Journal
CHEMICAL PHYSICS
Volume 357, Issue 1-3, Pages 45-53Publisher
ELSEVIER
DOI: 10.1016/j.chemphys.2008.10.015
Keywords
Ultrafast spectroscopy; Multi-dimensional electronic spectroscopy; J-aggregates
Funding
- Austrian Science Foundation (FWF) [F016-18]
- (Advanced Light Sources-ADLIS Special Research Program) [P18233]
- DOC-program of the Austrian Academy of Sciences
- Austrian Science Fund (FWF) [P18233] Funding Source: Austrian Science Fund (FWF)
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We investigate the first steps of exciton dynamics in the Course of nanometric band-to-band energy-transfer in a bi-tubular J-aggregate by employing two-dimensional (21)) coherent electronic spectroscopy. Coupled exciton states are mapped as typical off. diagonal signals in 2D frequency-frequency correlation spectra, with sub-20 femtosecond (is) time resolution. The experiments enable to look beneath conventional incoherent Population transfer by directly probing the early 100 fs quantum-kinetic regime. Our data, acquired at room temperature, indicate low-amplitude coherent motion, followed by quantum-dissipative population transfer. Exciton inter-band coherence with low intensity is observed in the high-energy cross-peak (omega(3) > vertical bar omega(1)vertical bar) as an electronic wave-packet following quantum-beat oscillation up to 100 is, whereas ongoing exciton relaxation is imaged in the low-energy cross-peak (omega(3) > vertical bar omega(1)vertical bar) as typical streaked signals along the coherence frequency omega(1). Solvent induced band symmetry breaking and tube expansion create spatial disorder and densities-of-states with dipoles of minor collectivity that affect both the morphology and electronic band features by broadening the peaks and streaks and promoting the irreversibility of tube-to-tube transfer on longer time-scales. (C) 2008 Elsevier B.V. All rights reserved.
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