Ultrathin Ni-Mo oxide nanoflakes for high-performance supercapacitor electrodesopen access
- Authors
- Chavan, Harish S.; Hou, Bo; Ahmed, Abu Talha Aqueel; Kim, Jongmin; Jo, Yongcheol; Cho, Sangeun; Park, Youngsin; Pawar, Sambhaji M.; Inamdar, Akbar I.; Cha, Seung Nam; Kim, Hyungsang; Im, Hyunsik
- Issue Date
- 30-Oct-2018
- Publisher
- ELSEVIER SCIENCE SA
- Keywords
- Supercapacitor; Ni-Mo oxide nanoflake; Electrochemical active surface area; Successive ionic layer adsorption and reaction
- Citation
- JOURNAL OF ALLOYS AND COMPOUNDS, v.767, pp 782 - 788
- Pages
- 7
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF ALLOYS AND COMPOUNDS
- Volume
- 767
- Start Page
- 782
- End Page
- 788
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/24439
- DOI
- 10.1016/j.jallcom.2018.07.179
- ISSN
- 0925-8388
1873-4669
- Abstract
- Supercapacitors based on nanomaterial electrodes exhibit great potential as power sources for advanced electronic devices. From a practical viewpoint, it is desirable to fabricate highly active and sustainable nanomaterial electrodes consisting of non-precious elements using a simple technique in a controllable way. In this work, we report the synthesis of a self-assembled ultra-thin porous nanoflake Ni-Mo oxide (NMO) film using the successive ionic layer adsorption and reaction (SILAR) technique. The nanoflake NMO thin film electrode with a large electrochemically active surface area of similar to 108 cm(-2) exhibits a high specific capacitance of 1180 Fg(-1) at a current density of 1 Ag-1 and excellent rate capability, with a negligible capacity loss of 0.075% per cycle. Even at a high current rate of 10 A g(-1) it retains a capacity of 600 Fg(-1). The highest energy and power densities obtained are 119 Whkg(-1) and 15.7 kWkg(-1), respectively. Electrochemical impedance spectroscopy analyses reveal that the electrode has considerably low charge transfer resistance. The observed excellent electrochemical energy storage performance of the nanoflake NMO electrode with a nanoporous surface is due to the synergetic effects of the large electrochemically active surface area, enhanced ion diffusion, and improved electrical conductivity. (C) 2018 Elsevier B.V. All rights reserved.
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- Appears in
Collections - College of Natural Science > Department of Physics > 1. Journal Articles
- College of Advanced Convergence Engineering > Division of System Semiconductor > 1. Journal Articles

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