-term cycling characteristics. First-principles calculations unravel a general principle that the competitive coordination between anions and solvents to Li ions is the origin of different interfacial chemistries. By bridging the gap between solution thermodynamics and interfacial chemistry in batteries, this work opens a brand-new way towards precise electrolyte engineering for energy storage devices with desired properties.

摘要

锂离子电池(LIBs)的性能高度依赖于其界面化学,而界面化学由电解质调节。传统电解质通常包含极性溶剂以解离锂盐。在此,我们报道了一种弱溶剂化电解质(WSE),它由纯非极性溶剂组成,这导致了一种特殊的溶剂化结构,在1.0 M的低盐浓度下,离子对和聚集体占主导。重要的是,WSE在石墨电极上形成独特的阴离子衍生界面,表现出快速充电和长期循环特性。第一性原理计算揭示了一个普遍原则,即阴离子与溶剂对锂离子的竞争配位是不同界面化学的起源。通过弥合电池中溶液热力学与界面化学之间的差距,这项工作为具有所需性能的储能装置的精确电解质工程开辟了一条全新的道路。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验