INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES

In this paper we compare two different approaches for the calculation of the enhancement factor W<sub>i</sub>, based on its definition as the ratio of the chemical and the component diffusion coefficients for species in mixed-conduction electrodes, originated from the "dilute soluti...

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Main Authors: M.D.Levi, D.Aurbach, M.A.Vorotyntsev
Format: Article
Language:English
Published: Institute for Condensed Matter Physics 2002-01-01
Series:Condensed Matter Physics
Subjects:
Online Access:http://dx.doi.org/10.5488/CMP.5.2.329
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spelling doaj-04bfcf0ea0734cac9f3c1f39093ba0a52020-11-24T22:51:13ZengInstitute for Condensed Matter PhysicsCondensed Matter Physics1607-324X2002-01-015232936210.5488/CMP.5.2.329INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODESM.D.LeviD.AurbachM.A.VorotyntsevIn this paper we compare two different approaches for the calculation of the enhancement factor W<sub>i</sub>, based on its definition as the ratio of the chemical and the component diffusion coefficients for species in mixed-conduction electrodes, originated from the "dilute solution" or "lattice gas" models for the ion system. The former approach is only applicable for small changes of the ion concentration while the latter allows one to consider a broad range of intercalation levels. The component diffusion coefficient of lithium ions has been determined for a series of lithium intercalation anodes and cathodes. A new "enhancement factor" for the ion transport has been defined and its relations to the intercalation capacitance and the intercalation isotherm have been established. A correlation between the dependences of the differential capacitance and the partial ion conductivity on the potential has been observed. It is considered as a prove that the intercalation process is controlled by the availability of sites for Li-ion insertion rather than by the concurrent insertion of the counter-balancing electronic species.http://dx.doi.org/10.5488/CMP.5.2.329Li-ion batterybinary componentchemical diffusion coefficientionic conductivitylattice gas model
collection DOAJ
language English
format Article
sources DOAJ
author M.D.Levi
D.Aurbach
M.A.Vorotyntsev
spellingShingle M.D.Levi
D.Aurbach
M.A.Vorotyntsev
INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES
Condensed Matter Physics
Li-ion battery
binary component
chemical diffusion coefficient
ionic conductivity
lattice gas model
author_facet M.D.Levi
D.Aurbach
M.A.Vorotyntsev
author_sort M.D.Levi
title INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES
title_short INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES
title_full INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES
title_fullStr INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES
title_full_unstemmed INTERPRETATION OF POTENTIAL INTERMITTENCE TITRATION TECHNIQUE EXPERIMENTS FOR VARIOUS Li-INTERCALATION ELECTRODES
title_sort interpretation of potential intermittence titration technique experiments for various li-intercalation electrodes
publisher Institute for Condensed Matter Physics
series Condensed Matter Physics
issn 1607-324X
publishDate 2002-01-01
description In this paper we compare two different approaches for the calculation of the enhancement factor W<sub>i</sub>, based on its definition as the ratio of the chemical and the component diffusion coefficients for species in mixed-conduction electrodes, originated from the "dilute solution" or "lattice gas" models for the ion system. The former approach is only applicable for small changes of the ion concentration while the latter allows one to consider a broad range of intercalation levels. The component diffusion coefficient of lithium ions has been determined for a series of lithium intercalation anodes and cathodes. A new "enhancement factor" for the ion transport has been defined and its relations to the intercalation capacitance and the intercalation isotherm have been established. A correlation between the dependences of the differential capacitance and the partial ion conductivity on the potential has been observed. It is considered as a prove that the intercalation process is controlled by the availability of sites for Li-ion insertion rather than by the concurrent insertion of the counter-balancing electronic species.
topic Li-ion battery
binary component
chemical diffusion coefficient
ionic conductivity
lattice gas model
url http://dx.doi.org/10.5488/CMP.5.2.329
work_keys_str_mv AT mdlevi interpretationofpotentialintermittencetitrationtechniqueexperimentsforvariousliintercalationelectrodes
AT daurbach interpretationofpotentialintermittencetitrationtechniqueexperimentsforvariousliintercalationelectrodes
AT mavorotyntsev interpretationofpotentialintermittencetitrationtechniqueexperimentsforvariousliintercalationelectrodes
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