Chem. Mater., 20 (4), 13761380, 2008. 10.1021/cm702033z
Web Release Date: January 10, 2008

Copyright © 2008 American Chemical Society

Hydrous Manganese Dioxide Nanowall Arrays Growth and Their Li+ Ions Intercalation Electrochemical Properties

Dawei Liu, Qifeng Zhang, Peng Xiao, Betzaida B. Garcia, Qing Guo, Richard Champion,§ and Guozhong Cao*

Department of Materials Science and Engineering, Department of Mechanical Engineering, and Department of Chemical Engineering, University of Washington, Seattle, Washington 98195, and Department of Physics, Chongqing University, P. R. China

Received July 26, 2007

Revised Manuscript Received November 13, 2007

Abstract:

Nanowall arrays of hydrous manganese dioxide MnO2·0.5H2O were deposited on cathodic substrates by the potentiostatic method from a mixed aqueous solution of manganese acetate and sodium sulfate, and the Li+ ions intercalation properties of such nanowall arrays were studied. The deposition was induced by a change of local pH resulting from electrolysis of H2O. Composition of this new nanowall structure was investigated by means of combined XRD, XPS, and TGA and determined to be hydrous manganese dioxide. SEM study revealed that the MnO2·0.5H2O nanowall arrays were homogeneous across the entire substrate of top thicknesses that varied from 50 to 100 nm with identical depth. The nanowall arrays of hydrous manganese dioxide exhibited an initial capacity of 270 mAh/g with a reversible capacity maintained at 220 mAh/g at the 50th charge/discharge cycle in the Li+ ions intercalation capacity measurement at a high charge/discharge rate of 0.1 mA/cm2 (C/2, 76 mAh/g). This greatly enhanced Li+ ions intercalation capacity is ascribed to the large active surface area of the nanowall arrays and a short facile diffusion path for Li+ ions. The nanowall arrays of hydrous manganese dioxide also displayed an improved cyclic stability attributed to the reduced strain accumulated in these nanostructures during Li+ ions intercalation.

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