## Abstract The kinetics of the charge transfer process of the ferroβ/ferricyanide Redox system on anodically formed titanium oxide layers is studied. The oxides were formed potentiodynamically in borate buffer solutions of pH = 8. Anodic and cathodic Tafel lines were measured at a scan rate of 1.0
Hydrogen evolution reaction on Titanium and oxide-covered titanium electrodes
β Scribed by M. W. Khalil; M. A. Abdel Rahim
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 465 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0933-5137
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β¦ Synopsis
Abstract
The kinetics of HER on Ti electrodes in H~2~SO~4~ of various concentrations in the pH range of 0.24β1.88 was studied. Cathodic Tafel lines were measured potentiodynamically at a scan rate 1.0 mVs^β1^ within the H~2~ evolution potential range. Linear parallel Tafel lines of a slope of 152 mVdecade^β1^ were obtained. A value of 0.73 was calculated for the reaction order wrt a~H~^+^ using the exchange cd, i~0~ Tafel lines measured on oxide covered electrodes showed three deviations from linearity. An attempt was made to explain the deviations in terms of hydride formation and chemical oxide dissolution. Tafel slopes of 152 mVdecade^β1^ were also observed for the HER on oxideβcovered electrodes. The nature and composition of the oxide did not depend on the electrolyte in which the oxides were formed.
π SIMILAR VOLUMES
Evidence is preseoted for a reversible reaction occurring within the bulk of the surface oxide She on Ti electrodes at negative poteutials. Higb frequency impedance measurements give results characteristic of a buIk phenomenon and clearly distinguish the behaviour of filmed Ti electrodes from that o
Ti/SnO, + CuCo,O, and Ti/RuO, + TiO, anodes were used to study oxygen evolution in alkaline solutions and to compare the kinetics on both electrodes. On each electrode the existence of two Tafel regions was confirmed. At low current density (cd) the Tafel slope is 39mV decade-', whereas at high cd i