Unilamellar Vesicle Formation and Microscopic Structure of Ionic Liquids in Aqueous Solutions
journal contributionposted on 14.01.2016, 00:00 authored by Xiaomin Liu, Guohui Zhou, Feng Huo, Jianji Wang, Suojiang Zhang
Imidazolium-based ionic liquid [Cnmim]Br (n = 10, 12, 14) without any additives in aqueous solutions could form unilamellar vesicles was first observed by TEM recently. As molecular aggregation is a complex phenomenon which is difficult to study in detail experimentally, we performed molecular simulations for [Cnmim]Br (n = 10, 12, 14) aqueous solutions. The entire process of spontaneous aggregation for [C12mim]Br into small unilamellar vesicle was elucidated. Radial distribution functions reveal that the strong spatial correlation between cation and anion still exists in the presence of a large amount of water. The inner layer of vesicle is packed denser than the outer layer by analyzing the radial density distribution. Furthermore, anions distribution provides the direct evidence for very little anions being dissolved in the water and verifies the experimental speculation. By analyzing hydrogen bond number and coordination number in the solution, it is implied that binding between counterions enhanced with increasing IL concentration, and the distribution density of ions in vesicle is close to the neat system. Moreover, it is observed that aggregation is facilitated with increasing the alkyl chains by comparing three aqueous solution systems. Additionally, spatial correlation between chain terminal C becomes stronger with increasing the alkyl chain length.
Read the peer-reviewed publication
alkyl chain lengthIonic Liquidsalkyl chainsTEMsolution systemsdensity distributiondistribution densityanions distributionhydrogen bond numberIL concentrationRadial distribution functionschain terminal CCnmimaggregationMicroscopic StructureC 12mimunilamellar vesiclescoordination numberUnilamellar Vesicle Formationcorrelationunilamellar vesicle