双金属片
电子顺磁共振
吸附
材料科学
光谱学
化学工程
化学
物理化学
核磁共振
冶金
金属
物理
量子力学
工程类
作者
Kavipriya Thangavel,Andrea Folli,Marcus Fischer,Martin Hartmann,Damien M. Murphy,Andreas Pöppl
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2024-01-01
卷期号:14 (6): 4244-4251
被引量:1
摘要
The flexibility of the MIL-53(M) metal-organic framework (MOF) has been elucidated through various characterization methodologies, particularly in gas and liquid adsorption processes. However, to the best of our knowledge, there has been no prior electron paramagnetic resonance (EPR) characterization of liquid-phase adsorption in the MOF MIL-53(M), which offers insights into local geometric changes at the oxygen octahedron containing the metal ions of the framework. In this study, we investigate, for the first time, the pore transformations within the MIL-53(Al0.99Cr0.01) framework during liquid-phase adsorption using EPR spectroscopy. Our investigation concentrates explicitly on the adsorption of pure solvents, including water, methanol, ethanol, isopropanol, pyridine, and mixed water/methanol phases. The EPR spectroscopy on the (Al0.99Cr0.01) MOF has allowed us to witness and comprehend the transitions between the narrow pore and large pore phases by examining changes in the zero-field splitting parameters of the S = 3/2 Cr(iii) species. Of all the solvents examined, a robust and distinct spectral feature observed during methanol adsorption unequivocally indicates the pore opening.
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