Synthesis of NiMoS4 for High-Performance Hybrid Supercapacitors

被引:68
作者
Du, Dongwei [1 ]
Lan, Rong [1 ]
Humphreys, John [1 ]
Xu, Wei [1 ]
Xie, Kui [2 ]
Wang, Huanting [3 ]
Tao, Shanwen [1 ,3 ]
机构
[1] Univ Warwick, Sch Engn, Coventry CV4 7AL, W Midlands, England
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[3] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
关键词
MICROWAVE-ASSISTED SYNTHESIS; ELECTRODE MATERIAL; ACTIVATED CARBON; ENERGY-STORAGE; LOW-COST; NANOSHEETS; GRAPHENE; COMOS4; FOAM;
D O I
10.1149/2.0071713jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Transition metal sulfides have been suggested as promising materials for efficient energy storage with superior electrochemical performances. Compound NiMoS4-A was synthesized by a facile chemical co-precipitation process, followed by calcining at 450 degrees C in Ar. The as-prepared NiMoS4-A electrode exhibits a high specific capacity of 313 C g(-1) at 1 A g(-1) and good rate capability (83% retention at 10 A g(-1)). Electrochemical impedance spectroscopy (EIS) results indicate that the good performances could be attributed to the low internal and charge transfer resistances. Additionally, the quantitative charge storage analysis reveals that the faradaic redox process dominates at lower scan rates (78% at 1 mV s(-1)), while the capacitive effect dominates at higher scan rates (56% at 20 mV s(-1)). Furthermore, a hybrid supercapacitor (HSC), with NiMoS4-A as the positive electrode and activated carbon (AC) as the negative electrode, displays a high energy density of 35 Wh kg(-1) at an average power density of 400 W kg(-1). Meanwhile, the HSC exhibits excellent cycle stability, maintaining 82% of the initial capacitance after 10000 charge-discharge cycles even at a high current density of 5 A g(-1). These good electrochemical performances indicate that NiMoS4-A is a promising positive electrode material for hybrid supercapacitors. (C) 2017 The Electrochemical Society. All rights reserved.
引用
收藏
页码:A2881 / A2888
页数:8
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