Insights to the formation of Zr-based metal-organic frameworks from in situ powder x-ray diffraction

被引:0
作者
Petersen, E. Eja [1 ,2 ]
Main, Russell M. [2 ]
Magdysyuk, Oxana, V [2 ]
Kelly, Nicole L. [2 ]
Borthwick, Emma A. L. [2 ]
Naden, Aaron B. [2 ]
Ashbrook, Sharon E. [2 ]
Morris, Russell E. [2 ]
Ettlinger, Romy [1 ,2 ]
机构
[1] Tech Univ Munich, TUM Sch Nat Sci, Dept Chem, Lichtenbergstr 4, D-85748 Garching, Germany
[2] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Scotland
来源
JOURNAL OF PHYSICS-MATERIALS | 2025年 / 8卷 / 01期
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
metal-organic framework; <italic>in situ</italic> powder x-ray diffraction; crystallisation kinetics;
D O I
10.1088/2515-7639/ad9b4f
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This study sheds light on the kinetics of crystallisation of two Zr-based metal-organic frameworks (MOFs), namely Zr6-MOF-808 and Zr6-MOF-801, using in situ powder x-ray diffraction (PXRD). Once a room temperature synthesis for the two MOFs was designed for the very small scale, a successful series of in situ PXRD experiments over the range of 10 degrees C-40 degrees C yielded high quality quantitative information on the kinetics of crystallisation for both MOFs. These findings indicate the importance of the solubility of the linker and its connectivity: while the rate of nucleation and the resulting particle size of the MOF (Zr6-MOF-801), with the less soluble and lower connected linker, was strongly temperature dependent, the growth and particle size of Zr6-MOF-808 was hardly impacted by an increase in temperature. This work highlights the importance of careful preliminary research and helps to improve future MOF synthesis design to efficiently achieve the desired particle size distribution.
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页数:8
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