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Cited 2 time in webofscience Cited 2 time in scopus
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Effect of potential and current on electrodeposited MnO2 as a pseudocapacitor electrode: Surface morphology/chemistry and stability

Authors
Han, SehunPark, SungjunYi, Seong-HoonIm, Won BinChun, Sang-Eun
Issue Date
Aug-2020
Publisher
ELSEVIER SCIENCE SA
Keywords
PseudocapacitorSurface morphology/chemistryElectrodepositionManganese oxide filmElectrochemical stabilityIrreversible reaction
Citation
JOURNAL OF ALLOYS AND COMPOUNDS, v.831, pp.1 - 11
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF ALLOYS AND COMPOUNDS
Volume
831
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/1810
DOI
10.1016/j.jallcom.2020.154838
ISSN
0925-8388
Abstract
Amorphous MnO2 (a-MnO2) that exhibits a high theoretical specific capacitance can be conveniently grown via electrodeposition as a pseudocapacitor electrode. However, the electrodeposited a-MnO2 exhibits lower electrochemical stability than a-MnO2 synthesized using other routes. We investigate the influence of the electrodeposition conditions on the evolution of the properties of a-MnO2 during electrodeposition and their corresponding effect on the electrochemical stability. MnO2 is electrodeposited at potentiostatic and galvanostatic mode. The different surface morphology/chemistry of a-MnO2 is obtained by applying high and low potentials or current. The applied potential or current determines the surface morphology based on a predominance between nucleation and growth of a-MnO2. The fine surface enables a higher specific capacitance because of the enlarged specific surface area but also leads to lower rate performance by limiting ion transport through the smaller microstructure. The opposite results are observed in a coarse MnO2 deposit. When the applied potential or current is high, the manganese has a lower average valence number. The lifetime of a-MnO2 is degraded by the irreversible reaction between Mn4+/Mn7+ and oxygen evolution. Particularly, finer MnO2 is less stable than coarse one, which can arise from multiple high-energy connecting sites. A narrow potential window without Mn4+/Mn7+ interconversion promotes long-term stability.
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