Photoluminescence (PL) quantum efficiency is a key issue in designing succe
ssful light-emitting polymer systems. Exciton relaxation is strongly affect
ed by exciton quenching at nonradiative trapping centers and the formation
of excimers. These factors reduce the PL quantum yield of light-emitting po
lymers. In this work, we have systematically investigated the effects of ex
citon confinement on the PL quantum yield of an oligomer, polymer, and alte
rnating block copolymer (ABC) PPV system. Time-resolved and temperature-dep
endent luminescence studies have been performed. The ABC design effectively
confine photoexcitations within the chromophores, preventing exciton migra
tion and excimer formation. An unusually high (PL) quantum yield (above 90%
) in the solid state is reported for the alternating block copolymer PPV, a
s compared to that of similar to 30% of the polymer and oligomer model comp
ounds. (C) 2000 Elsevier Science S.A. All rights reserved.