RESUMO
The non-isotropic alignment of molecules can increase the interaction efficiency with propagating light fields. This applies to both emissive and absorptive systems and can be exploited for achieving unprecedented efficiencies of organic opto-electronic devices such as organic light-emitting diodes. Optical analysis has revealed certain phosphorescent emitters to align spontaneously in an advantageous orientation. Unfortunately, established approaches only determine an average orientation because emission patterns solely depend on the second moments of the transition dipole vector distribution. In order to resolve further details of such a distribution, additional differences in the emission characteristics of parallel and perpendicularly oriented emitters need to be introduced. A thin metal layer near the emitters introduces plasmon mediated losses mostly for perpendicular emitters. Then, analyzing the emission at different polarizations allows one to measure emission lifetimes of mostly parallel or mostly perpendicular oriented emitters. This should alter the transient emission when observing the temporal phosphorescence decay under different directions and/or polarizations. The angular width of the orientation distribution can be derived from the degree of such lifetime splitting. Our results suggest a narrow but obliquely oriented molecular ensemble of Ir(MDQ)2(acac) doped into the α-NPD host inside an Organic LED stack.
RESUMO
In this perspective, we provide an overview of the emerging field of coupled conjugates of quantum dots and organic semiconductors, referred to as "coupled organic-inorganic nanostructures" (COIN). We summarize important aspects of their optical properties and highlight suitable descriptions of their electrical transport behavior. In particular, we discuss the key role of the electronic structure at the interface of COINs and the impact of structural/morphological features on the optoelectronic properties. Finally, we comment on the physics of current quantum dot-based devices and novel opportunities provided by the application of COINs in this respect.
RESUMO
Optically pumped organic semiconductor lasers are fabricated by evaporation of a thin film of tris(8-hydroxyquinoline) aluminum (Alq(3)) molecularly doped with a laser dye on top of a polyester substrate with an embossed grating structure. We achieve low-threshold, longitudinally monomode distributed-feedback laser operation. By varying the film thickness of the organic semiconductor film, we can tune the wavelength of the surface-emitting laser over 44 nm. The low laser threshold allows the use of a very compact all-solid-state pump laser ( approximately 10 cm long). This concept opens up a way to obtain inexpensive lasers that are tunable over the whole visible range.