Two-Scale Analysis of the Electrostatics of Dielectric Crystals: Emergence of Polarization Density and Boundary Charges
arXiv:2602.10927 · doi:10.1137/25M1747907
Abstract
Ionic crystals, such as solid electrolytes and complex oxides, are central to modern technologies for energy storage, sensing, actuation, and other functional applications. An important fundamental issue in the atomic and quantum-scale modeling of these materials is defining the macroscopic polarization. In a periodic crystal, the usual definition of the polarization as the first moment of the charge density in a unit cell is found to depend qualitatively - allowing even a change in the sign - and quantitatively on the choice of unit cell. We examine this issue using a rigorous approach based on the framework of 2-scale convergence. By examining the continuum limit of when the lattice spacing is much smaller than the characteristic dimensions of the body, we show that the 2-scale limit provides both a bulk polarization as well as a surface charge density supported on the boundary of the body. Further, different choices of the periodic unit cell of the body lead to correspondingly different partial unit cells at the boundary; these choices give to different bulk polarization and surface charges but compensate such that the electric field and energy are independent of the choice of unit cell.
References in corpus (11)
- Flexoelectricity in soft elastomers and the molecular mechanisms underpinning the design and emergence of giant flexoelectricity
- Architected Elastomer Networks for Optimal Electromechanical Response
- Statistical Mechanical Analysis of the Electromechanical Coupling in an Electrically-Responsive Polymer Chain
- Nonlinear Statistical Mechanics Drives Intrinsic Electrostriction and Volumetric Torque in Polymer Networks
- Statistical mechanics of a dielectric polymer chain in the force ensemble
- Statistical Field Theory of Polarizable Polymer Chains with Nonlocal Dipolar Interactions
- Discrete-to-Continuum Limits of Long-Range Electrical Interactions in Nanostructures
- Exploiting Instabilities to Enable Large Shape Transformations in Dielectric Elastomers
- Nonuniqueness in Defining the Polarization: Nonlocal Surface Charges and the Electrostatic, Energetic, and Transport Perspectives
- Soft Electromechanical Elastomers Impervious to Instability
- Dipolar Self-Interactions Drive Polymer Chain Collapse