Quantification of the resist dissolution process: an in situ analysis using high speed atomic force microscopy

J. Santillan, M. Shichiri, T. Itani
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Abstract

This work focuses on the application of a high speed atomic force microscope (HS-AFM) for the in situ visualization / quantification of the resist dissolution process. This technique, as reported in the past, has provided useful pointers on the formation of resist patterns during dissolution. This paper discusses about an investigation made on the quantification of what we refer to as “dissolution unit size” or the basic units of patterning material dissolution. This was done through the establishment of an originally developed analysis method which extracts the difference between two succeeding temporal states of the material film surface (images) to indicate the amount of change occurring in the material film at a specific span of time. Preliminary experiments with actual patterning materials were done using a positive-tone EUV model resist composed only of polyhydroxystyrene (PHS)-based polymer with a molecular weight of 2,500 and a polydispersity index of 1.2. In the absence of a protecting group, the material was utilized at a 50nm film thickness with post application bake of 90°C/60s. The resulting film is soluble in the alkali-based developer even without exposure. Results have shown that the dissolution components (dissolution unit size) of the PHS-based material are not of fixed size. Instead, it was found that aside from one constantly dissolving unit size, another, much larger dissolution unit size trend also occurs during material dissolution. The presence of this larger dissolution unit size suggests an occurrence of "polymer clustering". Such polymer clustering was not significantly present during the initial stages of dissolution (near the original film surface) but becomes more persistently obvious after the dissolution process reaches a certain film thickness below the initial surface.
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抗蚀剂溶解过程的定量:高速原子力显微镜原位分析
本文主要研究了高速原子力显微镜(HS-AFM)在抗蚀剂溶解过程中的原位可视化和定量应用。正如过去所报道的那样,这种技术为在溶解过程中形成抗蚀剂图案提供了有用的指导。本文讨论了一项关于我们所说的“溶解单位尺寸”或图案材料溶解基本单位的量化研究。这是通过建立一种原始开发的分析方法来实现的,该方法提取材料薄膜表面(图像)的两个连续时间状态之间的差异,以指示在特定时间跨度内材料薄膜中发生的变化量。用分子量为2500、多分散指数为1.2的聚羟基苯乙烯(PHS)基聚合物组成的正色调EUV模型抗蚀剂进行了初步实验。在没有保护组的情况下,使用50nm薄膜厚度的材料,涂后温度为90°C/60s。所得到的胶片即使不曝光也可溶于碱基显影剂。结果表明,phs基材料的溶解组分(溶解单位尺寸)不是固定尺寸的。相反,我们发现除了一个不断溶解的单位尺寸外,在材料溶解过程中还会出现另一个更大的溶解单位尺寸趋势。这种较大的溶解单位尺寸的存在表明发生了“聚合物聚集”。这种聚合物聚集在溶解的初始阶段(靠近原始膜表面)并不明显,但在溶解过程达到初始表面以下的一定膜厚后,这种聚合物聚集变得更加明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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