산화아연 막은 투명한 전도성 물질로써 다양한 분야의 광전자소자에 이용되고 있다. 그러므로 산화아연 막의 특성을 규명하는 것은 광전자소자의 성능을 높이는데 매우 중요한 역할을 할 것이다. 본 논 문에서는 이러한 산화아연 막을 용액공정 기반으로 제작하여 형태적, 구조적 특성을 평가하고자 한다. 구 체적으로는 졸-겔 방법을 반복적으로 시행하여, 시행 횟수에 따른 산화아연 막의 물성의 변화를 관찰할 것 이다. 일정한 용액 조건하에서, 5회의 반복적인 졸-겔 방법을 시행한 결과 결정화가 진행되는 것을 확인하 였다. 7회 이상에서는 원소 구성 및 결정화도가 특정 값에 수렴하는 경향을 보였다. 최종적인 산화아연 막 의 평균결정의 크기는 약 10.7 nm 정도로 계산되었다. 본 연구를 통해 최적의 결정화를 보이는 공정횟수 는 7회였다. 본 연구 결과 및 방법론은 다양한 용액공정 변수를 가변시키면서 적용할 수가 있고 최적의 공 정조건을 확립하는데 기여할 것으로 기대한다.

Polyoxometalates (POMs) are nanoclusters composed of transition metals with high oxidation states. Owing to their redox properties and structural diversity, POMs have been applied to broad fields, such as catalysis, materials, and medicine. Among various fields of application, POMs play an important role in radiochemistry. POMs can form complexes with tri- and tetravalent lanthanides and actinides (radioactive elements), which may be good sequestrators or agents for separating nuclear wastes. Among the most prominent POM structures, Anderson-type POMs with a general formula of [Hy(XO6)M6O18]n− (y=0–6, n=2–8, M=addenda atom, X=heteroatom) represent one of the basic topological structures of the POM family. An important feature of Anderson type POMs is incorporating a large number of various heteroatoms with different size and oxidation states, which can lead to tune chemical properties. Interestingly, no example of Anderson type POMs with early transition metal ions in the heteroatom site has been reported to date. Herein, we discovered that the Anderson POM Na2K6Ti0.92W6.08O24·12H2O, which consists of pure inorganic framework built from a central Ti core supported by six WO6 inorganic scaffold, and the crystal structure was confirmed and refined using single-crystal X-ray diffraction (SC-XRD). In addition, structural characterizations, including, Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and Inductively coupled plasma-optical emission spectroscopy (ICP-OES) were performed.

We prepare ZnO nanoparticles by environmentally friendly synthesis using Cyathea nilgiriensis leaf extract. Various phytochemical constituents are identified through the assessment of ethanolic extract of plant Cyathea nilgiriensis holttum by GC-MS analysis. The formation of ZnO nanoparticles is confirmed by FT-IR, XRD, SEM-EDX, TEM, SAED and PSA analysis. TEM observation reveals that the biosynthesized ZnO nanopowder has a hexagonal structure. The calculated average crystallite size from the high intense plane of (1 0 1) is 29.11 nm. The particle size, determined by TEM analysis, is in good agreement with that obtained by XRD analysis. We confirm the formation of biomolecules in plant extract by FT-IR analysis and propose a possible formation mechanism of ZnO nanoparticles. Disc diffusion method is used for the analyses of antimicrobial activity of ZnO nanoparticles. The synthesized ZnO nanoparticles exhibit antimicrobial effect in disc diffusion experiments. The biosynthesized ZnO nanoparticles display good antibacterial performance against B. subtilis (Gram-positive bacteria) and K. pneumonia (Gram-negative bacteria). Bio-synthesized nanoparticles using green method are found to possess good antimicrobial performance.

자연에서도 생합성이 되는 테트라하이드로-β-카볼린 화합물은 Pictet-Spengler반응을 통해서 화학적으로도 합성된다. 본 연구에서는 β-카볼린 화합물을 쉽고 효과적으로 합성할 수 있는 친환경 합성법을 개발하여 유기용매가 아닌 물을 사용하여 합성하였다. 이 화합물은 투명한 결정형의 생성물로 얻어지므로 복잡한 분리과정이 필요하지 않다. 합성된 화합물은 NMR 및 UPLC/MS를 이용하여 구조를 확인하 였다. 화합물 1의 이론적 분자량(C17H17N2 249.1392), 화합물 2 (C17H23N2 255.1861), 화합물 3(C19H21N2O3 325.1552), 화합물 4(C19H19N2O 279.1497)과 측정된 화합물들의 질량과 비교하였다. 그 결과 측정된 화합물 1의 분자량 ([M+H]+m/z detected 249.1315), 2 (detected 255.1789), 3 (detected 325.1460) 그리고 4 (detected 279.1364)와 거의 일치함으로써 생성된 화합물이 1~4의 구조를 가지고 있음을 확인하였다. 합성된 화합물들을 그람 음성균인 E. coli DH5α를 대상으로 항균효과를 조사한 결과 강한 저해효과를 확인할 수 있었다.

본 연구에서는 구조단열패널을 구조 벽체로서 활용하기 위하여 개구부를 설치한 후 편심축하중 실험 및 해석을 수행 하였다. 실험체의 크기는 1200×2400㎜이다. 실험체는 7개로서 개구부의 크기와 개구부 보강방법, 강재를 시용한 구조단열패널 보강을 변수로 하여 진행하였다. 구조단열패널에 대하여 개구부 설치에 따른 구조적 거동을 분석하기 위한 변수해석을 수행하였다. 구조성능 실험 결과와의 비교분석을 통해 해석에 대한 검증을 하였고, 개구부 크기를 변수로 하여 편심축하중을 받는 구조단열패널의 구조적 거동을 유한요소해석을 통하여 분석하였다. 이를 통해 구조단열패널에 적합한 최적의 개구부 형상을 제안 하고자 한다.

북미와 유럽 등지에서 주거용 주택소재로서 폭넓게 사용되고 있는 구조단열패널(SIP)의 구조적 성능을 평가하기 위해 면내전단하중 시험을 수행하였다. 국외의 경우, 구조단열패널의 기준과 관련된 연구들이 다양하게 진행되었다. 하지만, 국내의 경우, 구조단열패널에 대한 기준은 마련되어 있지 않으며, 성능평가와 관련된 연구는 극소수이다. 본 연구에서는 구조단열패널을 내력벽으로 활용하기 위한 구조성능평가 실험을 수행하였으며, 벽체에 개구부 설치 후 면내전단하중을 가력하였다. 실험체의 크기는 2,400×2,400㎜이며, 변수로는 개구부의 크기와 개구부 보강방법이다. 실험체의 수량은 총 8개이다. 개구부가 있는 구조단열패널의 구조 해석을 수행 하였다. 해석 결과는 구조 실험 시험 결과와 비교하였다. 이를 통해 구조단열패널의 구조 거동을 예측할 수 있는 해석 모델을 완성하였다. 개구 크기를 변수로 하여 면내전단하중을 받는 구조단열패널의 거동을 유한 요소 해석을 통해 분석하였다. 연구를 통해 구조단열패널의 최적 개구부 크기를 제안한다.

This study investigates the microstructural properties of CoCrFeMnNi high entropy alloy (HEA) oxynitride thin film. The HEA oxynitride thin film is grown by the magnetron sputtering method using nitrogen and oxygen gases. The grown CoCrFeMnNi HEA film shows a microstructure with nanocrystalline regions of 5~20 nm in the amorphous region, which is confirmed by high-resolution transmission electron microscopy (HR-TEM). From the TEM electron diffraction pattern analysis crystal structure is determined to be a face centered cubic (FCC) structure with a lattice constant of 0.491 nm, which is larger than that of CoCrFeMnNi HEA. The HEA oxynitride film shows a single phase in which constituting elements are distributed homogeneously as confirmed by element mapping using a Cs-corrected scanning TEM (STEM). Mechanical properties of the CoCrFeMnNi HEA oxynitride thin film are addressed by a nano indentation method, and a hardness of 8.13 GPa and a Young’s modulus of 157.3 GPa are obtained. The observed high hardness value is thought to be the result of hardening due to the nanocrystalline microstructure.

Activated carbons (ACs) have been used as EDLC (electric double-layer capacitor) electrode materials due to their high specific area, stability, and ecological advantages. In order to prepare ACs with high density and crystallinity, coal tar pitch (CTP) was activated by K2CO3 and the textural and electrochemical properties of the obtained ACs were investigated. Although the CTP ACs formed by K2CO3 activation had much smaller specific surface area and pore volume than did the CTP ACs formed by KOH activation, their volumetric specific capacitance (F/cc) levels as electrode materials for EDLC were comparable due to their higher density and micro-crystallinity. Structural characterization and EDLC-electrode performance were studied with different activation conditions of CTP/K2CO3 ratio, activation temperature, and activation period.

This study suggested comprehensive structural characterization methods for the commercial blue light emitting diodes(LEDs). By using the Z-contrast intensity profile of Cs-corrected high-angle annular dark field scanning transmission electron microscope(HAADF-STEM) images from a commercial lateral GaN-based blue light emitting diode, we obtained important structural information on the epilayer structure of the LED, which would have beendifficult to obtain by conventional analysis. This method was simple but very powerful to obtain structural and chemical information on epi-structures in a nanometer-scale resolution. One of the examples was that we could determine whether the barrier in the multi-quantum well(MQW) was GaN or InGaN. Plan-view TEM observations were performed from the commercial blue LED to characterize the threading dislocations(TDs) and the related V-pit defects. Each TD observed in the region with the total LED epilayer structure including the MQW showed V-pit defects for almost of TDs independent of the TD types: edge-, screw-, mixed TDs. The total TD density from the region with the total LED epilayer structure including the MQW was about 3.6 × 108 cm−2 with a relative ratio of Edge- : Screw- :Mixed-TD portion as 80%: 7%: 13%. However, in the mesa etched region without the MQW total TD density was about 2.5 × 108 cm−2 with a relative ratio of Edge- : Screw- :Mixed TD portion of 86%: 5%: 9 %. The higher TD density in the total LED epilayer structure implied new generation of TDs mostly from the MQW region.

Double walled carbon nanotubes (DWCNTs) are considered an ideal model for studying the coupling interactions between different concentric shells in multi-walled CNTs. Due to their intrinsic coaxial structures they are mechanically, thermally, and structurally more stable than single walled CNTs. Geometrically, owing to the buffer-like function of the outer tubes in DWCNTs, the inner tubes exhibit exciting transport and optical properties that lend them promise in the fabrication of field-effect transistors, stable field emitters, and lithium ion batteries. In addition, by utilizing the outer tube chemistry, DWCNTs can be useful for anchoring semiconducting quantum dots and also as effective multifunctional fillers in producing tough, conductive transparent polymer films. The inner tubes meanwhile preserve their excitonic transitions. This article reviews the synthesis of DWCNTs, their electronic structure, transport, and mechanical properties, and their potential uses.

Pure zirconia and x mol% calcia partially stabilized zirconia (x = 1.5, 3, and 8) nanopowders were synthesized by hydrothermal method with various reaction temperatures for 24 hrs. The precipitated precursor of pure zirconia and x mol% calcia doped zirconia was prepared by adding NH4OH to starting solutions; resulting sample was then put into an autoclave reactor. The optimal experimental conditions, such as reaction temperatures and times and amounts of stabilizer CaO, were carefully studied. The synthesized ZrO2 and x mol% CaO-ZrO2 (x = 1.5, 3, and 8) powders were characterized by XRD, SEM, TG-DTA, and Raman spectroscopy. When the hydrothermal temperature was as low as 160˚C, pure ZrO2 and x mol% CaO-ZrO2 (x = 1.5 and 3) powders were identified as a mixture of monoclinic and tetragonal phases. However, a stable tetragonal phase of zirconia was observed in the 8 mol% calcia doped zirconia nanopowder at hydrothermal temperature above 160˚C. To observe the phase transition, the 3 mol% CaO-ZrO2 and 8 mol% CaO-ZrO2 nanopowders were heat treated from 600 to 1000˚C for 2h. The 3 mol% CaO-ZrO2 heat treated at above 1000˚C was found to undergo a complete phase transition from mixture phase to monoclinic phase. However, the 8 mol% calcia doped zirconia appeared in the stable tetragonal phase after heat treatment. The result of this study therefore should be considered as the preparation of 8 mol% CaO-ZrO2 nanopowders via the hydrothermal method.

We report the structural characterization of BixZn1-xO thin films grown on c-plane sapphire substrates by plasma-assisted molecular beam epitaxy. By increasing the Bi flux during the growth process, BixZn1-xO thin films with various Bi contents (x = 0~13.17 atomic %) were prepared. X-ray diffraction (XRD) measurements revealed the formation of Bi-oxide phase in (Bi)ZnO after increasing the Bi content. However, it was impossible to determine whether the formed Bi-oxide phase was the monoclinic structure α-Bi2O3 or the tetragonal structure β-Bi2O3 by means of XRD θ-2θ measurements, as the observed diffraction peaks of the 2θ value at ~28 were very close to reflection of the (012) plane for the monoclinic structure α-Bi2O3 at 28.064 and the reflection of the (201) plane for the tetragonal structure β-Bi2O3 at 27.946. By means of transmission electron microscopy (TEM) using a diffraction pattern analysis and a high-resolution lattice image, it was finally determined as the monoclinic structure α-Bi2O3 phase. To investigate the distribution of the Bi and Bi-oxide phases in BiZnO films, elemental mapping using energy dispersive spectroscopy equipped with TEM was performed. Considering both the XRD and the elemental mapping results, it was concluded that hexagonal-structure wurtzite BixZn1-xO thin films were grown at a low Bi content (x = ~2.37 atomic %) without the formation of α-Bi2O3. However, the increased Bi content (x = 4.63~13.17 atomic %) resulted in the formation of the α-Bi2O3 phase in the wurtzite (Bi)ZnO matrix.

사용후핵연료를 파이로 건식처리하면 사용후핵연료 자체 내에 존재하는 세슘, 스트론튬, 초우라늄 계열등이 중간저장 되어 영구처분 방사선원항에서 제외되므로 사용후핵연료집합체를 구성하는 구조재, 즉 금 속폐기물의 방사선원항이 중요해지게 된다. 따라서 본 연구에서는 17×17 KOFA 사용후핵연료 10 톤이 파 이로 건식처리 되었을 경우를 가정하여 각 구조재 부품별로 방사선원항 특성을 분석하였다. 우선 구조재 부품별로 질량 및 부피를 상세히 계산하였다. 핵연료 상단 및 하단 고정체에서의 중성자스펙트럼이 노심과 다르므로 각 구조재 부품별로 핵반응단면적라이브러리를 KENO-VI/ORIGEN-S 모듈로 직접 생산하였으 며, 이를 적용하여 ORIGEN-S 코드로 방사화 방사선원항을 평가하였다. 평가결과 원자로 방출후 10 년 시 점에서의 방사능세기, 붕괴열, 위해지수 값은 각각 1.40×1015 Bequerels, 236 Watts, 4.34×109 m3-water 로 나타났으며, 이는 사용후핵연료 자체 값의 0.7 %, 1.1 %, 0.1 %에 해당하는 값이다. 방사능세기, 붕괴 열, 위해지수 모든 측면에서는 금속폐기물 전체물량의 1 %만을 차지하는 인코넬 718 그리드판이 가장 중 요한 것으로 평가되었으며, 특히 이를 따로 분리하여 관리하면 금속폐기물 전체 방사능세기를 20∼45 % 정도, 위해지수를 30∼45 % 정도 감소시킬 수 있는 것으로 나타났다. 전체적으로 볼 때, 금속폐기물의 방 사능세기 및 위해지수는 처분시스템 설계 시 중요한 인자로 고려되어야 하나, 붕괴열은 그 열량이 작아 중 요하지 않은 것으로 나타났다.

This paper presents results and observations obtained from a study of the optical and thermal properties of alkali tellurite depending on the composition. Fourier transform infrared (FT-IR) spectra showed evidence of chemical modification from TeO4 trigonal bipyramids (tbp) to TeO3 trigonal pyramids (tp) in tellurite glasses. The optical band gaps of the different glass samples calculated using Tauc's method were found to range from 3.5-3.8 eV. The glass transition temperature (Tg) and glass stability (δT) of alkali tellurite glasses were investigated, as M2O [M: Li, Na, K] amounted to 25 mol%, through the use of differential thermal analysis (DTA). The coefficient of thermal expansion (CTE) was measured in a thermo mechanical analysis (TMA) with a slow heating rate after the glass samples were annealed. The results confirm that the optical band gap of alkali tellurite glasses depends on the Te-O-Te structural relaxation related to the ratio of bridging/non bridging oxygen (BO/NBO). In contrast, the thermal properties are related to the ionic field strength of the Te-O-M and M-O-M bonds, and the Te-O-Te breakage depends on the ratio of BO/NBO.

MBS에 의해(001)GaAs기판 위에 성장된 Zn1-xCoxSe(x=1.0, 7.4, 9.5 %)반도체 박막과 (ZnSe/FeSe)반도체 초격자 박막의 미세구조를 투과전자현미경을 이용하여 연구하였다. Zn1-xCoxSe 박막 시편의 경우, 박막과 기판 사이의 격자 불일치때문에 a/2<110>형태의 버거즈 벡터를 가지는 부정합 전위를 관찰하였다. 모든 Zn1-xCoxSe 박막과 기판의 계면은 뚜렷이 구별되었고, 계면에서 산화물이나 이물질이 존재하지 않았다. 또한, (ZnSe/FeSe)초격자를 성장시키기 전에 GaAs기판 위에 ZnSe바닥층을 넣음으로써 고품질의 (ZnSe/FeSe)초격자를 얻었다. (ZnSe/FeSe)초격자에 있는 FeSe는 섬아연광 결정구조로 존재하였다.