• 제목/요약/키워드: Dy2O3

검색결과 165건 처리시간 0.028초

Dy3+와 Eu3+ 이온이 동시 도핑된 Y2WO6 형광체의 구조와 발광 특성

  • 이동규;조선욱;조신호
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2015년도 제49회 하계 정기학술대회 초록집
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    • pp.152-152
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    • 2015
  • 최근에 백색 발광체 개발에 많은 관심이 고조되고 있다. 본 연구에서는 고상반응법을 사용하여 활성제 이온 $Dy^{3+}$의 함량을 0.05 mol로 고정하고, $Eu^{3+}$ 이온의 함량을 각각 0, 0.5, 1, 5, 10, 15 mol%로 변화시켜 $Y_2WO_6:Dy^{3+}$, $Eu^{3+}$ 형광체 분말을 합성하였다. $Dy^{3+}$ 이온만 도핑된 $Y_2WO_6$ 형광체의 흡광 수펙트럼은 전하 전달 밴드 ($Dy^{3+}-O^{2-}$)에 의한 250~350 nm에 존재 하는 밴드폭이 넓은 전이 신호와 360~500 nm 영역에 걸쳐 있는 상대적으로 흡광 세기가 약한 다수의 $Dy^{3+}$ 이온의 전이 신호가 관측 되었다. $Dy^{3+}$$Eu^{3+}$가 동시 도핑된 $Y_2WO_6$ 형광체의 발광 스펙트럼의 경우에, $Eu^{3+}$ 이온의 몰 비가 증가함에 따라 $Dy^{3+}$ 이온에 의한 577 nm에 주 피크를 갖는 황색 발광 파장의 세기는 감소하였고, $Eu^{3+}$ 이온에 의해 발생하는 612 nm의 적색 발광 파장의 세기는 순차적으로 증가하였다. 이 결과는 $Dy^{3+}$$Eu^{3+}$ 이온의 몰 비를 적절히 조절함으로써 최적의 백색 발광 형광체를 제조할 수 있음을 제시한다.

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Photoluminescence properties and energy transfer of $Dy^{3+}$ and $Tm^{3+}$ co-activated $CaZrO_3$ phosphor for white LEDs

  • Li, Yezhou;Wang, Yuhua
    • Journal of Information Display
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    • 제12권2호
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    • pp.93-96
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    • 2011
  • Single-phased $CaZrO_3:Dy^{3+}$, $Tm^{3+}$ series have been successfully synthesized by solid-state reaction, and their luminescence properties were investigated. Under 355 nm excitation, $CaZrO_3:Dy^{3+}$ series showed characteristic emission of $Dy^{3+}$, which exhibited yellowish white color. By introducing $Tm^{3+}$ into the matrix, the emitted hue of the $Dy^{3+}$-doped sample could be easily tailored to white, and simultaneously, energy transfer from $Tm^{3+}$ to $Dy^{3+}$ was observed. The color coordinates of the optimum white-emitting sample were (0.321, 0.323), which were very close to the data of the National Television Standard Committee (0.33, 0.33). The co-activated phosphors presented good match to ultraviolet light-emitting diodes (LEDs), which revealed that they could be novel promising phosphors utilized in white LED application.

희토류 첨가 광소재의 나노구조 : Dy 첨가 Ge-As-S 유리의 X-선 흡수 스펙트럼 분석 (Nanostructure of Optical Materials Doped with Rare-Earths: X-Ray Absorption Spectroscopy of Dy-Doped Ge-As-S Glass)

  • 최용규;송재혁;신용범;;허종
    • 한국세라믹학회지
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    • 제43권3호
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    • pp.177-184
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    • 2006
  • Dy $L_3$-edge XANES and EXAFS spectra of chalcogenide Ge-As-S glass doped with ca. 0.2 wt% dysprosium have been investigated along with some reference Dy-containing crystals. Amplitude of the white-line peak in XANES spectrum of the glass sample turns out to be stronger than that of other reference crystals, i.e., $DY_2S_3,\;Dy_2O_3\;and\;DyBr_3$. It has been verified from the Dy $L_3$-edge EXAFS spectra that a central Dy atom is surrounded by $6.7{\pm}0.5$ sulfur atoms in its first coordination shell in the Ge-As-S glass, which is relatively smaller than 7.5 of the $Dy_2S_3$ crystal. Averaged Dy-S inter-atomic-distance of the glass ($2.78{\pm}0.01{\AA}$) also turns out to be somewhat shorter than that of the $Dy_2S_3$ crystal ($2.82{\pm}0.01{\AA}$). Such nanostructural changes occurring at Dy atoms imply there being stronger covalency of Dy-S chemical bonds in the Ge-As-S glass than in the crystal counterpart. The enhanced covalency in the nanostructural environment of $Dy^{3+}$ ions inside the glass would then be responsible for optical characteristics of the $4f{\leftrightarrow}4f$ transitions of the dopants, i.e., increase of oscillator strengths and spontaneous radiative transition probabilities.

충남 태안 철마산 일대의 지질 및 희토류 광화작용 (REE Mineralization and Geology of Chulmasan Area, Taean, Chungchungnamdo)

  • 유봉철
    • 한국광물학회지
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    • 제32권2호
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    • pp.127-143
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    • 2019
  • 철마산 일대의 지질은 하부로부터 선캠브리아기의 소근리층, 화강암질편마암, 엽리상 흑운모화강암, 엽리상 운모화강암, 염기성암맥 및 산성암맥으로 구성된다. 이 일대의 희토류 광화작용은 화강암질편마암과 엽리상 운모화강암에서 관찰된다. 이들 암석에서 소량 희토류 원소 및 토륨을 함유한 광물들은 저어콘($Y_2O_3$ 0.00~1.18 wt.%, $Gd_2O_3$ 0.00~0.59 wt.%, $Er_2O_3$ 0.00~0.22 wt.%, $Yb_2O_3$ 0.00~0.34 wt.%, $Lu_2O_3$ 0.00~0.48 wt.%, $ThO_2$ 0.00~0.33 wt.%), 토리아나이트($Nd_2O_3$ 0.00~0.24 wt.%, $Lu_2O_3$ 0.00~0.26 wt.%), 베르시에린($La_2O_3$ 0.04~0.26 wt.%, $Nd_2O_3$ 0.00~0.20 wt.%, $Tb_2O_3$ 0.04~0.12 wt.%, $Dy_2O_3$ 0.17~0.26 wt.%, $Er_2O_3$ 0.33~0.44 wt.%, $Lu_2O_3$ 0.00~0.19 wt.%, $ThO_2$ 0.61~0.93 wt.%), 녹니석($La_2O_3$ 0.44~0.68 wt.%, $Ce_2O_3$ 0.12~0.13 wt.%, $Nd_2O_3$ 0.31~0.44 wt.%, $Eu_2O_3$ 0.03~0.08 wt.%, $Dy_2O_3$ 0.09~0.21 wt.%, $Ho_2O_3$ 0.04~0.14 wt.%, $Er_2O_3$ 0.18~0.32 wt.%, $Lu_2O_3$ 0.07~0.21 wt.%, $ThO_2$ 0.00~0.97 wt.%), 흑운모($Nd_2O_3$ 0.02~0.08 wt.%, $Gd_2O_3$ 0.07~0.08 wt.%, $Tb_2O_3$ 0.02~0.07 wt.%, $Dy_2O_3$ 0.35~0.43 wt.%, $Ho_2O_3$ 0.15~0.26 wt.%, $Er_2O_3$ 0.24~0.28 wt.%, $Yb_2O_3$ 0.06~0.18 wt.%, $ThO_2$ 0.00~0.12 wt.%), 정장석($Dy_2O_3$ 0.05~0.12 wt.%, $Ho_2O_3$ 0.05~0.06 wt.%, $Er_2O_3$ 0.28 wt.%, $Yb_2O_3$ 0.06~0.12 wt.%) 및 사장석($Ho_2O_3$ 0.01~0.03 wt.%, $Er_2O_3$ 0.10~0.27 wt.%, $ThO_2$ 0.11~0.13 wt.%)이며 희토류 광물로는 바스트나사이트와 퍼구소나이트이다. 희토류 광물들은 주로 장석류, 운모류, 저어콘, 인회석 및 티탄철석의 간극을 따라 산출된다. 따라서 철마산 일대의 희토류 광화작용 산물인 바스트나사이트와 퍼구소나이트는 화강암질편마암과 엽리상 운모화강암의 형성 시 희토류 원소 및 토륨이 구성광물 내에 소량 함유되어 있었으며 그후 계속된 화성활동 및 변성작용에 의하여 기존 광물 내에 함유되어 있던 희토류 원소가 재 농집에 의해 형성된 것으로 생각된다.

Dysprosium과 Erbium이 동시 첨가된 X7R MLCC용 페로브스카이트 BaTiO3의 전기적특성과 온도안정성 (Electrical Properties and Temperature Stability of Dysprosium and Erbium Co-doped Barium Titanate with Perovskite Structure for X7R MLCCs)

  • 노태민;김진성;류지승;이희수
    • 한국세라믹학회지
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    • 제48권4호
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    • pp.323-327
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    • 2011
  • The effects of $Dy_2O_3$ and $Er_2O_3$ co-doping on electrical properties and temperature stability of barium titanate ($BaTiO_3$) ceramics were investigated in terms of microstructure and structural analysis. The dielectric constant and the insulation resistance (IR) of 0.7 mol% $Dy_2O_3$ and 0.3 mol% $Er_2O_3$ co-doped dielectrics had about 60% and 20% higher than the values of undoped one, respectively, and the temperature coefficient of capacitance (TCC) met the X7R specification. The addition of $Dy_2O_3$ contributed to electrical properties caused by increase of tetragonality; however, preferential diffusion of $Dy^{3+}$ ions toward A site in $BaTiO_3$ grain exhibited an adverse effect on temperature stability by grain growth. On the other hand, The $Er_2O_3$ addition in $BaTiO_3$ could affect the TCC behavior and the IR with suppression of grain growth caused by reinforcement of grain boundary and electrical compensation. Therefore, the enhanced electrical properties and temperature stability through the co-doping could be deduced from the increase of tetragonality and the suppression of grain growth.

위조 방지 분야에 응용 가능한 다양한 희토류 이온이 도핑된 SrMoO4 형광체의 제조 및 특성 (Synthesis and Properties of SrMoO4 Phosphors Doped with Various Rare Earth Ions for Anti-Counterfeiting Applications)

  • 문태옥;정재용;조신호
    • 한국재료학회지
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    • 제30권8호
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    • pp.406-412
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    • 2020
  • SrMoO4:RE3+ (RE=Dy, Sm, Tb, Eu, Dy/Sm) phosphors are prepared by co-precipitation method. The effects of the type and the molar ratio of activator ions on the structural, morphological, and optical properties of the phosphor particles are investigated. X-ray diffraction data reveal that all the phosphors have a tetragonal system with a main (112) diffraction peak. The emission spectra of the SrMoO4 phosphors doped with several activator ions indicate different multicolor emissions: strong yellow-emitting light at 573 nm for Dy3+, red light at 643 nm for Sm3+, green light at 545 nm for Tb3+, and reddish orange light at 614 nm for Eu3+ activator ions. The Dy3+ singly-doped SrMoO4 phosphor shows two dominant emission peaks at 479 and 573 nm corresponding to the 4F9/26H15/2 magnetic dipole transition and 4F9/26H13/2 electric dipole transition, respectively. For Dy3+ and Sm3+ doubly-doped SrMoO4 phosphors, two kinds of emission peaks are observed. The two emission peaks at 479 and 573 nm are attributed to 4F9/26H15/2 and 4F9/26H13/2 transitions of Dy3+ and two emission bands centered at 599 and 643 nm are ascribed to 4G5/26H7/2 and 4G5/26H9/2 transitions of Sm3+. As the concentration of Sm3+ increases from 1 to 5 mol%, the intensities of the emission bands of Dy3+ gradually decrease; those of Sm3+ slowly increase and reach maxima at 5 mol% of Sm3+ ions, and then rapidly decrease with increasing molar ratio of Sm3+ ions due to the concentration quenching effect. Fluorescent security inks based on as-prepared phosphors are synthesized and designed to demonstrate an anti-counterfeiting application.

$ZnO-Pr_6O_{11}-CoO-Dy_2O_3$계 바리스터의 I-V 특성에 $Pr_6O_{11}/CoO$ 조성비 영향 (Influence of $Pr_6O_{11}/CoO$ Composition Ratio on I-V Characteristics of $ZnO-Pr_6O_{11}-CoO-Dy_2O_3$ Based varistors)

  • 남춘우;류정선;윤한수
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2000년도 영호남학술대회 논문집
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    • pp.179-184
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    • 2000
  • The I-V characteristics of $ZnO-Pr_6O_{11}-CoO-Dy_2O_3$ based varistors were investigated in the $Pr_6O_{11}/CoO$ composition ratio range of 0.5/0.5 to 1.0/1.0 and sintering temperature range of 1300 to $1350^{\circ}C$ as the basic study to develop the advanced $Pr_6O_{11}$-based ZnO varistors. All varistors except for $Pr_6O_{11}$/CoO = 0.5/1.0 exhibited the best I-V characteristics at $1350^{\circ}C$. However, the varistors with $Pr_6O_{11}$/CoO= 0.5/1.0 exhibited the best I-V characteristics at $1350^{\circ}C$. The varistors with $Pr_6O_{11}$/CoO= 0.5/1.0 of all varistors exhibited the best I-V characteristics, which the nonlinear exponent is 36.9 and the leakage current is 7.6 ${\mu}A$ Therefore, it was estimated that ZnO-$Pr_6O_{11}-CoO-Dy_2O_3$ ceramics with $Pr_6O_{11}$/CoO= 0.5/1.0 will be usefully used as varistor materials in the future.

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고상반응법으로 합성된 SrAl_2O_4:Eu^{+2}, Dy^{+3}$ 장잔광 형광체 분말의 빛발광 특성

  • 김병규;유연태;엄기석;이영기
    • 한국결정성장학회지
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    • 제9권3호
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    • pp.315-319
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    • 1999
  • 고상반응법으로 Eu와 Dy을 공부활제로 한$SrAl_2O_4$ 형광체 분말을 합성한 후, PL(Photoluminescence) 측정 장치를 이용하여 장잔광 축광재료소서 가장 중요한 발광특성과 장잔광특성을 조사하였다. 10K의 발광스펙트럼은 청색파장의 450nm(2.755 eV)와 녹색 파장의 520nm(2.384 eV)의 위치에서 뚜렷한 발광피크를 나타내었는데 반하여 300K에서는 450nm의 발광피크는 관측되지 않고 주로 520nm의 발광피크가 관측되었다. 그리고$SrAl_2O_4$:$Eu^{+2},Dy^{+3}$ 형광체의 잔광세기는 시간에 따라 지수 함수적으로 감소되나 발광의 감쇠속도가 작은 뛰어난 장잔광 특성을 나타내었다.

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SrAl2O4(Eu,Dy,Nd) 압광체를 이용한 균열첨단에서의 응력장 가시화 연구 (Direct Observation of Crack Tip Stress Field Using the Mechanoluminescence of SrAl2O4:(Eu,Dy,Nd))

  • 김지식;손기선
    • 소성∙가공
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    • 제12권5호
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    • pp.493-497
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    • 2003
  • The present investigation aims at visualizing the crack tip stress field using a mechanoluminescence material. The well known compound $SrAl_2O_4$:$Eu^{2+}$ was adopted as a mechanolurninescence material. Two more trivalent rare-earth elements such as Dy and Nd were taken into consideration as codopants to provide the appropriate trap levels. Samples of a variety of compositions were prepared by varing $Eu^{2+}$, $Dy^{3+}$, and $Nd^{3+}$ doping contents, for which the combinatorial chemistry method was used. In order to search for the optimum composition for the highest mechanoluminescence, the luminescence induced by a compressive device including a CCD camera. In parallel, a compact tension specimen was prepared by mixing the luminescence powders of optimum composition and epoxy resin. Crack initiation from the mechanically machined sharp note tip and its growth during loading were found to be associated with the extent of light emission from $SrAl_2O_4$.