微观结构
锂(药物)
锡
材料科学
兴奋剂
球体
碳纤维
离子
化学工程
纳米技术
复合材料
冶金
光电子学
化学
复合数
心理学
物理
有机化学
工程类
精神科
天文
作者
Yali Yang,Tianyu Li,Ning Sun,Bin Xu,Reiner Anwander,Yucang Liang
标识
DOI:10.1021/acsaem.5c01612
摘要
To enhance the Li storage capacity in carbon materials, incorporation of Sn into the carbon matrix fabricates Sn@C composites for lithium-ion batteries (LIBs). Due to the trade-off between the Sn content and particle size, high capacity and long-term stability cannot simultaneously be achieved in LIBs. Meanwhile, which factor holds importance and at what stage to influence the performance have remained unanswered due to the challenges of achieving a well-controlled morphology and Sn distribution. Herein, a multistep strategy using functional polymer-mediated Sn loading, layer encapsulation, and carbonization was utilized to embed Sn into N-doped hollow carbon spheres for affording Sn-content- and particle-size-tunable Sn@h-NCs. Adjusting the SnCl2 addition can fine-tune the Sn content up to 27.1 wt %, while Sn aggregation causes structure transformation from hollow to yolk–shell configurations. When employed as anodes for LIBs, Sn@h-NCs exhibit a high initial discharge capacity of 1314 mAh g–1 at 30 mA g–1, along with a superior cycling-stability, maintaining 705 mAh g–1 at 0.5 A g–1 after 150 cycles, much higher than the performance of NCs. However, aggregation-induced increase in Sn particle size results in elevated overpotential and resistance, suggesting that higher Sn-content Sn@h-NCs deliver superior capacity at a lower current density, while Sn@h-NCs with a lower content offer comparable capacity but improved stability at a higher current density.
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