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Residual Stress Behavior in Methylsilsesquioxane-Based Dielectric Thin Films 甲基硅氧烷基介电薄膜的残余应力行为
W. Oh, T. Shin, M. Ree, M. Jin, K. Char
Abstract Residual stress of methylsilsequioxane film, which was spin-coated on silicon substrate and followed by soft-baking, was measured in-situ during curing and subsequent cooling with varying processing conditions. The thickness and refractive index of the cured films were measured using ellipsometry. Their structure was also examined by X-ray diffraction.
摘要:对在硅衬底上自旋涂覆甲基硅氧烷薄膜进行软焙后,在不同工艺条件下固化和冷却过程中的残余应力进行了原位测量。利用椭偏仪测量了固化膜的厚度和折射率。用x射线衍射对其结构进行了分析。
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引用次数: 8
Uniaxial Stretching of Polypyrrole Cast Film 聚吡咯铸膜的单轴拉伸
Kitae Song, H. Rhee, Sang Yun Lee, J. Joo, J. Y. Lee
Abstract Uniaxial stretching of polypyrrole (PPy) cast film significantly improved the electrical conductivity and break strength of the film in the stretching direction. The electrostatic effect of nitrogen atoms in pyrrole rings was also increased from 44% to 56% by stretching without change in the doping level. These phenomena indicate that stretching can induce more extended conformation of PPy molecules in the cast film.
摘要对聚吡咯(PPy)浇铸薄膜进行单轴拉伸,可以显著提高薄膜在拉伸方向上的导电性和断裂强度。在不改变掺杂水平的情况下,拉伸吡咯环中氮原子的静电效应也从44%提高到56%。这些现象表明拉伸可以诱导铸膜中PPy分子的延伸构象。
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引用次数: 0
Preparation of Heteropoly Acid Entraped in Nano Silica Matrix 纳米二氧化硅包埋杂多酸的制备
Hyun Jong Kim, Y. Chu, J. Moon, Haksoo Han, Y. Shul
Abstract Heteropoly acid entraped in nano silica matrix was prepared by the microemulsions method. The primary particle size was less than 400nm and it decreased with the content of the heteropoly acid. When these silica particles were blended with sulfonated polyethersulfone, the HPA could be effectively immobilized in aqueous environment. The conductivity of this composite electrolyte was 1.4×10−3 S/cm with the 15% HPA.
摘要:采用微乳液法制备杂多酸包埋在纳米二氧化硅基体上。初始粒径小于400nm,随杂多酸含量的增加而减小。当这些二氧化硅颗粒与磺化聚醚砜混合时,HPA在水环境中可以有效地固定化。当HPA浓度为15%时,复合电解质的电导率为1.4×10−3 S/cm。
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引用次数: 5
Anionic Polymerization of Isocyanates with Optically Active Properties 具有光学活性的异氰酸酯的阴离子聚合
Yeong-Deuk Shin, Jun-Hwan Ahn, Jae‐Suk Lee
Abstract Random copolymers, an optically functionalized isocyanate containing disperse red 1 (DR1NCO) with a chiral isocyanate containing (s)-(-)-2-methylbutanol (MBI), were prepared by anionic polymerization in THF at -98°C with Na-Naph as a two-directional initiator. As the contents of MBI in the copolymer increased, the optical rotation of the polymer was also increased. To study about the optical activity change with initiator systems, homo polymer of MBI was synthesized with one-directional and two-directional initiator. The difference of optical activity in both systems was investigated using Circular Dichroism (CD) spectroscopy and optical rotation.
摘要以Na-Naph为双向引发剂,在-98℃THF中阴离子聚合制备了含分散红1的光学官能化异氰酸酯(DR1NCO)与含(s)-(-)-2-甲基丁醇(MBI)的手性异氰酸酯(MBI)无规共聚物。随着共聚物中MBI含量的增加,聚合物的旋光度也随之增加。为了研究引发剂体系对MBI的旋光性的影响,分别用单向和双向引发剂合成了MBI的homo聚合物。利用圆二色(CD)光谱和旋光性研究了两种体系的旋光性差异。
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引用次数: 0
Effect of Cation-Mixing on Photo Luminescence of PbI2-based Organic/Inorganic Perovskite Thin Films 阳离子混合对pbi2基有机/无机钙钛矿薄膜光致发光的影响
Yumeko Komatsu, N. Sakamoto, M. Era
Abstract The influence of cation-mixing on photo luminescence(PL) of PbI2-based organic/inorganic perovskite thin films expressed by chemical formula (C6H9C2H4NH3)2PbI4 was investigated. Cation-mixing to inorganic layer by addition of ZnI2 or CdI2 did not affect the character of exciton in the films because all optical spectra of the (CHE)2(Pb,M)I4 films were the same profile. Dependence of PL intensity at 2.4eV of photon energy(PL2.4) on inorganic layer compositions was changed by kind of additive cation. In the case of Zn addition, PL2.4 was uniformly decreased with an increase of additive amounts of Zn. On the other hand, PL2.4 of the (C6H9C2H4NH3)2(Pb, Cd)I4 films remarkably increased with increasing of Cd concentration up to 20mol%Cd. It was obvious that cation-mixing with Cd is effective to advance the optical properties of the (C6H9C2H4NH3)2PbI4 films. Relationships between PL2.4 and layer structure of the films were discussed according to structural analysis using XRD.
摘要研究了阳离子混合对化学式(C6H9C2H4NH3)2PbI4表示的pbi2基有机/无机钙钛矿薄膜光致发光(PL)的影响。由于(CHE)2(Pb,M)I4薄膜的所有光谱都是相同的,因此通过添加ZnI2或CdI2将阳离子混合到无机层中不会影响薄膜中激子的特性。在2.4eV光子能量(PL2.4)下,外加阳离子的种类改变了无机层组成对PL强度的依赖性。在添加Zn的情况下,随着Zn添加量的增加,PL2.4均匀降低。另一方面,(C6H9C2H4NH3)2(Pb, Cd)I4薄膜的PL2.4随着Cd浓度的增加而显著增加,Cd浓度达到20mol%Cd。结果表明,与Cd的阳离子混合可以有效地提高(C6H9C2H4NH3)2PbI4薄膜的光学性能。通过XRD结构分析,探讨了PL2.4与薄膜层状结构的关系。
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引用次数: 1
The Highly Efficient Polymeric Photorefractive Materials: Influence of Alkyl End Group of Chromophore on Photorefractive Properties 高效聚合物光折变材料:发色团烷基端基对光折变性能的影响
H. Chun, I. Moon, Dong-Ho Shin, Nakjoong Kim
Abstract Photorefractive composites based on carbazole-substituted polysiloxane, doped with a series of NLO chromophores and photo-sensitizer were presented. The alkyl end group of chromophore was observed to influence electro-optic and photoconductivity of composite, in addition to device stability. And the gain coefficient of composite containing 4-diethylaminobenzylidene malonitrile as a chromophore was over 100 cm −1 at 60 V/μm. And gain of composite was ca.2.0 at 90 V/μm, which indicates that the pump beam was almost transferred to the signal beam.
摘要:研究了以咔唑取代的聚硅氧烷为基础,掺杂一系列NLO发色团和光敏剂的光折变复合材料。除了器件稳定性外,还观察到发色团的烷基端基对复合材料的电光和光电导率有影响。在60 V/μm下,以4-二乙基氨基对酶二腈为发色团的复合材料的增益系数大于100 cm−1。复合材料在90 V/μm时的增益为ca.2.0,表明泵浦光束几乎被转移到信号光束。
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引用次数: 1
Optically Induced Diffraction Grating on the Film of Polyurethane Bearing an Azobenzene Chromophore 含偶氮苯发色团聚氨酯薄膜上的光致衍射光栅
D. Choi, J. H. Kim, Y. Cha, Hyun Taig Hong
Abstract Polyurethane bearing an aminonitroazobenzene was synthesized for fabricating the diffraction grating on the film surface. Two beam coupling method was employed for fabricating the diffraction grating. The dynamics of diffraction grating was studied in term of the variation of the diffraction efficiency. The long-term stability of the diffraction efficiency was also investigated.
摘要合成了含氨基硝基偶氮苯的聚氨酯,用于在薄膜表面制备衍射光栅。采用双光束耦合法制作衍射光栅。从衍射效率变化的角度研究了衍射光栅的动力学特性。并对衍射效率的长期稳定性进行了研究。
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引用次数: 0
Crystal and Molecular Structure of 3,5,6-Trichloro-2-Pyridinol Complexes 3,5,6-三氯-2-吡啶醇配合物的晶体和分子结构
M. A. Sridhar, N. K. Lokanath, J. S. Prasad, A. Pasha
Abstract The complex (A), 3,5,6-trichloro-2-pyridinol-piperazine, C9H12N3OCl3, crystallizes in the monoclinic space group P21/n with the parameters a=8.915(4) A, b=7.062(3) Å, c=19.039(5) Å, β=102.79(3)°, V=1168.9(8) Å3, Z=4. The structure was solved by direct methods using SHELXS-86 (Sheldrick, 1990) and refined using SHELXL-93 (Sheldrick, 1993). The final residual factor is R1=0.0662 for 1273 reflections with I > 2[sgrave](I). The structure has intermolecular hydrogen bonds. The molecules which are stacked in layers are interconnected through the hydrogen bonds. The complex B, 3,5,6-trichloro-2-pyridinol-piperdine, C10H13N2OCl3, crystallizes in the monoclinic space group P21/c with the parameters a=12.514(4) Å, b=22.464(2) Å, c=13.765(3) Å, β=98.02(2)°, V=3831.9(2) Å3, Z=12. The structure was solved by direct methods using SHELXS-86 and refined using SHELXL-93. The final residual factor is R1=0.072 for 2662 reflections with I > 2[sgrave](I). The structure has both intra and intermolecular hydrogen bonds.
摘要配合物(A), 3,5,6-三氯-2-吡啶-哌嗪C9H12N3OCl3在单斜空间群P21/n中结晶,参数为A =8.915(4) A, b=7.062(3) Å, c=19.039(5) Å, β=102.79(3)°,V=1168.9(8) Å3, Z=4。使用SHELXS-86 (Sheldrick, 1990)直接求解该结构,并使用SHELXL-93 (Sheldrick, 1993)对其进行细化。对于I > 2[sgrave](I)的1273个反射,最终残差因子为R1=0.0662。这种结构具有分子间氢键。层层叠叠的分子通过氢键相互连接。配合物B, 3,5,6-三氯-2-吡啶-哌替啶C10H13N2OCl3在单斜空间群P21/c中结晶,参数为a=12.514(4) Å, B =22.464(2) Å, c=13.765(3) Å, β=98.02(2)°,V=3831.9(2) Å3, Z=12。用SHELXS-86直接求解,用SHELXL-93细化。对于I > 2[sgrave](I)的2662个反射,最终残差因子R1=0.072。该结构具有分子内氢键和分子间氢键。
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引用次数: 0
The Optical Characteristics of the Light Emitting Device with TPD and PBD Thin Films TPD和PBD薄膜发光器件的光学特性
D. Shin, Jung-Hyun Kim
Abstract The emission spectra generated from the electroluminescence (EL) devices on CuPC (copper phthalocyanine) / TPD (N,N′-diphenyl-N,N′-di(m-tolyl)-benzidine) / PBD (2-(4-biphenylyl)-5(4-tert-butyl-phenyl)-1,3,4-oxadiazole) had been studied. The EL devices emitted blue light two emission maxima, and one of them is about 50 nm bathochromic shifted from the photoluminescence maximum [2]. The bathochromic shift is caused by the new energy state generated under a high electric field [1].
摘要研究了CuPC(酞菁铜)/ TPD (N,N′-二苯基-N,N′-二(间甲基苯基)-联苯胺)/ PBD(2-(4-联苯基)-5(4-叔丁基苯基)-1,3,4-恶二唑)的电致发光(EL)器件的发射光谱。EL器件发出的蓝光有两个发射最大值,其中一个距离光致发光最大值约50 nm的深色偏移[2]。这种色移是在高电场作用下产生的新能态引起的[1]。
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引用次数: 0
Orientational Behavior of Discotic Nematic Phase for a Discotic Liquid Crystalline Triphenylene on Polyimide and Alkylammoniumbromide Coated Substrates 盘状液晶三苯在聚酰亚胺和烷基溴化铵涂覆基底上的盘状向列相取向行为
H. Monobe, Shoji Mima, M. Ukon, T. Sugino, Y. Shimizu
Abstract Orientational behavior of a discotic liquid crystalline triphenylene (C8OBT) on the substrates coated with a polyimide and a cetyltrimethylammoniumbromide (CTAB) was investigated by polarizing microscopy. The averaged direction and the order parameters of the triphenylene core plane and carbonyl groups of C8OBT were evaluated by an infrared dichroic method. C8OBT exhibits a homeotropic alignment on a polyimide film as for the discotic nematic (ND) phase, while it shows a tilt or homogeneous alignment on a CTAB-coated substrate. The order parameter of triphenylene ND phase is higher on the polyimide (S = 0.6) than a CTAB-coated substrate (0.2), in contrast to that of the carbonyl groups is comparable (0.2).
用偏光显微镜研究了圆盘状液晶三苯(C8OBT)在聚酰亚胺和十六烷基三甲基溴化铵(CTAB)包覆基底上的取向行为。用红外二向色法测定了C8OBT的三苯基核心面和羰基的平均方向和有序参数。C8OBT在聚酰亚胺薄膜上表现为盘状向列相(ND)的同向取向,而在ctab涂层的衬底上表现为倾斜或均匀取向。三苯基ND相在聚酰亚胺上的有序参数(S = 0.6)高于ctab涂层的有序参数(S = 0.2),而羰基的有序参数与之相当(S = 0.2)。
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引用次数: 2
期刊
Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals
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