Dielectric modulation of ion transport near interfaces
arXiv:1809.05213 · doi:10.1103/PhysRevLett.120.135501
Abstract
Ion mobility and ionic conductance in nanodevices are known to deviate from bulk behavior, a phenomenon often attributed to surface effects. We demonstrate that dielectric mismatch between the electrolyte and the surface can qualitatively alter ionic transport in a counterintuitive manner. Instead of following the polarization-induced modulation of the concentration profile, mobility is enhanced or reduced by changes in the ionic atmosphere near the interface and affected by a polarization force parallel to the surface. In addition to revealing this mechanism, we explore the effect of salt concentration and electrostatic coupling.
References in corpus (4)
- Salt-induced collapse and reexpansion of highly charged flexible polyelectrolytes
- Universality class of criticality in the restricted primitive model electrolyte
- Ionic transport through sub-10 nm diameter hydrophobic high-aspect ratio nanopores: experiment, theory and simulation
- Ionic exclusion phase transition in neutral and weakly charged cylindrical nanopores
Cited by in corpus (10)
- Accelerated simulation method for charge regulation effects
- Effects of Surface Trapping and Contact Ion Pairing on Ion Transport in Nanopores
- Asymmetric electrolytes near structured dielectric interfaces
- Manipulation of confined polyelectrolyte conformations through dielectric mismatch
- Frequency and field-dependent response of confined electrolytes from Brownian dynamics simulations
- Accurate and Efficient Numerical Simulation of Dielectrically Anisotropic Particles
- HSMA: An O(N) electrostatics package implemented in LAMMPS
- Broken Symmetries in Quasi-2D Charged Systems via Negative Dielectric Confinement
- Ewald summation for ion-dipole mixture under dielectric confinement
- Competition between Born solvation, dielectric exclusion, and Coulomb attraction in spherical nanopores