• 제목/요약/키워드: morphological transition

검색결과 110건 처리시간 0.026초

Diamine의 구조적 이성질체에 따른 내열성 폴리이미드 박막의 잔류응력거동 (Residual Stress Behavior of High Temperature Polyimide Thin Films depending on the Structural Isomers of Diamine)

  • 임창호;정현수;한학수
    • 마이크로전자및패키징학회지
    • /
    • 제6권2호
    • /
    • pp.23-30
    • /
    • 1999
  • 이성질체에 따른 폴리이미드 박막의 잔류응력 영향과 모폴로지와의 상관관계가 조사되었다. 이를 위해, Poly(phenylene biphenyltetracarboximide) (BPDA-PDA)와 poly (oxydiphenylene biphenyltetracar-boximide) (BPDA-ODA)를 여러 다른 diamine인 1, 3-phenylene diamine (1, 3-PDA), 1.4-phenylene diamine (1,4-PDA)과 3.4'-oxydiphenylene diamine (3,4'-ODA) , 4,4'-oxydiphenylene diamine (4.4'-ODA)으로부터 제조하였다. 이들 박막에 대하여, Thin Film Stress Analyzer (TFSA)를 이용하여 공정온도 (25~$400^{\circ}C$)하에서 전구체의 열적 이미드화에 따라 실시간으로 폴리이미드 박막의 잔류응력 거동을 측정하였다. 폴리이미드 박막의 잔류응력은 면 방향 배향성과 사슬 질서도가 우수한 BPDA-1,4-PDA가 7MPa로 가장 낮게 나타났으며 BPDA-1,3-PDA, BPDA-3,4'-ODA, BPDA-4,4'-ODA의 경우 40~50Mpa 범위에 있었다. 이성질체에 따른 폴리이미드 박막의 잔류응력은 모폴로지 (사슬 강직도, 질서도, 배향성) 변화 및 유리전이 거동과 관련된 사슬 운동성을 이용하여 분석되었다.

  • PDF

고성능 에너지 저장 소자를 위한 니켈 구조체에 담지된 니켈 코발트 수산화물의 나노 형상 제어 (Nano-Morphology Design of Nickel Cobalt Hydroxide on Nickel Foam for High-Performance Energy Storage Devices)

  • 신동요;윤종천;하철우
    • 한국재료학회지
    • /
    • 제31권12호
    • /
    • pp.710-718
    • /
    • 2021
  • Recently, due to high theoretical capacitance and excellent ion diffusion rate caused by the 2D layered crystal structure, transition metal hydroxides (TMHs) have generated considerable attention as active materials in supercapacitors (or electrochemical capacitors). However, TMHs should be designed using morphological or structural modification if they are to be used as active materials in supercapacitors, because they have insulation properties that induce low charge transfer rate. This study aims to modify the morphological structure for high cycling stability and fast charge storage kinetics of TMHs through the use of nickel cobalt hydroxide [NiCo(OH)2] decorated on nickel foam. Among the samples used, needle-like NiCo(OH)2 decorated on nickel foam offers a high specific capacitance (1110.9 F/g at current density of 0.5 A/g) with good rate capability (1110.9 - 746.7 F/g at current densities of 0.5 - 10.0 A/g). Moreover, at a high current density (10.0 A/g), a remarkable capacitance (713.8 F/g) and capacitance retention of 95.6% after 5000 cycles are noted. These results are attributed to high charge storage sites of needle-like NiCo(OH)2 and uniformly grown NiCo(OH)2 on nickel foam surface.

서로 다른 증착 온도에서 성장된 BaWO4:Sm3+ 형광체 박막의 구조, 광학, 표면 형상의 특성 (Structural, optical, and morphological properties of BaWO4:Sm3+ phosphor thin films grown at different deposition temperature)

  • 조신호
    • 한국표면공학회지
    • /
    • 제55권2호
    • /
    • pp.96-101
    • /
    • 2022
  • The effects of the growth temperature on the structural, optical, and morphological properties of BaWO4:Sm3+ phosphor thin films were investigated. The BaWO4:Sm3+ thin films were grown on quartz substrates at several growth temperatures by radio-frequency magnetron sputtering. All the thin films crystallized in a tetragonal structure with a main BaWO4 (112) diffraction peak. The 830 nm-thick BaWO4:Sm3+ thin films grown at 300 ℃ exhibited numerous polygon-shaped particles. The excitation spectra of BaWO4:Sm3+ thin films consisted of a broad excitation band in the 200-270 nm with a maximum at 236 nm due to the O2--Sm3+ charge transfer and two small bands peaked at 402 and 463 nm, respectively. Under 236 nm excitation, the BaWO4:Sm3+ thin films showed an intense red emission peak at 641 nm due to the 4G5/26H9/2 transition of Sm3+, indicating that the Sm3+ ions occupied sites of non-inversion symmetry in the BaWO4 host lattice. The highest emission intensity was observed for the thin film grown at 300 ℃, with a 51.8% transmittance and 5.09 eV bandgap. The average optical transmittance in the wavelength range of 500-1100 nm was increased from 53.2% at 200 ℃ to 60.8% after growing at 400 ℃. These results suggest that 300 ℃ is the optimum temperature for growing redemitting BaWO4:Sm3+ thin films.

Eu3+와 Tb3+ 활성제 이온이 SrSnO3 형광체의 특성에 미치는 영향 (Effects of Eu3+ and Tb3+ Activator Ions on the Properties of SrSnO3 Phosphors)

  • 김정대;조신호
    • 한국재료학회지
    • /
    • 제24권9호
    • /
    • pp.469-473
    • /
    • 2014
  • $SrSnO_3$ phosphor powders were synthesized with two different contents of activator ions $Eu^{3+}$ and $Tb^{3+}$ using the solid-state reaction method. The structural, morphological, and optical properties of the phosphors were investigated using X-ray diffractometry, field-emission scanning electron microscopy, and fluorescence spectrophotometry, respectively. All the phosphors showed a cubic structure, irrespective of the type and the content ratio of activator ions. For $Eu^{3+}$-doped $SrSnO_3$ phosphors, the intensity of the 620 nm red emission spectrum resulting from the $^5D_0{\rightarrow}^7F_2$ transition of $Eu^{3+}$ was stronger than that of the 595 nm orange emission signal due to the $^5D_0{\rightarrow}^7F_1$ transition in the range 0.01-0.05 mol of $Eu^{3+}$, but the ratio of the intensity was reversed in the range 0.10-0.20 mol of $Eu^{3+}$. The variation in the emission intensity indicates that the site symmetry of the $Eu^{3+}$ ions around the host crystal was changed from non-inversion symmetry to inversion. For the $Tb^{3+}$-doped $SrSnO_3$ phosphors under excitation at 281 nm, one strong green emission band at 550 nm and several weak bands were observed. These results suggest that the optimum red and green emission signals can be realized when the activator ion content for $Eu^{3+}$- or $Tb^{3+}$-doped $SrSnO_3$ phosphors is 0.20 mol and 0.15 mol, respectively.

Establishment of Hertwig's Epithelial Root Sheath/Epithelial Rests of Malassez Cell Line from Human Periodontium

  • Nam, Hyun;Kim, Ji-Hye;Kim, Jae-Won;Seo, Byoung-Moo;Park, Joo-Cheol;Kim, Jung-Wook;Lee, Gene
    • Molecules and Cells
    • /
    • 제37권7호
    • /
    • pp.562-567
    • /
    • 2014
  • Human Hertwig's epithelial root sheath/epithelial rests of Malassez (HERS/ERM) cells are epithelial remnants of teeth residing in the periodontium. Although the functional roles of HERS/ERM cells have yet to be elucidated, they are a unique epithelial cell population in adult teeth and are reported to have stem cell characteristics. Therefore, HERS/ERM cells might play a role as an epithelial component for the repair or regeneration of dental hard tissues; however, they are very rare population in periodontium and the primary isolation of them is considered to be difficult. To overcome these problems, we immortalized primary HERS/ERM cells isolated from human periodontium using SV40 large T antigen (SV40 LT) and performed a characterization of the immortalized cell line. Primary HERS/ERM cells could not be maintained for more than 6 passages; however, immortalized HERS/ERM cells were maintained for more than 20 passages. There were no differences in the morphological and immunophenotypic characteristics of HERS/ERM cells and immortalized HERS/ERM cells. The expression of epithelial stem cell and embryonic stem cell markers was maintained in immortalized HERS/ERM cells. Moreover, immortalized HERS/ERM cells could acquire mesenchymal phenotypes through the epithelial-mesenchymal transition via TGF-${\beta}1$. In conclusion, we established an immortalized human HERS/ERM cell line with SV40 LT and expect this cell line to contribute to the understanding of the functional roles of HERS/ERM cells and the tissue engineering of teeth.

Synthesis of New Spiro[benzo[c]fluorene-7,9'-fluorene] Dimers and Their Optical Properties

  • Seo, Jeong-A;Lee, Chil-Won;Gong, Myoung-Seon
    • Bulletin of the Korean Chemical Society
    • /
    • 제34권5호
    • /
    • pp.1414-1420
    • /
    • 2013
  • Five novel spiro[benzo[c]fluorene-7,9'-fluorene] based dyes, including 5-[spiro[benzo[c]fluorene-7,9'-fluoren]-5-yl] spiro[benzo[c]fluorene-7,9'-fluorene] (7), 5-[spiro[benzo[c]fluorene-7,9'-fluoren]-9-yl] spiro[benzo[c]fluorene-7,9'-fluorene] (8), 5-[spiro[benzo[c]fluorene-7,9'-fluoren]-2'-yl] spiro[benzo[c]fluorene-7,9'-fluorene] (9), 9-[spiro[benzo[c]fluorene-7,9'-fluoren]-9-yl] spiro[benzo[c]fluorene-7,9'-fluorene] (10), and 2'-[spiro[benzo[c]-fluorene-7,9'-fluoren]-2'-yl] spiro[benzo[c]fluorene-7,9'-fluorene] (11) were successfully prepared from the corresponding halogen and boronic acid derivatives through the Suzuki coupling reaction, respectively. Chemical structures were confirmed by $^1H$ nuclear magnetic resonance (NMR), $^{13}C$ NMR, Fourier transforminfrared spectrscopy, mass spectroscopy, and elemental analysis. The thermal properties were determined by differential scanning calorimetry and thermal gravimetric analysis. The relationships between the optical and electrochemical properties and the combined positions between these dimers were systematically investigated using UV-vis, photoluminescence (PL), and photoelectron spectroscopy. These five dimers exhibited high fluorescent quantum yields and good morphological stability with high glass transition states > $174^{\circ}C$. Dimer 7 showed a UV absorbance peak at 353 nm, emission PL peak at 424 nm, and quantum efficiency of 0.62 in a cyclohexane solution.

NOx 제거용 WO3-TiO2 계 SCR 촉매 제조 및 열적열화거동연구 (Preparation and Thermal Degradation Behavior of WO3-TiO2 Catalyst for Selective Catalytic Reduction of NOx)

  • 신병길;김장훈;윤상현;이희수;신동우;민화식
    • 대한금속재료학회지
    • /
    • 제49권8호
    • /
    • pp.596-600
    • /
    • 2011
  • Thermal degradation behavior of a $WO_3-TiO_2$ monolithic catalyst was investigated in terms of structural, morphological, and physico-chemical analyses. The catalyst with 4 wt.% $WO_3$ contents were prepared by a wet-impregnation method, and a durability test of the catalysts were performed in a temperature range between $400^{\circ}C$ and $800^{\circ}C$ for 3 h. An increase of thermal stress decreased the specific surface area, which was caused by grain growth and agglomeration of the catalyst particles. The phase transition from anatase to rutile occurred at around $800^{\circ}C$ and a decrease in the Brønsted acid sites was confirmed by structural analysis and physico-chemical analysis. A change in Brønsted acidity can affect to the catalytic efficiency; therefore, the thermal degradation behavior of the $WO_3-TiO_2$ catalyst could be explained by the transition to a stable rutile phase of $TiO_2$ and the decrease of specific surface area in the SCR catalyst.

용매 어닐링에 의한 박막에서 Polystyrene-Poly(1,4-butadiene) 블록공중합체의 모폴로지 전이 (Morphological Transitions of Symmetric Polystyrene-block-Poly(1,4-butadiene) Copolymers in Thin Films upon Solvent-Annealing)

  • 이동은;김응건;이동현
    • 폴리머
    • /
    • 제36권4호
    • /
    • pp.542-548
    • /
    • 2012
  • 본 연구에서는 용매 증기 하에서 박막으로 제조된 polystyrene-poly(1,4-butadiene) 블록공중합체(PS-b-PBD)의 모폴로지 형성과 특성이 원자주사현미경(AFM)을 사용하여 연구되었다. 사이클로헥산으로만 용매 어닐링된 박막의 경우 폴리스티렌의 매트릭스 내부에 PBD가 미세상을 형성하는 perforated lamellae가 형성되었지만, n-헥산만으로 용매 어닐링 된 박막은 불규칙한 패턴만이 관측되었다. 그러나 사이클로헥산과 n-헥산의 혼합 용매를 사용하여 용매 어닐링할 경우 기질에 수직으로 배향된 라멜라가 관측되었다. 이러한 모폴로지 전이는 혼합 용매의 혼합비에 의해 조절되며 n-헥산의 양이 증가하면서 라멜라의 형성이 뚜렷이 관측되었다. 그러나 용매 어닐링에 사용된 혼합 용매 중 n-헥산의 주요 성분이 될 경우 n-헥산의 PBD로의 용매 친화력에 의해 모폴로지 형성이 오히려 지연되는 것을 확인하였다. 이러한 사이클로헥산과 n-헥산의 혼합비에 따른 모폴로지 전이는 블록공중합체에 대한 두 용매들의 친화력과 관련 있으며, 이를 이해하기 위해 이들의 용해도 상수 및 Flory 상호인력 인자들이 고려되었다. 또한 본 연구로부터 얻어진 두 가지 모폴로지를 이용하여 실리카 나노 패턴의 제조를 위한 템플레이트로 활용하였다.

버네사이트 합성 시 에이징 시간에 따른 중간생성물 페이크네타이트 상전이 및 표면 형태학적 특성 (Phase Transition and Surface Morphological Characteristics of Intermediate Product Feitknechtite According to Aging Time during the Synthesis of Birnessite)

  • 민소영;김영규
    • 한국광물학회지
    • /
    • 제32권3호
    • /
    • pp.213-222
    • /
    • 2019
  • 버네사이트(birnessite, $7{\AA}$ manganate, ${\delta}-MnO_2$)는 망간단괴를 구성하는 주요한 광물이다. 버네사이트는 또한 이온교환제와 배터리 재충전 물질로서 사용될 수 있기 때문에 다양한 합성법이 연구되고 있다. 그러나 버네사이트는 화학양론적으로 성립하지 않는 화학조성을 가지기 때문에 합성 시 단일 상을 수득하기에는 어려움이 존재한다. 버네사이트 합성과정 중에서 중간생성물로 페이크네타이트(${\beta}-MnOOH$)가 나타나는데, 본 연구에서는 이 중간생성물이 버네사이트로 상전이 하는 특성 차이를 XRD와 SEM 결과를 통해 비교하였다. 이번 연구에서는 기존에 연구된 합성 방법 중에서 산화-환원(redox)반응을 기작으로 하는 Feng et al. (2004)와 Luo et al. (1998) 두 방법을 이용하였다. Feng et al. (2004) 방법으로는 $27^{\circ}C$에서 60일, Luo et al. (1998) 방법으로는 $60^{\circ}C$에서 3일 에이징 한 시료에서 단일 상의 버네사이트를 수득할 수 있는 것으로 나타났다. 이러한 두 시료의 상전이 특성은 $Mg^{2+}$ 도핑여부에 따라 차이가 나타나는 것으로 판단되며 $Mg^{2+}$ 도핑된 Luo et al. (1998) 방법으로 합성된 버네사이트의 경우 페이크네타이트 상전이 속도가 느리게 나타났고 고온에서 거의 단일 상 버네사이트를 확인할 수 있었으며 결정 표면 및 형태 또한 두 방법 간의 차이를 확인하였다.

Cyclopolymerization of 1,6-Heptadiyne by Molybdenum and Tungsten-Based Catalysts

  • Gal, Yeong-Soon;Lee, Won-Chul;Gui, Tae-Long;Jin, Sung-Ho;Kwangnak Koh;Kim, Sung-Hoon;Kim, Dong-Won;Ko, Jang-Myoun;Chun, Jong-Han
    • Macromolecular Research
    • /
    • 제9권4호
    • /
    • pp.220-227
    • /
    • 2001
  • The polymerization of 1,6-heptadiyne was carried out by molybdenum and tungsten-based transition metal catalysts. This polymerization by MoCl$\_$5/ alone proceeded well to give a quantitative yield of polymer. The effect of monomer to catalyst mole ratio (M/C), initial monomer concentration ([M]$\_$0/), and the polymerization temperature for the cyclopolymerization of 1,6-heptadiyne was studied and discussed. The polymerization solution exhibited red color even after 30 min of polymerization time. The resulting polymers were mostly brown powders and mostly insoluble in any organic solvents although the polymerization proceeded in homogeneous manner in some cases. The polymer structure was characterized by various instrumental methods to have the conjugated polymer backbone structure carrying cyclic recurring unit. The thermal and morphological properties of the resulting poly(1,6-heptadiyne) were also discussed.

  • PDF