One-step synthesis of graphene nanoribbon-MnO2 hybrids and their all-solid-state asymmetric supercapacitors

被引:182
作者
Liu, Mingkai [1 ]
Tjiu, Weng Weei [2 ]
Pan, Jisheng [2 ]
Zhang, Chao [1 ]
Gao, Wei [1 ]
Liu, Tianxi [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, Adv Mat Lab, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[2] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
基金
中国国家自然科学基金;
关键词
PERFORMANCE ELECTROCHEMICAL CAPACITORS; SENSITIZED SOLAR-CELLS; CARBON NANOTUBE CARPET; ENERGY DENSITY; MANGANESE-DIOXIDE; POWER-DENSITY; SURFACE-AREA; SP(2) CARBON; MNO2; ELECTRODES;
D O I
10.1039/c3nr06650a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three-dimensional (3D) hierarchical hybrid nanomaterials (GNR-MnO2) of graphene nanoribbons (GNR) and MnO2 nanoparticles have been prepared via a one-step method. GNR, with unique features such as high aspect ratio and plane integrity, has been obtained by longitudinal unzipping of multi-walled carbon nanotubes (CNTs). By tuning the amount of oxidant used, different mass loadings of MnO2 nanoparticles have been uniformly deposited on the surface of GNRs. Asymmetric supercapacitors have been fabricated with the GNR-MnO2 hybrid as the positive electrode and GNR sheets as the negative electrode. Due to the desirable porous structure, excellent electrical conductivity, as well as high rate capability and specific capacitances of both the GNR and GNR-MnO2 hybrid, the optimized GNR//GNR-MnO2 asymmetric supercapacitor can be cycled reversibly in an enlarged potential window of 0-2.0 V. In addition, the fabricated GNR//GNR-MnO2 asymmetric supercapacitor exhibits a significantly enhanced maximum energy density of 29.4 W h kg(-1) (at a power density of 12.1 kW kg(-1)), compared with that of the symmetric cells based on GNR-MnO2 hybrids or GNR sheets. This greatly enhanced energy storage ability and high rate capability can be attributed to the homogeneous dispersion and excellent pseudocapacitive performance of MnO2 nanoparticles and the high electrical conductivity of the GNRs.
引用
收藏
页码:4233 / 4242
页数:10
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