Radiation Chemistry in Chemically Amplified Resists

被引:337
|
作者
Kozawa, Takahiro [1 ]
Tagawa, Seiichi [1 ]
机构
[1] Osaka Univ, Inst Sci & Ind Res, Osaka 5670047, Japan
关键词
LINE-EDGE ROUGHNESS; ELECTRON-BEAM LITHOGRAPHY; EXTREME-ULTRAVIOLET RESISTS; PICOSECOND PULSE-RADIOLYSIS; POST-OPTICAL LITHOGRAPHY; ACID GENERATION EFFICIENCY; PHENOL RADICAL CATIONS; PRIMARY PHOTOCHEMICAL PROCESSES; GEMINATE ION RECOMBINATION; MONTE-CARLO SIMULATION;
D O I
10.1143/JJAP.49.030001
中图分类号
O59 [应用物理学];
学科分类号
摘要
Historically, in the mass production of semiconductor devices, exposure tools have been repeatedly replaced with those with a shorter wavelength to meet the resolution requirements projected in the International Technology Roadmap for Semiconductors issued by the Semiconductor Industry Association. After ArF immersion lithography, extreme ultraviolet (EUV; 92.5 eV) radiation is expected to be used as an exposure tool for the mass production at or below the 22nm technology node. If realized, 92.5 eV EUV will be the first ionizing radiation used for the mass production of semiconductor devices. In EUV lithography, chemically amplified resists, which have been the standard resists for mass production since the use of KrF lithography, will be used to meet the sensitivity requirement. Above the ionization energy of resist materials, the fundamental science of imaging, however, changes from photochemistry to radiation chemistry. In this paper, we review the radiation chemistry of materials related to chemically amplified resists. The imaging mechanisms from energy deposition to proton migration in resist materials are discussed. (C) 2010 The Japan Society of Applied Physics
引用
收藏
页数:19
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