in polarography technique there is electrical double layer how the process occurs i. e.. diffusion
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The model which gave rise to the term 'electrical double layer' was first put forward in the 1850's by Helmholtz. In this model he assumed that no electron transfer reactions occur at the electrode and the solution is composed only of electrolyte. The interactions between the ions in solution and the electrode surface were asssumed to be electrostatic in nature and resulted from the fact that the electrode holds a charge density (qm)which arises from either an excess or deficiency of electrons at the electrode surface. In order for the interface to remain neutral the charge held on the electrode is balanced by the redistribution of ions close to the electrode surface. Helmholtz's view of this region
The attracted ions are assumed to approach the electrode surface and form a layer balancing the electrode charge, the distance of approach is assumed to be limited to the radius of the ion and a single sphere of solvation round each ion. The overall result is two layers of charge (the double layer) and a potential drop which is confined to only this region (termed the outer Helmholtz Plane, OHP) in solution. The result is absolutely analogous to an electrical capacitor which has two plates of charge separated by some distance with the potential drop occurring in a linear manner between the two plates. It is perhaps no surprise that when impedance analysis is performed on electrochemical systems the response due to the electrolyte redistribution is modelled in terms of capacitative elements.