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Register a new user90 degree polarization rotator using a bilayered chiral metamaterial with giant optical activity
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A bilayered chiral metamaterial (CMM) is proposed to realize a 90 degree polarization rotator, whose giant optical activity is due to the transverse magnetic dipole coupling among the metallic wire pairs of enantiomeric patterns. By transmission through this thin bilayered structure of less than lambda/30 thick, a linearly polarized wave is converted to its cross polarization with a resonant polarization conversion efficiency (PCE) of over 90%. Meanwhile, the axial ratio of the transmitted wave is better than 40 dB. It is demonstrated that the chirality in the propagation direction makes this efficient cross-polarization conversion possible. The transversely isotropic property of this polarization rotator is also experimentally verified. The optical activity of the present structure is about 2700 degree/lambda, which is the largest optical activity that can be found in literature.
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Motivated by the theoretical observation that isotropic chirality can exist even in completely random systems, we design a dielectric metamaterial consisting of a random colloid of meta-atoms, which exhibits unprecedentedly high isotropic optical activity. Each meta-atom is composed of a helically arranged cluster of silicon nanospheres. Such clusters can be fabricated by large-scale DNA self-assembly techniques. It is demonstrated that the use of a high concentration of the meta-atoms in the colloid provides significant suppressions of incoherent scattering losses. As a result, the proposed system shows three orders of magnitude improvement of isotropic optical activity as compared with the previous metamaterial designs. This work highlights the significant potential of completely random system, which are commonly produced in colloidal sciences, for applications as metamaterials towards novel photonic effects and devices.
We study theoretically and experimentally a novel type of metamaterial with hybrid elements composed of twisted pairs of cross-shaped meta-atoms and their complements. We reveal that such two-layer metasurfaces demonstrate large, dispersionless optical activity at the transmission resonance accompanied by very low ellipticity. We develop a retrieval procedure to determine the effective material parameters for this structure, which has lower-order symmetry ($mathrm {C}_4$) than other commonly studied chiral structures. We verify our new theoretical approach by reproducing numerical and experimental scattering parameters.
We demonstrate numerically and experimentally a conjugated gammadion chiral metamaterial that uniaxially exhibits huge optical activity and circular dichroism, and gives a negative refractive index. This chiral design provides smaller unit cell size and larger chirality compared with other published planar designs. Experiments are performed at GHz frequencies (around 6GHz) and in good agreement with the numerical simulations.
Optical activity is the ability of chiral materials to rotate linearly-polarized (LP) electromagnetic waves. Because of their intrinsic asymmetry, traditional chiral molecules usually lack isotropic performance, or at best only possess a weak form of chirality. Here we introduce a knotted chiral meta-molecule that exhibits optical activity corresponding to a 90{deg} polarization rotation of the incident waves. More importantly, arising from the continuous multi-fold rotational symmetry of the chiral torus knot structure, the observed polarization rotation behavior is found to be independent of how the incident wave is polarized. In other words, the proposed chiral knot structure possesses two-dimensional (2-D) isotropic optical activity as illustrated in Fig. 1, which has been experimentally validated in the microwave spectrum. The proposed chiral torus knot represents the most optically active meta-molecule reported to date that is intrinsically isotropic to the incident polarization.
In the close vicinity of a chiral nanostructure, the circular dichroism of a biomolecule could be greatly enhanced, due to the interaction with the local superchiral fields. Modest enhancement of optical activity using a planar metamaterial, with some chiral properties, and achiral nanoparticles has been previously reported. A more substantial chirality enhancement can be achieved in the local filed of a chiral nanostructure with a three-dimensional arrangement. Using an embossed chiral nanostructure designed for chiroptical sensing, we measure the circular dichroism spectra of two biomolecules, Chlorophylls A and B, at the molecular level, using a simple polarization resolved reflection measurement. This experiment is the first realization of the on-resonance surface-enhanced circular dichroism, achieved by matching the chiral resonances of a strongly chiral metamaterial with that of a chiral molecule, resulting in an unprecedentedly large differential CD spectrum from a monolayer of a chiral material.
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