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Compatibility of chemically amplified photoresists with bottom antireflective coatings

机译:具有底部抗反射涂层的化学扩增的光致抗蚀剂的相容性

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The effects of acid structures and blocking groups in chemically amplified resists on compatibility with bottom anti-reflective coatings (BARCs), were investigated. The resists consisted of tert-butoxy carbonyl (t-BOC) or acetal blocked polyhydroxystyrene with three types of photoacid generators (PAGs) which generate trifluoromethanesulfonic acid (acid 1), 2,4-dimethyl benzensulfonic acid (acid 2) and cyclohexanesulfonic acid (acid 3). Three types of commercially available BARCs, Brewer Science CD9, DUV11 and DUV18 were used for this study. CD9 was decomposed by exposure and generated an acid substance, which induced the necking at the bottom of the resist films. In the case of DUV11, the generated acid from the PAG was neutralized, and footing was observed in t-BOC type resists. Acetal type resists had no footing on DUV11 because the deblocking reaction progressed without post-exposure baking. DUV18 had good compatibility with most of the resist materials because of its neutral acidity. From the viewpoint of resist materials, it was found that the acetal type resists tended to have necking, because the deblocking reaction occurred at lower acid concentration compared with t-BOC type resists. Moreover, the tendency to have a necking profile, in increasing order, was acid 3 $GRT acid 2 $GRT acid 1. This order corresponded with the reverse order of the efficiency of the deblocking reaction. A weak acid might be greatly affected by some substance diffused from a BARC. The acetal type resist with acid 1 had excellent compatibility with various BARCs. However, the resolution capability of the acetal type resist with acid 1 was lower than that of the acetal type resist with acid 3, because the acid diffusion length of acid 1 was larger than that of acid 3. It was concluded that good compatibility of the resist with the BARC is achieved by the high deblocking reaction efficiency and moderate diffusion length of acid in acetal type resists.
机译:酸结构和封闭基团在与底部抗反射涂层(的BARC)的兼容性化学放大抗蚀剂的影响,进行了调查。抗蚀剂由叔丁氧基羰基(叔BOC)或缩醛保护的聚羟基苯乙烯的三种类型的光产酸剂,其生成三氟甲磺酸(酸1)(的PAG),2,4-二甲基苯磺酸(酸2)和环己烷磺酸(酸3)。三种类型的市售的BARC的,布鲁尔科技CD9,DUV11和DUV18被用于这项研究。 CD9通过暴露分解产生的酸物质,其诱导的颈缩在抗蚀膜的底部。在DUV11的情况下,从PAG产生的酸进行中和,并在叔BOC型抗蚀剂中观察到的基础上。缩醛型抗蚀剂,没有立足点上DUV11因为解封反应的进行,而不暴露后烘烤。 DUV18曾与大多数的反抗,因为它的中性酸度的材料相容性好。从抗蚀剂材料的观点出发,发现,缩醛型抗蚀剂趋于具有缩颈的,因为解块反应发生在较低的酸浓度与叔BOC型抗蚀剂进行比较。此外,该倾向为具有缩颈轮廓,以递增次序,呈酸3 $ GRT酸2 $ GRT酸1.本顺序对应了与脱保护反应的效率的顺序相反。弱酸可以通过从BARC扩散一些物质受到很大的影响。缩醛型抗蚀剂用酸1具有与各种的BARC优异的相容性。然而,缩醛型的分辨能力用酸1比缩醛型酸3抗蚀剂的抗蚀剂下,由于酸1的酸扩散长度比的酸3可以得出结论认为较大的良好的相容性与BARC抗蚀剂是由缩醛型抗蚀剂的高解封反应效率和酸的适度扩散长度来实现。

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