The search for stable vesicular structures is a long-standing topic of research because of the usefulness of these structures and the scarcity of surfactant systems that spontaneously form vesicles in true thermodynamic equilibrium. We report the first experimental evidence of spontaneous formation of vesicles for a pure cationic double tail surfactant (didodecyldimethylammonium bromide, DDAB) in a protic ionic liquid (ethylammonium nitrate, EAN). Using small and ultra-small angle neutron scattering, rheology and bright field microscopy, we identify the coexistence of two vesicle containing phases in compositions ranging from 2 to 68 wt %. A low density highly viscous solution containing giant vesicles (D ~ 30 μm) and a sponge (L(3)) phase coexists with a dilute high density phase containing large vesicles (D ~ 2.5 μm). Vesicles form spontaneously via different thermodynamic routes, with the same size distribution, which strongly supports that they exist in a true thermodynamic equilibrium. The formation of equilibrium vesicles and the L(3) phase is facilitated by ion exchange between the cationic surfactant and the ionic liquid, as well as the strength of the solvophobic effect in the protic ionic liquid.

The self-assembly of didodecyldimethylammonium bromide (DDAB) in a protic ionic liquid, ethylammonium nitrate (EAN), in the high surfactant concentration regime is studied using five different experimental techniques. A thermoreversible first-order sponge (L(3)) to lamellar (L(α)) transition occurring at [DDAB] > 80 wt % was identified by (1) a sharp increase in the elastic and viscous moduli, (2) a transition peak recorded by differential scanning calorimetry, (3) formation of Maltese cross birefringence textures observed via polarizing optical microscopy, (4) a decrease in the interbilayer mean distance measured by small angle neutron scattering, and (5) an abrupt increase in the conductivity obstruction factor. In contrast to aqueous DDAB solutions, this surfactant forms a stable L(3) phase in EAN in a wide window of compositions and temperatures, which is potentially useful for the synthesis of nanoporous materials. To the best of our knowledge, this is the first evidence of the formation of the L(3) phase in an ionic liquid.