• 대한화학회지
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• 제54권3호
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• pp.291-294
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• 2010

본 연구에서는 다양한 농도의 BCzVBi를 청색 형광도판트, DPVBi를 청색 호스트 물질로 적용한 청색OLED 소자를 제작하였다. 최적화된 고효율 청색 OLED 소자의 적층 구조는 NPB (500 ${\AA}$)/DPVBi:BCzVBi-6%(150 ${\AA}$)/$Alq_3$(300 ${\AA}$)/Liq(20 ${\AA}$)/Al (1000 ${\AA}$)으로 구성되었다. 청색 OLED의 최대휘도는 구동전압 13.8V에서13200 cd/$m^2$이고 전류밀도 및 최대효율은 각각 1000 cd/$m^2$의 휘도에서 26.4 mA/$cm^2$, 구동전압 3.9 V에서 4.24 cd/A 이었다. 도핑된 청색 OLED 소자의 발광효율은 도핑되지 않은 소자의 2배에 이른 반면 색좌표는 (0.16, 0.19)로 서로 비슷하였다. BCzVBi가 6% 도핑된 청색 OLED 445 nm와 470 nm에 2개의 EL 스펙트럼의 Peak이 존재하는 반면 도핑되지 않은 순수한 DPVBi 청색OLED 소자는 456 nm에서의 유일한 Peak만을 보여주고 있다. 이는 호스트 물질인 DPVBi의 LUMO와 도판트 물질인 BCzVBI의 LUMO 사이에 분자 진동에 의한 페르스터 에너지 전이에 기인한 것이다.

• 대한전기학회:학술대회논문집
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• 대한전기학회 1999년도 하계학술대회 논문집 D
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• pp.1800-1802
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• 1999

Electroluminescence is occurred when phosphor is located in electric field. In this paper, we made powder electroluminescent device (PELD) with structured ITO film/phosphor/Insulator/silver paste. The transparent electrode was ITO film and green(2704-01) and orange(2702-02) and blue-green(2703-01) were used as phosphor. The insulator was $BaTiO_3$ and $Y_2O_3$, back electrode was silver paste. To investigate electrical and optical properties of PELDs, EL spectrum, Brightness, Transferred charge density using Sawyer-Towers circuit was measured.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2001년도 하계학술대회 논문집
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• pp.343-346
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• 2001

To implementation of white electroluminescnet device in this paper, two methods were tried without synthesis of new white EL phosphor. At first, ZnS:Mn,Cl was mixed with ZnS:Cu from 20 to 50 weight percents. Second, ZnS:Mn,Cl was mixed with blue dye from 0 to 1.2 weight percents. The devices for experiments were measured as following; current-voltage, emission spectrum, brightness-voltage and CIE coordinate system and frequency properties.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2005년도 International Meeting on Information Displayvol.II
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• pp.1416-1418
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• 2005

A new DCM derivative containing a phenothiazine moiety, 4-(dicyanomethylene)-2-t-butyl-6-(9-ethylphenothiazine-2- enyl)-4H-pyran (DCPTZ), has been synthesized as an orange-red fluorescent dye molecule for organic lightemitting diodes (OLEDs). EL devices with the structure of $ITO/PEDOT-PSS/{\alpha}-NPD/Alq_3:DCPTZ/Alq_3/LiF/Al$ have been fabricated with changing the doping concentration of the DCPTZ. Maximum EL spectra of the devices ranged from $580{\sim}620$ nm depending on the doping concentration of the dye molecule. An EL device with 0.5 % doping concentration showed CIE coordinate (0.51, 0.47) at luminance of 100 $cd/m^2$. White light-emitting devices with the structure of $ITO/PEDOT-PSS/{\alpha}-NPD/{\alpha}-NPD:DCPTZ/DPVBi/Alq_3/$ LiF/Al have been also fabricated. The thickness of blue light-emitting 1,4-bis(2,2- diphenylvinyl)benzene (DPVBi) layer was changed to obtain a white light-emission. A white light-emission from the device was observed when the thickness of the DPVBi layer became thicker than 10 nm.

• 폴리머
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• 제29권4호
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• pp.357-362
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• 2005

중합체의 공액길이를 제어하고 이들이 갖는 에너지 준위를 조절하며, 발광성능향상과 발광파장을 조절하려는 목적으로 설폰기가 포함된 페닐렌-비닐렌계의 새로운 전기발광 고분자들을 Witting 중합을 통해 합성하였다. 합성된 고분자들은 일반 유기 용매에 좋은 용해성을 보였고 $400^{circ}C$ 정도의 초기분해온도와 $200^{circ}C$ 전후의 높은 유리전이온도를 가짐으로써 열적 안정성이 매우 높음을 확인하였다. 각각의 고분자는 용액과 필름상태에서 모두 설폰기의 꺾임에 의해 공액길이가 짧아질수록 UV 흡수와 발광 스펙트럼이 단파장으로 이동하였고 이를 통해 설폰기가 효율적으로 발광파장을 제어하는 것을 확인하였다. 또한 CV측정과 이론적인 계산을 통해 전자친화도가 큰 설폰기에 의해서 합성된 고분자들의 HOMO 및 LUMO 에너지 준위가 상대적으로 낮아짐으로써 소자의 전기발광특성이 향상됨을 확인하였다.

• 대한전자공학회논문지TE
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• 제39권1호
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• pp.9-15
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• 2002

본 논문은 청색 유기 EL 소자를 진공증착법으로 제작하여 그 특성을 분석하였다. 발광층 물질(A1q/sub 3/)에 게스트물질(Type I-TPB와 Type II-DPA)의 도핑농도(0.5∼2 wt%)를 변화시켜 청색발광소자를 제작하여 전기적, 광학적 특성을 조사하였다. Alq3에 도펀트의 농도를 증가함에 따라 청색에 해당하는 색좌표 점으로 이동하였다. Type I이 Type II의 경우보다 동작개시전압 및 구동전압이 낮게 나타났으며 휘도에서는 Type II가 밝게 나타났다. Alq/sub 3/에 DPA(2wt%)를 도펀트로 사용한 소자의 경우 인가전압 15V에서 휘도는 1282cd/m/sup 2/, 최대발광 파장은 476nm, 색좌표는(0.1273, 0.0672)으로 우수한 특성을 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제33권11호
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• pp.3645-3650
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• 2012

Two new blue emitting cationic iridium(III) complexes with two substituted 2-phenlypyridine ligands as main ligands and one 2,2'-biimidazole as an ancillary ligand, $[(L1)_2Ir(biim)]Cl$ (1) and $[(L2)_2Ir(biim)]Cl$ (2), where L1 = 2-(2',4'-difluorophenyl)-4-methylpyridine, L2 = 2-(2',4'-difluoro-3'-trifluoromethylphenyl)-4-methylpyridine and biim = 2,2'-biimidazole, were synthesized for applications in phosphorescent organic light-emitting diodes (PhOLEDs). Their photophysical, electrochemical and electroluminescent (EL) device performances were examined. The photoluminescent (PL) spectra revealed blue phosphorescence in the 450 to 485 nm range with a quantum yield of more than 10%. The iridium(III) compounds studied showed good solubility in organic solvents with no solvatochromism dependent on the solvent polarity. The solution-processed OLEDs were prepared with the configuration, ITO/PEDOT:PSS (40 nm)/mCP:Ir(III) (70 nm)/OXD-7 (20 nm)/LiF (1 nm)/Al (100 nm), by spin coating the emitting layer containing the mCP host doped with the iridium phosphors. The best performance of the fabricated OLEDs based on compound 1 showed an external quantum efficiency of 4.5%, luminance efficiency of 8.52 cd $A^{-1}$ and blue emission with the CIE coordinates (x,y) of (0.16, 0.33).

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2006년도 6th International Meeting on Information Display
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• pp.1583-1586
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• 2006

All non-dopant white organic light-emitting diodes (WOLEDs) have been realized by using solid state highly fluorescent red bis(4-(N-(1- naphthyl)phenylamino)phenyl)fumaronitrile (NPAFN) and amorphous bipolar blue light-emitting 2-(4- diphenylamino)phenyl-5-(4-triphenylsilyl)phenyl- 1,3,4-oxadiazole (TPAOXD), together with well known green fluorophore tris(8- hydroxyquinolinato)aluminum $(Alq_3)$. The fabrication of multilayer WOLEDs did not involve the hard-tocontrol doping process. Two WOLEDs, Device I and II, different in layer thickness of $Alq_3$, 30 and 15 nm, respectively, emitted strong electroluminescence (EL) as intense as $25,000\;cd/m^2$. For practical solid state lighting application, EL intensity exceeding $1,000\;cd/m^2$ was achieved at current density of $18-19\;mA/cm^2$ or driving voltage of 6.5-8 V and the devices exhibited external quantum efficiency $({\eta}_{ext})$ of $2.6{\sim}2.9%$ corresponding to power efficiency $({\eta}_P)$ of $2.1{\sim}2.3\;lm/W$ at the required brightness.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2008년도 추계학술대회 논문집 Vol.21
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• pp.50-50
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• 2008

ZnO has been extensively studied for optoelectronic applications such as blue and ultraviolet (UV) light emitters and detectors, because it has a wide band gap (3.37 eV) anda large exciton binding energy of ~60 meV over GaN (~26 meV). However, the fabrication of the light emitting devices using ZnO homojunctions is suffered from the lack of reproducibility of the p-type ZnO with high hall concentration and mobility. Thus, the ZnO-based p-n heterojunction light emitting diode (LED) using p-Si and p-GaN would be expected to exhibit stable device performance compared to the homojunction LED. The n-ZnO/p-GaN heterostructure is a good candidate for ZnO-based heterojunction LEDs because of their similar physical properties and the reproducibleavailability of p-type GaN. Especially, the reduced lattice mismatch (~1.8 %) and similar crystal structure result in the advantage of acquiring high performance LED devices with low defect density. However, the electroluminescence (EL) of the device using n-ZnO/p-GaN heterojunctions shows the blue and greenish emissions, which are attributed to the emission from the p-GaN and deep-level defects. In this work, the n-ZnO:Ga/p-GaN:Mg heterojunction light emitting diodes (LEDs) were fabricated at different growth temperatures and carrier concentrations in the n-type region. The effects of the growth temperature and carrier concentration on the electrical and emission properties were investigated. The I-V and the EL results showed that the device performance of the heterostructure LEDs, such as turn-on voltage and true ultraviolet emission, developed through the insertion of a thin intrinsic layer between n-ZnO:Ga and p-GaN:Mg. This observation was attributed to a lowering of the energy barriers for the supply of electrons and holes into intrinsic ZnO, and recombination in the intrinsic ZnO with the absence of deep level emission.

• 한국재료학회지
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• 제15권8호
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• pp.543-547
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• 2005

Organic electroluminescence devices were made from 1,4-bis-(9-anthrylvinyl)benzene (AVB) and 1,4-bis-(9-aminoanthryl)benzene (AAB) anthracene derivatives. Device structure was ITO/AVB/PANI(EB)/Al (multi-layer device) and ITO/AAB:DCM/Al(single-layer device). In these devices, AVB, polyaniline(emeraldine base) (PANI(EB)) and AAB were used as the emitting material. 4-(dicyanomethylene)-2-methyl-6-p-(dimethylamino)styryl-4H -pyran(DCM) was used as red fluorescent dopant. We studied change of fluorescence wavelength with concentration of DCM doped in AAB. The ionization potential (IP) and optical band gap (Eg) were measured by cyclic voltammetry and UV-visible spectrum. We compared with difference of emitting wavelength between photoluminescence and electroluminescence spectrum. In case of the multi-layer device, PANI and AVB EL spectra have similar wave pattern to each PL spectrum and when PAM and AVB were used at the same time, and multi-layer device showed that a balanced recombination and radiation kom PANI and AVB. In case of the single-layer device, with the increase of DCM concentration, the blue emission decreases and red emission increases. This indicates that DCM was excited by the energy transfer from AAB to DCM or the direct recombination at the dopant sites due to carrier trapping, or both. The device with $1.0wt\%$ DCM concentration gave white light.