Graphoepitaxial Assembly of Symmetric Block Copolymers on Weakly Preferential Substrates
Graphoepitaxial Assembly of Symmetric Block Copolymers on Weakly Preferential Substrates
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DOI:
10.1002/adma.201001669
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发表时间:
2010-10-08
影响因子:
29.4
通讯作者:
Gopalan, Padma
中科院分区:
文献类型:
--
作者:
Han, Eungnak;Kang, Huiman;Gopalan, Padma
Self-assembly of block copolymers (BCPs) has emerged as a simple and robust “bottom-up” method for fabricating dense and periodic nanostructures as they microphase separate into nanoscale domains.[1–5] In general, microphase separation of BCPs in thin films on unpatterned surfaces leads to the formation of randomly oriented grains. This low degree of lateral ordering in thin films has led to the use of chemically [6–10] or topographically [11–16] patterned substrates for the directed assembly of BCPs.Graphoepitaxy of BCPs uses a topographically patterned substrate where spatial confinement of BCP induces nucleation and propagation of microdomains from the confining hard walls. In a seminal work, Segalman et al. demonstrated the use of a topographically patterned substrate to align sphere-forming BCP with long-range lateral order.[11] In the case of anisotropic domains such as cylinder-or lamella-forming BCP, controlling the orientation of domains along the vertical and lateral directions is essential for generation of desired pattern geometry. For example, cylinder-forming BCP can be used to create either line or dot arrays depending on the domain orientation with respect to the substrate. Similarly perpendicularly oriented lamellar domains can also generate line arrays. Hydroxyl-terminated random copolymer P (S-r-MMA), composed of styrene (St) and methyl methacrylate (MMA), is widely used as a nonpreferential layer for inducing perpendicular orientation of PS-b-PMMA. From earlier studies, it is known that a P (S-r-MMA), copolymer containing∼ 0.60 styrene is effective as a nonpreferential buffer layer.[17, 18] More recently, we [19–21] and others [22] have shown that there is a compositional window (so-called perpendicular window) of the copolymer that results in perpendicular orientation of the BCP domains, which is different for the lamella-and the cylinder-forming BCP. The perpendicular window also depends on the film thickness of the overlaying BCP.