Hydrogen evolution on electrodeposited nickel-cobalt-molybdenum in alkaline water electrolysis
โ Scribed by Chonglun Fan; D.L. Piron; P. Paradis
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 628 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
B a constant/V b Tafel slope/V b, Tafel slope in the low overpotential range/ mV bh Tafel slope in the high overpotential range/ mV C capacitance at electrode-solution interface/ Fcm -2 or mF cm" 2 Cd , double layer capacitance/Fcm -2 or mF cm -2 Cd pseudocapacitance/Fcm -2 or mFcm 2 E potential/V F Faraday constant/C mot -' ie, hydrogen exchange current density extrapolated from the Tafel relation in the low overpotential range/mA cm -2 hydrogen exchange current density extrapolated from the Tafel relation in the high overpotential range/mA cm -2 m a constant > 1 q charge required to form a surface monolayer of adsorbed hydrogen/C cm -2 R gas constant/J K -' mot -' T temperature/K Greek symbols a transfer coefficient a, transfer coefficient in the low overpotential range
๐ SIMILAR VOLUMES
In micro-electrolysis cells (4 cm' electrode area) which possess a sandwichconfiguration as used irradvanced water electrolysis[ l] different anodic and cathodic electrocatalysts, which did not contain noble metals were investigated over the current density range from 10ea to 1.0 Acm-' and a tempera
The possibility of in situ activation of oxygen evolving anodes and hydrogen evolving cathodes in alkaline water electrolysers has been investigated. It is possible to activate anodes by depositing on them cobalt oxide or iron oxide or an even more active mixture of both. In all three cases the oxyg