Abstract
We found an unusual way in improving electroluminescence efficiency of blue organic light-emitting diodes (OLEDs). Two electron deficient 4,5-diazafluorene- or di(2,2′-pyridyl)-containing blue fluorophores, PhSPN2N2DPV (4,5-diaza-2′-diphenylamino-7′-(2,2″-diphenylvinyl)-9,9′-spirobifluorene) and PhFpy2py2DPV (N-[7-(2,2-diphenylvinyl)-9,9′-di(2,2″-pyridyl)-2-fluorenyl]-N,N-diphenylamine), were synthesized and characterized for non-doped blue OLEDs. Whereas PhFpy2py2DPVOLED performs ordinarily, PhSPN2N2DPVOLED outperforms previously known PhSPDPV (2-diphenylamino-7-diphenylvinyl-9,9′-spirobifluorene) OLED significantly: maximum external quantum efficiency of ∼5% (4.6% at 20 mA cm−2) and the peak electroluminance of 60510 cd m−2 (1810 cd m−2 at 20 mA cm−2) versus 3.4% (2.9% at 20 mA cm−2) and 33020 cd m−2 (910 cd m−2 at 20 mA cm−2) ofPhSPDPVOLED. We attribute the superior performance of PhSPN2N2DPVOLED to the good charge balancing, which is in turn due to the very low hole mobility of PhSPN2N2DPV. The experimental results reveal that the electron-deficient moiety, 4,5-diazafluorene or di(2,2′-dipyridyl), increases electron affinity but reduces the hole mobility. Electron mobility, determined by time-of-flight (TOF) method, is 5 × 10−5 and 5 × 10−4 cm2V−1 s−1 (at an electric field of 4.9 × 105 V cm−1) for PhSPN2N2DPV and PhFpy2py2DPV, respectively. Surprisingly, they are not higher than 8 × 10−4 cm2V−1 s−1 of nonpolar PhSPDPV. On the other hand, hole mobility is 2 × 10−6 and 2 × 10−4 cm2V−1 s−1 for PhSPN2N2DPV and PhFpy2py2DPV, respectively, and they are both significantly lower than 6 × 10−3 cm2V−1 s−1 of PhSPDPV. For PhSPN2N2DPV and PhFpy2py2DPV bipolar blue fluorophores, we have demonstrated that electron-transporting and light-emitting functions involve different molecular halves. The design of such molecular halves greatly facilitates the optical and electronic optimizations of fluorophores for high-performance OLEDs.
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