Spectro-temporal symmetry in action-detected optical spectroscopy: Highlighting excited-state dynamics in large systems

Datum vydání
2025Publikováno v
Journal of Chemical PhysicsNakladatel / Místo vydání
American Institute of PhysicsRočník / Číslo vydání
162 (12)ISBN / ISSN
ISSN: 0021-9606ISBN / ISSN
eISSN: 1089-7690Informace o financování
MSM//PRIMUS/24/SCI/007
UK//COOP
Metadata
Zobrazit celý záznamKolekce
Tato publikace má vydavatelskou verzi s DOI 10.1063/5.0255316
Abstrakt
Multidimensional optical spectroscopy observes transient excitation dynamics through time evolution of spectral correlations. Its action-detected variants offer several advantages over the coherent detection and are thus becoming increasingly widespread. Nevertheless, a drawback of action-detected spectra is the presence of a stationary background of the so-called incoherent mixing of excitations from independent states that resembles a product of ground-state absorption spectra and obscures the excited-state signal. This issue is especially problematic in fluorescence-detected two-dimensional electronic spectroscopy (F-2DES) and fluorescence-detected pump-probe spectroscopy (F-PP) of extended systems, where large incoherent mixing arises from efficient exciton-exciton annihilation. In this work, we demonstrate on the example of F-2DES and F-PP an inherent spectro-temporal symmetry of action-detected spectra, which allows general, system-independent subtraction of any stationary signals including incoherent mixing. We derive the expressions for spectra with normal and reversed time ordering of the pulses, relating these to the symmetry of the system response. As we show both analytically and numerically, the difference signal constructed from spectra with normal and reversed pulse ordering is free of incoherent mixing and highlights the excited-state dynamics. We further verify the approach on the experimental F-PP spectra of a molecular squaraine heterodimer and the F-2DES spectra of the photosynthetic antenna light-harvesting complex 2 of purple bacteria. The approach is generally applicable to action-detected 2DES and pump-probe spectroscopy without experimental modifications and is independent of the studied system, enabling their application to large systems such as molecular complexes. (c) 2025 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license(https://creativecommons.org/licenses/by/4.0/).
Klíčová slova
fluorescence, spectroscopy, 2DES
Trvalý odkaz
https://hdl.handle.net/20.500.14178/3539Licence
Licence pro užití plného textu výsledku: Creative Commons Uveďte původ 4.0 International
