首页 > 最新文献

Journal of Photopolymer Science and Technology最新文献

英文 中文
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 Q3 Materials Science Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.49
Yosuke Ohta, A. Sekiguchi, Shinji Yamakawa, T. Harada, Takeo Watanabe, Hiroki Yamamoto
{"title":"Comparison of Photoresist Sensitivity between KrF, EB and EUV Exposure","authors":"Yosuke Ohta, A. Sekiguchi, Shinji Yamakawa, T. Harada, Takeo Watanabe, Hiroki Yamamoto","doi":"10.2494/photopolymer.35.49","DOIUrl":"https://doi.org/10.2494/photopolymer.35.49","url":null,"abstract":"","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2022-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76579671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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 Q3 Materials Science Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.261
Masaya Jukei, Hitoshi Araki, Hisashi Ogasawara, Akira Shimada, T. Fujiwara, Masao Tomikawa
{"title":"Low Temperature Curable Low Dk & Df Polyimide for Redistribution Layer","authors":"Masaya Jukei, Hitoshi Araki, Hisashi Ogasawara, Akira Shimada, T. Fujiwara, Masao Tomikawa","doi":"10.2494/photopolymer.35.261","DOIUrl":"https://doi.org/10.2494/photopolymer.35.261","url":null,"abstract":"","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2022-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75570134","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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 Q3 Materials 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
{"title":"Biomimetic Diamond-like Carbon Coating on a Lumen of Small-diameter Long-sized Tube Modified Surface Uniformly with Carboxyl Group using Oxygen Plasma","authors":"Yuichi Imai, Hiroyuki Fukue, T. Nakatani, S. Kunitsugu, K. Kanda, Tsuneo Suzuki, S. Watari, Y. Fujii, D. Ousaka, Susumu Oozawa, Tomio Uchi","doi":"10.2494/photopolymer.35.289","DOIUrl":"https://doi.org/10.2494/photopolymer.35.289","url":null,"abstract":"","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2022-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85874843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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 Q3 Materials Science Pub Date : 2022-12-16 DOI: 10.2494/photopolymer.35.313
Takashi Doi, Isao Nishimura, M. Kaneko, T. Shimokawa
{"title":"Development of Low-Residual-Stress Photosensitive Adhesive Materials for Wafer-Scale Microfluidic Device Fabrication","authors":"Takashi Doi, Isao Nishimura, M. Kaneko, T. Shimokawa","doi":"10.2494/photopolymer.35.313","DOIUrl":"https://doi.org/10.2494/photopolymer.35.313","url":null,"abstract":"","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2022-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84237988","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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 Q3 Materials 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
{"title":"EUV Metal Oxide Resist Development Technology for Improved Sensitivity, Roughness and Pattern Collapse Margin for High Volume Manufacturing","authors":"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","doi":"10.2494/photopolymer.35.87","DOIUrl":"https://doi.org/10.2494/photopolymer.35.87","url":null,"abstract":"","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2022-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78107535","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
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 Q3 Materials 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
{"title":"High Speed Ashing of Ion Implanted Photoresist by Microwave Excited Water Vapor Plasma with Powered Substrate","authors":"Takeshi Aizawa, Tasuku Sakurai, Khant Nyar Paing, Yusuke Kayamori, Y. Nakano, Yasunori Tanaka, T. Ishijima","doi":"10.2494/photopolymer.35.365","DOIUrl":"https://doi.org/10.2494/photopolymer.35.365","url":null,"abstract":"","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80087345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nodule Deformation on Cleaning of PVA Roller Brushes and its Relation to Cross-contamination PVA辊刷清洗时的结瘤变形及其与交叉污染的关系
IF 0.8 4区 化学 Q3 Materials Science Pub Date : 2021-06-11 DOI: 10.2494/photopolymer.34.505
Atsuki Hosaka, Tsubasa Miyaki, Y. Mizushima, Satomi Hamada, Ryota Koshino, A. Fukunaga, T. Sanada
This study investigates nodule deformation and contact area during PVA roller-type brush scrubbing to clarify their relationship with cross-contamination. Two high-speed video cameras with collimating LED light sources and an evanescent field on a prism enabled us to observe brush nodule deformation and contact area. Deformation analysis showed that the volume of a roller-type brush changes gradually at the beginning of compression, deforms more when vertically pushed at maximum compression, and then recovers rapidly at the end of compression. The brush contact area changes according to the brush and wafer rotation speed. The contact area can be categorized into three: the front, rear side face in the brush traveling direction, and vertically pushed bottom face on the surface. We analyzed the three types of brush contacts on a 100 mm type wafer and observed that the vertical compression type significantly affected the cross-contamination region.
本研究研究了PVA辊刷擦洗过程中结核的变形和接触面积,以阐明它们与交叉污染的关系。我们利用两台高速摄像机,通过准直LED光源和棱镜上的倏逝场,观察电刷结节的变形和接触面积。变形分析表明,滚筒式电刷的体积在压缩开始时逐渐变化,在最大压缩时垂直推压变形较大,压缩结束后迅速恢复。电刷接触面积根据电刷和晶圆的转速而变化。接触区域可分为三种:前、后侧面在毛刷移动方向上,以及垂直推底面在表面上。在100mm晶圆片上分析了三种类型的电刷接触,发现垂直压缩类型对交叉污染区域有显著影响。
{"title":"Nodule Deformation on Cleaning of PVA Roller Brushes and its Relation to Cross-contamination","authors":"Atsuki Hosaka, Tsubasa Miyaki, Y. Mizushima, Satomi Hamada, Ryota Koshino, A. Fukunaga, T. Sanada","doi":"10.2494/photopolymer.34.505","DOIUrl":"https://doi.org/10.2494/photopolymer.34.505","url":null,"abstract":"This study investigates nodule deformation and contact area during PVA roller-type brush scrubbing to clarify their relationship with cross-contamination. Two high-speed video cameras with collimating LED light sources and an evanescent field on a prism enabled us to observe brush nodule deformation and contact area. Deformation analysis showed that the volume of a roller-type brush changes gradually at the beginning of compression, deforms more when vertically pushed at maximum compression, and then recovers rapidly at the end of compression. The brush contact area changes according to the brush and wafer rotation speed. The contact area can be categorized into three: the front, rear side face in the brush traveling direction, and vertically pushed bottom face on the surface. We analyzed the three types of brush contacts on a 100 mm type wafer and observed that the vertical compression type significantly affected the cross-contamination region.","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2021-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74006296","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Orientation Control of the Microphase-separated Nanostructures of Block Copolymers on Polyimide Substrates 聚酰亚胺基嵌段共聚物微相分离纳米结构的取向控制
IF 0.8 4区 化学 Q3 Materials Science Pub Date : 2021-06-11 DOI: 10.2494/photopolymer.34.439
Hayato Maeda, Y. Nabae, T. Hayakawa
This study aimed to form a perpendicularly orientated lamellar structure with polystyrene-block -poly(methyl methacrylate) (PS- b -PMMA) by its microphase separation on a polyimide substrate. Eight types of polyimides were prepared from different combinations of monomers and tested as the bottom layer for the microphase separation of PS- b -PMMA. The surface free energies of those polyimide substrates were evaluated by the Owens-Wendt method. Thin films of PS- b -PMMA were prepared on the polyimide substrates and the self-assembly was induced by thermal annealing, and the surface architecture was observed by atomic force microscopy. In the tested polyimide substrates, only one from 2,2-bis[4-(3,4-dicarboxyphenoxy) phenyl]propane dianhydride (tetracarboxylic dianhydride) and 1,12-bis (4-aminophenoxy) dodecane (diamine) showed a perpendicularly oriented lamellar structure. This polyimide substrate shows one of the smallest polar components in its surface free energy. Relatively large domain size and long correlation length in the PS- b -PMMA layer were obtained by optimizing the conditions for fabrication of the polyimide substrate, which were prepared by casting the polyimide onto a silicon wafer, followed by thermal annealing. These results suggest that the combination of one monomer with relatively large molecular weight, which will result in a low density of imide groups, and the other monomer with long alkyl chains, which will reduce the polarity of the resulting polyimide, contributes to providing a perpendicular orientation.
本研究旨在利用聚苯乙烯-嵌段聚甲基丙烯酸甲酯(PS- b - pmma)在聚酰亚胺基底上的微相分离形成垂直取向的层状结构。以不同的单体组合制备了8种不同类型的聚酰亚胺,并对其作为微相分离PS- b - pmma的底层进行了测试。用Owens-Wendt法计算了这些聚酰亚胺衬底的表面自由能。在聚酰亚胺基底上制备了PS- b - pmma薄膜,通过热退火诱导其自组装,并用原子力显微镜观察其表面结构。在测试的聚酰亚胺底物中,只有2,2-二[4-(3,4-二氧基苯氧基)苯基]丙烷二酐(四羧基二酐)和1,12-二(4-氨基苯氧基)十二烷(二胺)表现出垂直取向的层状结构。这种聚酰亚胺衬底在其表面自由能中显示出最小的极性组分之一。通过优化聚酰亚胺衬底的制备条件,将聚酰亚胺浇铸在硅片上,然后进行热处理,得到了较大的畴尺寸和较长的相关长度。这些结果表明,一个相对较大分子量的单体的组合将导致亚胺基团的密度低,而另一个具有长烷基链的单体的组合将降低所得聚酰亚胺的极性,有助于提供垂直取向。
{"title":"Orientation Control of the Microphase-separated Nanostructures of Block Copolymers on Polyimide Substrates","authors":"Hayato Maeda, Y. Nabae, T. Hayakawa","doi":"10.2494/photopolymer.34.439","DOIUrl":"https://doi.org/10.2494/photopolymer.34.439","url":null,"abstract":"This study aimed to form a perpendicularly orientated lamellar structure with polystyrene-block -poly(methyl methacrylate) (PS- b -PMMA) by its microphase separation on a polyimide substrate. Eight types of polyimides were prepared from different combinations of monomers and tested as the bottom layer for the microphase separation of PS- b -PMMA. The surface free energies of those polyimide substrates were evaluated by the Owens-Wendt method. Thin films of PS- b -PMMA were prepared on the polyimide substrates and the self-assembly was induced by thermal annealing, and the surface architecture was observed by atomic force microscopy. In the tested polyimide substrates, only one from 2,2-bis[4-(3,4-dicarboxyphenoxy) phenyl]propane dianhydride (tetracarboxylic dianhydride) and 1,12-bis (4-aminophenoxy) dodecane (diamine) showed a perpendicularly oriented lamellar structure. This polyimide substrate shows one of the smallest polar components in its surface free energy. Relatively large domain size and long correlation length in the PS- b -PMMA layer were obtained by optimizing the conditions for fabrication of the polyimide substrate, which were prepared by casting the polyimide onto a silicon wafer, followed by thermal annealing. These results suggest that the combination of one monomer with relatively large molecular weight, which will result in a low density of imide groups, and the other monomer with long alkyl chains, which will reduce the polarity of the resulting polyimide, contributes to providing a perpendicular orientation.","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2021-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73034268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis of Photo-degradable Polyphthalaldehyde Macromonomer and Adhesive Property Changes of its Copolymer with Butyl Acrylate on UV-irradiation 光降解聚邻苯二醛大单体的合成及其与丙烯酸丁酯共聚物在紫外线照射下粘附性能的变化
IF 0.8 4区 化学 Q3 Materials Science Pub Date : 2021-06-11 DOI: 10.2494/photopolymer.34.219
H. Hayashi, Hideki Tachi, K. Suyama
We prepared a new polyphthalaldehyde (PPA) macromonomer by introducing a polymerizable methacryloyl group at the terminal of PPA main-chain. Resulting macromonomer was copolymerized with butyl acrylate to obtain pressure-sensitive adhesives (PSAs). We also compared the behavior of the copolymers with those of polymer blends of poly(butyl acrylate) and linear PPA polymers to clarify the role of polymerization. Higher peel strengths were observed for copolymers than those of corresponding polymer blends. As an increase in irradiation time, the strength generally decreased, although once increased for the copolymer films at the early stage. These results suggest that the introduction and the depolymerization of PPA side-chains caused drastic changes in adhesive properties.
通过在PPA主链末端引入可聚合的甲基丙烯酰,制备了一种新的聚邻苯二醛(PPA)大单体。所得的高分子单体与丙烯酸丁酯共聚得到压敏胶(psa)。我们还将共聚物的行为与聚丙烯酸丁酯和线性PPA聚合物的共混聚合物的行为进行了比较,以阐明聚合的作用。共聚物的剥离强度高于相应的共混聚合物。随着辐照时间的增加,共聚物膜的强度普遍下降,但在初期有一次增加。这些结果表明,PPA侧链的引入和解聚引起了胶粘剂性能的剧烈变化。
{"title":"Synthesis of Photo-degradable Polyphthalaldehyde Macromonomer and Adhesive Property Changes of its Copolymer with Butyl Acrylate on UV-irradiation","authors":"H. Hayashi, Hideki Tachi, K. Suyama","doi":"10.2494/photopolymer.34.219","DOIUrl":"https://doi.org/10.2494/photopolymer.34.219","url":null,"abstract":"We prepared a new polyphthalaldehyde (PPA) macromonomer by introducing a polymerizable methacryloyl group at the terminal of PPA main-chain. Resulting macromonomer was copolymerized with butyl acrylate to obtain pressure-sensitive adhesives (PSAs). We also compared the behavior of the copolymers with those of polymer blends of poly(butyl acrylate) and linear PPA polymers to clarify the role of polymerization. Higher peel strengths were observed for copolymers than those of corresponding polymer blends. As an increase in irradiation time, the strength generally decreased, although once increased for the copolymer films at the early stage. These results suggest that the introduction and the depolymerization of PPA side-chains caused drastic changes in adhesive properties.","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2021-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74249396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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 Q3 Materials 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。
{"title":"Analyses of Charge Accumulation of PTzBT Ternary Polymer Solar Cells Using ESR Spectroscopy","authors":"D. Xue, M. Saito, I. Osaka, K. Marumoto","doi":"10.2494/photopolymer.34.351","DOIUrl":"https://doi.org/10.2494/photopolymer.34.351","url":null,"abstract":"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.","PeriodicalId":16810,"journal":{"name":"Journal of Photopolymer Science and Technology","volume":null,"pages":null},"PeriodicalIF":0.8,"publicationDate":"2021-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78503331","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
期刊
Journal of Photopolymer Science and Technology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1