电解质
材料科学
电化学
法拉第效率
水溶液
电化学窗口
二甲基乙酰胺
无机化学
电池(电)
分析化学(期刊)
化学工程
电极
溶剂
化学
离子电导率
物理化学
有机化学
热力学
功率(物理)
工程类
物理
作者
Shigang Chen,Pan Sun,John Humphreys,Peimiao Zou,Mengfei Zhang,Georgina Jeerh,Boyao Sun,Shanwen Tao
标识
DOI:10.1021/acsami.1c12911
摘要
N,N-Dimethylacetamide (DMA) cooperated with LiNO3 salt has previously shown to be a promising electrolyte for a Li//O2 battery, showing good stability against both the O2 electrode reaction and Li stripping/plating. In this work, DMA is hybridized with a concentrated nitrate electrolyte [2.5 m Zn(NO3)2 + 13 m LiNO3 aqueous solution] for better electrochemical stability while using less dissolved salts. The widest electrochemical stability window for this DMA-diluted electrolyte is determined as 3.1 V, the negative critical stability potential of which is −1.6 V versus Ag/AgCl, indicating desirable stability against hydrogen evolution and Zn deposition. The findings can be attributed to the weakened Li+/Zn2+ solvation sheath caused by low permittivity of DMA, as revealed through Raman spectra characterization and molecular dynamics simulation. A Zn//Zn symmetrical cell and Zn//LiMn2O4 hybrid ion batteries are assembled in air directly, attributed to the stability of DMA toward O2. Zn stripping/plating with a dendrite-free morphology is delivered for 110 h and 200 charge/discharge cycles under 1 C rate, achieving 99.0% Coulombic efficiency. The maximum capacity of the battery is 121.0 mA h·g–1 under 0.2 C rate (based on the mass of LiMn2O4), delivering an energy density of 165.8 W h·kg–1 together with 2.0 V working voltage. This work demonstrates the feasibility and validity of utilizing a relatively dilute electrolyte dissolved in oxygen for a highly stable aqueous rechargeable battery.
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