Published May 20, 2008 | Version v1
Journal article

Manganese films electrodeposited at different potentials and temperatures in ionic liquid and their application as electrode materials for supercapacitors

  • 1. Department of Materials Science and Engineering, National Cheng Kung University, 1 Ta-Hsueh Road, Tainan 701, Taiwan (China)
  • 2. Department of Chemistry, National Cheng Kung University, Tainan, Taiwan (China)
  • 3. Faculty of Medicinal and Applied Chemistry, Kaohsiung Medical University, Kaohsiung, Taiwan (China)

Description

Electrodeposition of manganese (Mn) in butylmethylpyrrolidinium bis(trifluoromethylsulfony)imide (BMP-NTf2) ionic liquid is demonstrated in this study. Crystal structures and surface morphologies of the Mn films deposited at various potentials (from -1.8 V to -2.2 V) and temperatures (from 50 deg. C to 110 deg. C) were examined with an X-ray diffractometer (XRD) and a scanning electron microscope (SEM), respectively. Experimental results indicate that the deposited Mn films were amorphous in nature; however, their morphologies strongly depended on the deposition conditions. After being anodized in Na2SO4 solution, the deposited Mn was transformed to Mn oxide. Electrochemical properties of the Mn oxides were evaluated using cyclic voltammetry (CV). It was confirmed that the different Mn deposition conditions caused the variations in pseudocapacitive performance of the oxide electrodes. The oxide (∼0.1 mg) anodized from the Mn deposited at -1.8 V and 50 deg. C had the highest specific capacitance of 402 F/g measured at a CV scan rate of 5 mV/s. Its capacitance retained ratio after 500 CV testing cycles was as high as 94%

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2008.01.036

Additional details

Identifiers

DOI
10.1016/j.electacta.2008.01.036;
PII
S0013-4686(08)00085-6;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
53
Journal Issue
13
Journal Page Range
p. 4447-4453
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.