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Polymeric materials that couple deformation and electrostatics have the potential for use in soft sensors and actuators with potential applications ranging from robotic, biomedical, energy, aerospace and automotive technologies. In contrast to the mechanics of polymers that has been studied using statistical mechanics approaches for decades, the coupled response under deformation and electrical field has largely been modeled only phenomenologically at the continuum scale. In this work, we examine the physics of the coupled deformation and electrical response of an electrically-responsive polymer chain using statistical mechanics. We begin with a simple anisotropic model for the electrostatic dipole response to electric field of a single monomer, and use a separation of energy scales between the electrostatic field energy and the induced dipole field energy to reduce the nonlocal and infinite-dimensional statistical averaging to a simpler local finite-dimensional averaging. In this simplified setting, we derive the equations of the most likely monomer orientation density using the maximum term approximation, and a chain free energy is derived using this approximation. These equations are investigated numerically and the results provide insight into the physics of electro-mechanically coupled elastomer chains. Closed-form approximations are also developed in the limit of small electrical energy with respect to thermal energy; in the limit of small mechanical tension force acting on the chain; and using asymptotic matching for general chain conditions.
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DISCRETE-TO-CONTINUUM LIMITS OF LONG-RANGE ELECTRICAL INTERACTIONS IN NANOSTRUCTURES
We consider electrostatic interactions in two classes of nanostructures embedded in a three dimensional space: (1) helical nanotubes, and (2) thin films with uniform bending (i.e., constant mean curvature). Starting from the atomic scale with a discrete distribution of dipoles, we obtain the continuum limit of the electrostatic energy; the continuum energy depends on the geometric parameters that define the nanostructure, such as the pitch and twist of the helical nanotubes and the curvature of the thin film. We find that the limiting energy is local in nature. This can be rationalized by noticing that the decay of the dipole kernel is sufficiently fast when the lattice sums run over one and two dimensions, and is also consistent with prior work on dimension reduction of continuum micromagnetic bodies to the thin film limit. However, an interesting contrast between the discrete-to-continuum approach and the continuum dimension reduction approaches is that the limit energy in the latter depends only on the normal component of the dipole field, whereas in the discrete-to-continuum approach, both tangential and normal components of the dipole field contribute to the limit energy.
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- PAR ID:
- 10404561
- Date Published:
- Journal Name:
- Archive for rational mechanics and analysis
- Volume:
- 247
- ISSN:
- 0003-9527
- Page Range / eLocation ID:
- 29
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
-
Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1007/s00205-023-01869-6
