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Copper sulfide nanoparticles as high-performance cathode materials for Mg-ion batteries

机译:硫化铜纳米颗粒作为Mg离子电池的高性能正极材料

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摘要

Rechargeable magnesium batteries are appealing as safe, low-cost systems with high-energy-density storage that employ predominantly dendrite-free magnesium metal as the anode. While significant progress has been achieved with magnesium electrolytes in recent years, the further development of Mg-ion batteries, however, is inherently limited by the lack of suitable cathode materials, mainly due to the slow diffusion of high-charge-density Mg-ions in the intercalation-type host structures and kinetic limitations of conversion-type cathodes that often causes poor cyclic stability. Nanostructuring the cathode materials offers an effective means of mitigating these challenges, due to the reduced diffusion length and higher surface areas. In this context, we present the highly reversible insertion of Mg-ions into nanostructured conversion-type CuS cathode, delivering high capacities of 300 mAh g−1 at room temperature and high cyclic stability over 200 cycles at a current density of 0.1 A g−1 with a high coulombic efficiency of 99.9%. These materials clearly outperform bulk CuS, which is electrochemically active only at an elevated temperature of 50 °C. Our results not only point to the important role of nanomaterials in the enhancement of the kinetics of conversion reactions but also suggest that nanostructuring should be used as an integral tool in the exploration of new cathodes for multivalent, i.e., (Mg, Ca, Al)-ion batteries.
机译:可充电镁电池作为安全,低成本,具有高能量密度存储的系统而吸引人,该系统主要使用无枝晶的镁金属作为阳极。尽管近年来镁电解质已取得了重大进展,但镁离子电池的进一步发展因缺乏合适的阴极材料而受到固有的限制,这主要是由于高电荷密度镁离子的缓慢扩散插层型主体结构中的自由基和转化型阴极的动力学局限性通常会导致较差的循环稳定性。由于减小了扩散长度和增加了表面积,对阴极材料进行纳米结构化提供了缓解这些挑战的有效方法。在此背景下,我们展示了Mg离子高度可逆地插入纳米结构转化型CuS阴极中的能力,在室温下可提供300 mAh g -1 的高容量,并且在200次循环中可提供高循环稳定性。电流密度为0.1 A g -1 ,库仑效率高达99.9%。这些材料明显优于块状CuS,后者仅在50 C的高温下才具有电化学活性。我们的研究结果不仅指出了纳米材料在增强转化反应动力学方面的重要作用,而且还表明,纳米结构应作为探索多价新阴极(例如,Mg,Ca,Al)的不可或缺的工具。离子电池。

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