RESUMEN
The nanoscale organization of electrolyte solutions at interfaces is often described well by the electrical double-layer model. However, a recent study has shown that this model breaks down in solutions of LiClO4 in acetonitrile at a silica interface, because the interface imposes a strong structuring in the solvent that in turn determines the preferred locations of cations and anions. As a surprising consequence of this organisation, the effective surface potential changes from negative at low electrolyte concentration to positive at high electrolyte concentration. Here we combine previous ion-current measurements with vibrational sum-frequency-generation spectroscopy experiments and molecular dynamics simulations to explore how the localization of ions at the acetonitrile-silica interface depends on the sizes of the anions and cations. We observe a strong, synergistic effect of the cation and anion identities that can prompt a large difference in the ability of ions to partition to the silica surface, and thereby influence the effective surface potential. Our results have implications for a wide range of applications that involve electrolyte solutions in polar aprotic solvents at nanoscale interfaces.
RESUMEN
Dielectric permittivity is central to many biological and physiochemical systems, as it affects the long-range electrostatic interactions. Similar to many fluid properties, confinement greatly alters the dielectric response of polar liquids. Many studies have focused on the reduction of the dielectric response of water under confinement. Here, using molecular dynamics simulations, statistical-mechanical theories, and multiscale methods, we study the out-of-plane (z-axis) dielectric response of protic and aprotic fluids confined inside slit-like graphene channels. We show that the reduction in perpendicular permittivity is universal for all the fluids and exhibits a Langevin-like behavior as a function of channel width. We show that this reduction is due to the favorable in-plane (x-y plane) dipole-dipole electrostatic interactions of the interfacial fluid layer. Furthermore, we observe an anomalously low dielectric response under an extreme confinement.
RESUMEN
Enhancement of parallel (x-y plane) dielectric permittivity of confined fluids has been shown previously. However, a theoretical model that explains this enhancement is lacking thus far. In this study, using statistical-mechanical theories and molecular dynamics simulations, we show an explicit relation between the parallel dielectric permittivity, density variations, and dipolar correlations for protic and aprotic fluids confined in slit-like channels. We analyze the importance of dipolar correlations on enhancement of parallel dielectric permittivity inside large channels and extreme confinements. In large channels, beyond the interfacial region, dipolar correlations exhibit bulk-like behavior. Under extreme confinement, the correlations become stronger to the extent that they give rise to a giant increase in the parallel dielectric permittivity. This sudden increase in dielectric permittivity can be a signature of a liquid transition into higher-ordered structures and has important consequences for understanding ion transport, molecular dissociation, and chemical reactions inside nanoconfined environments.
RESUMEN
We develop coarse-grained force fields (CGFFs) for computationally efficient and accurate molecular simulation of imidazolium-based ionic liquids. To obtain CGFF parameters, we employ a systematic coarse-graining approach based on the relative entropy (RE) method to reproduce not only the structure but also the thermodynamic properties of the reference all-atom molecular model. Our systematic coarse-graining approach adds a constraint to the RE minimization using the Lagrange multiplier method in order to reproduce thermodynamic properties such as pressure. The Boltzmann inversion technique is used to obtain the bonded interactions, and the non-bonded and long-range electrostatic interactions are obtained using the constrained relative entropy method. The structure and pressure obtained from the coarse-grained (CG) models for different alkyl chain lengths are in agreement with the all-atom molecular dynamics simulations at different thermodynamic states. We also find that the dynamical properties, such as diffusion, of the CG model preserve the faster dynamics of bulky cation compared to the anion. The methodology developed here for reproduction of thermodynamic properties and treatment of long-range Coulombic interactions is applicable to other soft-matter.