The defect structure evolution in magnesium hydride/metal-organic framework structures MIL-101 (Cr) composite at high temperature hydrogen sorption-desorption processes

被引:7
作者
Kudiiarov, Viktor N. [1 ]
Kurdyumov, Nikita [1 ]
Elman, Roman R. [1 ]
Laptev, Roman S. [1 ]
Kruglyakov, Mark A. [1 ]
Ushakov, Ivan A. [1 ]
V. Tereshchenko, Andrei [1 ]
Lider, Andrey M. [1 ]
机构
[1] Tomsk Polytech Univ, Lenin Ave 30, Tomsk 634050, Russia
关键词
Hydrogen; Phase transitions; Defects structure; Sorption-desorption processes; Composite; Magnesium hydride; Metal-organic frameworks; Positron annihilation; POSITRON-ANNIHILATION SPECTROSCOPY; STORAGE PROPERTIES; LATTICE-DEFECTS; MG; NANOCOMPOSITES; KINETICS; FE; TM;
D O I
10.1016/j.jallcom.2023.171534
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This paper describes the microstructural changes in the process of high temperature hydrogen sorption of composite based on MgH2 and metal-organic framework structures (MOFs) MIL-101 (Cr). The microstructure of the composite was analyzed by X-ray diffraction, electron microscopy and positron annihilation spectroscopy (PAS). The PAS complex allows in situ measurements in a vacuum chamber at elevated temperature and pressure ranges during hydrogenation or dehydrogenation. Based on the results obtained, the composite structure represents a core-shell in which nano-sized particles of chromium oxide and MIL-101(Cr) residues are evenly distributed on the surface of larger magnesium hydride particles. The MOFs MIL-101(Cr) is partially retained after mechanical synthesis and remains relatively stable when heated to 340 & DEG;C. The defect structure formed as a result of the synthesis contributes to the rapid diffusion of hydrogen into the bulk of magnesium particles. This defect structure affects the absorption of hydrogen by composites at temperatures up to 400 & DEG;C and have a negligible effect at 450 & DEG;C.
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页数:14
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