Chemically amplified negative-tone resist using novel acryl polymer for 193-nm lithography

Hideo Hada; Takeshi Iwai; Toshimasa Nakayama

doi:10.1117/12.350254

11 June 1999 Chemically amplified negative-tone resist using novel acryl polymer for 193-nm lithography

Hideo Hada, Takeshi Iwai, Toshimasa Nakayama

Author Affiliations +

Proceedings Volume 3678, Advances in Resist Technology and Processing XVI; (1999) https://doi.org/10.1117/12.350254
Event: Microlithography '99, 1999, Santa Clara, CA, United States

Abstract

We report the development of a novel acryl polymer with an (alpha) -hydroxymethyl acrylate in the application to 193nm chemically amplified negative-tone resist. This new polymer structure consists of ((alpha) -hydroxymethyl)acrylate and MAA. The ester and alcohol group in the polymer contribute to an intramolecule and/or intermolecular hybrid crosslinking reactions without crosslinker and in the presence of a photo generated acid as a catalysis. In an intramolecular crosslink reaction, the ester group reacts to a neighboring hydroxymethyl group within the polymer chain. As a result, a lactone group is made in the main polymer chain. On the other hand, in an intermolecular crosslink reaction, the ester group reacts to a hydroxymethyl group of another polymer chain to make an ester chain. In this reaction, the new polymer is densely crosslinked and fine resist pattern is obtained without having any swelling problem. Consequently, the resist is optimized and contains the new polymer, photoacid generator and a small amount of crosslinker. Under conventional illumination condition, 180nm line and space pattern are achieved without any kind of swelling problem. The sensitivity is 40 mJ/cm² with the standard developer, NMD-3 2.38 percent.

Citation Download Citation

Hideo Hada, Takeshi Iwai, and Toshimasa Nakayama "Chemically amplified negative-tone resist using novel acryl polymer for 193-nm lithography", Proc. SPIE 3678, Advances in Resist Technology and Processing XVI, (11 June 1999); https://doi.org/10.1117/12.350254

ACCESS THE FULL ARTICLE

INSTITUTIONAL
Select your institution to access the SPIE Digital Library.

SELECT YOUR INSTITUTION

PERSONAL
Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.

PERSONAL SIGN IN

No SPIE Account? Create one

;

PURCHASE THIS CONTENT

SUBSCRIBE TO DIGITAL LIBRARY

50 downloads per 1-year subscription

Members: $195

Non-members: $335 ADD TO CART

25 downloads per 1 - year subscription

Members: $145

Non-members: $250 ADD TO CART

PURCHASE SINGLE ARTICLE