CVD법으로 제조한 탄소 나노튜브의 전계 전자 방출 특성

이임렬,Lee, Rhim-Youl 한국재료학회 2003 한국재료학회지 Vol.13 No.7

The microstructure and field emission properties of carbon nanotubes(CNT) grown by Ni-catalytic chemical vapor deposition(CVD) were investigated. CVD-grown CNT had a high density of curved shape with randomly oriented. It was found that an increase in electric field caused an increase in field emission current and field emission sites of CNT. The maximum field emission current density was measured to be 3.6 ㎃/$\textrm{cm}^2$ at 2.5 V/$\mu\textrm{m}$, while the brightness of 56 cd/$\textrm{cm}^2$ was observed for the CNT-grown area of 0.8 $\textrm{cm}^2$ from a phosphor screen. Field emission current at constant electric field gradually decreased initially and then stabilized with time.

산소와 구리의 공정반응에 의한 구리와 알루미나의 직접접합

이임렬(Rhim Youl Lee),유환성(Hwan Song Yu) 단국대학교 신소재기술연구소 1991 신소재 연구논집 Vol.1 No.-

초음파 분무법으로 제조한 $(Y,Gd)BO_3:Eu^{3+}$ 형광체의 발광특성에 관한 연구

김대수,이임렬,Kim, Dae-Su,Lee, Rhim-Youl 한국재료학회 2000 한국재료학회지 Vol.10 No.3

초음파 분무법으로 $(Y,Gd)BO_3:Eu$의 PDP 적색 형광체를 제조하여 147nm VUV 여기에 따른 발광 특성을 분석하였다. 초음파 분무에 사용된 전구체 용액은 Y, Gd, Eu의 아세트산염과 $H_3BO_3$를 증류수에 용해하여 1.7MHz의 초음파 분무기로 고온의 반응관내로 분무하였다. 분무된 액적은 반응관내에서 통과시 불충분한 반응으로 C-C와 C-H를 함유한 비정질 상이었으나, $1100^{\circ}C$에서 추가 열처리 한 시편은 고상반응법으로 제조한 형광체와 동일한 결정구조와 성분을 보였다. 고상반응법으로 제조한 형광체의 분말 크기는 $3{\mu\textrm{m}}$으로 조대하고 불균일한 분포를 보인 반면, $500^{\circ}C$에서 분무한 후 $900^{\circ}C$에서 열처리하여 제조한 $(Y_{0.7}Gd_{0.3})_{0.95}BO_3:Eu_{0.05}\;^{3+}$ 형광체의 모양은 비교적 구형이었으며 평균 입자크기는 $0.7{\mu\textrm{m}}$로 미세하고 균일한 분포를 하고 있었다. 147nm VUV 여기시 초음파 분무로 제조한 $(Y_{0.7}Gd_{0.3})_{0.95}BO_3:Eu_{0.05}\;^{3+}$ 형광체의 적색 발광강도는 고상반응법으로 제조한 시편이나 상용품인 $(Y,Gd)BO_3:Eu$ 형광체에 비해 그 휘도가 증가되었다. The $(Y,Gd)BO_3:Eu$ red phosphors for PDP application were synthesized by ultrasonic spray method and then their photoluminance properties were investigated under 147nm VUV irradiation. The precursor solution of acetates of Y, GD and Eu and boric acid diluted in water was sprayed using 1.7 MHz ultra-sonic sprayer into the reaction tube held at high temperature. The as-sprayed particles were amorphous phase having C-C and C-H bonds due to the insufficient thermal reaction during the pass along the tube. But the sprayed samples followed by heat treatment at $1100^{\circ}C$ had the same crystal structure and chemical composition as those samples followed by solid state reaction. It was found that the $(Y_{0.7}Gd_{0.3})_{0.95} BO_3:Eu_{0.05}^{3+}$ phosphor particles synthesized by spray at $500^{\circ}C$ and then heat treated at $900^{\circ}C$ had a spherical-like shape and fine particle size at $0.7{\mu\textrm{m}}$ having a narrow size distribution, while the phosphor particles made by solid state reaction was $3{\mu\textrm{m}}$ coarse and non-uniform size distribution. The emitting intensity under 147nm VUV excitation for $(Y_{0.7}Gd_{0.3})_{0.95}BO_3:Eu_{0.05}^{3+}$ phosphor prepared by spray method was found to be higher than those phosphor made by solid state reaction and the commercial $(Y,Gd)BO_3:Eu$ product.

탄소나노 튜브위에 성장된 Pd 및 Pt 나노 입자의 제조 및 특성

김형균,이임렬,Kim, Hyung-Kun,Lee, Rhim-Youl 한국재료학회 2009 한국재료학회지 Vol.19 No.4

Carbon nanotubes (CNT) were used as a catalyst support where catalytically active Pd and Pt metal particles decorated the outside of the external CNT walls. In this study, Pd and Pt nanoparticles supported on $HNO_3$-treated CNT were prepared by microwave-assisted heating of the polyol process using $PdCl_2$ and $H_2PtCl_6{\codt}6H_2O$ precursors, respectively, and were then characterized by SEM, TEM, and Raman. Raman spectroscopy showed that the acid treated CNT had a higher intensity ratio of $I_D/I_G$ compared to that of non-treated CNT, indicating the formation of defects or functional groups on CNT after chemical oxidation. Microwave irradiation for total two minutes resulted in the formation of Pd and Pt nanoparticles on the acid treated CNT. The sizes of Pd and Pt nanoparticles were found to be less than 10 nm and 3 nm, respectively. Furthermore, the $SnO_2$ films doped with CNT decorated by Pd and Pt nanoparticles were prepared, and then the $NO_2$ gas response of these sensor films was evaluated under $1{\sim}5\;ppm$ $NO_2$ concentration at $200^{\circ}C$. It was found that the sensing property of the $SnO_2$ film sensor on $NO_2$ gas was greatly improved by the addition of CNT-supported Pd and Pt nanoparticles.

BaO-MgO-$Al_2O_3$계에서 조성변화에 따른 청색 형광체의 발광특성

박상현,공명선,이임렬,Park, Sang-Hyun,Kong, Myung-Sun,Lee, Rhim-Youl 한국재료학회 1998 한국재료학회지 Vol.8 No.6

활성제로 $Eu^{+2}$을 사용한 BaO-MgO-$AI_2O_3$에서 화학조성 변화에 따른 청색 형광체의 광학특성을 254nm 자외선 및 147nm의 진공자외선 하에서 측정하였다. 동 형광체는 자외선 및 진공자외선 조사를 받아 주 파장이 445nm 인 가시광선의 청색을 발하는 형광체이다. $BaMgAI_{14}O_{23}$ : Eu 농도에 따라 증가하였으며 진공자외선의 경우에는 5%농도에서 최대가 됨을 알 수 있었다. 자외선 및 진공자외선 모두에서 $BaMgAI_{10}O_{17}$형광체의 청색 발광강도는$BaMgAI_{14}O_{23}$보다 좋았다. 또한 $BaMgAI_{10}O_{17}$에서 Ba대신 Ca이나 Sr을 0.1mole 치환시킨 $Ba_{0.9}Ca_{0.1}MgAI_{10}O_{17}$과 $Ba_{0.9}Sr_{0.1}MgAI_{10}O_{17}$ 형광체로 광특성을 더욱 개선할 수 있었다. The optical properties with chemical composition change in BaO- MgO-$AI_2O_3$, system activated by divalent Eu ion were investigated under 254nm ultraviolet(UV) and 147nm vacuum ultraviolet(VUV). These phosphors emitted a blue light at a dominant wavelength of $\lambda$=445nm under UV and VUV irradiations. It was found that the brightness of $BaMgAI_{14}O_{23}$ phosphor increased with Eu concentration up to 10% under UV but it showed a maximum emitting intensity at 5% Eu for VUV. The emitting intensity of blue color of $BaMgAl_{10}O_{l7}$ phosphor was higher than that of $BaMgAI_{14}O_{23}$for both excitation. A further improvement in brightness was obtained for $Ba_{o.9}Ca_{0.1}MaAl_{14}O_{23}$ and $Ba_{0.9}Sr_{0.1}MgAl_{10}O_{17}$ phosphor synthesized by the substition of $Ba^{+2}$ ion with O.lmole of $Ca^{+2}$ or $Sr^{+2}$ ions in $BaMgAl_{IO}O_{17}$: Eu phosphor.

산소와 구리의 공정반응에 의한 구리와 알루미나의 직접접합

이임렬,유환성 단국대학교 신소재기술연구소 1991 신소재 Vol.1 No.-

본 연구에서는 구리표면의 구리-산소간의 공정반응에 의하여 형성된 Cu-Cu_2O 공용액상 피막으로 고체 Cu금속과 Al_2O_3세라믹을 압력없이 직접접합시키는 방법을 조사하였으며 접합조건에 따른 접합특성, 파면 및 계면분석을 SEM, EDS, XRD 및 peeling 시험을 통하여 분석하였다. 1.5×10^-1 torr 진공하에서 1015℃의 온도에서 산화시킨 구리시편은 미세한 산화물 Cu_2O가 표면에 잘 형성되었다. 그후 공정온도 1065℃ 이상의 접합온도 1075℃에서 5분간 10^-3 torr의 진공하에서 직접접합시킨 시편은 접합력이 우수한 Cu/Al_2O_3 접합이 되었으며 접합후 구리기니 내에는 Cu2O가 석출된 공융조직을 갖고 있었다. 3분 산화조건에서 충분한 액상이 형성되어 29kg의 최대 접합강도를 보였으며 산회시간이 이보다 짧거나 불충분한 액상의 형성이나 산화물내의 균열 등으로 결합력이 저하하였다. 파단후 Al_2O_3 표면에는 Cu_2O nodule이 존재하였고 Cu족에는 nodule이 빠진홈을 관찰할 수 있었는바 cu2O/Al_2O_3계면 접착력은 Cu.Cu_2O계면보다 강함을 알 수 있었다. 또한 파단면에는 반응 생성물 CuAlO_2가 접합중 형성되었으나 이 반응층 두께는 SEM분해능 이하인 매우 얇은 것으로 생각된다. The direct bonding between Cu and Al_2O_3, utilizing Cu-Cu_2O skin melt formed on Cu surface by eutectic reation of Cu-O, is investigated in this study. The bond strength, fracture surface and interface structure with bonding conditions have been studied using SEM, EDS, XRD and peeling test. A fine Cu_2O is formed on the surface of Cu with oxidation at 1015℃ under 1.5×10^-1torr vacuum. After oxidation, the bonded specimen conducted at 1075℃ in 10^-3torr vacuum for 5minutes, higher temperature than its eutectic temperature of 1065℃, has a good strength having a Cu_2O precipitated structure in Cu matrix upon cooling. It has been found that the maximum bonding force of 29kg is obtatined for 3 minutes of oxidation. However, the adhesion forces are decreased with shorter or longer oxidation than this due to the formation of insufficient liquid skin or crack within oxide. After peeling test, Al_2O_3 surface is covered with Cu_2O nodules which are pulled out of Cu surface indication that Cu_2O/Al_2O_3 adhesion force is stronger than that of Cu/Cu_2O. Moreover a reaction phase of CuAlO_2, thought to be very thin layer below the resolution of SEM, is also formed during the bonding process.