文摘
To examine the quenching of a triplet exciton by low triplet energy (ET) polymer hosts with differentchain configurations for high ET phosphor guests, the quenching rate constant measurements were carriedout and analyzed by the standard Stern-Volmer equation. We found that an effective shielding of tripletenergy transfer from a high ET phosphor guest to a low ET polymer host is possible upon introducing denseside chains to the polymer to block direct contact from the guest such that the possibility of Dexter energytransfer between them is reduced to a minimum. Together with energy level matching to allow chargetrapping on the guest, high device efficiency can be achieved. The extent of shielding for the systems ofphenylene-based conjugated structures from iridium complexes follows the sequence di-substituted (octoxylchain) in the para position (dC8OPPP) is greater than monosubstituted (mC8OPPP) and the PPPs withlonger side chains are much higher than a phenylene tetramer (P4) with two short methyl groups. Further,capping the dialkoxyl-susbstituents with a carbazole (Cz) moiety (CzPPP) provides enhanced extent ofshielding. Excellent device efficiency of 30 cd/A (8.25%) for a green electrophosphorescent device can beachieved with CzPPP as a host, which is higher than that of dC8OPPP as host (15 cd/A). The efficiencyis higher than those of high ET conjugated polymers, poly(3,6-carbazole) derivatives, as hosts (23 cd/A).This observation suggests a new route for molecular design of electroluminescent polymers as a host fora phosphorescent dopant.