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

机译:氢中反应性球磨生产的镁碳储氢杂化材料

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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).
机译:时间分辨的研究揭示了在存在各种类型的碳(包括石墨(G),活性炭(AC),多壁碳纳米管)的情况下,在氢(HRBM)中高能反应球磨过程中Mg与氢相互作用的动力学和机理。 MWCNT),可膨胀(EG)和热膨胀(TEG)石墨。碳的引入会显着改变氢化行为,而氢化行为在很大程度上取决于碳添加剂的性质和数量。对于含1%(重量)的AC或TEG和5%(重量)的MWCNT的材料,氢化作用优于单个镁,并在1小时内完成。数据分析表明,碳通过溢出机制充当“活化”氢的载体。对于Mg-G,氢化从潜伏期开始并进行得较慢。 EG和TEG含量的增加超过1重量%导致氢化动力学的恶化。碳添加剂的作用源于其在HRBM过程中的破坏,从而形成包裹MgH2纳米颗粒并阻止晶粒生长的石墨烯层。与单独的Mg(180 nm)相比,这导致了重新氢化的Mg-C杂化材料(40-125 nm)中吸收-解吸循环稳定性的提高和MgH2晶粒尺寸的减小。

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