• 분석과학
• /
• 제27권6호
• /
• pp.314-320
• /
• 2014

$La_{2-x}(MoO_4)_3:Er^{3+}/Yb^{3+}$ particles with doping concentrations of $Er^{3+}$ and $Yb^{3+}$ ($x=Er^{3+}+Yb^{3+}$, $Er^{3+}$=0.05, 0.1, 0.2 and $Yb^{3+}$ = 0.2, 0.45) were successfully prepared by the microwave-modified sol-gel method, and the upconversion photoluminescence properties were investigated. Well-crystallized particles, formed after heat-treatment at $900^{\circ}C$ for 16 h, showed a fine and homogeneous morphology with particle sizes of $2-5{\mu}m$. Under excitation at 980 nm, $La_{1.7}(MoO_4)_3:Er_{0.1}Yb_{0.2}$ and $La_{1.5}(MoO_4)_3:Er_{0.05}Yb_{0.45}$ particles exhibited a strong 525 nm emission band, a weak 550 nm emission band in the green region, and a very weak 655 nm emission band in the red region. The Raman spectra of the doped particles indicated the presence of strong peaks at higher frequencies of 752, 846, 922, 1358 and $1435cm^{-1}$ and lower frequency of $314cm^{-1}$ induced by the disorder of the $[MoO_4]^{2-}$ groups with the incorporation of the $Er^{3+}$ and $Yb^{3+}$ elements into the crystal lattice or by a new phase formation.

• 한국세라믹학회지
• /
• 제29권2호
• /
• pp.107-118
• /
• 1992

Alumina supports for TiO2 ultrafiltration membrane coating were prepared by presintering disk-type preforms at 140$0^{\circ}C$. These supports showed uniform microstructures which had the apparent porosity of 40%, the pore size distribution in the range of 0.1~0.5${\mu}{\textrm}{m}$, and the water flux of 1400ι/$m^2$.h at the pressure difference of 10 atm. The optimum pH and concentration of the TiO2 sol for coating were 0.8 and 1.0 wt%, respectively, and sol particles were identified as rutile forms of 20 nm size. Crack-free alumina-supported rutile TiO2 membranes could be prepared through well controlled drying and heating the gel layer coated by the sol-gel dipping. The pore size of the TiO2 membranes heat-treated at 50$0^{\circ}C$ for 2 hrs was 30~80$\AA$, and their thickness varied from 1.1 to 3.8 ${\mu}{\textrm}{m}$ in accordence with the dipping time (4~40 min). The flux of water through this composite membrane at 10 atm was found to be in the range from 800 to 1100ι/$m^2$.hr depending on the dipping time (10~40 min). The membrane thickness increased linearly with the square root of the dipping time and the slope was 0.62 ${\mu}{\textrm}{m}$/{{{{ SQRT { min} }}.

• 한국전기전자재료학회:학술대회논문집
• /
• 한국전기전자재료학회 2001년도 하계학술대회 논문집
• /
• pp.315-318
• /
• 2001

The optical and dielectric properties of TiO$_2$ thin films prepared with mixtures of Epoxy, bits-(4, 4'-p-toluenesulfonylacidic isoproplylidene)-cyclohexadiol and UVI 6990 in dry sol-gel process were investigated. The absorption peak of the films was showed at 360nm. Photocurrent of the thin films doped with 50 wt% of TiO$_2$was higher than that of nondoped thin films. Energy gap was lowered from 3.6 to 3.3 eV with increasing amount of TiO$_2$. Relative dielectric constants of samples were 1.5 to 3 and showed a characteristics of lower dielectric materials.

• Transactions on Electrical and Electronic Materials
• /
• 제16권1호
• /
• pp.5-9
• /
• 2015

Optical and electrical properties were studied for Antimony doped tin oxide thin films from precursors containing 10, 30, 50, and 70 atom% of Sb deposited on bare sodalime silica, barrier layer coated sodalime silica, and pure silica glass substrates by sol-gel spinning technique. The direct band gaps were found to vary from 3.13~4.12 eV when measured in the hv range of 2.5~5.0 eV, and varied from 4.22~5.08 eV when measured in the range of 4.0~7.0 eV. Indirect band gap values were in the range of 2.35~3.11 eV. Blue shift of band gap with respect to bulk band gap and Moss-Burstein shift were observed. Physical thickness of the films decreased with the increase in % Sb. Resistivity of the films deposited on SLS substrate was in the order of $10^{-2}$ ohm cm. Sheet resistance of the films deposited on barrier layer coated soda lime silica glass substrate was found to be relatively less.

• 공학논문집
• /
• 제6권1호
• /
• pp.161-168
• /
• 2004

In the present study, a simple method was successfully used for hydroxyapatite coatings on Ti-6AL-4V substrates deposited by using a sol-gel derived precursor. Prior to hydroxyapatite coating the samples were micropolished (0.1 micron) and divided into three sets. The first set, were the micropolished samples kept as such. The second set were coated with titania sol and the third set was treated with 5M NaOH. After three repetitions of hydroxyapatite coating procedures on each set and heat treatment at $600^{\circ}C$, the formation of hydroxyapatite has been confirmed by XRD analyses and the substrate material was found to be oxidized with negligible amount of CaO in the coating. The SEM studies revealed surface morphology. Hydroxyapatite, calcined at $600^{\circ}C$, displaying a porous structure arisen from heating of the bulk

• 한국자기학회지
• /
• 제11권4호
• /
• pp.168-172
• /
• 2001

Sol-gel법을 이용하여 Co$_{0.9}$Zn$_{0.1}$Fe$_2$O$_4$ 박막을 제조하였다. 성장한 박막의 구조 및 자기적 성질에 관하여 x선 회절분석기 (XRD), atomic force microscopy(AFM) 및 Auger electron spectroscopy(AES), 진동시료자화측정기 (VSM)을 이용하였다. Co-Zn 페라이트 박막의 경우, 400 $^{\circ}C$ 이상의 열처리 온도에서 단일상의 spinel 구조만을 가지고 있으며, 아무런 방향성이 없이 성장함을 나타내고 있다. 열처리 온도가 600 $^{\circ}C$ 이하에서 성장된 박막 표면의 거칠기는 3 nm 이하였으며, 형성된 입자의 크기는 약 40nm이하임을 알 수 있었다. 또한, 40$0^{\circ}C$에서 열처리한 경우 기판에서 Si이 Co-Zn 페라이트 박막내로 확산이 거의 나타나지 않았으나, 870 $^{\circ}C$에서 열처리한 경우 계면에서 기판과 박막의 상호 확산을 확인할 수 있었다. 제작한 박막은 외부 자기장의 방향과는 무관한 등방성의 자기적 특성을 보이며, 최대 보자력은 600 $^{\circ}C$에선 열처리한 자성박막이 약 1,900 Oe을 가짐을 알 수 있었다.있었다.

• 한국표면공학회지
• /
• 제38권4호
• /
• pp.167-173
• /
• 2005

Surface characteristics of HA(hydroxyapatite) coated dental implant alloy by Sol-Gel method were investigated using potentiostat, ICP, SEM, EDX, EPMA and surface roughness tester. Surface roughness of HA coated specimen by Sol-Gel showed higher than that of PVD coated specimen. Corrosion resistance increased in the order of $1\%$ lactic acid, artificial saliva, $0.5\%$ HCI and $0.9\%$ NaCl solution. Amount of Ca element release was higher than that of V and P in the $0.5\%$ HCI and $0.9\%$ NaCl solution.

• 한국자기학회지
• /
• 제16권1호
• /
• pp.1-5
• /
• 2006

결정구조는 같은 spinel 구조이나, 자기적으로는 각각 반강자성과 준강자성 특성을 띠고 있는 $Co_3O_4$와 자철광 $Fe_3O_4$의 혼성 Co-ferrite인 $Co_xFe_{1-x}O_4$ 박막을 sol-gel법으로 제조하여, Fe 이온에 대한 Co 이온 치환으로 발생된 양이온 거동이 Co-ferrite 박막의 결정구조 및 자기적 특성에 미치는 효과를 XRB 실험, VSM 측정, 그리고 Conversion Electron Mossbauer Spectroscopy (CEMS) 실험으로 조사하였다. 그 결과 $Co^{3+}$ 이온이 주로 $Fe^{3+}$ 이온을 치환하여 단위정의 크기가 감소를 가져오며, 결정구조는 inverse spinel 구조에서 normal spinel 구조로 변환된다. CEMS 분광실험을 통하여 확인된 Fe 이온의 site preference는 주로 $Fe^{3+}$ 이온이 $Co^{3+}$ 치환됨을 보여주고 있으며, 동시에 B-site의 $Co^{2+}$ 이온은 A-site로 이동된다. 자화곡선 측정결과 Co 조성값의 증가로 자기 moment값이 감소되는 것으로 나타났는데, 이것은 low spin상태의 $Co^{3+}$이 high spin상태의 $Fe^{3+}$이온을 치환하여 주로 발생한 것이다.

• 한국분말재료학회지
• /
• 제30권5호
• /
• pp.394-401
• /
• 2023

Li_1.5Al_0.5Ti_1.5(PO₄)₃ (LATP) is considered to be one of the promising solid-state electrolytes owing to its excellent chemical and thermal stability, wide potential range (~5.0 V), and high ionic conductivity (~10^-4 S/cm). LATP powders are typically prepared via the sol-gel method by adding and mixing nitrate or alkoxide precursors with chelating agents. Here, the thermal properties, crystallinity, density, particle size, and distribution of LATP powders based on chelating agents (citric acid, acetylacetone, EDTA) are compared to find the optimal conditions for densely sintered LATP with high purity. In addition, the three types of LATP powders are utilized to prepare sintered solid electrolytes and observe the microstructure changes during the sintering process. The pyrolysis onset temperature and crystallization temperature of the powder samples are in the order AC-LATP > CA-LATP > ED-LATP, and the LATP powder utilizing citric acid exhibits the highest purity, as no secondary phase other than LiTi₂PO₄ phase is observed. LATP with citric acid and acetylacetone has a value close to the theoretical density (2.8 g/cm³) after sintering. In comparison, LATP with EDTA has a low sintered density (2.2 g/cm³) because of the generation of many pores after sintering.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
• /
• pp.508-508
• /
• 2013

백색 유기발광소자는 전색 디스플레이, 액정디스플레이의 backlights, 조명에서 잠재적인 가능성 때문에 디스플레이와 조명 업계에서 각광 받고 있다. 백색 유기발광소자를 제작하기 위한 방법으로 형광체를 이용한 백색 유기발광소자가 연구되고 있지만, 아직 색순도와 색좌표에 대한 연구가 필요하다. 본 연구에서는 무기물 형광체를 이용한 백색 유기발광소자의 전기적 특성과 광학적 특성을 관찰하였다. 광원으로 사용된 청색 유기발광소자에 적색과 녹색의 무기물 형광체를 결합하는 방법으로 백색 유기발광소자를 제작하였다. 광원으로 사용한 청색 유기발광소자의 양극으로는 투명전극으로 널리 쓰이고 있는 ITO를 사용하였고 정공 수송층으로는 N,N'-bis-(1-naphthyl)-N,N'-diphenyl-1,1'-biphenyl-4,4'-diamine, 청색 발광층으로는 1,3-bis(carbazol-9-yl) benzene 호스트에 bis (3,5-difluoro-2-(2-pyridyl)phenyl)-(2-carboxypyridyl) iridium (III) 청색인광도 펀트를 사용하였다. 정공 저지층과 전자 수송층으로는 각각 2,9-dimethyl-4,7-diphenyl-1,10-phenanthorlene와 4,7-diphenyl-1,10-phenanthroline을 사용하고 전자 주입층으로는 lithium quinolate를 사용하였으며 음극으로는 Al을 사용하였다. 색 변환층으로 사용된 유기물 형광체는 sol-gel 방법으로 제작된 적색 형광체와 녹색 형광체를 사용하였다. Sol-gel 방법으로 제작된 형광체에 대한 주사현미경 측정 결과 입자의 표면이 고르고 크기가 작고 균일하였고, 높은 온도 열처리에 따라서 용매제가 대부분 제거되어 형광체 발광 특성이 잘 일어났음을 확인하였다. 제작한 백색유기발광소자에서 혼합비율에 따른 전계발광 특성 변화를 관찰하였다.