堆积
解耦(概率)
金属有机骨架
吸附
材料科学
化学
纳米技术
遮罩(插图)
密度泛函理论
计算机科学
选择性吸附
化学稳定性
分子
水准点(测量)
蓝图
组合化学
工作(物理)
理论(学习稳定性)
树枝状大分子
二聚体
产品(数学)
羧酸
曲面(拓扑)
多孔性
作者
Shengjie Lin,Yaning Qiao,Yuxuan Du,Y Wang,Yi Xie,Yabing He,Li Li,Banglin Chen
摘要
ABSTRACT Hydrogen‐bonded organic frameworks (HOFs) are promising porous materials, yet their development is hindered by an inherent trade‐off between structural stability and functional site accessibility. Conventional stabilization strategies relying on extensive π–π stacking inevitably shield aromatic surfaces, compromising adsorption performance. Herein, we report a synergistic design strategy that integrates high hydrogen‐bonding connectivity with inherently nonplanar molecular conformations to overcome this challenge. The strategically designed tetraisophthalate linker, featuring a hexamethylbiphenyl core, adopts a nonplanar conformation that suppresses extended π–π stacking, while its eight carboxylic acid groups form a dense hydrogen‐bonded network ensuring framework robustness. The resulting HOF‐ZJNU‐10 exhibits a high BET surface area (2500 m 2 g −1 ), exceptional stability, and crucially, fully accessible aromatic surfaces lining the pore channels. This unique combination enables outstanding methanol‐to‐olefins (MTO) product purification, delivering polymer‐grade ethylene and propylene with record‐high productivity. This work establishes a general blueprint for decoupling stability from functional site masking in HOFs.
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