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April 4, 2026The Journal of Physical Chemistry Letters1 citations

Heterogeneity-Resolved Ultrafast Transient Absorption Spectroscopy of Single Supramolecular Light-Harvesting Antennas

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SAShun AraiSMS. MatsubaraTKTorû Kondô

Key Points

  • This research aims to investigate the excitation dynamics of chlorophyll-derivative aggregates in light-harvesting systems, focusing on structural heterogeneity.
  • Utilized a transient absorption microscope integrating single-objective absorption microscopy with balanced detection.
  • Employed lock-in amplification for sensitive quantitative analysis of excitation dynamics.
  • Analyzed individual chlorophyll aggregates to assess variations in kinetic components and their time-constant distributions.
  • Identified two kinetic components with similar time constants but distinct time-constant distributions.
  • Quantified several photophysical properties, including absorbance change and fluorescence efficiency.
  • Established a framework for evaluating excitation dynamics beyond mean values to include distribution profiles.

Abstract

Photosynthetic light harvesting proceeds rapidly and robustly through precisely arranged pigment molecules. However, the molecular arrangements are not uniform because they exhibit structural heterogeneity among individual complexes and across spatial regions and undergo dynamic fluctuations. Such static and dynamic disorder can substantially perturb excitation dynamics. Here, we report a highly sensitive transient absorption microscope that integrates single-objective absorption microscopy, balanced detection, and lock-in amplification, enabling the quantitative analysis of heterogeneity and temporal fluctuations in excitation dynamics. By analyzing individual chlorophyll-derivative aggregates mimicking photosynthetic light-harvesting antennas, we demonstrated that two kinetic components with nearly identical time constants can be resolved based on differences in their time-constant distributions. We further quantified the photophysical properties of each component, including the absorbance change, fluorescence intensity, fluorescence efficiency, and fluorescence peak intensity ratio. These results establish an analytical framework for excitation dynamics that leverages not only the mean values of time constants but also their distribution profiles.

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Cite This Study

Arai et al. (2026) studied this question.

synapsesocial.com/papers/69d0af9a659487ece0fa58c9https://doi.org/10.1021/acs.jpclett.6c00164
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