We compare picosecond time-resolved photoluminescence spectra of thin polyc
rystalline films of quaterthiophene (4T) vapour deposited on two different
substrates: highly oriented pyrolytic graphite (HOPG) and glass. At zero ti
me delay, both films show the same highly resolved vibrational fine structu
re as isolated 4T molecules. The fine structure remains over time on HOPG,
but vanishes within the first 100 ps on glass and is replaced by emission f
rom two luminescent traps. The results explain the line broadening in time-
integrated (cw) spectra and yield information on the luminescence quenching
in polycrystalline organic films. (C) 1999 Elsevier Science B.V. All right
s reserved.