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Photoinduced singlet and triplet energy transfer in fullerene-oligothiophene-fullerene triads

机译:富勒烯-低聚噻吩-富勒烯三联体中的光诱导单重态和三重态能量转移

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摘要

Photophysical properties of fullerene-oligothiophene-fullerene (C_(60)-nT-C_(60)) triads with n = 3, 6, or 9 thiophene units have been investigated using photoinduced absorption (PIA) and (time-resolved) fluorescence spectroscopy in toluene and compared to mixtures of oligothiophenes (nT) with N-methylfulleropyrrolidine (MP-C_(60)). Photoexcitation of the oligothiophene moiety of the C_(60)-nT-C_(60) triads in toluene results in a very fast singlet-energy transfer reaction to the fullerene moiety with rates varying between 10~(12) and 10~(13) s~(-1). In the mixtures, an inter-molecular triplet-energy transfer reaction occurs. The preference for intra- and inter-molecular energy instead of electron transfer reactions in these triads in toluene is in full agreement with predictions that can be made for the change in free energy upon charge separation.
机译:使用光诱导吸收(PIA)和(时间分辨)荧光光谱法研究了n = 3、6或9个噻吩单元的富勒烯-低聚噻吩-富勒烯(C_(60)-nT-C_(60))三单元组的光物理性质与甲苯中的低聚噻吩(nT)和N-甲基全氟吡咯烷(MP-C_(60))的混合物进行比较。甲苯中C_(60)-nT-C_(60)三联体的寡噻吩部分的光激发导致非常快的单线态能量转移至富勒烯部分,反应速率在10〜(12)和10〜(13)之间变化s〜(-1)。在混合物中,发生分子间三重态能量转移反应。这些三元组在甲苯中优先选择分子内和分子间的能量,而不是电子转移反应,这与电荷分离后自由能变化的预测完全一致。

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