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通过等离子体处理实现可控各向异性润湿用于高χ嵌段共聚物的定向自组装

Controlled Anisotropic Wetting by Plasma Treatment for Directed Self-Assembly of High-χ Block Copolymers.

作者信息

Putranto Achmad Fajar, Petit-Etienne Camille, Cavalaglio Sébastien, Cabannes-Boué Benjamin, Panabiere Marie, Forcina Gianluca, Fleury Guillaume, Kogelschatz Martin, Zelsmann Marc

机构信息

CNRS, CEA/LETI Minatec, Laboratoire des Technologies de la Microélectronique (LTM), Université Grenoble Alpes, 38000 Grenoble, France.

CNRS, Bordeaux INP, LCPO, UMR 5629, Univ. Bordeaux, F-33600 Pessac, France.

出版信息

ACS Appl Mater Interfaces. 2024 May 29;16(21):27841-27849. doi: 10.1021/acsami.4c01657. Epub 2024 May 17.

Abstract

The directed self-assembly (DSA) of block copolymers (BCPs) is a promising next-generation lithography technique for high-resolution patterning. However, achieving lithographically applicable BCP organization such as out-of-plane lamellae requires proper tuning of interfacial energies between the BCP domains and the substrate, which remains difficult to address effectively and efficiently with high-χ BCPs. Here, we present the successful generation of anisotropic wetting by plasma treatment on patterned spin-on-carbon (SOC) substrates and its application to the DSA of a high-χ Si-containing material, poly(1,1-dimethylsilacyclobutane)--polystyrene (PDMSB--PS), with a 9 nm half pitch. Exposing the SOC substrate to different plasma chemistries promotes the vertical alignment of the PDMSB--PS lamellae within the trenches. In particular, a patterned substrate treated with HBr/O plasma gives both a neutral wetting at the bottom interface and a strong PS-affine wetting at the sidewalls of the SOC trenches to efficiently guide the vertical BCP lamellae. Furthermore, prolonged exposure to HBr/O plasma enables an adjustment of the trench width and an increased density of BCP lines on the substrate. Experimental observations are in agreement with a free energy configurational model developed to describe the system. These advances, which could be easily implemented in industry, could contribute to the wider adoption of self-assembly techniques in microelectronics, and beyond to applications such as metasurfaces, surface-enhanced Raman spectroscopy, and sensing technologies.

摘要

嵌段共聚物(BCP)的定向自组装(DSA)是一种很有前景的用于高分辨率图案化的下一代光刻技术。然而,要实现光刻适用的BCP结构,如面外薄片,需要适当调整BCP域与衬底之间的界面能,而对于高χ值的BCP来说,这仍然难以有效且高效地解决。在此,我们展示了通过对图案化旋涂碳(SOC)衬底进行等离子体处理成功产生各向异性润湿性,并将其应用于具有9nm半节距的高χ值含硅材料聚(1,1 - 二甲基硅环丁烷)-聚苯乙烯(PDMSB - PS)的DSA。将SOC衬底暴露于不同的等离子体化学环境中可促进PDMSB - PS薄片在沟槽内垂直排列。特别是,用HBr/O等离子体处理的图案化衬底在底部界面具有中性润湿性,在SOC沟槽的侧壁具有强烈的PS亲和润湿性,从而有效地引导垂直的BCP薄片。此外,长时间暴露于HBr/O等离子体能够调整沟槽宽度并增加衬底上BCP线的密度。实验观察结果与为描述该系统而开发的自由能构型模型一致。这些进展能够很容易地在工业中实现,有助于在微电子领域更广泛地采用自组装技术,并且还能应用于诸如超表面、表面增强拉曼光谱和传感技术等领域。

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