The hydrogen evolution reaction on nickel surfaces stabilized by H-absorption
β Scribed by S.A.S. Machado; L.A. Avaca
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 637 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0013-4686
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β¦ Synopsis
The hydrogen evolution reaction (her) was studied on bright nickel electrodes in alkaline solutions at several temperatures. The formation of nickel hydrides in the potential region of the her was previously analyzed by cyclic voltammetry and the electrode surface was pre-conditioned to minimize the effect of the hydrides in the experimental response of the system. Data from polarization curves was conveniently analyzed by non-linear regression fitting resulting in a Volmer-Heyrovsky mechanism in which the second reaction must be the rds to explain the characteristics of the hydride formation. The calculated value of the rate constant for the electrochemical desorption step was 165 x lo-" mol cm" s-l at 25Β°C. The apparent energy of activation was 58 kJ mol-', a value somewhat higher than those in the literature and that was justified in terms of the specific pre-treatment of the surface. A voltammetric method for determining the real electrochemical active area of Ni electrodes is also described.
π SIMILAR VOLUMES
## Ahtract -The effect of electrode surface roughness on the kinetics of the hydrogen evolution reaction has been studied for mild steel and nickel cathodes in 10 M NaOH at 348 0 K. With the nickel cathodes, the 'T'afel slope was independent of whether the electrode surface was smooth or roughened
Nickel was modtfied at the surface from alkalme solution contamrng dtfferent concentrattons of WO,% or MoG4= It was shown that improvement in the overpotential (n) and in the exchange current density of the hydrogen evolution reaction m KOH 3M on the electrode depends on the nature of the heteropoly