School of Materials Science and Engineering, Tongji University, 201804, Shanghai, P. R. China.
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 200240, Shanghai, P. R. China.
Angew Chem Int Ed Engl. 2023 Jun 19;62(25):e202302617. doi: 10.1002/anie.202302617. Epub 2023 May 10.
Rechargeable magnesium batteries (RMBs) are seriously plagued by the direct exposure of the Mg anode to the electrolyte components, leading to spontaneous and electrochemical side reactions and interfacial passivation. Herein, a benign coordination layer is constructed at the Mg/electrolyte interface where aniline with a strong magnesiophilic amine group and high stability to Mg is chosen as representative, which has higher adsorption energy than DME (1,2-dimethoxyethane) and trace water. This Mg coordination environment mitigates side reactions, forming a non-passivating interface consisting of aniline and much fewer by-products after several cycles. Therefore, the Mg symmetrical cell operates with a low overpotential and uniform Mg deposition. This interfacial coordination can also be adopted for Mg anode protection in various electrolyte cases of Mg(TFSI) electrolyte systems.
可充电镁电池 (RMBs) 严重受到镁阳极与电解质成分直接接触的困扰,导致自发和电化学副反应以及界面钝化。在此,在 Mg/电解质界面构建了良性的配位层,选择具有强镁亲和性胺基团和对镁高稳定性的苯胺作为代表性物质,其对 DME(1,2-二甲氧基乙烷)和痕量水的吸附能更高。这种镁配位环境减轻了副反应,在经过几个循环后形成了由苯胺和更少副产物组成的非钝化界面。因此,镁对称电池的过电位较低,镁沉积均匀。这种界面配位也可以用于 Mg(TFSI)电解质体系的各种电解质情况下的镁阳极保护。