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2D lamellar structured Bi Sb1-@NC toward cycle-stable lithium/sodium-ion storage with high-capacity

阳极 材料科学 合金 碳纤维 锂(药物) 电化学 插层(化学) 层状结构 化学工程 储能 纳米技术 电极 纳米颗粒 电池(电) 兴奋剂 法拉第效率 钠离子电池 锂离子电池 复合数 氧化还原
作者
Faxiu Zhang,Jing Xie,Xinhui Liu,Zhenjiang Lu,Jindou Hu,Yali Cao
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:137: 118512-118512
标识
DOI:10.1016/j.est.2025.118512
摘要

The structural instability and capacity limitations of bismuth (Bi) and antimony (Sb) pose significant challenges for their implementation in Li + /Na + energy storage systems. Therefore, designing two-dimensional (2D) Bi and Sb alloy materials with a specialized structure serves as an efficacious method for addressing their defects. In this work, we successfully synthesized a BiSb binary alloy nanoparticles in 2D N-doped carbon nanosheets with controlled ratios via thermal-drying and pyrolysis. Notably, outstanding performance is demonstrated by the Bi 0.5 Sb 0.5 @NC anode, showing both high capacity and exceptional cycling stability during Li + and Na + intercalation processes. In lithium-ion batteries (LIBs), the Bi 0.5 Sb 0.5 @NC anode specifically reaches a capacity of 570 mAh g −1 after 300 cycles at 0.5 A g −1 and exhibits exceptional cycling stability, maintaining 430 mAh g −1 after 1000 cycles at 3 A g −1 . Comparable performance is also shown in sodium-ion batteries (SIBs), which maintains 345.3 mAh g −1 after 500 cycles at 3 A g −1 . The proposed strategy, which integrates binary alloy with nitrogen-enriched carbon matrix, demonstrates promising viability for implementing alloy-type anodes in both LIBs and SIBs. This architectural design effectively addresses challenges associated with alloy-based electrodes while enhancing electrochemical performance. • Structurally stable 2D Bi x Sb 1 -x @NC nanosheets anode with controlled ratios are successfully prepared. • The Bi 0.5 Sb 0.5 @NC anode exhibits exceptional lithium and sodium storage performance. • The alloy strategy and nitrogen doping in carbon co-improving sodium ion storage performance.
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