Li Cheng-Dun, Lin Ting-An, Chen Po-Hsiung, Gau Tsai-Sheng, Lin Burn-Jeng, Chiu Po-Wen, Liu Jui-Hsiung
Department of Chemistry, National Tsing Hua University Hsinchu 30013 Taiwan
TSMC-NTHU Joint Research Center, National Tsing Hua University Hsinchu 30013 Taiwan.
Nanoscale Adv. 2024 Apr 9;6(11):2928-2944. doi: 10.1039/d4na00006d. eCollection 2024 May 29.
This work reports the synthesis and characterization of a novel pentameric tin chloro cluster, (vinylSn)SnClO(OH)(-BuCO) (1), and explores its application as an efficient negative-tone photoresist in a 1 : 2 weight ratio blend with (-BuSn)O(OH) (2). Through e-beam lithography, a small high-resolution pattern (HP = 20 nm) is achieved for the blend photoresist (3) at a dose of 2080 μC cm. Additionally, EUV lithography demonstrates the development of a high-resolution pattern (HP = 16 nm) at an EUV dose of 70 mJ cm. Mechanistic studies by reflective FTIR indicate a significant decomposition of Sn-carbon and SnO(-Bu) moieties starting at = 35 mJ cm, which is accompanied by growth of the Sn-O absorption intensity. A collapse of the cluster frameworks of clusters (1) and (2) is observed at > 70 mJ cm. High-resolution X-ray photoelectron spectroscopy (HRXPS) reveals that low EUV light predominantly decomposes Sn-butyl and Sn-Cl bonds. As EUV doses increase, primary photolytic reactions involve cleavage of Sn-butyl, Sn-OCBu, and Sn-vinyl bonds. Notably, the photolytic decomposition of Sn-Cl bonds is distinctive, with only two out of five bonds being cleaved, even at high EUV doses, resulting in a break in film growth at = 27-35 mJ cm in the EUV contrast curve. Moreover, HRXPS analysis suggests that radical propagation on the vinyltin end of the blend is unlikely, providing concise mechanistic insights into the photochemical processes governing the behavior of this advanced photoresist.
本工作报道了一种新型五聚体氯锡簇合物(乙烯基锡)SnClO(OH)(-BuCO) (1)的合成与表征,并探索了其在与(-BuSn)O(OH) (2)按1:2重量比混合时作为高效负性光刻胶的应用。通过电子束光刻,在剂量为2080 μC cm时,混合光刻胶(3)实现了20 nm的小尺寸高分辨率图案(HP = 20 nm)。此外,极紫外光刻表明在70 mJ cm的极紫外剂量下可形成16 nm的高分辨率图案(HP = 16 nm)。反射傅里叶变换红外光谱的机理研究表明,从 = 35 mJ cm开始,Sn-碳和SnO(-Bu)部分发生显著分解,同时伴随着Sn-O吸收强度的增加。在 > 70 mJ cm时观察到簇合物(1)和(2)的簇框架坍塌。高分辨率X射线光电子能谱(HRXPS)显示,低剂量极紫外光主要分解Sn-丁基和Sn-氯键。随着极紫外剂量的增加,主要的光解反应涉及Sn-丁基、Sn-OCBu和Sn-乙烯基键的断裂。值得注意的是,Sn-氯键的光解分解具有独特性,即使在高极紫外剂量下,五个键中也只有两个被断裂,导致在极紫外对比度曲线中 = 27 - 35 mJ cm时膜生长中断。此外,HRXPS分析表明,混合体系中乙烯基锡端的自由基传播不太可能发生,这为控制这种先进光刻胶行为的光化学过程提供了简洁的机理见解。