We
have designed and synthesized three nona-coordinated organoeuropium
complexes (OEuCs) with the general formula [Eu(btfa)3(FurTerPy)]
(Eu1), [Eu(btfa)3(ThioTerPy)] (Eu2), and [Eu(btfa)3(NapTerPy)] (Eu3) by employing
a primary 4,4,4-trifluoro-1-phenyl-1,3-butanedione (btfa) antenna
ligand and three functionalized 2,2′:6′,2″-terpyridine
(TerPy) ligands bearing different electron-donating groups at the
4′ position, namely, FurTerPy = 4′-(furan-2-yl)-2,2′:6′,2″-terpyridine;
ThioTerPy = 4′-(thiophen-2-yl)-2,2′:6′,2″-terpyridine;
and NapTerPy = 4′-(naphthalen-1-yl)-2,2′:6′,2″-terpyridine.
The detailed photophysical properties of Eu1, Eu2, and Eu3 were analyzed using both experimental and
computational methods. By analyzing the experimental and time-dependent
density functional theory (TD-DFT) data in conjunction with the Lanthanide
Luminescence Software Package (LUMPAC), we further elucidated the
energy transfer processes in the OEuCs. Finally, the complexes were
tested as the emitting layer (EML) in a multilayered device to fabricate
red organic light-emitting diodes (R-OLED). Through optimization and
device engineering, we have achieved a remarkable electroluminescence
(EL) performance of maximum current efficiency (ηc) = 12.32 cd/A, maximum power efficiency (ηp) =
11.73 lm/W, and maximum external quantum efficiency (EQEmax) = 10.20%, respectively, for the Eu3-based double-EML
OLED. To the best of our knowledge, this is the highest reported overall
EL performance among the OEuCs until now.