The electric double layer has a life of its own

Using molecular dynamics simulations with recently developed importance sampling methods, we show that the differential capacitance of a model ionic liquid based double-layer capacitor exhibits an anomalous dependence on the applied electrical potential. Such behavior is qualitatively incompatible with standard mean-field theories of the electrical double layer, but is consistent with observations made in experiment. The anomalous response results from structural changes induced in the interfacial region of the ionic liquid as it develops a charge density to screen the charge induced on the electrode surface. These structural changes are strongly influenced by the out-of-plane layering of the electrolyte and are multifaceted, including an abrupt local ordering of the ions adsorbed in the plane of the electrode surface, reorientation of molecular ions, and the spontaneous exchange of ions between different layers of the electrolyte close to the electrode surface. The local ordering exhibits signatures of a first-order phase transition, which would indicate a singular charge-density transition in a macroscopic limit

Competitive Solvation of (Bis)(trifluoromethanesulfonyl)imide Anion by Acetonitrile and Water

Competitive solvation of an ion by two or more solvents is one of the key phenomena determining the identity of our world. Solvation in polar solvents frequently originates from non-additive non-covalent interactions. Pre-parametrized potentials poorly capture these interactions, unless the force field derivation is repeated for every new system. Development cost increases drastically as new chemical species are supplied. This work represents an alternative simulation approach, PM7-MD, by coupling the latest semiempirical parametrization, PM7, with equation-of-motion propagation scheme and temperature coupling. Using a competitive solvation of (bis)(trifluoromethanesulfonyl)imide anion in acetonitrile and water, the work demonstrates efficiency and robustness of PM7-MD

NMR and Rheological Study of Anion Size Influence on the Properties of Two Imidazolium-based Ionic Liquids

NMR self-diffusion and relaxation, coupled with viscosity, were used to study the properties and structure of two imidazolium-based ionic liquids, 1-ethyl-3-methylimidazolium acetate [C2MIM][OAc] and 1-ethyl-3-methylimidazolium octanoate [C2MIM][OOct]. The experimental results point to the formation of different types of aggregates in each ionic liquid. These aggregates are small and stable under flow and temperature in [C2MIM][OAc], whereas the aggregates are large and sensitive to flow and temperature in [C2MIM][OOct]. In the latter case the size of aggregates decreases both under flow and temperature increase

Solvation Structure of Uracil in Ionic Liquids

The local solvation environment of uracil dissolved in the ionic liquid 1-ethyl-3-methylimidazolium acetate has been studied using neutron diffraction techniques. At solvent:solute ratios of 3:1 and 2:1 ionic liquid:uracil, little perturbation of the ion-ion correlations compared to those of the neat ionic liquid are observed. We find that solvation of the uracil is driven predominantly by the acetate anion of the solvent. While short distance correlations exist between uracil and the imidazolium cation, the geometry of these contacts suggest that they cannot be considered as hydrogen bonds, in contrast to other studies by Araújo et al. (J. M. Araújo, A. B. Pereiro, J. N. Canongia-Lopes, L. P. Rebelo, I. M. Marrucho, J. Phys. Chem. B 2013, 117, 4109-4120). Nevertheless, this combination of interactions of the solute with both the cation and anion components of the solvents helps explain the high solubility of the nucleobase in this media. In addition, favorable uracil-uracil contacts are observed, of similar magnitude to those between cation and uracil, and are also likely to aid dissolutio

Solvation behavior of cellulose and xylan in the MIM/EMIMAc ionic liquid solvent system – parameters for small scale solvation

Ionic liquid treatment has been reported by several researchers as a possible step in the process of fractionating lignocellulosic biomass within the biorefinery concept. However, understanding how solvation can be achieved and how the feedstock biopolymers are affected is needed prior to a viable implementation. An effective two component solvent system for the wood components cellulose and xylan has been developed. Furthermore, the solvation of these components in the system consisting of the ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate (EMIMAc) in a novel combination with the co-solvent 1-methylimidazole (MIM) is investigated. Focused beam reflectance measurement (FBRM) particle characterization in combination with microscopic analysis and molecular weight determinations (xylan) shows that cellulose and xylan can be most efficiently solvated using only 3 to 4% IL (n/n anhydro-glucose units and n/n anhydro-xylose units) and 9% IL, respectively, while still avoiding any significant polymer degradation. A model for a two-step process of cellulose solvation in the present system is proposed

Dimerization of ion radicals in ionic liquids. An example of favourable "Coulombic" solvation.

International audienceThe irreversible dimerization of the acetophenone radical anion, chosen as an example of a carbon-carbon coupling reaction between two charged species, was investigated in a series of 1,3-dialkylimidazolium and 1,2,3-trialkylimidazolium ionic liquids. Indeed, such ion dimerizations which display slow kinetics despite small activation energies, are controlled by a subtle competition between bond formation, Coulombic repulsion and solvation. The effects of viscosity, "polarity" and ionic solvation on the reactivity of the radical anions were examined. The dimerization rate constants were demonstrated to be only weakly affected by the high viscosity of the medium or its apparent polarity. When the acetophenone radical anion is "solvated" in imidazolium-based ionic liquids, a strong interaction between the negatively-charged intermediates and the imidazolium cation occurs. The ensuing charge stabilization allows a fast dimerization step in all the ionic liquids used. The kinetic effect is even enhanced in the 1,3-dialkylimidazolium salts as compared to the 1,2,3-trialkylimidazolium ones because the interaction between the radical anions and the 1,3-dialkylimidazolium cations are stronger, probably due to the formation of H-bond. The reactivity of the ion radical is demonstrated not only to be mainly dominated by electrostatic interactions, but also that the nature of the ionic liquid cations with respect to that of the ion radical is a major factor that affects the reaction kinetics

Computational approaches to understanding reaction outcomes of organic processes in ionic liquids

This review considers how various computational methods have been applied to explain the changes in reaction outcome on moving from a molecular to an ionic liquid solvent. Initially, different conceptual approaches to modelling ionic liquids are discussed, followed by a consideration of the limitations and constraints of these approaches. A series of case studies demonstrating the utility of computational approaches to explain processes in ionic liquids are considered; some of these address the solubility of species in ionic liquids while others examine classes of reaction where the outcome in ionic liquids can be explained through the application of computational approaches. Overall, the utility of computational methods to explain, and potentially predict, the effect of ionic liquids on reaction outcome is demonstrated