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Spectroscopy
Volume 22 (2008), Issue 2-3, Pages 199-211
http://dx.doi.org/10.3233/SPE-2008-0334

Electronic coherence transfer in photosynthetic complexes and its signatures in optical spectroscopy

Tomáš Mančal,1,6 Leonas Valkunas,2,3 Elizabeth L. Read,4,5 Gregory S. Engel,4,5 Tessa R. Calhoun,4,5 and Graham R. Fleming4,5

1Institute of Physics, Faculty of Mathematics and Physics, Charles University in Prague, Prague, Czech Republic
2Institute of Physics, Vilnius, Lithuania
3Department of Theoretical Physics, Faculty of Physics of Vilnius University, Vilnius, Lithuania
4Department of Chemistry, University of California, Berkeley, CA, USA
5Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
6Institute of Physics, Faculty of Mathematics and Physics, Charles University in Prague, Ke Karlovu 5, CZ-121 16 Prague, Czech Republic

Copyright © 2008 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Effects of electronic coherence transfer after photoexcitation of excitonic complexes and their manifestation in optical spectroscopy are discussed. A general excitonic model Hamiltonian is considered in detail to elucidate the origin of energy relaxation in excitonic complexes. We suggest that the second-order quantum master equation for the reduced density matrix of electronic degrees of freedom provides the most suitable theoretical framework for the study of coherence transfer in photosynthetic bacteriochlorophyll complexes. Temperature dependence of the absorption band maximum of a simple excitonic dimer is interpreted in terms of coherence transfer between two excited states. The role of reorganization energy of the transitions in the magnitude of the effect is discussed. A large reorganization energy difference between the two states is found to induce significant band shift. The predictions of the theory are compared to experimental measurements of the bacterial reaction center absorption spectra of Rhodobacter sphaeroides As an example of a time-dependent spectroscopic method sensitive to coherences and possibly to their transfer, we present recent two-dimensional photon echo measurements of energy relaxation in the so-called Fenna–Matthews–Olson complex of Chlorobium tepidum, where distinct oscillatory patters predicted to be signatures of electronic coherence have been observed.