Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), School of Materials Science and Engineering , Shandong University , Jingshi Road 17923 , Jinan 250061 , PR China.
School of Applied Physics and Materials , Wuyi University , 22 Dongcheng Village , Jiangmen 529020 , PR China.
ACS Nano. 2018 Apr 24;12(4):3568-3577. doi: 10.1021/acsnano.8b00643. Epub 2018 Apr 5.
Metal-based anodes have recently aroused much attention in sodium ion batteries (SIBs) owing to their high theoretical capacities and low sodiation potentials. However, their progresses are prevented by the inferior cycling performance caused by severe volumetric change and pulverization during the (de)sodiation process. To address this issue, herein an alloying strategy was proposed and nanoporous bismuth (Bi)-antimony (Sb) alloys were fabricated by dealloying of ternary Mg-based precursors. As an anode for SIBs, the nanoporous BiSb alloy exhibits an ultralong cycling performance (10 000 cycles) at 1 A/g corresponding to a capacity decay of merely 0.0072% per cycle, due to the porous structure, alloying effect and proper Bi/Sb atomic ratio. More importantly, a (de)sodiation mechanism ((Bi,Sb) ↔ Na(Bi,Sb) ↔ Na(Bi,Sb)) is identified for the discharge/charge processes of Bi-Sb alloys by using operando X-ray diffraction and density functional theory calculations.
基于金属的阳极由于其高的理论容量和低的钠化电势,最近在钠离子电池(SIBs)中引起了广泛关注。然而,由于在(去)钠化过程中严重的体积变化和粉碎,它们的循环性能较差,阻碍了它们的发展。为了解决这个问题,本文提出了一种合金化策略,并通过三元 Mg 基前体的脱合金化制备了纳米多孔铋(Bi)-锑(Sb)合金。作为 SIBs 的阳极,纳米多孔 BiSb 合金在 1 A/g 下表现出超长的循环性能(10000 次循环),每循环的容量衰减仅为 0.0072%,这归因于多孔结构、合金化效应和适当的 Bi/Sb 原子比。更重要的是,通过原位 X 射线衍射和密度泛函理论计算,确定了 Bi-Sb 合金在放电/充电过程中的脱钠/钠化机制((Bi,Sb)↔Na(Bi,Sb)↔Na(Bi,Sb))。