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Amphiphilic complexes with luminescent rare earth metal ions suitable for Lanmuir-Blodgett (LB) deposition have been synthesized. LB monolayers with closely packed Eu complexes deposited directly on silver demonstrate significant far-field emission in contrast to the theoretical predictions of full quenching. Angular radiation and polarization patterns of the electric and magnetic dipole emission of Eu³⁺point to a high excitation efficiency of surface plasmon polaritons. Different luminescent behavior of closely packed emitters in comparison to diluted systems is tentatively attributed to the collective state of emitters in LB layers formed via near-field coupling with surface plasmons.

We have studied emission kinetics in dye-doped polymeric films (HITC:PMMA), deposited on top of glass and silver and embedded in Fabry–Perot cavities (metal-insulator-metal waveguides). For highly doped films on glass, we observed strong concentration quenching, as evidenced by a dramatic shortening of the emission kinetics, consistent with our previous studies. However, for the same dye-doped films on top of silver, slower emission kinetics were observed despite the high decay rates of individual dye molecules near the metallic surface. The concentration quenching rates in Fabry–Perot cavities were nearly identical to those of HITC:PMMA films deposited on top of silver. These findings are explained within a theoretical model for the inhibition of Förster energy transfer near a metallic surface. Furthermore, the emission kinetics of the dye-doped films on top of silver were approximately single exponential—consistent with the strong coupling of excited molecules with propagating surface plasmons.