Published August 2007 | Version v1
Journal article

Superior hydrogen storage kinetics of MgH2 nanoparticles doped with TiF3

  • 1. Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)
  • 2. Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China) and College of Engineering, Peking University, Beijing 100871 (China)

Description

MgH2 nanoparticles were obtained by hydriding ultrafine magnesium particles which were prepared by hydrogen plasma-metal reaction. The X-ray diffraction (XRD) and transmission electron microscopy (TEM) results show that the obtained sample is almost pure MgH2 phase, without residual magnesium and with an average particle size of ∼300 nm. Milled with 5 wt.% TiF3 as a doping precursor in a hydrogen atmosphere, the sample desorbed 4.5 wt.% hydrogen in 6 min under an initial hydrogen pressure of ∼0.001 bar at 573 K and absorbed 4.2 wt.% hydrogen in 1 min under ∼20 bar hydrogen at room temperature. Compared with MgH2 micrometer particles doped with 5 wt.% TiF3 under the same conditions as the MgH2 nanoparticles, it is suggested that decrease of particle size is beneficial for enhancing absorption capacity at low temperatures, but has no effect on desorption. In addition, the catalyst was mainly responsible for improving the sorption kinetics and its catalytic mechanism is discussed

Additional details

Identifiers

DOI
10.1016/j.actamat.2007.04.020;
PII
S1359-6454(07)00267-4;

Publishing Information

Journal Title
Acta Materialia
Journal Volume
55
Journal Issue
13
Journal Page Range
p. 4585-4591
ISSN
1359-6454
CODEN
ACMAFD

Optional Information

Copyright
Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.