抵抗
光刻胶
共聚物
聚合物
材料科学
平版印刷术
单体
热分解
化学工程
光刻
制作
高分子化学
玻璃化转变
溶解度
纳米技术
三元运算
热稳定性
剥离(纤维)
薄膜
薄脆饼
自组装
环己烷
预聚物
紫外线
纳米光刻
分解
同系序列
聚合
热的
极紫外光刻
作者
Yuting Tang,Weiwei Li,Xinyan Huang,Min Zhang,Han Han,Jialong Zhang,Qinyu Luo,Jiangli Fan,Pengzhong Chen,Xiaojun Peng
出处
期刊:
[Wiley]
日期:2026-05-28
卷期号:: e70062-e70062
被引量:1
摘要
Abstract In response to the increasing demands in advanced lithography for high‐resolution and highly stable photoresists, the development of high‐performance resist materials has become critically important. In this study, a series of poly (tert‐butyl methacrylate‐ co ‐adamantyl methacrylate‐ co ‐[trifluoroethyl methacrylate/1,1,1,3,3,3‐hexafluoroisopropyl isobutyrate methacrylate]) copolymers (PTAF) were rationally designed and synthesized, and their preparation conditions were systematically optimized via a single‐factor experimental design. The molecular weight distribution, thermal properties, hydrophobicity, and electron‐beam lithography (EBL) performance of the resulting polymers were comprehensively investigated. The results show that PTAF exhibits a narrow molecular weight distribution (polydispersity index = 1.2–1.3) and a number‐average molecular weight ( M n ) of approximately 4271 g mol −1 . The polymer demonstrates good thermal stability, with an initial decomposition temperature ( T d ) of 212°C and a glass transition temperature ( T g ) of 105°C, along with pronounced hydrophobicity. EBL results reveal that PTAF displays intrinsic negative‐tone behavior in the absence of externally added photoacid generators, enabling fabrication of high‐resolution patterns with a minimum linewidth of 16.5 nm. Mechanistic studies indicate that fluorinated monomers undergo ionization upon irradiation, initiating in situ acid generation, which subsequently triggers the deprotection of tert‐butyl ester groups during post‐exposure baking. This process leads to a polarity reversal and a corresponding solubility switch in the resist system. Overall, this work establishes a high‐performance ternary copolymer photoresist platform and elucidates its negative‐tone imaging mechanism, providing valuable insights for the design of polymer‐based resists in advanced lithography, particularly for extreme ultraviolet applications.
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