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嵌段共聚物在乳液液滴中自组装的最新进展。

Recent progress in the self-assembly of block copolymers confined in emulsion droplets.

机构信息

College of Materials, Chemistry and Chemical Engineering, Hangzhou Normal University, No. 2318 Yuhangtang Rd., Cangqian, Yuhang District, Hangzhou, 311121, China.

出版信息

Chem Commun (Camb). 2018 Nov 22;54(94):13183-13195. doi: 10.1039/c8cc05812a.

Abstract

When the self-assembly of block copolymers (BCPs) occurs within a deformable emulsion droplet, BCPs can aggregate into a variety of nanoscaled particles with unique nanostructures and properties since the confinement effect can effectively break the symmetry of a structure. On the other hand, the self-assembled BCP particles can serve as the scaffolds to further direct the spatial arrangement of functional inorganic nanoparticles (NPs) via co-assembly or in situ deposition, thus generating diverse hybrid functional BCP/NP composites with enhanced properties. Here, we summarize the recent progress in the confined self-assembly of BCPs within the emulsion droplet and spatial arrangement of NPs on the resulting BCP scaffolds. This feature article focuses on the influence of multiple factors, including the oil/water interfacial properties, confinement degree, intrinsic properties of BCPs, additives, pH value, and temperature, on the nanostructures of the self-assembled BCP particles as well as the spatial arrangement of NPs on the BCP scaffolds from both experiment and simulation studies.

摘要

当嵌段共聚物(BCPs)在可变形乳液液滴内自组装时,由于受限效应可以有效地打破结构的对称性,BCPs 可以聚集形成具有独特纳米结构和性能的各种纳米级颗粒。另一方面,自组装的 BCP 颗粒可以作为支架,通过共组装或原位沉积进一步指导功能无机纳米颗粒(NPs)的空间排列,从而生成具有增强性能的各种混合功能 BCP/NP 复合材料。在这里,我们总结了乳液液滴内 BCP 受限自组装和所得 BCP 支架上 NPs 空间排列的最新进展。本文重点介绍了多种因素对自组装 BCP 颗粒的纳米结构以及 BCP 支架上 NPs 空间排列的影响,这些因素包括油/水界面性质、受限程度、BCPs 的固有性质、添加剂、pH 值和温度等,这是通过实验和模拟研究得出的。

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