The patterning of conjugated polymers for multicolored electroluminescence applications is a current topic of research in polymer device technology. Several techniques including direct writing approaches such as ink-jet printing have been proposed to solve this challenge. We present an approach to tuning the (electro)luminescence color of a film consisting of a blend of conjugated polymers after its deposition by means of UV-irradiation in the presence of an active agent. This promises to be an alternative, highly parallel approach towards multicolored electroluminescence.

The realization of a polymeric injection laser diode is an important aim in organic electronics. A crucial step towards this goal lies in the understanding and fabrication of feedback structures for lasers. Such feedback structures may be fabricated either in the substrate or directly in the active polymer layer.

Soft Lithography has proven itself as a useful tool to pattern a wide variety of materials. Typically one uses elastomeric molds (stamps) to pattern materials and structures whereby dimensions as low as 30 nm can be achieved.

Different types of Soft Lithographic processes are applied to produce optical feedback structures for optically pumped laser arrays.

The cw absorption, steady state photoluminescence (PL), photoinduced absorption (PA), PL-detected magnetic resonance (PLDMR), and the time resolved PL of a novel polyfluorene (PF) prepared with bulky polyphenylene dendrimer substituents are compared with those of (PF) with ethyl-hexyl substituents. We show that the dendronic sidechains suppress the contribution from unwanted low energetic emission, yielding a polymer with pure blue emission. The sidechains also strongly alter the dynamics of the excited entities. In particular, the time-resolved PL and temperature-dependence of the cw PL from 20-320 K reveal distinct singlet exciton (SE) dynamics in the polymer films, while the behavior in solution is essentially the same. However, the PA results show that the dynamics of polarons and triplet excitons (TEs) are similar, and the PLDMR shows that the interaction between the SEs and polarons are also similar.

Photochemical methods were developed to obtain a variation of the refractive index in aromatic polymer surfaces and a change in the photoluminescence characteristics of phenylene-vinylene-based polymers. Films of aromatic polymers, among them polystyrene (PS), poly(2-vinylnaphthalene) (PVN) and derivatives of poly(-phenylene-vinylene) (PPV) were UV irradiated in the presence of gaseous hydrazine (N2H4). The photoreaction led to a strongreduction of the refractive index of the polymers due to a hydrogenation of the aromatic units. In the case of PPV, we observed reductive photobleaching. This new technique was employed to produce photogenerated patterns in PPV. The results are compared to oxidative bleaching.

Photochemical methods were developed to obtain a variation of the refractive index in aromatic polymer surfaces and a change in the photoluminescence characteristics of phenylenevinylene-based polymers. Films of aromatic polymers, among them polystyrene (PS), poly(2-vinylnaphthalene) (PVN) and derivatives of poly(p-phenylene-vinylene) (PPV) were UV irradiated in the presence of gaseous hydrazine (N2H4). The photoreaction led to a strong reduction of the refractive index of the polymers due to a hydrogenation of the aromatic units. In the case of PPV, we observed reductive photobleaching. This new technique was employed to produce photogenerated patterns in PPV. The results are compared to oxidative bleaching.