Statistical Field Theory of Polarizable Polymer Chains with Nonlocal Dipolar Interactions
arXiv:2404.02848 · doi:10.1103/PhysRevE.109.044501
Abstract
The electromechanical response of polymeric soft matter to applied electric fields is of fundamental scientific interest as well as relevant to technologies for sensing and actuation. Several existing theoretical and numerical approaches for polarizable polymers subject to a combined applied electric field and stretch are based on discrete monomer models. In these models, accounting for the interactions between the induced dipoles on monomers is challenging due to the nonlocality of these interactions. On the other hand, the framework of statistical field theory provides a continuous description of polymer chains that potentially enables a tractable way to account for these interactions. However, prior formulations using this framework have been restricted to the case of weak anisotropy of the monomer polarizability. This paper formulates a general approach based in the framework of statistical field theory to account for the nonlocal nature of the dipolar interactions without any restrictions on the anisotropy or nonlinearity of the polarizability of the monomer. The approach is based on 3 key elements: (1) the statistical field theory framework, in which the discrete monomers are regularized to a continuous dipole distribution; (2) a replacement of the nonlocal dipole-dipole interactions by the local electrostatics PDE with the continuous dipole distribution as the forcing; (3) the use of a completely general relation between the polarization and the local electric field. Rather than treat the dipole-dipole interactions directly, the continuous description in the field theory enables the computationally-tractable nonlocal-to-local transformation. Further, it enables the use of a realistic statistical-mechanical ensemble wherein the average far-field applied electric field is prescribed, rather than prescribing the applied field at every point in the polymer domain.
References in corpus (12)
- Modeling of emergent memory and voltage spiking in ionic transport through angström-scale slits
- Flexoelectricity in soft elastomers and the molecular mechanisms underpinning the design and emergence of giant flexoelectricity
- The interplay between symmetry-breaking and symmetry-preserving bifurcations in soft dielectric films and the emergence of giant electro-actuation
- 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
- A finite element approach to self-consistent field theory calculations of multiblock polymers
- Statistical mechanics of a dielectric polymer chain in the force ensemble
- Polymer networks which locally rotate to accommodate stresses, torques, and deformation
- Statistical field theory for nonlinear elasticity of polymer networks with excluded volume interactions
- Modulation of ionic conduction using polarizable surfaces
- A Dimensionally-Reduced Nonlinear Elasticity Model for Liquid Crystal Elastomer Strips with Transverse Curvature
Cited by in corpus (5)
- Active matter as the underpinning agency for extraordinary sensitivity of biological membranes to electric fields
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- Nonuniqueness in Defining the Polarization: Nonlocal Surface Charges and the Electrostatic, Energetic, and Transport Perspectives
- Soft Electromechanical Elastomers Impervious to Instability
- Two-Scale Analysis of the Electrostatics of Dielectric Crystals: Emergence of Polarization Density and Boundary Charges