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Oligomer-Fullerene Dyads:Photophysics and Performance as Active Layer Material in Photovoltaic Cells

机译:低聚物-富勒烯染料:光物理性质和作为光伏电池活性层材料的性能

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摘要

The photophysics of a homologous series of oligo(p-phenylene vinylene)-fulleropyrrolidine (OPVn-C60, n = 1 to 4, with n the number of phenyl rings) donor-acceptor dyads and the corresponding single moiety model compounds were studied. Fast intramolecular singlet-energy transfer occurs after photoexcitation of the OPVn moiety in an apolar solvent. Photoexcitation in a polar solvent results in electron transfer for OPV3-C60, OPV4-C60, and to some extent for OPV2-C60, but not for OPV1-C60. These results are compared to the results obtained for mixtures of the single moiety model compounds in the same solvents. In these dyads electron transfer is likely to occur via a two-step process, i.e. a very fast singlet-energy transfer prior to charge separation. In thin films of OPV3-C60 and OPV4-C60, a long-lived charge-separated state is formed after photoexcitation. This long lifetime is attributed to the migration of charges to different molecules. A flexible photovoltaic device, prepared from OPV4-C60, is presented.
机译:研究了低聚(对亚苯基亚乙烯基)-全吡咯烷(OPVn-C60,n = 1-4,n个苯环数)同源的供体-受体二元组和相应的单部分模型化合物的光物理性质。在非极性溶剂中对OPVn部分进行光激发后,分子内单线态能量快速转移。在极性溶剂中进行光激发会导致OPV3-C60,OPV4-C60的电子转移,并且在某种程度上导致OPV2-C60的电子转移,但对于OPV1-C60则不会。将这些结果与在相同溶剂中单部分模型化合物的混合物获得的结果进行比较。在这些二单元组中,电子转移很可能通过两步过程发生,即在电荷分离之前非常快速的单重态能量转移。在OPV3-C60和OPV4-C60的薄膜中,在光激发之后形成长寿命的电荷分离状态。如此长的寿命归因于电荷向不同分子的迁移。提出了一种由OPV4-C60制备的柔性光伏器件。

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