The increasing demand for precise chemical and biological sensing has led to the development of highly efficient plasmonic optical fiber sensors. Therefore, it is essential to optimize and match the operating wavelength region of both the optical fiber configuration and localized surface plasmon resonance of nanoparticles (NPs). This can be achieved by developing NPs that can reach resonance at near-infrared wavelengths, where refractive index sensitivity is enhanced, and silica optical fibers have lower losses. High aspect-ratio bimetallic Au@Ag nanorods and different side-polished fiber structures are tested using numerical simulations. The selected optical fiber configuration was based on a side- polished fiber with a 1 mm polished section. It is compared power losses and power at the NP interface for two configurations: a step-index single-mode fiber (SMF) with core/cladding diameters of 8.2/125 µm and a multimode graded-index fiber (GIF) with 62.5/125 µm at various polishing depths. The results showed that the best performance for both configurations was achieved at similar polishing depths, namely 59.5 and 55.2 µm for the SMF and GIF, respectively. The optical impact of retardation effects due to the proximity with the fiber structure were also observed, which caused a reduction in sensitivity from 1750 nm/RIU to 1500 nm/RIU and a red-shift of
The transport of quantum states without loss of "coherence" is extremely important for realizing quantum information systems. Quantum effects have been demonstrated in exotic systems, such as cold atoms suspended in magnetic fields, but these systems are extremely challenging to realise. In this work we will translate this work into the chemical domain, using thin films of "J-aggregates". These J-aggregates are quantum many-body systems characterized by the sharing of excitonic states over two or more molecules. This novel organic quantum soft-matter platform can confine the light at the nanoscale taking the advantages of supramolecular chemistry to design properties on demand.
Plasmonic materials are well stablished and used in fields like biomedicine or energy harvesting due to their exceptional optical properties. One of the most interesting characteristics of plasmonic nanoparticles is their ability to confine light at the nanoscale. Nevertheless, such behaviour can also be found in some non-metallic materials as in organic-excitonic materials based on J-aggregates. Herein, we evaluate the synthetic route to obtain colloidal dispersions of excitonic core-shell nanoparticles that can mimicking plasmonic behaviour.
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