Abstract
The spectral evolution of an intrachain neutral singlet exciton toward a charge-transfer (CT) state in solvents of increasing polarity has been monitored by time-resolved photoluminescence and ultrafast transient-absorption spectroscopy in a model conjugated random copolymer composed of electron donor and electron acceptor units. In polar solvents, a charge-like absorption superimposes the region of stimulated emission and leads to a dramatic reduction in gain implying that CT states can be detrimental for light amplification and lasing.
- Received 20 January 2010
DOI:https://doi.org/10.1103/PhysRevB.81.205421
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