Mao Yu, Gleason Karen K
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Langmuir. 2006 Feb 14;22(4):1795-9. doi: 10.1021/la0521701.
Terpolymers of methyl alpha-chloroacrylate (MCA), methacrylic acid (MAA), and methacrylic anhydride (MAH) were synthesized by initiated chemical vapor deposition (iCVD) of MCA and MAA followed by low-temperature annealing that partially converts MAA into MAH. The MAA composition in the iCVD copolymer can be systematically varied between 37 and 85 mol % by adjusting the gas feed fractions of monomers. Study of the monomer reactivity ratios and the copolymer molecular weights supports the hypothesis of a surface propagation mechanism during the iCVD copolymerization. The carboxylic dehydration reaction at the annealing temperature of 160 degrees C is dominated by a mechanism of intramolecular cyclization, resulting in intramolecular MAH anhydride formation while preventing crosslink formation. The incorporation of highly electron-withdrawing anhydride functionality enhances chain scission susceptibility under electron-beam irradiation. P(MCA-MAA-MAH) terpolymer thin films can be completely developed at dosages as low as 20 microC/cm2 at 50 kV. High-quality positive-tone patterns were created with 60 nm feature size achieved in the vapor deposited films.
通过引发化学气相沉积(iCVD)法先沉积甲基-α-氯丙烯酸酯(MCA)和甲基丙烯酸(MAA),然后进行低温退火,使部分MAA转化为甲基丙烯酸酐(MAH),从而合成了甲基-α-氯丙烯酸酯(MCA)、甲基丙烯酸(MAA)和甲基丙烯酸酐(MAH)的三元共聚物。通过调节单体的气体进料比例,iCVD共聚物中的MAA组成可以在37至85摩尔%之间系统地变化。对单体反应比和共聚物分子量的研究支持了iCVD共聚过程中表面传播机制的假设。在160℃退火温度下的羧酸脱水反应以分子内环化机制为主,导致分子内形成MAH酸酐,同时防止交联形成。高吸电子性酸酐官能团的引入增强了电子束辐照下的断链敏感性。P(MCA-MAA-MAH)三元共聚物薄膜在50 kV下剂量低至20 μC/cm2时即可完全显影。在气相沉积薄膜中实现了60 nm特征尺寸的高质量正性图案。