Analysis of charging-induced structural damage in electrochemical systems

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2 Scopus citations

Abstract

Electrochemical charging of an electrochemical system results in Maxwell stress and a variation in the surface energy of the electrode. The charging-induced variation in the surface energy of the electrode and Maxwell stress introduce mechanical deformation and create stresses in the electrode. To relax the strain energy stored in the electrode, surface cracking and buckling can occur. Under the condition that the charging-induced change in the surface energy is the dominant factor controlling the in-plane deformation of a planar electrode, i.e. the bonding between the adsorbate and the substrate is weak, the variation in the surface energy of the electrode can be described by the Lippmann equation. Using the Lippmann equation, both the surface charge density on the electrode and the surface energy of the electrode are formulated as a function of the electrode potential. Analytical relations between the critical electrode potential and average damage size have been obtained for the charging-induced cracking and buckling in a planar, thin-film electrode. The results show that surface cracking will prevail over local buckling in accordance with experimental observations. Both critical electrode potentials are inversely proportional to the square root of the magnitude of the differential capacity of the electrical double layer at the electrode potential of zero charge.

Original languageEnglish
Pages (from-to)7072-7077
Number of pages6
JournalPhysical Chemistry Chemical Physics
Volume19
Issue number10
DOIs
StatePublished - 2017

Bibliographical note

Funding Information:
This work was supported by the NSF through grant CMMI-1634540, monitored by Dr Khershed Cooper, and was supported by the KSEF through grant KSEF-148-502-15-341.

Publisher Copyright:
© the Owner Societies 2017.

Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.

ASJC Scopus subject areas

  • Physics and Astronomy (all)
  • Physical and Theoretical Chemistry

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