Facile Synthesis and Characterization of Cu3(MoO4)2(OH)2Nanorods for High Performance Supercapacitor Electrode Application

被引:6
作者
Harichandran, Gurusamy [1 ]
Radha, Sivasubramanian [1 ]
Yesuraj, Johnbosco [2 ]
Muthuraaman, Bhagavathiachari [2 ]
机构
[1] Univ Madras, Dept Polymer Sci, Guindy Campus, Chennai 600025, Tamil Nadu, India
[2] Univ Madras, Dept Energy, Guindy Campus, Chennai 600025, Tamil Nadu, India
来源
CHEMISTRYSELECT | 2020年 / 5卷 / 35期
关键词
Copper molybdate hydrate; Conducting materials; CTAB; Energy conversion; supercapacitors; ELECTROCHEMICAL PERFORMANCE; SONOCHEMICAL SYNTHESIS; HOLLOW MICROSPHERES; MNMOO4; NANORODS; FLOWER-LIKE; GRAPHENE; HYBRID; NANOSTRUCTURES; NANOSPHERES; MORPHOLOGY;
D O I
10.1002/slct.202002610
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present study, Cu-3(MoO4)(2)(OH)(2)electrode materials were prepared by CTAB assisted hydrothermal method. Thermal, crystalline and bonding properties of freshly prepared samples were confirmed by thermo gravimetric analysis (TGA), x-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman analyses. The surface morphological features of Cu-3(MoO4)(2)(OH)(2)electrode materials were observed via Scanning electron microscopy (SEM) analysis. The concentration of cetyl trimethyl ammonium bromide (CTAB) template has much influenced in nanomaterial formation and the high concentration (3 mM) of CTAB provides nanorod structures. The electrochemical analysis of Cu-3(MoO4)(2)(OH)(2) electrodes were demonstrated via cyclic voltammetry (CV), chronopotentiometry (CP) and cyclic stability analyses. The electrochemical investigations of Cu-3(MoO4)(2)(OH)(2)electrode provide remarkable specific capacitance of 532 F g(-1)at a scan rate of 5 mV s(-1)and good cyclic stability of 98 % retention even after 5000 cycles at a scan rate of 20 mV s(-1)with good rate capability. These outcomes prompted to assign a probable application for the synthesized Cu-3( MoO4)(2)(OH)(2)to utilize as a capable electrode material for supercapacitor applications.
引用
收藏
页码:11037 / 11047
页数:11
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