Synthesis of MnNb2O6 with hierarchical structure as a novel electrode material for high-performance supercapacitors

被引:31
|
作者
Wang, Ting [1 ]
Ma, Tengfei [1 ]
Ge, Tao [2 ]
Shi, Shaojun [1 ]
Ji, Hongmei [1 ]
Li, Weili [2 ]
Yang, Gang [1 ]
机构
[1] Changshu Inst Technol, Sch Chem & Mat Engn, Jiangsu Lab Adv Funct Mat, Changshu 215500, Jiangsu, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Mat Sci & Engn, Zhenjiang 212003, Peoples R China
关键词
Columbite compounds; Hierarchical structure; Supercapacitor; Electrode materials; Electrochemical performance; HIGH-ENERGY DENSITY; ENHANCED PERFORMANCE; SURFACE-AREA; OXIDE; CAPACITANCE; NIOBIUM; SHEETS; MN;
D O I
10.1016/j.jallcom.2018.04.031
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Columbite compound MnNb2O6, consisted the layers with slightly distorted hexagonal-closed-packed oxygen sublattice, has abundant reaction sites whereby the interlayered ions can occur faradic reaction to enhance the charge storage capability. Here, we first report three-dimensional nanostructure of MnNb2O6 as electrode materials for electrochemical pseudocapacitor synthesized through hydrothermal method. The crystal morphologies of MnNb2O6 show an evolution with the hydrothermal time, from primary spindle-like particles grown for 12 h and undergrown star-like crystals for 18 h, to hierarchical star-like crystals for 1 day and overgrown crystals for 3 days. MNO-1d sample synthesized for 1 day possesses ordered six-leaf nanostructure composed of hierarchical nano-sheets (thickness-30 nm). To explore its potential applications for supercapacitor, MnNb2O6 sample as electrode material is characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge-discharge measurements. MNO-1d demonstrates an outstanding specific capacitance of 350 F g(-1) and rate capability with a high capacitance retention of-90% of its initial capacitance after 10000 cycles at a high current density of 10 A g(-1). (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:428 / 435
页数:8
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