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Abstract The direct electrooxidation reaction of ammonia borane (ABOR) as the anodic reaction of direct ammonia borane fuel cells (DABFCs) is greatly dependent on the properties of electrocatalysts. Both the active sites and charge/mass transfer characteristics are the key to promoting the processes of kinetics and thermodynamics, which can further improve the electrocatalytic activity. Hence, the catalyst double‐heterostructured Ni2P/Ni2P2O7/Ni12P5 (d‐NPO/NP) with the optimistic redistribution of electrons and active sites is prepared for the first time. The d‐NPO/NP‐750 catalyst obtained after pyrolysis at 750 °C shows the outstanding electrocatalytic activity toward ABOR with an onset potential of −0.329 V vs RHE which is better than all the published catalysts. The density functional theory (DFT) computations illustrate that the Ni2P2O7/Ni2P acts as the activity enhancement heterostructure with a high d‐band center (−1.60 eV) and the low activation energy barrier, while the Ni2P2O7/Ni12P5 acts as the conductivity enhancement heterostructure with the highest density of valence electrons.
Jia et al. (2023) studied this question.