Two-dimensional spectroscopy of electronic couplings in photosynthesis

Tobias Brixner, Jens Stenger, Harsha M. Vaswani, Minhaeng Cho (), Robert E. Blankenship and Graham R. Fleming ()
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Tobias Brixner: University of California
Jens Stenger: University of California
Harsha M. Vaswani: University of California
Minhaeng Cho: Korea University
Robert E. Blankenship: Arizona State University
Graham R. Fleming: University of California

Nature, 2005, vol. 434, issue 7033, 625-628

Abstract: Abstract Time-resolved optical spectroscopy is widely used to study vibrational and electronic dynamics by monitoring transient changes in excited state populations on a femtosecond timescale1. Yet the fundamental cause of electronic and vibrational dynamics—the coupling between the different energy levels involved—is usually inferred only indirectly. Two-dimensional femtosecond infrared spectroscopy based on the heterodyne detection of three-pulse photon echoes2,3,4,5,6,7 has recently allowed the direct mapping of vibrational couplings, yielding transient structural information. Here we extend the approach to the visible range3,8 and directly measure electronic couplings in a molecular complex, the Fenna–Matthews–Olson photosynthetic light-harvesting protein9,10. As in all photosynthetic systems, the conversion of light into chemical energy is driven by electronic couplings that ensure the efficient transport of energy from light-capturing antenna pigments to the reaction centre11. We monitor this process as a function of time and frequency and show that excitation energy does not simply cascade stepwise down the energy ladder. We find instead distinct energy transport pathways that depend sensitively on the detailed spatial properties of the delocalized excited-state wavefunctions of the whole pigment–protein complex.

Date: 2005
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DOI: 10.1038/nature03429

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