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利用电子束光刻技术对氨硅烷进行气相纳米图案化:理解和最小化背景功能化。

Vapor-Phase Nanopatterning of Aminosilanes with Electron Beam Lithography: Understanding and Minimizing Background Functionalization.

机构信息

Department of Chemistry , University of Alberta , 11227 Saskatchewan Drive , Edmonton , Alberta T6G 2G2 , Canada.

National Institute for Nanotechnology, National Research Council Canada , 11421 Saskatchewan Drive , Edmonton , Alberta T6G 2M9 , Canada.

出版信息

Langmuir. 2018 Apr 24;34(16):4780-4792. doi: 10.1021/acs.langmuir.8b00679. Epub 2018 Apr 12.

Abstract

Electron beam lithography (EBL) is a highly precise, serial method for patterning surfaces. Positive tone EBL resists enable patterned exposure of the underlying surface, which can be subsequently functionalized for the application of interest. In the case of widely used native oxide-capped silicon surfaces, coupling an activated silane with electron beam lithography would enable nanoscale chemical patterning of the exposed regions. Aminoalkoxysilanes are extremely useful due to their reactive amino functionality but have seen little attention for nanopatterning silicon surfaces with an EBL resist due to background contamination. In this work, we investigated three commercial positive tone EBL resists, PMMA (950k and 495k) and ZEP520A (57k), as templates for vapor-phase patterning of two commonly used aminoalkoxysilanes, 3-aminopropyltrimethoxysilane (APTMS) and 3-aminopropyldiisopropylethoxysilane (APDIPES). The PMMA resists were susceptible to significant background reaction within unpatterned areas, a problem that was particularly acute with APTMS. On the other hand, with both APTMS and APDIPES exposure, unpatterned regions of silicon covered by the ZEP520A resist emerged pristine, as shown both with SEM images of the surfaces of the underlying silicon and through the lack of electrostatically driven binding of negatively charged gold nanoparticles. The ZEP520A resist allowed for the highly selective deposition of these alkoxyaminosilanes in the exposed areas, leaving the unpatterned areas clean, a claim also supported by contact angle measurements with four probe liquids and X-ray photoelectron spectroscopy (XPS). We investigated the mechanistic reasons for the stark contrast between the PMMA resists and ZEP520A, and it was found that the efficacy of resist removal appeared to be the critical factor in reducing the background functionalization. Differences in the molecular weight of the PMMA resists and the resulting influence on APTMS diffusion through the resist films are unlikely to have a significant impact. Area-selective nanopatterning of 15 nm gold nanoparticles using the ZEP520A resist was demonstrated, with no observable background conjugation noted in the unexposed areas on the silicon surface by SEM.

摘要

电子束光刻 (EBL) 是一种高度精确的、用于表面图案化的串行方法。正性电子束光刻胶可实现底层表面的图案化曝光,然后可以对其进行功能化以应用于感兴趣的领域。对于广泛使用的天然氧化物封端的硅表面,将活化硅烷与电子束光刻结合使用,可以对暴露区域进行纳米级化学图案化。由于其反应性氨基官能团,氨丙基三甲氧基硅烷 (APTMS) 和氨丙基二异丙氧基硅烷 (APDIPES) 等氨基烷氧基硅烷非常有用,但由于背景污染,它们在使用电子束光刻胶对硅表面进行纳米图案化方面的应用很少受到关注。在这项工作中,我们研究了三种商业正性电子束光刻胶,聚甲基丙烯酸甲酯 (PMMA,950k 和 495k) 和 ZEP520A (57k),作为两种常用的氨基烷氧基硅烷,即 3-氨丙基三甲氧基硅烷 (APTMS) 和 3-氨丙基二异丙氧基硅烷 (APDIPES),气相图案化的模板。PMMA 光刻胶在未图案化区域容易发生显著的背景反应,而 APTMS 问题尤其严重。另一方面,在 APTMS 和 APDIPES 暴露时,用 ZEP520A 光刻胶覆盖的硅的未图案化区域仍然保持原状,这一点从下面硅的表面 SEM 图像以及负电荷的金纳米粒子的静电驱动结合缺失中都可以看出。ZEP520A 光刻胶允许这些烷氧基氨基硅烷在暴露区域中高度选择性地沉积,而未图案化的区域保持清洁,这一说法也得到了四探针液体接触角测量和 X 射线光电子能谱 (XPS) 的支持。我们研究了 PMMA 光刻胶和 ZEP520A 之间明显差异的机理原因,发现去除光刻胶的效果似乎是减少背景功能化的关键因素。PMMA 光刻胶的分子量差异及其对 APTMS 扩散通过光刻胶膜的影响不太可能产生重大影响。使用 ZEP520A 光刻胶对 15nm 金纳米粒子进行了面积选择性的纳米图案化,通过 SEM 观察到硅表面未暴露区域没有观察到背景结合。

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