School of Materials and Energy , Guangdong University of Technology , Guangzhou 510006 , China.
School of Materials Science and Energy Engineering , Foshan University , Foshan 528000 , P. R. China.
ACS Appl Mater Interfaces. 2019 Sep 25;11(38):35050-35059. doi: 10.1021/acsami.9b14287. Epub 2019 Sep 12.
A yolk-double shell cube-like SnS@N-S codoped carbon (YDSC-SnS@NSC) was delicately tailored by a self-templated and selective etching method as well as a self-assembly strategy. Herein, the ZnSn(OH) (ZHS) solid nanocubes were used as templates for the formation of a thin carbon shell that encapsulated the active material, thereby preventing the aggregation and maintaining the uniformity. ZHS is then converted into an intermediate ZnS-SnS hybrid by a facile thermal sulfidation process. Because SnS is insoluble in acidic condition, it is easy to create a yolk-shell architecture by selectively removing the ZnS component. Further heat treatment promoted the melting of SnS and resulted in the decomposition of SnS into SnS, which is simultaneously accompanied with a heat- and capillary-driven self-assembly to form a SnS inner core and SnS/C double shell. Such nanostructures with an inner void space and robust double shells are useful in buffering the volume expansion of SnS during lithiation and sodiation. Furthermore, N and S atoms doped into the carbon shell can enhance the electrical conductivity, which is beneficial to the fast charge-transfer kinetics. Because of these advantages, YDSC-SnS@NSC as the anode for Li-ion batteries exhibits improved electrochemical properties. Especially, the YDSC-SnS@NSC anode for Na-ion batteries shows an outstanding rate capability of 257 mA h g at 8 A g and an ultrastable long-term cyclic performance at a current density of 1 A g with a capacity retention of 83.5% (340 mA h g at the first cycle and ultimately reached 284 mA h g) and only 0.012% capacity decay per cycle for over 1500 cycles. Such superior electrochemical performance demonstrated that this rationally designed anode is promising for application in both Li- and Na-ion storages.
采用自模板和选择性刻蚀方法以及自组装策略,巧妙地制备了蛋黄-双壳立方状 SnS@N-S 共掺杂碳 (YDSC-SnS@NSC)。在此,ZnSn(OH)(ZHS)固体纳米立方用作形成薄碳壳的模板,该碳壳封装了活性材料,从而防止了聚集并保持了均匀性。然后,通过简便的热硫化过程将 ZHS 转化为中间的 ZnS-SnS 杂化物。由于 SnS 不溶于酸性条件,因此通过选择性去除 ZnS 组分很容易制造出蛋黄壳结构。进一步的热处理促进了 SnS 的熔化,并导致 SnS 分解为 SnS,同时伴随着热和毛细驱动力的自组装,形成 SnS 内核和 SnS/C 双壳。这种具有内部空隙和坚固双壳的纳米结构有助于缓冲 SnS 在锂化和钠化过程中的体积膨胀。此外,掺杂到碳壳中的 N 和 S 原子可以提高电导率,有利于快速的电荷转移动力学。由于这些优势,作为锂离子电池的阳极,YDSC-SnS@NSC 表现出改进的电化学性能。特别是,作为钠离子电池的 YDSC-SnS@NSC 阳极具有出色的倍率性能,在 8 A g 时为 257 mA h g,在 1 A g 的电流密度下具有超稳定的长期循环性能,容量保持率为 83.5%(首次循环时为 340 mA h g,最终达到 284 mA h g),并且在 1500 次循环以上的循环中,容量衰减率仅为 0.012%/循环。这种卓越的电化学性能表明,这种合理设计的阳极在锂离子和钠离子存储中具有广阔的应用前景。