Synthesis of three-dimensional honeycomb-like Fe3N@NC composites with enhanced lithium storage properties

被引:0
|
作者
Liu, Shenghong [1 ]
Zheng, Wenrui [1 ]
Xie, Wenhe [1 ]
Cui, Hong [1 ]
Li, Ya [1 ]
Zhang, Chao [1 ]
Ji, Zhichao [1 ]
Liu, Fuwei [1 ]
Chen, Rui [1 ]
Sun, Haibin [1 ]
Xu, Jiantie [2 ]
机构
[1] Xinyang Normal Univ, Dept Phys & Elect Engn, Key Lab Microelect & Energy Henan Prov, Xinyang 464000, Peoples R China
[2] South China Univ Technol, Sch Environm & Energy, Guangdong Prov Key Lab Atmospher Environm & Pollut, Natl Engn Lab VOCs Pollut Control Technol & Equipm, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
Iron nitrides; Nitrogen doping; Pore structure; Lithium ion batteries;
D O I
暂无
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
Iron nitrides have been recognized as attractive anode candidates for lithium ion batteries (LIBs) due to their high theoretical capacities, high tap densities, cost-effectiveness, multiple electron transfer and good ionic diffusion. The strategies of pore structure engineering and carbon coating have been proven to be effective ways to address the critical issues of iron nitrides as anodes for LIBs. Herein, we synthesized a series of Fe3N@NC-x with 3D honeycomb nanostructures by a simple heating-controlled and ammoniation-assisted approach. The Fe3N@NC-x as anodes for LIBs display outstanding lithium storage properties with high reversible capacity of 767.8 mA h g(-1) at 0.1 A g(-1) and long-term cycling performance (814.5 mA h g(-1) at 1 A g(-1) over 2000 cycles). Such outstanding properties were attributed to the interconnected conductive pathways (honeycomb walls, hexagonal channels) for rapid ionic/electronic transport, the macro-/meso porous structure for the quick penetration of electrolytes and the accommodation of electrode volume variation during the cycles, meso-/micro porous structure for the additional storage of Lit, and efficient utilization of the Fe3N nanoparticles unifomly distributed through highly conductive interconnected network.(C) 2022 Elsevier Ltd. All rights reserved.
引用
收藏
页码:162 / 169
页数:8
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