Hong Yongseok, Kim Woojae, Kim Taeyeon, Kaufmann Christina, Kim Hyungjun, Würthner Frank, Kim Dongho
Department of Chemistry, Spectroscopy Laboratory for Functional π-Electronic Systems, Yonsei University, 03722, Seoul, Republic of Korea.
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, 14853, New York, USA.
Angew Chem Int Ed Engl. 2022 Mar 21;61(13):e202114474. doi: 10.1002/anie.202114474. Epub 2022 Feb 7.
In π-conjugated organic photovoltaic materials, an excimer state has been generally regarded as a trap state which hinders efficient excitation energy transport. But despite wide investigations of the excimer for overcoming the undesirable energy loss, the understanding of the relationship between the structure of the excimer in stacked organic compounds and its properties remains elusive. Here, we present the landscape of structural dynamics from the excimer formation to its relaxation in a co-facially stacked archetypical perylene bisimide folda-dimer using ultrafast time-domain Raman spectroscopy. We directly captured vibrational snapshots illustrating the ultrafast structural evolution triggering the excimer formation along the interchromophore coordinate on the complex excited-state potential surfaces and following evolution into a relaxed excimer state. Not only does this work showcase the ultrafast structural dynamics necessary for the excimer formation and control of excimer characteristics but also provides important criteria for designing the π-conjugated organic molecules.
在π共轭有机光伏材料中,激基缔合物态通常被视为一种陷阱态,它会阻碍有效的激发能传输。尽管人们对激基缔合物进行了广泛研究以克服不良的能量损失,但对于堆叠有机化合物中激基缔合物的结构与其性质之间的关系仍缺乏深入了解。在此,我们利用超快时域拉曼光谱展示了在共面堆叠的典型苝二酰亚胺折叠二聚体中,从激基缔合物形成到弛豫的结构动力学全貌。我们直接捕捉到了振动快照,这些快照说明了在复杂的激发态势能面上,沿着发色团间坐标触发激基缔合物形成并随后演化为弛豫激基缔合物态的超快结构演化过程。这项工作不仅展示了激基缔合物形成以及控制激基缔合物特性所需的超快结构动力学,还为设计π共轭有机分子提供了重要标准。