posted on 2018-08-13, 16:20authored byPeter C. Jones
Preliminary passivation studies established that
kinetic measurements could be made at α- and β-lead
dioxide electrodes, in perchloric acid electrolytes,
without the intrusion of solid films.
The kinetics of the rate controlling exchange
reaction at α- and β-PbO2 have been investigated using
the galvanostatic pulse technique. The overpotential-current
density data was interpreted in terms of two
rate controlling charge transfer mechanisms. Around
the equilibrium potential the reaction mechanism appears
as a simultaneous two-electron transfer which changed
to two consecutive single-electron transfer steps at
high overpotential. Possible reaction mechanisms have
been discussed on the basis of the observed kinetic
parameters.
Differential capacitance-potential data for α- and β-PbO2 has been measured in inert electrolytes.
A comparison of the electrochemical behaviour of α- and β-PbO2 has been made.
Funding
Loughborough University of Technology (scholarship).
This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/
Publication date
1968
Notes
A Doctoral Thesis. Submitted in partial fulfilment of the requirements for the award of Doctor of Philosophy at Loughborough University.