材料科学
钨
硫化物
离子
冶金
纳米技术
化学工程
工程物理
有机化学
工程类
化学
作者
Jiarui Zhang,Hang He,Ruihang Wen,Jian-Cheng Jin,Kun Luo
标识
DOI:10.1002/adfm.202503917
摘要
Abstract Magnesium ion batteries (MIBs) receive concentrated attention owing to their high intrinsic advantages such as theoretical volumetric energy densities. However, poor cycling performances and low‐temperature electrochemical properties remain major technical issues in MIBs. Electrode materials impose a great influence on the electrochemical characteristics of MIBs. 2D transition metal dichalcogenides (TMDs) are potentially excellent electrode materials for MIBs on account of their open framework and outstanding electrochemical characteristics. In this work, the pre‐intercalation modification strategy is adopted to design the K + pre‐intercalated WS 2 material as the electrode material of MIBs. Structural characterizations and density functional theory (DFT) calculations demonstrate that the Mg 2+ diffusion barrier in the K + pre‐intercalated WS 2 is effectively lowered accompanied by the interlayer expansion in the layered structure, aiding quick ion diffusion and reliable Mg 2+ ion storage. Consequently, the K‐WS 2 electrode demonstrates excellent electrochemical performances, a reversible capacity of 217 mA h g −1 at 0.2 A g −1 with outstanding cycling stability. In addition, the K‐WS 2 electrode is capable of running smoothly at low temperatures, showing superior capacity preservation of 97% upon completion of 1000 cycles at −30 °C. This work supplies an uplifting means to the modification and optimization of cutting‐edge electrode materials for MIBs.
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