• Korean Journal of Materials Research
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• v.8 no.2
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• pp.141-146
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• 1998

Ball mill을 이용하여 Ar 분위기에서 기계적 합금법으로 $Fe_{ 5}$$Si_{x}$ $B_{5-x}$ 분말을 제조하고, 제조된 분말을 연속 진공 열처리 시킨 후 Si첨가에 따른 결정구조 및 자기적성질을 조사하였다. 250시간 볼밀처리한 Fe$_{5}$ $B_{5}$ 합금에서 전체적으로 비정질 구조가 형성되었으나 일부분에 결정질이 존재하고 있었으며, $800^{\circ}C$에서 2시간 열처리하면 FeB와 $Fe_{2}$B 상이 혼재된 구조를 얻었다. 250시간 볼밀처리한 $Fe_{5}$ $Si_{2}$$B_{3}$합금에서 전체적으로 비정질 구조를 얻을 수 있었고, 이 시료를 2시간, $800^{\circ}C$로 열처리 하였을 때 $Fe_{2}$B상은 사라지고, 대부분 FeB의 균질한 상을 나타내었다. $Fe_{5}$ $B_{5}$ /조성에서는 분말 입자크기가 약 $1\mu\textrm{m}$이었으나, Si이 첨가되면 분말 입자크기가 약 $10\mu\textrm{m}$로 커졌다. Si의 첨가에 의해서 비정질상의 형성을 촉진시켜 단일 FeB상의 합성시간을 단축시킬 수 있었다.

• Journal of the Korean Ceramic Society
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• v.39 no.6
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• pp.604-609
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• 2002

Nanosized $BaCeO_3$ powders with the stoichiometric composition of a molecular level were synthesized by the citrate process based on the Pechini method. Polymeric precursor was formed by use of citric acid and ethylen glycol, as chelating agent of metal ions and reaction medium, respectively. Single phase orthorhombic structured $BaCeO_3$powders, about 100 nm sized and uniform shaped were obtained through the calcination of the polymeric precursor at $900^{\circ}C$ for 4 h. Extremely small quantities of carbonate ions($CO_^{2-}$) were completely decomposed at over $1100^{\circ}C$. The mean size of the powders was increased twice, however, it has very uniform distribution in its size and shape.

• Journal of the Korean Chemical Society
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• v.33 no.1
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• pp.65-69
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• 1989

Barium titanyl oxalate was synthesized by adding ethanol solution of oxalic acid to the mixed aqueous solution which contained barium or lanthanum radiotracers in addition to Ba(NO$_3)_2$ and TiO(NO$_3)_2$. The oxalate was finally converted to BaTiO$_3$ by calcination at 1000$^{\circ}$C in air. The chemical formula of the oxalate was confirmed to be BaTiO(CTEX>$_2O_4)_2{\cdot}4H_2O$ by the thermal analysis of the barium titanyl oxalate. When the mixture's molar ratio(Ba/Ti) was within a range of 0.950-1.05, the formation of stoichiometric Barium titanate was confirmed with the help of barium tracers. The homogeneity of lanthanum deposite in the final product was also confirmed through the behavior of lanthanum tracers. The results as well as those obtained by XRD and SEM have been explained on the basis of the fact that the reaction occurs on the molecular level in solution and the barium titanate is formed in crystals of single phase.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.22 no.4
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• pp.194-199
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• 2012

The $LiMn_{1.5}Ni_{0.5}O_4$, substituting a part of Mn with Ni in the $LiMn_2O_4$, the spinel structure has good charge-discharge cycle stability and high discharge capacity at 4.7 V. In this study $LiMn_{1.5}Ni_{0.5}O_4$ powders were synthesized by polymerization complex method. The effect on the characteristics of synthesized $LiMn_{1.5}Ni_{0.5}O_4$ powders was studied with citric acid (CA) : metal ion (ME) molar ratio (5 : 1, 10 : 1, 15 : 1, 30 : 1) and calcination temperature ($500{\sim}900^{\circ}C$). Single phase of $LiMn_{1.5}Ni_{0.5}O_4$ was observed from XRD analysis on the powders calcined at low ($500^{\circ}C$) and high temperatures ($900^{\circ}C$). The crystalline size and crystallinity increased with calcination temperature. At low calcination temperature the particle size decreased and specific surface area increased as the CA molar ratio increased. On the other hand, high particle growth rate at high calcination temperature interfered the particle size reduction and specific surface area increase induced by the increase of CA molar ratio.

• The Journal of the Convergence on Culture Technology
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• v.9 no.5
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• pp.523-528
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• 2023

The applicability as a material to improve solar cell performance was reviewed by synthesizing a phosphor that emits red wavelengths by a liquid synthesis method using a metal salt aqueous solution and a polymer medium as a starting material. An aqueous solution was prepared using nitrate of metals such as Ca, Zn, Al, and Eu, and a precursor impregnated with starch, a natural polymer, was sintered to synthesize CaZnAlO:Eu phosphor powder. The surface structure and composition analysis of the synthesized CaZnAlO:Eu phosphor powder were analyzed by scanning electron microscope(SEM) and energy-dispersed X-ray spectroscopy(EDS). The crystal structure of CaZnAlO:Eu phosphor particles was analyzed by an X-ray diffraction analyzer (XRD). As a result of measuring the photoluminescence(PL) characteristics of the phosphor, it was confirmed that a red phosphor with a light emitting wavelength of 650-780nm was successfully synthesized. According to SEM and EDS analysis, the synthesized Ca₁₄Zn₆Al_9.93O₃₅:Eu³⁺_0.07 phosphor powder has a uniform particle size, and Eu ions used as an activator are present. The synthesized CZA:Eu³⁺ phosphor can be used as a material that can increase the light absorption efficiency of the solar cell by converting ultraviolet or visible light down conversion into a wavelength in the near-infrared region.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2016.11a
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• pp.191.2-191.2
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• 2016

$TiO_2$는 우수한 화학적 및 물리적 안정성 때문에 수전해 장기간 사용에 적합한 전기화학 전극으로 여겨진다. 큰 표면적을 갖는 $TiO_2$를 제조하기 위한 수많은 방법 중 양극산화(anodization)는 비교적 간단하고 저렴한 공정으로 인하여 매우 실용적인 방법으로서 알려져 있다. 특히, 고도로 정렬 된 $TiO_2$ 나노튜브($TiO_2$ NTs) 의 경우에는 분말상과 달리 전극제조를 위해 추가적인 접착제를 필요하지 않다. 그러나, $TiO_2$는 일반적으로 절연 특성을 나타내기 때문에 전극의 활용을 위해서는 본질적으로 촉매의 사용이 불가피하다. 다수의 전기 촉매 중, $IrO_2$와 $RuO_2$는 수전해 분야에 잘 알려진 산화 촉매이다. 그럼에도 불구하고, 특유의 높은 종횡비 때문에 $TiO_2$ 나노튜브에 전기 촉매를 균일하게 도핑하는 것은 많은 어려움이 따른다. 이를 해결하기 위한 방법으로 $RuO_2$를 도핑하기 위한 단일공정 $TiO_2$ 양극산화 기술이 보고된 바 있다. 본 연구에서는 2원 촉매($IrO_2$ 및 $RuO_2$)를 $TiO_2$ 나노튜브에 도핑하기 위한 단일공정 양극산화 기술에 대하여 연구하였다. 전구물질로써 $KRuO_4$($RuO_2$ 전구체)와 IrOx 나노입자(IrOx NPs, $IrO_2$ 전구체)를 사용하였다. 특히, IrOx를 나노 입자는 $IrCl_3$로부터 중간 매체로 합성된다. IrOx는 단일공정 양극산화 중에 $TiO_2$ 나노튜브 상에 도핑 가능한 이온 형태인 $IrO_4$-로 전환될 수 있다. 제조된 시료는 열처리 후 바로 전극으로 사용되었으며 SEM, XPS, TEM, ICP-OES 등으로 정성, 정량 분석을 수행하였다. LSV와 EIS를 통해 전기화학적 성능 평가가 이루어졌으며, LSV를 통해 포집한 기체는 가스 크로마토그래피를 사용하여 정량분석한 후 그 효율을 측정하였다.

• 한국신재생에너지학회:학술대회논문집
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• 2010.11a
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• pp.89.1-89.1
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• 2010

본 연구는 세라믹 연결재로 사용되는 Perovskite 구조의 LSTO조성의 실제 SOFC stack 적용을 위한 소결온도를 낮출 수 있는 방법에 관해 연구하였다. SOFC 단전지에서 IC 소재는 $1300{\sim}1400^{\circ}C$에서 소결이 이루어져야만 하나 현재 사용하고 있는 LCO계 조성의 경우 $1500{\sim}1600^{\circ}C$의 높은 온도에서 소결이 이루어지며 고온에서 $Cr_2O_3$의 휘발로 인해 낮은 전기전도성을 갖는 문제점을 가지고 있다. 이러한 문제점을 해결하기 위해 IC 소재에 소결조제를 첨가하여 소결특성을 평가하였고, SEM과 XRD분석을 통하여 perovskite 단일상이 합성된 것을 확인하였다. 또한 Archimedes법을 사용하여 흡수율 및 겉기공율을 측정하였고, DC analyzer를 사용하여 전기전도도를 측정한 결과 대기분위기 $750^{\circ}C$에서 높은 값을 나타냄을 확인할 수 있었다.

• Journal of the Korean Magnetics Society
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• v.18 no.6
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• pp.217-220
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• 2008

We have investigated the magnetic properties of $ErFe_2O_4$. Stoichiometric polycrystalline sample of $ErFe_2O_4$ was prepared by solid-state reaction method in a stream of CO/$CO_2$ gas. The X-ray power diffraction pattern shows that the diffraction peaks are indexed with respect to the rhombohedral structure with a space group of R3m. The temperature dependent magnetization for $ErFe_2O_4$ shows two-step phase transitions at about 220 and 250 K. The transition at 250 K is an antiferromagnetic transition and that at 220 K is a structural transition.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.22 no.4
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• pp.207-212
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• 2012

A single phase $Mg_3Sb_2$ alloy was synthesized by melting the mixture of Mg and Sb metal powders at 1173 K. The figure of merit of the $Mg_3Sb_2$ prepared by melting method increased with temperature and showed a value of $2.39{\times}10^{-2}$ at 593 K. When the $Mg_3Sb_2$ powders were milled at high speed in a planetary ball mill for 12~48 h, Zintle phase ($Mg_3Sb_2$) was maintained as a main phase, but its crystallinity became deteriorated and elemental Sb phase appeared. Sb phase free $Mg_3Sb_2$ could be obtained by the mechanical alloying of high speed ball milling for 24 h using elemental Mg and Sb powder mixtures.

• Journal of the Korean Magnetics Society
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• v.21 no.5
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• pp.157-162
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• 2011

The effect of ferrous/ferric molar ratio and precipitants on the formation of nano size magnetite particle was investigated by coprecipitation method. Ferrous sulfate and ferric sulfate were used as iron sources and sodium hydroxide and ammonium hydroxide was used as a precipitant. Single phase magnetite was synthesized with all of experiment conditions (ferrous/ferric molar ratios and precipitants). Particle size was smaller, and particle size distribution was narrower when NaOH was used than $NH_4OH$ was used. The crystallinity and particle size was increased and narrower particle size distribution with increasing molar ratio ferrous/ferric sulfate with the same precipitant. Super paramagnetism could be obtained at all of experiment conditions. The highest saturation magnetization (72 emu/g) was obtained when the ferrous/ferric molar ratio was 2.5 and precipitant was used $NH_4OH$.