Rashad Muhammad, Ngoipala Apinya, Vandichel Matthias, Geaney Hugh
Department of Chemical Sciences and Bernal Institute, University of Limerick, Limerick V94 T9PX, Ireland.
ACS Appl Mater Interfaces. 2024 Oct 5;16(41):55383-94. doi: 10.1021/acsami.4c11272.
Magnesium-ion batteries (MIBs) are a "beyond Li-ion" technology that are hampered by Mg metal reactivity, which motivates the development of anode materials such as tin (Sn) with high theoretical capacity (903 mAh g). However, pure Sn is inactive for Mg storage. Herein, Mg alloying with Sn is enabled within dual-phase Bi-Sn anodes, where the optimal composition (BiSn) outperformed single-phase Bi and Sn electrodes to deliver high specific capacity (462 mAh g at 100 mA g), good cycle life (84% after 200 cycles), and significantly improved rate capability (403 mAh g at 1000 mA g). Density functional theory (DFT) calculations revealed that Mg alloys first with Bi and the subsequent formation of the MgBi//Sn interfaces is energetically more favorable compared to the individual MgBi and Sn phases. Mg insertion into Sn is facilitated when MgBi is present. Moreover, dealloying Mg from MgBi:MgSn systems requires the creation of Mg vacancies and subsequent Mg diffusion. Mg vacancy creation is easier for MgSn compared to MgBi, while the latter has slightly lower activated Mg-diffusion pathways. The computational findings point toward easier magnesiation/demagnesiation for BiSn alloys over pure Bi or pure Sn, corroborating the superior Mg storage performance of Bi-Sn electrodes over the corresponding single-phase electrodes.
镁离子电池(MIBs)是一种“超越锂离子”的技术,但其受到镁金属反应活性的阻碍,这推动了诸如具有高理论容量(903 mAh g)的锡(Sn)等负极材料的开发。然而,纯锡对镁存储不活跃。在此,在双相Bi-Sn负极中实现了镁与锡的合金化,其中最佳组成(BiSn)的性能优于单相Bi和Sn电极,可提供高比容量(100 mA g时为462 mAh g)、良好的循环寿命(200次循环后为84%)以及显著改善的倍率性能(1000 mA g时为403 mAh g)。密度泛函理论(DFT)计算表明,与单独的MgBi和Sn相相比,镁首先与Bi合金化,随后形成MgBi//Sn界面在能量上更有利。当存在MgBi时,镁插入锡更容易。此外,从MgBi:MgSn体系中脱合金化镁需要产生镁空位并随后进行镁扩散。与MgBi相比,MgSn产生镁空位更容易,而后者具有略低的活化镁扩散途径。计算结果表明,BiSn合金比纯Bi或纯Sn更容易进行镁化/脱镁,这证实了Bi-Sn电极在镁存储性能上优于相应的单相电极。