%0 Journal Article %1 Hong_2022 %A Hong, Yongseok %A Kim, Woojae %A Kim, Taeyeon %A Kaufmann, Christina %A Kim, Hyungjun %A Würthner, Frank %A Kim, Dongho %D 2022 %I Wiley %J Angew. Chem. Int. Ed. %K myown %R 10.1002/anie.202114474 %T Real-time Observation of Structural Dynamics Triggering Excimer Formation in a Perylene Bisimide Folda-dimer by Ultrafast Time-Domain Raman Spectroscopy %U https://doi.org/10.1002%2Fanie.202114474 %X 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.

@article{Hong_2022, abstract = {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.}, added-at = {2022-02-09T11:22:22.000+0100}, author = {Hong, Yongseok and Kim, Woojae and Kim, Taeyeon and Kaufmann, Christina and Kim, Hyungjun and Würthner, Frank and Kim, Dongho}, biburl = {https://www.bibsonomy.org/bibtex/2bab46545789c16915ad6117e3af1e123/wuerthner_group}, doi = {10.1002/anie.202114474}, interhash = {3573a02662f4600281c742fb215fe009}, intrahash = {bab46545789c16915ad6117e3af1e123}, journal = {Angew. Chem. Int. Ed.}, keywords = {myown}, month = feb, publisher = {Wiley}, timestamp = {2022-02-09T11:22:22.000+0100}, title = {Real-time Observation of Structural Dynamics Triggering Excimer Formation in a Perylene Bisimide Folda-dimer by Ultrafast Time-Domain Raman Spectroscopy}, url = {https://doi.org/10.1002%2Fanie.202114474}, year = 2022 }