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Comparison of Photoresist Sensitivity between KrF, EB and EUV Exposure KrF、EB和EUV曝光光刻胶灵敏度的比较
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.49
Yosuke Ohta, A. Sekiguchi, Shinji Yamakawa, T. Harada, Takeo Watanabe, Hiroki Yamamoto
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引用次数: 0
Development of Low-Residual-Stress Photosensitive Adhesive Materials for Wafer-Scale Microfluidic Device Fabrication 用于晶圆级微流控器件制造的低残余应力光敏胶粘剂材料的研制
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.313
Takashi Doi, Isao Nishimura, M. Kaneko, T. Shimokawa
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引用次数: 0
EUV Metal Oxide Resist Development Technology for Improved Sensitivity, Roughness and Pattern Collapse Margin for High Volume Manufacturing EUV金属氧化物抗蚀剂开发技术,用于提高灵敏度,粗糙度和大批量生产的图案崩溃裕度
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.87
C. Dinh, S. Nagahara, Yuhei Kuwahara, Arnaud Dauendorffer, Keisuke Yoshida, Soichiro Okada, T. Onitsuka, S. Kawakami, S. Shimura, M. Muramatsu, Kosuke Yoshihara, J. Petersen, D. D. Simone, P. Foubert, G. Vandenberghe, L. Huli, Steven Grzeskowiak, Alexandra Krawicz, Nayoung Bae, Kanzo Kato, K. Nafus, Angélique Raley
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引用次数: 8
Low Temperature Curable Low Dk & Df Polyimide for Redistribution Layer 重分配层用低温固化低Dk & Df聚酰亚胺
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.261
Masaya Jukei, Hitoshi Araki, Hisashi Ogasawara, Akira Shimada, T. Fujiwara, Masao Tomikawa
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引用次数: 1
Biomimetic Diamond-like Carbon Coating on a Lumen of Small-diameter Long-sized Tube Modified Surface Uniformly with Carboxyl Group using Oxygen Plasma 用氧等离子体均匀修饰小直径长管管腔表面的仿生类金刚石涂层
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.289
Yuichi Imai, Hiroyuki Fukue, T. Nakatani, S. Kunitsugu, K. Kanda, Tsuneo Suzuki, S. Watari, Y. Fujii, D. Ousaka, Susumu Oozawa, Tomio Uchi
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引用次数: 1
High Speed Ashing of Ion Implanted Photoresist by Microwave Excited Water Vapor Plasma with Powered Substrate 微波激发水蒸气等离子体对离子注入光刻胶的高速灰化研究
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2022-01-01 DOI: 10.2494/photopolymer.35.365
Takeshi Aizawa, Tasuku Sakurai, Khant Nyar Paing, Yusuke Kayamori, Y. Nakano, Yasunori Tanaka, T. Ishijima
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引用次数: 0
Synthesis, Properties, and Photovoltaic Characteristics of Arch- and S-shaped Naphthobisthiadiazole-based Acceptors 拱形和s型萘双噻二唑基受体的合成、性质和光伏特性
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2021-06-11 DOI: 10.2494/photopolymer.34.285
Seihou Jinnai, Y. Ie
Fine-tuning physical properties by structural modification is important for developing organic semiconducting materials. In this work, we designed and synthesized new electron-accepting compounds containing or naphtho[1,2- c :5,6- c' ]bis[1,2,5]thiadiazole (NTz) groups as electron-accepting units; these units are structural isomers. The vNTz-based compounds have an arch-shaped molecular backbone with C 2v symmetry, whereas the NTz-based compound forms an S-shaped molecular backbone with C 2h symmetry. Property measurements showed unique behavior originating from the vNTz core. An organic solar cell comprising the vNTz-based compound and poly(3-hexylthiopehene) showed a power conversion efficiency of 2.06%. This result demonstrates the potential of vNTz as an electron-accepting unit in organic semiconducting materials.
通过结构修饰来微调物理性质是开发有机半导体材料的重要手段。本文设计并合成了以萘[1,2- c:5,6- c']二[1,2,5]噻二唑(NTz)为电子接受单位的新型电子接受化合物;这些单位是结构异构体。vntz基化合物具有c2v对称的拱形分子骨架,而ntz基化合物具有c2h对称的s形分子骨架。性能测量显示了vNTz核的独特行为。由vntz基化合物和聚(3-己基噻吩)组成的有机太阳能电池的功率转换效率为2.06%。这一结果证明了vNTz在有机半导体材料中作为电子接受单元的潜力。
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引用次数: 1
Photoluminescence Properties of Copolyimides Containing Naphthalene Core and Analysis of Excitation Energy Transfer between the Dianhydride Moieties 含萘核共聚亚胺的光致发光性质及二氢基间激发能转移分析
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2021-06-11 DOI: 10.2494/photopolymer.34.423
Marina Doi, Koichiro Muto, Mayuko Nara, Naiqiang Liang, K. Sano, Hiroaki Mori, R. Ishige, S. Ando
The photoluminescence (PL) properties of semi-aromatic polyimide (PI) films and their model compounds (MCs) prepared from dianhydrides having a rigid naphthalene core were analyzed. The PMMA-dispersed MC and copolymerized PI (CoPI) films derived from 2,3,6,7-naphthalenetetracarboxylic dianhydride (NTDA) exhibited long-lived phosphorescence owing to the suppression of molecular motion by the rigidity of a naphthalene core. Additionally, the PMMA-dispersed MC and the CoPI films derived from 1,5-dibromo derivative of NTDA (DBrNT) exhibited room-temperature phosphorescence due to the enhancement of spin-orbit coupling by bromine atoms. The photophysical processes of the CoPI films prepared from NTDA/DBrNT and 4,4'-oxydiphtalic dianhydride (ODPA) in which the latter absorption band is located at a shorter wavelength than the former were analyzed. After UV irradiation, efficient excitation energy transfer occurs from the ODPA to NTDA/DBrNT moieties, and only the emission from the latter moieties was observed. These results demonstrate that the CoPI films derived from two dianhydrides absorbing different UV wavelengths can be used as spectral conversion films that convert a wide range of UV-light into longer wavelength visible
研究了以刚性萘为核心的二酐为原料制备的半芳香族聚酰亚胺(PI)薄膜及其模型化合物的光致发光性能。由2,3,6,7-萘四羧酸二酐(NTDA)制备的聚甲基丙烯酸甲酯(pmma)分散MC和共聚PI (CoPI)薄膜由于萘核的刚性抑制了分子的运动而表现出长寿命的磷光。此外,pmma分散的MC和由NTDA的1,5-二溴衍生物(DBrNT)衍生的CoPI薄膜由于溴原子增强了自旋-轨道耦合而表现出室温磷光。分析了NTDA/DBrNT与4,4′-氧化二苯二酐(ODPA)制备的CoPI膜的光物理过程,后者的吸收波段位于较短的波长。紫外辐照后,ODPA向NTDA/DBrNT发生了有效的激发能转移,仅观察到后一部分的发射。这些结果表明,由两种二酐吸收不同紫外波长的CoPI膜可以作为光谱转换膜,将大范围的紫外转换成波长较长的可见光
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引用次数: 2
Analyses of Charge Accumulation of PTzBT Ternary Polymer Solar Cells Using ESR Spectroscopy PTzBT三元聚合物太阳能电池电荷积累的ESR分析
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2021-06-11 DOI: 10.2494/photopolymer.34.351
D. Xue, M. Saito, I. Osaka, K. Marumoto
phenomenon, we hypothesize that energy transfer from 1,2-dioxetanedione to DNSE occurred momentarily in the THF and water solution because of their miscibility. Note that, in highly polar solvents, the emission of DNSE was not visualized, probably because the rate of chemiluminescent reaction is too fast to visually detect the emission caused by the miscibility of their solvents with water in comparison with the case observed using low-polarity solvents. Moreover, no emission was observed with ethyl acetate, although it is immiscible with water. This is probably because the reaction of ethyl acetate with hydrogen peroxide was faster than the oxidation of bis(2,4,6-trichlorophenyl) oxalate. As a result, DNSE was not excited because 1,2-dioxetanedione was not produced.
现象,我们假设从1,2-二氧乙二酮到DNSE的能量转移在四氢呋喃和水溶液中瞬间发生,因为它们的互溶性。值得注意的是,在高极性溶剂中,DNSE的发射没有被观察到,可能是因为化学发光反应的速度太快,与使用低极性溶剂观察到的情况相比,肉眼无法检测到由溶剂与水的混溶引起的发射。此外,虽然乙酸乙酯不与水混溶,但未观察到有排放物。这可能是因为乙酸乙酯与过氧化氢的反应比二(2,4,6-三氯苯基)草酸酯的氧化快。结果,DNSE没有被激发,因为没有产生1,2-二氧乙二酮。
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引用次数: 2
Glass Microchannel Formation by Mycelium 菌丝体形成玻璃微通道
IF 0.8 4区 化学 Q4 POLYMER SCIENCE Pub Date : 2021-06-11 DOI: 10.2494/photopolymer.34.381
D. Sato, F. Tsumori
We propose a new method to fabricate complicated 3-dimensional glass microchannels. We employed mycelium for this purpose. Mycelium possesses a complicated, fine and three-dimensional network structure. We cultivated mycelium in silica compounds, and subsequently silica compounds were heated to be sintered. During this heating process, all the mycelium was burned off and remained a fine network channel structure in a transparent glass chip. We also tried to control of the growth of this mycelium. The growth could be changed by growth conditions. In this work, we used cyclic mechanical stimuli for this purpose. We set cyclic tensile strain to the sample under growing mycelium. This cyclic strain caused anisotropic growth of the mycelium in some condition.
提出了一种制备复杂三维玻璃微通道的新方法。我们利用菌丝体来达到这个目的。菌丝体具有复杂精细的三维网状结构。我们在二氧化硅化合物中培养菌丝体,然后将二氧化硅化合物加热烧结。在加热过程中,所有菌丝体都被烧毁,在透明的玻璃芯片中保留了精细的网状通道结构。我们也试图控制这种菌丝体的生长。生长条件可以改变其生长。在这项工作中,我们为此目的使用了循环机械刺激。我们对生长菌丝下的样品设置循环拉伸应变。这种循环应变在一定条件下引起菌丝的各向异性生长。
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引用次数: 0
期刊
Journal of Photopolymer Science and Technology
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