• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2001.07a
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• pp.211-214
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• 2001

The undesirable phase transformation of zirconium dioxide at high temperatures can be eliminated by stabilization of the cubic phase with an addition of a selected alkaline earth or rare-earth oxide. In this paper the ionic conductivity of cubic solid solutions in the stabilized ZrO$_2$ by CaO-Y$_2$O$_3$ system was examined. The higher ionic conductivity appears to be related to lower activation energy rather than to the number of oxygen vacancies dictated by composition. Those compositions of highest conductivity lie close to the cubic-monoclinic solid-solution phase boundary. Conductivity temperature data are presented that indicate a reversible order-disorder transition for Zr$_2$2-Y$_2$O$_3$cubic solid solutions containing 20 and 25 mole % $Y_2$O$_3$.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 1998.11a
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• pp.331-334
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• 1998

Crystal structure and surface morphology of Se thin film fabricated by EBE method had been studied. Se thin film was deposited with amorphous structure until substrate temperature of l00$^{\circ}C$. But Se thin film was grown with monoclinic structure at substrate temperature af over 150$^{\circ}C$, and its lattice constant of a, b and c was 12.76${\AA}$, 9.15${\AA}$ and 10.41${\AA}$ respectively. Also, after heat-treatment at 150。 for 15 min with substrate temperature of l00。, amorphous Se was proved to be hexagonal structure, and its lattice constant of a and c was 4.27${\AA}$ and 4.83${\AA}$ respectively.

• Journal of Integrative Natural Science
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• v.8 no.4
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• pp.250-257
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• 2015

The crystal structure of the potential active 3-(4-ethylphenyl)-3H-chromeno[4,3-c]isoxazole-3a(4H)-carbonitrile ($C_{19}H_{16}N_2O_2$) has been determined from single crystal X-ray diffraction data. In the title compound crystallizes in the monoclinic space group $P2_1/c$ with unit cell dimension a=6.6869 (8) ${\AA}$, b=15.8326 (19) ${\AA}$ and c= 15.237 (2) ${\AA}$ [${\alpha}=90^{\circ}$, ${\beta}=100.663^{\circ}$ and ${\gamma}=90^{\circ}$]. In the structure chromene, isoxazole and carboxylate are almost coplanar each other. All geometrical parameters revelled that chromene ring of pyran ring adopt sofa conformation. The crystal packing is stabilized by intermolecular C-H...N and C-H...O hydrogen bond interaction.

• Transactions of Materials Processing
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• v.12 no.3
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• pp.244-250
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• 2003

Sheets of aluminum alloy 1100 were asymmetrically cold rolled in a rolling mill with different roll speeds. In order to promote the shear deformation during asymmetrical rolling, cold rolling without lubrication was performed with a roll speed ratio of 1.5/l.0. The evolution of texture components during asymmetrical rolling was investigated by the calculation of the orientation distribution function (ODF) using the monoclinic sample symmetry. The strain state during asymmetrical rolling was tackled by means of FEM calculations. Asymmetrical rolling gave rise to the development of pronounced strain gradients throughout the thickness layers which resulted in the formation of strong texture gradients in the aluminum sheet.

• Proceedings of the Korea Crystallographic Association Conference
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• 2000.11a
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• pp.21-21
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• 2000

• Korean Journal of Crystallography
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• v.12 no.1
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• pp.5-9
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• 2001

Nd/sub 0.05/Y/sub 0.95/Ca₄O(BO₃)₃(Nd:YCOB) single crystals were grown by the Czochralski method using a iridium crucible under N₂ atmosphere. Optimum growth parameters to get high quality of single crystals were 1.5∼2 mm/hr of growth rate and 10∼20 rpm of rotation rate. The grown crystals were transparent with light purple color and well-developed in cleavage planes. The crystal structure of Nd;YCOB were identified to monoclinic by XRD method. Crystal defects acting as light scattering centers, such as micro-pores, secondary phases, inclusions and cracks were not observed under the He-Ne laser illuminations. Three red, green, blue laser devices for the RGB laser oscillations were designed and then fabricated from the grown Nd:YCOB crystals according to the phase-matching angles of negative type-I which were φ=16.40°, 33.95° and θ=22.59° with the flatness of λ/6 at least, respectively.

• Korean Journal of Crystallography
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• v.10 no.1
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• pp.71-75
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• 1999

융액인상법에 의하여 Nd3+ 이온이 15 at% 주입된 LaSc3(BO3)4 단결정을 성장하였다. 최적의 결정성장 조건하에서 성장된 결정은 결정형이 잘 발달되고 보라색 투명하였다. 편광 현미경에 의한 결정결함 분석결과 성장된 결정 중심부에서 0.1 mm 크기의 기포가 검출되었고, B2O3가 증발하여 결정에 증착된 shoulder 부위에서는 균열이 발생되었으나 body에서는 결함이 검출되지 않았다. X선 회절에 의하여 cell parameter를 측정한 결과 a=7.73 , b=9.85 , c=12.05 , β=105.48o 및 공간군 C2/c의 monoclinic 구조로 분석되었다. 양질의 단결정을 성장하기 위한 결정성장 요소는 회전속도 10 rmp, 인상속도 1.5 mm/h이었다. 성장된 결정은 808 nm에서 강하고 넓은 흡수대와 1050∼1080 nm에 걸친 형광 방출대가 관찰되었다. 성장된 결정을 이용하여 직경 3 mm, 두께 1mm 크기의 micro-chip laser 소자의 제조기술을 확립하였다.

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.10-15
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• 2000

Compound trans-[FeH(NCS(i-Pr)-S)(dppe)₂](1) reacted with isopropyl iodide (i-PrI) to give an Fe(II)-organic isothiocyanide complex, trans-[FeH(NCS(i-Pr)-S)(dppe)₂]I (2). Compound 2 was structurally characterized, in which the hydride ligand appears to be involved in the "dihydrogen" bonding, M-H…H-C. Crystallographic data for 2: monoclinic space group P2₁/n, a=13.490(2)Å, b=17.269(3)Å, c=21.384(3)Å, β=90.682(7)°, Z=4, R(wR₂)=0.0348(0.0894).

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.42-45
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• 2000

The complex [Zn(L)Cl](H₂O)(ClO₄) (1) (L=3,14-dimethyl-2,6,13,17-tetraazatricyclo[14,4,O/sup 1.18/,O/sup 7.12/]docosane) has been prepared and characterized by X-ray crystallography. 1 crystallizes in the monoclinic space group P2₁/c, with a=8.883(1), b=19.319(9), c=15.124(2)Å, β=101.65(1)°, V=2542.0(13) ų, Z=4, R₁(wR₂) for 4457 observed reflections of [I>2σ(I)] was 0.0640(0.1557). The coordination geometry around the zinc is a distorted square-pyramid with four nitrogen atoms of the macrocycle occupying the basal sites(Zn-N/sub av/=2.131(2)Å) and a chloride atom at the axial position with the Zn-Cl distance of 2.315(2)Å.

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.46-51
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• 2000

The molecular structures of 2-SC₄H₃CH=NN(H)C/sub 6/H/sub 5/(C/sub 11/H/sub 10/N₂S) and (GaMe₂)₂(2-SC₄H₃CH=NNC/sub 6/H/sub 5/)₂(C/sub 26/H/sub 30/Ga₂N₄S₂) have been determined by X-ray diffraction. Crystallographic data for 2-SC₄H₃CH=NN(H)C/sub 6/H/sub 5/:orthorhombic space group P2₁2₁2₁, a=6.108(1)Å, b=7.593(1)Å, c=22.356(2)Å, V=1037.1(3)ų, Z=4, R=0.0613. Crystallographic data for (GaMe₂)₂(2-SC₄H₃CH=NNC/sub 6/H/sub 5/)₂:monoclinic space group P2₁/n, a=15.996(2) Å, c=9.879(3)Å, β=100.07.(2)°, V=2764.599)ų, Z=4, R=0.0503.