Issue 17, 2012

Enhancement of the electrocapacitive performance of manganese dioxide by introducing a microporous carbon spheres network

Abstract

An amorphous MnO2·nH2O/microporous carbon spheres (α-MnO2·nH2O/MCS) composite electrode material is prepared by a chemical co-precipitation method. It is observed that the amorphous MnO2 particles are deposited on the surface of the MCS, which form a network with a uniquely developed three-dimensional open porous system containing macropores, mesopores and micropores. The electrochemical measurements reveal that the composite electrode material presents a much more stable and reversible capacitance behavior compared to the pure α-MnO2·nH2O in 1 M of Na2SO4 electrolyte. The composite containing 25 wt% MCS exhibits optimal specific capacitance of 218.2 F g−1 at 2 mV s−1, and is still as high as 112.4 F g−1 at 100 mV s−1, while a drastic reduction from 197.0 F g−1 at 2 mV s−1 to only 40.7 F g−1 at 100 mV s−1 occurs for the pure α-MnO2·nH2O. The composite also shows a rather high electrode-specific capacitance of 3.13 F cm−2 and a long cycle life. The remarkable enhancement in the electrochemical performance is mainly attributed to the microporous structure of the MCS contributing to the deposition of MnO2 particles on the surface of the MCS, and the uniquely developed porous network of the composite facilitating the rapid transport of the electrolyte. These factors result in the high electrochemical utilization of MnO2, a great reduction of the equivalent series resistance, and hence the relatively high and stable electrochemical behavior.

Graphical abstract: Enhancement of the electrocapacitive performance of manganese dioxide by introducing a microporous carbon spheres network

Supplementary files

Article information

Article type
Paper
Submitted
14 Oct 2011
Accepted
28 Feb 2012
First published
29 Feb 2012

Phys. Chem. Chem. Phys., 2012,14, 5966-5972

Enhancement of the electrocapacitive performance of manganese dioxide by introducing a microporous carbon spheres network

W. Wei, X. Huang, Y. Tao, K. Chen and X. Tang, Phys. Chem. Chem. Phys., 2012, 14, 5966 DOI: 10.1039/C2CP23235A

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