In this study the charge dissociation at the donor/acceptor heterointerface of thermally evaporated planar heterojunction merocyanine/C 60 organic solar cells is investigated. Deposition of the donor material on a heated substrate as well as post-annealing of the complete devices at temperatures above the glass transition temperature of the donor material results in a twofold increase of the fill factor. An analytical model employing an electric-fielddependent exciton dissociation mechanism reveals that geminate recombination is limiting the performance of as-deposited cells. Fourier-transform infrared ellipsometry shows that, at temperatures above the glass transition temperature of the donor material, the orientation of the dye molecules in the donor films undergoes changes upon annealing. Based on this finding, the influence of the dye molecules' orientations on the charge-transfer state energies is calculated by quantum mechanical/molecular mechanics methods. The results of these detailed studies provide new insight into the exciton dissociation process in organic photovoltaic devices, and thus valuable guidelines for designing new donor materials.

Cyclometallated iridium carbene complexes are introduced as efficient blue triplet emitters. Quantum mechanical calculations have been used to design and to optimize this class of materials predominantely with respect to color coordinates and luminescence quantum yield. To complete the set of materials required for deep blue OLED devices we engineered suitable host and blocker materials for the use in combination with large triplet energy carbene emitters. These tailor-made materials were applied to develop deep blue electroluminescent devices with excellent efficiency.

Thermal co-evaporation of C(60) fullerene and two merocyanine dyes affords bulk heterojunction solar cells with improved short-circuit currents and power conversion efficiencies in comparison with the respective single donor cells. These results are rationalized by the formation of three distinct subphases driven by differences in molecular shape and electrostatic interactions.

Graphene nanoribbons (GNRs) have the potential for next-generation functional devices. So far, GNRs with defined stereochemistry are rarely reported in literature and their optical response is usually bound to the ultraviolet or visible spectral region, while covering the near-infrared (NIR) regime is still challenging. Herein, we report two novel quaterrylene bisimides with either one-or twofold-twisted π-backbones enabled by the steric congestion of a fourfold bay arylation leading to an end-toend twist of up to 76°. The strong interlocking effect of the πstacked aryl substituents introduces a rigidification of the chromophore unambiguously proven by single-crystal X-ray analysis. This leads to unexpectedly strong NIR emissions at 862 and 903 nm with quantum yields of 1.5 and 0.9%, respectively, further ensuring high solubility as well as resolvable and highly stable atropo-enantiomers. Circular dichroism spectroscopy of these enantiopure chiral compounds reveals a strong Cotton effect Δε of up to 67 M −1 cm −1 centered far in the NIR region at 849 nm.

The application of an ultra-fast low angle RARE technique for the 19F imaging of perfluorocarbons (PFCs) used as temporary blood substitutes is described. This sequence is attractive for fast 19F imaging studies that measure the biodistribution of PFCs in vivo, due to its high signal-to-noise ratio. Extensions of this technique for the chemical shift selective measurement of fluorine T1 values are presented. Using the linear dependence between the oxygen partial pressure (pO2) and the T1 relaxation rate of PFC resonances this technique makes possible the fast in vivo measurement of oxygen tension. Using the sequence in a diffusion sensitized form 19F measurements of the diffusion constants of PFCs are also presented. Phantom experiments to test the methods, and in vivo images obtained in rat studies are given and discussed.