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Real-time Observation of Structural Dynamics Triggering Excimer Formation in a Perylene Bisimide Folda-dimer by Ultrafast Time-Domain Raman Spectroscopy.
Hong, Yongseok; Kim, Woojae; Kim, Taeyeon; Kaufmann, Christina; Kim, Hyungjun; Würthner, Frank; Kim, Dongho.
Afiliação
  • Hong Y; Department of Chemistry, Spectroscopy Laboratory for Functional π-Electronic Systems, Yonsei University, 03722, Seoul, Republic of Korea.
  • Kim W; Department of Chemistry, Spectroscopy Laboratory for Functional π-Electronic Systems, Yonsei University, 03722, Seoul, Republic of Korea.
  • Kim T; Department of Chemistry and Chemical Biology, Cornell University, Ithaca, 14853, New York, USA.
  • Kaufmann C; Department of Chemistry, Spectroscopy Laboratory for Functional π-Electronic Systems, Yonsei University, 03722, Seoul, Republic of Korea.
  • Kim H; The Institute for Sustainability and Energy at Northwestern, Northwestern University, Evanston, 60208, Illinois, USA.
  • Würthner F; Institut für Organische Chemie & Center for Nanosystems Chemistry, Universitat Würzburg, Am Hubland, 97074, Würzburg, Germany.
  • Kim D; Department of Chemistry, Incheon National University, 119 Academy-ro, Yeonsu-gu, 22012, Incheon, Republic of Korea.
Angew Chem Int Ed Engl ; 61(13): e202114474, 2022 Mar 21.
Article em En | MEDLINE | ID: mdl-35075813
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article