The time-resolved photoluminescence spectrum of a polythiophene derivative
has been analyzed from the viewpoint of the vibronic structure and its dyna
mics. We found that the photoluminescence (PL) originates from two vibronic
coupled states which consist of the odd-parity 1B(u) component and the eve
n-parity 2A(g) component. Since the fluorescences from the two states have
different time constants and different vibronic structures, the PL shows a
biexponential decay and a spectral change.