Enhanced hydrogen sorption properties of Ni and Co-catalyzed MgH2

Jianfeng Mao, Zaiping Guo, Xuebin Yu, Huakun Liu, Zhu Wu, Jun Ni

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

166 Citations (Scopus)

Abstract

MgH2 is one of the most promising hydrogen storage materials due to its high capacity and low cost. In an effort to develop MgH2 with a low dehydriding temperature and fast sorption kinetics, doping MgH2 with NiCl2 and CoCl2 has been investigated in this paper. Both the dehydrogenation temperature and the absorption/desorption kinetics have been improved by adding either NiCl2 or CoCl2, and a significant enhancement was obtained in the case of the NiCl2 doped sample. For example, a hydrogen absorption capacity of 5.17 wt% was reached at 300 °C in 60 s for the MgH2/NiCl2 sample. In contrast, the ball-milled MgH2 just absorbed 3.51 wt% hydrogen at 300 °C in 400 s. An activation energy of 102.6 kJ/mol for the MgH2/NiCl2 sample has been obtained from the desorption data, 18.7 kJ/mol and 55.9 kJ/mol smaller than those of the MgH2/CoCl2, which also exhibits an enhanced kinetics, and of the pure MgH2 sample, respectively. In addition, the enhanced kinetics was observed to persist even after 9 cycles in the case of the NiCl2 doped MgH2 sample. Further kinetic investigation indicated that the hydrogen desorption from the milled MgH2 is controlled by a slow, random nucleation and growth process, which is transformed into two-dimensional growth after NiCl2 or CoCl2 doping, suggesting that the additives reduced the barrier and lowered the driving forces for nucleation. Crown Copyright © 2010.
Original languageEnglish
Pages (from-to)4569-4575
JournalInternational Journal of Hydrogen Energy
Volume35
Issue number10
DOIs
Publication statusPublished - May 2010
Externally publishedYes

Bibliographical note

Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to <a href="mailto:[email protected]">[email protected]</a>.

Funding

The authors are grateful for financial support from Australian Research Council (ARC) Discovery projects ( DP0771193, DP0878661 ) and the CSIRO Flagship Program. Dr. X. B. Yu would also like to thank the Shanghai Leading Academic Discipline Project (B113) and the Pujiang Programs (08PJ14014) for financial support.

Research Keywords

  • Catalyst
  • Hydrogen storage
  • Kinetics
  • MgH2

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