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We report the first experimental observation of an Excitonic Optical Tamm State supported at the interface between a periodic multilayer dielectric structure and an organic dye-doped polymer layer. The existence of such states is enabled by the metal-like optical properties of the excitonic layer based on aggregated dye molecules. Experimentally determined dispersion curves, together with simulated data, including field profiles, allow us to identify the nature of these new modes. Our results demonstrate the potential of organic excitonic materials as a powerful means to control light at the nanoscale, offering the prospect of a new alternative type of nanophotonics based on molecular materials.

We examine the problem of efficiently collecting the photons produced by solid-state single photon sources. The extent of the problem is first established with the aid of simple physical concepts. Several approaches to improving the collection efficiency are then examined and are broadly categorized into two types. First are those based on cavity quantum dynamics, in which the pathways by which the source may emit a photon are restricted, thus channeling emission into one desired mode. Second are those where we try to reshape the free space modes into a target mode in an optimal way, by means of refraction, without fundamentally altering the way in which the source emits. Respectively, we examine a variety of microcavities and solid immersion lenses. Whilst we find that the micropillar microcavities offer the highest collection efficiency (similar to70%), choosing this approach may not always be appropriate due to other constraints. Details of the different approaches, their merits and drawbacks are discussed in detail., QC 20100525