4.7 Article

De/hydrogenation kinetics against air exposure and microstructure evolution during hydrogen absorption/desorption of Mg-Ni-Ce alloys

Journal

RENEWABLE ENERGY
Volume 113, Issue -, Pages 1399-1407

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.renene.2017.06.102

Keywords

Mg alloy; Hydrogen storage; Nucleation and growth; Oxidation resistance; Ceria

Funding

  1. Research Fund of the State Key Laboratory of Solidification Processing (NWPU), China [95-QZ-2014]
  2. Natural Science Foundation of Shaanxi Province, China [2017JM5079]
  3. National Natural Science Foundation of China [21406174]
  4. 111 project [B08040]

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Aiming at elucidating the positive effects of Ce element on the oxidation resistance of Mg-based hydrogen storage alloys, Mg-Ni-Ce alloys with different Ce contents have been prepared in a resistance furnace with furnace cooling. The mass fraction of Mg in each sample is 80% to maintain high and consistent hydrogen storage capacity. An 18R-type long-period stacking ordered phase (LPSO) is observed within the Mg12Ce matrix in Mg-Ni-Ce alloys. A two-step activation process is observed in Ce containing alloys. Detailed microstructural characterization of activated samples during air exposure and in-depth analysis of absorption/desorption kinetics on air-exposed samples based on Johnson-MehlAvrami (JMA) model are performed to discuss the mechanism underlying improved anti-oxidation properties. CeH2.73 forms after activation and transforms to CeO2 during air exposure, which is earlier and faster than the MgO formation during initial air contact preventing forming a compact and uniform MgO layer on the surface. The formed CeH2.73/CeO2 particles with average particle size less than 60 nm act as catalysts accelerating the hydrogen dissociation and nucleation sites for the MgH2 formation during hydrogenation. After de -/hydrogenation cycles, CeO2 turns back to CeH2.73, which can react with oxygen again when the sample is exposed to air. (C) 2017 Elsevier Ltd. All rights reserved.

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