Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, College Park, Maryland 20740, USA.
Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China.
Nat Commun. 2017 Jan 10;8:14083. doi: 10.1038/ncomms14083.
Rechargeable magnesium batteries have attracted considerable attention because of their potential high energy density and low cost. However, their development has been severely hindered because of the lack of appropriate cathode materials. Here we report a rechargeable magnesium/iodine battery, in which the soluble iodine reacts with Mg to form a soluble intermediate and then an insoluble final product magnesium iodide. The liquid-solid two-phase reaction pathway circumvents solid-state Mg diffusion and ensures a large interfacial reaction area, leading to fast reaction kinetics and high reaction reversibility. As a result, the rechargeable magnesium/iodine battery shows a better rate capability (180 mAh g at 0.5 C and 140 mAh g at 1 C) and a higher energy density (∼400 Wh kg) than all other reported rechargeable magnesium batteries using intercalation cathodes. This study demonstrates that the liquid-solid two-phase reaction mechanism is promising in addressing the kinetic limitation of rechargeable magnesium batteries.
可充电镁电池因其潜在的高能量密度和低成本而受到广泛关注。然而,由于缺乏合适的阴极材料,其发展受到了严重阻碍。在这里,我们报告了一种可充电镁/碘电池,其中可溶性碘与 Mg 反应生成可溶性中间产物,然后生成不溶性最终产物碘化镁。液-固两相反应途径绕过了固态 Mg 扩散,确保了较大的界面反应面积,从而实现了快速的反应动力学和高的反应可逆性。因此,与所有其他使用插层阴极的报道的可充电镁电池相比,可充电镁/碘电池具有更好的倍率性能(在 0.5 C 时为 180 mAh g-1,在 1 C 时为 140 mAh g-1)和更高的能量密度(约 400 Wh kg-1)。本研究表明,液-固两相反应机制在解决可充电镁电池的动力学限制方面具有广阔的应用前景。