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Abstract Recent theoretical work has predicted that dislocation patterning induces anisotropic flat bands in the electronic band diagram, which can lead to unusual effects such as unconventional superconductivity. This work develops a reduced-dimensional framework to provide insights into their origin. An effective one-dimensional dislocation potential is constructed by averaging over the spatial distributions of dislocations along a singular direction. The resulting model introduces a parameter that quantifies the strain modulation, thereby providing a transparent approach to analyze the role of dislocation strain in leading to flat band formation. 

Two-dimensional (2D) electronic materials are of significant technological interest due to their exceptional properties and broad applicability in engineering. The transition from nanoscale physics, which dictates their stable configurations, to macroscopic engineering applications requires the use of multiscale methods to systematically capture their electronic properties at larger scales. A key challenge in coarse-graining is the rapid and near-periodic variation of the charge density, which exhibits significant spatial oscillations at the atomic scale. Therefore, the polarization density field—the first moment of the charge density over the periodic unit cell—is used as a multiscale mediator that enables efficient coarse-graining by exploiting the almost-periodic nature of the variation. Unlike the highly oscillatory charge density, the polarization varies over lengthscales that are much larger than the atomic, making it suitable for continuum modeling. In this paper, we investigate the electrostatic potential arising from the charge distribution of arbitrarily-deformed 2D materials. Specifically, we consider a sequence of problems wherein the underlying lattice spacing vanishes and thus obtain the continuum limit. We consider three distinct limits: where the thickness is much smaller than, comparable to, and much larger than the in-plane lattice spacing. These limiting procedures provide the homogenized potential expressed in terms of the boundary charge and dipole distribution, subject to the appropriate boundary conditions that are also obtained through the limit process. Furthermore, we demonstrate that despite the intrinsic non-uniqueness in the definition of polarization, accounting for the boundary charges ensures that the total electrostatic potential, the associated electric field, and the corresponding energy of the homogenized system are uniquely determined. 

We report that a dielectric polymer chain, constrained at both ends, sharply collapses when exposed to a high electric field. The chain collapse is driven by nonlocal dipolar interactions and anisotropic polarization of monomers, a characteristic of real polymers that prior theories were unable to incorporate. Once collapsed, a large number of chain monomers accumulate at the center location between the chain ends, locally increasing the electric field and polarization by orders of magnitude. The chain collapse is sensitive to the orientation of the applied electric field and chain stretch. Our findings not only offer new ways for rapid actuation and sensing but also provide a pathway to discover the critical physics behind instabilities and electrical breakdown in dielectric polymers. 

This paper addresses a two-dimensional sharp interface variational model for solid-state dewetting of thin films with surface energies, introduced byWang, Jiang, Bao, and Srolovitz in Jiang et al. (Scr Mater 115:123–127, 2016). Using the H−1-gradient flow structure of the evolution law, short-time existence for a surface diffusion evolution equation with curvature regularization is established in the context of epitaxially strained two-dimensional films. The main novelty, as compared to the study of the wetting regime, is the presence of moving contact lines.