Scalable, large-area synthesis of heteroatom-doped few-layer graphene-like microporous carbon nanosheets from biomass for high-capacitance supercapacitors

被引:89
作者
Gopalakrishnan, Arthi [1 ]
Kong, Chang Yi [2 ,3 ]
Badhulika, Sushmee [1 ]
机构
[1] Indian Inst Technol Hyderabad, Dept Elect Engn, Hyderabad 502285, India
[2] Shizuoka Univ, Grad Sch Integrated Sci & Technol, Hamamatsu, Shizuoka 4328561, Japan
[3] Shizuoka Univ, Res Inst Green Sci & Technol, Hamamatsu, Shizuoka 4328561, Japan
关键词
ACTIVATED CARBON; SELF-ACTIVATION; POROUS CARBON; GINGER; PYROLYSIS; ELECTRODE; LEAVES;
D O I
10.1039/c8nj05128c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
High-capacitance electrochemical supercapacitors are promising devices due to their long-term stability and simple device construction. Unlike available reports on biomass-derived carbon as supercapacitor electrodes, in this paper, we report novel few-layer graphene-like microporous carbon nanosheets obtained from a single biomass precursor, which yield very high specific capacitance. A simple, ultra-low cost, one-step activation-free approach yields few-layer graphene-like microporous carbon nanosheets in the presence of heteroatoms by using ginger root as a biomass precursor. Suitable heteroatom content combined with porous graphene-like carbon nanosheet structure enhances the specific capacitance. The as-prepared carbon nanosheets from ginger roots possessing few-layer graphene-like structures are confirmed by X-ray diffraction and transmission electron microscopy, and the presence of few heteroatoms is confirmed by energy dispersive spectroscopy. The electrochemical measurements reveal that the ginger root-derived carbon electrode exhibits very high specific capacitance of 390 F g(-1) at 1 A g(-1) of current density. The ginger-derived carbon electrode also has 93.3% capacitance retention until 3500 charge/discharge cycles. This approach indicates great potential to achieve sustainable, low-cost, simple and large-scale production of renewable biomass-derived carbon materials for efficient energy storage applications in the future.
引用
收藏
页码:1186 / 1194
页数:9
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