材料科学
层状结构
共聚物
环氧乙烷
掺杂剂
氢键
自组装
结晶
无定形固体
高分子化学
化学工程
两亲性
聚合物
相(物质)
液晶
分子
兴奋剂
纳米技术
结晶学
有机化学
化学
复合材料
光电子学
工程类
作者
Shuai Huang,Linlin Pang,Yuxuan Chen,Liming Zhou,Shaoming Fang,Haifeng Yu
标识
DOI:10.1002/marc.201700783
摘要
Microphase-separated structures of block copolymers (BCs) with a size of sub-10 nm are usually obtained by hydrogen-bond-induced self-assembly of BCs through doping with small molecules as functional additives. Here, fabrication of hierarchically self-assembled sub-10 nm structures upon microphase separation of amphiphilic liquid-crystalline BCs (LCBCs) at the existence of hydrogen bonds but without any dopants is reported. The newly introduced urethane groups in the side chain of the hydrophobic block of LCBCs interact with the ether groups of the hydrophilic poly(ethylene oxide) (PEO) block, leading to imperfect crystallization of the PEO blocks. Both crystalline and amorphous domains coexist in the separated PEO phase, enabling a lamellar structure to appear inside the PEO nanocylinders. This provides an elegant method to fabricate controllable sub-10 nm microstructures in well-defined polymer systems without the introduction of any dopants.
科研通智能强力驱动
Strongly Powered by AbleSci AI