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Semiconducting Oxides: Effects of Electronic and Surface Structure on Dissolution Kinetics of Nickel Oxide

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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


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