Selective excitation of plasmons superlocalized at sharp perturbations of metal nanoparticles

Sharp metal corners and tips support plasmons localized on the scale of the curvature radius -- superlocalized plasmons. We analyze plasmonic properties of nanoparticles with small and sharp corner- and tip-shaped surface perturbations in terms of hybridization of the superlocalized plasmons, which frequencies are determined by the perturbations shape, and the ordinary plasmons localized on the whole particle. When the frequency of a superlocalized plasmon gets close to that of the ordinary plasmon, their strong hybridization occurs and facilitates excitation of an optical hot-spot near the corresponding perturbation apex. The particle is then employed as a nano-antenna that selectively couples the free-space light to the nanoscale vicinity of the apex providing precise local light enhancement by several orders of magnitude

Tunability of wire-grid metamaterial immersed into nematic liquid crystal

We propose electrically tunable hybrid metamaterial consisting of special wire grid immersed into nematic liquid crystal. The plasma-like permittivity of the structure can be substantially varied due to switching of the liquid crystal alignment by external voltages applied to the wires. Depending on the scale of the structure, the effect is available for both microwave and optical frequency ranges.Comment: 3 page

Effect of nanoparticle chain formation on dielectric anisotropy of nematic composites

A general theory of the dielectric constant of nematic liquid crystal mixtures is presented including the particular case of nematics doped with polar nanoparticles. The results are used to estimate the contribution of chains of polar nanoparticles to the static dielectric anisotropy and birefringence of the nematic composite taking into account contributions from chains of different lengths. The dependence of the dielectric anisotropy on the dipolar interaction strength is considered in detail and it is shown that formation of polar chains of nanoparticles enables one to explain a significant increase of the dielectric constant of the composite as observed experimentally

Phase behavior and orientational ordering in block copolymers doped with anisotropic nanoparticles

A molecular field theory and coarse-grained computer simulations with dissipative particle dynamics have been used to study the spontaneous orientational ordering of anisotropic nanoparticles in the lamellar and hexagonal phases of diblock copolymers and the effect of nanoparticles on the phase behavior of these systems. Both the molecular theory and computer simulations indicate that strongly anisotropic nanoparticles are ordered orientationally mainly in the boundary region between the domains and the nematic order parameter possesses opposite signs in adjacent domains. The orientational order is induced by the boundary and by the interaction between nanoparticles and the monomer units in different domains. In simulations, sufficiently long and strongly selective nanoparticles are ordered also inside the domains. The nematic order parameter and local concentration profiles of nanoparticles have been calculated numerically using the model of a nanoparticle with two interaction centers and also determined using the results of computer simulations. A number of phase diagrams have been obtained which illustrate the effect of nanoparticle selectivity and molar fraction of the stability ranges of various phases. Different morphologies have been identified by analyzing the static structure factor and a phase diagram has been constructed in coordinates' nanoparticle concentration-copolymer composition. Orientational ordering of even a small fraction of nanoparticles may result in a significant increase of the dielectric anisotropy of a polymer nanocomposite, which is important for various applications

Nonlinear properties of left-handed metamaterials

We analyze nonlinear properties of microstructured materials with negative refraction, the so-called left-handed metamaterials. We consider a two-dimensional periodic structure created by arrays of wires and split-ring resonators embedded into a nonlinear dielectric, and calculate the effective nonlinear electric permittivity and magnetic permeability. We demonstrate that the hysteresis-type dependence of the magnetic permeability on the field intensity allows changing the material from left- to right-handed and back. These effects can be treated as the second-order phase transitions in the transmission properties induced by the variation of an external field.Comment: 4 pages, 3 figure

Molecular theory of the tilting transition and computer simulations of the tilted lamellar phase of rod-coil diblock copolymers

Symmetric rod-coil diblock copolymers have been simulated using the method of dissipative particle dynamics in the broad range of the Flory-Huggins parameter. It has been found that the tilted lamellar phase appears to be the most stable one at strong segregation. The rod-coil copolymer tilt angle and orientational order parameters have been determined as functions of the segregation strength. The density functional theory of rod-coil diblock copolymers has been generalized to the case of the tilted lamellar phase and used to study the stability of the orthogonal lamellar phase with respect to tilt. The orthogonal phase indeed appears to be unstable in the broad region of the parameter space in the case of relatively strong segregation. It has also been shown that the transition into the tilted lamellar phase is determined by a strong coupling between two independent tilt order parameters

Molecular theory of liquid-crystal ordering in rod-coil diblock copolymers

Molecular-statistical theory of rod-coil diblock copolymers is proposed using the general density functional approach which enables one to consider the cases of both weak and strong segregation. The free energy of the system is expressed as a functional of the phase-space densities of rod and coil monomers, which depend on the orientational and translational order parameters. Temperature-concentration phase diagrams are obtained and the profiles of all order parameters are calculated numerically by minimizing the polymer free energy. The lamellar phase is shown to possess strong orientational order which is partially induced by the phase structural anisotropy. The enhanced stability of the lamellar phase is determined by a combination of the microphase separation effects and the emergence of long-range smectic order