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用于可充电镁电池的非晶态多硫化钼阴极

An Amorphous Molybdenum Polysulfide Cathode for Rechargeable Magnesium Batteries.

作者信息

Zhao Xinyi, Xu Fei

机构信息

Key Laboratory of Hydraulic Machinery Transients, Ministry of Education, School of Power and Mechanical Engineering, Wuhan University, Wuhan, 430072, China.

出版信息

Chemphyschem. 2023 Aug 15;24(16):e202300333. doi: 10.1002/cphc.202300333. Epub 2023 Jun 22.

Abstract

Rechargeable magnesium batteries (RMBs) attract research interest owing to the low cost and high reliability, but the design of cathode materials is the major difficulty of their development. The bivalent magnesium cation suffers from a strong interaction with the anion and is difficult to intercalate into traditional magnesium intercalation cathodes. Herein, an amorphous molybdenum polysulfide (a-MoS ) is synthesized via a simple one-step solvothermal reaction and used as the cathode material for RMBs. The a-MoS cathode provides a high capacity (185 mAh g ) and a good rate performance (50 mAh g at 1000 mA g ), which are much superior compared with crystalline MoS and demonstrate the privilege of amorphous RMB cathodes. A mechanism study demonstrates both of molybdenum and sulfur undergo redox reactions and contribute to the capacity. Further optimizations indicate low-temperature synthesis would favor the magnesium storage performance of a-MoS .

摘要

可充电镁电池(RMBs)因其低成本和高可靠性而吸引了研究兴趣,但阴极材料的设计是其发展的主要难点。二价镁阳离子与阴离子存在强烈相互作用,难以嵌入传统的镁嵌入阴极。在此,通过简单的一步溶剂热反应合成了一种非晶态多硫化钼(a-MoS),并将其用作可充电镁电池的阴极材料。a-MoS阴极具有高容量(185 mAh g)和良好的倍率性能(在1000 mA g下为50 mAh g),与结晶态MoS相比有很大优势,证明了非晶态可充电镁电池阴极的优越性。机理研究表明钼和硫都发生了氧化还原反应并对容量有贡献。进一步的优化表明低温合成有利于a-MoS的镁存储性能。

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