• Proceedings of the Korean Vacuum Society Conference
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• 2013.08a
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• pp.166-166
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• 2013

최근에 희토류 이온이 도핑된 형광체를 발광 소자, 레이저, 섬광재료, 광섬유, 촉매, 디스플레이와 같은 다양한 분야에 응용하기 위한 연구에 상당한 관심이 집중되고 있으며, 희토류 이온이 도핑된 발광 물질은 음극선관, 램프 조명, 플라즈마 디스플레이, X선 검출기, 전계 방출 디스플레이 소자를 포함한 다양한 영역에 응용되고 있다. 본 연구에서는 고상 반응법을 사용하여 발광 효율이 높은 적색과 주황색 형광체를 제조하고자 서로 다른 활성체 이온 Eu3+, Sm3+의 농도를 변화 시키면서 두 종류 Ca1-1.5xTa2O6:Eux3+와 Ca1-1.5xTa2 O6:Smx3+ 형광체 분말을 합성하였다. 특히, 활성제 이온의 농도비에 따른 형광체 분말의 결정 구조, 표면 형상, 입자의 크기, 흡광과 발광 특성을 측정하였다. 그림은 활성체 이온의 함량비를 달리하여 합성한 Ca1-1.5xTa2O6:Eux3+, Ca1-1.5xTa2O6:Smx3+ 형광체 분말에서 측정한 흡광(photoluminescence excition) 스펙트럼의 결과를 나타낸 것이다. 여기 파장 399 nm로 여기 시킨 Ca1-1.5xTa2O6:Eux3+ 형광체 분말의 경우에, 발광 세기가 가장 강한 617 nm의 주 피크가 관측되었다. 또한, 여기 파장 410 nm로 여기 시킨 Ca1-1.5xTa2O6:Smx3+ 형광체 분말의 경우에는 발광 세기가 가장 강한 주 피크는 609 nm에서 나타났다. 실험 결과로부터, Eu3+와 Sm3+ 이온이 각각 도핑된 CaTa2O6 형광체의 경우에는 색 순도가 높은 파장과 발광 세기는 Eu3+ 이온인 경우에 0.15 mol, Sm3+ 이온이 도핑되는 경우에는 0.05 mol이 최적의 합성 조건임을 알 수 있었다.

• Journal of the Microelectronics and Packaging Society
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• v.22 no.4
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• pp.77-82
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• 2015

To increase the performance of solid oxide fuel cell operating at intermediate temperature ($600^{\circ}C{\sim}800^{\circ}C$), $Sm_{0.2}Ce_{0.8}O_2$ (SDC) thin layer was applied to the $La_{0.8}Sr_{0.2}Mn_{0.8}Cu_{0.2}O_3$ (LSMCu) cathode by sol-gel coating method. The SDC was employed as a diffusion barrier layer on the yttria-stabilized zirconia(YSZ) to prevent the interlayer by-product formation of $SrZrO_3$ or $La_2Zr_2O_7$. The by-products were hardly formed at the electrolyte-cathode interlayer resulting to reduce the cathode polarization resistance. Moreover, SDC thin film was coated on the cathode pore wall surface to extend the triple phase boundary (TPB) area.

• Progress in Superconductivity
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• v.7 no.1
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• pp.69-76
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• 2005

Complex single buffer composed of yttrium and samarium oxide was deposited on the metallic substrates by MOCVD (metal organic chemical vapor deposition) method using single liquid source. Two different types of the substrates with in-plane textures of about $8{\sim}10$ degree of Ni and $3at.\%W-Ni$ alloy were used. Y(tmhd: 2,2,6,6-tetramethyl-3,5-heptane dionate)$_3$:Sm(tmhd)$_3$ of liquid source was adjusted to 0.4:0.6 to minimize the lattice mismatch between the complex single buffer and the YBCO. The epitaxial growth of $(Y_{x}Sm_{1-x})_{2}O_3$ was achieved at the temperature higher than $500^{\circ}C$ in $O_2$ atmosphere. However, it was found that the formation of NiO accelerated with increasing deposition temperature. By supplying $H_{2}O$ vapor, this oxidation of the substrate could be suppressed throughout the deposition temperatures. We could get the epitaxial growth on pure Ni substrate without the formation of NiO. The competitive (222) and (400) growths were observed at the deposition temperatures of $650\~750^{\circ}C$, but the (400) growth became dominant above $800^{\circ}C$. The $(Y_{x}Sm_{1-x})_{2}O_3$-buffered metallic substrates can be used as the buffer for YBCO coated conductor.

• Korean Journal of Metals and Materials
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• v.48 no.11
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• pp.995-1002
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• 2010

This study investigated the effect of process temperature on the alloying process during synthesis of $Sm_2Fe_{17}$ powder from ball-milled samarium oxide ($Sm_2O_3$) powders and a solid reducing agent of calcium hydrides ($CaH_2$) using iron nanopowder (n-Fe powder) by a reduction-diffusion (R-D) process. The $n-Fe-Sm_2O_3-CaH_2$ mixed powders were subjected to heat treatment at $850{\sim}1100^{\circ}C$ in $Ar-H_2$ for 5 h. It was found that the iron nanopowders in the mixed powders are sintered below $850^{\circ}C$ during the R-D process and the $SmH_2$ is synthesized by a reduced Sm that combines with $H_2$ around $850^{\circ}C$. The results showed that $SmH_2$ is able to separate Sm and $H_2$ respectively depending on an increase in process temperature, and the formed $Sm_2Fe_{17}$ phase on the surface of the sintered Fe nanopowder agglomerated at temperatures of $950{\sim}1100^{\circ}C$ in this study. The formation of the $Sm_2Fe_{17}$ layer is mainly due to the diffusion reaction of Sm atoms into the sintered Fe nanopowder, which agglomerates above $950^{\circ}C$. We concluded that nanoscale $Sm_2Fe_{17}$ powder can be synthesized by controlling the diffusion depth using well-dispersed Fe nanopowders.

• 한국초전도학회:학술대회논문집
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• v.14
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• pp.35-35
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• 2004

• 한국초전도학회:학술대회논문집
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• v.14
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• pp.45-45
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• 2004

• Proceedings of the Korean Vacuum Society Conference
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• 2015.08a
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• pp.190.2-190.2
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• 2015

최근에 최적의 모체 결정과 활성제 이온을 선택하여 우수한 발광과 흡광 특성을 갖는 산화물 형광체를 합성하여 디스플레이, 고체 레이저, 백색 발광 소자를 제작하는데 관심이 고조되고 있다. 본 연구에서는 열 및 화학적으로 안정한 $Gd_2MoO_6$를 모체 결정으로 선택하고 $Eu^{3+}$, $Sm^{3+}$ 이온을 활성제 이온으로 각각 도핑하여 다양한 종류의 색을 구현하는 새로운 종류의 형광체를 제조하고자 한다. 비교적 간단한 장비로 구성되고 볼밀 작업을 통하여 쉽게 초기 물질을 혼합 분쇄하고 소결할 수 있는 고상반응법을 사용하여 합성하였다. 특히, 모체 결정에 주입되는 활성제 이온을 둘러싸고 있는 국소적인 환경이 반전 대칭에서 벗어나는 정도를 파악하여 활성제 이온의 발광 파장의 세기가 최대가 되는 최적의 조건을 규명하고자 한다. $Eu^{3+}$ 이온이 도핑된 $Gd_2MoO_6$ 형광체의 발광 스펙트럼은 $Eu^{3+}$ 이온의 함량에 관계없이 모든 시료에서 전형적인 $Eu^{3+}$ 이온의 $^5D_0-^7F_j$ (j=1-4) 전이에 의한 발광 스펙트럼을 나타내었고, 가장 강한 적색 발광 파장은 611 nm에서 관측되었다. $Sm^{3+}$ 이온이 도핑된 $Gd_2MoO_6$ 형광체의 경우에, $Sm^{3+}$ 이온의 함량에 관계없이 모든 시료에서 $Sm^{3+}$ 이온의 $^4G_{5/2}-^6H_j$ (j=5/2, 7/2, 9/2) 전이에 의한 발광 스펙트럼을 나타내었고, 가장 강한 발광 파장은 616 nm에서 관측되었다. 이외에도, 결정 입자와 발광 세기의 상관 관계를 조사하였다.

• Advances in materials Research
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• v.1 no.2
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• pp.115-128
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• 2012

The structural and electrical properties of $(1-x)Ba(Sm_{1/2}Nb_{1/2})O_3-xBaTiO_3$; ($0{\leq}x{\leq}1$) ceramics were prepared by conventional ceramic technique at $1375^{\circ}C$/7 h in air atmosphere. The crystal symmetry, space group and unit cell dimensions were derived from the X-ray diffraction (XRD) data using FullProf software whereas crystallite size and lattice strain were estimated from Williamson-Hall approach. XRD analysis of the compound indicated the formation of a single-phase cubic structure with the space group Pm m. Dielectric study revealed that the compound $0.75Ba(Sm_{1/2}Nb_{1/2})O_3-0.25BaTiO_3$ is having low and ${\varepsilon}^{\prime}$ and ${\varepsilon}^{{\prime}{\prime}}$ a low $T_{CC}$ (< 5%) in the working temperature range (up to+$100^{\circ}C$) which makes this composition suitable for capacitor application and may be designated as 'Stable Low-K' Class I material as per the specifications of the Electronic Industries Association. The correlated barrier hopping model was employed to successfully explain the mechanism of charge transport in the system. The ac conductivity data were used to evaluate the density of states at Fermi level, minimum hopping length and apparent activation energy of the compounds.

• Journal of the Korean institute of surface engineering
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• v.50 no.4
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• pp.282-288
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• 2017

$Eu^{3+}$- or $Sm^{3+}$-doped $La_2MoO_6$ phosphors were synthesized with different concentrations of activator ions via a solid-state reaction. The X-ray diffraction patterns exhibited that crystalline structures of all the phosphors were tetragonal systems with the dominant peak occurring at (103) plane, irrespective of the concentration and the type of activator ions. The crystallites showed the pebble-like crystalline shapes and the average crystallite size increased with a tendency to agglomerate as the concentration of $Eu^{3+}$ ions increased. The excitation spectra of $Eu^{3+}$-doped $La_2MoO_6$ phosphors contained an intense charge transfer band centered at 331 nm in the range of 250-370 nm and three weak peaks at 381, 394, and 415 nm, respectively, due to the $^7F_0{\rightarrow}^5L_7$, $^7F_0{\rightarrow}^5L_6$, and $^7F_0{\rightarrow}^5D_3$ transitions of $Eu^{3+}$ ions. The emission spectra under excitation at 331 nm exhibited a strong red band centered at 620 nm and two weak bands at 593 and 704 nm. As the concentration of $Eu^{3+}$ increased from 1 to 20 mol%, the intensities of all the emission bands gradually increased. For the $Sm^{3+}$-doped $La_2MoO_6$ phosphors, the emission spectra consisted of an intense emission band at 607 nm arising from the $^4G_{5/2}{\rightarrow}^6H_{7/2}$ transition and three relatively small bands at 565, 648, and 707 nm originating from the $^4G_{5/2}{\rightarrow}^6H_{5/2}$, $^4G_{5/2}{\rightarrow}^6H_{9/2}$, and $^4G_{5/2}{\rightarrow}^6H_{11/2}$ transitions of $Sm^{3+}$, respectively. The intensities of all the emission bands approached maxima when concentration of $Sm^{3+}$ ions was 5 mol%. These results indicate that the optimum concentrations for highly-luminescent red and orange emission are 20 mol% of $Eu^{3+}$ and 5 mol% of $Sm^{3+}$ ions, respectively.

• Progress in Superconductivity and Cryogenics
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• v.8 no.3
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• pp.27-31
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• 2006

We propose a replication method to solve the problem of large percent failure in texturing processes of coated conductors. This problem is due to the individual texturing process for each coated conductor that is very long tape having no single defect spot. We tested two different methods of replication process that are based on a well-textured Ni template. First method has structure of Ni/BaO/STO/$CeO_2$/SmBCO/Ag. So BaO layer is dissolved in water that we can separate STO/$CeO_2$/SmBCO/Ag layers. In this processing, the property of STO is conserved but the superconductivity of SmBCO is deteriorated. So we can consider another method. Second method has structure of template(STO)/BaO/STO/Pt/STO. After dissolving BaO then we deposited YBCO. The result of these experiments showed the feasibility of replication.