Porous Fe-Mn-O nanocomposites: Synthesis and supercapacitor electrode application

被引:26
作者
Zhu, Guoxing [1 ,3 ]
Yang, Jing [1 ]
Liu, Yuanjun [2 ]
Xie, Xulan [1 ]
Ji, Zhenyuan [1 ]
Yin, Jinxiu [1 ]
Shen, Xiaoping [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxide; Fe-Mn-O; Porous structure; Capacitors; Electrodes; HIGH-PERFORMANCE; CARBON NANOTUBES; ARCHITECTURE; FACILE; ENERGY; HOLLOW; FABRICATION; NANOWIRES; NANORODS; DESIGN;
D O I
10.1016/j.pnsc.2016.05.016
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Transition metal oxide micro-/nanostructures demonstrate high potential applications in energy storage devices. Here, we report a facile synthesis of highly homogeneous oxide composites with porous structure via a coordination polymer precursor, which was prepared with the assistance of tartaric acid. The typical product, Fe-Mn-O composite was demonstrated here. The obtained Fe-Mn-O product was systemically characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, elemental mapping analysis, and X-ray photoelectron spectroscopy. It was demonstrated that the Fe-Mn-O nanocomposite shows interconnected porous structure, in which iron, manganese, and oxygen are uniformly distributed. In addition, the Fe-Mn-O nanocomposite was then fabricated as capacitor electrodes. Operating in an aqueous neutral solution, the Fe-Mn-O composite electrodes showed an wide working potential window from 0.2 to 1.0 V (vs. SCE), and a specific capacitance of 86.7 Fg(-1) or 0.4 F cm(-2) at a constant current density of 1 Ag-1 with good cycle life. This study offers a new precursor approach to prepare porous metal oxide composites, which would be applied in energy-storage/conversion devices, catalysts, sensors, and so on. (C) 2016 Chinese Materials Research Society. Production and hosting by Elsevier B.V.
引用
收藏
页码:264 / 270
页数:7
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