材料科学
微型多孔材料
膜
三嗪
聚合物
选择性
气体分离
化学工程
纳米技术
共轭体系
合理设计
共轭微孔聚合物
多孔性
合成膜
偶极子
分子间力
基质(化学分析)
磁导率
作者
Ding Xh,W. Q. He,Daijun Meng,Ali A. AL‐Thuraya,Bizi Yu,Yuting Zhang,Ayan Yao,Yumo Fan,Jian Guan,Pengbo Liao,Hongjun Zhang,Sheng Yang
标识
DOI:10.1002/adfm.202528057
摘要
ABSTRACT The development of conjugated microporous polymers (CMPs) with extended π ‐conjugation has positioned them as promising candidates for advanced gas separation membranes. Realizing their superior performance hinges on the rational design of their porous frameworks. Herein, we report a novel strategy to create tunable localized electric fields within CMPs by incorporating triazine rings at varied molecular positions, thereby achieving highly efficient CO 2 separation in Pebax‐based mixed matrix membranes (MMMs). As designed, the fine‐tuning of the triazine units enables the construction of an optimized donor‐ π ‐acceptor (D‐ π ‐A) electronic structure in the CMP‐PT framework. This tailored structure enhances intermolecular interactions, confers a larger dipole moment, improves coordination capability, and ultimately optimizes the microporous environment of the resultant MMM. Compared to the pristine Pebax membrane, the optimal Pebax‐CMP‐PT‐1% MMM exhibits a remarkable 83.4% enhancement in CO 2 permeability and a CO 2 /N 2 selectivity of 167.31 at 20 bar, surpassing the 2019 Robeson upper bound. This work provides a valuable strategy for the development of next‐generation high‐performance CO 2 separation membranes.
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