Controlling the microdomain orientation in block copolymer thin films via cross-linkable random copolymer neutral layer

被引:13
|
作者
Kim, Seyong [1 ]
Wang, Hyun Suk [1 ]
Choe, Youngson [2 ]
Choi, Soo-Hyung [3 ]
Bang, Joona [1 ]
机构
[1] Korea Univ, Dept Chem & Biol Engn, Anam Dong 5-1, Seoul 136713, South Korea
[2] Pusan Natl Univ, Dept Chem Engn, Busan, South Korea
[3] Hongik Univ, Dept Chem Engn, Seoul 121791, South Korea
基金
新加坡国家研究基金会;
关键词
SURFACE-INDUCED ORIENTATION; PERPENDICULAR ORIENTATION; INTERFACIAL INTERACTIONS; BOTTOM-UP; NANOPARTICLES; CHEMISTRY; LITHOGRAPHY; FABRICATION; TEMPLATES; PATTERNS;
D O I
10.1038/pj.2016.9
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Block copolymer (BCP) thin films are capable of producing periodic nanoscale features that are hardly accessible by conventional 'top-down' lithography. Such is the potential of BCP thin films that many research groups are intensively studying this field. Notwithstanding their advantages, BCP thin films suffer from an inherent tendency to produce microdomains parallel to the substrate due to selective wetting. To date, various approaches to induce perpendicular orientation have been reported using surface neutralization, solvent annealing, external fields and nano-fillers. Of these approaches, surface neutralization using random copolymers is the most widely used because of its straightforward and intuitive methodology. Surface neutralization alleviates the preferential interaction of one block with the substrate, and thus selective wetting, which enables the formation of microdomains perpendicular to the substrate. In this review, advances in surface neutralization are covered by introducing four efficient cross-linkable random copolymers incorporated with benzocyclobutene, glycidyl methacrylate, azide and ketene functional groups.
引用
收藏
页码:333 / 340
页数:8
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