摘要

A novel furo[3,2-c] pyridine based Ir complex, namely (pfupy) 2Ir(acac), has been developed by replacing sulfurwith oxygen in the C<^> N ligand. Compared with the thiophene-containing (pthpy) 2Ir(acac), the LUMO level is elevated while the HOMO level remains almost unchanged for the resultant furan-containing (pfupy) 2Ir(acac). As a consequence, the emissive maximum is blue-shifted from 556 nm of (pthpy) 2Ir(acac) to 538 nm of (pfupy) 2Ir(acac) together with an improved photoluminescence quantum yield of 0.80. The corresponding device based on (pfupy) 2Ir(acac) realizes a record-high external quantum efficiency (EQE) of 30.5% (110.5 cd A(-1)) without any out-coupling technology. Even at a luminance of 1000 and 5000 cd m(-2), the EQE still remains at 26.6% (96.4 cd A(-1)) and 25.6% (92.7 cd A(-1)), respectively, indicative of the gentle efficiency roll-off. The results clearly demonstrate the great potential of furan-based functional materials applied in OLEDs.