Free-standing macro-porous nitrogen doped graphene film for high energy density supercapacitor

被引:34
作者
Jin, Yanan [1 ,2 ]
Meng, Yuena [1 ]
Fan, Wei [2 ]
Lu, Hengyi [2 ]
Liu, Tianxi [2 ]
Wu, Sixin [1 ]
机构
[1] Henan Univ, Natl & Local Joint Engn Res Ctr High Efficiency D, Collaborat Innovat Ctr Nano Funct Mat & Applicat, Sch Mat & Engn,Minist Educ,Key Lab Special Funct, Kaifeng, Peoples R China
[2] Donghua Univ, State Key Lab Modificat Chem Fibers & Polymer Mat, Coll Mat Sci & Engn, 2999 North Renmin Rd, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Graphene aerogel film; Supercapacitors; N-doped carbon material; Free-standing; HIGH-PERFORMANCE; ASYMMETRIC SUPERCAPACITOR; NANOSTRUCTURED MATERIALS; ELECTRODE MATERIAL; CARBON MATERIALS; POLYPYRROLE; ACTIVATION; COMPOSITE; CAPACITANCE; NANOSHEETS;
D O I
10.1016/j.electacta.2019.06.107
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this paper, a porous free-standing nitrogen-doped graphene (NG) film for high energy density supercapacitor is prepared via a facile hydrogel strategy. Taking advantage of the hydrogel behavior together with the mechanical stability of GO sheets, an interconnected macro-porous nitrogen-doped free-standing film is constructed. The nitrogen doping structure ensures sufficient pseudocapacitance and conductivity of the film, while the macro-porous structure favors fast ion adsorption. When assembled in a symmetric two-electrode supercapacitor, not any conductive agent or binder is used. The free-standing NG film shows specific capacitance of 455.4 F g(-1) based on the mass of whole electrode, while no capacitance loss after 5000 cycles. Furthermore, an asymmetric supercapacitor is assembled with this NG film as negative electrode and a macro-porous graphene/polypyrrole composite film synthesized using the similar strategy as positive electrode. An energy density of 34.51 Wh kg(-1) at a power density of 849.77 W kg(-1) is obtained, suggesting great potential of this film for application in energy storage field. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:865 / 874
页数:10
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