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Conjugated oligothiophene derivatives based on bithiophene with unsaturated bonds as building blocks for solution-processed bulk heterojunction organic solar cells

机译:基于具有不饱和键的联噻吩的共轭低聚噻吩衍生物,作为溶液处理的本体异质结有机太阳能电池的构建基块

摘要

A new building block ATVTA that uses stiff carbon–carbon triple bonds (A) on 1,2-di(2-thienyl)-ethene (TVT) has been developed. Oligothiophene derivatives S-01 with a TVT unit, S-02 with a 5,5′-diethynyl-2,2′-dithienyl (AT2) unit and S-03 with ATVTA were synthesized to compare their effects in a systematic study. Due to the better π-conjugation extension of the TVT unit, S-01 exhibits the most red-shifted absorption profile among them, whereas S-02 possesses the deepest HOMO level. While the HOMO level of S-03 is down-shifted by 0.02 eV relative to that of S-01, the alkyne linkages can effectively down-shift the HOMO level. By replacing the terminal units of S-03 with stronger electron acceptors, S-04 and S-05 exhibited broader absorption profiles and lower HOMO levels than those of S-03. Organic solar cells based on these molecules were fabricated and an S-03:PC60BM (1:1, w/w) based device afforded the highest Voc value of 0.96 V and a power conversion efficiency (PCE) of 2.19 %.
机译:已经开发出一种新的结构单元ATVTA,它在1,2-二(2-噻吩基)-乙烯(TVT)上使用硬碳-碳三键(A)。在系统研究中,合成了具有TVT单元的寡噻吩衍生物S-01,具有5,5'-二乙炔基-2,2'-二噻吩基(AT2)单元的S-02和具有ATVTA的S-03。由于TVT单元具有更好的π共轭扩展性,因此S-01在其中具有最大的红移吸收曲线,而S-02具有最深的HOMO能级。尽管S-03的HOMO能级相对于S-01降低了0.02 eV,但是炔键可以有效地降低HOMO的能级。通过用更强的电子受体取代S-03的末端单元,与S-03相比,S-04和S-05表现出更宽的吸收曲线和更低的HOMO水平。制造了基于这些分子的有机太阳能电池,并且基于S-03:PC60BM(1:1,w / w)的设备提供了0.96 V的最高Voc值和2.19%的功率转换效率(PCE)。

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