| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 218159 | Journal of Electroanalytical Chemistry | 2015 | 8 Pages |
•Ionic liquid(IL)/water(W) interface has been studied using x-ray reflectometry.•Surface of the IL shows multilayering of ions with low-density topmost layer.•Cation bilayer is formed at the IL/W interface when IL side is positively charged.•A model for the electrical double layer at the IL/W interface is presented.
The structure at air interface and water (W) interface of a hydrophobic ionic liquid (IL), trioctylmethylammonium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate ([TOMA+][TFPB−]), has been studied using x-ray reflectometry. Multilayering of ions has been found at the IL/air interface, with the topmost ionic layer having lower density than the IL bulk. For the IL/W interface, x-ray reflectivity data depends on the phase-boundary potential across the IL/W interface. When the phase-boundary potential of W with respect to IL, ΔILWϕ, is + 0.20 V, TFPB− ions are accumulated at the topmost ionic layer on the IL side of the IL/W interface. On the other hand, when ΔILWϕ = - 0.27 V, the accumulation of TOMA+ ions occurs with bilayer thickness, which is probably due to local interaction between TOMA+ ions at the topmost layer and at the second layer through interdigitation of their alkyl chains. To quantitatively analyze the x-ray reflectivity data, we construct a model of the electrical double layer (EDL) at the IL/W interface, by combining the Gouy–Chapman–Stern model on the W side and the Oldham model on the IL side. The constructed model predicts that the EDL on the IL side is within the topmost layer for the phase-boundary potentials in the present study, suggesting that the TOMA+ bilayer found at the negative potential results from the local interaction beyond the framework of the present mean-field theory. Even at the positive potential the surface charge density predicted by the EDL theory is significantly smaller than that estimated from x-ray reflectivity data, which implies that densification of the topmost ionic layer leads us to overestimate the surface charge density.
