Edge-nitrogen enriched carbon nanosheets for potassium-ion battery anodes with an ultrastable cycling stability

被引:57
作者
Chu, Kainian [1 ,2 ]
Zhang, Xiaojuan [1 ,2 ]
Yang, Yang [3 ,4 ]
Li, Zhiqiang [1 ,2 ]
Wei, Lingzhi [1 ,2 ]
Yao, Ge [1 ,2 ]
Zheng, Fangcai [1 ,2 ]
Chen, Qianwang [1 ,2 ,3 ,4 ]
机构
[1] Anhui Univ, Inst Phys Sci & Informat Technol, Hefei 230601, Peoples R China
[2] Anhui Univ, Lab Struct & Funct Regulat Hybrid Mat, Minist Educ, Hefei 230601, Peoples R China
[3] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
[4] Univ Sci & Technol China, Dept Mat Sci & Engn, Hefei 230026, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Nitrogen doping; Carbon; Porous structures; Anode materials; Potassium ion battery; DOPED POROUS CARBON; HOLLOW CARBON; CAPACITY; SODIUM;
D O I
10.1016/j.carbon.2021.08.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Edge-nitrogen (pyridinic/pyrrolic nitrogen) doped carbon materials have been considered as promising anodes for potassium ion batteries (KIBs), which can provide a high surface-induced capacitive capacity beyond the K+-intercalated mechanism. However, achieving a high-level edge-nitrogen doping is still a great challenge owning to inevitable introduction of graphitic nitrogen into carbon materials via conventional pyrolysis process. Herein, we design porous carbon nanosheets with bundant defects and edge sites to graft nitrogen atoms to achieve a high-level edge-nitrogen doping (88.36%). The optimized edge nitrogen doped carbon nanosheets (ENCNs-60 0) exhibits a high reversible capacity of 443 mAh g(-1) at 0.1 A g(-1) after 200 cycles, excellent rate performance (175 mAh g(-1) at 20 A g(-1)), and ultrastable cycling stability (246 mAh g(-1) at 5 A g(-1) over 10,000 cycles). Density functional theory calculations and kinetic studies confirm that both edge-nitrogen doping and explanded interlayer distance are greatly conducive for the adsorption and diffusion of K+ , thereby ensuring enhanced potassium-storage performance with a synergistic adsorption-intercalation mechanism. (C) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页码:277 / 286
页数:10
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