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Title: Theory of femtosecond coherent double-pump single-molecule spectroscopy: Application to light harvesting complexes

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4919240· OSTI ID:22415698
;  [1]; ;  [2]
  1. Division of Materials Science, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore)
  2. Department of Chemistry, Technische Universität München, Garching D-85747 (Germany)

We develop a first principles theoretical description of femtosecond double-pump single-molecule signals of molecular aggregates. We incorporate all singly excited electronic states and vibrational modes with significant exciton-phonon coupling into a system Hamiltonian and treat the ensuing system dynamics within the Davydov D{sub 1} Ansatz. The remaining intra- and inter-molecular vibrational modes are treated as a heat bath and their effect is accounted for through lineshape functions. We apply our theory to simulate single-molecule signals of the light harvesting complex II. The calculated signals exhibit pronounced oscillations of mixed electron-vibrational (vibronic) origin. Their periods decrease with decreasing exciton-phonon coupling.

OSTI ID:
22415698
Journal Information:
Journal of Chemical Physics, Vol. 142, Issue 16; Other Information: (c) 2015 AIP Publishing LLC; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
Country of Publication:
United States
Language:
English