Abstract
The great significance of boosting the design of percolating nanopore structures in block copolymers (BCPs) for varied use cases has been widely demonstrated in the past several decades. However, it still remains challenging to prepare the desired porous structures in a rapid, facile, and universal manner. Here we develop an unconventional and benchtop strategy to rapidly generate the nanoporous BCPs with arbitrary structural characters regardless of the BCP bulk morphology. This universal pore-forming strategy enables the sustainable CO2-based BCPs to form the advanced membranes with 1 s soaking for efficiently rejecting 94.2% brilliant blue R (826 g/mol). At the same time, the water permeance retains around 1020 L/(m2·h·bar), which is 1~3 orders of magnitude higher than that of other membranes. This strategy may offer a fantastic opportunity to introduce percolating pore structures in those newly developed BCPs with which the previously reported pore-forming methods may not deal.
Original language | English (US) |
---|---|
Journal | Angewandte Chemie (International ed. in English) |
DOIs | |
State | Published - Nov 8 2022 |
Bibliographical note
KAUST Repository Item: Exported on 2022-11-11Acknowledgements: Dr. Yunlong Hou in Prof. Hadjichristidis' lab helped finish the nitrogen physisorption experiments; Dr. Wojciech Ogieglo and Prof. Ingo Pinnau (Advanced Membranes and Porous Materials Centre, KAUST) contributed to the experiments on the in-situcmonitoring of the film thickness. The authors greatly thank and acknowledge these collaborators for their valuable contributions to this work. Research reported in this work was supported by the King Abdullah University of Science and Technology (KAUST).
ASJC Scopus subject areas
- General Chemistry
- Catalysis