A theoretical analysis of emission in oligo-p-phenylene vinylene herringbon
e aggregates shows that the radiative decay rate of the lower exciton band-
edge can exceed that of a single molecule. Such superradiant H-aggregates r
equire long-range orientational order and constructive interference between
the off-axis molecular transition dipole moments. Excellent agreement with
the experimental emission spectrum of p-distyrylbenzene nanoaggregates is
obtained. Extensions are made to superradiant polymer aggregates, which cou
ld have important optical device applications. (C) 2000 Elsevier Science B.
V. All rights reserved.