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1.
Efficient blue organic light‐emitting diodes using N2,N2,N11,N11,5,6,7,8‐octaphenyltriphenylene‐2,11‐diamine derivatives
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Young Seok Kim Su Jin Jeong Hyun Woo Lee Jwajin Kim Song Eun Lee Young Kwan Kim Seung Soo Yoon 《Luminescence》2016,31(4):1031-1036
In this study, we have synthesized phenyl‐substituted triphenylene derivatives, using the Diels–Alder reaction and the Buchwald–Hartwig reaction. To investigate electroluminescence properties of these materials, multilayer organic light‐emitting diode (OLED) devices were fabricated with a structure of indium–tin–oxide (ITO) (180 nm)/4,4′‐bis(N‐(1‐naphthyl)‐N‐phenylamino)biphenyl (NPB) (50 nm)/blue‐emitting materials (1–3) (30 nm)/bathophenanthroline (Bphen) (35 nm)/lithium quinolate (Liq) (2 nm)/Al (100 nm). A device using N2,N2,N11,N11,5,6,7‐heptaphenyltriphenylene‐2,11‐diamine (2) exhibited efficient blue emission with luminous, power, and external quantum efficiencies of 0.92 cd/A, 0.67 lm/W, and 1.17% at 20 mA/cm2, respectively. The Commission International de L'Éclairage coordinates of this device were (x = 0.15, y = 0.09) at 6.0 V. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
2.
Blue organic light‐emitting diodes based on fluorene‐bridged quinazoline and quinoxaline derivatives
Dong Young Kim Jisu Kang Song Eun Lee Young Kwan Kim Seung Soo Yoon 《Luminescence》2017,32(7):1180-1185
Two blue emitters based on fluorene‐bridged quinazoline and quinoxaline derivatives were prepared via the Suzuki reaction. Their photoluminescent properties were investigated. Furthermore, theoretical studies on these materials using the density functional theory calculation were conducted. To explore their electroluminescent properties, multilayered organic light‐emitting diodes were fabricated with the following device structure: indium–tin–oxide (180 nm)/4,4′‐bis(N‐(1‐naphthyl)‐N‐phenylamino)biphenyl (50 nm)/blue emitting materials ( 1 and 2 ) (30 nm)/bathophenanthroline (35 nm)/8‐hydroxy‐quinolinato lithium (2 nm)/Al (100 nm). Two devices showed efficient blue emission with the external quantum efficiencies of 1.58% and 1.30%, respectively, at 20 mA/cm2, and Commission Internationale dÉclairage coordinates of (0.18, 0.24) and (0.19, 0.27) at 6.0 V. These results suggest that the self‐aggregation properties of emitters would have considerable effects on their photoluminescent and electroluminescent properties. 相似文献
3.
2‐(4‐Ethoxy phenyl)‐4‐phenyl quinoline organic phosphor for solution processed blue organic light‐emitting diodes
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This paper reports the synthesis and characterization of 2‐(4‐ethoxyphenyl)‐4‐phenyl quinoline (OEt‐DPQ) organic phosphor using an acid‐catalyzed Friedlander reaction and the preparation of blended thin films by molecularly doping OEt‐DPQ in poly(methyl methacrylate) (PMMA) at different wt%. The molecular structure of the synthesized phosphor was confirmed by Fourier transform infra‐red (FTIR) spectroscopy and nuclear magnetic resonance spectra (NMR). Surface morphology and percent composition of the elements were assessed by scanning electron microscopy (SEM) and energy dispersive analysis of X‐rays (EDAX). The thermal stability and melting point of OEt‐DPQ and thin films were probed by thermo‐gravimetric analysis (TGA)/differential thermal analysis (DTA) and were found to be 80°C and 113.6°C, respectively. UV–visible optical absorption spectra of OEt‐DPQ in the solid state and blended films produced absorption bands in the range 260–340 nm, while photoluminescence (PL) spectra of OEt‐DPQ in the solid state and blended thin films demonstrated blue emission that was registered at 432 nm when excited at 363–369 nm. However, solvated OEt‐DPQ in chloroform, tetrahydrofuran or dichloromethane showed a blue shift of 31–43 nm. Optical absorption and emission parameters such as molar extinction coefficient (ε), energy gap (Eg), transmittance (T), reflectance (R), refractive index (n), oscillator energy (E0) and oscillator strength (f), quantum yield (φf), oscillator energy (E0), dispersion energy (Ed), Commission Internationale de l'Éclairage (CIE) co‐ordinates and energy yield fluorescence (EF) were calculated to assess the phosphor's suitability as a blue emissive material for opto‐electronic applications such as organic light‐emitting diodes (OLEDs), flexible displays and solid‐state lighting technology. 相似文献
4.
Near‐UV excited narrow line red‐emitting phosphors, Eu3+‐activated Y2MoO6 systems, were synthesized using a simple molten salt reaction. The structure and photoluminescence characteristics were investigated using X‐ray powder diffraction, UV–Vis absorption and fluorescent spectrophotometry. The excitation spectra show strong broad‐band absorptions in the near‐UV to blue light regions which match the radiation of near‐UV light‐emitting diode chips well. Under excitation of either near‐UV or blue light, intense red emission with a main peak of 611 nm is observed, ascribed to the 5D0–7F2 transition of Eu3+ ions; the optimal doping concentration is 20 mol%. The chromaticity coordinates (x = 0.65, y = 0.34) of the as‐obtained phosphor are very close to the National Television Standard Committee standard values (x = 0.67, y = 0.33). All these characteristics suggest that this material is a promising red‐emitting phosphor candidate for white‐LEDs based on near‐UV LED chips. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
5.
A new series of blue light‐emitting 2,4‐diphenylquinoline (DPQ) substituted blue light‐emitting organic phosphors namely, 2‐(4‐methoxy‐phenyl)‐4‐phenyl‐quinoline (OMe–DPQ), 2‐(4‐methyl‐phenyl)‐4‐phenylquinoline (M‐DPQ), and 2‐(4‐bromo‐phenyl)‐4‐phenylquinoline (Br‐DPQ) were synthesized by substituting methoxy, methyl and bromine at the 2‐para position of DPQ, respectively by Friedländer condensation of 2‐aminobenzophenone and corresponding acetophenone. The synthesized phosphors were characterized by different techniques, e.g., Fourier transform infra‐red (FTIR), differential scanning calorimeter (DSC), UV‐visible absorption and photoluminescence spectra. FTIR spectra confirms the presence of chemical groups such as C=O, NH, or OH in all the three synthesized chromophores. DSC studies show that these complexes have good thermal stability. Although they are low‐molecular‐weight organic compounds, they have the potential to improve the stability and operating lifetime of a device made out of these complexes. The synthesized polymeric compounds demonstrate a bright emission in the blue region in the wavelength range of 405–450 nm in solid state. Thus the attachment of methyl, methoxy and bromine substituents to the diphenyl quinoline ring in these phosphors results in colour tuning of the phosphorescence. An electroluminescence (EL) cell of Br‐DPQ phosphor was made and its EL behaviour was studied. A brightness–voltage characteristics curve of Br‐DPQ cell revealed that EL begins at 400 V and then the brightness increases exponentially with applied AC voltage, while current–voltage (I–V) characteristics revealed that the turn on voltage of the fabricated EL cell was 11 V. Hence this phosphor can be used as a promising blue light material for electroluminescent devices. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
6.
A series of Ce3+‐activated blue‐emitting phosphors BaY2Si3O10 (BYSO) was designed and synthesized by a conventional solid‐state method. Upon ultraviolet light (250–370 nm) excitation, the obtained phosphors showed an intense blue emission band centered at 400–427 nm depending on doping concentration, and corresponding to the 5d→4f transition of Ce3+. The effects of doping concentration on crystal structure, emitting color, photoluminescence and photoluminescence excitation spectra, as well as the concentration quenching mechanism were studied in detail. The optimal doping concentration of Ce3+ in this phosphor was demonstrated to be about 0.75% and the concentration quenching mechanism can be ascribed to electric dipole–dipole interactions with a critical distance of ~38 Å. These fine luminescence properties indicate that BYSO:Ce3+ may be a potential blue phosphor for full‐color ultra‐violet (UV) white light emitting diodes (WLEDs). 相似文献
7.
Yongfu Teng 《Luminescence》2021,36(1):256-260
A near‐ultraviolet (NUV) blue‐emitting phosphor Ba9Al2Si6O24:Ce3+ (BAS:Ce3+) was synthesized using a high‐temperature solid‐state reaction. BAS:Ce3+ had an excitation band peak at about 328 nm and showed a blue emission band. The NUV‐blue emission band had a peak at about 386 nm with a band width of about 60 nm, attributed to the 5d–4f transition of Ce3+. Fluorescent decay showed an exponential model with a lifetime of 27.2 nsec. At 150°C, the luminescence intensity decreased to 68.7% compared with the intensity at room temperature. 相似文献
8.
A variety of chiral derivatives of benzo[d]naphtho[1,2‐b]pyran‐6‐one were prepared in a single step by Et3N‐mediated condensation of homophthalic anhydride with different derivatives of (S)‐amino acid chlorides at –5 °C by employing a chiral pool methodology. Chirality 27:951–957, 2015. © 2015 Wiley Periodicals, Inc. 相似文献
9.
This paper presents a green and cost‐effective recipe for the synthesis of blue‐emitting ZnO nanoparticles (NPs) using cellulose bio‐templates. Azadirachta indica (neem) leaf extract prepared in different solvents were used as biological templates to produce nanostructures of wurtzite ZnO with a particle size ~12–36 nm. A cellulose‐driven capping mechanism is used to describe the morphology of ZnO NPs. The scanning electron microscopy (SEM), transmission electron microscopy (TEM), X‐ray diffraction (XRD), Fourier transform infra‐red (FTIR) and photoluminescence (PL) studies showed that solvents affect the growth process and the capping mechanism of bio‐template severely. Structural changes in ZnO NPs were evident with variation in pH, dielectric constants (DC) and boiling points (BP) of solvents. Furthermore, an energy band model is proposed to explain the origin of the blue emission in the as‐obtained ZnO NPs. PL excitation studies and the theoretical enthalpy values of individual defects were used to establish the association between the interstitial‐zinc‐related defect levels and the blue emission. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
10.
CaS:Ce3+ is an efficient green‐emitting (535 nm) phosphor, excitable with blue light (450–470 nm) and was synthesized via a solid‐state reaction method by heating under a reducing atmosphere. The luminescent properties, photoluminescent (PL) excitation and emission of the phosphor were analyzed by spectrofluorophotometry. The excitation and emission peaks of the CaS:Ce3+ phosphor lay in the visible region, which made them relevant for light‐emitting diode (LED) application for the generation of white light. Judd‐Oflet parameters were calculated and revealed that green light emitted upon blue illumination. The prepared phosphor had strong blue absorption at 470 nm and a broad green emission band range from 490–590 nm with the peak at 537 nm. The characteristics of the CaS:Ce3+ phosphor make it suitable for use as a wavelength tunable green emitting phosphor for three band white LEDs pumped by a blue LED (470 nm). The Commission International de l'Eclairage co‐ordinates were calculated by a spectrophotometric method using the spectral energy distribution (0.304, 0.526) and confirm the green emission. The potential application of this phosphor is as a phosphor‐converted white light‐emitting diode. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
11.
Photoluminescence,cathodoluminescence and thermal stability of Sm3+‐activated Sr3La(VO4)3 red‐emitting phosphors
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A series of Sm3+‐activated Sr3La(VO4)3 phosphors were synthesized by a facile sol‐gel method. X‐ray diffraction patterns and photoluminescence (PL)/cathodoluminescence (CL) spectra as well as PL decay curves were employed to characterize the obtained samples. Upon 402 nm light excitation, the characteristic emissions of Sm3+ ions corresponding to 4G5/2→6HJ transitions were observed in all the as‐prepared products. The PL emission intensity was increased with increase in Sm3+ ion concentration, while concentration quenching occurred when the doping concentration was over 4 mol%. The non‐radiative energy transfer mechanism for concentration quenching of Sm3+ ions was dominated by dipole–dipole interaction and the critical distance was around 21.59 Å. Furthermore, temperature‐dependent PL emission spectra revealed that the obtained phosphors possessed good thermal stability with an activation energy of 0.19 eV. In addition, the CL spectra of the samples were almost the same as the PL spectra, and the CL emission intensity showed a tendency to increase with increase in accelerating voltage and filament current. These results suggest that the Sm3+‐activated Sr3La(VO4)3 phosphors with good color coordinates, high color purity and superior thermal stability may be a potential candidate for applications in white light‐emitting diodes and field‐emission displays as red‐emitting phosphors. 相似文献
12.
Sr2ZnWO6:Eu3+,Bi3+,Li+: a potential white‐emitting phosphor for near‐ultraviolet white light‐emitting diodes
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Yuanyuan Ma Weiguang Ran Weina Li Chunyan Ren Haiyan Jiang Jinsheng Shi 《Luminescence》2016,31(3):665-670
A series of Sr2ZnWO6 phosphors co‐doped with Eu3+, Bi3+ and Li+ were prepared using the Pechini method. The samples were tested using X‐ray diffraction and luminescence spectroscopy. The results show that the samples can be effectively excited by near‐ultraviolet (UV) and UV light. The introduction of Bi3+ and Li+ significantly enhances the fluorescence emission of Sr2ZnWO6:Eu3+ and changes the light emitted by the phosphors from bluish‐green to white. When excited at 371 nm, Sr2–x–zZn1–yWO6:xEu3+,yBi3+,zLi+ (x = 0.05, y = 0.05, z = 0.05, 0.1 and 0.15) samples emit high‐performance white light. Intense red–orange emission is also observed when excited by UV light. The obtained phosphor is a potential white‐emitting phosphor that could meet the needs of excitation sources with near‐UV chips. In addition, this phosphor might have promising application as a red–orange emitting phosphor for white light‐emitting diodes based on UV light‐emitting diodes. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
13.
Crystal structure and luminescence properties of the blue‐green‐emitting Ba9(Lu,Y)2Si6O24:Ce3+ phosphor
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Huawei Xu Zhi Zhou Yongfu Liu Qunxing Liu Zhiyuan He Shen Wang Linyi Huang Hongbo Zhu 《Luminescence》2017,32(5):812-816
Samples of the Ba9(Lu2‐xYx)Si6O24:Ce3+ (x = 0–2) blue‐green phosphors were synthesized by solid‐state reactions. All the samples exhibited a rhombohedral crystal structure. As the Y3+ concentration increased, the diffraction peaks shifted to the small angle region and the lattice parameters increased due to the larger ionic radius of Y3+ (r = 0.900 Å) compared with that of Lu3+ (r = 0.861 Å). Under 400 nm excitation, samples exhibited strong blue‐green emissions around 490 nm. The emission bands had a slight blue shift that resulted from weak crystal‐field splitting with increasing Y3+ concentration. Luminescence intensity and quantum efficiency (QE) decreased with increasing Y3+ concentration. The internal QE decreased from 74 to 50% and the external QE decreased from 50 to 34% as x increased from 0 to 2. The thermal stability of the Lu series was better than that of the Y‐series. The excitation band peak around 400 nm matched well with the emission light from the efficient near‐ultraviolet (NUV) chip. These results indicate promising applications for these NUV‐based white light‐emitting diodes. 相似文献
14.
Eu2+‐activated SrMg2Al16O27 novel phosphor was synthesized by a combustion method (550°C furnace). The prepared phosphor was first characterized by X‐ray diffraction (XRD) for confirmation of phase purity. SEM analysis showed the morphology of the phosphor. The photoluminescence characteristics showed broad‐band excitation at 324 nm, which was monitored at 465 nm emission wavelength. The SrMg2Al16O27:Eu2+ phosphor shows broad blue emission centred at 465 nm, emitting a blue light corresponding to 4f65d1 → 4f7 transition. Here we report the photoluminescence characteristics of the prepared phosphor and compare it with commercial BAM:Eu2+ phosphor. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
15.
Synthesis and characterization of pure and Li+ activated Alq3 complexes for green and blue organic light emitting diodes and display devices
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Pure and Li+‐doped Alq3 complexes were synthesized by simple precipitation method at room temperature, maintaining the stoichiometric ratio. These complexes were characterized by X‐ray diffraction, ultraviolet‐visible absorption and Fourier transform infrared and photoluminescence (PL) spectra. X‐ray diffraction analysis reveals the crystalline nature of the synthesized complexes, while Fourier transform infrared spectroscopy confirm the molecular structure, the completion of quinoline ring formation and presence of quinoline structure in the metal complex. Ultraviolet‐visible and PL spectra revealed that Li+ activated Alq3 complexes exhibit the highest intensity in comparison to pure Alq3 phosphor. Thus, Li+ enhances PL emission intensity when doped into Alq3 phosphor. The excitation spectra lie in the range of 383–456 nm. All the synthesized complexes other than Liq give green emission, while Liq gives blue emission with enhanced intensity. Thus, he synthesized phosphors are the best suitable candidates for green‐ and blue‐emitting organic light emitting diode, PL liquid‐crystal display and solid‐state lighting applications. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
16.
Synthesis and luminescence properties of blue‐emitting phosphor Ca12Al14O32F2:Eu2+ for white light‐emitting diode
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A blue‐emitting phosphor Ca12Al14O32F2:Eu2+ was synthesized using a high‐temperature solid‐state reaction under a reductive atmosphere. The X‐ray diffraction measurements indicate that a pure phase Ca12Al14O32F2:Eu2+ can be obtained for low doping concentration of Eu2+. The phosphor has a strong absorption in the range 270–420 nm with a maximum at ~340 nm and blue emission in the range 400–500 nm with chromatic coordination of (0.152, 0.045). The optimal doping concentration is ~0.24. In addition, the luminescence properties of the as‐synthesized phosphor were evaluated by comparison with those of Ca12Al14O32Cl2:Eu2+ and the commercially available phosphor BaMgAl10O17:Eu2+. The emission intensity of Ca12Al14O32F2:Eu2+ was ~72% that of BaMgAl10O17:Eu2+ under excitation at λ = 375 nm. The results indicate that Ca12Al14O32F2:Eu2+ has potential application as a near‐UV‐convertible blue phosphor for white light‐emitting diodes. 相似文献
17.
An orange‐emitting phosphor, Eu2+‐activated LiSr4(BO3)3, was synthesized using the conventional solid‐state reaction. The photoluminescence excitation and emission spectra, and temperature dependence of the luminescence intensity of the phosphor were investigated. The results showed that LiSr4(BO3)3:Eu2+ could be efficiently excited by incident light of 250–450 nm, and emits a strong orange light. With increasing temperature, the emission bands of LiSr4(BO3)3:Eu2+ show an abnormal blue‐shift with broadening bandwidth and decreasing emission intensity. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
18.
《Luminescence》2017,32(3):334-340
A series of Eu2+‐activated barium orthosilicates (BaZnSiO4) were synthesized using a high‐temperature solid‐state reaction. A photoluminescence excitation study of Eu2+ shows a broad absorption band in the range of 270–450 nm, with multiple absorption peak maxima (310, 350 and 400 nm) due to 4f–5d electronic transition. The emission spectra of all the compositions show green color emission (in the spectral region 450–550 nm with a peak maximum at 502 nm and a shoulder at ~ 490 nm) with appropriate Comission Internationale de l'Eclairage (CIE) color coordinates. The two emission peaks are due to the presence of Eu2+ in two different Ba sites in the BaZnSiO4 host lattice. The energy transfers between the Eu2+ ions in BaZnSiO4 host are elucidated from the critical concentration quenching data based on the electronic multipolar interaction. All Eu2+‐activated BaZnSiO4 phosphor materials can be efficiently excited in the ultraviolet (UV) to near UV‐region (270–420 nm), making them attractive candidate as a green phosphor for solid state lighting–white light‐emitting diodes. 相似文献
19.
Pure and Na+‐doped Alq3 complexes were synthesized by a simple precipitation method at room temperature, maintaining a stoichiometric ratio. These complexes were characterized by X‐ray diffraction, Fourier transform infrared (FTIR), UV/Vis absorption and photoluminescence (PL) spectra. The X‐ray diffractogram exhibits well‐resolved peaks, revealing the crystalline nature of the synthesized complexes, FTIR confirms the molecular structure and the completion of quinoline ring formation in the metal complex. UV/Vis absorption and PL spectra of sodium‐doped Alq3 complexes exhibit high emission intensity in comparison with Alq3 phosphor, proving that when doped in Alq3, Na+ enhances PL emission intensity. The excitation spectra of the synthesized complexes lie in the range 242–457 nm when weak shoulders are also considered. Because the sharp excitation peak falls in the blue region of visible radiation, the complexes can be employed for blue chip excitation. The emission wavelength of all the synthesized complexes lies in the bluish green/green region ranging between 485 and 531 nm. The intensity of the emission wavelength was found to be elevated when Na+ is doped into Alq3. Because both the excitation and emission wavelengths fall in the visible region of electromagnetic radiation, these phosphors can also be employed to improve the power conversion efficiency of photovoltaic cells by using the solar spectral conversion principle. Thus, the synthesized phosphors can be used as bluish green/green light‐emitting phosphors for organic light‐emitting diodes, flat panel displays, solid‐state lighting technology – a step towards the desire to reduce energy consumption and generate pollution free light. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
20.
Synthesis and investigation of the conversion reactions of pyrimidine‐thiones with nucleophilic reagent and evaluation of their acetylcholinesterase,carbonic anhydrase inhibition,and antioxidant activities
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Parham Taslimi Afsun Sujayev Fikret Turkan Emin Garibov Zübeyir Huyut Vagif Farzaliyev Sevgi Mamedova İlhami Gulçin 《Journal of biochemical and molecular toxicology》2018,32(2)
The conversion reactions of pyrimidine‐thiones with nucleophilic reagent were studied during this scientific research. For this purpose, new compounds were synthesized by the interaction between 1,2‐epoxy propane, 1,2‐epoxy butane, and 4‐chlor‐1‐butanol and pyrimidine‐thiones. These pyrimidine‐thiones derivatives ( A–K ) showed good inhibitory action against acetylcholinesterase (AChE), and human carbonic anhydrase (hCA) isoforms I and II. AChE inhibition was in the range of 93.1 ± 33.7–467.5 ± 126.9 nM. The hCA I and II were effectively inhibited by these compounds, with Ki values in the range of 4.3 ± 1.1–9.1 ± 2.7 nM for hCA I and 4.2 ± 1.1–14.1 ± 4.4 nM for hCA II. On the other hand, acetazolamide clinically used as CA inhibitor showed Ki value of 13.9 ± 5.1 nM against hCA I and 18.1 ± 8.5 nM against hCA II. The antioxidant activity of the pyrimidine‐thiones derivatives ( A–K ) was investigated by using different in vitro antioxidant assays, including Cu2+ and Fe3+ reducing, 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH?) radical scavenging, and Fe2+ chelating activities. 相似文献