The synthesis of a new thieno[3,2‐b]thiophene isoindigo (iITT) based monomer unit, and its subsequent incorporation into a series of alternating copolymers is reported. Copolymerisation with benzothiadiazole, bithiophene and thiophene comonomer units by palladium catalysed cross coupling gives three new narrow band gap semiconducting polymers for OFET applications. Extending the fused nature of the isoindigo core serves to further enhance molecular orbital overlap along the polymer backbones and facilitate good charge transport characteristics thus demonstrating the potential of extending the fused ring system that is attached to the isoindigo core. When used as the semiconducting channel in top‐gate/bottom‐contact OFET devices, good ambipolar properties are observed, with hole and electron mobilities up to 0.4 cm2/Vs and 0.7 cm2/Vs respectively. The three new polymers show good stability, with high temperature annealing showing an increase in the crystallinity of the polymers which corresponds directly to charge carrier mobility improvement as shown by X‐ray diffraction, atomic force microscopy and photothermal deflection spectroscopy.
A series of novel thiophene-flanked benzodipyrrolidone (BPT)-based alternating copolymers are synthesised, their optical and electrical properties evaluated. The BPT unit promotes a conjugated, planar polymer backbone, with a low bandgap, primarily due to low lying LUMO energy levels. Copolymerisation with thiophene exhibits well balanced ambipolar organic field-effect transistor performance, with electron and hole mobilities 0.1 and 0.2 cm(2) V(-1) s(-1), respectively.
Six phenyl-flanked benzodipyrrolidone-based copolymers are designed, synthesised and characterised. Three exhibit backbone in-plane curvature or out-of-plane twisting, while the other three remain planar and co-linear. While the first three appear less crystalline by X-ray diffraction, they afford a smoother solid-state film surface topology and increased electron mobility in top-gate, bottom-contact OFETs.
A series of four dihydropyrroloindoledione-based organic semi-conducting polymers are examined for performance in transistor and photovoltaic cell devices. The dihydropyrroloindoledione unit was alternately copolymerized with phenyl, thiophene and bithiophene comonomers, and the resultant polymers exhibit broad absorption, low-bandgaps and deep energy levels, with charge carrier mobilities approaching 0.1 cm 2 V À1 s À1 . Solar cells processed in a printing friendly solvent (m-xylene) exhibited >2% PCE with a high fill-factor of 0.62 and V oc of 0.75 V.
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