离子键合
多孔性
聚合物
材料科学
化学工程
比表面积
固碳
催化作用
高分子化学
化学
有机化学
二氧化碳
复合材料
离子
工程类
作者
Qing Yu,Yuanzhe Cheng,Zihao Li,Donghui Yang,Qing Meng,Bao‐Hang Han
标识
DOI:10.1016/j.cej.2022.136275
摘要
Ionic porous organic polymers (IPOPs) emerge as porous networks with charged characteristics for versatile applications. However, most of the reported IPOPs have suffered from poor porosity due to the presence of electric charges in the synthesis process. Until now, it is a challenge to obtain IPOPs with both great porosity and high ionic density. Herein, we demonstrate a simple crosslinking strategy to integrate large specific surface area and abundant ionic sites in IPOPs (named as IPOPs-XL). Especially, IPOP1-XL synthesized via crosslinking strategy exhibits a large Brunauer–Emmett–Teller (BET) specific surface area of 1830 m2 g−1, which is 18 times higher than that of the pyridine-based polymer before crosslinking (IPOP-1, 96 m2 g−1). The uptake capacity for carbon dioxide (CO2) of IPOP1-XL (11.7 wt%) is also much higher than that of IPOP-1 (4.5 wt%) at 273 K due to the enhanced porosity. Meanwhile, IPOP1-XL also possesses an improved ionic density (3.5 mmol g−1), which plays a pivotal role in CO2 chemical fixation. This work provides a feasible method to improve the porosity of IPOPs.
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