dc.contributor.author |
Jones, Colin F. |
|
dc.contributor.author |
Segall, Robert L. |
|
dc.contributor.author |
Smart, Roger St. C. |
|
dc.contributor.author |
Turner, Peter S. |
|
dc.date.accessioned |
2025-04-24T09:51:10Z |
|
dc.date.available |
2025-04-24T09:51:10Z |
|
dc.date.issued |
1978 |
|
dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18772 |
|
dc.description.abstract |
The effect of decreasing dissolution rate of nickel oxide per unit surface area in acid solution with increasing prior annealing temperature (700–1450°C) has been shown to occur over a wide range of pH. The linear dependence of log (rate) on pH may be explained on a model of non-oxidative dissolution in which the pH variation changes the overpotential at the surface. Electron microscopy shows a different mode of attack at pH < 0. The presence in solution of a strong oxidizing ion such as cobaltic causes a very large increase in dissolution rate (> 200 fold) for all prior annealing temperatures but the oxide annealed at 1450°C is still the slowest to dissolve in the presence of cobaltic ions. This is believed to be because it has the lowest kink site density, the role of the Co3+ being hole injection into the p-type semiconductor at kink sites. The general conclusion of the work is that the supply of the majority carriers (the holes) may be rate limiting in the dissolution process. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (07) |
en_US |
dc.subject |
Chemistry |
en_US |
dc.subject |
Semiconducting oxides |
en_US |
dc.subject |
Nickel oxide |
en_US |
dc.subject |
Journal of the Chemical Society : Faraday Transaction - I |
en_US |
dc.title |
Semiconducting Oxides: Effects of Electronic and Surface Structure on Dissolution Kinetics of Nickel Oxide |
en_US |
dc.type |
Article |
en_US |