脱氢
氢气储存
催化作用
材料科学
化学工程
煅烧
氢
碳纳米管
三聚氰胺
碳纤维
成核
氢化镁
纳米颗粒
碳化物
无机化学
化学
纳米技术
复合材料
有机化学
复合数
工程类
作者
Ziyin Dai,Lirong Xiao,Hideo Kimura,Chuanxin Hou,Xueqin Sun,Wei Du,Xiubo Xie
摘要
The high operating temperatures and slow kinetics limit the application of MgH2 based hydrogen storage materials. The Ni3ZnC0.7/carbon nanotubes loaded onto melamine sponge-derived carbon (MS) skeleton composites is produced by vacuum filtration followed by calcination method. The Ni3ZnC0.7 nanoparticles of about 5-30nm remain stable during the ball milling process and can not react with MgH2. After dehydrogenation, the Ni3ZnC0.7 reacts with MgH2 and in-situ changes to Mg2Ni/Zn. The MgH2-2.5wt%MS@Ni3ZnC0.7 can absorb 5.18wt% H2 with 200s at 423K and the initial hydrogen release temperature is reduced to 585K. After 20 hydrogen uptake/release cycles, the capacity retention rates are determined to be 88.4% and 94.6% for hydrogenation and dehydrogenation. The transformation of Mg2Ni/Mg2NiH4 provides additional diffusion channels for hydrogen atoms or molecules and can serve as “hydrogen pump” for promoting the de/hydrogenation. Moreover, Zn/MgZn2 provides the active sites for the nucleation of Mg/MgH2. The theoretical calculated MgH2 dissociation energy barrier on the Ni3ZnC0.7 surface is 0.49eV and the Mg-H bond is 1.995Å, much lower than that of MgH2 surface of 1.55eV and higher for Mg-H bond of 1.72Å. This study offers guidance for the design of porous carbon loaded non-stoichiometric metal carbides catalysts to enhance the hydrogen storage properties of MgH2.
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