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Faculty for Biology, Chemistry, and Earth Sciences

Macromolecular Chemistry I:

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Weller, T.; Rundel, K.; Krauss, G.; McNeill, Chris; Thelakkat, M.: Highly Efficient and Balanced Charge Transport in Thieno[3,4-c]pyrrole-4,6-dione Copolymers: Dramatic Influence of Thieno[3,2-b]thiophene Comonomer on Alignment and Charge Transport, Journal of Physical Chemistry C, 122(14), 7565-7574 (2018) -- DOI: 10.1021/acs.jpcc.7b11984
Abstract:
The design, synthesis, characterization, and application of a novel series of copolymers based on the electron deficient thieno[3,4-c]pyrrole-4,6-dione building block, copolymerized with either thieno[3,2-b]thiophene (PTPDTT) or thiophene (PTPDT), are reported. High molecular weights were obtained for PTPDTT via Stille polycondensation. For the PTPDTs, different molecular weights were achieved by varying the polymerization conditions. The increase in molecular weight (PTPDT-2) favors face-on alignment and increases the charge carrier mobility. Grazing-incidence wide-angle X-ray scattering measurements reveal higher crystallinity for PTPDTT with up to 5 orders of lamellar stacking compared to PTPDTs. All polymers show ambipolar charge transport with highly balanced hole and electron mobilities in organic field effect transistors (OFETs), which improve considerably upon thermal annealing. A shift of comonomer from simple thiophene in PTPDT-2 to planar and electron-dense thienothiophene in PTPDTT drastically changes the alignment from face-on to edge-on fashion. Consequently, the charge carrier mobility increases considerably by 1 order of magnitude in PTPDTT, reaching excellent charge carrier mobilities for both holes (0.11 cm2 V–1 s–1) and electrons (0.17 cm2 V–1 s–1). PTPDTT was tested as a donor material in combination with PC71BM as well as an acceptor material along with a donor polymer. As a donor material, a power conversion efficiency of 4.3% was reached in combination with PC71BM.
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