Direct measurement of the reaction front in chemically amplified photoresists

被引:88
作者
Lin, EK [1 ]
Soles, CL
Goldfarb, DL
Trinque, BC
Burns, SD
Jones, RL
Lenhart, JL
Angelopoulos, M
Willson, CG
Satija, SK
Wu, WL
机构
[1] Natl Inst Stand & Technol, Div Polymers, Gaithersburg, MD 20899 USA
[2] Natl Inst Stand & Technol, Ctr Neutron Res, Gaithersburg, MD 20899 USA
[3] IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA
[4] Univ Texas, Dept Chem, Austin, TX 78712 USA
[5] Univ Texas, Dept Chem Engn, Austin, TX 78712 USA
关键词
D O I
10.1126/science.1072092
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The continuing drive by the semiconductor industry to fabricate smaller structures using photolithography will soon require dimensional control at length scales comparable to the size of the polymeric molecules in the materials used to pattern them. The current technology, chemically amplified photoresists, uses a complex reaction-diffusion process to delineate patterned areas with high spatial resolution. However, nanometer-level control of this critical process is limited by the lack of direct measurements of the reaction front. We demonstrate the use of x-ray and neutron reflectometry as a general method to measure the spatial evolution of the reaction-diffusion process with nanometer resolution. Measuring compositional profiles, provided by deuterium-labeled reactant groups for neutron scattering contrast, we show that the reaction front within the material is broad rather than sharply defined and the compositional profile is altered during development. Measuring the density profile, we directly correlate the developed film structure with that of the reaction front.
引用
收藏
页码:372 / 375
页数:5
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