The energy relaxation of optical excitations in poly(p-phenyl-phenylen
evinylene) (PPPV) and PPPV blended in polycarbonate (PC) is investigat
ed by means of picosecond time-resolved luminescence spectroscopy. In
PPPV a pronounced dependence on the photon energy of the excitation la
ser is found. For excitation into the tail states of the inhomogeneous
ly broadened density of states distribution, the spectral shape of the
luminescence remains almost constant with time. However, a transient
red-shift is observed for excitation at higher energies. Experiments o
n the diluted system PPPV/PC allow us to distinguish between intra-and
inter-chain processes. The experimental results can be explained with
a hopping model.