Choudhury Snehashis, Tu Zhengyuan, Nijamudheen A, Zachman Michael J, Stalin Sanjuna, Deng Yue, Zhao Qing, Vu Duylinh, Kourkoutis Lena F, Mendoza-Cortes Jose L, Archer Lynden A
School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, NY, 14853, USA.
Department of Material Science and Engineering, Cornell University, Ithaca, NY, 14853, USA.
Nat Commun. 2019 Jul 12;10(1):3091. doi: 10.1038/s41467-019-11015-0.
Electrochemical cells that utilize lithium and sodium anodes are under active study for their potential to enable high-energy batteries. Liquid and solid polymer electrolytes based on ether chemistry are among the most promising choices for rechargeable lithium and sodium batteries. However, uncontrolled anionic polymerization of these electrolytes at low anode potentials and oxidative degradation at working potentials of the most interesting cathode chemistries have led to a quite concession in the field that solid-state or flexible batteries based on polymer electrolytes can only be achieved in cells based on low- or moderate-voltage cathodes. Here, we show that cationic chain transfer agents can prevent degradation of ether electrolytes by arresting uncontrolled polymer growth at the anode. We also report that cathode electrolyte interphases composed of preformed anionic polymers and supramolecules provide a fundamental strategy for extending the high voltage stability of ether-based electrolytes to potentials well above conventionally accepted limits.
利用锂和钠阳极的电化学电池因其实现高能电池的潜力而正在积极研究中。基于醚化学的液体和固体聚合物电解质是可充电锂和钠电池最有前景的选择之一。然而,这些电解质在低阳极电位下不受控制的阴离子聚合以及在最受关注的阴极化学的工作电位下的氧化降解,导致该领域出现了相当大的让步,即基于聚合物电解质的固态或柔性电池只能在基于低电压或中电压阴极的电池中实现。在此,我们表明阳离子链转移剂可以通过阻止阳极处不受控制的聚合物生长来防止醚电解质的降解。我们还报告说,由预制阴离子聚合物和超分子组成的阴极电解质界面提供了一种基本策略,可将基于醚的电解质的高电压稳定性扩展到远高于传统公认极限的电位。