Synthesis of Aminopyrene-tetraone-Modified Reduced Graphene Oxide as an Electrode Material for High-Performance Supercapacitors

被引:52
|
作者
Shi, Jianqiao [1 ]
Zhao, Zhipeng [1 ]
Wu, Jichuang [1 ]
Yu, Yibo [1 ]
Peng, Zhikun [1 ,2 ]
Li, Baojun [1 ]
Liu, Yushan [1 ]
Kang, Hongwei [3 ]
Liu, Zhongyi [1 ,4 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, 100 Kexue Ave, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Sch Chem Engn & Energy, 100 Kexue Ave, Zhengzhou 450001, Henan, Peoples R China
[3] Huanghe Sci & Technol Coll, Inst Nanostruct Funct Mat, Henan Prov Key Lab Nanocomposite & Applicat, Zhengzhou 450006, Henan, Peoples R China
[4] Henan Key Lab Green Catalyt Hydrogenat, Zhengzhou 450001, Henan, Peoples R China
来源
关键词
Asymmetric supercapacitor; Reduced graphene oxide; PYT-NH2/rGO; Pyrene-tetraone; NITROGEN-DOPED GRAPHENE; LITHIUM-ION BATTERIES; ONE-STEP SYNTHESIS; FUNCTIONALIZED GRAPHENE; GRAPHITE OXIDE; CARBON; NANOPARTICLES; REDUCTION; COMPOSITE; EFFICIENT;
D O I
10.1021/acssuschemeng.7b03814
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we successfully anchored 2-aminopyrene-3,4,9,10-tetraone (PYT-NH2), a small organic molecule, onto graphene oxide (GO) and then further chemically reduced it to obtain PYT-NH2/reduced graphene oxide (rGO). We observed that, as an electrode material for high-performance supercapacitor application, PYT-NH2/rGO exhibited higher capability and smaller charge transfer resistance in comparison with PYT-NH2/GO, rGO, and PYT-NH2. The specific capacitances were measured as 326.6 and 229.2 F g(-1) for PYT-NH2/rGO and PYT-NH2/GO, respectively, at a current density of 0.5 A g(-1) in 1 M sulfuric acid (H2SO4) electrolyte. In addition, we obtained the capacitance of 77.2 F g(-1) for PYT-NH2/rGO//activated carbon (AC) at 0.5 A g(-1) with an energy density of 15.4 W h kg(-1). Moreover, for the fabricated hybrid capacitor, the capacitance retention of 25 000 cycles was nearly 100% at 5 A g(-1), thus manifesting excellent electrochemical stability and signaling promising potential in energy storage applications.
引用
收藏
页码:4729 / 4738
页数:19
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