Novel multi-alicyclic polymers for enhancing plasma etch resistance in 193 nm lithography

Authors
Lee, JHAhn, KDCho, I
Issue Date
2001-02
Publisher
ELSEVIER SCI LTD
Citation
POLYMER, v.42, no.4, pp.1757 - 1761
Abstract
Fully multi-alkylic polymers designed for use as 193 nm photoresist materials have been synthesized by vinyl addition polymerization of tetracarbocyclic norbornene derivatives, t-butyl tetracyclo[4.4.0.1.(2,5) 1(7,10)]dodec-8-ene-3-carboxylate (t-BDN) and 3-acetoxytetracyclo-[4.4.0.1.(2,5) 1(7,10)]dodec-8-ene (AcODN). The alicyclic polymer backbones of these polymers provide plasma etch resistance and mechanical properties. Two pendant groups were introduced to provide the desired lithographic functions: the t-butyl carboxylate group as a carboxylic acid functionality masked by a protecting group undergoes acid-catalyzed thermolysis; and the acetoxy polar group influences adhesion, wettability and dissolution properties of the polymers. The polymer showed an acceptable high transmittance at 193 nm and good adhesion property. The plasma etch rates of the copolymer poly(t-BDN-co-AcODN) (85:15) using CF4/CHF3 mixed gas were 1.01 times with respect to a novolac based resist. The 0.2 mum line-and-space patterns were obtained with a dose of 45 mi cm(-2) using a KrF excimer laser stepper. (C) 2000 Elsevier Science Ltd. All rights reserved.
Keywords
ADDITION POLYMERIZATION; DERIVATIVES; ADDITION POLYMERIZATION; DERIVATIVES; 193 nm (ArF) resist materials; muliti-alicyclic polymers; norbornene polymers
ISSN
0032-3861
URI
https://pubs.kist.re.kr/handle/201004/140749
DOI
10.1016/S0032-3861(00)00559-0
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KIST Article > 2001
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