Youp Song Myoung, Kwak Young Jun, Choi Eunho
Division of Advanced Materials Engineering Hydrogen & Fuel Cell Research Center, Engineering Research Institute, Jeonbuk National University, 567 Baekje-daero Deokjin-gu Jeonju, 54896, Republic of Korea.
Department of Materials Engineering, Graduate School, Hydrogen &Fuel Cell Research Center, Engineering Research Institute, Jeonbuk National University, 567 Baekje-daero Deokjin-gu Jeonju, 54896, Republic of Korea.
J Nanosci Nanotechnol. 2020 Nov 1;20(11):7010-7017. doi: 10.1166/jnn.2020.18840.
Mg₂Ni samples were prepared by sintering a pelletized mixture under an argon atmosphere in a stainless steel crucible at 823 K. The XRD pattern of the prepared Mg₂Ni sample showed a well crystallized Mg₂Ni phase. The hydriding and dehydriding properties of the prepared samples were examined at 518-593 K under relatively low hydrogen pressures of 3-7 bar H₂. At 573 K under 7 bar H₂, the activation of the Mg₂Ni sample was completed at the number of cycles of six ( = 6). At = 7, the hydrided fractions of the sample were 0.53 (1.99 wt% H) at 4.97 min, 0.72 (2.71 wt% H) at 9.52 min, 0.81 (3.05 wt% H) at 31.15 min, and 0.81 (3.05 wt% H) at 60.07 min. The particle sizes of the prepared Mg₂Ni were not homogeneous and the particles had irregular shapes. We analyzed the rate-controlling steps for the hydriding reaction of the intermetallic compound Mg₂Ni by examining the dependences of hydriding rates on hydrogen pressure and temperature in the same reacted fraction ranges. The analyses in the same reacted fraction ranges were done in order to eliminate the influence of the interfacial area on the hydriding rate. When the driving force, which is the difference between the applied hydrogen pressure and equilibrium plateau pressure at a given temperature, was low, the nucleation of Mg₂Ni hydride controlled the hydriding rate of Mg₂Ni. After the nucleation of the Mg₂Ni hydride, the rate-controlling step of the hydriding reaction of Mg₂Ni was analyzed to be the forced flow of hydrogen molecules through pores, inter-particle channels, or cracks.
通过在不锈钢坩埚中于氩气气氛下在823 K烧结造粒混合物来制备Mg₂Ni样品。所制备的Mg₂Ni样品的XRD图谱显示出结晶良好的Mg₂Ni相。在518 - 593 K、相对较低的3 - 7 bar H₂氢气压力下检查所制备样品的吸氢和脱氢性能。在7 bar H₂、573 K时,Mg₂Ni样品在六个循环(= 6)时完成活化。在 = 7时,样品的吸氢分数在4.97分钟时为0.53(1.99 wt% H),在9.52分钟时为0.72(2.71 wt% H),在31.15分钟时为0.81(3.05 wt% H),在60.07分钟时为0.81(3.05 wt% H)。所制备的Mg₂Ni的粒径不均匀,颗粒形状不规则。通过在相同反应分数范围内检查吸氢速率对氢气压力和温度的依赖性,我们分析了金属间化合物Mg₂Ni吸氢反应的速率控制步骤。在相同反应分数范围内进行分析是为了消除界面面积对吸氢速率的影响。当驱动力(即给定温度下施加的氢气压力与平衡平台压力之间的差值)较低时,Mg₂Ni氢化物的成核控制了Mg₂Ni的吸氢速率。Mg₂Ni氢化物成核后,Mg₂Ni吸氢反应的速率控制步骤被分析为氢分子通过孔隙、颗粒间通道或裂缝的强制流动。