Photophysics of a Ruthenium 4H-Imidazole Panchromatic Dye in Interaction with Titanium Dioxide - Publication - Bridge of Knowledge

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Photophysics of a Ruthenium 4H-Imidazole Panchromatic Dye in Interaction with Titanium Dioxide

Abstract

The photophysics of bis(4,4′-di-tert-butyl-2,2′-bipyridine-κ2N,N′)[2-(4-carboxyphenyl)-4,5-bis(p-tolylimino-κN)imidazolato]ruthenium(II) hexafluorophosphate is investigated, both in solution and attached to a nanocrystalline TiO2 film. The studied substitution pattern of the 4H-imidazole ligand is observed to block a photoinduced structural reorganization pathway within the 4H-imidazole ligand that has been previously investigated. Protonation at the 4H-imidazole ring decreases the excited-state lifetime in solution. When the unprotonated dye is anchored to TiO2, photoinduced electron injection occurs from thermally nonrelaxed triplet metal-to-ligand charge transfer (3MLCT) states with a characteristic time constant of 0.5 ps and an injection efficiency of roughly 25 %. Electron injection from the subsequently populated thermalized 3MLCT state of the dye does not take place. The energy of this state seems to be lower than the conduction band edge of TiO2.

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Category:
Articles
Type:
artykuł w czasopiśmie wyróżnionym w JCR
Published in:
CHEMPHYSCHEM no. 16, edition 5, pages 1061 - 1070,
ISSN: 1439-4235
Language:
English
Publication year:
2015
Bibliographic description:
Schindler  J., Kupfer S., Wächtler M., Guthmuller J., Rau S., Dietzek B.: Photophysics of a Ruthenium 4H-Imidazole Panchromatic Dye in Interaction with Titanium Dioxide// CHEMPHYSCHEM. -Vol. 16, iss. 5 (2015), s.1061-1070
DOI:
Digital Object Identifier (open in new tab) 10.1002/cphc.201402856
Verified by:
Gdańsk University of Technology

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