Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637056
Title: Heterogeneous reactions in solar energy conversion
Author: Giddings, S. L.
Awarding Body: University College of Swansea
Current Institution: Swansea University
Date of Award: 1988
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Abstract:
Photochemical systems for the splitting of water into hydrogen and oxygen represent an attractive route for the conversion of solar energy into a chemical fuel. However, the success of such systems depends on the identification of suitable redox catalysts for the oxidation and reduction processes. While colloidal platinum has proved to be an efficient catalyst for the reduction of water, the development of stable and effective catalysts for water oxidation has been less successful. The work described in this thesis involves the study of ruthenium dioxide hydrate (RuO2.xH2)O as a heterogeneous catalyst for the oxidation of water to oxygen. Although this material has already been widely used as an oxygen catalyst, there have been many doubts as to its ability to act in this capacity. In Chapter Three an attempt is made to resolve this controversy via an investigation of the stability and catalytic activity of RuO2.xH2O when exposed to various oxidising agents. The results indicate that the catalytic activity and corrosion stability of an RuO2.xH2O sample is related to its degree of hydration. In Chapter Four an investigation is described into the effect of heat-treatment of RuO2.xH2O at different temperatures on its physical and chemical properties. From these results it appears that any sample of RuO2xH2O may be transformed into a stable, reproducible oxygen catalyst by simply heat-treating it at 140-150oC in air for ca. 5 hours. The latter conditions represent an optimum for catalytic activity where anodic corrosion is absent. This 'thermally-activated' RuO2.xH2O is shown to compare favourably with alternative oxygen catalysts. Chapters Five and Six involve a kinetic study of the RuO2.xH2O-catalysed oxidation of water by Ce(IV) ions in an attempt to elucidate the mechanism of catalysis of the oxide powder. The study is based on an electrochemical model in which the RuO2.xH2O particles are considered as microelectrodes. The initial charging of the RuO2.xH2O prior to water oxidation is discussed in Chapter Five and in Chapter Six the effect of an increase in the redox potential of the Ce4+/Ce3+ couple by changing the acid medium is investigated.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.637056  DOI: Not available
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