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dc.contributor.advisorVincent, Colin Angus
dc.contributor.authorSmith, Michael J.
dc.coverage.spatialv, 173 p.en_US
dc.date.accessioned2020-11-13T17:24:50Z
dc.date.available2020-11-13T17:24:50Z
dc.date.issued1983
dc.identifier.urihttp://hdl.handle.net/10023/20976
dc.description.abstractUsing a method based on the analysis of the voltage transient recorded during the application of a galvanostatic pulse to a solid state, three electrode cell, diffusion coefficients of silver electro-active species in AgₓTiS₁.₈ and AgₓNbS₂ were obtained. The activation energy of the diffusion process was found to be approximately 30 kJ mole⁻¹ for TiS₁.₈ and between 34 kJ mole⁻¹ and 24 kJ mole⁻¹, decreasing with increasing guest concentration, for NbS₂. Non-linearity at extended times in the experimental timescale was ascribed to finite length effects, variation of the thermodynamic enhancement factor during the pulse, or a combination of these influences. Temperature and composition variation of the cell emf, for AgₓTiS₁.₈ and AgₓNbS₂ systems, permitted thermodynamic parameters and the compositional variation of the enhancement factors to be obtained. Investigation of the effect of the temperature of oven pre-treatment on compressed powder samples of a lithium ion conducting vitreous electrolyte on the bulk conductivity was carried out using a scanning electron microscope and ac conductivity measurements. Electronic conductivity measurements, using Wagner's method were undertaken on samples of iodotungstate and iodoarsenate glass with a view to confirmation of the low levels necessary for the use of these electrolytes in galvanic cells.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subject.lccQD571.S6
dc.subject.lcc
dc.titleElectrochemical studies of solid solution electrodesen_US
dc.typeThesisen_US
dc.contributor.sponsorUniversity of St Andrewsen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US
dc.identifier.doihttps://doi.org/10.17630/sta/5


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