Aligned films of a semiconducting DPP‐based copolymer exhibit highly anisotropic charge transport with a band‐like temperature dependence along the alignment direction and hole mobilities of up to 6.7 cm2 V−1 s−1. X‐ray diffraction measurements reveal an exceptional degree of in‐plane alignment, high crystallinity, and a dominant face‐on orientation of the polymer backbones. The surprising charge‐transport properties are interpreted in a tie‐chain model consistent with anisotropic activation energies.
Hydrofluoroethers are shown to be benign solvents for a wide variety of organic electronic materials, even at extreme conditions such as boiling temperature (see figure). Coupled with fluorous functional materials they open new frontiers for “green” materials processing that can be readily adopted by industry.
Transfer of photoexcited charge from PbS nanocrystals to ligand molecules is investigated in different solvents. We find that the charge transfer rate increases dramatically with solvent dielectric constant. This trend is accounted for by a modified Marcus theory that incorporates only static dielectric effects. The choice of solvent allows significant control of the charge transfer process. As an important example, we find that PbS nanocrystals dispersed in water exhibit charge transfer rates 1000 times higher than the same nanocrystals in organic solvent. Rapid charge extraction will be important to efficient nanocrystal-based photovoltaic and photodetector devices.
The concept of chemical orthogonality has long been practiced in the field of inorganic semiconductor fabrication, where it is necessary to deposit and remove a layer of photoresist without damaging the underlying layers. However, these processes involving light sensitive polymers often damage organic materials, preventing the use of photolithography to pattern organic electronic devices. In this article we show that new photoresist materials that are orthogonal to organics allow the fabrication of complex devices, such as hybrid organic/inorganic circuitry and full-colour organic displays. The examples demonstrate that properly designed photoresists enable the fabrication of organic electronic devices using existing infrastructure.
Results and discussionAs a first target, we fabricated top-contact OTFTs having channel lengths which are difficult to achieve with conventional
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