• 제목/요약/키워드: Eu:Y2O3

검색결과 471건 처리시간 0.032초

합성공정이 Ba2SiO4:Eu2+ 형광체 분말의 합성과 발광특성에 미치는 영향 (Effects of the Preparation Process on the Synthesis and the Luminescence of Ba2SiO4:Eu2+ Phosphor Powders)

  • 박정혜;김영진
    • 전기화학회지
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    • 제16권3호
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    • pp.184-189
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    • 2013
  • 졸-겔법 및 졸-겔법과 연소법을 함께 사용한 하이브리드법으로 각각 얻어진 건식 젤을 열처리하여 $Ba_2SiO_4:Eu^{2+}$ ($B_2S:Eu^{2+}$) 분말을 합성하였으며, 이들 공정에 따른 구조 및 발광 특성 변화를 조사 하였다. Si 공급원으로서는 tetraethyl orthosilicate (TEOS)를 사용하였다. 졸-겔법에 의한 건식 젤로 하소 과정 없이 합성한 경우 TEOS 양의 변화에 따라서 상전이가 관찰되었으며, 1.2M TEOS에서 $B_2S:Eu^{2+}$ 단일상을 얻었을 수 있었다. 반면에 하소 과정을 거친 1.2M TEOS로 합성된 분말에서는 졸-겔법과 하이브리드법 모두 $B_2S:Eu^{2+}$와 미량의 $BaSiO_3:Eu^{2+}$ ($BS:Eu^{2+}$) 상이 혼재하는 분말을 얻을 수 있었으나, 이들 분말은 하소 과정 없이 합성된 것보다 발광특성이 약 두배 정도 우수하였다. 하이브리드법에 의한 $B_2S:Eu^{2+}$는 졸-겔법에 의한 것에 비하여 발광강도가 약간 떨어지나 공정 시간을 획기적으로 단축 시킬 수 있는 장점을 보이고 있었다. 1.1M TEOS로 하소 과정을 거쳐 하이브리드법으로 얻어진 분말은 $B_2S:Eu^{2+}$ 단일상으로 구성되어 있었으며, $Eu^{2+}$이온의 $4f^65d^1{\rightarrow}4f^7$ 전이에 의한 가장 강한 강도를 갖는 녹색 발광 (505 nm) 스펙트럼을 보이고 있었다.

$Tb^{3+}$ 와 Eu^{3+}$로 활성화시킨${Al_3}{GdB_4}{O_{12}}$ 형광체의 발광 특성 (Photoluminance Properties of ${Al_3}{GdB_4}{O_{12}}$ Phosphors Activated by $Tb^{3+} and Eu^{3+}$)

  • 김기운;강세선;이임렬
    • 한국재료학회지
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    • 제10권1호
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    • pp.49-54
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    • 2000
  • PDP용의 새로운 녹색 $Al_3GdB_4O_{12}:Tb^{3+} 형광체와 Al_3GdB_4O_{12}:Eu_{3+}$ 적색형광체를 제조한 후 광특성을 분석하였다. 또한 이들 형광체의 발광특성을 상용품인 $Zn_2SiO_4:Mn^{2+}$ 녹색 형광체와 $(Y,Gd)BO_3: Eu^{3+}$ 적색의 PDP 형광체와 상호 비교하였다. 형광체는 $1150^{\circ}C$에서 4시간 동안 공상 반응으로 제조하였다. 147nm의 진공자외선 조사시 $Al_3GdB_4O_{12}:Tb^{3+}$(15mol%) 녹색 형광체의 발광휘도는 상용품 $Zn_2SiO_4: Mn^{2+}$ 보다 증가하였으나 색좌표는 상대적으로 저하되었다. 한편 $Al_3GdB_4O_{12}:Eu^{3+}$(15mol%) 적색 형광체의 발광 휘도는 상용품$(Y,Gd)BO_3: Eu^{3+}$ 보다 작았으나 CIE 색좌표는 일부 개선되었다. $Al_3GdB_4O_{12}$ 형광체는 $\lambda=160nm$에서 모체 흡수에 의한 강한 여기밴드가 있으며, 진공자외선 영역에서 $Al_3GdB_4O_{12}:Tb^{3+}$ 녹색형광체의 여기강도는 $Zn_2SiO_4: Mn^{2+}$ 보다 컸으나 $Al_3GdB_4O_{12}:Eu^{3+}$ 적색 형광체의 여기강도는 $(Y,Gd)BO_3: Eu^{3+}$ 보다는 작았다.

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스핀코팅 및 급속열처리 공정을 통해 형성된 Y2O3:Eu3+ 박막의 발광특성 (Luminescent Properties of Y2O3:Eu3+ Thin Film Through Spin-coating and Rapid Thermal Annealing Process)

  • 박재홍;정용석
    • 반도체디스플레이기술학회지
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    • 제23권1호
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    • pp.88-91
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    • 2024
  • The europium doped yttrium oxide (Y2O3:Eu3+) thin film was formed on a Si substrate by the conventional spin-coating process followed by rapid thermal annealing (RTA) treatment. The spinning profiles such as rotation speed, acceleration and holding times were controlled during the spin-coating process for the best condition of the Y2O3:Eu3+ thin film. The RTA treatment was conducted for several temperature in order to crystallize the spin coated film. The Y2O3:Eu3+ thin film presented best performance in the conditions of 4000 rpm, 30 s and 10 s of rotation speed, acceleration time and holding time, respectively, at a fixed RTA temperature of 900 ℃.

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SrGa2S4 형광체의 합성과 발광 특성 (Synthesis of SrGa2S4 Phosphor and Its Luminescent Properties)

  • 허영덕;심재훈;도영락
    • 대한화학회지
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    • 제46권2호
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    • pp.164-168
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    • 2002
  • $SrGa_2S_4$:Eu는 녹색을 발광하는 형광체로 전계 방출 디스플레이, 음극선 발광 분야에 널리 응용되고 있다. 일반적으로 $SrGa_2S_4$:Eu의 합성은 $SrCO_3$,$Ga_2O_3$, 그리고 $Eu_2O_3$$H_2S$ 와 Ar 가스를 흘려주면서 고온에서 소송하는 고상반응법으로 합성하였다. 본 연구에서는 SrS, Eu 착물, 그리고 Ga 착물의 분해 반응을 통해서 $SrGa_2S_4$:Eu 형광체를 합성하였다. 이 방법의 장점은 Ar 가스 뿐 만 아니라 독성의 $H_2S$를 사용하지 않는 것이다. $SrGa_2S_4$:Eu 형광체의 합성 조건과 발광 특성을 검토하였다.

적색 형광체 나노 분말의 합성 및 특성 평가 (Formation and Characterization of Red Phosphor Nano Powders)

  • 유영철;김기도;임형섭;김희택
    • 공업화학
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    • 제19권1호
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    • pp.27-30
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    • 2008
  • 나노 형광체 합성에 있어서 입자 형상 및 입자 크기의 변화를 알아보기 위해 액상법으로 진행하였으며, 이를 바탕으로 최종적으로 약 80 nm급의 적색 나노 형광체의 합성이 가능하였다. 합성된 두 가지의 $Y_2O_3:Eu^{3+}$$YBO_3:Eu^{3+}$ 적색 나노 분말의 특성 평가를 비교하였으며, 그 결과 붕산염을 사용한 $YBO_3:Eu^{3+}$ 형광체 분말이 형상 면에서 약간의 응집이 발생하였으며, PL 특성 면에서도 $Y_2O_3:Eu^{3+}$ 대비 낮은 형광성을 보여주었다.

Preparation and Luminescence of Europium-doped Yttrium Oxide Thin Films

  • Chung, Myun Hwa;Kim, Joo Han
    • Applied Science and Convergence Technology
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    • 제26권2호
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    • pp.26-29
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    • 2017
  • Thin films of europium-doped yttrium oxide ($Y_2O_3$:Eu) were prepared on Si (100) substrates by using a radio frequency (RF) magnetron sputtering. After the deposition, the films were annealed at $1000^{\circ}C$ in an air ambient for 1 hour. X-ray diffraction analysis revealed that the $Y_2O_3$:Eu films had a polycrystalline cubic ${\alpha}-Y_2O_3$ structure. The as-deposited films showed no photoluminescence (PL), which was due to poor crystalline quality of the films. The crystallinity of the $Y_2O_3$:Eu films was significantly improved by annealing. The strong red PL emission was observed from the annealed $Y_2O_3$:Eu films and the highest intensity peak was centered at around 613 nm. This emission peak originated from the $^5D_0{\rightarrow}^7F_2$ transition of the trivalent Eu ions occupying the $C_2$ sites in the cubic ${\alpha}-Y_2O_3$ lattice. The broad PL excitation band was observed at wavelengths below 280 nm, which was attributed to the charge transfer transition of the trivalent Eu ion.

냉 음극 형광 램프용 Y2O3:Eu3+ 적색 형광체에 대한 이종 Flux 혼합첨가의 영향 (Effect of Different Fluxes in Preparation of Y2O3:Eu3+ Red Phosphor Used for Cold Cathode Fluorescence Lamp)

  • 구자인;김상문;신학기;박홍채;윤석영
    • 한국재료학회지
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    • 제19권3호
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    • pp.163-168
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    • 2009
  • $Eu^{3+}$-doped $Y_2O_3$ red phosphor was synthesized in a flux method using the chemicals $Y_2O_3,\;Eu_2O_3,\;H_3BO_3$ and $BaCl_2{\cdot}2H_2O$. The effect of a flux addition on the preparation of $Y_2O_3:Eu_{3+}$ red phosphor used as a cold cathode fluorescence lamp was investigated. $H_3BO_3$ and $BaCl_2{\cdot}2H_2O$ fluxes were used due to their different melting points. The crystallinity, thermal properties, morphology, and emission characteristics were measured using XRD, TG-DTA, SEM, and a photo-excited spectrometer. Under UV excitation of 254 nm, $Eu_2O_3$ 3.7 mol% doped $Y_2O_3$ exhibited a strong narrow-band red emission, peaking at 612 nm. From this result, the phosphor synthesized by firing $Y_2O_3$ with 3.7 mol% of $Eu_2O_3$, 0.25 mol% of $H_3BO_3$ and 0.5 mol% of $BaCl_2{\cdot}2H_2O$ fluxes at $1400^{\circ}C$ for 2 hours had a larger particle size of $4{\mu}m$ on average compared to the phosphor of the $H_3BO_3$ flux alone. In addition, a phosphor synthesized by the two fluxes together had a rounder corner shape, which led to the maximum emission intensity.

분무열분해 공정에 의해 합성되어진 나노 크기 Gd2O3:Eu형광체 (Nano-sized Gd2O3:Eu Phosphor Prepared by Spray Pyrolysis)

  • 김은정;강윤찬;박희동;유승곤
    • 한국재료학회지
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    • 제12권10호
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    • pp.771-775
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    • 2002
  • $Gd_2$$O_3$:Eu phosphor particles with nano-sized and non-aggregation characteristics were prepared by spray pyrolysis using the spray solution containing polymeric precursor and $Li_2$$CO_3$ flux material. Nano-sized $Gd_2$$O_3$:Eu phosphor particles had higher brightness than the commercial $Y_2$$O_3$:Eu phosphor particles. The $Gd_2$$O_3$:Eu phosphor particles had nano-size and non-aggregation characteristics after heat-treatment at $1000^{\circ}C$ when the addition amount of $Li_2$$CO_3$ flux was 1 wt.% and 3 wt.%. The mean size of particles were 200 nm and 400 nm when the amount of flux was 1 wt.% and 3 wt.%, respectively. The prepared phosphor particles had higher photoluminescence intensity than that of the commercial product regardless of the content of$ Li_2$$CO_3$ flux and had the maximum brightness when the content of flux was 5 wt %. The photoluminescence intensity of the nano-sized $Gd_2$$O_3$:Eu phosphor particles containing 3 wt.% $Li_2$$CO_3$ flux was 125% in comparison with that of the micron-sized $Y_2$$O_3$:Eu commercial product.

SrAl2O4계 축광재료의 습식공정에 의한 나노분말 합성 및 발광특성 (Synthesis of the Nano-sized SrAl2O4 Phosphors by Wet Processing and its Photoluminescence Properties)

  • 김정식
    • 한국세라믹학회지
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    • 제45권8호
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    • pp.477-481
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    • 2008
  • $Eu^{2+}$ and $Dy^{3+}$ co-doped strontium aluminate, $SrAl_2O_4$ long phosphorescent phoshor was fabricated and its photoluminescence was characterized. The phosphor, $SrAl_2O_4:Eu^{2+},Dy^{3+}$ was synthesized by a coprecipitation in which metal salts of $Sr(NO_3)_2$, $Al(NO_3)_3{\cdot}9H_2O$, were dissolved in $(NH_4)_2CO_3$ solution with adding $Eu(NO_3)_3{\cdot}5H_2O$ and $Dy(NO_3)_3{\cdot}5H_2O$ as a activator and co-activator, respectively. The coprecipitated products were separated from solution, washed, and dried in a vacuum dry oven. The dried powders were then mixed with 3 wt% $B_2O_3$ as a flux and heated at $800{\sim}1400^{\circ}C$ for 3 h under the reducing ambient atmosphere of 95%Ar+$5%H_2$ gases. For the synthesized $SrAl_2O_4:Eu^{2+},Dy^{3+}$, properties of photoluminescence such as emission, excitation and decay time were examined. The emission intensity increased as the annealing temperature increased and showed a maximum peak intensity at 510 nm with a broad band from $400{\sim}650\;nm$. Monitored at 520 nm, the excitation spectrum showed a maximum peak intensity at $315{\sim}320\;nm$ wavelength with a broad band from $200{\sim}500\;nm$ wavelength. The decay time of $SrAl_2O_4:Eu^{2+},Dy^{3+}$ increased as the annealing temperature increased.

Precipitation of Eu3+ - Yb3+ Codoped ZnAl2O4 Nanocrystals on Glass Surface by CO2 Laser Irradiation

  • Bae, Chang-hyuck;Lim, Ki-Soo;Babu, P.
    • Current Optics and Photonics
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    • 제2권1호
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    • pp.79-84
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    • 2018
  • We present a novel and simple method to enable spatially selective $ZnAl_2O_4$ nanocrystal formation on the surface of $B_2O_3$-$Al_2O_3$-ZnO-CaO-$K_2O$ glass by employing localized laser heating. Optimized precipitation of glass-ceramics containing nanocrystals doped with $Eu^{3+}$ and $Yb^{3+}$ ions was performed by controlling $CO_2$ laser power and scan speed. Micro-x-ray diffraction and transmission electron microscopy revealed the mean size and morphology of nanocrystals, and energy dispersive x-ray spectroscopy showed the lateral distribution of elements in the imaged area. Laser power and scan speed controled annealing temperature for crystalization in the range of 1.4-1.8 W and 0.01-0.3 mm/s, and changed the size of nanocrystals and distribution of dopant ions. We also report more than 20 times enhanced downshift visible emission under ultraviolet excitation, and 3 times increased upconversion emission from $Eu^{3+}$ ions assisted by efficient sensitizer $Yb^{3+}$ ions in nanocrystals under 980 nm excitation. The confocal microscope revealed the depth profile of $Eu^{3+}$ ions by showing their emission intensity variation.