Construction of Steady Amorphous Colloidal Array Patterns via Infiltration-Driven Assembly of Core–Shell Microparticles followed by Short-Time Heating

无定形固体 材料科学 聚苯乙烯 胶体 胶体晶体 分散性 玻璃化转变 化学工程 结构着色 纳米技术 复合材料 聚合物 高分子化学 光子晶体 化学 结晶学 光电子学 工程类
作者
Ting Lü,Mengwei Xu,Jujun Chen,Dongming Qi,Hongting Zhao
出处
期刊:Langmuir [American Chemical Society]
卷期号:39 (44): 15808-15816 被引量:7
标识
DOI:10.1021/acs.langmuir.3c02514
摘要

Although core-shell microparticles with a hard core and soft shell are often used to fabricate photonic crystal films, they are rarely applied to construct steady amorphous colloidal array (ACA) patterns. In this work, a series of monodisperse core-shell microparticles with a polystyrene (PS) core and poly(methyl methacrylate-butyl acrylate) (P(MMA-BA)) shell have been successfully synthesized, and the glass transition temperatures (Tg) of the shell layer have been well regulated. The synthesized core-shell microparticles were then used to fabricate ACA patterns via a convenient infiltration-driven assembly method. The results showed that the Tg of the shell significantly affected the microstructure of the amorphous colloidal arrays (ACAs). During the assembly process, the microparticles quickly contacted each other and the lower-Tg shells could merge with each other to form a continuous film. In this situation, the PS core was embedded and ranked in the P(MMA-BA) film, and both the refractive index contrast and order degree of the colloidal array became relatively low, resulting in a poor structural color. However, when the Tg of the shell layer was moderately high, a short-range ordered array was prepared via infiltration-driven assembly, thereby displaying a bright structural color. More importantly, the shell layers could merge with each other to some extent after short-time heating, resulting in fine mechanical stability. In brief, this study provides a facile and environmental approach to construct steady ACA patterns, which is promising in printing and painting industries.
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