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We studied dispersion in Rhodamine laser dyes (in the Kretschmann geometry) and found multi-branch 

Abstract We have studied effects of metal–dielectric substrates on photopolymerization of [2,2ʹ-Bi-1H-indene]-1,1ʹ-dione-3,3ʹ-diyl diheptanoate (BITh) monomer. We synthetized BITh and spin-coated it onto a variety of dielectric, metallic, and metal–dielectric substrates. The films were exposed to radiation of a UV–Visible Xe lamp, causing photo-polymerization of monomer molecules. The magnitude and the rate of the photo-polymerization were monitored by measuring the strength of the ~ 480 nm absorption band, which existed in the monomer but not in the polymer. Expectedly, the rate of photo-polymerization changed nearly linearly with the change of the pumping intensity. In contrast with our early study of photo-degradation of semiconducting polymer P3HT, the rate of photo-polymerization of BITh is getting modestly higher if the monomer film is deposited on top of silver separated from the monomer by a thin insulating MgF 2 layer preventing a charge transfer. This effect is partly due to a constructive interference of the incident and reflected light waves, as well as known in the literature effects of metal/dielectric substrates on a variety of spectroscopic and energy transfer parameters. At the same time, the rate of photopolymerization is getting threefold larger if monomer is deposited on Ag film directly and charge transfer is allowed. Finally, Au substrates cause modest (~ 50%) enhancement of both monomer film absorption and the rate of photo-polymerization. 

We have studied spectra and angular distribution of emission of Rhodamine 6G dye in Fabry-Perot cavities in weak and strong coupling regimes and demonstrated control of the strong coupling with the pumping intensity. 

We found that inhibition of concentration quenching of HITC dye in Fabry-Perot cavities is almost similar to that on top of silver. Low convexity of the emission kinetics suggests strong coupling mediated by surface plasmons. 

We show that concentration quenching of emission of dye molecules – an energy transfer to quenching centers – is inhibited in subwavelength Fabry-Perot cavities (or metal-insulator-metal, MIM, waveguides). 

We have synthesized a series of near-infrared rare-earth doped organic materials for nanophotonics applications and studied their absorption and emission properties. The developed materials show promise as research tools and (meta)device components. 

We studied emission kinetics of HITC dye in disordered metal-dielectric environments and found that the latter, contrary to expectations, can reverse emission kinetics shortening in highly concentrated dyes, caused by a combination of relaxation processes.