Dissolution behavior of chemically amplified resist polymers for 248-, 193-, and 157-nm lithography

被引:62
作者
Ito, H [1 ]
机构
[1] IBM Corp, Almaden Res Ctr, Div Res, San Jose, CA 95120 USA
关键词
D O I
10.1147/rd.455.0683
中图分类号
TP3 [计算技术、计算机技术];
学科分类号
0812 ;
摘要
The aqueous base development step is one of the most critical processes in modern lithographic imaging technology. Sinusoidal modulation of the exposing light intensity must be converted to a step function in the resist film during the development process. Thus, in designing high-performance resists, controlling the dissolution behavior of the resist polymer film in aqueous developer is of the utmost importance. This paper describes and compares the dissolution behavior of different polymers employed in chemically amplified imaging at 248, 193, and 157 nm. The polymers discussed in this paper are polyhydroxystyrene derivatives (248 nm), functionalized poly(cycloolefins) containing carboxylic acid (193 nm), and polymers bearing a hexafluoroisopropanol functionality for base solubility (157 nm).
引用
收藏
页码:683 / 695
页数:13
相关论文
共 38 条
[1]  
ALLEN RD, 1995, P SOC PHOTO-OPT INS, V2438, P474, DOI 10.1117/12.210396
[2]  
ALLEN RD, 1997, SEMICOND INT, V20, P73
[3]   The "living" free radical synthesis of poly(4-hydroxystyrene): Physical properties and dissolution behavior [J].
Barclay, GG ;
Hawker, CJ ;
Ito, H ;
Orellana, A ;
Malenfant, PRL ;
Sinta, RF .
MACROMOLECULES, 1998, 31 (04) :1024-1031
[4]   Narrow polydispersity polymers for microlithography: Synthesis and properties [J].
Barclay, GG ;
Hawker, CJ ;
Ito, H ;
Orellana, A ;
Malenfant, PRL ;
Sinta, RF .
ADVANCES IN RESIST TECHNOLOGY AND PROCESSING XIII, 1996, 2724 :249-260
[5]  
Chiba T., 2000, Journal of Photopolymer Science and Technology, V13, P657, DOI 10.2494/photopolymer.13.657
[6]   New ESCAP-type resist with enhanced etch resistance and its application to future DRAM and logic devices [J].
Conley, W ;
Brunsvold, B ;
Buehrer, F ;
Dellaguardia, R ;
Dobuzinsky, D ;
Farrell, T ;
Ho, H ;
Katnani, A ;
Keller, R ;
Marsh, J ;
Muller, P ;
Nunes, R ;
Ng, H ;
Oberschmidt, J ;
Pike, M ;
Ryan, D ;
CotlerWagner, T ;
Schulz, R ;
Ito, H ;
Hofer, D ;
Breyta, G ;
FenzelAlexander, D ;
Wallraff, G ;
Opitz, J ;
Thackeray, J ;
Barclay, G ;
Cameron, J ;
Lindsay, T ;
Cronin, M ;
Moynihan, M ;
Nour, S ;
Georger, J ;
Mori, M ;
Hagerty, P ;
Sinta, R ;
Zydowsky, T .
ADVANCES IN RESIST TECHNOLOGY AND PROCESSING XIV, 1997, 3049 :282-299
[7]   New materials for 157 nm photoresists: Characterization and properties [J].
Crawford, MK ;
Feiring, AE ;
Feldman, J ;
French, RH ;
Periyasamy, M ;
Schadt, FL ;
Smalley, RJ ;
Zumsteg, FC ;
Kunz, RR ;
Rao, V ;
Liao, L ;
Holl, SM .
ADVANCES IN RESIST TECHNOLOGY AND PROCESSING XVII, PTS 1 AND 2, 2000, 3999 :357-364
[8]  
Dammel R. R., 1998, Journal of Photopolymer Science and Technology, V11, P687, DOI 10.2494/photopolymer.11.687
[9]   GENERAL BASE CATALYSIS, STRUCTURE-REACTIVITY INTERACTIONS, AND MERGING OF MECHANISMS FOR ELIMINATION-REACTIONS OF (2-ARYLETHYL)QUINUCLIDINIUM IONS [J].
GANDLER, JR ;
JENCKS, WP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (07) :1937-1951
[10]   MEASUREMENT OF THIN-FILM DISSOLUTION KINETICS USING A QUARTZ CRYSTAL MICROBALANCE [J].
HINSBERG, WD ;
WILLSON, CG ;
KANAZAWA, KK .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1986, 133 (07) :1448-1451