吸附
金属有机骨架
氨
密度泛函理论
铝
傅里叶变换红外光谱
材料科学
金属
微量气体
氢键
化学工程
无机化学
化学
分子
物理化学
有机化学
计算化学
工程类
作者
Yaoqi Huang,Min Zhang,Zhenliang Zhu,Ruiyao Li,Shaojun Yuan
出处
期刊:Small
[Wiley]
日期:2025-07-23
标识
DOI:10.1002/smll.202504865
摘要
Abstract Effective removal of trace ammonia (NH 3 ) is essential to mitigate its adverse effects on human health and the environment. However, capturing NH 3 at ultra‐low concentrations remains challenging due to its weak interactions with conventional adsorbents. In this study, a novel ultramicroporous aluminum‐based metal–organic framework, MIL‐120, with 1D channels (5.4 Å × 4.7 Å) densely functionalized with µ 2 ‐OH groups is synthesized as a highly efficient adsorbent for NH 3 capture from polluted air. MIL‐120 exhibits a high static NH 3 uptake of 7.8 mmol g −1 at 298 K and 1 bar. Under trace conditions (100 ppm NH 3 ), dynamic breakthrough experiments reveal a notable adsorption capacity of 0.68 mmol g −1 , demonstrating a significant performance advantage over similar adsorbents. In situ FTIR spectroscopy combined with density functional theory (DFT) calculations confirms that the enhanced NH 3 affinity arises from a synergistic effect between ultramicropore confinement and strong hydrogen bonding at µ 2 ‐OH sites. This work highlights MIL‐120 as a promising candidate for trace NH 3 capture and provides critical insights for the rational design of next‐generation MOF‐based air purification materials.
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