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Evidence of Exciton Self-Trapping in Pseudoisocyanine J-Aggregates Formed in Layered Polymer Films
44
Citations
35
References
2015
Year
Charge ExcitationsOptical MaterialsEngineeringLayered Polymer FilmsExcitation Energy TransferPseudoisocyanine J-aggregates FormedChemistryLayered FilmSemiconductorsLuminescence SpectrumQuantum MaterialsExciton Self-trappingPhotophysical PropertyMaterials SciencePhysicsOptoelectronic MaterialsOrganic SemiconductorMolecular AggregateSolid-state PhysicElectronic MaterialsNatural SciencesSelf-assemblyPolymer ScienceApplied PhysicsCondensed Matter PhysicsPhononMolecule-based MaterialPolymer Self-assemblyFunctional Materials
At low temperatures in the luminescence spectrum of pseudoisocyanine (PIC) J-aggregates formed in a layered polymer film an unusual broad red-shifted band appears. The analysis of spectral properties of PIC J-aggregates allowed us to ascribe the additional red band to the exciton self-trapped state. In a layered polymer film, PIC J-aggregates are found to possess a 2D island-like structure, which results in a barrier type of the exciton self-trapping with coexisting free and self-trapped excitons. Both the strong topological disorder and exciton–phonon coupling are suggested to be the reason for the exciton self-trapping in J-aggregates. Nonradiative relaxation of self-trapped excitons at room temperature has been proposed to be responsible for a very low luminescence quantum yield and giant nonradiative rate constant for PIC J-aggregates formed in a layered film.
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