Surface adhesion and demolding force dependence on resist composition in ultraviolet nanoimprint lithography

被引:47
作者
Amirsadeghi, Alborz [1 ,2 ]
Lee, Jae Jong [3 ]
Park, Sunggook [1 ,2 ]
机构
[1] Louisiana State Univ, Dept Mech Engn, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Ctr Biomodular & Multiscale Syst, Baton Rouge, LA 70803 USA
[3] Korea Inst Machinery & Mat, Nanomech Syst Res Div, Taejon 305343, South Korea
关键词
UV nanoimprint lithography; Demolding force; Adhesion force; Young's modulus; Surface energy; IMPRINT; FABRICATION; RELEASE; FILMS; MOLD;
D O I
10.1016/j.apsusc.2011.09.090
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Demolding, the process to separate stamp from molded resist, is most critical to the success of ultraviolet nanoimprint lithography (UV-NIL). In the present study we investigated adhesion and demolding force in UV-NIL for different compositions of a model UV-curable resist system containing a base (either tripropyleneglycol diacrylate with shorter oligomer length or polypropyleneglycol diacrylate with longer oligomer length), a cross-linking agent (trimethylolpropane triacrylate) and a photoinitiator (Irgacure 651). The demolding force was measured using a tensile test machine with homemade fixtures after imprinting the UV resist on a silicon stamp. While decreasing the cross-linking agent content from 49 to 0 wt% has little effect on the resist surface energy, it reduces the resist's elastic modulus drastically. The decrease in elastic modulus results in a decreased adhesion force at the resist/stamp interface thereby facilitating the demolding. The decrease in elastic modulus and, therefore, demolding force by lowering the cross-linking agent content was markedly less pronounced in tripropyleneglycol diacrylate-based resists due to its shorter oligomer length. These general findings will be useful in designing new resists for UV-NIL process. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1272 / 1278
页数:7
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