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Synthesis, characterization, charge transport, and photovoltaic properties of dithienobenzoquinoxaline- and dithienobenzopyridopyrazine-based conjugated polymers

机译:二噻吩并苯并喹喔啉和二噻吩并苯并吡啶并吡嗪类共轭聚合物的合成,表征,电荷传输和光伏性质

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摘要

Two donor-acceptor polymers (P1 and P2) based on dithienobenzoquinoxaline (M1) and dithienobenzopyridopyrazine (M2) as acceptor and indacenodithiophene as donor were synthesized via Stille polycondensation. The fused dithienobenzene unit in M1 and M2 units can improve the intermolecular stacking of polymer and also decrease the steric hindrance. P1, with dithienobenzoquinoxaline acceptor, shows a band gap of 1.61 eV. The band gap of P2 was reduced to 1.48 eV after changing to dithienobenzopyridopyrazine as the acceptor unit. The mobilities of P1 and P2 reach 5.6 × 10-2 and 1.5 × 10~(-2) cm~2 V~(-1) s~(-1), respectively. The results from photovoltaic measurements showed a very promising PCE of 6.06% for the P1/PC_(71)BM blend system without any thermal or solvent treatments, showing a great offer for the roll-to-roll manufacturing of PSCs.
机译:通过Stille缩聚反应合成了两种以二硫代苯并喹喔啉(M1)和二硫代苯并吡啶并吡嗪(M2)为受体,茚满二噻吩为供体的供体-受体聚合物(P1和P2)。 M1和M2单元中稠合的二噻吩并苯单元可以改善聚合物的分子间堆积,也可以减少空间位阻。具有双硫杂苯并喹喔啉受体的P1显示带隙为1.61 eV。在改为二硫代苯并吡啶并吡嗪作为受体单元后,P2的带隙降低至1.48 eV。 P1和P2的迁移率分别达到5.6×10-2和1.5×10〜(-2)cm〜2 V〜(-1)s〜(-1)。光伏测量的结果表明,未经任何热处理或溶剂处理的P1 / PC_(71)BM共混体系的PCE非常有前途,为6.06%,这为PSC的卷对卷生产提供了很大的机会。

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