Effects of intramolecular vibrations on excitation energy transfer dynamics of the Fenna-Matthews-Olson complex

Sato, Yoshihiro; Hernández, Adrián Navarro; Gillespie, Lawson D.; Valete, Daniel

doi:10.1016/j.chemphys.2020.110940

Cited by 4 publications

(1 citation statement)

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“…[12][13][14][15] Following the experimentally consistent explanation 13 of reported spectroscopic signatures arising from vibronically coupled excitons, several experimental studies have reported [5][6][7][8][9][10][11] vibronic coherences between excited states of proteins, as well as persistent ground state vibrational coherences. Simulations of vibronic exciton models of extended multi-pigment proteins 6,7,[16][17][18][19] have further suggested a functional role 20 for excited state vibronic coherences in enhancing the rates of energy and charge delocalization. However, computationally expensive simulations on extended systems with explicit treatment of certain intramolecular vibrations often necessitate the use of reduced basis set descriptions.…”

Section: Introductionmentioning

confidence: 99%

Resonant Vibrational-Electronic Coupling between Photosynthetic Excitons is Inadequately Described by Reduced Basis Sets

Sahu¹,

Kurian²,

Tiwari³

2020

Preprint

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Vibrational-electronic (vibronic) resonance and its role in energy and charge transfer has been experimentally and theoretically investigated in several photosynthetic proteins. Using a dimer modeled on a typical photosynthetic protein, we contrast the description of such excitons provided by an exact basis set description, as opposed to a basis set with reduced vibrational dimensionality. Using a reduced analytical description of the full Hamiltonian, we show that in the presence of vibrational excitation both on electronically excited as well as unexcited sites, constructive interference between such basis states causes vibronic coupling between excitons to become progressively stronger with increasing quanta of vibrational excitation. This effect leads to three distinguishing features of excitons coupled through a vibronic resonance which are not captured in basis sets with reduced vibrational dimensionality -1. the vibronic resonance criterion itself, 2. vibronically assisted perfect delocalization between sites even though purely electronic mixing between the sites is imperfect due to energetic disorder, 3. the nuclear distortion accompanying vibronic excitons becoming increasingly larger for resonant vibronic coupling involving higher vibrational quanta. In terms of spectroscopically observable limitations of reduced basis set descriptions of vibronic resonance, several differences are seen in absorption and emission spectra, but may be obscured on account of overwhelming line broadening. However, we show that several features such as vibronic exciton delocalization and vibrational distortions associated with electronic excitations, which ultimately dictate the excited state wavepacket motions and relaxation processes, are fundamentally not described under reduced basis set descriptions of vibronic resonance.

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