The metal-electrolyte interface

Theories of the metal-electrolyte interface are reviewed with particular attention to the prediction of thermodynamic quantities. A comparison of the different theories is made using a range of experimental results on Hg-aqueous electrolyte systems. Certain widespread failings of the models are reve...

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Main Author: Painter, Katharine
Other Authors: March, Norman Henry
Published: University of Oxford 1983
Subjects:
541
Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.348154
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spelling ndltd-bl.uk-oai-ethos.bl.uk-3481542015-03-19T05:16:48ZThe metal-electrolyte interfacePainter, KatharineMarch, Norman Henry1983Theories of the metal-electrolyte interface are reviewed with particular attention to the prediction of thermodynamic quantities. A comparison of the different theories is made using a range of experimental results on Hg-aqueous electrolyte systems. Certain widespread failings of the models are revealed. These are identi- fied as being the results of a neglect of solvent structure and of chemical interactions. Next a solvent-free metal-molten salt system is investigated using a model based on the MSA. Thermodynamic properties, parti- cularly the capacitance and the potential at the point of zero charge and their variation with temperature, are calculated. The magnitudes for a range of ionic species are in agreement with experiments for Pb-alkali halide systems, but the (relatively weak) temperature dependence is not predicted correctly. The success of this application of the MSA compared to applications to aqueous systems shows the great importance of the solvent in determining the properties of these systems. To attempt to improve on the MSA model a new model based on the EXP approximation is developed. The predicted trend of the temperature dependence of capacitance is now given correctly but in other respects the predictions are worse than those of the MSA. In our first MSA model the metal is treated as a hard wall. A more realistic representation is now introduced which incorporates electron spill-out. By a phenomenological analysis the extent of spill-out into the electrolyte is estimated. No direct measurement of this quantity has been made. It is consistent with theoretical estimates made for aqueous systems when allowance ,is made for the effect of the solvent.541Electrolytes : Thermal properties : HalidesUniversity of Oxfordhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.348154http://ora.ox.ac.uk/objects/uuid:8457b005-b15e-4bee-9797-d1301edcb6e7Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 541
Electrolytes : Thermal properties : Halides
spellingShingle 541
Electrolytes : Thermal properties : Halides
Painter, Katharine
The metal-electrolyte interface
description Theories of the metal-electrolyte interface are reviewed with particular attention to the prediction of thermodynamic quantities. A comparison of the different theories is made using a range of experimental results on Hg-aqueous electrolyte systems. Certain widespread failings of the models are revealed. These are identi- fied as being the results of a neglect of solvent structure and of chemical interactions. Next a solvent-free metal-molten salt system is investigated using a model based on the MSA. Thermodynamic properties, parti- cularly the capacitance and the potential at the point of zero charge and their variation with temperature, are calculated. The magnitudes for a range of ionic species are in agreement with experiments for Pb-alkali halide systems, but the (relatively weak) temperature dependence is not predicted correctly. The success of this application of the MSA compared to applications to aqueous systems shows the great importance of the solvent in determining the properties of these systems. To attempt to improve on the MSA model a new model based on the EXP approximation is developed. The predicted trend of the temperature dependence of capacitance is now given correctly but in other respects the predictions are worse than those of the MSA. In our first MSA model the metal is treated as a hard wall. A more realistic representation is now introduced which incorporates electron spill-out. By a phenomenological analysis the extent of spill-out into the electrolyte is estimated. No direct measurement of this quantity has been made. It is consistent with theoretical estimates made for aqueous systems when allowance ,is made for the effect of the solvent.
author2 March, Norman Henry
author_facet March, Norman Henry
Painter, Katharine
author Painter, Katharine
author_sort Painter, Katharine
title The metal-electrolyte interface
title_short The metal-electrolyte interface
title_full The metal-electrolyte interface
title_fullStr The metal-electrolyte interface
title_full_unstemmed The metal-electrolyte interface
title_sort metal-electrolyte interface
publisher University of Oxford
publishDate 1983
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.348154
work_keys_str_mv AT painterkatharine themetalelectrolyteinterface
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