arXiv subjects

Harold S Park

Publications and source records attributed to Harold S Park.

3 recordsLinked to original sources

arXiv2026

Driven Odd Elasticity in Passive Mechanical Metamaterials

We present a mechanical mechanism leveraging passive mechanical components, i.e. chiral gears and a square lattice metamaterial, to demonstrate driven odd elasticity in a mechanical metamaterial. The mechanism couples tension and shear in a non-reciprocal way, resulting in an odd shear modulus. The emergence of this odd shear modulus enables non-conservative work in a standard quasistatic strain cycle, and further enables the non-Hermitian skin effect in dynamics. Our results demonstrate that odd elasticity can be achieved in mechanical structures using passive elements without electronic components coupled with feedback or robotic control systems.

cond-mat.soft↗

arXiv2022

High flexoelectric constants in Janus transition-metal dichalcogenides

Due to their combination of mechanical stiffness and flexibility, two-dimensional (2D) materials have received significant interest as potential electromechanical materials. Flexoelectricity is an electromechanical coupling between strain gradient and polarization. Unlike piezoelectricity, which exists only in non-centrosymmetric materials, flexoelectricity theoretically exists in all dielectric materials. However, most work on the electromechanical energy conversion potential of 2D materials has focused on their piezoelectric, and not flexoelectric behavior and properties. In the present work, we demonstrate that the intrinsic structural asymmetry present in monolayer Janus transition metal dichalcogenides (TMDCs) enables significant flexoelectric properties. We report these flexoelectric properties using a recently developed charge-dipole model that couples with classical molecular dynamics simulations. By employing a prescribed bending deformation, we directly calculate the flexoelectric constants while eliminating the piezoelectric contribution to the polarization. We find that the flexoelectric response of a Janus TMDC is positively correlated to its initial degree of asymmetry, which contributes to stronger $σ-σ$ interactions as the initial degree of asymmetry rises. In addition, the high transfer of charge across atoms in Janus TMDCs leads to larger electric fields due to $π-σ$ coupling. These enhanced $σ-σ$ and $π-σ$ interactions are found to cause the flexoelectric coefficients of the Janus TMDCs to be several times higher than traditional TMDCs such as MoS$_{2}$, whose flexoelectric constant is already ten times larger than graphene.

cond-mat.mtrl-sci↗

arXiv2012

A molecular simulation analysis of producing monatomic carbon chains by stretching ultranarrow graphene nanoribbons

Atomistic simulations were utilized to develop fundamental insights regarding the elongation process starting from ultranarrow graphene nanoribbons (GNRs) and resulting in monatomic carbon chains (MACCs). There are three key findings. First, we demonstrate that complete, elongated, and stable MACCs with fracture strains exceeding 100% can be formed from both ultranarrow armchair and zigzag GNRs. Second, we demonstrate that the deformation processes leading to the MACCs have strong chirality dependence. Specifically, armchair GNRs first form DNA-like chains, then develop into monatomic chains by passing through an intermediate configuration in which monatomic chain sections are separated by two-atom attachments. In contrast, zigzag GNRs form rope-ladder-like chains through a process in which the carbon hexagons are first elongated into rectangles; these rectangles eventually coalesce into monatomic chains through a novel triangle-pentagon deformation structure under further tensile deformation. Finally, we show that the width of GNRs plays an important role in the formation of MACCs, and that the ultranarrow GNRs facilitate the formation of full MACCs. The present work should be of considerable interest due to the experimentally demonstrated feasibility of using narrow GNRs to fabricate novel nanoelectronic components based upon monatomic chains of carbon atoms.

physics.comp-ph↗