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基于自洽场理论的锥形二嵌段共聚物的相行为

Phase Behavior of Tapered Diblock Copolymers from Self-Consistent Field Theory.

作者信息

Brown Jonathan R, Sides Scott W, Hall Lisa M

机构信息

William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, 140 W 19th Avenue, Columbus, Ohio 43210, United States.

National Renewable Energy Laboratory (NREL), 15013 Denver West Parkway, Golden, Colorado 80401, United States.

出版信息

ACS Macro Lett. 2013 Dec 17;2(12):1105-1109. doi: 10.1021/mz400546h. Epub 2013 Dec 6.

Abstract

Tapered diblock copolymers are similar to AB diblock copolymers, but the sharp junction between the A and B blocks is replaced with a gradient region in which composition varies from mostly A to mostly B along its length. The A side of the taper can be attached to the A block (normal) or the B block (inverse). We demonstrate how taper length and direction affect the phase diagrams and density profiles using self-consistent field theory. Adding tapers shifts the order-disorder transition to lower temperature versus the diblock, and this effect is larger for longer tapers and for inverse tapers. However, tapered systems' phase diagrams and interfacial profiles do not simply match those of diblocks at a shifted effective temperature. For instance, we find that normal tapering widens the bicontinuous gyroid region of the phase diagram, while inverse tapering narrows this region, apparently due to differences in polymer organization at the interfaces.

摘要

锥形双嵌段共聚物与AB双嵌段共聚物相似,但A段和B段之间的尖锐连接被一个渐变区域所取代,在该区域中,组成沿其长度方向从主要是A逐渐变化到主要是B。锥形的A侧可以连接到A段(正常情况)或B段(反向情况)。我们使用自洽场理论证明了锥长和方向如何影响相图和密度分布。与双嵌段相比,添加锥形会使有序-无序转变温度降低,并且对于更长的锥形和反向锥形,这种影响更大。然而,锥形体系的相图和界面分布并不简单地与在有效温度偏移时的双嵌段体系相匹配。例如,我们发现正向锥形会拓宽相图中的双连续螺旋状区域,而反向锥形会使该区域变窄,这显然是由于界面处聚合物排列的差异所致。

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