Abstract
The optical spectra of molecules are often highly congested, inhibiting definite assignment of features and dynamics. In this work, we demonstrate and apply a polarization-based strategy for the decomposition of time-resolved optical spectra to analyze the electronic structure and energy transfer in a molecular donor-acceptor (D-A) dyad. We choose a dyad with orthogonal transition dipole moments for D and A and high fluorescence quantum yield to show that polarization-controlled ultrafast transient absorption spectra can isolate the pure D and A parts of the total signal. This provides a strategy to greatly reduce spectral congestion in complex systems and thus allows for detailed studies of electronic structure and electronic energy transfer.
Original language | English |
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Pages (from-to) | 5390-5396 |
Number of pages | 7 |
Journal | Journal of Physical Chemistry Letters |
Volume | 14 |
Issue number | 23 |
DOIs | |
State | Published - 15 Jun 2023 |