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Isabel Pastoriza-Santos

Publications and source records attributed to Isabel Pastoriza-Santos.

4 recordsLinked to original sources

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

Bio-inspired polymers with polaritonic properties from visible to infrared: a material playground to mimic purple bacteria light-harvesting resonators

Light-harvesting complexes in natural photosynthetic systems, such as those in purple bacteria, consist of photo-reactive chromophores embedded in densely packed "antenna" systems organized in well-defined nanostructures. In the case of purple bacteria, the chromophore antennas are composed of natural J-aggregates such as bacteriochlorophylls and carotenoids. Inspired by the molecular composition of such biological systems, we create a library of organic materials composed of densely packed J-aggregates in a polymeric matrix, in which the matrix mimics a protein scaffold. This library of organic materials shows polaritonic properties which can be tuned from the visible to the infrared by choice of the model molecule. Inspired by the molecular architecture of the light-harvesting complexes of \textit{Rhodospirillum molischianum} bacteria, we study the light-matter interactions of J-aggregate-based nanorings with similar dimensions to the analogous natural nanoscale architectures. Electromagnetic simulations show that these nanorings of J-aggregates can act as resonators, with subwavelength confinement of light while concentrating the electric field in specific regions. These results open the door to bio-inspired building blocks for all-organic metamaterials while offering a new perspective on light-matter interactions at the nanoscale in densely packed organic matter in biological organisms including photosynthetic organelles.

physics.optics

Tunable narrowband Excitonic Optical Tamm States enabled by a metal-free all-organic structure

Optical Tamm States (OTS) are confined optical modes that can occur at the interface between two highly reflective structures. However, due to the strong reflectance required, their implemen-tation with highly processable and metal-free flexible materials has proven challenging. Herein, we develop the first structure supporting OTS based only on organic polymeric materials, demon-strating a photonic platform based on non-critical, widely available, and easily processable mate-rials. The structures fabricated present large areas and consist of a narrowband multi-layered polymeric Distributed Bragg Reflector (DBR) followed by a thin film of J-aggregate molecular exci-tonic material that can act as a highly reflective surface within a narrowband range. We take ad-vantage of the narrowband spectral response of the DBR and of the reflective molecular layer to tune the OTS band by varying the periodicity of the multilayer, opening the door for the fabrica-tion of OTS structures based on lightweight integrable excitonic devices with cost-effective proce-dures.

physics.optics