Structural evolution and nanodomain formation in blend films of a block copolymer and homopolymer

被引:0
|
作者
Sun, Ya-Sen [1 ]
Jian, Yi-Qing [2 ]
Yang, Shin-Tung [2 ]
Chiang, Pei-Hsuan [2 ]
Su, Chun-Jen [3 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 701, Taiwan
[2] Natl Cent Univ, Dept Chem & Mat Engn, Taoyuan 32001, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
关键词
X-RAY-SCATTERING; THIN-FILMS; DIBLOCK COPOLYMER; PHASE-BEHAVIOR; MULTIPLE-SCATTERING; ORDERED STRUCTURE; ULTRATHIN FILMS; BINARY BLENDS; IN-SITU; MORPHOLOGY;
D O I
10.1039/d4sm01029a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study explores the concurrent formation of surface perforations, parallel cylinders, and double gyroids in symmetric PS-b-PMMA/hPS blend films during isothermal annealing at 205 and 240 degrees C. By controlling the weight fraction ratio of PS-b-PMMA to hPS at 75/25, we systematically examined the impact of film thickness and annealing temperature on nanodomain development. Using in situ GISAXS and ex situ SEM, we observed that thin films rapidly formed surface perforations and underlying parallel cylinders at both annealing temperatures. For thicker films, annealing at 205 degrees C resulted in the coexistence of surface perforations and parallel cylinders, while annealing at 240 degrees C yielded the additional formation of double gyroids besides surface perforations and parallel cylinders. Furthermore, the double gyroids, which grew independently with {121}DG planes parallel to the substrate, did not exhibit in-plane epitaxial relationships with the other structures. These findings highlight the critical role of annealing temperature and film thickness in directing nanodomain morphology, offering new insights for the design of nanostructured materials with tailored properties.
引用
收藏
页码:277 / 290
页数:14
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