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阴极电解质中间相(CEI)赋予 MoS 快速的界面镁离子转移动力学。

Cathode Electrolyte Interphase (CEI) Endows Mo S with Fast Interfacial Magnesium-Ion Transfer Kinetics.

机构信息

College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, No. 53 Zhengzhou Road, Qingdao, 266042, Shandong, China.

Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No. 189 Songling Road, Qingdao, 266101, Shandong, China.

出版信息

Angew Chem Int Ed Engl. 2023 Mar 27;62(14):e202217709. doi: 10.1002/anie.202217709. Epub 2023 Feb 21.

Abstract

Magnesium (Mg) metal secondary batteries have attracted much attention for their high safety and high energy density characteristics. However, the significant issues of the cathode/electrolyte interphase (CEI) in Mg batteries are still being ignored. In this work, a significant CEI layer on the typical Mo S cathode surface has been unprecedentedly constructed through the oxidation of the chloride-free magnesium tetrakis(hexafluoroisopropyloxy)borate (Mg[B(hfip) ] ) salt under a proper charge cut-off voltage condition. The CEI has been identified to contain B O effective species originating from the oxidation of [B(hfip) ] anion. It is confirmed that the B O species is beneficial to the desolvation of solvated Mg , speeding up the interfacial Mg transfer kinetics, thereby improving the Mg -storage capability of Mo S host. The firstly reported CEI in Mg batteries will give deeper insights into the interface issues in multivalent electrochemical systems.

摘要

镁(Mg)金属二次电池因其高安全性和高能量密度特性而备受关注。然而,镁电池阴极/电解质界面(CEI)的重大问题仍未得到重视。在这项工作中,通过在适当的充电截止电压条件下,对无氯的镁四(六氟异丙氧基)硼酸酯(Mg[B(hfip)])盐进行氧化,在典型的 MoS 阴极表面前所未有地构建了一个显著的 CEI 层。已经确定 CEI 包含源自[B(hfip)]阴离子氧化的 BO 有效物质。据证实,BO 物质有利于溶剂化 Mg 的去溶剂化,加快了界面 Mg 转移动力学,从而提高了 MoS 主体的 Mg 存储能力。在镁电池中首次报道的 CEI 将深入了解多价电化学体系中的界面问题。

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