Low quantum efficiency of electroluminescence (EL) from solid state evapora
ted thin films of alpha-sexithiophene (alpha-6T) was accounted for by quenc
hing due to inter-chain interaction. The substitution of alpha-6T by volumi
nous substituants at the end of the chains led to an increase of the fluore
scence in the solid state with a concomitant decrease in conductivity down
to 10(-11) S cm(-1) due to the increase in spacing between molecules. A bil
ayer device alpha-6T/DPS6T improved hole blocking in the recombination regi
on between organic layers leading to creation of excitons away from the Al
electrode. By dispersing the molecules in a highly conducting hole transpor
ting host matrix of PVK the efficiency was further improved. Transient EL r
esponse of devices indicate that poor electron injection and mobility limit
s output efficiencies.