• 제목/요약/키워드: $SnO_{2}:Eu^{3+}$

검색결과 8건 처리시간 0.023초

2차원적 K2NiF4형 구조의 Sr2-2xEuxKxSnO4에서 Eu3+ 이온의 Luminescence (Eu3+ Luminescence in Two-Dimensional Sr2-2xEuxKxSnO4 with K2NiF4 Structure)

  • 여철현;;류광현
    • 대한화학회지
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    • 제41권4호
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    • pp.175-179
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    • 1997
  • 2차원적 $K_2NiF_4$형 구조를 갖는 $Sr_{2-2x}Eu_xK_xSnO_4$의 주격자 안에 존재하는 Eu3+ 이온의 luminescence에 대한 연구를 수행하였다. $Eu^{3+}$ 이온의 $^5D_o$$^7F_o$ 전이에 의한 방출선은 J=0 → J=0 전이로써 $Eu^{3+}$ 이온의 4f 껍질에서 전기 이중극자 전이에 대한 Judd-Ofelt 선택규칙(selection rule)에 의하여 금지된 전이이다. 그러나 $Sr_{2-2x}Eu_xK_xSnO_4$의 Eu3+ 이온의 방출 스펙트라에서는 $^5D_o$$^7F_o$$^5D_o$ → $^7F_o$

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증착 온도가 라디오파 마그네트론 스퍼터링으로 성장한 SnO2:Eu3+ 박막의 특성에 미치는 영향 (Effects of deposition temperature on the properties of SnO2:Eu3+ thin films grown by radio-frequency magnetron sputtering)

  • 조신호
    • 한국표면공학회지
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    • 제56권3호
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    • pp.201-207
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    • 2023
  • Eu3+-doped SnO2 (SnO2:Eu3+) phosphor thin films were grown on quartz substrates by radio-frequency magnetron sputtering. The deposition temperature was varied from 100 to 400 ℃. The X-ray diffraction patterns showed that all the thin films had two mixed phases of SnO2 and Eu2Sn2O7. The 880 nmthick SnO2:Eu3+ thin film grown at 100 ℃ exhibited numerous pebble-shaped particles. The excitation spectra of SnO2:Eu3+ thin films consisted of a strong and broad peak at 312 nm in the vicinity from 250 to 350 nm owing to the O2--Eu3+ charge transfer band, irrespective of deposition temperature. Upon 312 nm excitation, the SnO2:Eu3+ thin films showed a main emission peak at 592 nm arising from the 5D07F1 transition and a weak 615 nm red band originating from the 5D07F2 transition of Eu3+. As the deposition temperature increased, the emission intensities of two bands increased rapidly, approached a maximum at 100 ℃, and then decreased slowly at 400 ℃. The thin film deposited at 200 ℃ exhibited a band gap energy of 3.81 eV and an average transmittance of 73.7% in the wavelength range of 500-1100 nm. These results indicate that the luminescent intensity of SnO2:Eu3+ thin films can be controlled by changing the deposition temperature.

연소합성법에 의한 $SnO_{2}:Eu^{3+}$ 오렌지색 형광체의 제조 (Preparation of orange-emitting $SnO_{2}:Eu^{3+}$ phosphors by combustion synthesis)

  • 김진영;강종혁;전덕영
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2002년도 춘계학술대회 논문집 디스플레이 광소자 분야
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    • pp.61-64
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    • 2002
  • A novel ceramic synthesis technique, combustion synthesis, is explored to produce a orange-emitting $SnO_{2}:Eu^{3+}$ phosphors. This technique involves a reaction of metal salts with a citric acid as an organic fuel. The variation of the ratio of citric acid to metal introduces change in reaction temperature and atmosphere of the combustion reaction, which in turn influences crystallinity and luminescence properties of the final products seriously. And, the heat treatment of the as-synthesized product increases its luminescence intensity. Especially, the samples treated at above $1100^{\circ}C$ show a orange-emission peak, which is attributed to the formation of single phase and well-crystallized $SnO_{2}:Eu$ oxides in the rutile structure

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Synthesis of a new (Ta1-xSnx)Sr2EuCu2Oz superconductor

  • Kim, G.W.;Lee, H.K.
    • 한국초전도ㆍ저온공학회논문지
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    • 제16권2호
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    • pp.33-35
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    • 2014
  • We report here results of a study of superconductivity in the ($Ta_{1-x} Sn_x)Sr_2EuCu_2O_z$ system. We observe resistive superconducting transitions for the samples with x = 0.15-0.3, and the highest superconducting transition has been achieved for the sample with x = 0.2 which reveals onset $T_c$ of 43 K and zero-resistivity of 25 K. Thermoelectric power measurements indicate that Sn doping introduces holes into the system and thereby superconductivity can be achieved in the ($Ta_{1-x} Sn_x)Sr_2EuCu_2O_z$ system.

Eu3+와 Tb3+ 활성제 이온이 SrSnO3 형광체의 특성에 미치는 영향 (Effects of Eu3+ and Tb3+ Activator Ions on the Properties of SrSnO3 Phosphors)

  • 김정대;조신호
    • 한국재료학회지
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    • 제24권9호
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    • pp.469-473
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    • 2014
  • $SrSnO_3$ phosphor powders were synthesized with two different contents of activator ions $Eu^{3+}$ and $Tb^{3+}$ using the solid-state reaction method. The structural, morphological, and optical properties of the phosphors were investigated using X-ray diffractometry, field-emission scanning electron microscopy, and fluorescence spectrophotometry, respectively. All the phosphors showed a cubic structure, irrespective of the type and the content ratio of activator ions. For $Eu^{3+}$-doped $SrSnO_3$ phosphors, the intensity of the 620 nm red emission spectrum resulting from the $^5D_0{\rightarrow}^7F_2$ transition of $Eu^{3+}$ was stronger than that of the 595 nm orange emission signal due to the $^5D_0{\rightarrow}^7F_1$ transition in the range 0.01-0.05 mol of $Eu^{3+}$, but the ratio of the intensity was reversed in the range 0.10-0.20 mol of $Eu^{3+}$. The variation in the emission intensity indicates that the site symmetry of the $Eu^{3+}$ ions around the host crystal was changed from non-inversion symmetry to inversion. For the $Tb^{3+}$-doped $SrSnO_3$ phosphors under excitation at 281 nm, one strong green emission band at 550 nm and several weak bands were observed. These results suggest that the optimum red and green emission signals can be realized when the activator ion content for $Eu^{3+}$- or $Tb^{3+}$-doped $SrSnO_3$ phosphors is 0.20 mol and 0.15 mol, respectively.

Properties of Combustion Synthesized $SnO_2:Eu^{3+}$ Phosphors

  • Kang, Jong-Hyuk;Kim, Jin-Young;Jeon, Duk-Young
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2002년도 International Meeting on Information Display
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    • pp.831-834
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    • 2002
  • A novel ceramic synthesis technique, combustion synthesis, is explored to produce an orange-emitting $SnO_2:Eu^{3+}$ phosphors. This technique involves a reaction of metal salts with a citric acid as an organic fuel. The variation of the ratio of citric acid to metal introduces change in reaction temperature and atmosphere of the combustion reaction, which in turn influences crystallinity and luminescence properties of the final products significantly. And the heat treatment of the as-synthesized product improved the CL intensity of the products. Especially, the sample treated at above 1100 $^{\circ}C$ shows an orange-emission, which is attributed to the formation of single phase and well-crystallized $SnO_2$:Eu in rutile structure.

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수도(水稻)에서 여러 질소효율의 개념(槪念)과 상호관계(相互關係) (Concepts concerning various nitrogen efficiencies and their interrelation in rice plant)

  • 박훈
    • 한국토양비료학회지
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    • 제8권2호
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    • pp.69-80
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    • 1975
  • 수도(水稻)의 수량(收量)과 여러가지 질소효율간, 질소효율 상호간(相互間), 효율과 흡수량간(吸收量間)의 관계(關係)를 설정(設定)하고 3개(個) 연간(年間)의 3요소시험(要素試驗) (30~50개지역(個地域)) 결과자료(結果資料)로 검토(檢討)하였다. 설정(設定)된 상호관계(相互關係)는 고도유의상관(高度有意相關)을 보이므로 실험결과(實驗結果)에 잘 일치(一致)하였다. 시비하(施肥下)에서 다수성(多收性)은 시료(肥料)의 이용율(利用率)(Eu)을 증가(增加)시켜 일차적(一次的)으로 질소흡수(窒素吸收)를 증가(增加)시키고 흡수시료질소吸收肥料窒素(Nf) 효율(Ef) 및 시비효율(Fe)을 증가(增加)시키며 이차적(二次的)으로 질소효율(E)을 증가(增加)시키는데 의존(依存)한다. 흡수(吸收)된 토양질소(土壤窒素)(Ns) 효율(Es)은 Ef보다 E에 대(對)한 기여도(寄與度)가 컸으며 모든 질소효율은 동반질소(同伴窒素)의 흡수량(吸收量) 및 상대(相對)되는 다른 질소효율에 역상관(逆相關)을 보였다. Es와 Ef는 1. 감법(減法) 2. Cs (Cs=Ns/Ns+Nf) 대(對) E plotting 법(法)과 3. 표식비료(標識肥料)를 사용(使用)한 E-Cs 및 Y-Ns Plotting 법(法)이 있으며 Plotting 법(法)은 E-Es Cs+B 식(式) 또는 Y=Es Ns+Ef Nf식(式)을 사용(使用)하며 B=Ef Cf로 Ef Nf와 함께 주어진 조건하(條件下에서 상수(常數)로 본다. Es는 Ef보다 대부분(大部分)의 경우 (80%) 크며 포장간(圃場間)에 Es보다 Ef에 차이가 크며 Ef는 특히 비료(肥料)의 형태(形態)에 의존(依存)한다. 설정검토(設定檢討)된 상호관계(相互關係)는 다음과 같다. 1. Y=$Es{\cdot}Ns+Ef{\cdot}Nf$ (Y는 수량(收量)) 2. E=$Es{\cdot}Cs+Ef{\cdot}Cf(Cf=Nf/Ns/Nf)$ 3. E=b-aN, E=E, Es 또는 Ef이고 N=N, Ns 또는 Nf이다. (E=Y/N, N=Ns+Nf), b는 주어진 조건(條件)에서의 E의 이론적(理論的) 최대치(最大値)이고 a는 Y=EN 곡선(曲線)의 N=0에서의 접선(接線)의 기울기이다. 4. Fe=$Ef{\cdot}Eu$, Se=$Es{\cdot}Eu$ (Se는 토양유효질소의 종조생산효율) 5. E=$Se{\cdot}Cs/Eu+Fe{\cdot}Cf/Eu$ 6. Y=$Es{\cdot}Eu{\cdot}Sf+Ef{\cdot}Eu{\cdot}Fn$ 또는 Y=$Es{\cdot}Eu{\cdot}Ea{\cdot}Sn+Ef{\cdot}Eu{\cdot}Fn(Sf=Ea{\cdot}Sn$, Ea는 비료질소(肥料窒素)와 대등(對等)한 토양유효질소(Sf)를 전토양질소(全土壤窒素)(Sn)로 나눈 유효화율).

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Banded Iron Formations in Congo: A Review

  • Yarse Brodivier Mavoungou;Anthony Temidayo Bolarinwa;Noel Watha-Ndoudy;Georges Muhindo Kasay
    • 자원환경지질
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    • 제56권6호
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    • pp.745-764
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    • 2023
  • In the Republic of Congo, Banded iron formations (BIFs) occur in two areas: the Chaillu Massif and the Ivindo Basement Complex, which are segments of the Archean Congo craton outcropping in the northwestern and southwestern parts of the country. They show interesting potential with significant mineral resources reaching 2 Bt and grades up to 60% Fe. BIFs consist mostly of oxide-rich facies (hematite/magnetite), but carbonate-rich facies are also highlighted. They are found across the country within the similar geological sequences composed of amphibolites, gneisses and greenschists. The Post-Archean Australian Shale (PAAS)-normalized patterns of BIFs show enrichment in elements such as SiO2, Fe2O3, CaO, P2O5, Cr, Cu, Zn, Nb, Hf, U and depletion in TiO2, Al2O3, MgO, Na2O, K2O, Sc, Th, Ba, Zr, Rb, Ni, V. REE diagrams show slight light REEs (rare earth elements; LREEs) compared to heavy REEs (HREEs), and positive La and Eu anomalies. The lithological associations, as well as the very high (Eu/Eu*)SN ratios> 1.8 shown by the BIFs, suggest that they are related to Algoma-type BIFs. The positive correlations between Zr and TiO2, Al2O3, Hf suggest that the contamination comes mainly from felsic rocks, while the absence of correlations between MgO and Cr, Ni argues for negligeable contributions from mafic sources. Pr/Pr* vs. Ce/Ce* diagram indicates that the Congolese BIFs were formed in basins with redox heterogeneity, which varies from suboxic to anoxic and from oxic to anoxic conditions. They were formed through hydrothermal vents in the seawater, with relatively low proportions of detrital inputs derived from igneous sources through continental weathering. Some Congolese BIFs show high contents in Cr, Ni and Cu, which suggest that iron (Fe) and silicon (Si) have been leached through hydrothermal processes associated with submarine volcanism. We discussed their tectonic setting and depositional environment and proposed that they were deposited in extensional back-arc basins, which also recorded hydrothermal vent fluids.