A unique implementation of an organic image detector using resistive photo-switchable pixels is presented. This resistive photo-switch comprises the vertical integration of an organic photodiode and an organic resistive switching memory element. The photodiodes act as a photosensitive element while the resistive switching elements simultaneously store the detected light information.

We present a novel core-shell-surface multifunctional structure for dendrimers using a blue fluorescent pyrene core with triphenylene dendrons and triphenylamine surface groups. We find efficient excitation energy transfer from the triphenylene shell to the pyrene core, substantially enhancing the quantum yield in solution and the solid state (4-fold) compared to dendrimers without a core emitter, while TPA groups facilitate the hole capturing and injection ability in the device applications. With a luminance of up to 1400 cd/m(2), a saturated blue emission CIE(xy) = (0.15, 0.17) and high operational stability, these dendrimers belong to the best reported fluorescence-based blue-emitting organic molecules.

We report on solution processed polymer light emitting diodes (PLEDs) using inkjet-printed embedded and non-embedded metal grid anodes. Metal grids were inkjet-printed in a honeycomb layout. Honeycomb dimensions were varied from 3 mm to 8 mm to optimize device performance. Inkjetprinted grids were then coated with a highly conductive PEDOT:PSS formulation. First experiments on PEDOT:PSS coated, non-embedded metal grid anodes showed that grids with a 3 mm honeycomb diameter have a similar efficiency as optimized indium tin oxide (ITO) based reference devices. To further improve the efficiency of the devices, the honeycomb Ag-grids were embedded in an Ormocer V R-based material. A detailed performance analysis of PLEDs fabricated on ITO, nonembedded and embedded grids was carried out. It is shown that reduced leakage current and enhanced light outcoupling by embedding result in a significant efficiency enhancement of 250% in inkjet-printed embedded Ag-PEDOT:PSS ITO-free PLEDs, compared to the ITO-based reference PLEDs.

The origin of resistive switching in organic devices is studied by photovoltaic methods and impedance spectroscopy. The results show that the most commonly proposed charging/discharging mechanisms can be excluded as working mechanism. There is solid evidence that resistive switching is due to the formation/rupture of filaments. Further, it is shown that this is a universal property of metal/organic/metal thin-film devices.

Highly efficient and stable blue light emission is observed in novel copolymers that are produced from specially designed building blocks. A PEDOT:PSS-induced chemical degradation of the polymer light-emitting diodes (PLEDs) is identified at the interface, and it is found to be accompanied by a shift in the emission color. A method to prevent this highly undesirable interaction is presented.