Space-Confined Synthesis of Yolk-Shell Structured Co3O4/Nitrogen-Doped Carbon Nanocomposites with Hollow Mesoporous Carbon Nanocages as Advanced Functional Anodes for Lithium-Ion Batteries

被引:37
作者
Lu, Xiaojun [1 ]
Liu, Anran [1 ]
Zhang, Yuanjian [1 ]
Liu, Songqin [1 ]
机构
[1] Southeast Univ, Jiangsu Engn Lab Smart Carbon Rich Mat & Device C, Sch Chem & Chem Engn, Jiangsu Prov Hitech Key Lab Biomed Res, Nanjing 211189, Peoples R China
基金
中国国家自然科学基金;
关键词
metal oxides; nitrogen-doped carbon; carbon nanocages; yolk-shell; space-confined synthesis; lithium-ion batteries;
D O I
10.1021/acsaem.0c02098
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
Despite the high theoretical capacity as the anode material of lithium-ion batteries (LIBs), Co3O4 is subjected to rapid capacity decline and poor rate performance owing to its severe volume expansion and poor electronic conductivity. Herein, a yolk-shell structured Co3O4 nanocomposite with double carbon shells (Co3O4@NC@CNc) was fabricated as an electrode material to improve the properties of LIBs. The Co3O4@NC@CNC was derived from ZIF-67 within carbon nanocages (CNC) by carbonization. The hollow CNC acted as nanoreactors, which could effectively control the growth of ZIF-67 within the CNC and reduce the particle size of Co3O4 @nitrogen-doped carbon (Co3O4 PNC) nanocomposite derived from ZIF-67. When assessed as an LIBs anode material, the optimized Co3O4 @NC@CNC material exhibited outstanding properties with high capacity, superior cycling stability, and rate performance (960 mAh at 0.5 A and 772 mAh g(-1) at 2 A g(-1) after 100 cycles). The electrochemical properties were ascribed to the yolk-shell structure and the synergistic effect of the nanoscale Co3O4@NC and CNC, which improved the electronic conductivity, alleviated the volume expansion effect, shortened the diffusion distance of Li+, and accelerated Li+ transport kinetics. Moreover, the large specific surface and mesoporous structure were beneficial to the diffusion of electrolyte as well as capacitive contribution.
引用
收藏
页码:11153 / 11163
页数:11
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