Holzinger R, Baßler NS, Ritsch H, Genes C (2024)
Publication Type: Journal article
Publication year: 2024
Book Volume: 128
Pages Range: 3910-3915
Issue: 19
We study the photophysics of molecular aggregates from a quantum optics perspective, with emphasis on deriving scaling laws for the fast nonradiative relaxation of collective electronic excitations, referred to as Kasha’s rule. Aggregates exhibit an energetically broad manifold of collective states with delocalized electronic excitations originating from near-field dipole–dipole exchanges between neighboring monomers. Photoexcitation at optical wavelengths, much larger than the monomer–monomer average separation, addresses almost exclusively symmetric collective states, which for an arrangement known as H-aggregate show an upward hypsochromic shift. The extremely fast subsequent nonradiative relaxation via intramolecular vibrational modes populates lower energy, subradiant states, resulting in effective inhibition of fluorescence. Our analytical treatment allows for the derivation of an approximate scaling law of this relaxation process, linear in the number of available low-energy vibrational modes and directly proportional to the dipole–dipole interaction strength between neighboring monomers.
APA:
Holzinger, R., Baßler, N.S., Ritsch, H., & Genes, C. (2024). Scaling Law for Kasha’s Rule in Photoexcited Molecular Aggregates. Journal of Physical Chemistry A, 128, 3910-3915. https://doi.org/10.1021/acs.jpca.4c00342
MLA:
Holzinger, Raphael, et al. "Scaling Law for Kasha’s Rule in Photoexcited Molecular Aggregates." Journal of Physical Chemistry A 128 (2024): 3910-3915.
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