四烯
化学
单重态裂变
光激发
分子内力
激发态
光化学
超快激光光谱学
单重态
内部转换
系统间交叉
光谱学
吲哚
三重态
能量转换效率
原子物理学
蒽
谱线
立体化学
光电子学
分子
有机化学
物理
量子力学
天文
作者
Yifan Bo,Yuxuan Hou,Dominik Thiel,René Weiß,Timothy Clark,Michael J. Ferguson,Rik R. Tykwinski,Dirk M. Guldi
摘要
Photon energy conversion can be accomplished in many different ways, including the two opposing manners, down-conversion (i.e., singlet fission, SF) and up-conversion (i.e., triplet-triplet annihilation up-conversion, TTA-UC). Both processes have the potential to help overcome the detailed balance limit of single-junction solar cells. Tetracene, in which the energies of the lowest singlet excited state and twice the triplet excited state are comparable, exhibits both down- and up-conversion. Here, we have designed meta-diethynylphenylene- and 1,3-diethynyladamantyl-linked tetracene dimers, which feature different electronic coupling, to characterize the interplay between intramolecular SF (intra-SF) and intramolecular TTA-UC (intra-TTA-UC) via steady-state and time-resolved absorption and fluorescence spectroscopy. Furthermore, we have used Pd-phthalocyanine as a sensitizer to enable intra-TTA-UC in the two dimers via indirect photoexcitation in the near-infrared part of the solar spectrum. The work is rounded off by temperature-dependent measurements, which outline key aspects of how thermal effects impact intra-SF and intra-TTA-UC in different dimers.
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