4.5 Article

Dehydrogenation kinetics, reversibility, and reaction mechanisms of reversible hydrogen storage material based on nanoconfined MgH2-NaAlH4

Journal

JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
Volume 87, Issue -, Pages 16-22

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpcs.2015.07.018

Keywords

Intermetallic compounds; Microporous materials; Nanostructures; Differential scanning calorimetry (DSC); X-ray diffraction

Funding

  1. Suranaree University of Technology (SUT) [1/2558]

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Studies of dehydrogenation kinetics, reversibility, and reaction mechanisms during de/rehydrogenation of nanoconfined MgH2-NaAlH4 into carbon aerogel scaffold (CAS) for reversible hydrogen storage material are for the first time proposed. Two different MgH2-NaAlH4 molar ratios (1:1 and 2:1) of hydride composite are melt infiltrated into CAS under 1:1 (CAS:hydride composite) weight ratio. Successful nanoconfinement is confirmed by N-2 adsorption desorption. Multiple-step dehydrogenation of milled samples is reduced to two-step reaction due to nanoconfinement Peak temperatures corresponding to main dehydrogenation of nanoconfined samples significantly reduce as compared with those of milled samples, i.e., Delta T=up to 50 and 34 degrees C for nanoconfined sample with 1:1 and 2:1 (MgH2-NaAlH4) molar ratios, respectively. Hydrogen content released (the 1st cycle) and reproduced (the 2nd, 3rd, and 4th cycles) of nanoconfined samples enhance up to 80% and 68% with respect to theoretical hydrogen storage capacity, respectively, while those of milled samples are 71% and 38%, respectively. Remarkable hydrogen content reproduced after nanoconfinement is due to the fact that metallic Al obtained after dehydrogenation (T=300 degrees C under vacuum) of nanoconfined samples prefer to react with MgH2 and produces Al12Mg17, favorable for reversibility of MgH2-NaAlH4 system, whereas that of milled samples stays in the form of unreacted Al under the same temperature and pressure condition. (C) 2015 Elsevier Ltd. All rights reserved.

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