4.6 Article

The Improvement in Hydrogen Storage Performance of MgH2 Enabled by Multilayer Ti3C2

期刊

MICROMACHINES
卷 12, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/mi12101190

关键词

hydrogen storage; magnesium hydride; Ti3C2 MXene; catalyst

资金

  1. Science and Technology Research Project of Chongqing Municipal Education Commission [KJQN201912908]
  2. Science and Technology Research Program of Chongqing Municipal Education Commission [KJQN201912903]

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The MgH2+ML-Ti3C2 composite hydrogen storage system was successfully synthesized, reducing the initial desorption temperature to 142°C with a capacity of 6.56%. The kinetics of hydrogen absorption and desorption can be enhanced by ML-Ti3C2, attributed to two synergistic effects: Ti facilitates the dissociation or recombination of hydrogen molecules, and electron transfer generated by multivalent Ti promotes the conversion of hydrogen.
MgH2 has become a hot spot in the research of hydrogen storage materials, due to its high theoretical hydrogen storage capacity. However, the poor kinetics and thermodynamic properties of hydrogen absorption and desorption seriously hinder the development of this material. Ti-based materials can lead to good effects in terms of reducing the temperature of MgH2 in hydrogen absorption and desorption. MXene is a novel two-dimensional transition metal carbide or carbonitride similar in structure to graphene. Ti3C2 is one of the earliest and most widely used MXenes. Single-layer Ti3C2 can only exist in solution; in comparison, multilayer Ti3C2 (ML-Ti3C2) also exists as a solid powder. Thus, ML-Ti3C2 can be easily composited with MgH2. The MgH2+ML-Ti3C2 composite hydrogen storage system was successfully synthesized by ball milling. The experimental results show that the initial desorption temperature of MgH2-6 wt.% ML-Ti3C2 is reduced to 142 & DEG;C with a capacity of 6.56 wt.%. The E-a of hydrogen desorption in the MgH2-6 wt.% ML-Ti3C2 hydrogen storage system is approximately 99 kJ/mol, which is 35.3% lower than that of pristine MgH2. The enhancement of kinetics in hydrogen absorption and desorption by ML-Ti3C2 can be attributed to two synergistic effects: one is that Ti facilitates the easier dissociation or recombination of hydrogen molecules, while the other is that electron transfer generated by multivalent Ti promotes the easier conversion of hydrogen. These findings help to guide the hydrogen storage properties of metal hydrides doped with MXene.

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