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Two alcohol-soluble electron-transport materials (ETMs), diphenyl(4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl) phosphine oxide (pPBlPO) and (3,5-bis(1-phenyl-1H-benzo[ d]imidazol-2-yl)phenyl)diphenylphosphine oxide (mBPBIPO), have been synthesized. The physical properties of these ETMs were investigated and they both exhibited high electron-transport mobilities (1.67 x 10-4 and 2.15 x 10-4 cm2V-1 s-1), high glass-transition temperatures (81 and 110 °C), and low LUMO energy levels (-2.87 and -2.82 eV, respectively). The solubility of PBIPO in n-butyl alcohol was more than 20mgmL-1, which meets the requirement for fully solution-processed organic light-emitting diodes (OLEDs). Fully solution-processed green-phosphorescent OLEDs were fabricated by using alcohol-soluble PBIPO as electron-transport layers (ETLs), and they exhibited high current efficiencies, power efficiencies, and external quantum efficiencies of up to 38.43 cdA-1, 26.64 lmW-1, and 10.87%, respectively. Compared with devices that did not contain PBIPO as an ETM, the performance of these devices was much improved, which indicated the excellent electrontransport properties of PBIPO. [ABSTRACT FROM AUTHOR]

Aryl-substituted phenanthroimidazoles (PIs) have attracted tremendous attention in the field of organic light-emitting diodes (OLEDs), because they are simple to synthesize and have excellent thermal properties, high photoluminescence quantum yields (PLQYs), and bipolar properties. Herein, a novel blue-green emitting material, ( E)-2-{4′-[2-(anthracen-9-yl)vinyl]-[1,1′-biphenyl]-4-yl}-1-phenyl-1 H-phenanthro[9,10- d]imidazole (APE-PPI), containing a t-APE [1-(9-anthryl)-2-phenylethene] core and a PI moiety was designed and synthesized. Owing to the PI skeleton, APE-PPI possesses high thermal stability and a high PLQY, and the compound exhibits bipolar transporting characteristics, which were identified by single-carrier devices. Nondoped blue-green OLEDs with APE-PPI as the emitting layer show emission at λ=508 nm, a full width at half maximum of 82 nm, a maximum brightness of 9042 cd m−2, a maximum current efficiency of 2.14 cd A−1, and Commission Internationale de L'Eclairage (CIE) coordinates of (0.26, 0.55). Furthermore, a white OLED (WOLED) was fabricated by employing APE-PPI as the blue-green emitting layer and 4-(dicyanomethylene)-2- tert-butyl-6-(1,1,7,7-tetramethyljulolidin-4-yl-vinyl)-4 H-pyran (DCJTB) doped in tris-(8-hydroxyquinolinato)aluminum (Alq3) as the red-green emitting layer. This WOLED exhibited a maximum brightness of 10029 cd m−2, a maximum current efficiency of 16.05 cd A−1, CIE coordinates of (0.47, 0.47), and a color rendering index (CRI) of 85. The high performance of APE-PPI-based devices suggests that the t-APE and PI combination can potentially be used to synthesize efficient electroluminescent materials for WOLEDs. [ABSTRACT FROM AUTHOR]

Typical π-π stacking and aggregation-caused quenching could be suppressed in the film-state by the spiro conformation molecular design in the field of organic light-emitting diodes (OLEDs). Herein, a novel deep-blue fluorescent material with spiro conformation, 1-(4-( tert-butyl)phenyl)-2-(4-(10-phenyl-10 H-spiro[acridine-9,9′-fluoren]-2-yl)phenyl)-1 H-phenanthro[9,10- d]imidazole ( SAF-BPI), was designed and synthesized. The compound consists of spiro-acridine-fluorene (SAF) as donor part and phenanthroimidazole (BPI) as acceptor part. Owing to the rigid SAF skeleton, this compound exhibits a high thermal stability with a glass transition temperature ( Tg) of 198 °C. The compound exhibits bipolar transporting characteristics demonstrated by the single-carrier devices. The non-doped OLEDs based on the SAF-BPI as the emitting layer shows maximum emission at 448 nm, maximum luminance of 2122 cd m−2, maximum current efficiency (CE) of 3.97 cd A−1, and a maximum power efficiency of 2.08 lm W−1. The chromaticity coordinate is stable at (0.15, 0.10) at the voltage of 7-11 V. The device shows a slow efficiency roll-off with CE of 3.35 and 2.85 cd A−1 at 100 and 1000 cd m−2, respectively. [ABSTRACT FROM AUTHOR]