Comparative Analysis of Electrodeposited Cobalt oxide Thin Films by Chronoamperometry and Chronopotentiometry Modes for Supercapacitor Application

被引:2
作者
Gavande, S. S. [1 ,2 ]
Salunkhe, A. S. [3 ]
Navale, Y. H. [3 ]
Gavande, Shivani [3 ]
Kulkarni, P. S. [3 ]
Karche, B. R. [2 ]
机构
[1] Sangameshwar Coll, Dept Phys, Solapur 413003, MS, India
[2] Shankarrao Mohite Mahavidyala, Dept Phys, Akluj, MS, India
[3] Solapur Univ, Funct Mat Res Lab, Sch Phys Sci, Punyashlok Ahilyadevi Holkar, Solapur 413255, MS, India
来源
DAE SOLID STATE PHYSICS SYMPOSIUM 2019 | 2020年 / 2265卷
关键词
Cobalt oxide; Electrodeposition; Chronopotentiometry; Chronoamperometry; Cyclic voltammetry; PERFORMANCE;
D O I
10.1063/5.0017211
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Nanocrystalline and highly porous Cobalt oxide electrode was electrodeposited onto stainless steel substrates by two different electrodeposition modes, such as Chronopotentiometry and Chronoamperometry Methods. The deposited electrodes were then annealed at 5000C for 6 hours for metal oxide formation. The structural and morphological characteristics were investigated through X-ray diffraction analysis and SEM characterizations, wettability by Contact angle measurement. The electrochemical analysis was done through cyclic voltammetry and galvanostatic charge-discharge analysis. The electrochemical properties of the deposited thin films were studied using cyclic voltammetry and galvanostatic charge-discharge. The optimum value of specific capacitance of 294.67 Fg-1 at 5mVs-1 scan rate, specific energy 3.642Wh/kg, Specific Power 3 kW/kg was obtained in 1M aqueous Na2SO4 electrolyte at a current density of 1 A g-1 in 1M aqueous Na2SO4 electrolyte by Chronoamperometry mode. Similarly, using Chronopotentiometry mode of specific capacitance of 284.4 F g-1 at a scan rate of 5mVs-1, specific energy 4.325 Wh/kg, specific power 3 kW/kg was obtained at a current density of 1 A g-1 in 1M aqueous Na2SO4 electrolyte.
引用
收藏
页数:4
相关论文
共 11 条
[1]   Performance evaluation of symmetric supercapacitor based on cobalt hydroxide [Co(OH)2] thin film electrodes [J].
Jagadale, A. D. ;
Kumbhar, V. S. ;
Dhawale, D. S. ;
Lokhande, C. D. .
ELECTROCHIMICA ACTA, 2013, 98 :32-38
[2]   Influence of electrodeposition modes on the supercapacitive performance of Co3O4 electrodes [J].
Jagadale, Ajay D. ;
Kumbhar, Vijay S. ;
Bulakhe, Ravindra N. ;
Lokhande, Chandrakant D. .
ENERGY, 2014, 64 :234-241
[3]   Advancing the Supercapacitor Materials and Technology Frontier for Improving Power Quality [J].
Jampani, Prashanth ;
Manivannan, A. ;
Kumta, Prashant N. .
ELECTROCHEMICAL SOCIETY INTERFACE, 2010, 19 (03) :57-62
[4]   Chemical synthesis of cobalt oxide thin film electrode for supercapacitor application [J].
Kandalkar, S. G. ;
Dhawale, D. S. ;
Kim, Chang-Koo ;
Lokhande, C. D. .
SYNTHETIC METALS, 2010, 160 (11-12) :1299-1302
[5]   Nano-ceramic support materials for low temperature fuel cell catalysts [J].
Lv, Haifeng ;
Mu, Shichun .
NANOSCALE, 2014, 6 (10) :5063-5074
[6]   Electrochemical capacitance study on Co3O4 nanowires for super capacitors application [J].
Wang, Lu ;
Liu, Xiaoheng ;
Wang, Xin ;
Yang, Xujie ;
Lu, Lude .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS, 2011, 22 (06) :601-606
[7]   Template synthesis of hollow fusiform RuO2•xH2O nanostructure and its supercapacitor performance [J].
Wu, Xu ;
Zeng, Yan ;
Gao, Hairui ;
Su, Jun ;
Liu, Jinping ;
Zhu, Zhihong .
JOURNAL OF MATERIALS CHEMISTRY A, 2013, 1 (03) :469-472
[8]  
Xiao F, 2012, INT J ELECTROCHEM SC, V7, P7440
[9]   Nanocrystalline-Li2FeSiO4 synthesized by carbon frameworks as an advanced cathode material for Li-ion batteries [J].
Yang, Jinlong ;
Kang, Xiaochun ;
Hu, Lin ;
Gong, Xue ;
Mu, Shichun .
JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (19) :6870-6878
[10]   Oxygen-Rich Hierarchical Porous Carbon Derived from Artemia Cyst Shells with Superior Electrochemical Performance [J].
Zhao, Yufeng ;
Ran, Wei ;
He, Jing ;
Song, Yanfang ;
Zhang, Chunming ;
Xiong, Ding-Bang ;
Gao, Faming ;
Wu, Jinsong ;
Xia, Yongyao .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (02) :1132-1139