电解质
材料科学
电化学
化学工程
溶剂化
相间
溶剂
电极
化学
有机化学
物理化学
工程类
生物
遗传学
作者
Jie Wen,Hongwei Fu,Dianwei Zhang,Xuemei Ma,Lichen Wu,Ling Fan,Xinzhi Yu,Jiang Zhou,Bingan Lu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-08-10
卷期号:17 (16): 16135-16146
被引量:25
标识
DOI:10.1021/acsnano.3c05165
摘要
A robust interface between the electrode and electrolyte is essential for the long-term cyclability of potassium-ion batteries (PIBs). An effective strategy for achieving this objective is to enhance the formation of an anion-derived, robust, and stable solid-electrolyte interphase (SEI) via electrolyte structure engineering. Herein, inspired by the application of antisolvents in recrystallization, we propose a nonfluorinated antisolvent strategy to optimize the electrolyte solvation structure. In contrast to the conventional localized superconcentrated electrolyte introducing high-fluorinated ether solvent, the anion-cation interaction is considerably enhanced by introducing a certain amount of nonfluorinated antisolvent into a phosphate-based electrolyte, thereby promoting the formation of a thin and stable SEI to ensure excellent cycling performance of PIBs. Consequently, the nonfluorinated antisolvent electrolyte exhibits superior stability in the K||graphite cell (negligible capacity degradation after 1000 cycles) and long-term cycling in the K||K symmetric cell (>2200 h), as well as considerably improved oxidation stability. This study demonstrates the feasibility of optimized electrolyte engineering with a nonfluorinated antisolvent, providing an approach to realizing superior electrochemical energy storage systems in PIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI