选择性
多孔性
光催化
材料科学
化学工程
超分子化学
催化作用
多孔介质
阳离子聚合
还原(数学)
可见光谱
金属有机骨架
纳米技术
衍生工具(金融)
氮气
选择性还原
比表面积
化学
科技与社会
光化学
作者
Tingting Zhang,Fengqing Hu,Siao Shi,Waner Li,Jie Zhao,Yufan Xue,Haifeng Chen,Bo Wang,F Li,Chunhui Dai
出处
期刊:Chemsuschem
[Wiley]
日期:2026-04-21
卷期号:19 (8): e202502675-e202502675
标识
DOI:10.1002/cssc.202502675
摘要
Supramolecular organic frameworks (SOFs) with intrinsic porosity and appealing optoelectronic properties hold promise for the integrated capture and photocatalytic conversion of CO 2 from the air. Unfortunately, SOFs that can efficiently reduce CO 2 have never been reported so far. In this work, we demonstrate the construction of a porous SOF through host‐guest binding between cucurbit[8]uril (CB[8]) and a tetraphenylethylene‐based derivative for highly selective CO 2 reduction in the atmosphere of water vapor and air under solar light. The abundant cationic nitrogen sites within the framework endow the SOF with a CO 2 uptake capacity of 14.41 cm 3 g −1 at 298 K and 1 bar. Initial slope selectivity calculations demonstrated that SOF possessed high separation capability of CO 2 over N 2 with selectivity up to 57 at 273 K. In addition, the SOF showed efficient light harvesting in the visible region with an optical gap of 2.19 eV. Benefitting from these unique features, the SOF catalyzed the reduction of CO 2 with a stable CO production rate of 69.78 μmol h −1 g −1 . This research paves the way to design porous SOF‐based photocatalysts for biomimetic reduction of CO 2 in a practical environment.
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