RESUMO
Two new nonconjugated linked dicarbazole materials, dCzPSi and dCzPSO2, with high triplet energy were synthesized and characterized. dCzPSi and dCzPSO2 were adopted as unipolar host materials for the green thermally activated delayed fluorescence (TADF) emitter (4CzIPN) to achieve high-efficiency organic light-emitting diodes (OLEDs). The electron-transporting acceptor, PO-T2T, was introduced to mix with dCzPSi and dCzPSO2 to give two new exciplex-forming systems that can improve the exciton formation propensity in the emitting layer. The relevant properties of these new exciplexes were characterized, and they were suggested as promising cohosts for the green TADF emitter, 4CzIPN. The characteristics of the devices employing single hosts (dCzPSi and dCzPSO2) and exciplex-forming cohosts (dCzPSi:PO-T2T and dCzPSO2:PO-T2T) were explored. The obtained results indicate that the Si-bridged dicarbazole compound dCzPSi outperforms its counterpart dCzPSO2 in which two carbazole groups are linked by an SO2 group. The device employed with the dCzPSi:PO-T2T cohost with 10 wt % 4CzIPN achieved a low Von of 2.2 V and maximum efficiencies of 21.1% (external quantum efficiency), 56.4 cd A-1 (current efficiency), 59.1 lm W-1 (power efficiency), as compared to those (18.7%, 56.6 cd A-1, and 68.5 lm W-1) of the dCzPSO2:PO-T2T-hosted device. This work verifies the advantages of using a cohost that can form an exciplex for boosting the device efficiency with reduced efficiency roll-off of TADF-based OLEDs.
RESUMO
A star-shaped 1,3,5-triazine/cyano hybrid molecule CN-T2T was designed and synthesized as a new electron acceptor for efficient exciplex-based OLED emitter by mixing with a suitable electron donor (Tris-PCz). The CN-T2T/Tris-PCz exciplex emission shows a high ΦPL of 0.53 and a small ΔET-S = -0.59 kcal/mol, affording intrinsically efficient fluorescence and highly efficient exciton up-conversion. The large energy level offsets between Tris-PCz and CN-T2T and the balanced hole and electron mobility of Tris-PCz and CN-T2T, respectively, ensuring sufficient carrier density accumulated in the interface for efficient generation of exciplex excitons. Employing a facile device structure composed as ITO/4% ReO3:Tris-PCz (60 nm)/Tris-PCz (15 nm)/Tris-PCz:CN-T2T(1:1) (25 nm)/CN-T2T (50 nm)/Liq (0.5 nm)/Al (100 nm), in which the electron-hole capture is efficient without additional carrier injection barrier from donor (or acceptor) molecule and carriers mobilities are balanced in the emitting layer, leads to a highly efficient green exciplex OLED with external quantum efficiency (EQE) of 11.9%. The obtained EQE is 18% higher than that of a comparison device using an exciplex exhibiting a comparable ΦPL (0.50), in which TCTA shows similar energy levels but higher hole mobility as compared with Tris-PCz. Our results clearly indicate the significance of mobility balance in governing the efficiency of exciplex-based OLED. Exploiting the Tris-PCz:CN-T2T exciplex as the host, we further demonstrated highly efficient yellow and red fluorescent OLEDs by doping 1 wt % Rubrene and DCJTB as emitter, achieving high EQE of 6.9 and 9.7%, respectively.
RESUMO
A sequential single-flask multicomponent reactions is highly effective for the synthesis of 1,2-dihydroisoquinolines through amidealkylation from intermediate N-acylisoquinolinium salts under mild conditions. N-Acylisoquinolinium ions and trichloromethyl-1-(1H-indol-3-yl)isoquinoline-2(1H)-carboxylate have demonstrated their reactivity toward aromatic and aliphatic π-nucleophiles. One of the 1,2-dihydroisoquinoline derivatives was found to be a potent inhibitor for transcription factor NF-κB by blocking IκBα degradation, p65 nuclear translocation, and NF-κB DNA binding in TNF-α-induced NIH 3T3 cells.