Electrostatics of liquid interfaces

Abstract

The standard Maxwell formulation of the problem of polarized dielectrics suffers from a number of difficulties, both conceptual and practical. These difficulties are particularly significant in the case of liquid interfaces, where the ability of the interfacial multipoles to change their orientations to minimize their free energies leads to interfacial polarization localized within a thin microscopic layer. A formalism to capture this physical reality of localized interfacial polarization is proposed and is based on the surface charge as the source of microscopic electric fields in dielectrics. The surface charge density incorporates the local structure of the interface into electrostatic calculations. The corresponding surface susceptibility and interface dielectric constant provide local closures to the electrostatic boundary value problem. A robust approach to calculate the surface susceptibility from numerical simulations is proposed. The susceptibility can alternatively be extracted from a number of solution experiments, in particular those sensitive to the overall dipole moment of a closed dielectric surface. The theory is applied to the solvent-induced spectral shift and high-frequency dielectric response of solutions.

References in corpus (3)

• The vapor-liquid interface potential of (multi)polar fluids and its influence on ion solvation
• Electrostatics of liquid interfaces
• Electrostatic fluctuations in cavities within polar liquids and thermodynamics of polar solvation

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