The evolution of nanomorphology within thin solid‐state films of poly(3‐alkylthiophene):[6,6]‐phenyl‐C61 butyric acid methyl ester (P3AT:PCBM) blends during the film formation and subsequent thermal annealing is reported. In detail, the influence of the P3AT's alkyl side chain length on the polymer/fullerene phase separation is discussed. Butyl, hexyl, octyl, decyl, and dodecyl side groups are investigated. All of the P3ATs used were regioregular. To elucidate the nanomorphology, atomic force microscopy (AFM), X‐ray diffraction, and optical spectroscopy are applied. Furthermore, photovoltaic devices of each of the different P3ATs have been constructed, characterized, and correlated with the nanostructure of the blends. It is proposed that the thermal‐annealing step, commonly applied to these P3AT:PCBM blend films, controls two main issues at the same time: a) the crystallization of P3AT and b) the phase separation and diffusion of PCBM. The results show that PCBM diffusion is the main limiting process for reaching high device performances.

Mixtures of conjugated polymers and fullerenes command considerable attention for application in organic solar cells. To increase their efficiency, the design of new materials that absorb at longer wavelengths is of substantial interest. We have prepared such low band gap polymers using the donor-acceptor route, which is based on the concept that the interaction between alternating donors and acceptors results in a compressed band gap. Furthermore, for application in photovoltaic devices, sufficient polymer solubility is required. We have prepared four low band gap conjugated polymers, with a bis(1-cyano-2-thienylvinylene)phenylene base structure, and achieved an excellent solubility by the introduction of long alkoxy and alkyl side chains. The polymers were synthesized via an oxidative polymerization. Their electronic properties were determined from electrochemical and optical measurements, which confirm that they indeed have a low band gap. In the blend of such a low band gap polymer with PCBM, evidence for efficient charge transfer was obtained from PL and EPR measurements. However, bulk heterostructure solar cells made of such blends display only low efficiencies, which is attributed to low charge carrier mobilities.

This paper provides a photopolymerizing material suitable for stereolithography of complex submicrometer‐sized three‐dimensional (3D) structural elements to a broad scientific public. Here, we present the formulation of a polymer (LN1 resin) that allows further research in the field of nanofabrication and ‐technology as it surpasses current material limitations. The polymer consists of multifunctional acrylate oligomers as binder, polyfunctional monomers, and a photoinitiator (PI). The chemistry to form 3D structures is based on photopolymerization of the acrylate system initiated by free‐radical species that are triggered by two‐photon absorption of a PI. Important parameters of photocuring, such as the effects of PI concentration, temperature, and light intensity, were studied using photocalorimetry. The thermal stability of the material was tested using thermal gravimetric analysis, providing key information for electronic and photonic applications. Photonic‐crystal structures generated from this resin exhibiting photonic stop gaps in near‐infrared‐ and telecommunication‐wavelength regions are presented.

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