Non-Mie optical resonances in anisotropic biomineral nanoparticles

Abstract

A novel famility of optical resonances driven by Cartesian anisotropy is demonstrated in calcite and vaterite nanoparticles.

Abstract

The optical properties of nanoparticles have attracted continuous attention owing to their high fundamental and applied importance across many disciplines. A recently emerged field of all-dielectric nanophotonics employs optically induced electric and magnetic Mie resonances in dielectric nanoparticles with a high refractive index. This property allows obtaining additional valuable degrees of freedom to control the optical responses of nanophotonic structures. Here we propose a conceptually distinct approach towards reaching optical resonances in dielectric nanoparticles. We show that, lacking conventional Mie resonances, low-index nanoparticles can exhibit a novel anisotropy-induced family of non-Mie eigenmodes. Specifically, we investigate light interactions with calcite and vaterite nanospheres and compare them with the Mie scattering by a fused silica sphere. Having close permittivities and the same dimensions, these particles exhibit significantly different scattering behavior owing to their internal structure. While a fused silica sphere does not demonstrate any spectral features, the uniaxial structure of the permittivity tensor for calcite and the non-diagonal permittivity tensor for vaterite result in a set of distinguishable peaks in scattering spectra. Multipole decomposition and eigenmode analysis reveal that these peaks are associated with a new family of electric and magnetic resonances. We identify magnetic dipole modes of ordinary, extraordinary and hybrid polarization as well as complex electric dipole resonances, featuring a significant toroidal electric dipole moment. As both vaterite and calcite are biominerals, naturally synthesized and exploited by a variety of living organisms, our results provide an indispensable toolbox for understanding and elucidating the mechanisms behind the optical functionalities of true biological systems.