TiN nanotube supported Ni catalyst Ni@TiN-NTs: experimental evidence of structure–activity relations in catalytically hydrolyzing ammonia borane for hydrogen evolution

With commercial TiO(2) as the precursor, titanium nitride nanotubes (TiN-NTs) were fabricated through a hydrothermal – ammonia nitriding route, and next non-noble metal nanosized Ni particles were evenly and firmly anchored on the surface of the TiN-NTs via a PVP-mediated non-aqueous phase reduction–deposition strategy, to obtain the supported catalyst Ni@TiN-NTs. The X-ray powder diffraction (PXRD), field emission scanning and transmission electron microscopy (FE-SEM/TEM) and specific surface area measurements were used to characterize and analyze the phase composition, surface microstructure and morphological features of the product. The catalytic activity of the Ni@TiN-NTs for hydrolyzing ammonia borane to generate hydrogen (H(2)) under different conditions was evaluated systematically. The results reveal that the as-fabricated TiN-NTs are composed of TiN and a small amount of TiN(x)O(y) with the approximate molar atomic ratio of Ti to N at 1 : 1, existing as hollow microtubules with mean tube diameter of 130 nm and length of about 1 μm. Via in situ reduction and deposition, Ni nanoparticles can be uniformly anchored on the surface of TiN-NTs. The catalytic activities of Ni(x)@TiN-NTs with different Ni loading amounts are all higher than that of single metal Ni nanoparticles. The temperature has a positive effect on the catalytic activity of Ni(20)@TiN-NTs, and its total turnover frequency for hydrolyzing ammonia borane is 11.73 mol(H(2)) (mol Ni)(−1) min(−1), with an apparent activation energy of 52.05 kJ mol(−1) at 303 K. After 5 cycles, the Ni(20)@TiN-NTs catalyst still maintains 87% of the initial catalytic activity. It could be suggested that these tactics can also be extended to the fabrication of other metal or alloy catalysts supported by TiN-NTs, with great application potential and development prospects.