Aqueous, Mixed Micelles as a Means of Delivering the Hydrophobic Ionic Liquid EMIM TFSI to Graphene Oxide Surfaces

Most ionic liquids (ILs) are not surface-active and cannot, alone, be directed to assemble at surfaces-despite their potential as nonvolatile structure-directing agents and use as advanced materials in a multitude of applications. In this work, we investigate aqueous systems of common nonionic surfactants (Triton X-100 and Tween 20), which we use to solubilize 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide. The resulting solution of mixed micelle leads to spontaneous adsorption of the IL/surfactant complex onto graphene oxide (GO) surfaces, forming a compact film. Adsorption isotherms generated by fluorescence labeling of the IL and surfactant phases are used to quantify the extent of adsorption. While sensitive to the GO dispersion concentration, upwards of 3 g IL/g GO adsorb under dilute conditions. Atomic force microscopy is used to show that the adsorbed layer uniformly distributes as an similar to 1 nm thick coating (per GO side) as the system reaches the first plateau of a Langmuir-type isotherm. Adsorption beyond this plateau is possible but leads to thicker (>30 nm), inhomogeneous adsorbed layers. Both micellar size in solution and adsorbed layer thickness reduce upon the addition of IL to the surfactant phase, suggesting significant interactions among the materials and nonideal mixing of the components.

Automated summary

In this study, aqueous systems of common nonionic surfactants were used to investigate the adsorption of ionic liquids onto graphene oxide surfaces. The results showed that a compact film can be formed through the spontaneous adsorption of the IL/surfactant complex. The addition of IL to the surfactant phase led to a reduction in micellar size and adsorbed layer thickness, suggesting significant interactions and nonideal mixing among the components.