“…Nevertheless, because the BOR is a complex eight-electron process, the practical applications of DBFCs remain limited in scope due to the lack of highly efficient catalysts for the BOR at their anode. , So far, platinum group metals and coinage metals, as well as their alloys, are generally used to drive the proceeding of BOR. ,− Pt and Pd are suggested to favor a dissociative adsorption of BH 4 – on its surface, thereby facilitating a cleavage of B–H bond to promote the BOR. , However, these metals can also efficiently catalyze the parallel borohydride hydrolysis reaction due to their moderate binding with hydrogen, which is thus harmful for the selectivity of BOR and fuel utilization. , Au owes a better selectivity of BOR over the parallel reactions, but the weak binding with BH 4 – makes it less active toward the BOR. , Earth-abundant transition metals Co and Ni are regarded as alternative low cost catalysts for BOR, on account of the preferred dissociative adsorption of BH 4 – on them. ,, Low onset potentials of BOR approaching the theoretical value were observed in both metals, even more negative than those in the Pt and Pd materials, which can benefit larger open-circuit cell voltages of DBFCs. − However, the BOR activities of Co and Ni suffer from obvious degradations caused by the surface oxidation at high anodic polarization to reach large operation current densities. ,, …”