法拉第效率
材料科学
碳纤维
阳极
多孔性
化学工程
储能
超级电容器
电极
多孔介质
纳米技术
沉积(地质)
原子层沉积
钠
X射线光电子能谱
电容
能量转换
锂离子电池的纳米结构
作者
Y. Zhang,Biao Zheng,Qingfeng Fu,Yan Duan,Aiping Hu,Wenbin Zhong,Jilei Liu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-02-14
卷期号:26 (7): 2761-2768
被引量:1
标识
DOI:10.1021/acs.nanolett.5c06425
摘要
Porous carbon (PC) is widely used in energy storage devices such as supercapacitors due to its high surface area and abundant ion-accessible pores. However, its excessive open porosity in sodium-ion batteries (SIBs) leads to severe side reactions and low initial Coulombic efficiency. Regulating pore structures to transform PC into hard carbon (HC) with rich closed-pores is essential for improving sodium storage performance. Here, we report a direct microstructural conversion of PC into high-performance HC anodes for SIBs via the upcycling of polytetrafluoroethylene (PTFE) waste. Assisted by Brønsted-basic NH 3, the ultrastrong C–F bonds in PTFE are efficiently cleaved, inducing in situ carbon deposition that transforms open pores into a closed-pore structure with curved graphitic domains. The optimized YPT-1200 electrode achieves a high reversible capacity of 370.3 mAh g –1 with satisfactory initial Coulombic efficiency of 78.0% as well as impressive cycling stability (83.4% capacity retention over 300 cycles at 0.5C).
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