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Novel 9,9-dimethylfluorene-bridged D–π–A-type fluorophores with a hybridized local and charge-transfer excited state for deep-blue electroluminescence with CIE <sub/>y</sub> ～ 0.05
摘要： Deep-blue light emitting materials are of great significance in the fields of commercial full-color organic light-emitting diodes (OLEDs) and solid-state lighting. The hybridized local and charge-transfer excited state (HLCT) is a promising strategy to achieve deep-blue emission and high photoluminescence quantum yield. Based on HLCT, we designed and synthesized two novel donor–π–acceptor, 9,9-dimethylfluorene-bridged fluorophores (DFPBI & TFPBI) for efficient deep-blue OLED applications. Non-doped devices, with DFPBI and TFPBI as emitters, exhibit deep-blue emission with CIE coordinates of (0.154,0.042) and (0.152,0.054), accompanied by good EL performance with maximum external quantum efficiencies (EQEs) of 4.18% and 5.74%, respectively. In particular, the TFPBI-based non-doped device displays a slow efficiency roll-off at high luminance with an EQE of 5.50% and 4.80% at 100 cd m?2 and 1000 cd m?2, respectively. This work not only demonstrates the potential of these two fluorophores in deep-blue OLEDs, but also provides tactics for the design of deep-blue light emitting materials by using the 9,9-dimethylfluorene-bridged D–π–A architecture.
关键词： 9-dimethylfluorene,9,fluorophores,deep-blue emission,HLCT,OLEDs
更新于2025-09-19 17:15:36
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Asymmetric anthracene derivatives as multifunctional electronic materials for constructing simplified and efficient non-doped homogeneous deep blue fluorescent OLEDs
摘要： Herein, large π-conjugated core anthracene with an innate bipolar property was employed to construct multifunctional organic electronic materials. Delicate manipulating molecules via combining anthracene core and large periphery groups, two asymmetric anthracene derivatives namely (4-(10-(4-(9H-1,5-diazacarbazole-9-yl)phenyl)anthracen-9-yl)phenyl)diphenylphosphine oxide (p-PO15NCzDPA) and (3-(10-(3-(9H-1,5-diazarcarbazole-9-yl)phenyl)anthracen-9-yl)phenyl)diphenylphosphine oxide (m-PO15NCzDPA) were firstly designed and developed. The large periphery groups 1,5-diazarcarbazole (15NCz) and diphenylphosphine oxide (PO) efficiently interrupt the intramolecular π-conjugation, presenting an asymmetric bulky periphery enveloping strategy achieving highly twisted structures, which help to realize deep-blue emission. Meanwhile, due to the high PLQY and well-balanced bipolar transport characteristics, desired device addressing the contradiction of efficiency, color gamut and structure complexity is within reach. Detailed device engineering study was carried out, in which p-PO15NCzDPA and m-PO15NCzDPA were functioned as multifunction layers. As expected, p-PO15NCzDPA-based homogenous and unilateral homogenous OLEDs exhibited outstanding performance with impressive EQEmax of 4.55% and 6.40%, deep blue CIE coordinates of (0.152, 0.075) and (0.151, 0.066) at the voltage of 6 V, narrow FWHM of 46 nm and 50 nm, respectively. More importantly, the simplified homogenous device achieved extremely low efficiency roll-offs of 1.3% and 4.8% at 1000 and 5000 cd m-2, respectively. These results are among the most outstanding performance, which provided a guide for further improving the performance of deep blue fluorescent OLEDs and simplifying the structure of OLEDs.
关键词： asymmetric anthracene derivatives,homogenous device structure,multifunctional materials,deep-blue emission,fluorescent OLEDs
更新于2025-09-19 17:13:59
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Asymmetrically twisted phenanthrimidazole derivatives as host materials for blue fluorescent, green and red phosphorescent OLEDs
摘要： The electroluminescent properties of asymmetrically twisted phenanthrimidazole derivatives comprised of fluorescent anthracene or pyrene unit namely, 1-(1-(anthracen-10-yl)naphthalen-4-yl)-2-styryl-1H-phenanthro[9,10-d]imidazole (ANSPI), 1-(1-(pyren-1-yl) naphthalene-4-yl)-2-styryl-1H-phenanthro[9,10-d]imidazole (PNSPI), 4-(2-(4-(anthracen-9-yl) styryl)-1H-phenanthro[9,10-d]imidazol-1-yl)naphthalene-1-carbonitrile (ASPINC) and 4-(2-(4-(pyren-1-yl)styryl)-1H-phenanthro[9,10-d] imidazol-1-yl)naphthalene-1-carbonitrile (PSPINC) for blue OLEDs have been analyzed. The asymmetrically twisted conformation interrupt π-conjugation effectively results in deep-blue emission. The pyrene containing PSPINC based non-doped blue device (476 nm) shows maximium efficiencies (current efficiency (ηc)-4.23 cd/A; power efficiency (ηp)-2.86 lm/W; external quantum efficiency (ηex)-3.48%: CIE (0.16, 0.17) at 3.10 V. Among the doped blue devices, An(PPI)2:ASPINC shows high efficiencies (ηc-12.13 cd/A; ηp-5.98 lm/W; ηex-6.79%; L-23986 cd m?2; EL-458 nm) at 3.15 V with CIE (0.15, 0.17) than An(PPI)2:PSPINC based device which is inconsistent with non-doped device performances. The green and red PhOLEDs show higher efficiencies with Ir(ppy)3: ASPINC (ηc-50.6 cd/A; ηp-53.4 lm/W; ηex-17.0%; L-61581 cd m?2; EL-501 nm, CIE (0.31, 0.60) at 3.32 V and (bt)2Ir(dipba): ASPINC (ηc-15.2 cd/A; ηp-16.5 lm/W; ηex-14.5%; L-13456 cd m?2; EL-610 nm), CIE (0.63, 0.36) at 3.20 V, respectively. The complete energy transfer between the host and dopant molecules improved the efficiency of PHOLEDs.
关键词： asymmetrically twisted phenanthrimidazole derivatives,electroluminescent properties,energy transfer,blue OLEDs,deep-blue emission
更新于2025-09-11 14:15:04
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Efficient Deep-Blue Electrofluorescence with an External Quantum Efficiency Beyond 10%
摘要： The design of blue fluorescent materials combining both deep-blue emission (CIEy<0.06) and high-efficiency climbing over the typically limited exciton production efficiency of 25% is a challenge for organic light-emitting diodes (OLEDs). In this work, we have synthesized two blue luminogens, trans-9,10-bis(2-butoxyphenyl)anthracene (BBPA) and trans-9,10-bis (2,4-dimethoxyphenyl)anthracene with high photoluminescence quantum yields (PLQYs) of 89.5% and 87.0%, respectively. Intriguingly, we have proposed a strategy to avoid aggregation-caused quenching, which can effectively reduce the undesirable excimeric emission by introducing two host matrices with twisted molecular structure, 9,10-di(naphth-2-yl) anthracene and 10,100-bis-(4-fluorophenyl)-3,30-dimethyl-9,90-bianthracene (MBAn-(4)-F), in the BBPA emission layer. The device containing the EML of BBPA-doped MBAn-(4)-F exhibited a high external quantum efficiency of 10.27% for deep-blue emission with the Commission International de L’Eclairage CIE coordinates of (0.15, 0.05) via the steric effect. Importantly, this represents an advance in deep-blue-emitting fluorescent OLED architectures and materials that meet the requirements of high-definition display.
关键词： external quantum efficiency,deep-blue emission,fluorescent materials,OLEDs,steric effect
更新于2025-09-10 09:29:36