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Organic anti-reflective coating polymers, anti-reflective coating composition comprising the same and preparation methods thereof

a coating polymer and anti-reflective technology, applied in the field of organic anti-reflective coating polymers, anti-reflective coating compositions comprising the same, can solve the problems of cd (critical dimension) alteration, standing waves and reflective notching inevitably occurring, and no material has been known which enables control

Inactive Publication Date: 2002-09-12
SK HYNIX INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0046] Further, the anti-reflective coating resin dissolves well in all hydrocarbon solvent, while does not dissolve in any of the solvents during a hard-baking step and it does not experience undercutting and footing in a fabrication process of patterns. Particularly, because the anti-reflective coating resin is composed of acrylate polymer, its etching speed is higher than that of a photosensitive film and thus, the etching selectivity can be improved.
[0047] The present invention has been described in an illustrative manner, and it is to be understood the terminology used is intended to be in the nature of description rather than of limitation. It must be understood that many modifications and variations of the present invention are possible in light of the above teachings. Therefore, it is to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described.

Problems solved by technology

In a fabrication process of ultrafine patterns for preparing semiconductor devices, standing waves and reflective notching inevitably occur due to the optical properties of lower film layer on the wafer and due to the thickness change of photosensitive film.
In addition, there is another problem of the CD (critical dimension) alteration caused by diffracted and reflected light from the lower film layers.
However, in the case of an inorganic anti-reflective film, no material has been known which enables the control of the interference at 193 nm, the wavelength of light source.
But these two types of anti-reflective material have a problem in that the control of k value is almost impossible because the content of the chromophore is defined according to the ratio as originally designed at the time of polymerization.

Method used

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  • Organic anti-reflective coating polymers, anti-reflective coating composition comprising the same and preparation methods thereof
  • Organic anti-reflective coating polymers, anti-reflective coating composition comprising the same and preparation methods thereof
  • Organic anti-reflective coating polymers, anti-reflective coating composition comprising the same and preparation methods thereof

Examples

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Effect test

example 1

Composition of poly[acetoxystyrene-(2-hydroxyethylacrylate)]copolymer

[0037] A 500 ml round bottom flask was charged with 0.1 mole of acetoxystyrene / 0.1 mole of 2-hydroxyethylacrylate while stirring and 300 g of separately prepared tetrahydrofuran was added to a complete mixture. Thereafter, 0.1.about.3.0 g of 2,2'-azobisisobutyronitrile was added to allow a polymerization reaction at 60 to 75.degree. C. under a nitrogen atmosphere for 5 to 20 hours. After the completion of the reaction, the obtained solution was precipitated with ethyl ether or n-hexane solvent and then filtered and dried to obtain poly[acetoxystyrene-(2-hydroxyethyl- acrylate)] resin of the following Formula 7 (yield: 82%). 7

example 2

Composition of poly[acetoxystyrene-(3-hydroxypropylacrylate)]copolymer

[0038] A 500 ml round bottom flask was charged with 0.1 mole of acetoxystyrene / 0.1 mole of 3-hydroxypropylacrylate while stirring and 300 g of separately prepared tetrahydrofuran was added to a complete mixture. Thereafter, 0.1.about.3.0 g of 2,2'-azobisisobutyronitrile was added to allow a polymerization reaction at 60 to 75.degree. C. under a nitrogen atmosphere for 5 to 20 hours. After the completion of the reaction, the obtained solution was precipitated with ethyl ether or n-hexane solvent and then filtered and dried to obtain poly[acetoxystyrene-(3-hydroxypropy- lacrylate)] resin of the following Formula 8 (yield: 80%). 8

example 3

Composition of poly[acetoxystyrene-(4-hydroxybutylacrylate)]copolymer

[0039] A 500 ml round bottom flask was charged with 0.1 mole of acetoxystyrene / 0.1 mole of 4-hydroxybutylacrylate while stirring and 300 g of separately prepared tetrahydrofuran was added to a complete mixture. Thereafter, 0.1.about.3.0 g of 2,2'-azobisisobutyronitrile was added to allow a polymerization reaction at 60 to 75.degree. C. under a nitrogen atmosphere for 5 to 20 hours. After the completion of the reaction, the obtained solution was precipitated with ethyl ether or n-hexane solvent and then filtered and dried to obtain poly[acetoxystyrene-(4-hydroxybutyl- acrylate)] resin of the following Formula 9 (yield: 79%). 9

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Abstract

An organic anti-reflective polymer which prevents back reflection of lower film layers and eliminates standing wave that is occurred by a thickness change of photoresist and light, in a process for fabricating ultrafine patterns that use photoresist for lithography by using 193 nm ArF and its preparation method. More particularly, the organic anti-reflective polymer of the present invention is useful for fabricating ultrafine patterns of 64M, 256M, 1G, and 4G DRAM semiconductor devices. A composition containing such organic anti-reflective polymer, an anti-reflective coating layer made therefrom and a preparation method thereof.

Description

BACKGROUND[0001] 1. Technical Field[0002] An organic anti-reflective polymer which prevents back reflection of lower film layers and eliminates standing wave that occurs as a result of thickness changes of photoresist and light, in a process for fabricating ultrafine patterns that use photoresist for lithography by using 193 nm ArF and its preparation method are disclosed. More particularly, the organic anti-reflective polymer is disclosed that is useful for fabricating ultrafine patterns of 64M, 256M, 1G, and 4G DRAM semiconductor devices. A composition containing such organic anti-reflective polymer, an anti-reflective coating layer made therefrom and a preparation method thereof are also disclosed.[0003] 2. Description of the Background Art[0004] In a fabrication process of ultrafine patterns for preparing semiconductor devices, standing waves and reflective notching inevitably occur due to the optical properties of lower film layer on the wafer and due to the thickness change of...

Claims

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Application Information

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IPC IPC(8): G03F7/11C08F4/04C08F4/34C08F8/00C08F116/34C08F212/14C08F220/06C08F220/28C08L25/18C08L29/00C08L33/14C09D125/18C09D133/14G03F7/09H01L21/027
CPCC08F212/14C08F220/28G03F7/091C08F220/20C08F212/22C08F220/06
Inventor JUNG, MIN-HOJUNG, JAE-CHANGLEE, GEUN-SUSHIN, KI-SOO
Owner SK HYNIX INC