Gosselin Catherine, Huot Jacques
Hydrogen Research Institute, Université du Québec à Trois-Rivières, 3351 des Forges, Trois-Rivières, QC G9A 5H7, Canada.
Materials (Basel). 2015 Nov 20;8(11):7864-7872. doi: 10.3390/ma8115423.
The goal of this study was to optimize the activation behaviour of hydrogen storage alloy TiFe. We found that the addition of a small amount of Zr in TiFe alloy greatly reduces the hydrogenation activation time. Two different procedural synthesis methods were applied: co-melt, where the TiFe was melted and afterward re-melted with the addition of Zr, and single-melt, where Ti, Fe and Zr were melted together in one single operation. The co-melted sample absorbed hydrogen at its maximum capacity in less than three hours without any pre-treatment. The single-melted alloy absorbed its maximum capacity in less than seven hours, also without pre-treatment. The reason for discrepancies between co-melt and single-melt alloys was found to be the different microstructure. The effect of air exposure was also investigated. We found that the air-exposed samples had the same maximum capacity as the argon protected samples but with a slightly longer incubation time, which is probably due to the presence of a dense surface oxide layer. Scanning electron microscopy revealed the presence of a rich Zr intergranular phase in the TiFe matrix, which is responsible for the enhanced hydrogenation properties of these Zr-doped TiFe alloys.
本研究的目标是优化储氢合金TiFe的活化行为。我们发现,在TiFe合金中添加少量Zr可大大缩短氢化活化时间。应用了两种不同的程序合成方法:共熔法,即将TiFe熔化,然后在添加Zr的情况下再次熔化;单熔法,即将Ti、Fe和Zr在一次操作中一起熔化。共熔样品在未经任何预处理的情况下,不到三小时就吸收了其最大容量的氢气。单熔合金在不到七小时内也吸收了其最大容量的氢气,同样未经预处理。发现共熔和单熔合金之间存在差异的原因是微观结构不同。还研究了空气暴露的影响。我们发现,暴露在空气中的样品与氩气保护的样品具有相同的最大容量,但孕育期略长,这可能是由于存在致密的表面氧化层。扫描电子显微镜显示,在TiFe基体中存在富Zr的晶界相,这是这些Zr掺杂TiFe合金氢化性能增强的原因。