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Femtosekunden Pump-Probe Setup

Fachliche Zuordnung Physik der kondensierten Materie
Förderung Förderung in 2010
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 179616000
 
Erstellungsjahr 2016

Zusammenfassung der Projektergebnisse

When a solution of semiconducting polymers such as the light-emitting MEH-PPV (poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene]) is cooled down to cryogenic temperatures, the polymer chains start to aggregate into disordered and ordered domains. This is analogous to the aggregation process that occurs in thin films commonly used for organic semiconductor devices. By using the femtosecond pump-probe system, we could study how this aggregation impacts on the dynamics of the excited states in the sample. The pump-probe spectra show a different reduced absorption (ground state bleach) from either, disordered or ordered domains, as well as stimulated luminescence. By analysing the spectra and their evolution in time, we found that energy transfer takes place within less than 1 ps from disordered, unaggregated chain segments to highly planarized, aggregated chain segments. The short time scale of the energy transfer indicates intimate intermixing of the planarized and disordered polymeric chromophores, e.g. in a core-shell structure. When the femtosecond pump-probe spectra are correlated with coherent 2D spectroscopy, the time regimes dominated by localized and by mobile excitations can be differentiated. These spectroscopic results shed light on key morphological effects frequently encountered in organic semiconductors that are difficult to access by structural approaches. The efficiency of emiconducting polymer devices such as solar cells and light-emitting diodes strongly depend on the intermixing of disordered and ordered phases, so that spectroscopically obtained information is highly valuable.

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