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We report on Ni nanoparticles supported on boron nitride spheres (BNSP) and sheets (BNSH) as catalysts for hydrogen generation via hydrolysis of ammonia borane (NH 3 BH 3 , AB). The Ni/BN catalysts were prepared through a redox replacement reaction. The structure, morphology, and chemical composition of the obtained samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) equipped with energy dispersive X-ray spectroscopy (EDX), and inductively coupled plasma emission spectroscopy (ICP). The characterization results showed that Ni nanoparticles were well dispersed on the BNSP and BNSH supports for the four Ni/BN catalysts prepared (Ni atomic contents of 6.8, 9.0, 9.2, and 12 wt%). The catalytic activity toward the hydrolysis of AB was found to correlate with the loading of the Ni/BN catalysts, which showed great cycle performance. Theoretical calculations revealed that BN sheets significantly influenced the electric character of Ni catalysts and thereby their catalytic properties.

The wide band gap of boron nitride (BN) materials has been a major bottleneck for a wider application of BN in electronics. In this work, density functional theory computations were used to study the band structure of zigzag BN nanoribbons (BNNRs). Due to the ionic origin of the BN band gap, a heterogeneous edge decoration is an effective way to modulate the electronic band structure of BNNRs. This study demonstrates that a metallic behavior and magnetism can be realized by applying a NO 2 –NH 2 pair edge decoration. Although the lone electron pair of the NH 2 group is partly responsible for the metallic behavior, the effective potential difference induced by the donor–acceptor pair is also crucial for metallic behavior. Furthermore, these newly formed BNNRs were found to be more stable than H-passivated BNNRs. This simple chemical modification method offers great opportunities for the development of future BNNR-based electronic devices.