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.
Originalsprache | Englisch |
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Seiten (von - bis) | 5390-5396 |
Seitenumfang | 7 |
Fachzeitschrift | Journal of Physical Chemistry Letters |
Jahrgang | 14 |
Ausgabenummer | 23 |
DOIs | |
Publikationsstatus | Veröffentlicht - 15 Juni 2023 |