Ionic Liquid Solutions Show Anomalous Crowding Behavior at an Electrode Surface

X-ray reflectivity was used to study the several-nanometer-thick crowded layers that form at the interfaces between a planar electrode and concentrated solutions of ionic liquids. The ionic liquid [P-14,P-6,P-6,P-6](+)[NTf2](-) was dissolved in either strongly polar propylene carbonate or weakly polar dimethyl carbonate. In the range of 19-100 vol % ionic liquid, between working electrode potentials +2 and +2.75 V, uniform 2-7 nm thick interfacial layers were observed. These layers are not pure anions but contain three to five times as many anions as cations and about the same percentage of solvent as the bulk solution. On the other side of the layer, the density is that of the bulk solution. These features are inconsistent with a picture of the crowded layer as a region of pure, close-packed counterions. Not only the layer thickness but also the charge density decrease with increasing dilution at any given applied voltage. This appears to indicate, counterintuitively, that a thinner layer with lower net charge density will screen an electric field as effectively as a thicker layer with higher charge density.

Automated summary

X-ray reflectivity was used to study the crowded layers that form between a planar electrode and concentrated solutions of ionic liquids. The results show that the interfacial layers are not pure anions and contain more anions and solvent than the bulk solution. The thickness and charge density of the layer decrease with increasing dilution.