Broch K, Dieterle J, Branchi F, Hestand N J, Olivier Y, Tamura H, Cruz C, Nichols V M, Hinderhofer A, Beljonne D, Spano F C, Cerullo G, Bardeen C J, Schreiber F
Institute of Applied Physics and Center for Light Matter Interactions, Sensors and Analytics, LISA+, University of Tübingen, Auf der Morgenstelle 10, 72076, Tübingen, Germany.
Fritz-Haber Institute of the Max-Planck Society, Faradayweg 4-6, 14195, Berlin, Germany.
Nat Commun. 2018 Mar 5;9(1):954. doi: 10.1038/s41467-018-03300-1.
Singlet fission, the spin-allowed photophysical process converting an excited singlet state into two triplet states, has attracted significant attention for device applications. Research so far has focused mainly on the understanding of singlet fission in pure materials, yet blends offer the promise of a controlled tuning of intermolecular interactions, impacting singlet fission efficiencies. Here we report a study of singlet fission in mixtures of pentacene with weakly interacting spacer molecules. Comparison of experimentally determined stationary optical properties and theoretical calculations indicates a reduction of charge-transfer interactions between pentacene molecules with increasing spacer molecule fraction. Theory predicts that the reduced interactions slow down singlet fission in these blends, but surprisingly we find that singlet fission occurs on a timescale comparable to that in pure crystalline pentacene. We explain the observed robustness of singlet fission in such mixed films by a mechanism of exciton diffusion to hot spots with closer intermolecular spacings.
单重态裂变是一种自旋允许的光物理过程,可将激发单重态转化为两个三重态,因其在器件应用方面的潜力而备受关注。迄今为止,研究主要集中在对纯材料中单重态裂变的理解上,然而混合材料有望实现对分子间相互作用的可控调节,从而影响单重态裂变效率。在此,我们报告了一项关于并五苯与弱相互作用间隔分子混合物中单重态裂变的研究。实验测定的稳态光学性质与理论计算结果的比较表明,随着间隔分子比例的增加,并五苯分子间的电荷转移相互作用减弱。理论预测,相互作用的减弱会减缓这些混合物中的单重态裂变,但令人惊讶的是,我们发现单重态裂变发生的时间尺度与纯结晶并五苯相当。我们通过激子扩散到分子间距更近的热点区域的机制,解释了在这种混合薄膜中观察到的单重态裂变的稳健性。