电解质
电化学
电化学窗口
法拉第效率
氢
水溶液
阳极
无机化学
化学
化学工程
环丁砜
材料科学
电极
离子电导率
有机化学
物理化学
工程类
溶剂
作者
Yu Wang,Tairan Wang,Dejian Dong,Jing Xie,Yuepeng Guan,Yaqin Huang,Jun Fan,Yi‐Chun Lu
出处
期刊:Matter
[Elsevier BV]
日期:2021-11-10
卷期号:5 (1): 162-179
被引量:143
标识
DOI:10.1016/j.matt.2021.10.021
摘要
Conventional aqueous electrolytes suffer from a narrow voltage window due to water decomposition. Highly concentrated electrolytes expand the voltage window; however, they are limited by high cost and potential toxicity. Here, we develop a hydrogen bond-anchored electrolyte by introducing sulfolane as hydrogen bond acceptor to limit water activity. The designed electrolyte expands the voltage window to 3.4 V (1.3–4.7 V versus Li+/Li) and forms a hierarchical anode-electrolyte interphase to suppress the hydrogen evolution reaction. An aqueous Li4Ti5O12/LiMn2O4 full cell achieved 141 W h kg−1 for 300 cycles at 1 C and 125 W h kg−1 for 1,000 cycles at 5 C with a high Coulombic efficiency of 99.5%–99.9%. On-line electrochemical mass spectroscopy shows negligible hydrogen/oxygen gas evolution upon cycling, further confirming the stability of the designed electrolyte. This work demonstrates a rational and effective approach to suppress the hydrogen evolution reaction and achieve stable high-voltage aqueous batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI