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We study the optical response of a metamaterial surface created by a lattice of split-ring resonators covered with a nematic liquid crystal and demonstrate millisecond timescale switching between electric and magnetic resonances of the metasurface. This is achieved due to a high sensitivity of liquid-crystal molecular reorientation to the symmetry of the metasurface as well as to the presence of a bias electric field. Our experiments are complemented by numerical simulations of the liquid-crystal reorientation.

Core-shell nanoparticles have attracted surging interests due to their flexibly tunable resonances and various applications in medical diagnostics, biosensing, nanolasers, and many other fields. The core-shell nanoparticles can support simultaneously both electric and magnetic resonances, and when the resonances are properly engineered, entirely new properties can be achieved. Here we study core-shell nanoparticles that support both electric and artificial magnetic dipolar modes, which are engineered to coincide spectrally with the same strength. We reveal that the interferences of these two resonances result in azimuthally symmetric unidirectional scattering, which can be further improved by arranging the nanoparticles in a chain, with both azimuthal symmetry and vanishing backward scattering preserved over a wide spectral range. We also demonstrate that the vanishing backward scattering is preserved, even for random particle distributions, which can find applications in the fields of nanoantennas, photovoltaic devices, and nanoscale lasers that require backward scattering suppressions.

We propose a novel type of hybrid metal-dielectric structures composed of silicon nanoparticles and split-ring resonators for advanced control of optically induced magnetic response. We reveal that a hybrid "metamolecule" may exhibit a strong distance-dependent magnetic interaction that may flip the magnetization orientation and support "antiferromagnetic" ordering in a hybrid metamaterial created by a periodic lattice of such metamolecules. The propagation of magnetization waves in the hybrid structures opens new ways for manipulating artificial "antiferromagnetic" ordering at high frequencies., (© 2011 American Chemical Society)