等离子刻蚀过程中真空紫外线光子对超薄聚甲基丙烯酸甲酯的影响

Shikhar Arvind, Esben W. Larsen, Philippe Bezard, John Petersen, S. de Gendt
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摘要

最先进的极紫外光刻技术需要使用超薄光刻胶(或抗蚀剂),这是由于图案稳定性的考虑和极紫外光刻扫描仪焦距深度的减小。目前用于极紫外光刻的光阻厚度不到 50 纳米。这些超薄抗蚀剂使图案转移更加复杂,因为在干蚀刻过程中等离子体引起的意外损坏更加明显。更好地了解等离子体与超薄抗蚀剂之间的相互作用对于实现 10 纳米以下特征的图案转移至关重要。在此,我们研究了真空紫外线光子、氩离子和氩等离子体对 40 纳米厚的聚甲基丙烯酸甲酯薄膜的影响。我们使用氘灯、工业离子束蚀刻工具和工业电感耦合等离子体蚀刻工具,分别将聚合物暴露于光子、离子和等离子体中。然后使用不同的表征技术分析了暴露样品的化学和物理变化。我们观察到,真空紫外线光子与整个聚合物薄膜发生相互作用,而离子只影响表面和表层下区域。光子照射的样品在低剂量照射时形成较小的聚合物碎片,在高剂量照射时进一步开始交联。与此相反,离子改性只导致聚合物薄膜顶部几纳米的碳化,而底部则完好无损。等离子体暴露的样品显示出真空紫外线光子和离子及其协同作用所产生的变化。在 13.25 ± 0.12 nm 的光子诱导交联层上有 1.34 ± 0.03 nm 厚的离子诱导碳化层。通过研究等离子光子对超薄聚甲基丙烯酸甲酯的影响,我们能够为测试方法建立一个基准,该方法可扩展到新型超薄抗蚀剂平台。
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Impact of vacuum ultraviolet photons on ultrathin polymethylmethacrylate during plasma etching
State-of-the-art extreme ultraviolet lithography requires the use of ultrathin photoresists (or resists) due to pattern stability concerns and reduced depth of focus of the extreme ultraviolet lithography scanners. Current resists for extreme ultraviolet lithography are less than 50 nm thick. These ultrathin resists further complicate pattern transfer as unintended plasma-induced damage during dry etching is more pronounced. A better understanding of the interaction of plasma species with ultrathin resists is critical for enabling pattern transfer of sub-10 nm features. Here, we study the impact of vacuum ultraviolet photons, argon ions, and argon plasma on a 40 nm thick polymethylmethacrylate film. Using a deuterium lamp, an industrial ion beam etch tool, and an industrial inductively coupled plasma etch tool, we exposed the polymer to photons, ions, and plasma, respectively. The exposed samples were then analyzed for chemical and physical changes using different characterization techniques. It was observed that the vacuum ultraviolet photons interact with the entire bulk of polymer film, while the ions only affect the surface and subsurface region. The photon exposed samples formed smaller polymer fragments at low exposure doses and further started to cross-link at high doses. In contrast, the ion modification leads to carbonization of only the top few nanometers of the polymer film, leaving the bottom bulk intact. The plasma exposed sample showed changes characteristic to both vacuum ultraviolet photons and ions and their synergism. It was stratified with a 1.34 ± 0.03 nm thick ion-caused carbonized layer on top of a 13.25 ± 0.12 nm photon-induced cross-linked layer. By studying the impact of plasma photons on ultrathin polymethylmethacrylate, we were able to establish a baseline for a testing methodology that can be extended to novel ultrathin resist platforms.
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