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Adelaide Miranda

Publications and source records attributed to Adelaide Miranda.

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Surface Exciton Polaritons and Near-Zero Permittivity Surface Waves Supported by Artificial Organic Hyperbolic Metamaterials

Hyperbolic metamaterials enable extreme light confinement and control of photonic states, but their realization has been restricted to inorganic architectures. Here, a fully organic route to fabricate artificial hyperbolic metamaterials based on multilayered thin films of J-aggregate carbocyanine dyes alternated with polyelectrolytes is introduced. These structures exhibit strong optical anisotropy and experimentally support hyperbolic surface exciton polaritons and, for selected dyes, additional surface waves in near-zero permittivity regimes. Spectroscopic ellipsometry confirms a uniaxial dielectric tensor with negative in-plane and positive out-of-plane components, close to the absorption peaks of the constituent J-aggregates. This anisotropy is preserved across individual layers, demonstrating the robustness of the layer-by-layer approach and enabling the coupling of surface exciton polaritons and near-zero permittivity modes even in films only a few nanometres thick. Transfer-matrix simulations based on the obtained dielectric tensor reproduce the coupling conditions for all thicknesses, validating the optical model. Structural characterization reveals the link between optical anisotropy and supramolecular order, with preferential in-plane molecular orientation and the evolution from discrete nanostructures to continuous films as deposition progresses. These organic hyperbolic metamaterial architectures, associated with narrow excitonic resonances from J-aggregates, offer a unique platform for tailoring emission, energy transport, and exploring polariton dynamics at the nanoscale.

cond-mat.mtrl-sci

Room-Temperature Surface Exciton Polaritons in Colloidal J-Aggregate Flakes

J-aggregates are promising organic materials for nanophotonic applications due to their excitonic properties and ability to support surface exciton polaritons at room temperature, providing a robust platform for nanoscale light manipulation. While thin films composed of J-aggregates have demonstrated these advantages, colloidal J-aggregate nanoparticles remain underexplored. Herein, we report the synthesis of colloidal J-aggregate flakes by electrostatic interaction of cyanine molecules (TDBC) and oppositely charged polyelectrolytes (polydiallyldimethylammonium chloride, PDDA). These flakes exhibit colloidal stability maintaining the J-aggregate conformation even in solvents that favoured their monomeric state. The characterization of the colloidal J-aggregate flakes reveals their capability to support surface exciton polaritons at room temperature. This was further confirmed at single-particle level by observing an angular-independent Reststrahlen band near the excitonic resonance. In addition, the colloidal flakes exhibit a strong scattering component that broadens the extinction band and redshifts the photoluminescence, indicating that the colloidal architecture influences the optical response. These findings introduce a versatile colloidal system for constructing excitonic nanostructures tailored for advanced photonic applications.

physics.optics