Solvent Adsorption and Double-Layer Potential Drop at Electrodes

  • Sergio Trasatti

Abstract

Although the primary importance of the solvent dipole contribution [gs(dip)] to the inner-layer potential drop (∆ø) was recognized long ago,1 the problem appears to be still unsettled quantitatively. This is because gs(dip) is not amenable to experimental measurement2 and thus it can only be derived indirectly through assumptions involving a model. There has recently been a strong revival of interest in the topic and a number of attempts3–15 have been made to quantify \({{g}^{{{H}_{2}}O}}\) (dip) for Hg and other metals. However, results often are in quantitative disagreement with each other and qualitative differences may be found especially in the starting models.

Keywords

Potential Drop Capacity Curve Zero Charge Hydration Free Energy Nonaqueous Solvent 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Press, New York 1979

Authors and Affiliations

  • Sergio Trasatti
    • 1
  1. 1.University of MilanMilanItaly

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