期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 887, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.161380
关键词
MgH (2); Hydrogen storage properties; Density functional theory; MnO; Catalytic mechanism
资金
- National Natural Science Foundation of China [51571065, 51861002]
- Natural Science Foundation of Guangxi Province [2018GXNSFAA281266, 2018GXNSFAA281308, 2019GXNSFAA245050]
- Innovation-Driven Development Foundation of Guangxi Province [AA17204063]
The synthesis of a carbon-supported manganese monoxide nanocomposite (MnO@C) significantly improved the dehydrogenation/hydrogenation properties of magnesium hydride (MgH2), with reduced activation energies and enhanced hydrogen storage performance.
A carbon-supported manganese monoxide nanocomposite (MnO@C) was synthesized using a low-cost D113 cation exchange resin and manganese acetate tetrahydrate to improve the dehydrogenation/hydrogenation properties of magnesium hydride (MgH2). It was found that the dehydrogenated MnO@C-doped MgH2 composite could uptake 6.0 wt% of hydrogen within 60 min at 100 degrees C, and it could even uptake hydrogen at ambient temperature. Moreover, the synthesized composite could release approximately 5.0 wt% of hydrogen within 6 min at 300 degrees C. The dehydrogenation and hydrogenation apparent activation energies of MnO@C-doped MgH2 were calculated as 94.6 kJ mol(-1) and 22.5 kJ mol(-1), respectively, which were reduced by 38.8% and 67.2% when compared to the undoped sample. The density functional theory revealed that Mn and Mg0.9Mn0.1O facilitated the fracture of MgeH bonds, and thus improved the reversible hydrogen storage performance of MgH2. (C) 2021 Elsevier B.V. All rights reserved.
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