Electrochemically driven first-order phase transitions caused by elastic responses of ion-insertion electrodes under external kinetic control

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Abstract

This work is devoted to an extension of the continuum elasticity model combined with the classical lattice-gas (LG) model that recently appeared in the literature and described guest ion insertion into various host materials. The extension involves two important aspects: (i) derivation of intercalation isotherms with four different elastic parameters with the purpose to find their critical combination, leading to first-order phase transitions, and (ii) quantitative treatment of the first-order phase transition reactions controlled by slow external kinetics. This analysis helps to understand properly an important issue of the mechanism of electrochemically driven first-order phase transitions in various ion-insertion electrodes often disregarded in the literature: whatever the concerned electrochemical characteristics are measured, the underlying (often hidden, in practice) kinetic limitations must be considered. The analysis described herein refers to the dependence of the (chemical) differential intercalation capacitance, Cdif, and of the chemical diffusion coefficient, D, on the concentration of Li-ions in graphite in the course of electrochemical lithiation/delithiation of these electrodes.

Original languageEnglish
Pages (from-to)251-261
Number of pages11
JournalJournal of Electroanalytical Chemistry
Volume624
Issue number1-2
DOIs
StatePublished - 1 Dec 2008

Bibliographical note

Funding Information:
This work was supported by the GIF (German–Israel Foundation).

Funding

This work was supported by the GIF (German–Israel Foundation).

FundersFunder number
German–Israel Foundation
German-Israeli Foundation for Scientific Research and Development

    Keywords

    • Chemical diffusion coefficient
    • Differential intercalation capacitance
    • First-order phase transition
    • GITT
    • Intercalation
    • Li-ion batteries
    • PITT

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