| Literature DB >> 28523856 |
Zhixing Lin1, Shaohua Liu2, Wenting Mao1, Hao Tian1, Nan Wang1, Ninghe Zhang1, Feng Tian3, Lu Han1, Xinliang Feng4, Yiyong Mai1.
Abstract
We herein report the tunable self-assembly of simple block copolymers, namely polystyrene-block-poly(ethylene oxide) (PS-b-PEO) diblock copolymers, into porous cubosomes with inverse Im3‾m or Pn3‾m mesophases of controlled unit cell parameters as well as hexasomes with an inverse hexagonal (p6mm) structure, which have been rarely observed in polymer self-assembly. A new morphological phase diagram was constructed for the solution self-assembly of PS-b-PEO based on the volume fraction of the PS block against the initial copolymer concentration. The formation mechanisms of the cubosomes and hexasomes have also been revealed. This study not only affords a simple system for the controllable preparation and fundamental studies of ordered bicontinuous structures, but also opens up a new avenue towards porous architectures with highly ordered pores.Entities:
Keywords: block copolymers; colloidal particles; inverse mesophases; phase diagrams; self-assembly
Year: 2017 PMID: 28523856 DOI: 10.1002/anie.201702591
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336