LiBH4 is a high-capacity hydrogen storage
material; however, it suffers from high dehydrogenation temperature
and poor reversibility. To tackle those issues, we introduce a new
LiBH4-based system with in situ formed superfine and well-dispersed
Li3BO3 and NbH as co-reactants. Those are synthesized
by the addition of niobium ethoxide [Nb(OEt)5] to LiBH4, heat treatment of the mixture, and then hydrogenation, where
Li3BO3 and NbH are generated from the reaction
of Nb(OEt)5 and LiBH4. After optimization, the
system with a normalized composition of LiBH4-0.04(Li3BO3 + NbH) in molar fraction shows superior hydrogen
storage reversibility and kinetics. The initial and main dehydrogenation
temperatures of the system are 200 and 90 °C lower than those
of the pristine LiBH4, respectively, and 8.2 wt % H2 is released upon heating to 400 °C. A capacity of 7.2
wt % H2, corresponding to a capacity retention of 91%,
is sustained after 30 cycles in an isothermal cyclic regime of dwelling
at 400 °C for 60 min for dehydrogenation and dwelling at 500
°C and 50 bar H2 pressure for 20 min for hydrogenation.
Such a high cyclic stability for a LiBH4-based system has
never been reported to date. The in situ introduced Li3BO3 and NbH have a synergistic catalysis effect on the
improvement of the hydrogen storage performance of LiBH4, showing highly effective bidirectional action on both dehydrogenation
and hydrogenation.