Chemical Grafting-derived N, P Co-doped Hollow Microporous Carbon Spheres for High-Performance Sodium-ion Battery Anodes

被引:49
作者
Wang, Haijun [1 ]
Lan, Jin-Le [1 ]
Yuan, Haocheng [1 ]
Luo, Shicheng [1 ]
Huang, Yiqian [1 ]
Yu, Yunhua [1 ]
Cai, Qing [1 ]
Yang, Xiaoping [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Mat Sci & Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Chemical grafting; N; P co-doping; Porous carbon; DFT calculations; Sodium-ion battery; POROUS CARBON; HARD CARBON; LITHIUM-ION; NITROGEN; PHOSPHORUS; GRAPHENE; NANOSHEETS; STORAGE; ELECTRODE; CAPACITY;
D O I
10.1016/j.apsusc.2020.146221
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
Microstructure design combined with high-level heteroatoms doping has been considered the leading approach for preparing the high-performance carbon anodes for sodium-ion batteries (SIBs). Herein, a hollow porous carbon sphere (NP-HPCS) that exhibits a high N, P co-doping level (6.05 at% for N, 5.19 at% for P) and a large microporous specific area (339 m(2 )g(-1)) is reported. The microporous and N, P co-doping synergistic construction of the NP-HPCS was achieved by a high-efficiency chemical grafting of hexachlorocyclotriphosphazene (HCCP) onto polydopamine (PDA) shell, accompanied by the in situ micellar transformation of pore-forming agent F127 in the grafting process. The as-prepared NP-HPCS used as an anode for SIBs delivers a superior rate capacity (similar to 101 mAh g(-1) at 20 A g(-1)) and an excellent long cycle performance (similar to 120 mAh g(-1) after 5000 cycles at 5 A g(-1)). The kinetics analysis and density functional theory (DFT) calculations were carried out to further analyze the superior sodium storage performance of NP-HPCS. Our work suggests an effective way to develop high-performance carbon anode materials for SIBs.
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页数:9
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