产酸效率:EUV光子与光电子

D. Goldfarb, A. Afzali-Ardakani, M. Glodde
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引用次数: 24

摘要

EUV光酸的产生效率主要是根据PAG或抗蚀剂基质吸收EUV光子和产生低能光电子来描述的,据报道,这是EUV抗蚀剂中报道的高量子效率的最终原因(<1)。这种观察导致了最近对具有可变电子亲和力(EA)和还原电位(Ered)的pag的许多研究,这些研究可能有助于差分EUV光电子收集效率。然而,这些研究要么没有揭示PAG的化学结构,要么用电子束源代替EUV源,要么缺乏对EUV PAG分解背后潜在物理机制的基本讨论。在这项工作中,我们报告了一种甲基丙烯酸酯基抗蚀剂的EUV光速,该抗蚀剂由公开公开的等结构磺化膜组成,覆盖了广泛的EA和ed,以揭示任何优先的光电子清除作用。同时,为了比较直接的EUV光子吸收路径和基于光电子的分解路径,还测试了几种碘离子pag。与广泛报道的结果相反,我们发现,对于所研究的等结构磺胺pag,在计算EA和实验ed之间没有直接的相关性。相反,我们发现碘pag由于其更高的光吸收截面,可以更有效地利用可用的EUV功率。此外,我们确定了两个PAG组的阳离子尺寸效应,这能够进一步调节酸的产生效率。最后,我们根据大体积取代基对PAG阳离子的稳定性、瞬态光电子的时空范围以及不同系统中电子转移过程的差异,对光电子捕获的非选择性响应提出了正式的解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acid generation efficiency: EUV photons versus photoelectrons
EUV photoacid generation efficiency has been described primarily in terms of the EUV photon absorption by the PAG or the resist matrix and the production of low energy photoelectrons, which are reported as being ultimately responsible for the high quantum efficiencies reported in EUV resists (<1). Such observation led to a number of recent studies on PAGs with variable electron affinity (EA) and reduction potential (Ered) presumably conducive to a differential EUV photoelectron harvesting efficiency. However, such studies either did not disclose the PAG chemical structures, replaced the EUV source with an e-beam source, or lacked a fundamental discussion of the underlying physical mechanisms behind EUV PAG decomposition. In this work, we report the EUV photospeed of a methacrylatebased resist formulated with a battery of openly disclosed isostructural sulfonium PAGs covering a wide range of EA’s and Ered’s, to unveil any preferential photoelectron scavenging effect. In parallel, several iodonium PAGs are also tested in order to compare the direct EUV photon absorption route to the photoelectron-based decomposition path. Contrarily to what has been widely reported, we have found no direct correlation whatsoever between photospeed and the calculated EA’s or experimental Ered’s for the isostructural sulfonium PAGs studied. Instead, we found that iodonium PAGs make more efficient use of the available EUV power due to their higher photoabsorption cross-section. Additionally, we determined a cation size effect for both PAG groups, which is able to further modulate the acid generation efficiency. Finally, we present a formal explanation for the unselective response towards photoelectron harvesting based on the stabilization of the PAG cation by bulky substituent groups, the spatial and temporal range of the transient photoelectron and the differences in electron transfer processes for the different systems studied.
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