阳极
材料科学
动力学
电化学
化学工程
纳米颗粒
纳米技术
电极
化学
物理化学
量子力学
物理
工程类
作者
Bo Yan,Lichen Lin,Hao Sun,Tiantian Zhang,Changqing Xu,Chang Q. Sun,Lulu Zhang,Xuelin Yang
标识
DOI:10.1016/j.cej.2023.146950
摘要
Overcoming the sluggish reaction kinetics and volume effects of metal sulfides as anodic materials for sodium-ion batteries remains a challenging task. In this study, a multistep template-engaged strategy is employed for the first time to fabricate hierarchical double-shells NiS/SnS@nitrogen doped carbon (NiS/SnS@NC) nanoboxes, utilizing NiSn(OH)6 cubes as starting templates. The synergistic combination of sophisticated sulfide components and the double-shell structure effectively mitigates volume variation, reduces nanoparticle cohesion, and enhances electrode reaction kinetics. Notably, NiS/SnS@NC exhibits outstanding stability under high current density while maintaining a high capacity. Comprehensive kinetics analysis reveals that the enhanced sodium storage of NiS/SnS@NC can be attributed to its low interface reaction resistance, significant capacitive contribution, and rapid mass-transfer kinetics. The stepwise (de)sodiation processes of the NiS/SnS@NC anode are elucidated through various in/ex-situ characterization techniques, confirming the alternating reaction activity alternations between two components, which acts as a self-buffering and self-conductivity mechanism to enhance sodium storage. Finally, a practical application is demonstrated, where a well-designed NiS/SnS@NC||Na3V2(PO4)2F3/C full cell shows promising performance, achieving a high capacity of 265 mAh/g after 1000 cycles at 2.0 A/g. This work′s synthesis strategy and research findings contribute to advancing the exploration and application of NiSn(OH)6 and its derivatives in the field of energy storage and beyond.
科研通智能强力驱动
Strongly Powered by AbleSci AI