论文成果

Activation mechanism of conventional electrolytes with amine solvents: Species evolution and hydride-containing interphase formation

发布时间:2024-12-24  点击次数:

关键字:MG METAL; MAGNESIUM; DEPOSITION; BATTERIES; GROWTH

摘要:Rechargeable magnesium (Mg)-metal batteries have brought great expect to overcome the safety and energy density concerns of typical lithium-ion batteries. However, interfacial passivation of the Mg-metal anode impairs the reversible Mg plating/stripping chemistries, resulting in low Coulombic efficiency and large overpotential. In this work, a facile isobutylamine (IBA)-assisted activation strategy has been proposed and the fundamental mechanism has been unveiled in a specific way of evolving active species and forming MgH2-based solid-electrolyte interphase. After introducing IBA into a typical electrolyte of magnesium bis(trifluoromethanesulfonyl) imide (Mg(TFSI)(2)) in diglyme (G2) solvents, electrolyte species of [Mg2 (IBA)(5)](2 ) and protonated amine-based cations of [(IBA)H]( ) have been detected by nuclear magnetic resonance and mass spectra. This not only indicates direct solvation of IBA toward Mg2 but also suggests its ionization, which is central to mitigating the decomposition of G2 and TFSI anions by forming neutrally charged [(IBAH( ))(TFSI-)](0) and other complex ions. A series of experiments, including cryogenic-electron microscopy, D2O titration-mass spectra, and time of flight secondary ion mass spectrometry results, reveal a thin, non-passivated, and MgH2-containing interphase on the Mg-metal anode. Besides, uniform and dendrite-free Mg electrodeposits have been revealed in composite electrolytes. Benefiting from the activation effects of IBA, the composite electrolyte displays superior electrochemical performance (overpotential is approximately 0.16 V versus 2.00 V for conventional electrolyte; Coulombic efficiency is above 90% versus <10% for conventional electrolyte). This work offers a fresh direction to advanced electrolyte design for next-generation rechargeable batteries.(c) 2024 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.

卷号:98

期号:-

是否译文:

崂山校区 - 山东省青岛市松岭路99号   
四方校区 - 山东省青岛市郑州路53号   
中德国际合作区(中德校区) - 山东省青岛市西海岸新区团结路3698号
高密校区 - 山东省高密市杏坛西街1号   
济南校区 - 山东省济南市文化东路80号©2015 青岛科技大学    
管理员邮箱:master@qust.edu.cn

访问量: | 最后更新时间:-- | 开通时间:-- |手机版