“…[4][5][6] In 1974, the first successful results on hydrogen storage in TiFe at room temperature were reported by Reilly and Wiswall, but they found that the as-cast material should be activated by repeated exposure to vacuum and hydrogen atmosphere at temperatures as high as 673 K. [4] Later studies also showed that despite all advantages of TiFe, its difficult activation is a main drawback. [7][8][9][10] There have been several attempts to solve the activation problem of as-cast TiFe mainly using two strategies: 1) chemical activation by addition of a third element, such as Pd, [11] Ni, [12] Mn, [13][14][15][16] and Zr [17][18][19] and 2) mechanical activation by ball milling, [20][21][22] high-pressure torsion (HPT), [23][24][25] and cold rolling. [26,27] Although the exact mechanism for the activation of TiFe is still under argument, it is generally believed that the first strategy is based on the surface catalytic performance of elemental additives, and the second strategy is based on nanostructuring and introduction of hydrogen pathways into bulk, such as cracks, nanograin boundaries, and amorphous regions.…”