RESUMEN
We have examined the Coulombic interactions at the interface in a blend of two copolymers with intramolecular charge-transfer character and optimized band offsets for photoinduced charge generation. The combination of both time-resolved measurements of photoluminescence, and quantum-chemical modeling of the heterojunction allows us to show that relative orientation across the heterojunction can lead to either a repulsive barrier ( approximately 65 meV) or an attractive interaction which can enhance the charge-transfer processes. We conclude that polymer orientation at the heterojunction can be as important as energy-band offsets in determining the dynamics of charge separation and optical emission.
RESUMEN
The radiative and nonradiative decay rates of lissamine dye molecules, chemically attached to differently sized gold nanoparticles, are investigated by means of time-resolved fluorescence experiments. A pronounced fluorescence quenching is observed already for the smallest nanoparticles of 1 nm radius. The quenching is caused not only by an increased nonradiative rate but, equally important, by a drastic decrease in the dye's radiative rate. Assuming resonant energy transfer to be responsible for the nonradiative decay channel, we compare our experimental findings with theoretical results derived from the Gersten-Nitzan model.