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Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light
Published on: September 12, 2014
Fluorescence up-conversion study of excitation energy transport dynamics in oligothiophene-fullerene linked dyads
Takumi Nakamura1, Yasuyuki Araki, Osamu Ito
1Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Katahira, Sendai, Miyagi 980-8577, Japan.
Abstract:
Photoinduced excitation energy transport dynamics in oligothiophene-fullerene linked dyads, nT-C60 (n = 4, 8, and 12), have been investigated by femtosecond fluorescence up-conversion. In 8T-C60 and 12T-C60, each time profile of the fluorescence due to the 1nT* moiety consists of two components. The sub-picosecond component and a few picosecond components were experimentally evaluated depending on the lengths of oligothiophenes (n =8 and 12) and on the analyzing wavelength of the fluorescence. However, the time trace of the fluorescence due to 14T*-C60 decayed with a single short component in approximately 300 fs due to direct excited energy transfer (EET) from the 14T* moiety to the C60 moiety. On the basis of the kinetic models considering the short and long locally pi-conjugative thiophene segments in 8T-C60 and 12T-C60, the rate parameters of the elemental processes were evaluated. Sub-picosecond time constants of nT-C60 were found to be EET from the thiophene segment vicinal to the C60 moiety and intrachain energy transfer. Slower picosecond dynamics mainly corresponds to EET from the thiophene segments apart from the C60 moiety.
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