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Hybrid Resist Systems Based on α-Substituted Acrylate Copolymers

机译:基于α-取代丙烯酸酯共聚物的混合抗性体系

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Classical electron-beam resists such as poly(methyl methacrylate) (PMMA) and Nippon Zeon's ZEP function as high resolution and low roughness positive resists on the basis of radiation induced main chain scission to reduce the molecular weight while chemical amplification resists utilized in device manufacturing function on the basis of acid-catalyzed deprotection to change the polarity. In an attempt to increase the resolution and reduce the line roughness of chemical amplification resists, we prepared copolymers that undergo radiation induced main chain scission and acid-catalyzed deprotection. In another word, we wanted to increase the sensitivity of the PMMA resist by incorporating the acid-catalyzed deprotection mechanism in polymers that undergo main chain scission, maintaining the high resolution and low roughness of PMMA. To synthesize such hybrid resist polymers, we selected a-substituted acrylates and a-substituted styrenes. The former included methyl methacrylate (MMA), t-butyl methacrylate (TBMA), methyl a-fluoroacrylate (MFA), t-butyl a-fluoroacrylate (TBFA), and t-butyl a-trifluoromethylacrylate (TBTFMA) and the latter a-methylstyrene (aMEST), a-methyleneindane (aMEIN), and a-methylenetetralin (aMETL). The a-substituted t-butyl acrylic esters were copolymerized with the methyl esters and also with a-substituted styrenic monomers using 2, 2'-azobis(isobutyronitrile) (AIBN). Hybrid resists were formulated by adding a photochemical acid generator and a base quencher to the copolymers and developers were selected by studying the dissolution behavior of unexposed and 254 nm exposed resist films using a quartz crystal microbalance (QCM). In addition to the difference in the imaging mechanism, PMMA and ZEP differ from the chemical amplification resists in developers; organic solvent vs. aqueous base. We were interested in looking also into the influence of the developer on the lithographic performance. Contrast curves were generated by exposing the resist films to 100 keV electron beams and by changing the postexposure bake temperature (PEB) on a thermal gradient hot plate (TGP). The resists were imaged on our Leica 100 keV electron-beam system and line roughness was measured.
机译:传统的电子束抗蚀剂,例如聚甲基丙烯酸甲酯(PMMA)和Nippon Zeon的ZEP,在辐射诱导的主链断裂的基础上具有高分辨率和低粗糙度的正性抗蚀剂,以降低分子量,而化学放大抗蚀剂则用于器件制造中在酸催化脱保护的基础上改变极性。为了提高分辨率并减小化学放大抗蚀剂的线粗糙度,我们制备了经受辐射诱导的主链断裂和酸催化的脱保护的共聚物。换句话说,我们希望通过将酸催化的脱保护机理结合到发生主链断裂的聚合物中来保持PMMA的高分辨率和低粗糙度,从而提高PMMA抗蚀剂的灵敏度。为了合成这种杂化抗蚀剂聚合物,我们选择了α-取代的丙烯酸酯和α-取代的苯乙烯。前者包括甲基丙烯酸甲酯(MMA),甲基丙烯酸叔丁酯(TBMA),α-氟代丙烯酸甲酯(MFA),α-氟代丙烯酸叔丁酯(TBFA)和α-三氟甲基丙烯酸叔丁酯(TBTFMA),而后者a-甲基苯乙烯(aMEST),α-亚甲基茚满(aMEIN)和α-亚甲基四氢化萘(aMETL)。使用2,2'-偶氮二(异丁腈)(AIBN)将α-取代的叔丁基丙烯酸酯与甲酯以及α-取代的苯乙烯单体共聚。通过向共聚物中添加光化学产酸剂和碱淬灭剂来配制混合抗蚀剂,并通过使用石英晶体微天平(QCM)研究未曝光和254 nm曝光的抗蚀剂膜的溶解行为来选择显影剂。除了成像机理不同外,PMMA和ZEP与显影剂中的化学放大抗蚀剂也有所不同。有机溶剂与碱水溶液。我们也有兴趣研究显影剂对光刻性能的影响。通过将抗蚀剂膜暴露于100 keV电子束并通过改变热梯度热板(TGP)上的曝光后烘烤温度(PEB)来生成对比度曲线。光刻胶在我们的Leica 100 keV电子束系统上成像,并测量了线粗糙度。

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