Suchergebnisse

Homocoupling of monomers in a palladium-catalyzed copolymerization of donor-acceptor polymers affects the perfect alternating structure and may deteriorate the performance of such materials in solar cells. Here we investigate the effect of homocoupling bis(trialkylstannyl)-thiophene and -bithiophene monomers in two low band gap poly(diketopyrrolopyrrole-alt-oligothiophene) polymers by deliberately introducing extended oligothiophene defects in a controlled fashion. We find that extension of the oligothiophene by one or two thiophenes and creating defects up to at least 10% does not significantly affect the opto-electronic properties of the polymers or their photovoltaic performance as electron donor in solar cells in combination with [6,6]-phenyl C-71 butytic acid methyl ester as acceptor. By using model reactions, we further demonstrate that for the optimized synthetic protocol and palladium-catalyst system the naturally occurring defect concentration in the polymers is expected to be less than 0.5%. ; We thank Dr Koen Hendriks for valuable discussions. G. H. L. Heintges acknowledges the Agency for Innovation by Science and Technology in Flanders (IWT). This project has further received funding from the European Research Council under the European Union's Seventh Framework Programme (FP/2007-2013)/ERC Grant Agreement No. 339031 and from the Ministry of Education, Culture and Science (Gravity program 024.001.035).

The effect of gradually replacing the branched alkyl side chains of a diketopyrrolopyrrole (DPP) conjugated polymer by linear side chains containing branched siloxane end groups on the photovoltaic performance of blends of these polymers with a common fullerene acceptor is investigated. With an increasing proportion of siloxane side chains, the molecular weight and solubility of the polymers decreases. While the siloxane containing polymers exhibit a higher hole mobility in field-effect transistors, their performance in solar cells is less than the polymer with only alkyl sides chains. Using grazing-incidence wide-angle X-ray scattering, transmission electron microscopy, and fluorescence spectroscopy we identify two main reasons for the reduced performance of siloxane containing polymers in solar cells. The first one is a somewhat coarser phase-separated morphology with slightly wider polymer fibers. This is unexpected as often the fiber width is inversely correlated with polymer solubility. The second one is stronger non-radiative decay of the pristine polymers containing siloxane side chains. ; G. H. L. Heintges acknowledges the Agency for Innovation by Science and Technology in Flanders (IWT). This project has further received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No. 747422, from the European Research Council under the European Union's Seventh Framework Programme (FP/2007-2013)/ERC Grant Agreement No. 339031 and from the Ministry of Education, Culture and Science (Gravity program 024.001.035).

Polymorphism of organic semiconducting materials exerts critical effects on their physical properties such as optical absorption, emission and electrical conductivity, and provides an excellent platform for investigating structure-property relations. It is, however, challenging to efficiently tune the polymorphism of conjugated polymers in aggregated, semi-crystalline phases due to their conformational freedom and anisotropic nature. Here, two distinctly different semi-crystalline polymorphs (beta(1) and beta(2)) of a low-bandgap diketopyrrolopyrrole polymer are formed through controlling the solvent quality, as evidenced by spectroscopic, structural, thermal and charge transport studies. Compared to beta(1), the beta(2) polymorph exhibits a lower optical band gap, an enhanced photoluminescence, a reduced pi-stacking distance, a higher hole mobility in field-effect transistors and improved photocurrent generation in polymer solar cells. The beta(1) and beta(2) polymorphs provide insights into the control of polymer self-organization for plastic electronics and hold potential for developing programmable ink formulations for next-generation electronic devices. ; This project has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No. 747422, from the Netherlands Organisation for Scientific Research(016.Veni.192.106), from the Chinese Academy of Sciences (Grant No. XDB12020200), and from King Abdullah University of Science and Technology (KAUST). The research also received funding from the European Community's Seventh Framework Programme (FP7/2007-2013) (Grant Agreement no. 607585, project OSNIRO), the European Research Council (ERC Grant Agreement No. 33903), and the Ministry of Education, Culture, and Science (Gravity program 024.001.035). T.M. acknowledges the Foundation for Polish Science co-financed by the European Union under the European Regional Development Fund (First TEAM/2017-3/26). The authors acknowledge Beamline 9 of the DELTA electron storage ring in Dortmund for GIWAXS measurements. The authors thank Mateusz Brzezinski for the discussion about GIWAXS analysis, and Christ Weijtens for UPS measurements.

The interconnection layer (ICL) that connects adjacent subcells electrically and optically in solution-processed multi-junction polymer solar cells must meet functional requirements in terms of work functions, conductivity, and transparency, but also be compatible with the multiple layer stack in terms of processing and deposition conditions. Using a combination of poly(3,4-ethylenedioxythiophene):polystyrene sulfonate, diluted in near azeotropic water/n-propanol dispersions as hole transport layer, and ZnO nanoparticles, dispersed in isoamyl alcohol as electron transport layer, a novel, versatile ICL has been developed for solution-processed tandem and triple-junction solar cells in an n-i-p architecture. The ICL has been incorporated in six different tandem cells and three different triple-junction solar cells, employing a range of different polymer-fullerene photoactive layers. The new ICL provided an essentially lossless contact in each case, without the need of adjusting the formulations or deposition conditions. The approach permitted realizing complex devices in good yields, providing a power conversion efficiency up to 10%. ; European Community's Seventh Framework Programme (FP7) [607585]; European Research Council under the European Union's Seventh Framework Programme (FP)/ERC [339031]; Ministry of Education, Culture and Science [024.001.035]