4.8 Article

Magnesium-carbon hydrogen storage hybrid materials produced by reactive ball milling in hydrogen

Journal

CARBON
Volume 57, Issue -, Pages 146-160

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2013.01.058

Keywords

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Funding

  1. Hydrogen and Fuel Cell Technologies RDI Programme (HySA)
  2. Department of Science and Technology (DST) in South Africa [KP3-S04]
  3. Program of Research Co-operation between Norway and South Africa [180344]
  4. National Research Foundation (NRF) of South Africa

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Time-resolved studies uncovered kinetics and mechanism of Mg-hydrogen interactions during High energy reactive ball milling in hydrogen (HRBM) in presence of various types of carbon, including graphite (G), activated carbon (AC), multi-wall carbon nanotubes (MWCNT), expandable (EG) and thermally-expanded (TEG) graphite. Introduction of carbon significantly changes the hydrogenation behaviour, which becomes strongly dependent on the nature and amount of carbon additive. For the materials containing 1 wt.% AC or TEG, and 5 wt.% MWCNT, the hydrogenation becomes superior to that for the individual magnesium and finishes within 1 h. Analysis of the data indicates that carbon acts as a carrier of the activated hydrogen by a mechanism of spill-over. For Mg-G the hydrogenation starts from an incubation period and proceeds slower. An increase in the content of EG and TEG above 1 wt.% results in the deterioration of the hydrogenation kinetics. The effect of carbon additives has roots in their destruction during the HRBM to form graphene layers encapsulating the MgH2 nanoparticles and preventing the grain growth. This results in an increase of absorption-desorption cycle stability and a decrease of the MgH2 crystallite size in the re-hydrogenated Mg-C hybrid materials (40-125 nm) as compared to Mg alone (180 nm). (C) 2013 Elsevier Ltd. All rights reserved.

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