过电位
电解质
电化学
离子电导率
离解(化学)
无机化学
材料科学
电导率
电化学窗口
阴极
金属
离子键合
阳极
电化学电位
离子
位阻效应
化学工程
储能
盐(化学)
化学
离域电子
金属锂
离子液体
钠
快离子导体
作者
J. N. Zhang,Fang Chen,Bowen Liu,Liang Chen,Gang Wang
标识
DOI:10.1021/acsenergylett.6c02094
摘要
Abstract Mn metal batteries (MnMBs) are promising for stationary applications owing to the low cost and low working potential of Mn anodes. However, developing electrolytes that combine high ionic conductivity with low-overpotential Mn plating/stripping remains challenging because of the trade-off between salt dissociation and desolvation. Herein, we propose a weakly coordinating electrolyte, Mn[B(HFIP)4]2 (HFIP: hexafluoroisopropyl), for advanced MnMBs. The [B(HFIP)4]– anion, featuring full electron delocalization and steric hindrance, promotes complete salt dissociation in low-dielectric-constant ethers, yielding a pure ether-coordinated Mn2+ electrolyte with high ionic conductivity (4.7–8.5 mS/cm at 20 °C) and a wide electrochemical window (>3 V). Weak ether-Mn2+ coordination facilitates desolvation, affording a record-low Mn plating/stripping overpotential (<100 mV at 0.5 mA/cm2) and dendrite-free 3D growth. Coupling Mn anodes with polytriphenylamine or activated carbon cathodes enables quick-charge full cells, demonstrating the potential of anion engineering for high-performance multivalent metal batteries.
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