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MATERIALS RESEARCH BULLETIN · 2015 · IF 2.288

Organic solution-processible electroluminescent molecular glasses for non-doped standard red OLEDs with electrically stable chromaticity

Xiaoman Bi,Weiwei Zuo,Yingliang Liu,Zhenru Zhang,Cen Zeng,Shengang Xu,Shaokui Cao

Organic light-emitting molecular glasses (OEMGs) are synthesized through the introduction of nonplanar donor and branched aliphatic chain into electroluminescent emitters. The target OEMGs are characterized by 1 H NMR, 13 C NMR, IR, UV–vis and fluorescent spectra as well as elemental analysis, TG and DSC. The results indicated that the optical, electrochemical and electroluminescent properties of OEMGs are adjusted successfully by the replacement of electron-donating group. The non-doped OLED device with a standard red electroluminescent emission is achieved by spin-coating the THF solution of OEMG with a triphenylamine moiety. This non-doped red OLED device takes on an electrically stable electroluminescent performance, including the stable maximum electroluminescent wavelength of 640   nm, the stable luminous efficiency of 2.4   cd/A and the stable CIE1931 coordinate of ( x , y )   =   (0.64, 0.35), which is basically in accord with the CIE1931 coordinate ( x , y )   =   (0.64, 0.33) of standard red light in PAL system.

CAS / MDL: 100-39-0 14221-01-3
研究领域: 材料科学 · 光学 · 电子工程
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DYES AND PIGMENTS · 2024 · IF 4.1

Anthracene derivatives with electron-transport units for non-doped blue fluorescent organic light-emitting diodes

Zhiming Zhong,Tingxin Chen,Feng Peng,Pengfei Niu,Jin Xu,Lei Ying

Blue organic light-emitting diodes with non-doped emissive layer (EML) structures have been garnered increasing interest due to their convenience of manufacturing process. For this purpose, we designed and synthesized two novel anthracene derivatives, PO2PhAnTz and PO2PhAnBI. Both derivatives exhibited bright blue electroluminescence emission and a relatively low operating voltage with a simple bilayer device structure. The PO2PhAnBI with triphenyl-phosphine oxide moiety as host, anthracene core as dopant and benzimidazole as electron transport group, realized a balanced bipolar transport and attained a maximum external quantum efficiency of 5.74 %. The findings shed light on the molecule design role toward high-efficiency non-doped blue OLEDs.

研究领域: 材料科学 · 有机电子学
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TETRAHEDRON · 2022 · IF 2.388

Construction of biomass-based AIEgens with dehydroabietic acid triarylamine and tetraphenylethene Moieties for non-doped OLEDs

Yanan Gao,Xinwen Zhang,Jie Song,Liwei Dou,Hong Gao,Shibin Shang,Zhanqian Song

Dehydroabietic acid triarylamine (DTPA) synthesized from renewable natural rosin is an excellent hole-transporting material but is affected by aggregation-caused quenching in the solid state. Herein, two new biomass-based AIE luminogens (AIEgens), namely DTPA-TPE and 2DTPA-TPE, were synthesized through the attachment of DTPA to tetraphenylethene (TPE). Their aggregates in poor solvents and thin films have a strong emission with a fluorescence quantum yield of up to 67.4%. DTPA AIEgens exhibit superior thermal and morphological stability, showing high thermal degradation ( T 5d up to 412.0 °C) and glass transition ( T g up to 150.8 °C) temperatures. Electroluminescence (EL) devices with compounds used either as emitting layers (EMLs) or as EMLs and hole-transporting layers (HTLs) were constructed. The device with 2DTPA-TPE as the EML exhibits the best performance (turn-on voltage of 2.4 V, maximum luminance of 12,414 cd m −2 , current efficiency of 6.2 cd A −1 , and power efficiency of 6.5 lm W −1 ). The devices without the HTL ( N , N ′-di-1-naphthyl- N , N ′-diphenylbenzidine (NPB)) exhibit performances comparable with or better than those of the devices with NPB. These results indicate that these compounds are promising luminescent materials for non-doped organic light-emitting diodes.

研究领域: 有机化学 · 材料科学 · 光学工程
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MOLECULES · 2023 ·Vol. 28 ·期 7 ·3282 · IF 4.6

Tuning Photophysical Properties via Positional Isomerization of the Pyridine Ring in Donor–Acceptor-Structured Aggregation-Induced Emission Luminogens Based on Phenylmethylene Pyridineacetonitrile Derivatives

Haiya Sun,Shuixin Chen,Aiguo Zhong,Rong Sun,Jiajie Jin,Jiahao Yang,Dongzhi Liu,Junfeng Niu,Shengli Lu

A series of aggregation-induced emission (AIE)-featured phenylmethylene pyridineacetonitrile derivatives namedo-DBCNPy((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-2-yl)acrylonitrile),m-DBCNPy((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-3-yl)acrylonitrile), andp-DBCNPy((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-4-yl)acrylonitrile) have been synthesized by tuning the substitution position of the pyridine ring. The linkage manner of the pyridine ring had influences on the molecular configuration and conjugation, thus leading to different photophysical properties. The absorption and fluorescence emission peak showed a bathochromic shift when the linking position of the pyridine ring changed from themetato theorthoandparaposition. Meanwhile,o-DBCNPyexhibited the highest fluorescence quantum yield of 0.81 and the longest fluorescence lifetime of 7.96 ns as a neat film among all three isomers. Moreover, non-doped organic light-emitting diodes (OLEDs) were assembled in which the molecules acted as the light-emitting layer. Due to the relatively prominent emission properties, the electroluminescence (EL) performance of theo-DBCNPy-based OLED was superior to those of the devices based on the other two isomers with an external quantum efficiency (EQE) of 4.31%. The results indicate that delicate molecular modulation of AIE molecules could endow them with improved photophysical properties, making them potential candidates for organic photoelectronic devices.Keywords:aggregation-induced emission;phenylmethylene pyridineacetonitrile;positional isomerization;fluorescence emission;non-doped organic light-emitting diode

研究领域: 材料科学 · 光学 · 有机电子学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2016 ·Vol. 27 ·期 8 ·7839-7844 · IF 1.798

Application of ultra-thin CdS film as buffer layer in non-doped blue organic light-emitting diodes

Chang Xi,Jiang Wenlong,Ding Guiying,Wang Jin,Zhang Gang,Yao Guangxin

The device inserted 0.5 nm thick cadmium sulfide (CdS) as buffer layer, prepared by vacuum thermal evaporation method, has been studied on the non-doped blue organic light-emitting diode. Compared to the device without ultra-thin CdS film, the maximum luminance of the device with ultra-thin CdS film was 11,370 cd/m 2 at 11 V, and the maximum current efficiency reached 3.10 cd/A, increased 1.5 times and 1.2 times, respectively. In the optimized devices with the structure of ITO/MoO 3 (10 nm)/TPABBI (35 nm)/Bphen (40 nm)/CdS (0, 0.1, 0.3 and 0.5 nm)/LiF (0.5 nm)/Al (100 nm), the effects of CdS layer on the photoelectric performance of the devices were investigated in detail. When the CdS thickness was 0.3 nm, the maximum luminance was 13,590 cd/m 2 at 9 V and the turn on voltage was only 3 V. The maximum current efficiency of 3.42 cd/A was obtained. It is indicated that the simple structure of the device with inserted ultra-thin CdS film, cheap and stable inorganic photoelectric material, may be a promising way to fabricate hybrid organic–inorganic LEDs with high performances.

CAS / MDL: 1306-23-6
研究领域: 材料科学 · 光电子学 · 半导体物理
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