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Issues in deep-UV photoresist technology: Characterization and modeling of bulk and surface imaged resists for 248 and 213 nm lithography.

机译:深紫外光致抗蚀剂技术中的问题:用于248和213 nm光刻的本体和表面成像抗蚀剂的表征和建模。

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摘要

The drive for smaller feature sizes in integrated circuits has necessitated the use of shorter exposure wavelengths and the development of new resist technologies sensitive to the new wavelengths. An examination of chemical and physical mechanisms in resist materials has been made to support the applications of deep-UV lithography as the wavelength is shrunk to 248 nm and below. Resist models for chemically amplified resists and for surface imaging have been proposed and experimentally verified.;Airborne base contamination can significantly alter the lithographic properties of chemically amplified resists as a result of the small quantities of acid generated during the exposure. Techniques for characterizing the effect of contamination on resists and evaluations of the contamination susceptibility of the current available deep UV resists are described. In addition, a technique for estimating airborne contaminant concentration is described. Airborne amine concentrations of 4 to 5 parts per billion were detected in the University of California Microlab.;The use of new light sources has necessitated the development of novel resist materials based on chemical amplification. A fundamental understanding of the chemically amplified resist kinetics is necessary to produce more robust resist materials. Characterization and modeling techniques are described and used to verify a model for the chemically amplified deprotection kinetics in resists. The model proposes specific acid loss mechanisms that previously have been described only generically. In addition, we describe the use of 213 nm exposure wavelengths to characterize photo-acid diffusion in chemically amplified resists. Experimental data obtained to date do not allow a definitive separation of diffusion effects from the chemical kinetics.;Quantitative models for resist profile prediction are discussed for use with exposing wavelengths below 248 nm. A bi-layer surface-imaging resist process suitable for 213 nm exposure is described and demonstrated. Models for selective silylation and plasma etch dry development are proposed and experimentally verified. A methacrylate terpolymer is used as a bulk-imaging resist for 213 nm lithography. Models for the exposure, post-exposure bake and development of methacrylates are described.
机译:为了使集成电路中的特征尺寸更小,必须使用更短的曝光波长,并且需要开发对新波长敏感的新抗蚀剂技术。由于波长缩小到248 nm及以下,已经对抗蚀剂材料的化学和物理机理进行了研究,以支持深紫外光刻的应用。已经提出并通过实验验证了用于化学放大抗蚀剂的抗蚀剂模型和用于表面成像的抗蚀剂模型。由于在曝光过程中产生的少量酸,空气中的碱污染可以显着改变化学放大抗蚀剂的光刻性能。描述了表征污染物对抗蚀剂的影响的技术以及评估当前可用的深紫外线抗蚀剂的污染物敏感性的技术。另外,描述了一种估计空气中污染物浓度的技术。加州大学Microlab实验室检测出的空气中胺浓度为十亿分之4到5。;使用新光源必须开发基于化学放大的新型抗蚀剂材料。要生产出更坚固的抗蚀剂材料,必须对化学放大的抗蚀剂动力学有基本的了解。描述和表征技术并用于验证抗蚀剂中化学放大的脱保护动力学的模型。该模型提出了以前仅作一般性描述的特定酸损失机理。此外,我们描述了使用213 nm曝光波长来表征化学放大抗蚀剂中的光酸扩散。迄今为止获得的实验数据尚不能将扩散效应与化学动力学完全区分开。讨论了用于曝光量低于248 nm的抗蚀剂轮廓预测的定量模型。描述和演示了适用于213 nm曝光的双层表面成像抗蚀剂工艺。提出了选择性甲硅烷基化和等离子蚀刻干法显影的模型,并进行了实验验证。甲基丙烯酸酯三元共聚物用作213 nm光刻的整体成像抗蚀剂。描述了用于甲基丙烯酸酯的曝光,曝光后烘烤和显影的模型。

著录项

  • 作者

    Hutchinson, John Matthew.;

  • 作者单位

    University of California, Berkeley.;

  • 授予单位 University of California, Berkeley.;
  • 学科 Engineering Electronics and Electrical.
  • 学位 Ph.D.
  • 年度 1994
  • 页码 243 p.
  • 总页数 243
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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