V-free body-centered cubic (BCC) structured hydrogen
storage alloys
have gained significant attention for their low cost and high theoretical
hydrogen storage capacity (3.8 wt %). However, before practical application,
critical challenges, such as low dehydriding capacity, activation
difficulty, and poor cyclic stability, need to be solved. In this
work, an easily activated and high-performance V-free BCC-type alloy
(Ti40Cr50Mo10Ce1) was
successfully synthesized by heat treatment and Ce doping. The heat
treatment significantly increased its dehydriding capacity to 2.5
wt %, attributed to a reduced slope factor (0.76–0.17), making
it comparable to V-based BCC-type alloys. And the V-free BCC-type
alloy, after Ce doping, enabled room-temperature hydrogen absorption,
eliminating the need for high-temperature activation. Ce doping did
not significantly affect the activation energy, enthalpy change, or
hysteresis factor of the alloy during de/hydrogenation. Additionally,
the V-free BCC-type alloy, after heat treatment and Ce doping, exhibited
excellent cyclic stability, with a capacity retention rate of 90%
after 100 cycles. This study provides valuable guidance for designing
innovative and cost-effective hydrogen storage alloys.