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ABC三嵌段共聚物旋涂过程中有序微相分离图案的形成。

Formation of ordered microphase-separated pattern during spin coating of ABC triblock copolymer.

作者信息

Huang Weihuan, Luo Chunxia, Zhang Jilin, Han Yanchun

机构信息

State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, People's Republic of China.

出版信息

J Chem Phys. 2007 Mar 14;126(10):104901. doi: 10.1063/1.2710277.

Abstract

In this paper, the authors have systematically studied the microphase separation and crystallization during spin coating of an ABC triblock copolymer, polystyrene-b-poly(2-vinylpyridine)-b-poly(ethylene oxide) (PS-b-P2VP-b-PEO). The microphase separation of PS-b-P2VP-b-PEO and the crystallization of PEO blocks can be modulated by the types of the solvent and the substrate, the spinning speed, and the copolymer concentration. Ordered microphase-separated pattern, where PEO and P2VP blocks adsorbed to the substrate and PS blocks protrusions formed hexagonal dots above the P2VP domains, can only be obtained when PS-b-P2VP-b-PEO is dissolved in N,N-dimethylformamide and the films are spin coated onto the polar substrate, silicon wafers or mica. The mechanism of the formation of regular pattern by microphase separation is found to be mainly related to the inducement of the substrate (middle block P2VP wetting the polar substrate), the quick vanishment of the solvent during the early stage of the spin coating, and the slow evaporation of the remaining solvent during the subsequent stage. On the other hand, the probability of the crystallization of PEO blocks during spin coating decreases with the reduced film thickness. When the film thickness reaches a certain value (3.0 nm), the extensive crystallization of PEO is effectively prohibited and ordered microphase-separated pattern over large areas can be routinely prepared. When the film thickness exceeds another definite value (12.0 nm), the crystallization of PEO dominates the surface morphology. For films with thickness between these two values, microphase separation and crystallization can simultaneously occur.

摘要

在本文中,作者系统地研究了ABC三嵌段共聚物聚苯乙烯- b -聚(2-乙烯基吡啶)- b -聚环氧乙烷(PS- b -P2VP- b -PEO)旋涂过程中的微相分离和结晶情况。PS- b -P2VP- b -PEO的微相分离以及PEO嵌段的结晶可通过溶剂类型、基底类型、旋转速度和共聚物浓度进行调控。只有当PS- b -P2VP- b -PEO溶解于N,N-二甲基甲酰胺且将薄膜旋涂在极性基底(硅片或云母)上时,才能获得有序的微相分离图案,其中PEO和P2VP嵌段吸附在基底上,PS嵌段的突起在P2VP畴上方形成六边形点。发现微相分离形成规则图案的机制主要与基底的诱导作用(中间嵌段P2VP润湿极性基底)、旋涂早期溶剂的快速消失以及随后阶段剩余溶剂的缓慢蒸发有关。另一方面,旋涂过程中PEO嵌段结晶的概率随薄膜厚度减小而降低。当薄膜厚度达到某一值(3.0 nm)时,PEO的大量结晶被有效抑制,并且可以常规制备大面积的有序微相分离图案。当薄膜厚度超过另一确定值(12.0 nm)时,PEO的结晶主导表面形貌。对于厚度介于这两个值之间的薄膜,微相分离和结晶可同时发生。

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