吸附
检出限
硫化氢
解吸
选择性
傅里叶变换红外光谱
分析化学(期刊)
分子
多孔性
四氢呋喃
笼子
氢键
光谱学
胺气处理
材料科学
荧光
化学
化学工程
物理化学
色谱法
有机化学
溶剂
催化作用
数学
组合数学
工程类
硫黄
物理
量子力学
作者
Juan L. Obeso,Dingyue Hu,Valeria B. López‐Cervantes,Yoarhy A. Amador‐Sánchez,Catalina V. Flores,J. Gabriel Flores,Sanliang Ling,Enrique Lima,Aída Gutiérrez‐Alejandre,Marco A. Vera,Ricardo A. Peralta,J.A. de los Reyes,Diego Solís-Ibarra,Ilich A. Ibarra,Ming Liu
出处
期刊:Small
[Wiley]
日期:2024-11-06
标识
DOI:10.1002/smll.202408155
摘要
Abstract The first experimental investigation of a porous organic cage (POC) for the challenging task of H 2 S capture is reported. The N‐containing cage molecular material, a tertiary amine POC (6FT‐RCC3), demonstrates the highest H 2 S (hydrogen sulfide) capture (record capacity) for a porous material at room temperature and atmospheric pressure (20.6 mmol H 2 S g −1 ; 25 H 2 S molecules per cage) combined with excellent reversibility for at least five adsorption–desorption cycles. In situ FTIR spectroscopy, solid‐state 13 C, and 15 N CP MAS NMR spectroscopy experiments are applied to investigate the adsorption mechanism, identifying relatively weak interactions via hydrogen bonding. In addition, the fluorescence performances of this POC material are evaluated for the detection and sensing of H 2 S, where a clear H 2 S selectivity is observed over other gases. Remarkably, the limit of detection (LOD) is calculated to be 0.13 m m (≈4.43 ppm) in a tetrahydrofuran (THF) solution of H 2 S.
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