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Updated: Aug 16, 2025

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
TiO2 nanoparticle-supported Ni catalyst for the dehydrogenation of hydrazine hydrate
Ying Liu1, Xiaoya Liu2, Xinying Liu2
1State Key Laboratory of Separation Membranes and Membrane Processes, School of Environmental Science and Engineering, Tiangong University, Tianjin, 300387, China; School of Chemical Engineering and Technology, National Engineering Research Center of Distillation Technology, Tianjin University, Tianjin, 300072, China; Pei-yang National Distillation Technology Corporation Limited, Tianjin, 300072, China.
Abstract:
As one of the key factors that affect the application of hydrazine hydrate as a potential hydrogen source, efficient and cheap catalyst is particularly important. Nickel based catalysts have been widely studied because of their excellent catalytic performance for the decomposition of hydrazine hydrate to hydrogen. Herein, a Ni catalyst supported on anatase TiO2 through reduction and impregnation methods was prepared. Structure of the catalyst was investigated by transmission electron microscopy (TEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS). The effects of the amount of TiO2 and the concentration of NaOH on the activity of the catalyst were investigated. The results showed that the catalyst prepared with a metal nickel content of 0.2 mmol using 100 mg of the nano-TiO2 support had the best catalytic performance. Hydrazine hydrate could be completely decomposed at 343 K in 2.83 min, the hydrogen selectivity attained 100%, and the turnover frequency (TOF) value was 265.49 h-1. In this catalyst, transition metal Ni was dispersed on the support surface in the form of amorphous elemental or oxide. Anatase TiO2 support had the advantages of promoting the dispersion of metal Ni, exposing the active site, changing the electronic state of the active center, strengthening the strong metal-support interaction (SMSI), and improving the activity of the catalyst. After ten cycles of use, the performance of the catalyst stabilized and the hydrogen selectivity was still as high as 100%.
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