Journal
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Volume 178, Issue 2-3, Pages 192-200Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2005.10.037
Keywords
tetra(4-sulfonatophenyl)porphyrin; J-aggragate; fluorescence up-conversion spectroscopy; scanning near-field optical microscopy
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Fluorescence dynamics of tetra(4-sulfonatophenyl) porphyrin (TPPS) in aqueous solution and mesoscopic structures of TPPS in thin films have been investigated by femtosecond fluorescence up-conversion spectroscopy and scanning probe microscopy (AFM/SNOM), respectively. We observed very short lifetime in B-state fluorescence of J-aggregate (140 +/- 10 fs) which was shorter than that of monomer (200 +/- 10 fs) and protonated monomer (530 +/- 10 fs). In addition to the very short lifetime component in B state, we found very weak and short lifetime component in Q state of monomer TPPS. Fluorescence observed at the shorter wavelength edge of the monomer Q band has a comparable short lifetime of 240 +/- 20 fs as well as B-state component which has been assigned to the fluorescence from Q(y)(0, 0) state. TPPS J-aggregate prepared by spin coating on the substrate shows quasi-2D nano-rod structures originated from the interaction between I D J-aggregate. Large microcrystalline structures were observed in drop cast film. Near-field absorption and fluorescence images suggest the structural inhomogencities of J-aggregate microcrystals. (c) 2005 Elsevier B.V. All rights reserved.
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