Quantum Dynamics Simulations Reveal Ultrafast and Coherent Charge Transfer in the <i>Lhca4</i> Antenna of Photosystem I

Among the peripheral antenna complexes of Photosystem I, <i>Lhca4</i> exhibits the most striking signatures of low-lying exciton states, such as red-shifted absorption and fluorescence bands. These so-called "red forms" arise from strong coupling between locally excited (LE) and charge-transfer (CT) states within the a603-a609 chlorophyll (Chl) dimer. We employ ML-MCTDH quantum dynamics simulations and first-principles calculated Hamiltonians to investigate the CT mechanism between the two Chls. Our simulations reveal ultrafast (∼50 fs) population transfer, finely modulated by the protein environment via the LE-CT energy gap. Our analysis reveals the adiabatic and coherent nature of the process, providing mechanistic insight into the CT process in <i>Lhca4</i>. The system relaxes toward a coherent exciton-CT mixture with partial charge separation, a low lying state that still supports bright emission and energy transfer.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2025-12-12
DOI
https://doi.org/10.1021/acs.jpclett.5c02463
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
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article

Quantum Dynamics Simulations Reveal Ultrafast and Coherent Charge Transfer in the Lhca4 Antenna of Photosystem I

Piermarco Saraceno, Fabrizio Santoro, Lorenzo Cupellini
The Journal of Physical Chemistry Letters
Photosynthetic Processes and Mechanisms
article

Quantum Dynamics Simulations Reveal Ultrafast and Coherent Charge Transfer in the Lhca4 Antenna of Photosystem I

Piermarco Saraceno, Fabrizio Santoro, Lorenzo Cupellini
article en

Abstract

Among the peripheral antenna complexes of Photosystem I, <i>Lhca4</i> exhibits the most striking signatures of low-lying exciton states, such as red-shifted absorption and fluorescence bands. These so-called "red forms" arise from strong coupling between locally excited (LE) and charge-transfer (CT) states within the a603-a609 chlorophyll (Chl) dimer. We employ ML-MCTDH quantum dynamics simulations and first-principles calculated Hamiltonians to investigate the CT mechanism between the two Chls. Our simulations reveal ultrafast (∼50 fs) population transfer, finely modulated by the protein environment via the LE-CT energy gap. Our analysis reveals the adiabatic and coherent nature of the process, providing mechanistic insight into the CT process in <i>Lhca4</i>. The system relaxes toward a coherent exciton-CT mixture with partial charge separation, a low lying state that still supports bright emission and energy transfer.

The Journal of Physical Chemistry LettersVol. 16(51)
University of Pisa (IT), Institute for the Chemistry of OrganoMetallic Compounds (IT), Bologna Research Area (IT)
Openalex Percentile: Top 64%
Photosynthetic Processes and Mechanisms
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