纳米笼
杂原子
材料科学
阳极
沸石咪唑盐骨架
纳米复合材料
电化学
碳纤维
咪唑酯
化学工程
纳米技术
电极
化学
金属有机骨架
复合材料
有机化学
复合数
吸附
催化作用
工程类
物理化学
戒指(化学)
作者
Yong Zheng,Xuepeng Ni,Kunming Li,Xiaohui Yu,Hui Song,Shan Chen,Niaz Ali Khan,Dong Wang,Chao Zhang
标识
DOI:10.1016/j.coco.2022.101116
摘要
Carbon-based material is one of the most promising candidates of anode materials for sodium-ion batteries (SIBs). However, the poor rate performance and low capacity due to intrinsic nature greatly impact their practical application. Heteroatom-doped carbon material is an efficient method to optimize the electrochemical performance of anode electrodes for SIBs. Herein, we report a template-initiated strategy to fabricate nitrogen, phosphorus, fluorine co-doped hollow carbon nanocages (NPF–HCN) derived from a rationally designed zeolitic imidazolate [email protected] triazine polymer core-shell structured nanocomposites ([email protected]). High proportions of tailored multi-heteroatom species within the CTP network contribute to the in-situ generation of N, P, F-doping in the resultant hollow carbon nanocages. Additionally, the hierarchical porous and hollow nanostructures of the NPF-HCN can promote the penetration of electrolytes, thus reduce diffusion barrier of Na+. As anode materials of SIBs, the as-prepared NPF-HCN delivers a higher initial capacity of 569.6 mA h/g at 1 A/g and a superior cycling behavior with a high capacity of 220.3 mA h/g at 5 A/g after 5000 cycles.
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