Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4767244 | Electrochimica Acta | 2017 | 37 Pages |
Abstract
Herein the various steps in the electrodeposition mechanism of manganese dioxide from permanganate are elucidated. Two primary mechanisms are described, dependent on applied potential and hydrodynamics. The first is a combined reduction and disproportionation reaction involving the reduction of MnO4â to MnO42â, which subsequently hydrolyses and disproportionates to form the Mn(V) species H2MnO4â. This is then further reduced to form manganese dioxide. This reaction continues over the whole potential range, however whether the system is dynamic or static has an effect on this, with the former leading to continued reaction from an influx of MnO4â, and the latter not having available MnO4â to proceed. The second mechanism involves a dissolution of already existing manganese dioxide, through a MnOOH intermediate to form aqueous Mn2+. This Mn2+ then reacts with MnO4â in solution to form manganese dioxide. These mechanisms have been substantiated with scanning electron microscopy and X-ray photoelectron spectroscopy. The performance of these materials as capacitor electrodes has also been investigated, achieving 363Â F/g when cycled at 25Â mV/s.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Andrew J. Gibson, Kenneth G. Latham, Robert C. Burns, Scott W. Donne,