Dual-Functional Electrolyte Additives to Enhance Magnesium Plating/Stripping Performance for Rechargeable Magnesium Metal Batteries With Pure Amine Solvents
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引用次数: 0
Abstract
Reversible magnesium (Mg) plating/stripping is a key challenge for Mg metal batteries. Hence, a dual-functional additive, tin(II) fluoride (SnF2), is introduced into the simple Mg salts (Mg(OTf)2 and Mg(TFSI)2) electrolytes with a pure amine solvent (3-methoxypropylamine, MOPA). Interfacial characterizations and theoretical calculations reveal that the dissociated SnF2 can drive the in-situ formation of a multiphase Sn-based solid-electrolyte interphase (SEI) on the Mg anode. Such a robust and magnesiophilic SEI shields the Mg metal from MOPA-induced corrosion and parasitic reaction, while facilitates the interfacial kinetics of Mg2+. Concurrently, the competitive coordination of F− anions from SnF2 raises the contact ion pairs and further mitigates the MOPA decomposition. As a result, the reversibility of Mg metal anode is successfully enhanced, and Mg//Cu cells maintain over 1000 cycles at 2.0 mA cm−2 with an average Coulombic efficiency exceeding 99.8%. This work offering a promising pathway toward practical application of high-performance Mg metal batteries.
可逆镀/剥离镁是镁金属电池面临的一个关键挑战。因此,用纯胺溶剂(3-甲氧基丙胺,MOPA)将一种双功能添加剂氟化锡(SnF2)引入简单镁盐(Mg(OTf)2和Mg(TFSI)2)电解质中。界面表征和理论计算表明,解离的SnF2可以在Mg阳极上驱动多相sn基固体电解质界面(SEI)的原位形成。这种坚固的亲镁SEI保护了镁金属免受mopa诱导的腐蚀和寄生反应,同时促进了Mg2+的界面动力学。同时,SnF2中F−阴离子的竞争配位提高了接触离子对,进一步减轻了MOPA的分解。结果表明,Mg金属阳极的可逆性得到了增强,Mg/ Cu电池在2.0 mA cm−2下可维持1000次以上循环,平均库仑效率超过99.8%。这项工作为高性能镁金属电池的实际应用提供了一条有希望的途径。
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