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Photoinduced asymmetric charge trapping in a symmetric tetraazapyrene-fused bis(tetrathiafulvalene) conjugate

In fused donor–acceptor (D–A) ensembles, rapid charge recombination often occurs because the D and A units are spatially close and strongly coupled. To the best of our knowledge, a long-lived charge separated (CS) state is still elusive in such systems. The results presented here show that symmetric...

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Detalles Bibliográficos
Autores principales: Zhou, Ping, Nazari Haghighi Pashaki, Maryam, Frey, Hans-Martin, Hauser, Andreas, Decurtins, Silvio, Cannizzo, Andrea, Feurer, Thomas, Häner, Robert, Aschauer, Ulrich, Liu, Shi-Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646961/
https://www.ncbi.nlm.nih.gov/pubmed/38020370
http://dx.doi.org/10.1039/d3sc03184e
Descripción
Sumario:In fused donor–acceptor (D–A) ensembles, rapid charge recombination often occurs because the D and A units are spatially close and strongly coupled. To the best of our knowledge, a long-lived charge separated (CS) state is still elusive in such systems. The results presented here show that symmetric annulation of two tetrathiafulvalene (TTF) donors to a central tetraazapyrene (TAP) acceptor via two quinoxaline units leads to a CS state lifetime of a few ns. A detailed study of the electronic interactions between TTF and TAP units in the ground and excited states was performed and compared with the asymmetric counterpart by cyclic voltammetry, optical absorption and ultrafast transient absorption spectroscopy. The results demonstrate that the photoinduced asymmetric charge trapping between two TTFs significantly stabilizes the CS state, which is also verified theoretically.