Nitrogen and fluorine co-doped graphene as a high-performance anode material for lithium-ion batteries

被引:171
|
作者
Huang, Shizheng
Li, Yu
Feng, Yiyu
An, Haoran
Long, Peng
Qin, Chengqun
Feng, Wei [1 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
EXFOLIATED GRAPHITE OXIDE; OXYGEN REDUCTION REACTION; LI-ION; HIGH-CAPACITY; ELECTROCHEMICAL PROPERTIES; ELECTRODE MATERIALS; CHEMICAL-REDUCTION; CARBON NANOTUBES; NATURAL GRAPHITE; DOPING AGENTS;
D O I
10.1039/c5ta06012e
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
Nitrogen and fluorine co-doped graphene (NFG) with the N and F content as high as 3.24 and 10.9 at% respectively was prepared through the hydrothermal reaction of trimethylamine tri(hydrofluoride) [(C2H5)(3)N center dot 3HF] and aqueous-dispersed graphene oxide (GO) as the anode material for lithium ion batteries (LIBs). The N and F co-doping in graphene increased the disorder and defects of the framework, enlarged the space of the interlayer, wrinkled the nanosheets with many open-edge sites, and thus facilitated Li ion diffusion through the electrode compared with sole-N or F doped graphene. X-ray photoelectron spectroscopy (XPS) analysis of NFG demonstrated the presence of active pyridine and pyrrolic type N, and highly electrically conductive graphitic N and the semi-ionic C-F bond in the structure. The N and F doping content and the component types of N and F functional groups could be controlled by the hydrothermal temperature. The NFG prepared at 150 degrees C exhibited the best electrochemical performances when tested as the anode for LIBs, including the high coulombic efficiency in the first cycle (56.7%), superior reversible specific discharge capacity (1075 mA h g(-1) at 100 mA g(-1)), excellent rate capabilities (305 mA h g(-1) at 5 A g(-1)), and outstanding cycling stability (capacity retention of similar to 95% at 5 A g(-1) after 2000 cycles), which demonstrated that NFG was a promising candidate for anode materials of high-rate LIBs.
引用
收藏
页码:23095 / 23105
页数:11
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