Lee Seong Ho, Kwak Young Jun, Park Hye Ryoung, Song Myoung Youp
J Nanosci Nanotechnol. 2015 Nov;15(11):8777-82. doi: 10.1166/jnn.2015.11531.
In this work, MgH2 was employed as a starting material instead of Mg used in our previous work. Ni and LiBH4, which can absorb 18.4 wt% of hydrogen, were added. A sample with a composition of 86 wt% MgH2 + 10 wt% Ni + 4 wt% LiBH4 (named MgH2-10Ni-4LiBH4) was prepared by milling under hydrogen (reaction-involved milling) and its hydrogen-storage properties were examined. In addition, the rate-limiting step for the dehydriding reaction of the sample at the first cycle was analyzed. The activation of MgH2-10Ni-4LiBH4 for hydriding and dehydriding reactions was not required. The as-milled sample absorbed and released nearly 5 wt% H at 623 K for 60 min; it absorbed 4.90 wt% H under 12 bar H2 for 20 min and released 4.94 wt% H under 1.0 bar H2 for 60 min. The hydriding rate exhibited an inverse dependence on temperature. This is due to a decrease in the driving force for the hydriding reaction (the difference between the applied hydrogen pressure and the equilibrium plateau pressure) with the increase in temperature.
在这项工作中,使用MgH₂作为起始原料,而非我们之前工作中使用的Mg。添加了能够吸收18.4 wt%氢的Ni和LiBH₄。通过在氢气气氛下球磨(涉及反应的球磨)制备了组成为86 wt% MgH₂ + 10 wt% Ni + 4 wt% LiBH₄的样品(命名为MgH₂-10Ni-4LiBH₄),并对其储氢性能进行了研究。此外,分析了该样品在第一个循环中脱氢反应的限速步骤。MgH₂-10Ni-4LiBH₄的氢化和脱氢反应无需活化。球磨后的样品在623 K下60分钟内吸收和释放了近5 wt%的氢;在12 bar氢气下20分钟内吸收了4.90 wt%的氢,在1.0 bar氢气下60分钟内释放了4.94 wt%的氢。氢化速率与温度呈反比关系。这是由于随着温度升高,氢化反应的驱动力(外加氢气压力与平衡平台压力之差)减小所致。