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Vibronic Resonances Facilitate Excited-State Coherence in Light-Harvesting Proteins at Room Temperature

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posted on 2024-07-26, 13:58 authored by Fabio Novelli, Ahsan Nazir, Gethin H. Richards, Ashkan Roozbeh, Krystyna E. Wilk, Paul M. G. Curmi, Jeffrey DavisJeffrey Davis
Until recently it was believed that photosynthesis, a fundamental process for life on earth, could be fully understood with semiclassical models. However, puzzling quantum phenomena have been observed in several photosynthetic pigment-protein complexes, prompting questions regarding the nature and role of these effects. Recent attention has focused on discrete vibrational modes that are resonant or quasi-resonant with excitonic energy splittings and strongly coupled to these excitonic states. Here we unambiguously identify excited state coherent superpositions in photosynthetic light-harvesting complexes using a new experimental approach. Decoherence on the time scale of the excited state lifetime allows low energy (56 cm-1) oscillations on the signal intensity to be observed. In conjunction with an appropriate model, these oscillations provide clear and direct experimental evidence that the persistent coherences observed originate from quantum superpositions among vibronic excited states.

Funding

Quantum effects in photosynthesis: responsible for highly efficient energy transfer or trivial coincidence? Understanding the precise details of the highly efficient energy transfer processes in photosynthesis has the potential to impact the design of efficient solar energy solutions

Australian Research Council

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Quantitative multidimensional optical spectroscopy: revealing dynamics and structure in complex condensed matter systems

Australian Research Council

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History

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PDF (Accepted manuscript)

ISSN

1948-7185

Journal title

The Journal of Physical Chemistry Letters

Volume

6

Issue

22

Pagination

7 pp

Publisher

American Chemical Society

Copyright statement

Copyright © 2015. This document is the unedited versio of a Submitted Work that was subsequently accepted for publication in the Journal of Physical Chemistry Letters, 2015. Copyright © American Chemical Society after peer review. To access the final edited and published work, see https://doi.org/10.1021/acs.jpclett.5b02058.

Language

eng

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