溶剂化
电化学窗口
电解质
电化学
水溶液
离子
阳极
盐(化学)
电池(电)
溶解度
无机化学
化学
离子电导率
物理化学
电极
热力学
有机化学
物理
功率(物理)
作者
Long Chen,Jiaxun Zhang,Qin Li,Jenel Vatamanu,Xiao Ji,Travis P. Pollard,Chunyu Cui,Singyuk Hou,Ji Chen,Chongyin Yang,Lin Ma,Michael S. Ding,Mounesha N. Garaga,Steve Greenbaum,Hung-Sui Lee,Oleg Borodin,Kang Xu,Chunsheng Wang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-02-27
卷期号:5 (3): 968-974
被引量:239
标识
DOI:10.1021/acsenergylett.0c00348
摘要
A water-in-salt electrolyte (WiSE) offers an electrochemical stability window much wider than typical aqueous electrolytes but still falls short in accommodating high-energy anode materials, mainly because of the enrichment of water molecules in the primary solvation sheath of Li+. Herein, we report a new strategy in which a non-Li cosalt was introduced to alter the Li+-solvation sheath structure. The presence of an asymmetric ammonium salt (Me3EtN·TFSI) in water increases the solubility of LiTFSI by two times, pushes the salt/water molar ratio from 0.37 in WiSE to an unprecedented value of 1.13, and significantly suppresses the water activity in both bulk electrolyte and the Li+-solvation sheath. This new 63 m (mol kgsolvent–1) aqueous electrolyte (42 m LiTFSI + 21 m Me3EtN·TFSI) offers a wide potential window of 3.25 V and supports a 2.5 V aqueous Li-ion battery (LiMn2O4//Li4Ti5O12) to deliver a high energy density of 145 Wh kg–1 stably over 150 cycles.
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