We explore the evolution of plasmonic modes in two-dimensional nanocrystal oligomer "metamolecules" as the number of nanocrystals is systematically varied. Precise, hexagonally ordered Au nanocrystal oligomers with 1-31 members are assembled via capillary forces into polygonal topographic templates defined using electron-beam lithography. The visible and near-infrared scattering response of individual oligomers is measured by spatially resolved, polarized darkfield scattering spectroscopy. The response is highly sensitive to in-plane versus out-of-plane incident polarization, and we observe an exponentially saturating red shift in plasmon resonance wavelength as the number of nanocrystals per oligomer increases, in agreement with theoretical predictions. Simulations further elucidate the modes supported by the oligomers, including electric dipole and magnetic dipole resonances and their Fano interference. The single-oligomer sensitivity of our measurements also reveals the role of positional disorder in determining the wavelength and character of the plasmonic response. The progression of oligomer metamolecule structures studied here advances our understanding of fundamental plasmonic interactions in the transition regime between few-member plasmonic clusters and extended two-dimensional arrays.
Gold and silver nanoparticles, with different sizes, have been synthesized using ascorbic acid which allows a versatile and simple post-functionalisation.
Self-assembled plasmonic metamaterials are fabricated from silver nanoparticles covered with a silica shell. These metamaterials demonstrate topological darkness or selective suppression of reflection connected to global properties of the Fresnel coefficients. The optical properties of the studied structures are in good agreement with effective medium theory. The results suggest a practical way of achieving high phase sensitivity in plasmonic metamaterials.
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